Motif 1195 (n=122)
Position-wise Probabilities
Download
uniprot | genes | site | source | protein | function |
---|---|---|---|---|---|
A0A087WTJ2 | GIMAP1-GIMAP5 | Y14 | ochoa | GIMAP1-GIMAP5 readthrough | None |
A1L4K1 | FSD2 | T15 | ochoa | Fibronectin type III and SPRY domain-containing protein 2 (SPRY domain-containing protein 1) | None |
A2RRP1 | NBAS | T14 | ochoa | NBAS subunit of NRZ tethering complex (Neuroblastoma-amplified gene protein) (Neuroblastoma-amplified sequence) | Involved in Golgi-to-endoplasmic reticulum (ER) retrograde transport; the function is proposed to depend on its association in the NRZ complex which is believed to play a role in SNARE assembly at the ER (PubMed:19369418). Required for normal embryonic development (By similarity). May play a role in the nonsense-mediated decay pathway of mRNAs containing premature stop codons (By similarity). {ECO:0000250|UniProtKB:Q5TYW4, ECO:0000269|PubMed:19369418}. |
O00767 | SCD | Y14 | psp | Stearoyl-CoA desaturase (hSCD1) (EC 1.14.19.1) (Acyl-CoA desaturase) (Delta(9)-desaturase) (Delta-9 desaturase) (Fatty acid desaturase) | Stearoyl-CoA desaturase that utilizes O(2) and electrons from reduced cytochrome b5 to introduce the first double bond into saturated fatty acyl-CoA substrates (PubMed:15907797, PubMed:18765284). Catalyzes the insertion of a cis double bond at the delta-9 position into fatty acyl-CoA substrates including palmitoyl-CoA and stearoyl-CoA (PubMed:15907797, PubMed:18765284). Gives rise to a mixture of 16:1 and 18:1 unsaturated fatty acids (PubMed:15610069). Plays an important role in lipid biosynthesis. Plays an important role in regulating the expression of genes that are involved in lipogenesis and in regulating mitochondrial fatty acid oxidation (By similarity). Plays an important role in body energy homeostasis (By similarity). Contributes to the biosynthesis of membrane phospholipids, cholesterol esters and triglycerides (By similarity). {ECO:0000250|UniProtKB:P13516, ECO:0000269|PubMed:15610069, ECO:0000269|PubMed:15907797, ECO:0000269|PubMed:18765284}. |
O43482 | OIP5 | T14 | ochoa | Protein Mis18-beta (Cancer/testis antigen 86) (CT86) (Opa-interacting protein 5) (OIP-5) | Required for recruitment of CENPA to centromeres and normal chromosome segregation during mitosis. {ECO:0000269|PubMed:17199038}. |
O43768 | ENSA | T14 | ochoa | Alpha-endosulfine (ARPP-19e) | Protein phosphatase inhibitor that specifically inhibits protein phosphatase 2A (PP2A) during mitosis. When phosphorylated at Ser-67 during mitosis, specifically interacts with PPP2R2D (PR55-delta) and inhibits its activity, leading to inactivation of PP2A, an essential condition to keep cyclin-B1-CDK1 activity high during M phase (By similarity). Also acts as a stimulator of insulin secretion by interacting with sulfonylurea receptor (ABCC8), thereby preventing sulfonylurea from binding to its receptor and reducing K(ATP) channel currents. {ECO:0000250, ECO:0000269|PubMed:9653196}. |
O60306 | AQR | T14 | ochoa | RNA helicase aquarius (EC 3.6.4.13) (Intron-binding protein of 160 kDa) (IBP160) | Involved in pre-mRNA splicing as component of the spliceosome (PubMed:11991638, PubMed:25599396, PubMed:28076346, PubMed:28502770). Intron-binding spliceosomal protein required to link pre-mRNA splicing and snoRNP (small nucleolar ribonucleoprotein) biogenesis (PubMed:16949364). Plays a key role in position-dependent assembly of intron-encoded box C/D small snoRNP, splicing being required for snoRNP assembly (PubMed:16949364). May act by helping the folding of the snoRNA sequence. Binds to intron of pre-mRNAs in a sequence-independent manner, contacting the region between snoRNA and the branchpoint of introns (40 nucleotides upstream of the branchpoint) during the late stages of splicing (PubMed:16949364). Has ATP-dependent RNA helicase activity and can unwind double-stranded RNA molecules with a 3' overhang (in vitro) (PubMed:25599396). {ECO:0000269|PubMed:11991638, ECO:0000269|PubMed:16949364, ECO:0000269|PubMed:25599396, ECO:0000269|PubMed:28076346, ECO:0000269|PubMed:28502770}. |
O60503 | ADCY9 | T15 | ochoa | Adenylate cyclase type 9 (EC 4.6.1.1) (ATP pyrophosphate-lyase 9) (Adenylate cyclase type IX) (ACIX) (Adenylyl cyclase 9) (AC9) | Adenylyl cyclase that catalyzes the formation of the signaling molecule cAMP in response to activation of G protein-coupled receptors (PubMed:10987815, PubMed:12972952, PubMed:15879435, PubMed:9628827). Contributes to signaling cascades activated by CRH (corticotropin-releasing factor), corticosteroids and beta-adrenergic receptors (PubMed:9628827). {ECO:0000269|PubMed:10987815, ECO:0000269|PubMed:12972952, ECO:0000269|PubMed:15879435, ECO:0000269|PubMed:9628827}. |
O60664 | PLIN3 | T15 | ochoa | Perilipin-3 (47 kDa mannose 6-phosphate receptor-binding protein) (47 kDa MPR-binding protein) (Cargo selection protein TIP47) (Mannose-6-phosphate receptor-binding protein 1) (Placental protein 17) (PP17) | Structural component of lipid droplets, which is required for the formation and maintenance of lipid storage droplets (PubMed:34077757). Required for the transport of mannose 6-phosphate receptors (MPR) from endosomes to the trans-Golgi network (PubMed:9590177). {ECO:0000269|PubMed:34077757, ECO:0000269|PubMed:9590177}. |
O60711 | LPXN | T15 | ochoa | Leupaxin | Transcriptional coactivator for androgen receptor (AR) and serum response factor (SRF). Contributes to the regulation of cell adhesion, spreading and cell migration and acts as a negative regulator in integrin-mediated cell adhesion events. Suppresses the integrin-induced tyrosine phosphorylation of paxillin (PXN). May play a critical role as an adapter protein in the formation of the adhesion zone in osteoclasts. Negatively regulates B-cell antigen receptor (BCR) signaling. {ECO:0000269|PubMed:17640867, ECO:0000269|PubMed:18451096, ECO:0000269|PubMed:18497331, ECO:0000269|PubMed:20543562}. |
O75582 | RPS6KA5 | T14 | ochoa | Ribosomal protein S6 kinase alpha-5 (S6K-alpha-5) (EC 2.7.11.1) (90 kDa ribosomal protein S6 kinase 5) (Nuclear mitogen- and stress-activated protein kinase 1) (RSK-like protein kinase) (RSKL) | Serine/threonine-protein kinase that is required for the mitogen or stress-induced phosphorylation of the transcription factors CREB1 and ATF1 and for the regulation of the transcription factors RELA, STAT3 and ETV1/ER81, and that contributes to gene activation by histone phosphorylation and functions in the regulation of inflammatory genes (PubMed:11909979, PubMed:12569367, PubMed:12763138, PubMed:18511904, PubMed:9687510, PubMed:9873047). Phosphorylates CREB1 and ATF1 in response to mitogenic or stress stimuli such as UV-C irradiation, epidermal growth factor (EGF) and anisomycin (PubMed:11909979, PubMed:9873047). Plays an essential role in the control of RELA transcriptional activity in response to TNF and upon glucocorticoid, associates in the cytoplasm with the glucocorticoid receptor NR3C1 and contributes to RELA inhibition and repression of inflammatory gene expression (PubMed:12628924, PubMed:18511904). In skeletal myoblasts is required for phosphorylation of RELA at 'Ser-276' during oxidative stress (PubMed:12628924). In erythropoietin-stimulated cells, is necessary for the 'Ser-727' phosphorylation of STAT3 and regulation of its transcriptional potential (PubMed:12763138). Phosphorylates ETV1/ER81 at 'Ser-191' and 'Ser-216', and thereby regulates its ability to stimulate transcription, which may be important during development and breast tumor formation (PubMed:12569367). Directly represses transcription via phosphorylation of 'Ser-1' of histone H2A (PubMed:15010469). Phosphorylates 'Ser-10' of histone H3 in response to mitogenics, stress stimuli and EGF, which results in the transcriptional activation of several immediate early genes, including proto-oncogenes c-fos/FOS and c-jun/JUN (PubMed:12773393). May also phosphorylate 'Ser-28' of histone H3 (PubMed:12773393). Mediates the mitogen- and stress-induced phosphorylation of high mobility group protein 1 (HMGN1/HMG14) (PubMed:12773393). In lipopolysaccharide-stimulated primary macrophages, acts downstream of the Toll-like receptor TLR4 to limit the production of pro-inflammatory cytokines (By similarity). Functions probably by inducing transcription of the MAP kinase phosphatase DUSP1 and the anti-inflammatory cytokine interleukin 10 (IL10), via CREB1 and ATF1 transcription factors (By similarity). Plays a role in neuronal cell death by mediating the downstream effects of excitotoxic injury (By similarity). Phosphorylates TRIM7 at 'Ser-107' in response to growth factor signaling via the MEK/ERK pathway, thereby stimulating its ubiquitin ligase activity (PubMed:25851810). {ECO:0000250|UniProtKB:Q8C050, ECO:0000269|PubMed:11909979, ECO:0000269|PubMed:12569367, ECO:0000269|PubMed:12628924, ECO:0000269|PubMed:12763138, ECO:0000269|PubMed:12773393, ECO:0000269|PubMed:15010469, ECO:0000269|PubMed:18511904, ECO:0000269|PubMed:25851810, ECO:0000269|PubMed:9687510, ECO:0000269|PubMed:9873047}. |
O75694 | NUP155 | T14 | ochoa | Nuclear pore complex protein Nup155 (155 kDa nucleoporin) (Nucleoporin Nup155) | Essential component of nuclear pore complex. Could be essessential for embryogenesis. Nucleoporins may be involved both in binding and translocating proteins during nucleocytoplasmic transport. {ECO:0000250|UniProtKB:Q99P88}. |
O76021 | RSL1D1 | T15 | ochoa | Ribosomal L1 domain-containing protein 1 (CATX-11) (Cellular senescence-inhibited gene protein) (Protein PBK1) | Regulates cellular senescence through inhibition of PTEN translation. Acts as a pro-apoptotic regulator in response to DNA damage. {ECO:0000269|PubMed:18678645, ECO:0000269|PubMed:22419112}. |
O94804 | STK10 | T14 | ochoa | Serine/threonine-protein kinase 10 (EC 2.7.11.1) (Lymphocyte-oriented kinase) | Serine/threonine-protein kinase involved in regulation of lymphocyte migration. Phosphorylates MSN, and possibly PLK1. Involved in regulation of lymphocyte migration by mediating phosphorylation of ERM proteins such as MSN. Acts as a negative regulator of MAP3K1/MEKK1. May also act as a cell cycle regulator by acting as a polo kinase kinase: mediates phosphorylation of PLK1 in vitro; however such data require additional evidences in vivo. {ECO:0000269|PubMed:11903060, ECO:0000269|PubMed:12639966, ECO:0000269|PubMed:19255442}. |
P01583 | IL1A | Y15 | ochoa | Interleukin-1 alpha (IL-1 alpha) (Hematopoietin-1) | Cytokine constitutively present intracellularly in nearly all resting non-hematopoietic cells that plays an important role in inflammation and bridges the innate and adaptive immune systems (PubMed:26439902). After binding to its receptor IL1R1 together with its accessory protein IL1RAP, forms the high affinity interleukin-1 receptor complex (PubMed:17507369, PubMed:2950091). Signaling involves the recruitment of adapter molecules such as MYD88, IRAK1 or IRAK4 (PubMed:17507369). In turn, mediates the activation of NF-kappa-B and the three MAPK pathways p38, p42/p44 and JNK pathways (PubMed:14687581). Within the cell, acts as an alarmin and cell death results in its liberation in the extracellular space after disruption of the cell membrane to induce inflammation and alert the host to injury or damage (PubMed:15679580). In addition to its role as a danger signal, which occurs when the cytokine is passively released by cell necrosis, directly senses DNA damage and acts as a signal for genotoxic stress without loss of cell integrity (PubMed:26439902). {ECO:0000269|PubMed:14687581, ECO:0000269|PubMed:15679580, ECO:0000269|PubMed:17507369, ECO:0000269|PubMed:26439902, ECO:0000269|PubMed:2950091, ECO:0000269|PubMed:3258335}. |
P06241 | FYN | T15 | ochoa | Tyrosine-protein kinase Fyn (EC 2.7.10.2) (Proto-oncogene Syn) (Proto-oncogene c-Fyn) (Src-like kinase) (SLK) (p59-Fyn) | Non-receptor tyrosine-protein kinase that plays a role in many biological processes including regulation of cell growth and survival, cell adhesion, integrin-mediated signaling, cytoskeletal remodeling, cell motility, immune response and axon guidance (PubMed:11536198, PubMed:15489916, PubMed:15557120, PubMed:16387660, PubMed:20100835, PubMed:7568038, PubMed:7822789). Inactive FYN is phosphorylated on its C-terminal tail within the catalytic domain (PubMed:15489916). Following activation by PKA, the protein subsequently associates with PTK2/FAK1, allowing PTK2/FAK1 phosphorylation, activation and targeting to focal adhesions (PubMed:15489916). Involved in the regulation of cell adhesion and motility through phosphorylation of CTNNB1 (beta-catenin) and CTNND1 (delta-catenin) (PubMed:17194753). Regulates cytoskeletal remodeling by phosphorylating several proteins including the actin regulator WAS and the microtubule-associated proteins MAP2 and MAPT (PubMed:14707117, PubMed:15536091). Promotes cell survival by phosphorylating AGAP2/PIKE-A and preventing its apoptotic cleavage (PubMed:16841086). Participates in signal transduction pathways that regulate the integrity of the glomerular slit diaphragm (an essential part of the glomerular filter of the kidney) by phosphorylating several slit diaphragm components including NPHS1, KIRREL1 and TRPC6 (PubMed:14761972, PubMed:18258597, PubMed:19179337). Plays a role in neural processes by phosphorylating DPYSL2, a multifunctional adapter protein within the central nervous system, ARHGAP32, a regulator for Rho family GTPases implicated in various neural functions, and SNCA, a small pre-synaptic protein (PubMed:11162638, PubMed:12788081, PubMed:19652227). Involved in reelin signaling by mediating phosphorylation of DAB1 following reelin (RELN)-binding to its receptor (By similarity). Participates in the downstream signaling pathways that lead to T-cell differentiation and proliferation following T-cell receptor (TCR) stimulation (PubMed:22080863). Phosphorylates PTK2B/PYK2 in response to T-cell receptor activation (PubMed:20028775). Also participates in negative feedback regulation of TCR signaling through phosphorylation of PAG1, thereby promoting interaction between PAG1 and CSK and recruitment of CSK to lipid rafts (PubMed:18056706). CSK maintains LCK and FYN in an inactive form (By similarity). Promotes CD28-induced phosphorylation of VAV1 (PubMed:11005864). In mast cells, phosphorylates CLNK after activation of immunoglobulin epsilon receptor signaling (By similarity). Can also promote CD244-mediated NK cell activation (PubMed:15713798). {ECO:0000250|UniProtKB:P39688, ECO:0000269|PubMed:11005864, ECO:0000269|PubMed:11162638, ECO:0000269|PubMed:11536198, ECO:0000269|PubMed:12788081, ECO:0000269|PubMed:14707117, ECO:0000269|PubMed:14761972, ECO:0000269|PubMed:15536091, ECO:0000269|PubMed:15557120, ECO:0000269|PubMed:15713798, ECO:0000269|PubMed:16387660, ECO:0000269|PubMed:16841086, ECO:0000269|PubMed:17194753, ECO:0000269|PubMed:18056706, ECO:0000269|PubMed:18258597, ECO:0000269|PubMed:19179337, ECO:0000269|PubMed:19652227, ECO:0000269|PubMed:20028775, ECO:0000269|PubMed:20100835, ECO:0000269|PubMed:22080863, ECO:0000269|PubMed:7568038, ECO:0000269|PubMed:7822789, ECO:0000303|PubMed:15489916}. |
P06454 | PTMA | T14 | ochoa | Prothymosin alpha [Cleaved into: Prothymosin alpha, N-terminally processed; Thymosin alpha-1] | Prothymosin alpha may mediate immune function by conferring resistance to certain opportunistic infections. |
P06493 | CDK1 | T14 | ochoa|psp | Cyclin-dependent kinase 1 (CDK1) (EC 2.7.11.22) (EC 2.7.11.23) (Cell division control protein 2 homolog) (Cell division protein kinase 1) (p34 protein kinase) | Plays a key role in the control of the eukaryotic cell cycle by modulating the centrosome cycle as well as mitotic onset; promotes G2-M transition via association with multiple interphase cyclins (PubMed:16407259, PubMed:16933150, PubMed:17459720, PubMed:18356527, PubMed:19509060, PubMed:19917720, PubMed:20171170, PubMed:20935635, PubMed:20937773, PubMed:21063390, PubMed:2188730, PubMed:23355470, PubMed:2344612, PubMed:23601106, PubMed:23602554, PubMed:25556658, PubMed:26829474, PubMed:27814491, PubMed:30139873, PubMed:30704899). Phosphorylates PARVA/actopaxin, APC, AMPH, APC, BARD1, Bcl-xL/BCL2L1, BRCA2, CALD1, CASP8, CDC7, CDC20, CDC25A, CDC25C, CC2D1A, CENPA, CSNK2 proteins/CKII, FZR1/CDH1, CDK7, CEBPB, CHAMP1, DMD/dystrophin, EEF1 proteins/EF-1, EZH2, KIF11/EG5, EGFR, FANCG, FOS, GFAP, GOLGA2/GM130, GRASP1, UBE2A/hHR6A, HIST1H1 proteins/histone H1, HMGA1, HIVEP3/KRC, KAT5, LMNA, LMNB, LBR, MKI67, LATS1, MAP1B, MAP4, MARCKS, MCM2, MCM4, MKLP1, MLST8, MYB, NEFH, NFIC, NPC/nuclear pore complex, PITPNM1/NIR2, NPM1, NCL, NUCKS1, NPM1/numatrin, ORC1, PRKAR2A, EEF1E1/p18, EIF3F/p47, p53/TP53, NONO/p54NRB, PAPOLA, PLEC/plectin, RB1, TPPP, UL40/R2, RAB4A, RAP1GAP, RBBP8/CtIP, RCC1, RPS6KB1/S6K1, KHDRBS1/SAM68, ESPL1, SKI, BIRC5/survivin, STIP1, TEX14, beta-tubulins, MAPT/TAU, NEDD1, VIM/vimentin, TK1, FOXO1, RUNX1/AML1, SAMHD1, SIRT2, CGAS and RUNX2 (PubMed:16407259, PubMed:16933150, PubMed:17459720, PubMed:18356527, PubMed:19202191, PubMed:19509060, PubMed:19917720, PubMed:20171170, PubMed:20935635, PubMed:20937773, PubMed:21063390, PubMed:2188730, PubMed:23355470, PubMed:2344612, PubMed:23601106, PubMed:23602554, PubMed:25012651, PubMed:25556658, PubMed:26829474, PubMed:27814491, PubMed:30704899, PubMed:32351706, PubMed:34741373). CDK1/CDC2-cyclin-B controls pronuclear union in interphase fertilized eggs (PubMed:18480403, PubMed:20360007). Essential for early stages of embryonic development (PubMed:18480403, PubMed:20360007). During G2 and early mitosis, CDC25A/B/C-mediated dephosphorylation activates CDK1/cyclin complexes which phosphorylate several substrates that trigger at least centrosome separation, Golgi dynamics, nuclear envelope breakdown and chromosome condensation (PubMed:18480403, PubMed:20360007, PubMed:2188730, PubMed:2344612, PubMed:30139873). Once chromosomes are condensed and aligned at the metaphase plate, CDK1 activity is switched off by WEE1- and PKMYT1-mediated phosphorylation to allow sister chromatid separation, chromosome decondensation, reformation of the nuclear envelope and cytokinesis (PubMed:18480403, PubMed:20360007). Phosphorylates KRT5 during prometaphase and metaphase (By similarity). Inactivated by PKR/EIF2AK2- and WEE1-mediated phosphorylation upon DNA damage to stop cell cycle and genome replication at the G2 checkpoint thus facilitating DNA repair (PubMed:20360007). Reactivated after successful DNA repair through WIP1-dependent signaling leading to CDC25A/B/C-mediated dephosphorylation and restoring cell cycle progression (PubMed:20395957). Catalyzes lamin (LMNA, LMNB1 and LMNB2) phosphorylation at the onset of mitosis, promoting nuclear envelope breakdown (PubMed:2188730, PubMed:2344612, PubMed:37788673). In proliferating cells, CDK1-mediated FOXO1 phosphorylation at the G2-M phase represses FOXO1 interaction with 14-3-3 proteins and thereby promotes FOXO1 nuclear accumulation and transcription factor activity, leading to cell death of postmitotic neurons (PubMed:18356527). The phosphorylation of beta-tubulins regulates microtubule dynamics during mitosis (PubMed:16371510). NEDD1 phosphorylation promotes PLK1-mediated NEDD1 phosphorylation and subsequent targeting of the gamma-tubulin ring complex (gTuRC) to the centrosome, an important step for spindle formation (PubMed:19509060). In addition, CC2D1A phosphorylation regulates CC2D1A spindle pole localization and association with SCC1/RAD21 and centriole cohesion during mitosis (PubMed:20171170). The phosphorylation of Bcl-xL/BCL2L1 after prolongated G2 arrest upon DNA damage triggers apoptosis (PubMed:19917720). In contrast, CASP8 phosphorylation during mitosis prevents its activation by proteolysis and subsequent apoptosis (PubMed:20937773). This phosphorylation occurs in cancer cell lines, as well as in primary breast tissues and lymphocytes (PubMed:20937773). EZH2 phosphorylation promotes H3K27me3 maintenance and epigenetic gene silencing (PubMed:20935635). CALD1 phosphorylation promotes Schwann cell migration during peripheral nerve regeneration (By similarity). CDK1-cyclin-B complex phosphorylates NCKAP5L and mediates its dissociation from centrosomes during mitosis (PubMed:26549230). Regulates the amplitude of the cyclic expression of the core clock gene BMAL1 by phosphorylating its transcriptional repressor NR1D1, and this phosphorylation is necessary for SCF(FBXW7)-mediated ubiquitination and proteasomal degradation of NR1D1 (PubMed:27238018). Phosphorylates EML3 at 'Thr-881' which is essential for its interaction with HAUS augmin-like complex and TUBG1 (PubMed:30723163). Phosphorylates CGAS during mitosis, leading to its inhibition, thereby preventing CGAS activation by self DNA during mitosis (PubMed:32351706). Phosphorylates SKA3 on multiple sites during mitosis which promotes SKA3 binding to the NDC80 complex and anchoring of the SKA complex to kinetochores, to enable stable attachment of mitotic spindle microtubules to kinetochores (PubMed:28479321, PubMed:31804178, PubMed:32491969). {ECO:0000250|UniProtKB:P11440, ECO:0000250|UniProtKB:P39951, ECO:0000269|PubMed:16371510, ECO:0000269|PubMed:16407259, ECO:0000269|PubMed:16933150, ECO:0000269|PubMed:17459720, ECO:0000269|PubMed:18356527, ECO:0000269|PubMed:18480403, ECO:0000269|PubMed:19202191, ECO:0000269|PubMed:19509060, ECO:0000269|PubMed:19917720, ECO:0000269|PubMed:20171170, ECO:0000269|PubMed:20360007, ECO:0000269|PubMed:20395957, ECO:0000269|PubMed:20935635, ECO:0000269|PubMed:20937773, ECO:0000269|PubMed:21063390, ECO:0000269|PubMed:2188730, ECO:0000269|PubMed:23355470, ECO:0000269|PubMed:2344612, ECO:0000269|PubMed:23601106, ECO:0000269|PubMed:23602554, ECO:0000269|PubMed:25012651, ECO:0000269|PubMed:25556658, ECO:0000269|PubMed:26549230, ECO:0000269|PubMed:26829474, ECO:0000269|PubMed:27238018, ECO:0000269|PubMed:27814491, ECO:0000269|PubMed:28479321, ECO:0000269|PubMed:30139873, ECO:0000269|PubMed:30704899, ECO:0000269|PubMed:30723163, ECO:0000269|PubMed:31804178, ECO:0000269|PubMed:32351706, ECO:0000269|PubMed:32491969, ECO:0000269|PubMed:34741373, ECO:0000269|PubMed:37788673}.; FUNCTION: (Microbial infection) Acts as a receptor for hepatitis C virus (HCV) in hepatocytes and facilitates its cell entry. {ECO:0000269|PubMed:21516087}. |
P06493 | CDK1 | Y15 | ochoa|psp | Cyclin-dependent kinase 1 (CDK1) (EC 2.7.11.22) (EC 2.7.11.23) (Cell division control protein 2 homolog) (Cell division protein kinase 1) (p34 protein kinase) | Plays a key role in the control of the eukaryotic cell cycle by modulating the centrosome cycle as well as mitotic onset; promotes G2-M transition via association with multiple interphase cyclins (PubMed:16407259, PubMed:16933150, PubMed:17459720, PubMed:18356527, PubMed:19509060, PubMed:19917720, PubMed:20171170, PubMed:20935635, PubMed:20937773, PubMed:21063390, PubMed:2188730, PubMed:23355470, PubMed:2344612, PubMed:23601106, PubMed:23602554, PubMed:25556658, PubMed:26829474, PubMed:27814491, PubMed:30139873, PubMed:30704899). Phosphorylates PARVA/actopaxin, APC, AMPH, APC, BARD1, Bcl-xL/BCL2L1, BRCA2, CALD1, CASP8, CDC7, CDC20, CDC25A, CDC25C, CC2D1A, CENPA, CSNK2 proteins/CKII, FZR1/CDH1, CDK7, CEBPB, CHAMP1, DMD/dystrophin, EEF1 proteins/EF-1, EZH2, KIF11/EG5, EGFR, FANCG, FOS, GFAP, GOLGA2/GM130, GRASP1, UBE2A/hHR6A, HIST1H1 proteins/histone H1, HMGA1, HIVEP3/KRC, KAT5, LMNA, LMNB, LBR, MKI67, LATS1, MAP1B, MAP4, MARCKS, MCM2, MCM4, MKLP1, MLST8, MYB, NEFH, NFIC, NPC/nuclear pore complex, PITPNM1/NIR2, NPM1, NCL, NUCKS1, NPM1/numatrin, ORC1, PRKAR2A, EEF1E1/p18, EIF3F/p47, p53/TP53, NONO/p54NRB, PAPOLA, PLEC/plectin, RB1, TPPP, UL40/R2, RAB4A, RAP1GAP, RBBP8/CtIP, RCC1, RPS6KB1/S6K1, KHDRBS1/SAM68, ESPL1, SKI, BIRC5/survivin, STIP1, TEX14, beta-tubulins, MAPT/TAU, NEDD1, VIM/vimentin, TK1, FOXO1, RUNX1/AML1, SAMHD1, SIRT2, CGAS and RUNX2 (PubMed:16407259, PubMed:16933150, PubMed:17459720, PubMed:18356527, PubMed:19202191, PubMed:19509060, PubMed:19917720, PubMed:20171170, PubMed:20935635, PubMed:20937773, PubMed:21063390, PubMed:2188730, PubMed:23355470, PubMed:2344612, PubMed:23601106, PubMed:23602554, PubMed:25012651, PubMed:25556658, PubMed:26829474, PubMed:27814491, PubMed:30704899, PubMed:32351706, PubMed:34741373). CDK1/CDC2-cyclin-B controls pronuclear union in interphase fertilized eggs (PubMed:18480403, PubMed:20360007). Essential for early stages of embryonic development (PubMed:18480403, PubMed:20360007). During G2 and early mitosis, CDC25A/B/C-mediated dephosphorylation activates CDK1/cyclin complexes which phosphorylate several substrates that trigger at least centrosome separation, Golgi dynamics, nuclear envelope breakdown and chromosome condensation (PubMed:18480403, PubMed:20360007, PubMed:2188730, PubMed:2344612, PubMed:30139873). Once chromosomes are condensed and aligned at the metaphase plate, CDK1 activity is switched off by WEE1- and PKMYT1-mediated phosphorylation to allow sister chromatid separation, chromosome decondensation, reformation of the nuclear envelope and cytokinesis (PubMed:18480403, PubMed:20360007). Phosphorylates KRT5 during prometaphase and metaphase (By similarity). Inactivated by PKR/EIF2AK2- and WEE1-mediated phosphorylation upon DNA damage to stop cell cycle and genome replication at the G2 checkpoint thus facilitating DNA repair (PubMed:20360007). Reactivated after successful DNA repair through WIP1-dependent signaling leading to CDC25A/B/C-mediated dephosphorylation and restoring cell cycle progression (PubMed:20395957). Catalyzes lamin (LMNA, LMNB1 and LMNB2) phosphorylation at the onset of mitosis, promoting nuclear envelope breakdown (PubMed:2188730, PubMed:2344612, PubMed:37788673). In proliferating cells, CDK1-mediated FOXO1 phosphorylation at the G2-M phase represses FOXO1 interaction with 14-3-3 proteins and thereby promotes FOXO1 nuclear accumulation and transcription factor activity, leading to cell death of postmitotic neurons (PubMed:18356527). The phosphorylation of beta-tubulins regulates microtubule dynamics during mitosis (PubMed:16371510). NEDD1 phosphorylation promotes PLK1-mediated NEDD1 phosphorylation and subsequent targeting of the gamma-tubulin ring complex (gTuRC) to the centrosome, an important step for spindle formation (PubMed:19509060). In addition, CC2D1A phosphorylation regulates CC2D1A spindle pole localization and association with SCC1/RAD21 and centriole cohesion during mitosis (PubMed:20171170). The phosphorylation of Bcl-xL/BCL2L1 after prolongated G2 arrest upon DNA damage triggers apoptosis (PubMed:19917720). In contrast, CASP8 phosphorylation during mitosis prevents its activation by proteolysis and subsequent apoptosis (PubMed:20937773). This phosphorylation occurs in cancer cell lines, as well as in primary breast tissues and lymphocytes (PubMed:20937773). EZH2 phosphorylation promotes H3K27me3 maintenance and epigenetic gene silencing (PubMed:20935635). CALD1 phosphorylation promotes Schwann cell migration during peripheral nerve regeneration (By similarity). CDK1-cyclin-B complex phosphorylates NCKAP5L and mediates its dissociation from centrosomes during mitosis (PubMed:26549230). Regulates the amplitude of the cyclic expression of the core clock gene BMAL1 by phosphorylating its transcriptional repressor NR1D1, and this phosphorylation is necessary for SCF(FBXW7)-mediated ubiquitination and proteasomal degradation of NR1D1 (PubMed:27238018). Phosphorylates EML3 at 'Thr-881' which is essential for its interaction with HAUS augmin-like complex and TUBG1 (PubMed:30723163). Phosphorylates CGAS during mitosis, leading to its inhibition, thereby preventing CGAS activation by self DNA during mitosis (PubMed:32351706). Phosphorylates SKA3 on multiple sites during mitosis which promotes SKA3 binding to the NDC80 complex and anchoring of the SKA complex to kinetochores, to enable stable attachment of mitotic spindle microtubules to kinetochores (PubMed:28479321, PubMed:31804178, PubMed:32491969). {ECO:0000250|UniProtKB:P11440, ECO:0000250|UniProtKB:P39951, ECO:0000269|PubMed:16371510, ECO:0000269|PubMed:16407259, ECO:0000269|PubMed:16933150, ECO:0000269|PubMed:17459720, ECO:0000269|PubMed:18356527, ECO:0000269|PubMed:18480403, ECO:0000269|PubMed:19202191, ECO:0000269|PubMed:19509060, ECO:0000269|PubMed:19917720, ECO:0000269|PubMed:20171170, ECO:0000269|PubMed:20360007, ECO:0000269|PubMed:20395957, ECO:0000269|PubMed:20935635, ECO:0000269|PubMed:20937773, ECO:0000269|PubMed:21063390, ECO:0000269|PubMed:2188730, ECO:0000269|PubMed:23355470, ECO:0000269|PubMed:2344612, ECO:0000269|PubMed:23601106, ECO:0000269|PubMed:23602554, ECO:0000269|PubMed:25012651, ECO:0000269|PubMed:25556658, ECO:0000269|PubMed:26549230, ECO:0000269|PubMed:26829474, ECO:0000269|PubMed:27238018, ECO:0000269|PubMed:27814491, ECO:0000269|PubMed:28479321, ECO:0000269|PubMed:30139873, ECO:0000269|PubMed:30704899, ECO:0000269|PubMed:30723163, ECO:0000269|PubMed:31804178, ECO:0000269|PubMed:32351706, ECO:0000269|PubMed:32491969, ECO:0000269|PubMed:34741373, ECO:0000269|PubMed:37788673}.; FUNCTION: (Microbial infection) Acts as a receptor for hepatitis C virus (HCV) in hepatocytes and facilitates its cell entry. {ECO:0000269|PubMed:21516087}. |
P08473 | MME | T15 | psp | Neprilysin (EC 3.4.24.11) (Atriopeptidase) (Common acute lymphocytic leukemia antigen) (CALLA) (Enkephalinase) (Neutral endopeptidase 24.11) (NEP) (Neutral endopeptidase) (Skin fibroblast elastase) (SFE) (CD antigen CD10) | Thermolysin-like specificity, but is almost confined on acting on polypeptides of up to 30 amino acids (PubMed:15283675, PubMed:6208535, PubMed:6349683, PubMed:8168535). Biologically important in the destruction of opioid peptides such as Met- and Leu-enkephalins by cleavage of a Gly-Phe bond (PubMed:17101991, PubMed:6349683). Catalyzes cleavage of bradykinin, substance P and neurotensin peptides (PubMed:6208535). Able to cleave angiotensin-1, angiotensin-2 and angiotensin 1-9 (PubMed:15283675, PubMed:6349683). Involved in the degradation of atrial natriuretic factor (ANF) and brain natriuretic factor (BNP(1-32)) (PubMed:16254193, PubMed:2531377, PubMed:2972276). Displays UV-inducible elastase activity toward skin preelastic and elastic fibers (PubMed:20876573). {ECO:0000269|PubMed:15283675, ECO:0000269|PubMed:17101991, ECO:0000269|PubMed:20876573, ECO:0000269|PubMed:2531377, ECO:0000269|PubMed:27588448, ECO:0000269|PubMed:2972276, ECO:0000269|PubMed:6208535, ECO:0000269|PubMed:6349683}. |
P09234 | SNRPC | T14 | ochoa | U1 small nuclear ribonucleoprotein C (U1 snRNP C) (U1-C) (U1C) | Component of the spliceosomal U1 snRNP, which is essential for recognition of the pre-mRNA 5' splice-site and the subsequent assembly of the spliceosome. SNRPC/U1-C is directly involved in initial 5' splice-site recognition for both constitutive and regulated alternative splicing. The interaction with the 5' splice-site seems to precede base-pairing between the pre-mRNA and the U1 snRNA. Stimulates commitment or early (E) complex formation by stabilizing the base pairing of the 5' end of the U1 snRNA and the 5' splice-site region. {ECO:0000255|HAMAP-Rule:MF_03153, ECO:0000269|PubMed:1826349, ECO:0000269|PubMed:19325628, ECO:0000269|PubMed:2136774, ECO:0000269|PubMed:8798632}. |
P0CG47 | UBB | T14 | ochoa | Polyubiquitin-B [Cleaved into: Ubiquitin] | [Ubiquitin]: Exists either covalently attached to another protein, or free (unanchored). When covalently bound, it is conjugated to target proteins via an isopeptide bond either as a monomer (monoubiquitin), a polymer linked via different Lys residues of the ubiquitin (polyubiquitin chains) or a linear polymer linked via the initiator Met of the ubiquitin (linear polyubiquitin chains). Polyubiquitin chains, when attached to a target protein, have different functions depending on the Lys residue of the ubiquitin that is linked: Lys-6-linked may be involved in DNA repair; Lys-11-linked is involved in ERAD (endoplasmic reticulum-associated degradation) and in cell-cycle regulation; Lys-29-linked is involved in proteotoxic stress response and cell cycle; Lys-33-linked is involved in kinase modification; Lys-48-linked is involved in protein degradation via the proteasome; Lys-63-linked is involved in endocytosis, DNA-damage responses as well as in signaling processes leading to activation of the transcription factor NF-kappa-B. Linear polymer chains formed via attachment by the initiator Met lead to cell signaling. Ubiquitin is usually conjugated to Lys residues of target proteins, however, in rare cases, conjugation to Cys or Ser residues has been observed. When polyubiquitin is free (unanchored-polyubiquitin), it also has distinct roles, such as in activation of protein kinases, and in signaling. {ECO:0000269|PubMed:16543144, ECO:0000269|PubMed:34239127, ECO:0000303|PubMed:19754430}. |
P0CG48 | UBC | T14 | ochoa | Polyubiquitin-C [Cleaved into: Ubiquitin] | [Ubiquitin]: Exists either covalently attached to another protein, or free (unanchored). When covalently bound, it is conjugated to target proteins via an isopeptide bond either as a monomer (monoubiquitin), a polymer linked via different Lys residues of the ubiquitin (polyubiquitin chains) or a linear polymer linked via the initiator Met of the ubiquitin (linear polyubiquitin chains). Polyubiquitin chains, when attached to a target protein, have different functions depending on the Lys residue of the ubiquitin that is linked: Lys-6-linked may be involved in DNA repair; Lys-11-linked is involved in ERAD (endoplasmic reticulum-associated degradation) and in cell-cycle regulation; Lys-29-linked is involved in proteotoxic stress response and cell cycle; Lys-33-linked is involved in kinase modification; Lys-48-linked is involved in protein degradation via the proteasome; Lys-63-linked is involved in endocytosis, DNA-damage responses as well as in signaling processes leading to activation of the transcription factor NF-kappa-B. Linear polymer chains formed via attachment by the initiator Met lead to cell signaling. Ubiquitin is usually conjugated to Lys residues of target proteins, however, in rare cases, conjugation to Cys or Ser residues has been observed. When polyubiquitin is free (unanchored-polyubiquitin), it also has distinct roles, such as in activation of protein kinases, and in signaling. During ubiquitination, the acceptor ubiquitin is positioned in the active site via direct interaction with the E2 ubiquitin-conjugating enzymes such as UBE2R2 (PubMed:38326650). As a monoubiquitin, its C-terminal glycine is recognized as a C-degron by Cul2-RING (CRL2) E3 ubiquitin-protein ligase complexes (PubMed:39548056). {ECO:0000269|PubMed:16543144, ECO:0000269|PubMed:34239127, ECO:0000269|PubMed:38326650, ECO:0000269|PubMed:39548056, ECO:0000303|PubMed:19754430}. |
P10244 | MYBL2 | Y15 | psp | Myb-related protein B (B-Myb) (Myb-like protein 2) | Transcription factor involved in the regulation of cell survival, proliferation, and differentiation. Transactivates the expression of the CLU gene. {ECO:0000269|PubMed:10770937}. |
P11142 | HSPA8 | T14 | ochoa | Heat shock cognate 71 kDa protein (EC 3.6.4.10) (Heat shock 70 kDa protein 8) (Heat shock protein family A member 8) (Lipopolysaccharide-associated protein 1) (LAP-1) (LPS-associated protein 1) | Molecular chaperone implicated in a wide variety of cellular processes, including protection of the proteome from stress, folding and transport of newly synthesized polypeptides, chaperone-mediated autophagy, activation of proteolysis of misfolded proteins, formation and dissociation of protein complexes, and antigen presentation. Plays a pivotal role in the protein quality control system, ensuring the correct folding of proteins, the re-folding of misfolded proteins and controlling the targeting of proteins for subsequent degradation (PubMed:21148293, PubMed:21150129, PubMed:23018488, PubMed:24732912, PubMed:27916661, PubMed:2799391, PubMed:36586411). This is achieved through cycles of ATP binding, ATP hydrolysis and ADP release, mediated by co-chaperones (PubMed:12526792, PubMed:21148293, PubMed:21150129, PubMed:23018488, PubMed:24732912, PubMed:27916661). The co-chaperones have been shown to not only regulate different steps of the ATPase cycle of HSP70, but they also have an individual specificity such that one co-chaperone may promote folding of a substrate while another may promote degradation (PubMed:12526792, PubMed:21148293, PubMed:21150129, PubMed:23018488, PubMed:24732912, PubMed:27916661). The affinity of HSP70 for polypeptides is regulated by its nucleotide bound state. In the ATP-bound form, it has a low affinity for substrate proteins. However, upon hydrolysis of the ATP to ADP, it undergoes a conformational change that increases its affinity for substrate proteins. HSP70 goes through repeated cycles of ATP hydrolysis and nucleotide exchange, which permits cycles of substrate binding and release. The HSP70-associated co-chaperones are of three types: J-domain co-chaperones HSP40s (stimulate ATPase hydrolysis by HSP70), the nucleotide exchange factors (NEF) such as BAG1/2/3 (facilitate conversion of HSP70 from the ADP-bound to the ATP-bound state thereby promoting substrate release), and the TPR domain chaperones such as HOPX and STUB1 (PubMed:24121476, PubMed:24318877, PubMed:26865365, PubMed:27474739). Plays a critical role in mitochondrial import, delivers preproteins to the mitochondrial import receptor TOMM70 (PubMed:12526792). Acts as a repressor of transcriptional activation. Inhibits the transcriptional coactivator activity of CITED1 on Smad-mediated transcription. Component of the PRP19-CDC5L complex that forms an integral part of the spliceosome and is required for activating pre-mRNA splicing. May have a scaffolding role in the spliceosome assembly as it contacts all other components of the core complex. Binds bacterial lipopolysaccharide (LPS) and mediates LPS-induced inflammatory response, including TNF secretion by monocytes (PubMed:10722728, PubMed:11276205). Substrate recognition component in chaperone-mediated autophagy (CMA), a selective protein degradation process that mediates degradation of proteins with a -KFERQ motif: HSPA8/HSC70 specifically recognizes and binds cytosolic proteins bearing a -KFERQ motif and promotes their recruitment to the surface of the lysosome where they bind to lysosomal protein LAMP2 (PubMed:11559757, PubMed:2799391, PubMed:36586411). KFERQ motif-containing proteins are eventually transported into the lysosomal lumen where they are degraded (PubMed:11559757, PubMed:2799391, PubMed:36586411). In conjunction with LAMP2, facilitates MHC class II presentation of cytoplasmic antigens by guiding antigens to the lysosomal membrane for interaction with LAMP2 which then elicits MHC class II presentation of peptides to the cell membrane (PubMed:15894275). Participates in the ER-associated degradation (ERAD) quality control pathway in conjunction with J domain-containing co-chaperones and the E3 ligase STUB1 (PubMed:23990462). It is recruited to clathrin-coated vesicles through its interaction with DNAJC6 leading to activation of HSPA8/HSC70 ATPase activity and therefore uncoating of clathrin-coated vesicles (By similarity). {ECO:0000250|UniProtKB:P19120, ECO:0000269|PubMed:10722728, ECO:0000269|PubMed:11276205, ECO:0000269|PubMed:11559757, ECO:0000269|PubMed:12526792, ECO:0000269|PubMed:15894275, ECO:0000269|PubMed:21148293, ECO:0000269|PubMed:21150129, ECO:0000269|PubMed:23018488, ECO:0000269|PubMed:23990462, ECO:0000269|PubMed:24318877, ECO:0000269|PubMed:24732912, ECO:0000269|PubMed:27474739, ECO:0000269|PubMed:27916661, ECO:0000269|PubMed:2799391, ECO:0000269|PubMed:36586411, ECO:0000303|PubMed:24121476, ECO:0000303|PubMed:26865365}. |
P11142 | HSPA8 | Y15 | ochoa | Heat shock cognate 71 kDa protein (EC 3.6.4.10) (Heat shock 70 kDa protein 8) (Heat shock protein family A member 8) (Lipopolysaccharide-associated protein 1) (LAP-1) (LPS-associated protein 1) | Molecular chaperone implicated in a wide variety of cellular processes, including protection of the proteome from stress, folding and transport of newly synthesized polypeptides, chaperone-mediated autophagy, activation of proteolysis of misfolded proteins, formation and dissociation of protein complexes, and antigen presentation. Plays a pivotal role in the protein quality control system, ensuring the correct folding of proteins, the re-folding of misfolded proteins and controlling the targeting of proteins for subsequent degradation (PubMed:21148293, PubMed:21150129, PubMed:23018488, PubMed:24732912, PubMed:27916661, PubMed:2799391, PubMed:36586411). This is achieved through cycles of ATP binding, ATP hydrolysis and ADP release, mediated by co-chaperones (PubMed:12526792, PubMed:21148293, PubMed:21150129, PubMed:23018488, PubMed:24732912, PubMed:27916661). The co-chaperones have been shown to not only regulate different steps of the ATPase cycle of HSP70, but they also have an individual specificity such that one co-chaperone may promote folding of a substrate while another may promote degradation (PubMed:12526792, PubMed:21148293, PubMed:21150129, PubMed:23018488, PubMed:24732912, PubMed:27916661). The affinity of HSP70 for polypeptides is regulated by its nucleotide bound state. In the ATP-bound form, it has a low affinity for substrate proteins. However, upon hydrolysis of the ATP to ADP, it undergoes a conformational change that increases its affinity for substrate proteins. HSP70 goes through repeated cycles of ATP hydrolysis and nucleotide exchange, which permits cycles of substrate binding and release. The HSP70-associated co-chaperones are of three types: J-domain co-chaperones HSP40s (stimulate ATPase hydrolysis by HSP70), the nucleotide exchange factors (NEF) such as BAG1/2/3 (facilitate conversion of HSP70 from the ADP-bound to the ATP-bound state thereby promoting substrate release), and the TPR domain chaperones such as HOPX and STUB1 (PubMed:24121476, PubMed:24318877, PubMed:26865365, PubMed:27474739). Plays a critical role in mitochondrial import, delivers preproteins to the mitochondrial import receptor TOMM70 (PubMed:12526792). Acts as a repressor of transcriptional activation. Inhibits the transcriptional coactivator activity of CITED1 on Smad-mediated transcription. Component of the PRP19-CDC5L complex that forms an integral part of the spliceosome and is required for activating pre-mRNA splicing. May have a scaffolding role in the spliceosome assembly as it contacts all other components of the core complex. Binds bacterial lipopolysaccharide (LPS) and mediates LPS-induced inflammatory response, including TNF secretion by monocytes (PubMed:10722728, PubMed:11276205). Substrate recognition component in chaperone-mediated autophagy (CMA), a selective protein degradation process that mediates degradation of proteins with a -KFERQ motif: HSPA8/HSC70 specifically recognizes and binds cytosolic proteins bearing a -KFERQ motif and promotes their recruitment to the surface of the lysosome where they bind to lysosomal protein LAMP2 (PubMed:11559757, PubMed:2799391, PubMed:36586411). KFERQ motif-containing proteins are eventually transported into the lysosomal lumen where they are degraded (PubMed:11559757, PubMed:2799391, PubMed:36586411). In conjunction with LAMP2, facilitates MHC class II presentation of cytoplasmic antigens by guiding antigens to the lysosomal membrane for interaction with LAMP2 which then elicits MHC class II presentation of peptides to the cell membrane (PubMed:15894275). Participates in the ER-associated degradation (ERAD) quality control pathway in conjunction with J domain-containing co-chaperones and the E3 ligase STUB1 (PubMed:23990462). It is recruited to clathrin-coated vesicles through its interaction with DNAJC6 leading to activation of HSPA8/HSC70 ATPase activity and therefore uncoating of clathrin-coated vesicles (By similarity). {ECO:0000250|UniProtKB:P19120, ECO:0000269|PubMed:10722728, ECO:0000269|PubMed:11276205, ECO:0000269|PubMed:11559757, ECO:0000269|PubMed:12526792, ECO:0000269|PubMed:15894275, ECO:0000269|PubMed:21148293, ECO:0000269|PubMed:21150129, ECO:0000269|PubMed:23018488, ECO:0000269|PubMed:23990462, ECO:0000269|PubMed:24318877, ECO:0000269|PubMed:24732912, ECO:0000269|PubMed:27474739, ECO:0000269|PubMed:27916661, ECO:0000269|PubMed:2799391, ECO:0000269|PubMed:36586411, ECO:0000303|PubMed:24121476, ECO:0000303|PubMed:26865365}. |
P12883 | MYH7 | Y15 | ochoa | Myosin-7 (Myosin heavy chain 7) (Myosin heavy chain slow isoform) (MyHC-slow) (Myosin heavy chain, cardiac muscle beta isoform) (MyHC-beta) | Myosins are actin-based motor molecules with ATPase activity essential for muscle contraction. Forms regular bipolar thick filaments that, together with actin thin filaments, constitute the fundamental contractile unit of skeletal and cardiac muscle. {ECO:0000305|PubMed:26150528, ECO:0000305|PubMed:26246073}. |
P14923 | JUP | T14 | ochoa | Junction plakoglobin (Catenin gamma) (Desmoplakin III) (Desmoplakin-3) | Common junctional plaque protein. The membrane-associated plaques are architectural elements in an important strategic position to influence the arrangement and function of both the cytoskeleton and the cells within the tissue. The presence of plakoglobin in both the desmosomes and in the intermediate junctions suggests that it plays a central role in the structure and function of submembranous plaques. Acts as a substrate for VE-PTP and is required by it to stimulate VE-cadherin function in endothelial cells. Can replace beta-catenin in E-cadherin/catenin adhesion complexes which are proposed to couple cadherins to the actin cytoskeleton (By similarity). {ECO:0000250}. |
P15259 | PGAM2 | T15 | ochoa | Phosphoglycerate mutase 2 (EC 5.4.2.11) (EC 5.4.2.4) (BPG-dependent PGAM 2) (Muscle-specific phosphoglycerate mutase) (Phosphoglycerate mutase isozyme M) (PGAM-M) | Interconversion of 3- and 2-phosphoglycerate with 2,3-bisphosphoglycerate as the primer of the reaction. Can also catalyze the reaction of EC 5.4.2.4 (synthase), but with a reduced activity. |
P22460 | KCNA5 | T15 | psp | Potassium voltage-gated channel subfamily A member 5 (HPCN1) (Voltage-gated potassium channel HK2) (Voltage-gated potassium channel subunit Kv1.5) | Voltage-gated potassium channel that mediates transmembrane potassium transport in excitable membranes. Forms tetrameric potassium-selective channels through which potassium ions pass in accordance with their electrochemical gradient. The channel alternates between opened and closed conformations in response to the voltage difference across the membrane. Can form functional homotetrameric channels and heterotetrameric channels that contain variable proportions of KCNA1, KCNA2, KCNA4, KCNA5, and possibly other family members as well; channel properties depend on the type of alpha subunits that are part of the channel (PubMed:12130714). Channel properties are modulated by cytoplasmic beta subunits that regulate the subcellular location of the alpha subunits and promote rapid inactivation (PubMed:12130714). Homotetrameric channels display rapid activation and slow inactivation (PubMed:12130714, PubMed:8505626). Required for normal electrical conduction including formation of the infranodal ventricular conduction system and normal action potential configuration, as a result of its interaction with XIRP2 (By similarity). May play a role in regulating the secretion of insulin in normal pancreatic islets. {ECO:0000250|UniProtKB:Q61762, ECO:0000269|PubMed:12130714, ECO:0000269|PubMed:17267549, ECO:0000269|PubMed:20018952, ECO:0000269|PubMed:36917789, ECO:0000269|PubMed:8505626}.; FUNCTION: [Isoform 2]: Exhibits a faster depolarization rate, reduced voltage-dependent recovery from inactivation and an excessive cumulative inactivation. {ECO:0000269|PubMed:11524461}. |
P23588 | EIF4B | T14 | ochoa | Eukaryotic translation initiation factor 4B (eIF-4B) | Required for the binding of mRNA to ribosomes. Functions in close association with EIF4-F and EIF4-A. Binds near the 5'-terminal cap of mRNA in presence of EIF-4F and ATP. Promotes the ATPase activity and the ATP-dependent RNA unwinding activity of both EIF4-A and EIF4-F. |
P24941 | CDK2 | T14 | ochoa|psp | Cyclin-dependent kinase 2 (EC 2.7.11.22) (Cell division protein kinase 2) (p33 protein kinase) | Serine/threonine-protein kinase involved in the control of the cell cycle; essential for meiosis, but dispensable for mitosis (PubMed:10499802, PubMed:10884347, PubMed:10995386, PubMed:10995387, PubMed:11051553, PubMed:11113184, PubMed:12944431, PubMed:15800615, PubMed:17495531, PubMed:19966300, PubMed:20935635, PubMed:21262353, PubMed:21596315, PubMed:28216226, PubMed:28666995). Phosphorylates CABLES1, CTNNB1, CDK2AP2, ERCC6, NBN, USP37, p53/TP53, NPM1, CDK7, RB1, BRCA2, MYC, NPAT, EZH2 (PubMed:10499802, PubMed:10995386, PubMed:10995387, PubMed:11051553, PubMed:11113184, PubMed:12944431, PubMed:15800615, PubMed:19966300, PubMed:20935635, PubMed:21262353, PubMed:21596315, PubMed:28216226). Triggers duplication of centrosomes and DNA (PubMed:11051553). Acts at the G1-S transition to promote the E2F transcriptional program and the initiation of DNA synthesis, and modulates G2 progression; controls the timing of entry into mitosis/meiosis by controlling the subsequent activation of cyclin B/CDK1 by phosphorylation, and coordinates the activation of cyclin B/CDK1 at the centrosome and in the nucleus (PubMed:18372919, PubMed:19238148, PubMed:19561645). Crucial role in orchestrating a fine balance between cellular proliferation, cell death, and DNA repair in embryonic stem cells (ESCs) (PubMed:18372919, PubMed:19238148, PubMed:19561645). Activity of CDK2 is maximal during S phase and G2; activated by interaction with cyclin E during the early stages of DNA synthesis to permit G1-S transition, and subsequently activated by cyclin A2 (cyclin A1 in germ cells) during the late stages of DNA replication to drive the transition from S phase to mitosis, the G2 phase (PubMed:18372919, PubMed:19238148, PubMed:19561645). EZH2 phosphorylation promotes H3K27me3 maintenance and epigenetic gene silencing (PubMed:20935635). Cyclin E/CDK2 prevents oxidative stress-mediated Ras-induced senescence by phosphorylating MYC (PubMed:19966300). Involved in G1-S phase DNA damage checkpoint that prevents cells with damaged DNA from initiating mitosis; regulates homologous recombination-dependent repair by phosphorylating BRCA2, this phosphorylation is low in S phase when recombination is active, but increases as cells progress towards mitosis (PubMed:15800615, PubMed:20195506, PubMed:21319273). In response to DNA damage, double-strand break repair by homologous recombination a reduction of CDK2-mediated BRCA2 phosphorylation (PubMed:15800615). Involved in regulation of telomere repair by mediating phosphorylation of NBN (PubMed:28216226). Phosphorylation of RB1 disturbs its interaction with E2F1 (PubMed:10499802). NPM1 phosphorylation by cyclin E/CDK2 promotes its dissociates from unduplicated centrosomes, thus initiating centrosome duplication (PubMed:11051553). Cyclin E/CDK2-mediated phosphorylation of NPAT at G1-S transition and until prophase stimulates the NPAT-mediated activation of histone gene transcription during S phase (PubMed:10995386, PubMed:10995387). Required for vitamin D-mediated growth inhibition by being itself inactivated (PubMed:20147522). Involved in the nitric oxide- (NO) mediated signaling in a nitrosylation/activation-dependent manner (PubMed:20079829). USP37 is activated by phosphorylation and thus triggers G1-S transition (PubMed:21596315). CTNNB1 phosphorylation regulates insulin internalization (PubMed:21262353). Phosphorylates FOXP3 and negatively regulates its transcriptional activity and protein stability (By similarity). Phosphorylates ERCC6 which is essential for its chromatin remodeling activity at DNA double-strand breaks (PubMed:29203878). Acts as a regulator of the phosphatidylinositol 3-kinase/protein kinase B signal transduction by mediating phosphorylation of the C-terminus of protein kinase B (PKB/AKT1 and PKB/AKT2), promoting its activation (PubMed:24670654). {ECO:0000250|UniProtKB:P97377, ECO:0000269|PubMed:10499802, ECO:0000269|PubMed:10884347, ECO:0000269|PubMed:10995386, ECO:0000269|PubMed:10995387, ECO:0000269|PubMed:11051553, ECO:0000269|PubMed:11113184, ECO:0000269|PubMed:12944431, ECO:0000269|PubMed:15800615, ECO:0000269|PubMed:17495531, ECO:0000269|PubMed:18372919, ECO:0000269|PubMed:19966300, ECO:0000269|PubMed:20079829, ECO:0000269|PubMed:20147522, ECO:0000269|PubMed:20195506, ECO:0000269|PubMed:20935635, ECO:0000269|PubMed:21262353, ECO:0000269|PubMed:21319273, ECO:0000269|PubMed:21596315, ECO:0000269|PubMed:24670654, ECO:0000269|PubMed:28216226, ECO:0000269|PubMed:28666995, ECO:0000269|PubMed:29203878, ECO:0000303|PubMed:19238148, ECO:0000303|PubMed:19561645}. |
P24941 | CDK2 | Y15 | ochoa|psp | Cyclin-dependent kinase 2 (EC 2.7.11.22) (Cell division protein kinase 2) (p33 protein kinase) | Serine/threonine-protein kinase involved in the control of the cell cycle; essential for meiosis, but dispensable for mitosis (PubMed:10499802, PubMed:10884347, PubMed:10995386, PubMed:10995387, PubMed:11051553, PubMed:11113184, PubMed:12944431, PubMed:15800615, PubMed:17495531, PubMed:19966300, PubMed:20935635, PubMed:21262353, PubMed:21596315, PubMed:28216226, PubMed:28666995). Phosphorylates CABLES1, CTNNB1, CDK2AP2, ERCC6, NBN, USP37, p53/TP53, NPM1, CDK7, RB1, BRCA2, MYC, NPAT, EZH2 (PubMed:10499802, PubMed:10995386, PubMed:10995387, PubMed:11051553, PubMed:11113184, PubMed:12944431, PubMed:15800615, PubMed:19966300, PubMed:20935635, PubMed:21262353, PubMed:21596315, PubMed:28216226). Triggers duplication of centrosomes and DNA (PubMed:11051553). Acts at the G1-S transition to promote the E2F transcriptional program and the initiation of DNA synthesis, and modulates G2 progression; controls the timing of entry into mitosis/meiosis by controlling the subsequent activation of cyclin B/CDK1 by phosphorylation, and coordinates the activation of cyclin B/CDK1 at the centrosome and in the nucleus (PubMed:18372919, PubMed:19238148, PubMed:19561645). Crucial role in orchestrating a fine balance between cellular proliferation, cell death, and DNA repair in embryonic stem cells (ESCs) (PubMed:18372919, PubMed:19238148, PubMed:19561645). Activity of CDK2 is maximal during S phase and G2; activated by interaction with cyclin E during the early stages of DNA synthesis to permit G1-S transition, and subsequently activated by cyclin A2 (cyclin A1 in germ cells) during the late stages of DNA replication to drive the transition from S phase to mitosis, the G2 phase (PubMed:18372919, PubMed:19238148, PubMed:19561645). EZH2 phosphorylation promotes H3K27me3 maintenance and epigenetic gene silencing (PubMed:20935635). Cyclin E/CDK2 prevents oxidative stress-mediated Ras-induced senescence by phosphorylating MYC (PubMed:19966300). Involved in G1-S phase DNA damage checkpoint that prevents cells with damaged DNA from initiating mitosis; regulates homologous recombination-dependent repair by phosphorylating BRCA2, this phosphorylation is low in S phase when recombination is active, but increases as cells progress towards mitosis (PubMed:15800615, PubMed:20195506, PubMed:21319273). In response to DNA damage, double-strand break repair by homologous recombination a reduction of CDK2-mediated BRCA2 phosphorylation (PubMed:15800615). Involved in regulation of telomere repair by mediating phosphorylation of NBN (PubMed:28216226). Phosphorylation of RB1 disturbs its interaction with E2F1 (PubMed:10499802). NPM1 phosphorylation by cyclin E/CDK2 promotes its dissociates from unduplicated centrosomes, thus initiating centrosome duplication (PubMed:11051553). Cyclin E/CDK2-mediated phosphorylation of NPAT at G1-S transition and until prophase stimulates the NPAT-mediated activation of histone gene transcription during S phase (PubMed:10995386, PubMed:10995387). Required for vitamin D-mediated growth inhibition by being itself inactivated (PubMed:20147522). Involved in the nitric oxide- (NO) mediated signaling in a nitrosylation/activation-dependent manner (PubMed:20079829). USP37 is activated by phosphorylation and thus triggers G1-S transition (PubMed:21596315). CTNNB1 phosphorylation regulates insulin internalization (PubMed:21262353). Phosphorylates FOXP3 and negatively regulates its transcriptional activity and protein stability (By similarity). Phosphorylates ERCC6 which is essential for its chromatin remodeling activity at DNA double-strand breaks (PubMed:29203878). Acts as a regulator of the phosphatidylinositol 3-kinase/protein kinase B signal transduction by mediating phosphorylation of the C-terminus of protein kinase B (PKB/AKT1 and PKB/AKT2), promoting its activation (PubMed:24670654). {ECO:0000250|UniProtKB:P97377, ECO:0000269|PubMed:10499802, ECO:0000269|PubMed:10884347, ECO:0000269|PubMed:10995386, ECO:0000269|PubMed:10995387, ECO:0000269|PubMed:11051553, ECO:0000269|PubMed:11113184, ECO:0000269|PubMed:12944431, ECO:0000269|PubMed:15800615, ECO:0000269|PubMed:17495531, ECO:0000269|PubMed:18372919, ECO:0000269|PubMed:19966300, ECO:0000269|PubMed:20079829, ECO:0000269|PubMed:20147522, ECO:0000269|PubMed:20195506, ECO:0000269|PubMed:20935635, ECO:0000269|PubMed:21262353, ECO:0000269|PubMed:21319273, ECO:0000269|PubMed:21596315, ECO:0000269|PubMed:24670654, ECO:0000269|PubMed:28216226, ECO:0000269|PubMed:28666995, ECO:0000269|PubMed:29203878, ECO:0000303|PubMed:19238148, ECO:0000303|PubMed:19561645}. |
P25788 | PSMA3 | T14 | ochoa | Proteasome subunit alpha type-3 (Macropain subunit C8) (Multicatalytic endopeptidase complex subunit C8) (Proteasome component C8) (Proteasome subunit alpha-7) (alpha-7) | Component of the 20S core proteasome complex involved in the proteolytic degradation of most intracellular proteins. This complex plays numerous essential roles within the cell by associating with different regulatory particles. Associated with two 19S regulatory particles, forms the 26S proteasome and thus participates in the ATP-dependent degradation of ubiquitinated proteins. The 26S proteasome plays a key role in the maintenance of protein homeostasis by removing misfolded or damaged proteins that could impair cellular functions, and by removing proteins whose functions are no longer required. Associated with the PA200 or PA28, the 20S proteasome mediates ubiquitin-independent protein degradation. This type of proteolysis is required in several pathways including spermatogenesis (20S-PA200 complex) or generation of a subset of MHC class I-presented antigenic peptides (20S-PA28 complex). Binds to the C-terminus of CDKN1A and thereby mediates its degradation. Negatively regulates the membrane trafficking of the cell-surface thromboxane A2 receptor (TBXA2R) isoform 2. {ECO:0000269|PubMed:11350925, ECO:0000269|PubMed:14550573, ECO:0000269|PubMed:15244466, ECO:0000269|PubMed:17499743, ECO:0000269|PubMed:27176742}. |
P28066 | PSMA5 | T14 | ochoa | Proteasome subunit alpha type-5 (Macropain zeta chain) (Multicatalytic endopeptidase complex zeta chain) (Proteasome subunit alpha-5) (alpha-5) (Proteasome zeta chain) | Component of the 20S core proteasome complex involved in the proteolytic degradation of most intracellular proteins. This complex plays numerous essential roles within the cell by associating with different regulatory particles. Associated with two 19S regulatory particles, forms the 26S proteasome and thus participates in the ATP-dependent degradation of ubiquitinated proteins. The 26S proteasome plays a key role in the maintenance of protein homeostasis by removing misfolded or damaged proteins that could impair cellular functions, and by removing proteins whose functions are no longer required. Associated with the PA200 or PA28, the 20S proteasome mediates ubiquitin-independent protein degradation. This type of proteolysis is required in several pathways including spermatogenesis (20S-PA200 complex) or generation of a subset of MHC class I-presented antigenic peptides (20S-PA28 complex). {ECO:0000269|PubMed:15244466, ECO:0000269|PubMed:27176742, ECO:0000269|PubMed:8610016}. |
P35659 | DEK | T15 | ochoa|psp | Protein DEK | Involved in chromatin organization. {ECO:0000269|PubMed:17524367}. |
P37268 | FDFT1 | Y14 | ochoa | Squalene synthase (SQS) (SS) (EC 2.5.1.21) (FPP:FPP farnesyltransferase) (Farnesyl-diphosphate farnesyltransferase) (Farnesyl-diphosphate farnesyltransferase 1) | Catalyzes the condensation of 2 farnesyl pyrophosphate (FPP) moieties to form squalene. Proceeds in two distinct steps. In the first half-reaction, two molecules of FPP react to form the stable presqualene diphosphate intermediate (PSQPP), with concomitant release of a proton and a molecule of inorganic diphosphate. In the second half-reaction, PSQPP undergoes heterolysis, isomerization, and reduction with NADPH or NADH to form squalene. It is the first committed enzyme of the sterol biosynthesis pathway. {ECO:0000269|PubMed:10896663, ECO:0000269|PubMed:24531458}. |
P39687 | ANP32A | T15 | ochoa | Acidic leucine-rich nuclear phosphoprotein 32 family member A (Acidic nuclear phosphoprotein pp32) (pp32) (Leucine-rich acidic nuclear protein) (LANP) (Mapmodulin) (Potent heat-stable protein phosphatase 2A inhibitor I1PP2A) (Putative HLA-DR-associated protein I) (PHAPI) | Multifunctional protein that is involved in the regulation of many processes including tumor suppression, apoptosis, cell cycle progression or transcription (PubMed:10400610, PubMed:11360199, PubMed:16341127, PubMed:18439902). Promotes apoptosis by favouring the activation of caspase-9/CASP9 and allowing apoptosome formation (PubMed:18439902). In addition, plays a role in the modulation of histone acetylation and transcription as part of the INHAT (inhibitor of histone acetyltransferases) complex. Inhibits the histone-acetyltranferase activity of EP300/CREBBP (CREB-binding protein) and EP300/CREBBP-associated factor by histone masking (PubMed:11830591). Preferentially binds to unmodified histone H3 and sterically inhibiting its acetylation and phosphorylation leading to cell growth inhibition (PubMed:16341127). Participates in other biochemical processes such as regulation of mRNA nuclear-to-cytoplasmic translocation and stability by its association with ELAVL1 (Hu-antigen R) (PubMed:18180367). Plays a role in E4F1-mediated transcriptional repression as well as inhibition of protein phosphatase 2A (PubMed:15642345, PubMed:17557114). {ECO:0000269|PubMed:10400610, ECO:0000269|PubMed:11360199, ECO:0000269|PubMed:11830591, ECO:0000269|PubMed:15642345, ECO:0000269|PubMed:16341127, ECO:0000269|PubMed:17557114, ECO:0000269|PubMed:18180367, ECO:0000269|PubMed:18439902}.; FUNCTION: (Microbial infection) Plays an essential role in influenza A, B and C viral genome replication (PubMed:30666459, PubMed:32694517, PubMed:33045004, PubMed:33208942). Mechanistically, mediates the assembly of the viral replicase asymmetric dimers composed of PB1, PB2 and PA via its N-terminal region (PubMed:33208942). Also plays an essential role in foamy virus mRNA export from the nucleus (PubMed:21159877). {ECO:0000269|PubMed:21159877, ECO:0000269|PubMed:30666459, ECO:0000269|PubMed:32694517, ECO:0000269|PubMed:33045004, ECO:0000269|PubMed:33208942}. |
P41226 | UBA7 | Y15 | ochoa | Ubiquitin-like modifier-activating enzyme 7 (Ubiquitin-activating enzyme 7) (EC 6.2.1.-) (D8) (Ubiquitin-activating enzyme E1 homolog) | E1-activating enzyme that catalyzes the covalent conjugation of the ubiquitin-like protein product of ISG15 to additional interferon stimulated proteins (ISGs) as well as other cellular proteins such as P53 in a process termed protein ISGylation (PubMed:27545325). Plays an essential role in antiviral immunity together with ISG15 by restricting the replication of many viruses including rabies virus, influenza virus, sindbis virus, rotavirus or human cytomegalovirus (PubMed:16254333, PubMed:19073728, PubMed:29056542, PubMed:29743376, PubMed:37722521). For example, ISG15 modification of influenza A protein NS1 disrupts the association of the NS1 with importin-alpha leading to NS1 nuclear import inhibition (PubMed:20133869). ISGylation of human cytomegalovirs protein UL26 regulates its stability and inhibits its activities to suppress NF-kappa-B signaling (PubMed:27564865). {ECO:0000269|PubMed:16254333, ECO:0000269|PubMed:19073728, ECO:0000269|PubMed:20133869, ECO:0000269|PubMed:27545325, ECO:0000269|PubMed:27564865, ECO:0000269|PubMed:29056542, ECO:0000269|PubMed:29743376, ECO:0000269|PubMed:37722521}. |
P43487 | RANBP1 | T15 | ochoa | Ran-specific GTPase-activating protein (Ran-binding protein 1) (RanBP1) | Plays a role in RAN-dependent nucleocytoplasmic transport. Alleviates the TNPO1-dependent inhibition of RAN GTPase activity and mediates the dissociation of RAN from proteins involved in transport into the nucleus (By similarity). Induces a conformation change in the complex formed by XPO1 and RAN that triggers the release of the nuclear export signal of cargo proteins (PubMed:20485264). Promotes the disassembly of the complex formed by RAN and importin beta. Promotes dissociation of RAN from a complex with KPNA2 and CSE1L (By similarity). Required for normal mitotic spindle assembly and normal progress through mitosis via its effect on RAN (PubMed:17671426). Does not increase the RAN GTPase activity by itself, but increases GTP hydrolysis mediated by RANGAP1 (PubMed:7882974). Inhibits RCC1-dependent exchange of RAN-bound GDP by GTP (PubMed:7616957, PubMed:7882974). {ECO:0000250|UniProtKB:P34022, ECO:0000269|PubMed:17671426, ECO:0000269|PubMed:20485264, ECO:0000269|PubMed:7616957, ECO:0000269|PubMed:7882974}. |
P46782 | RPS5 | T14 | ochoa | Small ribosomal subunit protein uS7 (40S ribosomal protein S5) [Cleaved into: Small ribosomal subunit protein uS7, N-terminally processed (40S ribosomal protein S5, N-terminally processed)] | Component of the small ribosomal subunit (PubMed:23636399). The ribosome is a large ribonucleoprotein complex responsible for the synthesis of proteins in the cell (PubMed:23636399). Part of the small subunit (SSU) processome, first precursor of the small eukaryotic ribosomal subunit. During the assembly of the SSU processome in the nucleolus, many ribosome biogenesis factors, an RNA chaperone and ribosomal proteins associate with the nascent pre-rRNA and work in concert to generate RNA folding, modifications, rearrangements and cleavage as well as targeted degradation of pre-ribosomal RNA by the RNA exosome (PubMed:34516797). {ECO:0000269|PubMed:23636399, ECO:0000269|PubMed:34516797}. |
P49207 | RPL34 | T15 | ochoa | Large ribosomal subunit protein eL34 (60S ribosomal protein L34) | Component of the large ribosomal subunit (PubMed:12962325, PubMed:23636399, PubMed:25901680, PubMed:25957688, PubMed:32669547). The ribosome is a large ribonucleoprotein complex responsible for the synthesis of proteins in the cell (PubMed:12962325, PubMed:23636399, PubMed:25901680, PubMed:25957688, PubMed:32669547). {ECO:0000269|PubMed:23636399, ECO:0000269|PubMed:25901680, ECO:0000269|PubMed:25957688, ECO:0000269|PubMed:32669547, ECO:0000305|PubMed:12962325}. |
P49279 | SLC11A1 | Y15 | psp | Natural resistance-associated macrophage protein 1 (NRAMP 1) (Solute carrier family 11 member 1) | Macrophage-specific antiporter that fluxes metal ions in either direction against a proton gradient. Localized to late endosomal lysosomal membranes, delivers bivalent cations from the cytosol into these acidic compartments where they may directly affect antimicrobial activity (PubMed:11237855). Involved in iron metabolism and host natural resistance to infection with intracellular parasites. Pathogen resistance involves sequestration of Fe(2+) and Mn(2+), cofactors of both prokaryotic and eukaryotic catalases and superoxide dismutases, not only to protect the macrophage against its own generation of reactive oxygen species, but to deny the cations to the pathogen for synthesis of its protective enzymes (Probable). {ECO:0000269|PubMed:11237855, ECO:0000305|PubMed:16103355, ECO:0000305|PubMed:16395392}. |
P49757 | NUMB | Y15 | ochoa | Protein numb homolog (h-Numb) (Protein S171) | Regulates clathrin-mediated receptor endocytosis (PubMed:18657069). Plays a role in the process of neurogenesis (By similarity). Required throughout embryonic neurogenesis to maintain neural progenitor cells, also called radial glial cells (RGCs), by allowing their daughter cells to choose progenitor over neuronal cell fate (By similarity). Not required for the proliferation of neural progenitor cells before the onset of neurogenesis. Also involved postnatally in the subventricular zone (SVZ) neurogenesis by regulating SVZ neuroblasts survival and ependymal wall integrity (By similarity). May also mediate local repair of brain ventricular wall damage (By similarity). {ECO:0000250|UniProtKB:Q9QZS3, ECO:0000269|PubMed:18657069}. |
P50402 | EMD | T14 | ochoa | Emerin | Stabilizes and promotes the formation of a nuclear actin cortical network. Stimulates actin polymerization in vitro by binding and stabilizing the pointed end of growing filaments. Inhibits beta-catenin activity by preventing its accumulation in the nucleus. Acts by influencing the nuclear accumulation of beta-catenin through a CRM1-dependent export pathway. Links centrosomes to the nuclear envelope via a microtubule association. Required for proper localization of non-farnesylated prelamin-A/C. Together with NEMP1, contributes to nuclear envelope stiffness in germ cells (PubMed:32923640). EMD and BAF are cooperative cofactors of HIV-1 infection. Association of EMD with the viral DNA requires the presence of BAF and viral integrase. The association of viral DNA with chromatin requires the presence of BAF and EMD. {ECO:0000269|PubMed:15328537, ECO:0000269|PubMed:16680152, ECO:0000269|PubMed:16858403, ECO:0000269|PubMed:17785515, ECO:0000269|PubMed:19323649, ECO:0000269|PubMed:32923640}. |
P50851 | LRBA | T14 | ochoa | Lipopolysaccharide-responsive and beige-like anchor protein (Beige-like protein) (CDC4-like protein) | Involved in coupling signal transduction and vesicle trafficking to enable polarized secretion and/or membrane deposition of immune effector molecules (By similarity). Involved in phagophore growth during mitophagy by regulating ATG9A trafficking to mitochondria (PubMed:33773106). {ECO:0000250|UniProtKB:Q9ESE1, ECO:0000269|PubMed:33773106}. |
P52298 | NCBP2 | Y14 | ochoa | Nuclear cap-binding protein subunit 2 (20 kDa nuclear cap-binding protein) (Cell proliferation-inducing gene 55 protein) (NCBP 20 kDa subunit) (CBP20) (NCBP-interacting protein 1) (NIP1) | Component of the cap-binding complex (CBC), which binds co-transcriptionally to the 5' cap of pre-mRNAs and is involved in various processes such as pre-mRNA splicing, translation regulation, nonsense-mediated mRNA decay, RNA-mediated gene silencing (RNAi) by microRNAs (miRNAs) and mRNA export. The CBC complex is involved in mRNA export from the nucleus via its interaction with ALYREF/THOC4/ALY, leading to the recruitment of the mRNA export machinery to the 5' end of mRNA and to mRNA export in a 5' to 3' direction through the nuclear pore. The CBC complex is also involved in mediating U snRNA and intronless mRNAs export from the nucleus. The CBC complex is essential for a pioneer round of mRNA translation, before steady state translation when the CBC complex is replaced by cytoplasmic cap-binding protein eIF4E. The pioneer round of mRNA translation mediated by the CBC complex plays a central role in nonsense-mediated mRNA decay (NMD), NMD only taking place in mRNAs bound to the CBC complex, but not on eIF4E-bound mRNAs. The CBC complex enhances NMD in mRNAs containing at least one exon-junction complex (EJC) via its interaction with UPF1, promoting the interaction between UPF1 and UPF2. The CBC complex is also involved in 'failsafe' NMD, which is independent of the EJC complex, while it does not participate in Staufen-mediated mRNA decay (SMD). During cell proliferation, the CBC complex is also involved in microRNAs (miRNAs) biogenesis via its interaction with SRRT/ARS2, thereby being required for miRNA-mediated RNA interference. The CBC complex also acts as a negative regulator of PARN, thereby acting as an inhibitor of mRNA deadenylation. In the CBC complex, NCBP2/CBP20 recognizes and binds capped RNAs (m7GpppG-capped RNA) but requires NCBP1/CBP80 to stabilize the movement of its N-terminal loop and lock the CBC into a high affinity cap-binding state with the cap structure. The conventional cap-binding complex with NCBP2 binds both small nuclear RNA (snRNA) and messenger (mRNA) and is involved in their export from the nucleus (PubMed:26382858). {ECO:0000269|PubMed:11551508, ECO:0000269|PubMed:15361857, ECO:0000269|PubMed:17190602, ECO:0000269|PubMed:17363367, ECO:0000269|PubMed:17873884, ECO:0000269|PubMed:18369367, ECO:0000269|PubMed:19632182, ECO:0000269|PubMed:26382858}. |
P55072 | VCP | T14 | ochoa | Transitional endoplasmic reticulum ATPase (TER ATPase) (EC 3.6.4.6) (15S Mg(2+)-ATPase p97 subunit) (Valosin-containing protein) (VCP) | Necessary for the fragmentation of Golgi stacks during mitosis and for their reassembly after mitosis. Involved in the formation of the transitional endoplasmic reticulum (tER). The transfer of membranes from the endoplasmic reticulum to the Golgi apparatus occurs via 50-70 nm transition vesicles which derive from part-rough, part-smooth transitional elements of the endoplasmic reticulum (tER). Vesicle budding from the tER is an ATP-dependent process. The ternary complex containing UFD1, VCP and NPLOC4 binds ubiquitinated proteins and is necessary for the export of misfolded proteins from the ER to the cytoplasm, where they are degraded by the proteasome. The NPLOC4-UFD1-VCP complex regulates spindle disassembly at the end of mitosis and is necessary for the formation of a closed nuclear envelope. Regulates E3 ubiquitin-protein ligase activity of RNF19A. Component of the VCP/p97-AMFR/gp78 complex that participates in the final step of the sterol-mediated ubiquitination and endoplasmic reticulum-associated degradation (ERAD) of HMGCR. Mediates the endoplasmic reticulum-associated degradation of CHRNA3 in cortical neurons as part of the STUB1-VCP-UBXN2A complex (PubMed:26265139). Involved in endoplasmic reticulum stress-induced pre-emptive quality control, a mechanism that selectively attenuates the translocation of newly synthesized proteins into the endoplasmic reticulum and reroutes them to the cytosol for proteasomal degradation (PubMed:26565908). Involved in clearance process by mediating G3BP1 extraction from stress granules (PubMed:29804830, PubMed:34739333). Also involved in DNA damage response: recruited to double-strand breaks (DSBs) sites in a RNF8- and RNF168-dependent manner and promotes the recruitment of TP53BP1 at DNA damage sites (PubMed:22020440, PubMed:22120668). Recruited to stalled replication forks by SPRTN: may act by mediating extraction of DNA polymerase eta (POLH) to prevent excessive translesion DNA synthesis and limit the incidence of mutations induced by DNA damage (PubMed:23042605, PubMed:23042607). Together with SPRTN metalloprotease, involved in the repair of covalent DNA-protein cross-links (DPCs) during DNA synthesis (PubMed:32152270). Involved in interstrand cross-link repair in response to replication stress by mediating unloading of the ubiquitinated CMG helicase complex (By similarity). Mediates extraction of PARP1 trapped to chromatin: recognizes and binds ubiquitinated PARP1 and promotes its removal (PubMed:35013556). Required for cytoplasmic retrotranslocation of stressed/damaged mitochondrial outer-membrane proteins and their subsequent proteasomal degradation (PubMed:16186510, PubMed:21118995). Essential for the maturation of ubiquitin-containing autophagosomes and the clearance of ubiquitinated protein by autophagy (PubMed:20104022, PubMed:27753622). Acts as a negative regulator of type I interferon production by interacting with RIGI: interaction takes place when RIGI is ubiquitinated via 'Lys-63'-linked ubiquitin on its CARD domains, leading to recruit RNF125 and promote ubiquitination and degradation of RIGI (PubMed:26471729). May play a role in the ubiquitin-dependent sorting of membrane proteins to lysosomes where they undergo degradation (PubMed:21822278). May more particularly play a role in caveolins sorting in cells (PubMed:21822278, PubMed:23335559). By controlling the steady-state expression of the IGF1R receptor, indirectly regulates the insulin-like growth factor receptor signaling pathway (PubMed:26692333). {ECO:0000250|UniProtKB:P23787, ECO:0000269|PubMed:15456787, ECO:0000269|PubMed:16168377, ECO:0000269|PubMed:16186510, ECO:0000269|PubMed:20104022, ECO:0000269|PubMed:21118995, ECO:0000269|PubMed:21822278, ECO:0000269|PubMed:22020440, ECO:0000269|PubMed:22120668, ECO:0000269|PubMed:22607976, ECO:0000269|PubMed:23042605, ECO:0000269|PubMed:23042607, ECO:0000269|PubMed:23335559, ECO:0000269|PubMed:26265139, ECO:0000269|PubMed:26471729, ECO:0000269|PubMed:26565908, ECO:0000269|PubMed:26692333, ECO:0000269|PubMed:27753622, ECO:0000269|PubMed:29804830, ECO:0000269|PubMed:32152270, ECO:0000269|PubMed:34739333, ECO:0000269|PubMed:35013556}. |
P61978 | HNRNPK | T15 | ochoa | Heterogeneous nuclear ribonucleoprotein K (hnRNP K) (Transformation up-regulated nuclear protein) (TUNP) | One of the major pre-mRNA-binding proteins. Binds tenaciously to poly(C) sequences. Likely to play a role in the nuclear metabolism of hnRNAs, particularly for pre-mRNAs that contain cytidine-rich sequences. Can also bind poly(C) single-stranded DNA. Plays an important role in p53/TP53 response to DNA damage, acting at the level of both transcription activation and repression. When sumoylated, acts as a transcriptional coactivator of p53/TP53, playing a role in p21/CDKN1A and 14-3-3 sigma/SFN induction (By similarity). As far as transcription repression is concerned, acts by interacting with long intergenic RNA p21 (lincRNA-p21), a non-coding RNA induced by p53/TP53. This interaction is necessary for the induction of apoptosis, but not cell cycle arrest. As part of a ribonucleoprotein complex composed at least of ZNF827, HNRNPL and the circular RNA circZNF827 that nucleates the complex on chromatin, may negatively regulate the transcription of genes involved in neuronal differentiation (PubMed:33174841). {ECO:0000250, ECO:0000269|PubMed:16360036, ECO:0000269|PubMed:20673990, ECO:0000269|PubMed:22825850, ECO:0000269|PubMed:33174841}. |
P62979 | RPS27A | T14 | ochoa | Ubiquitin-ribosomal protein eS31 fusion protein (Ubiquitin carboxyl extension protein 80) [Cleaved into: Ubiquitin; Small ribosomal subunit protein eS31 (40S ribosomal protein S27a)] | [Ubiquitin]: Exists either covalently attached to another protein, or free (unanchored). When covalently bound, it is conjugated to target proteins via an isopeptide bond either as a monomer (monoubiquitin), a polymer linked via different Lys residues of the ubiquitin (polyubiquitin chains) or a linear polymer linked via the initiator Met of the ubiquitin (linear polyubiquitin chains). Polyubiquitin chains, when attached to a target protein, have different functions depending on the Lys residue of the ubiquitin that is linked: Lys-6-linked may be involved in DNA repair; Lys-11-linked is involved in ERAD (endoplasmic reticulum-associated degradation) and in cell-cycle regulation; Lys-29-linked is involved in proteotoxic stress response and cell cycle; Lys-33-linked is involved in kinase modification; Lys-48-linked is involved in protein degradation via the proteasome; Lys-63-linked is involved in endocytosis, DNA-damage responses as well as in signaling processes leading to activation of the transcription factor NF-kappa-B. Linear polymer chains formed via attachment by the initiator Met lead to cell signaling. Ubiquitin is usually conjugated to Lys residues of target proteins, however, in rare cases, conjugation to Cys or Ser residues has been observed. When polyubiquitin is free (unanchored-polyubiquitin), it also has distinct roles, such as in activation of protein kinases, and in signaling. {ECO:0000269|PubMed:16543144, ECO:0000269|PubMed:34239127, ECO:0000303|PubMed:19754430}.; FUNCTION: [Small ribosomal subunit protein eS31]: Component of the 40S subunit of the ribosome (PubMed:23636399, PubMed:9582194). Part of the small subunit (SSU) processome, first precursor of the small eukaryotic ribosomal subunit. During the assembly of the SSU processome in the nucleolus, many ribosome biogenesis factors, an RNA chaperone and ribosomal proteins associate with the nascent pre-rRNA and work in concert to generate RNA folding, modifications, rearrangements and cleavage as well as targeted degradation of pre-ribosomal RNA by the RNA exosome (PubMed:23636399, PubMed:34516797). {ECO:0000269|PubMed:23636399, ECO:0000269|PubMed:34516797, ECO:0000305|PubMed:9582194}. |
P62987 | UBA52 | T14 | ochoa | Ubiquitin-ribosomal protein eL40 fusion protein (CEP52) (Ubiquitin A-52 residue ribosomal protein fusion product 1) [Cleaved into: Ubiquitin; Large ribosomal subunit protein eL40 (60S ribosomal protein L40) (rpL40)] | [Ubiquitin]: Exists either covalently attached to another protein, or free (unanchored). When covalently bound, it is conjugated to target proteins via an isopeptide bond either as a monomer (monoubiquitin), a polymer linked via different Lys residues of the ubiquitin (polyubiquitin chains) or a linear polymer linked via the initiator Met of the ubiquitin (linear polyubiquitin chains). Polyubiquitin chains, when attached to a target protein, have different functions depending on the Lys residue of the ubiquitin that is linked: Lys-6-linked may be involved in DNA repair; Lys-11-linked is involved in ERAD (endoplasmic reticulum-associated degradation) and in cell-cycle regulation; Lys-29-linked is involved in proteotoxic stress response and cell cycle; Lys-33-linked is involved in kinase modification; Lys-48-linked is involved in protein degradation via the proteasome; Lys-63-linked is involved in endocytosis, DNA-damage responses as well as in signaling processes leading to activation of the transcription factor NF-kappa-B. Linear polymer chains formed via attachment by the initiator Met lead to cell signaling. Ubiquitin is usually conjugated to Lys residues of target proteins, however, in rare cases, conjugation to Cys or Ser residues has been observed. When polyubiquitin is free (unanchored-polyubiquitin), it also has distinct roles, such as in activation of protein kinases, and in signaling. {ECO:0000269|PubMed:16543144, ECO:0000269|PubMed:34239127, ECO:0000303|PubMed:19754430}.; FUNCTION: [Large ribosomal subunit protein eL40]: Component of the 60S subunit of the ribosome (PubMed:23169626, PubMed:23636399, PubMed:32669547, PubMed:39048817, PubMed:39103523). Ribosomal protein L40 is essential for translation of a subset of cellular transcripts, and especially for cap-dependent translation of vesicular stomatitis virus mRNAs (PubMed:23169626, PubMed:23636399, PubMed:32669547, PubMed:39048817, PubMed:39103523). {ECO:0000269|PubMed:23169626, ECO:0000269|PubMed:23636399, ECO:0000269|PubMed:32669547, ECO:0000269|PubMed:39048817, ECO:0000269|PubMed:39103523}. |
P78563 | ADARB1 | T14 | ochoa | Double-stranded RNA-specific editase 1 (EC 3.5.4.37) (RNA-editing deaminase 1) (RNA-editing enzyme 1) (dsRNA adenosine deaminase) | Catalyzes the hydrolytic deamination of adenosine to inosine in double-stranded RNA (dsRNA) referred to as A-to-I RNA editing. This may affect gene expression and function in a number of ways that include mRNA translation by changing codons and hence the amino acid sequence of proteins; pre-mRNA splicing by altering splice site recognition sequences; RNA stability by changing sequences involved in nuclease recognition; genetic stability in the case of RNA virus genomes by changing sequences during viral RNA replication; and RNA structure-dependent activities such as microRNA production or targeting or protein-RNA interactions. Can edit both viral and cellular RNAs and can edit RNAs at multiple sites (hyper-editing) or at specific sites (site-specific editing). Its cellular RNA substrates include: bladder cancer-associated protein (BLCAP), neurotransmitter receptors for glutamate (GRIA2 and GRIK2) and serotonin (HTR2C), GABA receptor (GABRA3) and potassium voltage-gated channel (KCNA1). Site-specific RNA editing of transcripts encoding these proteins results in amino acid substitutions which consequently alter their functional activities. Edits GRIA2 at both the Q/R and R/G sites efficiently but converts the adenosine in hotspot1 much less efficiently. Can exert a proviral effect towards human immunodeficiency virus type 1 (HIV-1) and enhances its replication via both an editing-dependent and editing-independent mechanism. The former involves editing of adenosines in the 5'UTR while the latter occurs via suppression of EIF2AK2/PKR activation and function. Can inhibit cell proliferation and migration and can stimulate exocytosis. {ECO:0000269|PubMed:18178553, ECO:0000269|PubMed:19908260, ECO:0000269|PubMed:21289159}.; FUNCTION: [Isoform 1]: Has a lower catalytic activity than isoform 2. {ECO:0000269|PubMed:9149227}.; FUNCTION: [Isoform 2]: Has a higher catalytic activity than isoform 1. {ECO:0000269|PubMed:9149227}. |
Q00526 | CDK3 | T14 | ochoa|psp | Cyclin-dependent kinase 3 (EC 2.7.11.22) (Cell division protein kinase 3) | Serine/threonine-protein kinase that plays a critical role in the control of the eukaryotic cell cycle; involved in G0-G1 and G1-S cell cycle transitions. Interacts with CCNC/cyclin-C during interphase. Phosphorylates histone H1, ATF1, RB1 and CABLES1. ATF1 phosphorylation triggers ATF1 transactivation and transcriptional activities, and promotes cell proliferation and transformation. CDK3/cyclin-C mediated RB1 phosphorylation is required for G0-G1 transition. Promotes G1-S transition probably by contributing to the activation of E2F1, E2F2 and E2F3 in a RB1-independent manner. {ECO:0000269|PubMed:15084261, ECO:0000269|PubMed:18794154, ECO:0000269|PubMed:8846921}. |
Q00526 | CDK3 | Y15 | ochoa|psp | Cyclin-dependent kinase 3 (EC 2.7.11.22) (Cell division protein kinase 3) | Serine/threonine-protein kinase that plays a critical role in the control of the eukaryotic cell cycle; involved in G0-G1 and G1-S cell cycle transitions. Interacts with CCNC/cyclin-C during interphase. Phosphorylates histone H1, ATF1, RB1 and CABLES1. ATF1 phosphorylation triggers ATF1 transactivation and transcriptional activities, and promotes cell proliferation and transformation. CDK3/cyclin-C mediated RB1 phosphorylation is required for G0-G1 transition. Promotes G1-S transition probably by contributing to the activation of E2F1, E2F2 and E2F3 in a RB1-independent manner. {ECO:0000269|PubMed:15084261, ECO:0000269|PubMed:18794154, ECO:0000269|PubMed:8846921}. |
Q00535 | CDK5 | T14 | ochoa | Cyclin-dependent kinase 5 (EC 2.7.11.1) (Cell division protein kinase 5) (Cyclin-dependent-like kinase 5) (Serine/threonine-protein kinase PSSALRE) (Tau protein kinase II catalytic subunit) (TPKII catalytic subunit) | Proline-directed serine/threonine-protein kinase essential for neuronal cell cycle arrest and differentiation and may be involved in apoptotic cell death in neuronal diseases by triggering abortive cell cycle re-entry. Interacts with D1 and D3-type G1 cyclins. Phosphorylates SRC, NOS3, VIM/vimentin, p35/CDK5R1, MEF2A, SIPA1L1, SH3GLB1, PXN, PAK1, MCAM/MUC18, SEPT5, SYN1, DNM1, AMPH, SYNJ1, CDK16, RAC1, RHOA, CDC42, TONEBP/NFAT5, MAPT/TAU, MAP1B, histone H1, p53/TP53, HDAC1, APEX1, PTK2/FAK1, huntingtin/HTT, ATM, MAP2, NEFH and NEFM. Regulates several neuronal development and physiological processes including neuronal survival, migration and differentiation, axonal and neurite growth, synaptogenesis, oligodendrocyte differentiation, synaptic plasticity and neurotransmission, by phosphorylating key proteins. Negatively regulates the CACNA1B/CAV2.2 -mediated Ca(2+) release probability at hippocampal neuronal soma and synaptic terminals (By similarity). Activated by interaction with CDK5R1 (p35) and CDK5R2 (p39), especially in postmitotic neurons, and promotes CDK5R1 (p35) expression in an autostimulation loop. Phosphorylates many downstream substrates such as Rho and Ras family small GTPases (e.g. PAK1, RAC1, RHOA, CDC42) or microtubule-binding proteins (e.g. MAPT/TAU, MAP2, MAP1B), and modulates actin dynamics to regulate neurite growth and/or spine morphogenesis. Also phosphorylates exocytosis associated proteins such as MCAM/MUC18, SEPT5, SYN1, and CDK16/PCTAIRE1 as well as endocytosis associated proteins such as DNM1, AMPH and SYNJ1 at synaptic terminals. In the mature central nervous system (CNS), regulates neurotransmitter movements by phosphorylating substrates associated with neurotransmitter release and synapse plasticity; synaptic vesicle exocytosis, vesicles fusion with the presynaptic membrane, and endocytosis. Promotes cell survival by activating anti-apoptotic proteins BCL2 and STAT3, and negatively regulating of JNK3/MAPK10 activity. Phosphorylation of p53/TP53 in response to genotoxic and oxidative stresses enhances its stabilization by preventing ubiquitin ligase-mediated proteasomal degradation, and induces transactivation of p53/TP53 target genes, thus regulating apoptosis. Phosphorylation of p35/CDK5R1 enhances its stabilization by preventing calpain-mediated proteolysis producing p25/CDK5R1 and avoiding ubiquitin ligase-mediated proteasomal degradation. During aberrant cell-cycle activity and DNA damage, p25/CDK5 activity elicits cell-cycle activity and double-strand DNA breaks that precedes neuronal death by deregulating HDAC1. DNA damage triggered phosphorylation of huntingtin/HTT in nuclei of neurons protects neurons against polyglutamine expansion as well as DNA damage mediated toxicity. Phosphorylation of PXN reduces its interaction with PTK2/FAK1 in matrix-cell focal adhesions (MCFA) during oligodendrocytes (OLs) differentiation. Negative regulator of Wnt/beta-catenin signaling pathway. Activator of the GAIT (IFN-gamma-activated inhibitor of translation) pathway, which suppresses expression of a post-transcriptional regulon of proinflammatory genes in myeloid cells; phosphorylates the linker domain of glutamyl-prolyl tRNA synthetase (EPRS) in a IFN-gamma-dependent manner, the initial event in assembly of the GAIT complex. Phosphorylation of SH3GLB1 is required for autophagy induction in starved neurons. Phosphorylation of TONEBP/NFAT5 in response to osmotic stress mediates its rapid nuclear localization. MEF2 is inactivated by phosphorylation in nucleus in response to neurotoxin, thus leading to neuronal apoptosis. APEX1 AP-endodeoxyribonuclease is repressed by phosphorylation, resulting in accumulation of DNA damage and contributing to neuronal death. NOS3 phosphorylation down regulates NOS3-derived nitrite (NO) levels. SRC phosphorylation mediates its ubiquitin-dependent degradation and thus leads to cytoskeletal reorganization. May regulate endothelial cell migration and angiogenesis via the modulation of lamellipodia formation. Involved in dendritic spine morphogenesis by mediating the EFNA1-EPHA4 signaling. The complex p35/CDK5 participates in the regulation of the circadian clock by modulating the function of CLOCK protein: phosphorylates CLOCK at 'Thr-451' and 'Thr-461' and regulates the transcriptional activity of the CLOCK-BMAL1 heterodimer in association with altered stability and subcellular distribution. {ECO:0000250|UniProtKB:Q03114, ECO:0000269|PubMed:12393264, ECO:0000269|PubMed:12691662, ECO:0000269|PubMed:15992363, ECO:0000269|PubMed:17009320, ECO:0000269|PubMed:17121855, ECO:0000269|PubMed:17591690, ECO:0000269|PubMed:17611284, ECO:0000269|PubMed:17671990, ECO:0000269|PubMed:18042622, ECO:0000269|PubMed:19081376, ECO:0000269|PubMed:19693690, ECO:0000269|PubMed:20061803, ECO:0000269|PubMed:20213743, ECO:0000269|PubMed:20826806, ECO:0000269|PubMed:21209322, ECO:0000269|PubMed:21220307, ECO:0000269|PubMed:21442427, ECO:0000269|PubMed:21465480, ECO:0000269|PubMed:21499257, ECO:0000269|PubMed:24235147, ECO:0000269|PubMed:9822744}. |
Q00535 | CDK5 | Y15 | ochoa|psp | Cyclin-dependent kinase 5 (EC 2.7.11.1) (Cell division protein kinase 5) (Cyclin-dependent-like kinase 5) (Serine/threonine-protein kinase PSSALRE) (Tau protein kinase II catalytic subunit) (TPKII catalytic subunit) | Proline-directed serine/threonine-protein kinase essential for neuronal cell cycle arrest and differentiation and may be involved in apoptotic cell death in neuronal diseases by triggering abortive cell cycle re-entry. Interacts with D1 and D3-type G1 cyclins. Phosphorylates SRC, NOS3, VIM/vimentin, p35/CDK5R1, MEF2A, SIPA1L1, SH3GLB1, PXN, PAK1, MCAM/MUC18, SEPT5, SYN1, DNM1, AMPH, SYNJ1, CDK16, RAC1, RHOA, CDC42, TONEBP/NFAT5, MAPT/TAU, MAP1B, histone H1, p53/TP53, HDAC1, APEX1, PTK2/FAK1, huntingtin/HTT, ATM, MAP2, NEFH and NEFM. Regulates several neuronal development and physiological processes including neuronal survival, migration and differentiation, axonal and neurite growth, synaptogenesis, oligodendrocyte differentiation, synaptic plasticity and neurotransmission, by phosphorylating key proteins. Negatively regulates the CACNA1B/CAV2.2 -mediated Ca(2+) release probability at hippocampal neuronal soma and synaptic terminals (By similarity). Activated by interaction with CDK5R1 (p35) and CDK5R2 (p39), especially in postmitotic neurons, and promotes CDK5R1 (p35) expression in an autostimulation loop. Phosphorylates many downstream substrates such as Rho and Ras family small GTPases (e.g. PAK1, RAC1, RHOA, CDC42) or microtubule-binding proteins (e.g. MAPT/TAU, MAP2, MAP1B), and modulates actin dynamics to regulate neurite growth and/or spine morphogenesis. Also phosphorylates exocytosis associated proteins such as MCAM/MUC18, SEPT5, SYN1, and CDK16/PCTAIRE1 as well as endocytosis associated proteins such as DNM1, AMPH and SYNJ1 at synaptic terminals. In the mature central nervous system (CNS), regulates neurotransmitter movements by phosphorylating substrates associated with neurotransmitter release and synapse plasticity; synaptic vesicle exocytosis, vesicles fusion with the presynaptic membrane, and endocytosis. Promotes cell survival by activating anti-apoptotic proteins BCL2 and STAT3, and negatively regulating of JNK3/MAPK10 activity. Phosphorylation of p53/TP53 in response to genotoxic and oxidative stresses enhances its stabilization by preventing ubiquitin ligase-mediated proteasomal degradation, and induces transactivation of p53/TP53 target genes, thus regulating apoptosis. Phosphorylation of p35/CDK5R1 enhances its stabilization by preventing calpain-mediated proteolysis producing p25/CDK5R1 and avoiding ubiquitin ligase-mediated proteasomal degradation. During aberrant cell-cycle activity and DNA damage, p25/CDK5 activity elicits cell-cycle activity and double-strand DNA breaks that precedes neuronal death by deregulating HDAC1. DNA damage triggered phosphorylation of huntingtin/HTT in nuclei of neurons protects neurons against polyglutamine expansion as well as DNA damage mediated toxicity. Phosphorylation of PXN reduces its interaction with PTK2/FAK1 in matrix-cell focal adhesions (MCFA) during oligodendrocytes (OLs) differentiation. Negative regulator of Wnt/beta-catenin signaling pathway. Activator of the GAIT (IFN-gamma-activated inhibitor of translation) pathway, which suppresses expression of a post-transcriptional regulon of proinflammatory genes in myeloid cells; phosphorylates the linker domain of glutamyl-prolyl tRNA synthetase (EPRS) in a IFN-gamma-dependent manner, the initial event in assembly of the GAIT complex. Phosphorylation of SH3GLB1 is required for autophagy induction in starved neurons. Phosphorylation of TONEBP/NFAT5 in response to osmotic stress mediates its rapid nuclear localization. MEF2 is inactivated by phosphorylation in nucleus in response to neurotoxin, thus leading to neuronal apoptosis. APEX1 AP-endodeoxyribonuclease is repressed by phosphorylation, resulting in accumulation of DNA damage and contributing to neuronal death. NOS3 phosphorylation down regulates NOS3-derived nitrite (NO) levels. SRC phosphorylation mediates its ubiquitin-dependent degradation and thus leads to cytoskeletal reorganization. May regulate endothelial cell migration and angiogenesis via the modulation of lamellipodia formation. Involved in dendritic spine morphogenesis by mediating the EFNA1-EPHA4 signaling. The complex p35/CDK5 participates in the regulation of the circadian clock by modulating the function of CLOCK protein: phosphorylates CLOCK at 'Thr-451' and 'Thr-461' and regulates the transcriptional activity of the CLOCK-BMAL1 heterodimer in association with altered stability and subcellular distribution. {ECO:0000250|UniProtKB:Q03114, ECO:0000269|PubMed:12393264, ECO:0000269|PubMed:12691662, ECO:0000269|PubMed:15992363, ECO:0000269|PubMed:17009320, ECO:0000269|PubMed:17121855, ECO:0000269|PubMed:17591690, ECO:0000269|PubMed:17611284, ECO:0000269|PubMed:17671990, ECO:0000269|PubMed:18042622, ECO:0000269|PubMed:19081376, ECO:0000269|PubMed:19693690, ECO:0000269|PubMed:20061803, ECO:0000269|PubMed:20213743, ECO:0000269|PubMed:20826806, ECO:0000269|PubMed:21209322, ECO:0000269|PubMed:21220307, ECO:0000269|PubMed:21442427, ECO:0000269|PubMed:21465480, ECO:0000269|PubMed:21499257, ECO:0000269|PubMed:24235147, ECO:0000269|PubMed:9822744}. |
Q01130 | SRSF2 | T14 | ochoa | Serine/arginine-rich splicing factor 2 (Protein PR264) (Splicing component, 35 kDa) (Splicing factor SC35) (SC-35) (Splicing factor, arginine/serine-rich 2) | Necessary for the splicing of pre-mRNA. It is required for formation of the earliest ATP-dependent splicing complex and interacts with spliceosomal components bound to both the 5'- and 3'-splice sites during spliceosome assembly. It also is required for ATP-dependent interactions of both U1 and U2 snRNPs with pre-mRNA. Interacts with other spliceosomal components, via the RS domains, to form a bridge between the 5'- and 3'-splice site binding components, U1 snRNP and U2AF. Binds to purine-rich RNA sequences, either 5'-AGSAGAGTA-3' (S=C or G) or 5'-GTTCGAGTA-3'. Can bind to beta-globin mRNA and commit it to the splicing pathway. The phosphorylated form (by SRPK2) is required for cellular apoptosis in response to cisplatin treatment. {ECO:0000269|PubMed:19592491, ECO:0000269|PubMed:21157427}. |
Q03135 | CAV1 | Y14 | ochoa|psp | Caveolin-1 | May act as a scaffolding protein within caveolar membranes (PubMed:11751885). Forms a stable heterooligomeric complex with CAV2 that targets to lipid rafts and drives caveolae formation. Mediates the recruitment of CAVIN proteins (CAVIN1/2/3/4) to the caveolae (PubMed:19262564). Interacts directly with G-protein alpha subunits and can functionally regulate their activity (By similarity). Involved in the costimulatory signal essential for T-cell receptor (TCR)-mediated T-cell activation. Its binding to DPP4 induces T-cell proliferation and NF-kappa-B activation in a T-cell receptor/CD3-dependent manner (PubMed:17287217). Recruits CTNNB1 to caveolar membranes and may regulate CTNNB1-mediated signaling through the Wnt pathway (By similarity). Negatively regulates TGFB1-mediated activation of SMAD2/3 by mediating the internalization of TGFBR1 from membrane rafts leading to its subsequent degradation (PubMed:25893292). Binds 20(S)-hydroxycholesterol (20(S)-OHC) (By similarity). {ECO:0000250|UniProtKB:P49817, ECO:0000269|PubMed:11751885, ECO:0000269|PubMed:17287217, ECO:0000269|PubMed:19262564, ECO:0000269|PubMed:25893292}. |
Q03135 | CAV1 | T15 | ochoa | Caveolin-1 | May act as a scaffolding protein within caveolar membranes (PubMed:11751885). Forms a stable heterooligomeric complex with CAV2 that targets to lipid rafts and drives caveolae formation. Mediates the recruitment of CAVIN proteins (CAVIN1/2/3/4) to the caveolae (PubMed:19262564). Interacts directly with G-protein alpha subunits and can functionally regulate their activity (By similarity). Involved in the costimulatory signal essential for T-cell receptor (TCR)-mediated T-cell activation. Its binding to DPP4 induces T-cell proliferation and NF-kappa-B activation in a T-cell receptor/CD3-dependent manner (PubMed:17287217). Recruits CTNNB1 to caveolar membranes and may regulate CTNNB1-mediated signaling through the Wnt pathway (By similarity). Negatively regulates TGFB1-mediated activation of SMAD2/3 by mediating the internalization of TGFBR1 from membrane rafts leading to its subsequent degradation (PubMed:25893292). Binds 20(S)-hydroxycholesterol (20(S)-OHC) (By similarity). {ECO:0000250|UniProtKB:P49817, ECO:0000269|PubMed:11751885, ECO:0000269|PubMed:17287217, ECO:0000269|PubMed:19262564, ECO:0000269|PubMed:25893292}. |
Q13277 | STX3 | T14 | psp | Syntaxin-3 | Potentially involved in docking of synaptic vesicles at presynaptic active zones. Apical receptor involved in membrane fusion of apical vesicles. {ECO:0000269|PubMed:24726755}.; FUNCTION: [Isoform B]: Essential for survival of retinal photoreceetors. {ECO:0000269|PubMed:33974130}.; FUNCTION: [Isoform 3]: Functions as a regulator of gene expression. {ECO:0000269|PubMed:29475951}. |
Q13322 | GRB10 | Y15 | ochoa | Growth factor receptor-bound protein 10 (GRB10 adapter protein) (Insulin receptor-binding protein Grb-IR) | Adapter protein which modulates coupling of a number of cell surface receptor kinases with specific signaling pathways. Binds to, and suppress signals from, activated receptors tyrosine kinases, including the insulin (INSR) and insulin-like growth factor (IGF1R) receptors. The inhibitory effect can be achieved by 2 mechanisms: interference with the signaling pathway and increased receptor degradation. Delays and reduces AKT1 phosphorylation in response to insulin stimulation. Blocks association between INSR and IRS1 and IRS2 and prevents insulin-stimulated IRS1 and IRS2 tyrosine phosphorylation. Recruits NEDD4 to IGF1R, leading to IGF1R ubiquitination, increased internalization and degradation by both the proteasomal and lysosomal pathways. May play a role in mediating insulin-stimulated ubiquitination of INSR, leading to proteasomal degradation. Negatively regulates Wnt signaling by interacting with LRP6 intracellular portion and interfering with the binding of AXIN1 to LRP6. Positive regulator of the KDR/VEGFR-2 signaling pathway. May inhibit NEDD4-mediated degradation of KDR/VEGFR-2. {ECO:0000269|PubMed:12493740, ECO:0000269|PubMed:15060076, ECO:0000269|PubMed:16434550, ECO:0000269|PubMed:17376403}. |
Q13451 | FKBP5 | T15 | ochoa | Peptidyl-prolyl cis-trans isomerase FKBP5 (PPIase FKBP5) (EC 5.2.1.8) (51 kDa FK506-binding protein) (51 kDa FKBP) (FKBP-51) (54 kDa progesterone receptor-associated immunophilin) (Androgen-regulated protein 6) (FF1 antigen) (FK506-binding protein 5) (FKBP-5) (FKBP54) (p54) (HSP90-binding immunophilin) (Rotamase) | Immunophilin protein with PPIase and co-chaperone activities (PubMed:11350175). Component of unligated steroid receptors heterocomplexes through interaction with heat-shock protein 90 (HSP90). Plays a role in the intracellular trafficking of heterooligomeric forms of steroid hormone receptors maintaining the complex into the cytoplasm when unliganded (PubMed:12538866). Acts as a regulator of Akt/AKT1 activity by promoting the interaction between Akt/AKT1 and PHLPP1, thereby enhancing dephosphorylation and subsequent activation of Akt/AKT1 (PubMed:28147277, PubMed:28363942). Interacts with IKBKE and IKBKB which facilitates IKK complex assembly leading to increased IKBKE and IKBKB kinase activity, NF-kappa-B activation, and IFN production (PubMed:26101251, PubMed:31434731). {ECO:0000269|PubMed:11350175, ECO:0000269|PubMed:12538866, ECO:0000269|PubMed:26101251, ECO:0000269|PubMed:28147277, ECO:0000269|PubMed:28363942, ECO:0000269|PubMed:31434731}. |
Q13576 | IQGAP2 | Y14 | psp | Ras GTPase-activating-like protein IQGAP2 | Binds to activated CDC42 and RAC1 but does not seem to stimulate their GTPase activity. Associates with calmodulin. |
Q15019 | SEPTIN2 | T14 | ochoa | Septin-2 (Neural precursor cell expressed developmentally down-regulated protein 5) (NEDD-5) | Filament-forming cytoskeletal GTPase. Forms a filamentous structure with SEPTIN12, SEPTIN6, SEPTIN2 and probably SEPTIN4 at the sperm annulus which is required for the structural integrity and motility of the sperm tail during postmeiotic differentiation (PubMed:25588830). Required for normal organization of the actin cytoskeleton. Plays a role in the biogenesis of polarized columnar-shaped epithelium by maintaining polyglutamylated microtubules, thus facilitating efficient vesicle transport, and by impeding MAP4 binding to tubulin. Required for the progression through mitosis. Forms a scaffold at the midplane of the mitotic splindle required to maintain CENPE localization at kinetochores and consequently chromosome congression. During anaphase, may be required for chromosome segregation and spindle elongation. Plays a role in ciliogenesis and collective cell movements. In cilia, required for the integrity of the diffusion barrier at the base of the primary cilium that prevents diffusion of transmembrane proteins between the cilia and plasma membranes: probably acts by regulating the assembly of the tectonic-like complex (also named B9 complex) by localizing TMEM231 protein. May play a role in the internalization of 2 intracellular microbial pathogens, Listeria monocytogenes and Shigella flexneri. {ECO:0000269|PubMed:15774761, ECO:0000269|PubMed:17803907, ECO:0000269|PubMed:18209106, ECO:0000269|PubMed:19145258, ECO:0000305|PubMed:25588830}. |
Q15233 | NONO | T15 | ochoa | Non-POU domain-containing octamer-binding protein (NonO protein) (54 kDa nuclear RNA- and DNA-binding protein) (p54(nrb)) (p54nrb) (55 kDa nuclear protein) (NMT55) (DNA-binding p52/p100 complex, 52 kDa subunit) | DNA- and RNA binding protein, involved in several nuclear processes (PubMed:11525732, PubMed:12403470, PubMed:26571461). Binds the conventional octamer sequence in double-stranded DNA (PubMed:11525732, PubMed:12403470, PubMed:26571461). Also binds single-stranded DNA and RNA at a site independent of the duplex site (PubMed:11525732, PubMed:12403470, PubMed:26571461). Involved in pre-mRNA splicing, probably as a heterodimer with SFPQ (PubMed:11525732, PubMed:12403470, PubMed:26571461). Interacts with U5 snRNA, probably by binding to a purine-rich sequence located on the 3' side of U5 snRNA stem 1b (PubMed:12403470). Together with PSPC1, required for the formation of nuclear paraspeckles (PubMed:22416126). The SFPQ-NONO heteromer associated with MATR3 may play a role in nuclear retention of defective RNAs (PubMed:11525732). The SFPQ-NONO heteromer may be involved in DNA unwinding by modulating the function of topoisomerase I/TOP1 (PubMed:10858305). The SFPQ-NONO heteromer may be involved in DNA non-homologous end joining (NHEJ) required for double-strand break repair and V(D)J recombination and may stabilize paired DNA ends (PubMed:15590677). In vitro, the complex strongly stimulates DNA end joining, binds directly to the DNA substrates and cooperates with the Ku70/G22P1-Ku80/XRCC5 (Ku) dimer to establish a functional preligation complex (PubMed:15590677). NONO is involved in transcriptional regulation. The SFPQ-NONO-NR5A1 complex binds to the CYP17 promoter and regulates basal and cAMP-dependent transcriptional activity (PubMed:11897684). NONO binds to an enhancer element in long terminal repeats of endogenous intracisternal A particles (IAPs) and activates transcription (By similarity). Regulates the circadian clock by repressing the transcriptional activator activity of the CLOCK-BMAL1 heterodimer (By similarity). Important for the functional organization of GABAergic synapses (By similarity). Plays a specific and important role in the regulation of synaptic RNAs and GPHN/gephyrin scaffold structure, through the regulation of GABRA2 transcript (By similarity). Plays a key role during neuronal differentiation by recruiting TET1 to genomic loci and thereby regulating 5-hydroxymethylcytosine levels (By similarity). Plays a role in the regulation of DNA virus-mediated innate immune response by assembling into the HDP-RNP complex, a complex that serves as a platform for IRF3 phosphorylation and subsequent innate immune response activation through the cGAS-STING pathway (PubMed:28712728, PubMed:30270045). Promotes activation of the cGAS-STING pathway in response to HIV-2 infection: acts by interacting with HIV-2 Capsid protein p24, thereby promoting detection of viral DNA by CGAS, leading to CGAS-mediated inmmune activation (PubMed:30270045). In contrast, the weak interaction with HIV-1 Capsid protein p24 does not allow activation of the cGAS-STING pathway (PubMed:30270045). {ECO:0000250|UniProtKB:Q99K48, ECO:0000269|PubMed:10858305, ECO:0000269|PubMed:11525732, ECO:0000269|PubMed:11897684, ECO:0000269|PubMed:12403470, ECO:0000269|PubMed:15590677, ECO:0000269|PubMed:22416126, ECO:0000269|PubMed:26571461, ECO:0000269|PubMed:28712728, ECO:0000269|PubMed:30270045}. |
Q16254 | E2F4 | T14 | ochoa | Transcription factor E2F4 (E2F-4) | Transcription activator that binds DNA cooperatively with DP proteins through the E2 recognition site, 5'-TTTC[CG]CGC-3' found in the promoter region of a number of genes whose products are involved in cell cycle regulation or in DNA replication. The DRTF1/E2F complex functions in the control of cell-cycle progression from G1 to S phase. E2F4 binds with high affinity to RBL1 and RBL2. In some instances can also bind RB1. Specifically required for multiciliate cell differentiation: together with MCIDAS and E2F5, binds and activate genes required for centriole biogenesis. {ECO:0000250|UniProtKB:Q6DE14, ECO:0000269|PubMed:7958924, ECO:0000269|PubMed:7958925}. |
Q5UIP0 | RIF1 | T15 | ochoa | Telomere-associated protein RIF1 (Rap1-interacting factor 1 homolog) | Key regulator of TP53BP1 that plays a key role in the repair of double-strand DNA breaks (DSBs) in response to DNA damage: acts by promoting non-homologous end joining (NHEJ)-mediated repair of DSBs (PubMed:15342490, PubMed:28241136). In response to DNA damage, interacts with ATM-phosphorylated TP53BP1 (PubMed:23333306, PubMed:28241136). Interaction with TP53BP1 leads to dissociate the interaction between NUDT16L1/TIRR and TP53BP1, thereby unmasking the tandem Tudor-like domain of TP53BP1 and allowing recruitment to DNA DSBs (PubMed:28241136). Once recruited to DSBs, RIF1 and TP53BP1 act by promoting NHEJ-mediated repair of DSBs (PubMed:23333306). In the same time, RIF1 and TP53BP1 specifically counteract the function of BRCA1 by blocking DSBs resection via homologous recombination (HR) during G1 phase (PubMed:23333306). Also required for immunoglobulin class-switch recombination (CSR) during antibody genesis, a process that involves the generation of DNA DSBs (By similarity). Promotes NHEJ of dysfunctional telomeres (By similarity). {ECO:0000250|UniProtKB:Q6PR54, ECO:0000269|PubMed:15342490, ECO:0000269|PubMed:23333306, ECO:0000269|PubMed:28241136}. |
Q68CQ4 | UTP25 | T15 | ochoa | U3 small nucleolar RNA-associated protein 25 homolog (Digestive organ expansion factor homolog) (UTP25 small subunit processor component) | Component of the ribosomal small subunit processome for the biogenesis of ribosomes, functions in pre-ribosomal RNA (pre-rRNA) processing (By similarity). Essential for embryonic development in part through the regulation of p53 pathway. Controls the expansion growth of digestive organs and liver (PubMed:23357851, PubMed:25007945, PubMed:27657329). Also involved in the sympathetic neuronal development (By similarity). Mediates, with CAPN3, the proteasome-independent degradation of p53/TP53 (PubMed:23357851, PubMed:27657329). {ECO:0000250|UniProtKB:Q6PEH4, ECO:0000269|PubMed:23357851, ECO:0000269|PubMed:25007945, ECO:0000269|PubMed:27657329}. |
Q7Z3C6 | ATG9A | Y15 | ochoa|psp | Autophagy-related protein 9A (APG9-like 1) (mATG9) | Phospholipid scramblase involved in autophagy by mediating autophagosomal membrane expansion (PubMed:22456507, PubMed:27510922, PubMed:29437695, PubMed:32513819, PubMed:32610138, PubMed:33106659, PubMed:33468622, PubMed:33850023). Cycles between the preautophagosomal structure/phagophore assembly site (PAS) and the cytoplasmic vesicle pool and supplies membrane for the growing autophagosome (PubMed:16940348, PubMed:22456507, PubMed:33106659). Lipid scramblase activity plays a key role in preautophagosomal structure/phagophore assembly by distributing the phospholipids that arrive through ATG2 (ATG2A or ATG2B) from the cytoplasmic to the luminal leaflet of the bilayer, thereby driving autophagosomal membrane expansion (PubMed:33106659). Also required to supply phosphatidylinositol 4-phosphate to the autophagosome initiation site by recruiting the phosphatidylinositol 4-kinase beta (PI4KB) in a process dependent on ARFIP2, but not ARFIP1 (PubMed:30917996). In addition to autophagy, also plays a role in necrotic cell death (By similarity). {ECO:0000250|UniProtKB:Q68FE2, ECO:0000269|PubMed:16940348, ECO:0000269|PubMed:22456507, ECO:0000269|PubMed:27510922, ECO:0000269|PubMed:29437695, ECO:0000269|PubMed:30917996, ECO:0000269|PubMed:32513819, ECO:0000269|PubMed:32610138, ECO:0000269|PubMed:33106659, ECO:0000269|PubMed:33468622, ECO:0000269|PubMed:33850023}. |
Q86TU7 | SETD3 | T14 | ochoa | Actin-histidine N-methyltransferase (EC 2.1.1.85) (Protein-L-histidine N-tele-methyltransferase) (SET domain-containing protein 3) (hSETD3) | Protein-histidine N-methyltransferase that specifically mediates 3-methylhistidine (tele-methylhistidine) methylation of actin at 'His-73' (PubMed:30526847, PubMed:30626964, PubMed:30785395, PubMed:31388018, PubMed:31993215). Histidine methylation of actin is required for smooth muscle contraction of the laboring uterus during delivery (PubMed:30626964). Does not have protein-lysine N-methyltransferase activity and probably only catalyzes histidine methylation of actin (PubMed:30626964, PubMed:30785395, PubMed:31388018). {ECO:0000269|PubMed:30526847, ECO:0000269|PubMed:30626964, ECO:0000269|PubMed:30785395, ECO:0000269|PubMed:31388018, ECO:0000269|PubMed:31993215}. |
Q86YV0 | RASAL3 | T15 | ochoa | RAS protein activator like-3 | Functions as a Ras GTPase-activating protein. Plays an important role in the expansion and functions of natural killer T (NKT) cells in the liver by negatively regulating RAS activity and the down-stream ERK signaling pathway. {ECO:0000250|UniProtKB:Q8C2K5}. |
Q8IWA5 | SLC44A2 | T14 | ochoa | Choline transporter-like protein 2 (Solute carrier family 44 member 2) | [Isoform 1]: Choline/H+ antiporter, mainly in mitochodria (PubMed:10677542, PubMed:20665236, PubMed:23651124, PubMed:33789160). Also acts as a low-affinity ethanolamine/H+ antiporter, regulating the supply of extracellular ethanolamine (Etn) for the CDP-Etn pathway, redistribute intracellular Etn and balance the CDP-Cho and CDP-Etn arms of the Kennedy pathway (PubMed:33789160). {ECO:0000269|PubMed:10677542, ECO:0000269|PubMed:20665236, ECO:0000269|PubMed:23651124, ECO:0000269|PubMed:33789160}.; FUNCTION: [Isoform 3]: Does not exhibit choline transporter activity. {ECO:0000269|PubMed:10677542, ECO:0000269|PubMed:20665236}. |
Q8IWJ2 | GCC2 | T14 | ochoa | GRIP and coiled-coil domain-containing protein 2 (185 kDa Golgi coiled-coil protein) (GCC185) (CLL-associated antigen KW-11) (CTCL tumor antigen se1-1) (Ran-binding protein 2-like 4) (RanBP2L4) (Renal carcinoma antigen NY-REN-53) | Golgin which probably tethers transport vesicles to the trans-Golgi network (TGN) and regulates vesicular transport between the endosomes and the Golgi. As a RAB9A effector it is involved in recycling of the mannose 6-phosphate receptor from the late endosomes to the TGN. May also play a role in transport between the recycling endosomes and the Golgi. Required for maintenance of the Golgi structure, it is involved in the biogenesis of noncentrosomal, Golgi-associated microtubules through recruitment of CLASP1 and CLASP2. {ECO:0000269|PubMed:16885419, ECO:0000269|PubMed:17488291, ECO:0000269|PubMed:17543864}. |
Q8IY95 | TMEM192 | T15 | ochoa | Transmembrane protein 192 | None |
Q8IZV2 | CMTM8 | T14 | ochoa | CKLF-like MARVEL transmembrane domain-containing protein 8 (Chemokine-like factor superfamily member 8) | None |
Q8N4S9 | MARVELD2 | Y14 | ochoa | MARVEL domain-containing protein 2 (Tricellulin) | Plays a role in the formation of tricellular tight junctions and of epithelial barriers (By similarity). Required for normal hearing via its role in the separation of the endolymphatic and perilymphatic spaces of the organ of Corti in the inner ear, and for normal survival of hair cells in the organ of Corti (PubMed:17186462). {ECO:0000250|UniProtKB:Q3UZP0, ECO:0000269|PubMed:17186462}. |
Q8NAV1 | PRPF38A | T15 | ochoa | Pre-mRNA-splicing factor 38A | Involved in pre-mRNA splicing as a component of the spliceosome. {ECO:0000269|PubMed:26673105, ECO:0000269|PubMed:28781166}. |
Q8NHG8 | ZNRF2 | T15 | ochoa | E3 ubiquitin-protein ligase ZNRF2 (EC 2.3.2.27) (Protein Ells2) (RING finger protein 202) (RING-type E3 ubiquitin transferase ZNRF2) (Zinc/RING finger protein 2) | E3 ubiquitin-protein ligase that plays a role in the establishment and maintenance of neuronal transmission and plasticity. Ubiquitinates the Na(+)/K(+) ATPase alpha-1 subunit/ATP1A1 and thereby influences its endocytosis and/or degradation (PubMed:22797923). Acts also as a positive regulator of mTORC1 activation by amino acids, which functions upstream of the V-ATPase and of Rag-GTPases (PubMed:27244671). In turn, phosphorylation by mTOR leads to its inhibition via targeting to the cytosol allowing a self-regulating feedback mechanism (PubMed:27244671). {ECO:0000269|PubMed:14561866, ECO:0000269|PubMed:22797923, ECO:0000269|PubMed:27244671}. |
Q8WTQ4 | C16orf78 | T14 | ochoa | Uncharacterized protein C16orf78 | None |
Q8WWP7 | GIMAP1 | Y14 | ochoa | GTPase IMAP family member 1 (Immunity-associated protein 1) (hIMAP1) | May regulate lymphocyte survival. Required for normal levels of mature T-lymphocytes and mature B-cells (By similarity). {ECO:0000250}. |
Q8WXS3 | BAALC | Y15 | ochoa | Brain and acute leukemia cytoplasmic protein | May play a synaptic role at the postsynaptic lipid rafts possibly through interaction with CAMK2A. {ECO:0000250|UniProtKB:Q920K5}. |
Q92688 | ANP32B | T15 | ochoa | Acidic leucine-rich nuclear phosphoprotein 32 family member B (Acidic protein rich in leucines) (Putative HLA-DR-associated protein I-2) (PHAPI2) (Silver-stainable protein SSP29) | Multifunctional protein that is involved in the regulation of many processes including cell proliferation, apoptosis, cell cycle progression or transcription (PubMed:18039846, PubMed:20015864). Regulates the proliferation of neuronal stem cells, differentiation of leukemic cells and progression from G1 to S phase of the cell cycle. As negative regulator of caspase-3-dependent apoptosis, may act as an antagonist of ANP32A in regulating tissue homeostasis (PubMed:20015864). Exhibits histone chaperone properties, able to recruit histones to certain promoters, thus regulating the transcription of specific genes (PubMed:18039846, PubMed:20538007). Also plays an essential role in the nucleocytoplasmic transport of specific mRNAs via the uncommon nuclear mRNA export receptor XPO1/CRM1 (PubMed:17178712). Participates in the regulation of adequate adaptive immune responses by acting on mRNA expression and cell proliferation (By similarity). {ECO:0000250|UniProtKB:Q9EST5, ECO:0000269|PubMed:17178712, ECO:0000269|PubMed:18039846, ECO:0000269|PubMed:20015864, ECO:0000269|PubMed:20538007}.; FUNCTION: (Microbial infection) Plays an essential role in influenza A and B viral genome replication (PubMed:31217244, PubMed:33045004). Also plays a role in foamy virus mRNA export from the nucleus to the cytoplasm (PubMed:21159877). {ECO:0000269|PubMed:21159877, ECO:0000269|PubMed:31217244, ECO:0000269|PubMed:33045004}. |
Q92997 | DVL3 | T15 | ochoa|psp | Segment polarity protein dishevelled homolog DVL-3 (Dishevelled-3) (DSH homolog 3) | Involved in the signal transduction pathway mediated by multiple Wnt genes. {ECO:0000250|UniProtKB:Q61062}. |
Q969T4 | UBE2E3 | T15 | ochoa | Ubiquitin-conjugating enzyme E2 E3 (EC 2.3.2.23) (E2 ubiquitin-conjugating enzyme E3) (UbcH9) (Ubiquitin carrier protein E3) (Ubiquitin-conjugating enzyme E2-23 kDa) (Ubiquitin-protein ligase E3) | Accepts ubiquitin from the E1 complex and catalyzes its covalent attachment to other proteins. In vitro catalyzes 'Lys-11'- and 'Lys-48'-, as well as 'Lys-63'-linked polyubiquitination. Participates in the regulation of transepithelial sodium transport in renal cells. {ECO:0000269|PubMed:10343118, ECO:0000269|PubMed:20061386, ECO:0000269|PubMed:27237050}. |
Q96BX8 | MOB3A | T15 | psp | MOB kinase activator 3A (MOB-LAK) (Mob1 homolog 2A) (Mps one binder kinase activator-like 2A) | May regulate the activity of kinases. {ECO:0000250}. |
Q96FC7 | PHYHIPL | T14 | ochoa | Phytanoyl-CoA hydroxylase-interacting protein-like | May play a role in the development of the central system. {ECO:0000250}. |
Q96LR5 | UBE2E2 | T14 | ochoa | Ubiquitin-conjugating enzyme E2 E2 (EC 2.3.2.23) (E2 ubiquitin-conjugating enzyme E2) (UbcH8) (Ubiquitin carrier protein E2) (Ubiquitin-protein ligase E2) | Accepts ubiquitin from the E1 complex and catalyzes its covalent attachment to other proteins. In vitro catalyzes 'Lys-11'- and 'Lys-48'-, as well as 'Lys-63'-linked polyubiquitination. Catalyzes the ISGylation of influenza A virus NS1 protein. {ECO:0000269|PubMed:20061386, ECO:0000269|PubMed:20133869, ECO:0000269|PubMed:27237050, ECO:0000269|PubMed:9371400}. |
Q96LT9 | RNPC3 | T15 | ochoa | RNA-binding region-containing protein 3 (RNA-binding motif protein 40) (RNA-binding protein 40) (U11/U12 small nuclear ribonucleoprotein 65 kDa protein) (U11/U12 snRNP 65 kDa protein) (U11/U12-65K) | Participates in pre-mRNA U12-dependent splicing, performed by the minor spliceosome which removes U12-type introns. U12-type introns comprises less than 1% of all non-coding sequences. Binds to the 3'-stem-loop of m(7)G-capped U12 snRNA. {ECO:0000269|PubMed:16096647, ECO:0000269|PubMed:19447915, ECO:0000269|PubMed:24480542, ECO:0000269|PubMed:29255062}. |
Q96QD9 | FYTTD1 | T14 | ochoa | UAP56-interacting factor (Forty-two-three domain-containing protein 1) (Protein 40-2-3) | Required for mRNA export from the nucleus to the cytoplasm. Acts as an adapter that uses the DDX39B/UAP56-NFX1 pathway to ensure efficient mRNA export and delivering to the nuclear pore. Associates with spliced and unspliced mRNAs simultaneously with ALYREF/THOC4. {ECO:0000269|PubMed:19836239}. |
Q96S97 | MYADM | T14 | ochoa | Myeloid-associated differentiation marker (Protein SB135) | None |
Q96S97 | MYADM | T15 | ochoa | Myeloid-associated differentiation marker (Protein SB135) | None |
Q99962 | SH3GL2 | T14 | psp | Endophilin-A1 (EEN-B1) (Endophilin-1) (SH3 domain protein 2A) (SH3 domain-containing GRB2-like protein 2) | Implicated in synaptic vesicle endocytosis. May recruit other proteins to membranes with high curvature. Required for BDNF-dependent dendrite outgrowth. Cooperates with SH3GL2 to mediate BDNF-NTRK2 early endocytic trafficking and signaling from early endosomes. {ECO:0000250|UniProtKB:Q62420}. |
Q9H0H3 | KLHL25 | T15 | ochoa | Kelch-like protein 25 (Ectoderm-neural cortex protein 2) (ENC-2) | Substrate-specific adapter of a BCR (BTB-CUL3-RBX1) E3 ubiquitin ligase complex involved in various processes, such as translation homeostasis and lipid synthesis (PubMed:22578813, PubMed:27664236, PubMed:34491895). The BCR(KLHL25) ubiquitin ligase complex acts by mediating ubiquitination of hypophosphorylated EIF4EBP1 (4E-BP1): ubiquitination and subsequent degradation of hypophosphorylated EIF4EBP1 (4E-BP1) probably serves as a homeostatic mechanism to maintain translation and prevent eIF4E inhibition when eIF4E levels are low (PubMed:22578813). The BCR(KLHL25) complex does not target EIF4EBP1 (4E-BP1) when it is hyperphosphorylated or associated with eIF4E (PubMed:22578813). The BCR(KLHL25) complex also acts as a regulator of lipid synthesis by mediating ubiquitination and degradation of ACLY, thereby inhibiting lipid synthesis (PubMed:27664236, PubMed:34491895). BCR(KLHL25)-mediated degradation of ACLY promotes fatty acid oxidation and is required for differentiation of inducible regulatory T (iTreg) cells (PubMed:34491895). {ECO:0000269|PubMed:22578813, ECO:0000269|PubMed:27664236, ECO:0000269|PubMed:34491895}. |
Q9H0U9 | TSPYL1 | T15 | ochoa | Testis-specific Y-encoded-like protein 1 (TSPY-like protein 1) | None |
Q9H6S3 | EPS8L2 | T14 | ochoa | Epidermal growth factor receptor kinase substrate 8-like protein 2 (EPS8-like protein 2) (Epidermal growth factor receptor pathway substrate 8-related protein 2) (EPS8-related protein 2) | Stimulates guanine exchange activity of SOS1. May play a role in membrane ruffling and remodeling of the actin cytoskeleton. In the cochlea, is required for stereocilia maintenance in adult hair cells (By similarity). {ECO:0000250|UniProtKB:Q99K30, ECO:0000269|PubMed:14565974}. |
Q9H8V3 | ECT2 | T14 | ochoa | Protein ECT2 (Epithelial cell-transforming sequence 2 oncogene) | Guanine nucleotide exchange factor (GEF) that catalyzes the exchange of GDP for GTP. Promotes guanine nucleotide exchange on the Rho family members of small GTPases, like RHOA, RHOC, RAC1 and CDC42. Required for signal transduction pathways involved in the regulation of cytokinesis. Component of the centralspindlin complex that serves as a microtubule-dependent and Rho-mediated signaling required for the myosin contractile ring formation during the cell cycle cytokinesis. Regulates the translocation of RHOA from the central spindle to the equatorial region. Plays a role in the control of mitotic spindle assembly; regulates the activation of CDC42 in metaphase for the process of spindle fibers attachment to kinetochores before chromosome congression. Involved in the regulation of epithelial cell polarity; participates in the formation of epithelial tight junctions in a polarity complex PARD3-PARD6-protein kinase PRKCQ-dependent manner. Plays a role in the regulation of neurite outgrowth. Inhibits phenobarbital (PB)-induced NR1I3 nuclear translocation. Stimulates the activity of RAC1 through its association with the oncogenic PARD6A-PRKCI complex in cancer cells, thereby acting to coordinately drive tumor cell proliferation and invasion. Also stimulates genotoxic stress-induced RHOB activity in breast cancer cells leading to their cell death. {ECO:0000269|PubMed:10579713, ECO:0000269|PubMed:14645260, ECO:0000269|PubMed:15254234, ECO:0000269|PubMed:15545273, ECO:0000269|PubMed:15642749, ECO:0000269|PubMed:16103226, ECO:0000269|PubMed:16170345, ECO:0000269|PubMed:16236794, ECO:0000269|PubMed:16495035, ECO:0000269|PubMed:19129481, ECO:0000269|PubMed:19468300, ECO:0000269|PubMed:19617897, ECO:0000269|PubMed:21189248, ECO:0000269|PubMed:21373644, ECO:0000269|PubMed:25068414, ECO:0000269|PubMed:31888991}. |
Q9NQC7 | CYLD | Y15 | ochoa|psp | Ubiquitin carboxyl-terminal hydrolase CYLD (EC 3.4.19.12) (Deubiquitinating enzyme CYLD) (Ubiquitin thioesterase CYLD) (Ubiquitin-specific-processing protease CYLD) | Deubiquitinase that specifically cleaves 'Lys-63'- and linear 'Met-1'-linked polyubiquitin chains and is involved in NF-kappa-B activation and TNF-alpha-induced necroptosis (PubMed:18313383, PubMed:18636086, PubMed:26670046, PubMed:26997266, PubMed:27458237, PubMed:27591049, PubMed:27746020, PubMed:29291351, PubMed:32185393). Negatively regulates NF-kappa-B activation by deubiquitinating upstream signaling factors (PubMed:12917689, PubMed:12917691, PubMed:32185393). Contributes to the regulation of cell survival, proliferation and differentiation via its effects on NF-kappa-B activation (PubMed:12917690). Negative regulator of Wnt signaling (PubMed:20227366). Inhibits HDAC6 and thereby promotes acetylation of alpha-tubulin and stabilization of microtubules (PubMed:19893491). Plays a role in the regulation of microtubule dynamics, and thereby contributes to the regulation of cell proliferation, cell polarization, cell migration, and angiogenesis (PubMed:18222923, PubMed:20194890). Required for normal cell cycle progress and normal cytokinesis (PubMed:17495026, PubMed:19893491). Inhibits nuclear translocation of NF-kappa-B (PubMed:18636086). Plays a role in the regulation of inflammation and the innate immune response, via its effects on NF-kappa-B activation (PubMed:18636086). Dispensable for the maturation of intrathymic natural killer cells, but required for the continued survival of immature natural killer cells (By similarity). Negatively regulates TNFRSF11A signaling and osteoclastogenesis (By similarity). Involved in the regulation of ciliogenesis, allowing ciliary basal bodies to migrate and dock to the plasma membrane; this process does not depend on NF-kappa-B activation (By similarity). Ability to remove linear ('Met-1'-linked) polyubiquitin chains regulates innate immunity and TNF-alpha-induced necroptosis: recruited to the LUBAC complex via interaction with SPATA2 and restricts linear polyubiquitin formation on target proteins (PubMed:26670046, PubMed:26997266, PubMed:27458237, PubMed:27591049). Regulates innate immunity by restricting linear polyubiquitin formation on RIPK2 in response to NOD2 stimulation (PubMed:26997266). Involved in TNF-alpha-induced necroptosis by removing linear ('Met-1'-linked) polyubiquitin chains from RIPK1, thereby regulating the kinase activity of RIPK1 (By similarity). Negatively regulates intestinal inflammation by removing 'Lys-63' linked polyubiquitin chain of NLRP6, thereby reducing the interaction between NLRP6 and PYCARD/ASC and formation of the NLRP6 inflammasome (By similarity). Does not catalyze deubiquitination of heterotypic 'Lys-63'-/'Lys-48'-linked branched ubiquitin chains (PubMed:27746020). Removes 'Lys-63' linked polyubiquitin chain of MAP3K7, which inhibits phosphorylation and blocks downstream activation of the JNK-p38 kinase cascades (PubMed:29291351). Also removes 'Lys-63'-linked polyubiquitin chains of MAP3K1 and MA3P3K3, which inhibit their interaction with MAP2K1 and MAP2K2 (PubMed:34497368). {ECO:0000250|UniProtKB:Q80TQ2, ECO:0000269|PubMed:12917689, ECO:0000269|PubMed:12917690, ECO:0000269|PubMed:12917691, ECO:0000269|PubMed:17495026, ECO:0000269|PubMed:18222923, ECO:0000269|PubMed:18313383, ECO:0000269|PubMed:18636086, ECO:0000269|PubMed:19893491, ECO:0000269|PubMed:20194890, ECO:0000269|PubMed:20227366, ECO:0000269|PubMed:26670046, ECO:0000269|PubMed:26997266, ECO:0000269|PubMed:27458237, ECO:0000269|PubMed:27591049, ECO:0000269|PubMed:27746020, ECO:0000269|PubMed:29291351, ECO:0000269|PubMed:32185393, ECO:0000269|PubMed:34497368}. |
Q9NR30 | DDX21 | T15 | ochoa | Nucleolar RNA helicase 2 (EC 3.6.4.13) (DEAD box protein 21) (Gu-alpha) (Nucleolar RNA helicase Gu) (Nucleolar RNA helicase II) (RH II/Gu) | RNA helicase that acts as a sensor of the transcriptional status of both RNA polymerase (Pol) I and II: promotes ribosomal RNA (rRNA) processing and transcription from polymerase II (Pol II) (PubMed:25470060, PubMed:28790157). Binds various RNAs, such as rRNAs, snoRNAs, 7SK and, at lower extent, mRNAs (PubMed:25470060). In the nucleolus, localizes to rDNA locus, where it directly binds rRNAs and snoRNAs, and promotes rRNA transcription, processing and modification. Required for rRNA 2'-O-methylation, possibly by promoting the recruitment of late-acting snoRNAs SNORD56 and SNORD58 with pre-ribosomal complexes (PubMed:25470060, PubMed:25477391). In the nucleoplasm, binds 7SK RNA and is recruited to the promoters of Pol II-transcribed genes: acts by facilitating the release of P-TEFb from inhibitory 7SK snRNP in a manner that is dependent on its helicase activity, thereby promoting transcription of its target genes (PubMed:25470060). Functions as a cofactor for JUN-activated transcription: required for phosphorylation of JUN at 'Ser-77' (PubMed:11823437, PubMed:25260534). Can unwind double-stranded RNA (helicase) and can fold or introduce a secondary structure to a single-stranded RNA (foldase) (PubMed:9461305). Together with SIRT7, required to prevent R-loop-associated DNA damage and transcription-associated genomic instability: deacetylation by SIRT7 activates the helicase activity, thereby overcoming R-loop-mediated stalling of RNA polymerases (PubMed:28790157). Involved in rRNA processing (PubMed:14559904, PubMed:18180292). May bind to specific miRNA hairpins (PubMed:28431233). Component of a multi-helicase-TICAM1 complex that acts as a cytoplasmic sensor of viral double-stranded RNA (dsRNA) and plays a role in the activation of a cascade of antiviral responses including the induction of pro-inflammatory cytokines via the adapter molecule TICAM1 (By similarity). {ECO:0000250|UniProtKB:Q9JIK5, ECO:0000269|PubMed:11823437, ECO:0000269|PubMed:14559904, ECO:0000269|PubMed:18180292, ECO:0000269|PubMed:25260534, ECO:0000269|PubMed:25470060, ECO:0000269|PubMed:25477391, ECO:0000269|PubMed:28431233, ECO:0000269|PubMed:28790157, ECO:0000269|PubMed:9461305}. |
Q9UHR5 | SAP30BP | Y14 | ochoa | SAP30-binding protein (Transcriptional regulator protein HCNGP) | Plays a role in transcriptional repression by promoting histone deacetylase activity, leading to deacetylation of histone H3 (PubMed:21221920). May be involved in the regulation of beta-2-microglobulin genes (By similarity). {ECO:0000250|UniProtKB:Q02614, ECO:0000269|PubMed:21221920}.; FUNCTION: (Microbial infection) Involved in transcriptional repression of HHV-1 genes TK and gC. {ECO:0000269|PubMed:21221920}. |
Q9ULM3 | YEATS2 | Y15 | ochoa | YEATS domain-containing protein 2 | Chromatin reader component of the ATAC complex, a complex with histone acetyltransferase activity on histones H3 and H4 (PubMed:18838386, PubMed:19103755, PubMed:27103431). YEATS2 specifically recognizes and binds histone H3 crotonylated at 'Lys-27' (H3K27cr) (PubMed:27103431). Crotonylation marks active promoters and enhancers and confers resistance to transcriptional repressors (PubMed:27103431). {ECO:0000269|PubMed:18838386, ECO:0000269|PubMed:19103755, ECO:0000269|PubMed:27103431}. |
Q9UPY5 | SLC7A11 | Y15 | ochoa | Cystine/glutamate transporter (Amino acid transport system xc-) (Calcium channel blocker resistance protein CCBR1) (Solute carrier family 7 member 11) (xCT) | Heterodimer with SLC3A2, that functions as an antiporter by mediating the exchange of extracellular anionic L-cystine and intracellular L-glutamate across the cellular plasma membrane (PubMed:11133847, PubMed:11417227, PubMed:14722095, PubMed:15151999, PubMed:34880232, PubMed:35245456, PubMed:35352032). Provides L-cystine for the maintenance of the redox balance between extracellular L-cystine and L-cysteine and for the maintenance of the intracellular levels of glutathione that is essential for cells protection from oxidative stress (By similarity). The transport is sodium-independent, electroneutral with a stoichiometry of 1:1, and is drove by the high intracellular concentration of L-glutamate and the intracellular reduction of L-cystine (PubMed:11133847, PubMed:11417227). In addition, mediates the import of L-kynurenine leading to anti-ferroptotic signaling propagation required to maintain L-cystine and glutathione homeostasis (PubMed:35245456). Moreover, mediates N-acetyl-L-cysteine uptake into the placenta leading to subsequently down-regulation of pathways associated with oxidative stress, inflammation and apoptosis (PubMed:34120018). In vitro can also transport L-aspartate (PubMed:11417227). May participate in astrocyte and meningeal cell proliferation during development and can provide neuroprotection by promoting glutathione synthesis and delivery from non-neuronal cells such as astrocytes and meningeal cells to immature neurons (By similarity). Controls the production of pheomelanin pigment directly (By similarity). {ECO:0000250|UniProtKB:Q9WTR6, ECO:0000269|PubMed:11133847, ECO:0000269|PubMed:11417227, ECO:0000269|PubMed:14722095, ECO:0000269|PubMed:15151999, ECO:0000269|PubMed:34120018, ECO:0000269|PubMed:34880232, ECO:0000269|PubMed:35245456, ECO:0000269|PubMed:35352032}. |
Q9UPZ9 | CILK1 | Y15 | psp | Serine/threonine-protein kinase ICK (EC 2.7.11.1) (Ciliogenesis associated kinase 1) (Intestinal cell kinase) (hICK) (Laryngeal cancer kinase 2) (LCK2) (MAK-related kinase) (MRK) | Required for ciliogenesis (PubMed:24797473). Phosphorylates KIF3A (By similarity). Involved in the control of ciliary length (PubMed:24853502). Regulates the ciliary localization of SHH pathway components as well as the localization of IFT components at ciliary tips (By similarity). May play a key role in the development of multiple organ systems and particularly in cardiac development (By similarity). Regulates intraflagellar transport (IFT) speed and negatively regulates cilium length in a cAMP and mTORC1 signaling-dependent manner and this regulation requires its kinase activity (By similarity). {ECO:0000250|UniProtKB:Q62726, ECO:0000250|UniProtKB:Q9JKV2, ECO:0000269|PubMed:24797473, ECO:0000269|PubMed:24853502}. |
Q9Y314 | NOSIP | Y14 | ochoa | Nitric oxide synthase-interacting protein (E3 ubiquitin-protein ligase NOSIP) (EC 2.3.2.27) (RING-type E3 ubiquitin transferase NOSIP) (eNOS-interacting protein) | E3 ubiquitin-protein ligase that is essential for proper development of the forebrain, the eye, and the face. Catalyzes monoubiquitination of serine/threonine-protein phosphatase 2A (PP2A) catalytic subunit PPP2CA/PPP2CB (By similarity). Negatively regulates nitric oxide production by inducing NOS1 and NOS3 translocation to actin cytoskeleton and inhibiting their enzymatic activity (PubMed:11149895, PubMed:15548660, PubMed:16135813). {ECO:0000250|UniProtKB:Q9D6T0, ECO:0000269|PubMed:11149895, ECO:0000269|PubMed:15548660, ECO:0000269|PubMed:16135813}. |
Q9Y3L3 | SH3BP1 | T15 | ochoa | SH3 domain-binding protein 1 | GTPase activating protein (GAP) which specifically converts GTP-bound Rho-type GTPases including RAC1 and CDC42 in their inactive GDP-bound form. By specifically inactivating RAC1 at the leading edge of migrating cells, it regulates the spatiotemporal organization of cell protrusions which is important for proper cell migration (PubMed:21658605). Also negatively regulates CDC42 in the process of actin remodeling and the formation of epithelial cell junctions (PubMed:22891260). Through its GAP activity toward RAC1 and/or CDC42 plays a specific role in phagocytosis of large particles. Specifically recruited by a PI3 kinase/PI3K-dependent mechanism to sites of large particles engagement, inactivates RAC1 and/or CDC42 allowing the reorganization of the underlying actin cytoskeleton required for engulfment (PubMed:26465210). It also plays a role in angiogenesis and the process of repulsive guidance as part of a semaphorin-plexin signaling pathway. Following the binding of PLXND1 to extracellular SEMA3E it dissociates from PLXND1 and inactivates RAC1, inducing the intracellular reorganization of the actin cytoskeleton and the collapse of cells (PubMed:24841563). {ECO:0000269|PubMed:21658605, ECO:0000269|PubMed:22891260, ECO:0000269|PubMed:24841563, ECO:0000269|PubMed:26465210}. |
Q9Y5S1 | TRPV2 | T14 | ochoa | Transient receptor potential cation channel subfamily V member 2 (TrpV2) (Osm-9-like TRP channel 2) (OTRPC2) (Vanilloid receptor-like protein 1) (VRL-1) | Calcium-permeable, non-selective cation channel with an outward rectification. Seems to be regulated, at least in part, by IGF1, PDGF and neuropeptide head activator. May transduce physical stimuli in mast cells. Activated by temperatures higher than 52 degrees Celsius; is not activated by vanilloids and acidic pH. {ECO:0000269|PubMed:10201375}. |
P62280 | RPS11 | T15 | Sugiyama | Small ribosomal subunit protein uS17 (40S ribosomal protein S11) | Component of the small ribosomal subunit. The ribosome is a large ribonucleoprotein complex responsible for the synthesis of proteins in the cell. Part of the small subunit (SSU) processome, first precursor of the small eukaryotic ribosomal subunit. During the assembly of the SSU processome in the nucleolus, many ribosome biogenesis factors, an RNA chaperone and ribosomal proteins associate with the nascent pre-rRNA and work in concert to generate RNA folding, modifications, rearrangements and cleavage as well as targeted degradation of pre-ribosomal RNA by the RNA exosome (PubMed:34516797). {ECO:0000269|PubMed:23636399, ECO:0000269|PubMed:34516797}. |
P63173 | RPL38 | T14 | Sugiyama | Large ribosomal subunit protein eL38 (60S ribosomal protein L38) | Component of the large ribosomal subunit. The ribosome is a large ribonucleoprotein complex responsible for the synthesis of proteins in the cell. {ECO:0000269|PubMed:23636399, ECO:0000269|PubMed:32669547}. |
Q15427 | SF3B4 | T14 | Sugiyama | Splicing factor 3B subunit 4 (Pre-mRNA-splicing factor SF3b 49 kDa subunit) (Spliceosome-associated protein 49) (SAP 49) | Component of the 17S U2 SnRNP complex of the spliceosome, a large ribonucleoprotein complex that removes introns from transcribed pre-mRNAs (PubMed:10882114, PubMed:12234937, PubMed:27720643, PubMed:32494006). The 17S U2 SnRNP complex (1) directly participates in early spliceosome assembly and (2) mediates recognition of the intron branch site during pre-mRNA splicing by promoting the selection of the pre-mRNA branch-site adenosine, the nucleophile for the first step of splicing (PubMed:12234937, PubMed:32494006). Within the 17S U2 SnRNP complex, SF3B4 is part of the SF3B subcomplex, which is required for 'A' complex assembly formed by the stable binding of U2 snRNP to the branchpoint sequence in pre-mRNA (PubMed:12234937, PubMed:27720643). Sequence independent binding of SF3A and SF3B subcomplexes upstream of the branch site is essential, it may anchor U2 snRNP to the pre-mRNA (PubMed:12234937). May also be involved in the assembly of the 'E' complex (PubMed:10882114). Also acts as a component of the minor spliceosome, which is involved in the splicing of U12-type introns in pre-mRNAs (PubMed:15146077, PubMed:33509932). {ECO:0000269|PubMed:10882114, ECO:0000269|PubMed:12234937, ECO:0000269|PubMed:15146077, ECO:0000269|PubMed:27720643, ECO:0000269|PubMed:32494006, ECO:0000269|PubMed:33509932}. |
P61513 | RPL37A | Y14 | Sugiyama | Large ribosomal subunit protein eL43 (60S ribosomal protein L37a) | Component of the large ribosomal subunit. The ribosome is a large ribonucleoprotein complex responsible for the synthesis of proteins in the cell. {ECO:0000269|PubMed:23636399, ECO:0000269|PubMed:32669547}. |
P62942 | FKBP1A | T15 | Sugiyama | Peptidyl-prolyl cis-trans isomerase FKBP1A (PPIase FKBP1A) (EC 5.2.1.8) (12 kDa FK506-binding protein) (12 kDa FKBP) (FKBP-12) (Calstabin-1) (FK506-binding protein 1A) (FKBP-1A) (Immunophilin FKBP12) (Rotamase) | Keeps in an inactive conformation TGFBR1, the TGF-beta type I serine/threonine kinase receptor, preventing TGF-beta receptor activation in absence of ligand. Recruits SMAD7 to ACVR1B which prevents the association of SMAD2 and SMAD3 with the activin receptor complex, thereby blocking the activin signal. May modulate the RYR1 calcium channel activity. PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides. {ECO:0000269|PubMed:16720724, ECO:0000269|PubMed:1696686, ECO:0000269|PubMed:1701173, ECO:0000269|PubMed:9233797}. |
P18077 | RPL35A | Y14 | Sugiyama | Large ribosomal subunit protein eL33 (60S ribosomal protein L35a) (Cell growth-inhibiting gene 33 protein) | Component of the large ribosomal subunit (PubMed:23636399, PubMed:32669547). The ribosome is a large ribonucleoprotein complex responsible for the synthesis of proteins in the cell (PubMed:23636399, PubMed:32669547). Required for the proliferation and viability of hematopoietic cells (PubMed:18535205). {ECO:0000269|PubMed:18535205, ECO:0000269|PubMed:23636399, ECO:0000269|PubMed:32669547}. |
P50914 | RPL14 | Y14 | Sugiyama | Large ribosomal subunit protein eL14 (60S ribosomal protein L14) (CAG-ISL 7) | Component of the large ribosomal subunit (PubMed:12962325, PubMed:23636399, PubMed:32669547). The ribosome is a large ribonucleoprotein complex responsible for the synthesis of proteins in the cell (PubMed:12962325, PubMed:23636399, PubMed:32669547). {ECO:0000269|PubMed:23636399, ECO:0000269|PubMed:32669547, ECO:0000305|PubMed:12962325}. |
Q13557 | CAMK2D | Y14 | Sugiyama | Calcium/calmodulin-dependent protein kinase type II subunit delta (CaM kinase II subunit delta) (CaMK-II subunit delta) (EC 2.7.11.17) | Calcium/calmodulin-dependent protein kinase involved in the regulation of Ca(2+) homeostatis and excitation-contraction coupling (ECC) in heart by targeting ion channels, transporters and accessory proteins involved in Ca(2+) influx into the myocyte, Ca(2+) release from the sarcoplasmic reticulum (SR), SR Ca(2+) uptake and Na(+) and K(+) channel transport. Targets also transcription factors and signaling molecules to regulate heart function. In its activated form, is involved in the pathogenesis of dilated cardiomyopathy and heart failure. Contributes to cardiac decompensation and heart failure by regulating SR Ca(2+) release via direct phosphorylation of RYR2 Ca(2+) channel on 'Ser-2808'. In the nucleus, phosphorylates the MEF2 repressor HDAC4, promoting its nuclear export and binding to 14-3-3 protein, and expression of MEF2 and genes involved in the hypertrophic program (PubMed:17179159). Is essential for left ventricular remodeling responses to myocardial infarction. In pathological myocardial remodeling acts downstream of the beta adrenergic receptor signaling cascade to regulate key proteins involved in ECC. Regulates Ca(2+) influx to myocytes by binding and phosphorylating the L-type Ca(2+) channel subunit beta-2 CACNB2. In addition to Ca(2+) channels, can target and regulate the cardiac sarcolemmal Na(+) channel Nav1.5/SCN5A and the K+ channel Kv4.3/KCND3, which contribute to arrhythmogenesis in heart failure. Phosphorylates phospholamban (PLN/PLB), an endogenous inhibitor of SERCA2A/ATP2A2, contributing to the enhancement of SR Ca(2+) uptake that may be important in frequency-dependent acceleration of relaxation (FDAR) and maintenance of contractile function during acidosis (PubMed:16690701). May participate in the modulation of skeletal muscle function in response to exercise, by regulating SR Ca(2+) transport through phosphorylation of PLN/PLB and triadin, a ryanodine receptor-coupling factor. In response to interferon-gamma (IFN-gamma) stimulation, catalyzes phosphorylation of STAT1, stimulating the JAK-STAT signaling pathway (By similarity). {ECO:0000250|UniProtKB:Q6PHZ2, ECO:0000269|PubMed:16690701, ECO:0000269|PubMed:17179159}. |
Q8IXH7 | NELFCD | Y14 | SIGNOR | Negative elongation factor C/D (NELF-C/D) (TH1-like protein) | Essential component of the NELF complex, a complex that negatively regulates the elongation of transcription by RNA polymerase II (PubMed:12612062). The NELF complex, which acts via an association with the DSIF complex and causes transcriptional pausing, is counteracted by the P-TEFb kinase complex (PubMed:10199401). {ECO:0000269|PubMed:10199401, ECO:0000269|PubMed:12612062}.; FUNCTION: (Microbial infection) The NELF complex is involved in HIV-1 latency possibly involving recruitment of PCF11 to paused RNA polymerase II. {ECO:0000269|PubMed:23884411}. |
Q96B26 | EXOSC8 | Y14 | Sugiyama | Exosome complex component RRP43 (Exosome component 8) (Opa-interacting protein 2) (OIP-2) (Ribosomal RNA-processing protein 43) (p9) | Non-catalytic component of the RNA exosome complex which has 3'->5' exoribonuclease activity and participates in a multitude of cellular RNA processing and degradation events. In the nucleus, the RNA exosome complex is involved in proper maturation of stable RNA species such as rRNA, snRNA and snoRNA, in the elimination of RNA processing by-products and non-coding 'pervasive' transcripts, such as antisense RNA species and promoter-upstream transcripts (PROMPTs), and of mRNAs with processing defects, thereby limiting or excluding their export to the cytoplasm. The RNA exosome may be involved in Ig class switch recombination (CSR) and/or Ig variable region somatic hypermutation (SHM) by targeting AICDA deamination activity to transcribed dsDNA substrates. In the cytoplasm, the RNA exosome complex is involved in general mRNA turnover and specifically degrades inherently unstable mRNAs containing AU-rich elements (AREs) within their 3' untranslated regions, and in RNA surveillance pathways, preventing translation of aberrant mRNAs. It seems to be involved in degradation of histone mRNA. The catalytic inactive RNA exosome core complex of 9 subunits (Exo-9) is proposed to play a pivotal role in the binding and presentation of RNA for ribonucleolysis, and to serve as a scaffold for the association with catalytic subunits and accessory proteins or complexes. EXOSC8 binds to ARE-containing RNAs. {ECO:0000269|PubMed:16912217, ECO:0000269|PubMed:17545563}. |
P55036 | PSMD4 | Y15 | Sugiyama | 26S proteasome non-ATPase regulatory subunit 4 (26S proteasome regulatory subunit RPN10) (26S proteasome regulatory subunit S5A) (Antisecretory factor 1) (AF) (ASF) (Multiubiquitin chain-binding protein) | Component of the 26S proteasome, a multiprotein complex involved in the ATP-dependent degradation of ubiquitinated proteins. This complex plays a key role in the maintenance of protein homeostasis by removing misfolded or damaged proteins, which could impair cellular functions, and by removing proteins whose functions are no longer required. Therefore, the proteasome participates in numerous cellular processes, including cell cycle progression, apoptosis, or DNA damage repair. PSMD4 acts as an ubiquitin receptor subunit through ubiquitin-interacting motifs and selects ubiquitin-conjugates for destruction. Displays a preferred selectivity for longer polyubiquitin chains. {ECO:0000269|PubMed:1317798, ECO:0000269|PubMed:15826667}. |
P55010 | EIF5 | Y14 | Sugiyama | Eukaryotic translation initiation factor 5 (eIF-5) | Component of the 43S pre-initiation complex (43S PIC), which binds to the mRNA cap-proximal region, scans mRNA 5'-untranslated region, and locates the initiation codon (PubMed:11166181, PubMed:22813744, PubMed:24319994). In this complex, acts as a GTPase-activating protein, by promoting GTP hydrolysis by eIF2G (EIF2S3) (PubMed:11166181). During scanning, interacts with both EIF1 (via its C-terminal domain (CTD)) and EIF1A (via its NTD) (PubMed:22813744). This interaction with EIF1A contributes to the maintenance of EIF1 within the open 43S PIC (PubMed:24319994). When start codon is recognized, EIF5, via its NTD, induces eIF2G (EIF2S3) to hydrolyze the GTP (PubMed:11166181). Start codon recognition also induces a conformational change of the PIC to a closed state (PubMed:22813744). This change increases the affinity of EIF5-CTD for EIF2-beta (EIF2S2), which allows the release, by an indirect mechanism, of EIF1 from the PIC (PubMed:22813744). Finally, EIF5 stabilizes the PIC in its closed conformation (PubMed:22813744). {ECO:0000269|PubMed:11166181, ECO:0000269|PubMed:22813744, ECO:0000269|PubMed:24319994}. |
Q9NPI1 | BRD7 | Y15 | Sugiyama | Bromodomain-containing protein 7 (75 kDa bromodomain protein) (Protein CELTIX-1) | Acts both as coactivator and as corepressor. May play a role in chromatin remodeling. Activator of the Wnt signaling pathway in a DVL1-dependent manner by negatively regulating the GSK3B phosphotransferase activity. Induces dephosphorylation of GSK3B at 'Tyr-216'. Down-regulates TRIM24-mediated activation of transcriptional activation by AR (By similarity). Transcriptional corepressor that down-regulates the expression of target genes. Binds to target promoters, leading to increased histone H3 acetylation at 'Lys-9' (H3K9ac). Binds to the ESR1 promoter. Recruits BRCA1 and POU2F1 to the ESR1 promoter. Coactivator for TP53-mediated activation of transcription of a set of target genes. Required for TP53-mediated cell-cycle arrest in response to oncogene activation. Promotes acetylation of TP53 at 'Lys-382', and thereby promotes efficient recruitment of TP53 to target promoters. Inhibits cell cycle progression from G1 to S phase. {ECO:0000250, ECO:0000269|PubMed:16265664, ECO:0000269|PubMed:16475162, ECO:0000269|PubMed:20215511, ECO:0000269|PubMed:20228809, ECO:0000269|PubMed:20660729}. |
P61158 | ACTR3 | T14 | Sugiyama | Actin-related protein 3 (Actin-like protein 3) | ATP-binding component of the Arp2/3 complex, a multiprotein complex that mediates actin polymerization upon stimulation by nucleation-promoting factor (NPF) (PubMed:9000076). The Arp2/3 complex mediates the formation of branched actin networks in the cytoplasm, providing the force for cell motility (PubMed:9000076). Seems to contact the pointed end of the daughter actin filament (PubMed:9000076). In podocytes, required for the formation of lamellipodia downstream of AVIL and PLCE1 regulation (PubMed:29058690). In addition to its role in the cytoplasmic cytoskeleton, the Arp2/3 complex also promotes actin polymerization in the nucleus, thereby regulating gene transcription and repair of damaged DNA (PubMed:17220302, PubMed:29925947). The Arp2/3 complex promotes homologous recombination (HR) repair in response to DNA damage by promoting nuclear actin polymerization, leading to drive motility of double-strand breaks (DSBs) (PubMed:29925947). Plays a role in ciliogenesis (PubMed:20393563). {ECO:0000269|PubMed:17220302, ECO:0000269|PubMed:20393563, ECO:0000269|PubMed:29058690, ECO:0000269|PubMed:29925947, ECO:0000269|PubMed:9000076}. |
Q9HCX4 | TRPC7 | T15 | SIGNOR | Short transient receptor potential channel 7 (TrpC7) (Transient receptor protein 7) (TRP-7) (hTRP7) | Forms a receptor-activated non-selective calcium permeant cation channel. Probably is operated by a phosphatidylinositol second messenger system activated by receptor tyrosine kinases or G-protein coupled receptors. Activated by diacylglycerol (DAG) (By similarity). May also be activated by intracellular calcium store depletion. {ECO:0000250|UniProtKB:Q9WVC5}. |
P61160 | ACTR2 | T15 | Sugiyama | Actin-related protein 2 (Actin-like protein 2) | ATP-binding component of the Arp2/3 complex, a multiprotein complex that mediates actin polymerization upon stimulation by nucleation-promoting factor (NPF) (PubMed:9000076). The Arp2/3 complex mediates the formation of branched actin networks in the cytoplasm, providing the force for cell motility (PubMed:9000076). Seems to contact the pointed end of the daughter actin filament (PubMed:9000076). In podocytes, required for the formation of lamellipodia downstream of AVIL and PLCE1 regulation (PubMed:29058690). In addition to its role in the cytoplasmic cytoskeleton, the Arp2/3 complex also promotes actin polymerization in the nucleus, thereby regulating gene transcription and repair of damaged DNA (PubMed:17220302, PubMed:29925947). The Arp2/3 complex promotes homologous recombination (HR) repair in response to DNA damage by promoting nuclear actin polymerization, leading to drive motility of double-strand breaks (DSBs) (PubMed:29925947). {ECO:0000269|PubMed:17220302, ECO:0000269|PubMed:29058690, ECO:0000269|PubMed:29925947, ECO:0000269|PubMed:9000076}. |
Q8NG66 | NEK11 | T15 | Sugiyama | Serine/threonine-protein kinase Nek11 (EC 2.7.11.1) (Never in mitosis A-related kinase 11) (NimA-related protein kinase 11) | Protein kinase which plays an important role in the G2/M checkpoint response to DNA damage. Controls degradation of CDC25A by directly phosphorylating it on residues whose phosphorylation is required for BTRC-mediated polyubiquitination and degradation. {ECO:0000269|PubMed:12154088, ECO:0000269|PubMed:19734889, ECO:0000269|PubMed:20090422}. |
Download
reactome_id | name | p | -log10_p |
---|---|---|---|
R-HSA-9948299 | Ribosome-associated quality control | 3.552714e-15 | 14.449 |
R-HSA-9010553 | Regulation of expression of SLITs and ROBOs | 1.665335e-14 | 13.778 |
R-HSA-422475 | Axon guidance | 1.276756e-14 | 13.894 |
R-HSA-9954716 | ZNF598 and the Ribosome-associated Quality Trigger (RQT) complex dissociate a ri... | 4.163336e-14 | 13.381 |
R-HSA-9954709 | Ribosome Quality Control (RQC) complex extracts and degrades nascent peptide | 4.762857e-14 | 13.322 |
R-HSA-8953854 | Metabolism of RNA | 6.838974e-14 | 13.165 |
R-HSA-9675108 | Nervous system development | 6.195044e-14 | 13.208 |
R-HSA-72706 | GTP hydrolysis and joining of the 60S ribosomal subunit | 2.766676e-13 | 12.558 |
R-HSA-975956 | Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) | 4.535261e-13 | 12.343 |
R-HSA-72613 | Eukaryotic Translation Initiation | 8.545387e-13 | 12.068 |
R-HSA-72737 | Cap-dependent Translation Initiation | 8.545387e-13 | 12.068 |
R-HSA-376176 | Signaling by ROBO receptors | 1.390998e-12 | 11.857 |
R-HSA-156827 | L13a-mediated translational silencing of Ceruloplasmin expression | 4.408029e-12 | 11.356 |
R-HSA-156902 | Peptide chain elongation | 4.845346e-12 | 11.315 |
R-HSA-9954714 | PELO:HBS1L and ABCE1 dissociate a ribosome on a non-stop mRNA | 7.042700e-12 | 11.152 |
R-HSA-927802 | Nonsense-Mediated Decay (NMD) | 6.774692e-12 | 11.169 |
R-HSA-975957 | Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) | 6.774692e-12 | 11.169 |
R-HSA-156842 | Eukaryotic Translation Elongation | 8.977707e-12 | 11.047 |
R-HSA-72689 | Formation of a pool of free 40S subunits | 1.437450e-11 | 10.842 |
R-HSA-6791226 | Major pathway of rRNA processing in the nucleolus and cytosol | 1.402212e-11 | 10.853 |
R-HSA-72764 | Eukaryotic Translation Termination | 1.437450e-11 | 10.842 |
R-HSA-2408557 | Selenocysteine synthesis | 2.814038e-11 | 10.551 |
R-HSA-192823 | Viral mRNA Translation | 3.490486e-11 | 10.457 |
R-HSA-9633012 | Response of EIF2AK4 (GCN2) to amino acid deficiency | 3.881562e-11 | 10.411 |
R-HSA-8868773 | rRNA processing in the nucleus and cytosol | 5.271594e-11 | 10.278 |
R-HSA-1799339 | SRP-dependent cotranslational protein targeting to membrane | 5.878908e-11 | 10.231 |
R-HSA-168273 | Influenza Viral RNA Transcription and Replication | 5.008208e-10 | 9.300 |
R-HSA-72312 | rRNA processing | 8.834465e-10 | 9.054 |
R-HSA-2262752 | Cellular responses to stress | 1.297060e-09 | 8.887 |
R-HSA-8953897 | Cellular responses to stimuli | 1.267113e-09 | 8.897 |
R-HSA-72766 | Translation | 2.777652e-09 | 8.556 |
R-HSA-168255 | Influenza Infection | 2.758841e-09 | 8.559 |
R-HSA-9711097 | Cellular response to starvation | 6.267531e-09 | 8.203 |
R-HSA-2408522 | Selenoamino acid metabolism | 9.272985e-09 | 8.033 |
R-HSA-453279 | Mitotic G1 phase and G1/S transition | 2.721289e-08 | 7.565 |
R-HSA-450531 | Regulation of mRNA stability by proteins that bind AU-rich elements | 4.496322e-08 | 7.347 |
R-HSA-9766229 | Degradation of CDH1 | 4.859765e-08 | 7.313 |
R-HSA-9828211 | Regulation of TBK1, IKKε-mediated activation of IRF3, IRF7 upon TLR3 ligation | 5.743566e-08 | 7.241 |
R-HSA-9613829 | Chaperone Mediated Autophagy | 6.761471e-08 | 7.170 |
R-HSA-9014325 | TICAM1,TRAF6-dependent induction of TAK1 complex | 1.305803e-07 | 6.884 |
R-HSA-450408 | AUF1 (hnRNP D0) binds and destabilizes mRNA | 1.274796e-07 | 6.895 |
R-HSA-9764561 | Regulation of CDH1 Function | 1.311198e-07 | 6.882 |
R-HSA-5689877 | Josephin domain DUBs | 1.305803e-07 | 6.884 |
R-HSA-4641258 | Degradation of DVL | 1.486621e-07 | 6.828 |
R-HSA-176408 | Regulation of APC/C activators between G1/S and early anaphase | 2.287524e-07 | 6.641 |
R-HSA-9824878 | Regulation of TBK1, IKKε (IKBKE)-mediated activation of IRF3, IRF7 | 2.633671e-07 | 6.579 |
R-HSA-9013973 | TICAM1-dependent activation of IRF3/IRF7 | 2.633671e-07 | 6.579 |
R-HSA-69615 | G1/S DNA Damage Checkpoints | 2.543856e-07 | 6.595 |
R-HSA-5362768 | Hh mutants are degraded by ERAD | 2.655844e-07 | 6.576 |
R-HSA-5610780 | Degradation of GLI1 by the proteasome | 3.046194e-07 | 6.516 |
R-HSA-5387390 | Hh mutants abrogate ligand secretion | 3.973004e-07 | 6.401 |
R-HSA-187577 | SCF(Skp2)-mediated degradation of p27/p21 | 4.518798e-07 | 6.345 |
R-HSA-9706377 | FLT3 signaling by CBL mutants | 5.221228e-07 | 6.282 |
R-HSA-69202 | Cyclin E associated events during G1/S transition | 5.129767e-07 | 6.290 |
R-HSA-5678895 | Defective CFTR causes cystic fibrosis | 5.126283e-07 | 6.290 |
R-HSA-69206 | G1/S Transition | 5.068583e-07 | 6.295 |
R-HSA-69601 | Ubiquitin-Mediated Degradation of Phosphorylated Cdc25A | 5.126283e-07 | 6.290 |
R-HSA-69613 | p53-Independent G1/S DNA Damage Checkpoint | 5.126283e-07 | 6.290 |
R-HSA-8866652 | Synthesis of active ubiquitin: roles of E1 and E2 enzymes | 5.493710e-07 | 6.260 |
R-HSA-174143 | APC/C-mediated degradation of cell cycle proteins | 5.639013e-07 | 6.249 |
R-HSA-453276 | Regulation of mitotic cell cycle | 5.639013e-07 | 6.249 |
R-HSA-69656 | Cyclin A:Cdk2-associated events at S phase entry | 6.190875e-07 | 6.208 |
R-HSA-975163 | IRAK2 mediated activation of TAK1 complex upon TLR7/8 or 9 stimulation | 6.417824e-07 | 6.193 |
R-HSA-9615710 | Late endosomal microautophagy | 7.709314e-07 | 6.113 |
R-HSA-937072 | TRAF6-mediated induction of TAK1 complex within TLR4 complex | 8.351560e-07 | 6.078 |
R-HSA-168927 | TICAM1, RIP1-mediated IKK complex recruitment | 8.351560e-07 | 6.078 |
R-HSA-2173791 | TGF-beta receptor signaling in EMT (epithelial to mesenchymal transition) | 8.351560e-07 | 6.078 |
R-HSA-8875360 | InlB-mediated entry of Listeria monocytogenes into host cell | 8.351560e-07 | 6.078 |
R-HSA-69563 | p53-Dependent G1 DNA Damage Response | 8.288682e-07 | 6.082 |
R-HSA-69580 | p53-Dependent G1/S DNA damage checkpoint | 8.288682e-07 | 6.082 |
R-HSA-9694493 | Maturation of protein E | 8.847309e-07 | 6.053 |
R-HSA-9683683 | Maturation of protein E | 8.847309e-07 | 6.053 |
R-HSA-5658442 | Regulation of RAS by GAPs | 9.294595e-07 | 6.032 |
R-HSA-5358346 | Hedgehog ligand biogenesis | 1.040092e-06 | 5.983 |
R-HSA-211733 | Regulation of activated PAK-2p34 by proteasome mediated degradation | 1.060827e-06 | 5.974 |
R-HSA-936440 | Negative regulators of DDX58/IFIH1 signaling | 1.060827e-06 | 5.974 |
R-HSA-1362300 | Transcription of E2F targets under negative control by p107 (RBL1) and p130 (RBL... | 1.071826e-06 | 5.970 |
R-HSA-174184 | Cdc20:Phospho-APC/C mediated degradation of Cyclin A | 1.161556e-06 | 5.935 |
R-HSA-9931269 | AMPK-induced ERAD and lysosome mediated degradation of PD-L1(CD274) | 1.161556e-06 | 5.935 |
R-HSA-68949 | Orc1 removal from chromatin | 1.161556e-06 | 5.935 |
R-HSA-9692914 | SARS-CoV-1-host interactions | 1.125709e-06 | 5.949 |
R-HSA-1538133 | G0 and Early G1 | 1.236088e-06 | 5.908 |
R-HSA-179419 | APC:Cdc20 mediated degradation of cell cycle proteins prior to satisfation of th... | 1.294684e-06 | 5.888 |
R-HSA-936964 | Activation of IRF3, IRF7 mediated by TBK1, IKKε (IKBKE) | 1.358457e-06 | 5.867 |
R-HSA-69017 | CDK-mediated phosphorylation and removal of Cdc6 | 1.440359e-06 | 5.842 |
R-HSA-176409 | APC/C:Cdc20 mediated degradation of mitotic proteins | 1.599510e-06 | 5.796 |
R-HSA-180534 | Vpu mediated degradation of CD4 | 1.657816e-06 | 5.780 |
R-HSA-176814 | Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins | 1.773116e-06 | 5.751 |
R-HSA-75815 | Ubiquitin-dependent degradation of Cyclin D | 1.908949e-06 | 5.719 |
R-HSA-349425 | Autodegradation of the E3 ubiquitin ligase COP1 | 1.908949e-06 | 5.719 |
R-HSA-8948747 | Regulation of PTEN localization | 2.131056e-06 | 5.671 |
R-HSA-9824446 | Viral Infection Pathways | 2.011331e-06 | 5.697 |
R-HSA-8854050 | FBXL7 down-regulates AURKA during mitotic entry and in early mitosis | 2.190292e-06 | 5.659 |
R-HSA-174113 | SCF-beta-TrCP mediated degradation of Emi1 | 2.190292e-06 | 5.659 |
R-HSA-169911 | Regulation of Apoptosis | 2.190292e-06 | 5.659 |
R-HSA-174048 | APC/C:Cdc20 mediated degradation of Cyclin B | 2.593786e-06 | 5.586 |
R-HSA-937041 | IKK complex recruitment mediated by RIP1 | 2.593786e-06 | 5.586 |
R-HSA-110320 | Translesion Synthesis by POLH | 2.593786e-06 | 5.586 |
R-HSA-180585 | Vif-mediated degradation of APOBEC3G | 2.504566e-06 | 5.601 |
R-HSA-912631 | Regulation of signaling by CBL | 2.593786e-06 | 5.586 |
R-HSA-9663891 | Selective autophagy | 2.556265e-06 | 5.592 |
R-HSA-6804757 | Regulation of TP53 Degradation | 2.504566e-06 | 5.601 |
R-HSA-5689896 | Ovarian tumor domain proteases | 2.854654e-06 | 5.544 |
R-HSA-4641257 | Degradation of AXIN | 2.854654e-06 | 5.544 |
R-HSA-9762114 | GSK3B and BTRC:CUL1-mediated-degradation of NFE2L2 | 2.854654e-06 | 5.544 |
R-HSA-3785653 | Myoclonic epilepsy of Lafora | 3.099121e-06 | 5.509 |
R-HSA-1253288 | Downregulation of ERBB4 signaling | 3.099121e-06 | 5.509 |
R-HSA-9637628 | Modulation by Mtb of host immune system | 3.099121e-06 | 5.509 |
R-HSA-8849469 | PTK6 Regulates RTKs and Their Effectors AKT1 and DOK1 | 3.099121e-06 | 5.509 |
R-HSA-6807004 | Negative regulation of MET activity | 3.159040e-06 | 5.500 |
R-HSA-8852276 | The role of GTSE1 in G2/M progression after G2 checkpoint | 3.179908e-06 | 5.498 |
R-HSA-9929356 | GSK3B-mediated proteasomal degradation of PD-L1(CD274) | 3.674657e-06 | 5.435 |
R-HSA-69541 | Stabilization of p53 | 3.674657e-06 | 5.435 |
R-HSA-6806003 | Regulation of TP53 Expression and Degradation | 3.674657e-06 | 5.435 |
R-HSA-162909 | Host Interactions of HIV factors | 3.981087e-06 | 5.400 |
R-HSA-8941858 | Regulation of RUNX3 expression and activity | 4.151200e-06 | 5.382 |
R-HSA-9604323 | Negative regulation of NOTCH4 signaling | 4.151200e-06 | 5.382 |
R-HSA-937042 | IRAK2 mediated activation of TAK1 complex | 4.359797e-06 | 5.361 |
R-HSA-8876384 | Listeria monocytogenes entry into host cells | 4.577512e-06 | 5.339 |
R-HSA-110313 | Translesion synthesis by Y family DNA polymerases bypasses lesions on DNA templa... | 4.676824e-06 | 5.330 |
R-HSA-9932298 | Degradation of CRY and PER proteins | 5.255299e-06 | 5.279 |
R-HSA-5610785 | GLI3 is processed to GLI3R by the proteasome | 5.255299e-06 | 5.279 |
R-HSA-5610783 | Degradation of GLI2 by the proteasome | 5.255299e-06 | 5.279 |
R-HSA-9929491 | SPOP-mediated proteasomal degradation of PD-L1(CD274) | 4.676824e-06 | 5.330 |
R-HSA-5676590 | NIK-->noncanonical NF-kB signaling | 4.676824e-06 | 5.330 |
R-HSA-9607240 | FLT3 Signaling | 4.676824e-06 | 5.330 |
R-HSA-9664873 | Pexophagy | 5.964704e-06 | 5.224 |
R-HSA-1168372 | Downstream signaling events of B Cell Receptor (BCR) | 6.403308e-06 | 5.194 |
R-HSA-5610787 | Hedgehog 'off' state | 6.790596e-06 | 5.168 |
R-HSA-5632684 | Hedgehog 'on' state | 6.950396e-06 | 5.158 |
R-HSA-69231 | Cyclin D associated events in G1 | 7.348438e-06 | 5.134 |
R-HSA-69236 | G1 Phase | 7.348438e-06 | 5.134 |
R-HSA-9645460 | Alpha-protein kinase 1 signaling pathway | 7.968977e-06 | 5.099 |
R-HSA-8876493 | InlA-mediated entry of Listeria monocytogenes into host cells | 7.968977e-06 | 5.099 |
R-HSA-69052 | Switching of origins to a post-replicative state | 8.161525e-06 | 5.088 |
R-HSA-4608870 | Asymmetric localization of PCP proteins | 8.179917e-06 | 5.087 |
R-HSA-5607761 | Dectin-1 mediated noncanonical NF-kB signaling | 8.179917e-06 | 5.087 |
R-HSA-174084 | Autodegradation of Cdh1 by Cdh1:APC/C | 9.086052e-06 | 5.042 |
R-HSA-8852135 | Protein ubiquitination | 9.542892e-06 | 5.020 |
R-HSA-5358351 | Signaling by Hedgehog | 1.000504e-05 | 5.000 |
R-HSA-5663205 | Infectious disease | 9.006147e-06 | 5.045 |
R-HSA-9678108 | SARS-CoV-1 Infection | 8.908968e-06 | 5.050 |
R-HSA-174154 | APC/C:Cdc20 mediated degradation of Securin | 1.007182e-05 | 4.997 |
R-HSA-1266738 | Developmental Biology | 1.010029e-05 | 4.996 |
R-HSA-2122948 | Activated NOTCH1 Transmits Signal to the Nucleus | 1.033851e-05 | 4.986 |
R-HSA-209560 | NF-kB is activated and signals survival | 1.043112e-05 | 4.982 |
R-HSA-5357956 | TNFR1-induced NF-kappa-B signaling pathway | 1.197453e-05 | 4.922 |
R-HSA-4086400 | PCP/CE pathway | 1.197457e-05 | 4.922 |
R-HSA-5619084 | ABC transporter disorders | 1.197457e-05 | 4.922 |
R-HSA-162906 | HIV Infection | 1.222102e-05 | 4.913 |
R-HSA-73893 | DNA Damage Bypass | 1.230328e-05 | 4.910 |
R-HSA-5656169 | Termination of translesion DNA synthesis | 1.584864e-05 | 4.800 |
R-HSA-1358803 | Downregulation of ERBB2:ERBB3 signaling | 1.341289e-05 | 4.872 |
R-HSA-2691230 | Signaling by NOTCH1 HD Domain Mutants in Cancer | 1.341289e-05 | 4.872 |
R-HSA-2691232 | Constitutive Signaling by NOTCH1 HD Domain Mutants | 1.341289e-05 | 4.872 |
R-HSA-1234176 | Oxygen-dependent proline hydroxylation of Hypoxia-inducible Factor Alpha | 1.491849e-05 | 4.826 |
R-HSA-937039 | IRAK1 recruits IKK complex | 1.341289e-05 | 4.872 |
R-HSA-975144 | IRAK1 recruits IKK complex upon TLR7/8 or 9 stimulation | 1.341289e-05 | 4.872 |
R-HSA-8866427 | VLDLR internalisation and degradation | 1.341289e-05 | 4.872 |
R-HSA-1169091 | Activation of NF-kappaB in B cells | 1.491849e-05 | 4.826 |
R-HSA-5205685 | PINK1-PRKN Mediated Mitophagy | 1.380590e-05 | 4.860 |
R-HSA-209543 | p75NTR recruits signalling complexes | 1.341289e-05 | 4.872 |
R-HSA-2559582 | Senescence-Associated Secretory Phenotype (SASP) | 1.599515e-05 | 4.796 |
R-HSA-8866654 | E3 ubiquitin ligases ubiquitinate target proteins | 1.638480e-05 | 4.786 |
R-HSA-174490 | Membrane binding and targetting of GAG proteins | 1.697911e-05 | 4.770 |
R-HSA-174178 | APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins ... | 1.796529e-05 | 4.746 |
R-HSA-8948751 | Regulation of PTEN stability and activity | 1.796529e-05 | 4.746 |
R-HSA-9755511 | KEAP1-NFE2L2 pathway | 1.967368e-05 | 4.706 |
R-HSA-5687128 | MAPK6/MAPK4 signaling | 1.969309e-05 | 4.706 |
R-HSA-182971 | EGFR downregulation | 2.063600e-05 | 4.685 |
R-HSA-9909615 | Regulation of PD-L1(CD274) Post-translational modification | 2.107219e-05 | 4.676 |
R-HSA-174495 | Synthesis And Processing Of GAG, GAGPOL Polyproteins | 2.119762e-05 | 4.674 |
R-HSA-205043 | NRIF signals cell death from the nucleus | 2.119762e-05 | 4.674 |
R-HSA-5684264 | MAP3K8 (TPL2)-dependent MAPK1/3 activation | 2.119762e-05 | 4.674 |
R-HSA-72702 | Ribosomal scanning and start codon recognition | 2.345854e-05 | 4.630 |
R-HSA-5656121 | Translesion synthesis by POLI | 3.187679e-05 | 4.497 |
R-HSA-110312 | Translesion synthesis by REV1 | 2.613905e-05 | 4.583 |
R-HSA-1295596 | Spry regulation of FGF signaling | 2.613905e-05 | 4.583 |
R-HSA-9758274 | Regulation of NF-kappa B signaling | 3.187679e-05 | 4.497 |
R-HSA-193639 | p75NTR signals via NF-kB | 2.613905e-05 | 4.583 |
R-HSA-9708530 | Regulation of BACH1 activity | 3.187679e-05 | 4.497 |
R-HSA-9706369 | Negative regulation of FLT3 | 3.187679e-05 | 4.497 |
R-HSA-9759194 | Nuclear events mediated by NFE2L2 | 2.731834e-05 | 4.564 |
R-HSA-9680350 | Signaling by CSF1 (M-CSF) in myeloid cells | 3.353299e-05 | 4.475 |
R-HSA-168638 | NOD1/2 Signaling Pathway | 3.353299e-05 | 4.475 |
R-HSA-5205647 | Mitophagy | 3.353299e-05 | 4.475 |
R-HSA-8939902 | Regulation of RUNX2 expression and activity | 3.555763e-05 | 4.449 |
R-HSA-5655862 | Translesion synthesis by POLK | 3.848678e-05 | 4.415 |
R-HSA-3134975 | Regulation of innate immune responses to cytosolic DNA | 3.848678e-05 | 4.415 |
R-HSA-975110 | TRAF6 mediated IRF7 activation in TLR7/8 or 9 signaling | 3.848678e-05 | 4.415 |
R-HSA-69481 | G2/M Checkpoints | 3.891139e-05 | 4.410 |
R-HSA-4641263 | Regulation of FZD by ubiquitination | 4.604745e-05 | 4.337 |
R-HSA-3229121 | Glycogen storage diseases | 4.604745e-05 | 4.337 |
R-HSA-68882 | Mitotic Anaphase | 4.649912e-05 | 4.333 |
R-HSA-2173796 | SMAD2/SMAD3:SMAD4 heterotrimer regulates transcription | 4.674912e-05 | 4.330 |
R-HSA-2555396 | Mitotic Metaphase and Anaphase | 4.815391e-05 | 4.317 |
R-HSA-1234174 | Cellular response to hypoxia | 4.847024e-05 | 4.315 |
R-HSA-6804760 | Regulation of TP53 Activity through Methylation | 5.463959e-05 | 4.262 |
R-HSA-69278 | Cell Cycle, Mitotic | 5.690983e-05 | 4.245 |
R-HSA-382556 | ABC-family proteins mediated transport | 5.971661e-05 | 4.224 |
R-HSA-9020702 | Interleukin-1 signaling | 6.313151e-05 | 4.200 |
R-HSA-9646399 | Aggrephagy | 6.367381e-05 | 4.196 |
R-HSA-72203 | Processing of Capped Intron-Containing Pre-mRNA | 6.825556e-05 | 4.166 |
R-HSA-983168 | Antigen processing: Ubiquitination & Proteasome degradation | 7.452062e-05 | 4.128 |
R-HSA-179409 | APC-Cdc20 mediated degradation of Nek2A | 8.744548e-05 | 4.058 |
R-HSA-69275 | G2/M Transition | 8.606153e-05 | 4.065 |
R-HSA-1640170 | Cell Cycle | 6.787675e-05 | 4.168 |
R-HSA-450321 | JNK (c-Jun kinases) phosphorylation and activation mediated by activated human ... | 8.744548e-05 | 4.058 |
R-HSA-1632852 | Macroautophagy | 8.142190e-05 | 4.089 |
R-HSA-9636383 | Prevention of phagosomal-lysosomal fusion | 8.744548e-05 | 4.058 |
R-HSA-2979096 | NOTCH2 Activation and Transmission of Signal to the Nucleus | 8.744548e-05 | 4.058 |
R-HSA-9931295 | PD-L1(CD274) glycosylation and translocation to plasma membrane | 8.744548e-05 | 4.058 |
R-HSA-195253 | Degradation of beta-catenin by the destruction complex | 6.962067e-05 | 4.157 |
R-HSA-3322077 | Glycogen synthesis | 7.525245e-05 | 4.123 |
R-HSA-512988 | Interleukin-3, Interleukin-5 and GM-CSF signaling | 8.497428e-05 | 4.071 |
R-HSA-5637815 | Signaling by Ligand-Responsive EGFR Variants in Cancer | 8.744548e-05 | 4.058 |
R-HSA-1236382 | Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants | 8.744548e-05 | 4.058 |
R-HSA-162599 | Late Phase of HIV Life Cycle | 8.874870e-05 | 4.052 |
R-HSA-9013694 | Signaling by NOTCH4 | 9.136211e-05 | 4.039 |
R-HSA-69239 | Synthesis of DNA | 9.178169e-05 | 4.037 |
R-HSA-453274 | Mitotic G2-G2/M phases | 9.256258e-05 | 4.034 |
R-HSA-8856828 | Clathrin-mediated endocytosis | 9.261220e-05 | 4.033 |
R-HSA-2173789 | TGF-beta receptor signaling activates SMADs | 9.317040e-05 | 4.031 |
R-HSA-2672351 | Stimuli-sensing channels | 9.662373e-05 | 4.015 |
R-HSA-1169408 | ISG15 antiviral mechanism | 9.756196e-05 | 4.011 |
R-HSA-5696397 | Gap-filling DNA repair synthesis and ligation in GG-NER | 1.010143e-04 | 3.996 |
R-HSA-175474 | Assembly Of The HIV Virion | 1.010143e-04 | 3.996 |
R-HSA-450302 | activated TAK1 mediates p38 MAPK activation | 1.010143e-04 | 3.996 |
R-HSA-9705462 | Inactivation of CSF3 (G-CSF) signaling | 1.010143e-04 | 3.996 |
R-HSA-69002 | DNA Replication Pre-Initiation | 1.016718e-04 | 3.993 |
R-HSA-5689603 | UCH proteinases | 1.040919e-04 | 3.983 |
R-HSA-5684996 | MAPK1/MAPK3 signaling | 1.107069e-04 | 3.956 |
R-HSA-69242 | S Phase | 1.140838e-04 | 3.943 |
R-HSA-2173788 | Downregulation of TGF-beta receptor signaling | 1.160499e-04 | 3.935 |
R-HSA-9013507 | NOTCH3 Activation and Transmission of Signal to the Nucleus | 1.160499e-04 | 3.935 |
R-HSA-5357905 | Regulation of TNFR1 signaling | 1.214417e-04 | 3.916 |
R-HSA-6781823 | Formation of TC-NER Pre-Incision Complex | 1.214417e-04 | 3.916 |
R-HSA-1169410 | Antiviral mechanism by IFN-stimulated genes | 1.451279e-04 | 3.838 |
R-HSA-110314 | Recognition of DNA damage by PCNA-containing replication complex | 1.508931e-04 | 3.821 |
R-HSA-71291 | Metabolism of amino acids and derivatives | 1.509373e-04 | 3.821 |
R-HSA-532668 | N-glycan trimming in the ER and Calnexin/Calreticulin cycle | 1.558654e-04 | 3.807 |
R-HSA-9612973 | Autophagy | 1.569062e-04 | 3.804 |
R-HSA-5668541 | TNFR2 non-canonical NF-kB pathway | 1.601419e-04 | 3.795 |
R-HSA-162587 | HIV Life Cycle | 1.630843e-04 | 3.788 |
R-HSA-72172 | mRNA Splicing | 1.664253e-04 | 3.779 |
R-HSA-983705 | Signaling by the B Cell Receptor (BCR) | 1.694615e-04 | 3.771 |
R-HSA-8939236 | RUNX1 regulates transcription of genes involved in differentiation of HSCs | 1.697915e-04 | 3.770 |
R-HSA-69620 | Cell Cycle Checkpoints | 1.759670e-04 | 3.755 |
R-HSA-8878166 | Transcriptional regulation by RUNX2 | 1.808595e-04 | 3.743 |
R-HSA-5633007 | Regulation of TP53 Activity | 1.828328e-04 | 3.738 |
R-HSA-5689901 | Metalloprotease DUBs | 1.927342e-04 | 3.715 |
R-HSA-9637687 | Suppression of phagosomal maturation | 1.927342e-04 | 3.715 |
R-HSA-1643713 | Signaling by EGFR in Cancer | 1.927342e-04 | 3.715 |
R-HSA-9692916 | SARS-CoV-1 activates/modulates innate immune responses | 1.972934e-04 | 3.705 |
R-HSA-6804756 | Regulation of TP53 Activity through Phosphorylation | 2.015252e-04 | 3.696 |
R-HSA-901032 | ER Quality Control Compartment (ERQC) | 2.165225e-04 | 3.664 |
R-HSA-72649 | Translation initiation complex formation | 2.292475e-04 | 3.640 |
R-HSA-1236974 | ER-Phagosome pathway | 2.377642e-04 | 3.624 |
R-HSA-5654732 | Negative regulation of FGFR3 signaling | 2.423550e-04 | 3.616 |
R-HSA-202424 | Downstream TCR signaling | 2.509203e-04 | 3.600 |
R-HSA-917729 | Endosomal Sorting Complex Required For Transport (ESCRT) | 2.703326e-04 | 3.568 |
R-HSA-6782210 | Gap-filling DNA repair synthesis and ligation in TC-NER | 2.649951e-04 | 3.577 |
R-HSA-6782135 | Dual incision in TC-NER | 3.048256e-04 | 3.516 |
R-HSA-75893 | TNF signaling | 2.649951e-04 | 3.577 |
R-HSA-8863795 | Downregulation of ERBB2 signaling | 3.005569e-04 | 3.522 |
R-HSA-162588 | Budding and maturation of HIV virion | 3.331308e-04 | 3.477 |
R-HSA-72662 | Activation of the mRNA upon binding of the cap-binding complex and eIFs, and sub... | 3.048256e-04 | 3.516 |
R-HSA-177929 | Signaling by EGFR | 2.649951e-04 | 3.577 |
R-HSA-2173795 | Downregulation of SMAD2/3:SMAD4 transcriptional activity | 3.681581e-04 | 3.434 |
R-HSA-450294 | MAP kinase activation | 3.728824e-04 | 3.428 |
R-HSA-2173793 | Transcriptional activity of SMAD2/SMAD3:SMAD4 heterotrimer | 2.649951e-04 | 3.577 |
R-HSA-5654733 | Negative regulation of FGFR4 signaling | 2.703326e-04 | 3.568 |
R-HSA-9764274 | Regulation of Expression and Function of Type I Classical Cadherins | 3.028283e-04 | 3.519 |
R-HSA-9764265 | Regulation of CDH1 Expression and Function | 3.028283e-04 | 3.519 |
R-HSA-1227986 | Signaling by ERBB2 | 3.490377e-04 | 3.457 |
R-HSA-9833109 | Evasion by RSV of host interferon responses | 3.331308e-04 | 3.477 |
R-HSA-5607764 | CLEC7A (Dectin-1) signaling | 3.780236e-04 | 3.422 |
R-HSA-5621481 | C-type lectin receptors (CLRs) | 2.825436e-04 | 3.549 |
R-HSA-168928 | DDX58/IFIH1-mediated induction of interferon-alpha/beta | 3.423552e-04 | 3.466 |
R-HSA-9909396 | Circadian clock | 3.432509e-04 | 3.464 |
R-HSA-5683057 | MAPK family signaling cascades | 3.950341e-04 | 3.403 |
R-HSA-9705683 | SARS-CoV-2-host interactions | 3.493716e-04 | 3.457 |
R-HSA-68867 | Assembly of the pre-replicative complex | 3.093790e-04 | 3.510 |
R-HSA-9674555 | Signaling by CSF3 (G-CSF) | 2.703326e-04 | 3.568 |
R-HSA-170834 | Signaling by TGF-beta Receptor Complex | 3.969145e-04 | 3.401 |
R-HSA-8878159 | Transcriptional regulation by RUNX3 | 3.969145e-04 | 3.401 |
R-HSA-5673001 | RAF/MAP kinase cascade | 4.038845e-04 | 3.394 |
R-HSA-5675482 | Regulation of necroptotic cell death | 4.057430e-04 | 3.392 |
R-HSA-5654726 | Negative regulation of FGFR1 signaling | 4.057430e-04 | 3.392 |
R-HSA-3858494 | Beta-catenin independent WNT signaling | 4.179266e-04 | 3.379 |
R-HSA-201681 | TCF dependent signaling in response to WNT | 4.229209e-04 | 3.374 |
R-HSA-8848021 | Signaling by PTK6 | 4.242455e-04 | 3.372 |
R-HSA-9006927 | Signaling by Non-Receptor Tyrosine Kinases | 4.242455e-04 | 3.372 |
R-HSA-5696394 | DNA Damage Recognition in GG-NER | 4.459909e-04 | 3.351 |
R-HSA-168643 | Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signali... | 4.518438e-04 | 3.345 |
R-HSA-5696400 | Dual Incision in GG-NER | 4.890076e-04 | 3.311 |
R-HSA-9735869 | SARS-CoV-1 modulates host translation machinery | 4.890076e-04 | 3.311 |
R-HSA-5654727 | Negative regulation of FGFR2 signaling | 4.890076e-04 | 3.311 |
R-HSA-901042 | Calnexin/calreticulin cycle | 4.890076e-04 | 3.311 |
R-HSA-1980145 | Signaling by NOTCH2 | 4.890076e-04 | 3.311 |
R-HSA-983712 | Ion channel transport | 5.118725e-04 | 3.291 |
R-HSA-2559585 | Oncogene Induced Senescence | 5.348996e-04 | 3.272 |
R-HSA-5218859 | Regulated Necrosis | 5.759704e-04 | 3.240 |
R-HSA-9682385 | FLT3 signaling in disease | 5.837737e-04 | 3.234 |
R-HSA-72163 | mRNA Splicing - Major Pathway | 5.970858e-04 | 3.224 |
R-HSA-168164 | Toll Like Receptor 3 (TLR3) Cascade | 6.021849e-04 | 3.220 |
R-HSA-9759476 | Regulation of Homotypic Cell-Cell Adhesion | 6.342304e-04 | 3.198 |
R-HSA-3769402 | Deactivation of the beta-catenin transactivating complex | 6.357374e-04 | 3.197 |
R-HSA-448424 | Interleukin-17 signaling | 6.468619e-04 | 3.189 |
R-HSA-1834949 | Cytosolic sensors of pathogen-associated DNA | 6.468619e-04 | 3.189 |
R-HSA-975138 | TRAF6 mediated induction of NFkB and MAP kinases upon TLR7/8 or 9 activation | 6.863239e-04 | 3.163 |
R-HSA-1236975 | Antigen processing-Cross presentation | 6.863239e-04 | 3.163 |
R-HSA-5213460 | RIPK1-mediated regulated necrosis | 6.908985e-04 | 3.161 |
R-HSA-975155 | MyD88 dependent cascade initiated on endosome | 7.163033e-04 | 3.145 |
R-HSA-5688426 | Deubiquitination | 7.279210e-04 | 3.138 |
R-HSA-166166 | MyD88-independent TLR4 cascade | 7.472867e-04 | 3.127 |
R-HSA-937061 | TRIF (TICAM1)-mediated TLR4 signaling | 7.472867e-04 | 3.127 |
R-HSA-202403 | TCR signaling | 7.472867e-04 | 3.127 |
R-HSA-9648002 | RAS processing | 7.493649e-04 | 3.125 |
R-HSA-8964043 | Plasma lipoprotein clearance | 7.493649e-04 | 3.125 |
R-HSA-204998 | Cell death signalling via NRAGE, NRIF and NADE | 7.652037e-04 | 3.116 |
R-HSA-446652 | Interleukin-1 family signaling | 7.739059e-04 | 3.111 |
R-HSA-69306 | DNA Replication | 8.006085e-04 | 3.097 |
R-HSA-5696395 | Formation of Incision Complex in GG-NER | 8.112450e-04 | 3.091 |
R-HSA-8982491 | Glycogen metabolism | 8.112450e-04 | 3.091 |
R-HSA-168181 | Toll Like Receptor 7/8 (TLR7/8) Cascade | 8.464886e-04 | 3.072 |
R-HSA-5357801 | Programmed Cell Death | 8.490036e-04 | 3.071 |
R-HSA-68886 | M Phase | 8.495804e-04 | 3.071 |
R-HSA-6781827 | Transcription-Coupled Nucleotide Excision Repair (TC-NER) | 8.526171e-04 | 3.069 |
R-HSA-983169 | Class I MHC mediated antigen processing & presentation | 8.666946e-04 | 3.062 |
R-HSA-1980143 | Signaling by NOTCH1 | 8.990144e-04 | 3.046 |
R-HSA-5675221 | Negative regulation of MAPK pathway | 9.456802e-04 | 3.024 |
R-HSA-9683701 | Translation of Structural Proteins | 9.456802e-04 | 3.024 |
R-HSA-168138 | Toll Like Receptor 9 (TLR9) Cascade | 9.555583e-04 | 3.020 |
R-HSA-9711123 | Cellular response to chemical stress | 1.003862e-03 | 2.998 |
R-HSA-109581 | Apoptosis | 1.075187e-03 | 2.969 |
R-HSA-5654743 | Signaling by FGFR4 | 1.095073e-03 | 2.961 |
R-HSA-9637690 | Response of Mtb to phagocytosis | 1.095073e-03 | 2.961 |
R-HSA-5654738 | Signaling by FGFR2 | 1.103609e-03 | 2.957 |
R-HSA-6806834 | Signaling by MET | 1.103609e-03 | 2.957 |
R-HSA-2467813 | Separation of Sister Chromatids | 1.145212e-03 | 2.941 |
R-HSA-5693607 | Processing of DNA double-strand break ends | 1.159742e-03 | 2.936 |
R-HSA-418990 | Adherens junctions interactions | 1.211772e-03 | 2.917 |
R-HSA-6783310 | Fanconi Anemia Pathway | 1.260292e-03 | 2.900 |
R-HSA-5654741 | Signaling by FGFR3 | 1.260292e-03 | 2.900 |
R-HSA-8951664 | Neddylation | 1.310895e-03 | 2.882 |
R-HSA-9006925 | Intracellular signaling by second messengers | 1.336365e-03 | 2.874 |
R-HSA-2565942 | Regulation of PLK1 Activity at G2/M Transition | 1.340854e-03 | 2.873 |
R-HSA-72165 | mRNA Splicing - Minor Pathway | 1.349107e-03 | 2.870 |
R-HSA-72695 | Formation of the ternary complex, and subsequently, the 43S complex | 1.349107e-03 | 2.870 |
R-HSA-9861718 | Regulation of pyruvate metabolism | 1.349107e-03 | 2.870 |
R-HSA-445989 | TAK1-dependent IKK and NF-kappa-B activation | 1.442204e-03 | 2.841 |
R-HSA-9909648 | Regulation of PD-L1(CD274) expression | 1.505837e-03 | 2.822 |
R-HSA-9694516 | SARS-CoV-2 Infection | 1.538021e-03 | 2.813 |
R-HSA-5689880 | Ub-specific processing proteases | 1.550819e-03 | 2.809 |
R-HSA-2122947 | NOTCH1 Intracellular Domain Regulates Transcription | 1.641674e-03 | 2.785 |
R-HSA-74160 | Gene expression (Transcription) | 1.770853e-03 | 2.752 |
R-HSA-2559583 | Cellular Senescence | 1.895783e-03 | 2.722 |
R-HSA-162582 | Signal Transduction | 2.025226e-03 | 2.694 |
R-HSA-9754678 | SARS-CoV-2 modulates host translation machinery | 2.222777e-03 | 2.653 |
R-HSA-9012852 | Signaling by NOTCH3 | 2.353976e-03 | 2.628 |
R-HSA-5619115 | Disorders of transmembrane transporters | 2.468133e-03 | 2.608 |
R-HSA-5654736 | Signaling by FGFR1 | 2.490411e-03 | 2.604 |
R-HSA-6807070 | PTEN Regulation | 2.572714e-03 | 2.590 |
R-HSA-5663202 | Diseases of signal transduction by growth factor receptors and second messengers | 2.630424e-03 | 2.580 |
R-HSA-421270 | Cell-cell junction organization | 2.701233e-03 | 2.568 |
R-HSA-975871 | MyD88 cascade initiated on plasma membrane | 2.785121e-03 | 2.555 |
R-HSA-168176 | Toll Like Receptor 5 (TLR5) Cascade | 2.785121e-03 | 2.555 |
R-HSA-168142 | Toll Like Receptor 10 (TLR10) Cascade | 2.785121e-03 | 2.555 |
R-HSA-190236 | Signaling by FGFR | 2.785121e-03 | 2.555 |
R-HSA-1500931 | Cell-Cell communication | 2.839585e-03 | 2.547 |
R-HSA-3295583 | TRP channels | 2.867262e-03 | 2.543 |
R-HSA-8869496 | TFAP2A acts as a transcriptional repressor during retinoic acid induced cell dif... | 2.887491e-03 | 2.539 |
R-HSA-193704 | p75 NTR receptor-mediated signalling | 2.895315e-03 | 2.538 |
R-HSA-9033241 | Peroxisomal protein import | 2.932170e-03 | 2.533 |
R-HSA-5693565 | Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at... | 2.932170e-03 | 2.533 |
R-HSA-913531 | Interferon Signaling | 2.950586e-03 | 2.530 |
R-HSA-388841 | Regulation of T cell activation by CD28 family | 3.016460e-03 | 2.521 |
R-HSA-2644603 | Signaling by NOTCH1 in Cancer | 3.090580e-03 | 2.510 |
R-HSA-2644602 | Signaling by NOTCH1 PEST Domain Mutants in Cancer | 3.090580e-03 | 2.510 |
R-HSA-2894862 | Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants | 3.090580e-03 | 2.510 |
R-HSA-2894858 | Signaling by NOTCH1 HD+PEST Domain Mutants in Cancer | 3.090580e-03 | 2.510 |
R-HSA-2644606 | Constitutive Signaling by NOTCH1 PEST Domain Mutants | 3.090580e-03 | 2.510 |
R-HSA-2871837 | FCERI mediated NF-kB activation | 3.093756e-03 | 2.510 |
R-HSA-1280215 | Cytokine Signaling in Immune system | 3.113832e-03 | 2.507 |
R-HSA-168249 | Innate Immune System | 3.143026e-03 | 2.503 |
R-HSA-6798695 | Neutrophil degranulation | 3.209773e-03 | 2.494 |
R-HSA-389948 | Co-inhibition by PD-1 | 3.215109e-03 | 2.493 |
R-HSA-2454202 | Fc epsilon receptor (FCERI) signaling | 3.461858e-03 | 2.461 |
R-HSA-166016 | Toll Like Receptor 4 (TLR4) Cascade | 3.482472e-03 | 2.458 |
R-HSA-8856825 | Cargo recognition for clathrin-mediated endocytosis | 3.494091e-03 | 2.457 |
R-HSA-2426168 | Activation of gene expression by SREBF (SREBP) | 3.600691e-03 | 2.444 |
R-HSA-9006934 | Signaling by Receptor Tyrosine Kinases | 3.717622e-03 | 2.430 |
R-HSA-1643685 | Disease | 3.719979e-03 | 2.429 |
R-HSA-5696398 | Nucleotide Excision Repair | 3.756845e-03 | 2.425 |
R-HSA-5693532 | DNA Double-Strand Break Repair | 4.018180e-03 | 2.396 |
R-HSA-9725370 | Signaling by ALK fusions and activated point mutants | 4.033482e-03 | 2.394 |
R-HSA-9700206 | Signaling by ALK in cancer | 4.033482e-03 | 2.394 |
R-HSA-73887 | Death Receptor Signaling | 4.132258e-03 | 2.384 |
R-HSA-9958517 | SLC-mediated bile acid transport | 4.264734e-03 | 2.370 |
R-HSA-449147 | Signaling by Interleukins | 4.343848e-03 | 2.362 |
R-HSA-5693606 | DNA Double Strand Break Response | 4.365887e-03 | 2.360 |
R-HSA-5685942 | HDR through Homologous Recombination (HRR) | 4.365887e-03 | 2.360 |
R-HSA-168256 | Immune System | 4.643959e-03 | 2.333 |
R-HSA-446728 | Cell junction organization | 4.758455e-03 | 2.323 |
R-HSA-9006936 | Signaling by TGFB family members | 4.867770e-03 | 2.313 |
R-HSA-9613354 | Lipophagy | 5.046695e-03 | 2.297 |
R-HSA-2465910 | MASTL Facilitates Mitotic Progression | 5.046695e-03 | 2.297 |
R-HSA-5693567 | HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA) | 5.116768e-03 | 2.291 |
R-HSA-399956 | CRMPs in Sema3A signaling | 1.097622e-02 | 1.960 |
R-HSA-159236 | Transport of Mature mRNA derived from an Intron-Containing Transcript | 5.708256e-03 | 2.243 |
R-HSA-72202 | Transport of Mature Transcript to Cytoplasm | 8.197681e-03 | 2.086 |
R-HSA-5696399 | Global Genome Nucleotide Excision Repair (GG-NER) | 8.833613e-03 | 2.054 |
R-HSA-9907900 | Proteasome assembly | 1.085211e-02 | 1.964 |
R-HSA-3371556 | Cellular response to heat stress | 6.793725e-03 | 2.168 |
R-HSA-168898 | Toll-like Receptor Cascades | 1.050256e-02 | 1.979 |
R-HSA-9029558 | NR1H2 & NR1H3 regulate gene expression linked to lipogenesis | 9.845951e-03 | 2.007 |
R-HSA-195721 | Signaling by WNT | 6.934269e-03 | 2.159 |
R-HSA-3928662 | EPHB-mediated forward signaling | 1.085211e-02 | 1.964 |
R-HSA-166058 | MyD88:MAL(TIRAP) cascade initiated on plasma membrane | 6.391862e-03 | 2.194 |
R-HSA-168188 | Toll Like Receptor TLR6:TLR2 Cascade | 6.391862e-03 | 2.194 |
R-HSA-168179 | Toll Like Receptor TLR1:TLR2 Cascade | 7.001152e-03 | 2.155 |
R-HSA-181438 | Toll Like Receptor 2 (TLR2) Cascade | 7.001152e-03 | 2.155 |
R-HSA-73894 | DNA Repair | 6.255727e-03 | 2.204 |
R-HSA-111932 | CaMK IV-mediated phosphorylation of CREB | 5.889398e-03 | 2.230 |
R-HSA-977225 | Amyloid fiber formation | 7.891311e-03 | 2.103 |
R-HSA-69205 | G1/S-Specific Transcription | 6.492095e-03 | 2.188 |
R-HSA-111933 | Calmodulin induced events | 6.492095e-03 | 2.188 |
R-HSA-111997 | CaM pathway | 6.492095e-03 | 2.188 |
R-HSA-8864260 | Transcriptional regulation by the AP-2 (TFAP2) family of transcription factors | 1.085211e-02 | 1.964 |
R-HSA-111996 | Ca-dependent events | 9.768892e-03 | 2.010 |
R-HSA-3700989 | Transcriptional Regulation by TP53 | 1.032924e-02 | 1.986 |
R-HSA-157118 | Signaling by NOTCH | 7.994062e-03 | 2.097 |
R-HSA-1655829 | Regulation of cholesterol biosynthesis by SREBP (SREBF) | 7.301380e-03 | 2.137 |
R-HSA-5693538 | Homology Directed Repair | 6.197332e-03 | 2.208 |
R-HSA-70268 | Pyruvate metabolism | 1.020032e-02 | 1.991 |
R-HSA-1236394 | Signaling by ERBB4 | 5.955857e-03 | 2.225 |
R-HSA-917937 | Iron uptake and transport | 6.210512e-03 | 2.207 |
R-HSA-5663084 | Diseases of carbohydrate metabolism | 5.708256e-03 | 2.243 |
R-HSA-9694635 | Translation of Structural Proteins | 6.741330e-03 | 2.171 |
R-HSA-1489509 | DAG and IP3 signaling | 1.141874e-02 | 1.942 |
R-HSA-9820952 | Respiratory Syncytial Virus Infection Pathway | 1.152992e-02 | 1.938 |
R-HSA-8876725 | Protein methylation | 1.216088e-02 | 1.915 |
R-HSA-9679506 | SARS-CoV Infections | 1.222656e-02 | 1.913 |
R-HSA-9772573 | Late SARS-CoV-2 Infection Events | 1.249588e-02 | 1.903 |
R-HSA-174824 | Plasma lipoprotein assembly, remodeling, and clearance | 1.249588e-02 | 1.903 |
R-HSA-437239 | Recycling pathway of L1 | 1.260244e-02 | 1.900 |
R-HSA-73857 | RNA Polymerase II Transcription | 1.304214e-02 | 1.885 |
R-HSA-9705671 | SARS-CoV-2 activates/modulates innate and adaptive immune responses | 1.340034e-02 | 1.873 |
R-HSA-382551 | Transport of small molecules | 1.389711e-02 | 1.857 |
R-HSA-9912633 | Antigen processing: Ub, ATP-independent proteasomal degradation | 1.468930e-02 | 1.833 |
R-HSA-6804114 | TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest | 1.468930e-02 | 1.833 |
R-HSA-3371571 | HSF1-dependent transactivation | 1.517358e-02 | 1.819 |
R-HSA-72187 | mRNA 3'-end processing | 1.585915e-02 | 1.800 |
R-HSA-9909505 | Modulation of host responses by IFN-stimulated genes | 1.603108e-02 | 1.795 |
R-HSA-5602566 | TICAM1 deficiency - HSE | 1.723883e-02 | 1.763 |
R-HSA-77042 | Formation of editosomes by ADAR proteins | 1.723883e-02 | 1.763 |
R-HSA-9609507 | Protein localization | 1.734173e-02 | 1.761 |
R-HSA-4419969 | Depolymerization of the Nuclear Lamina | 1.742328e-02 | 1.759 |
R-HSA-2559580 | Oxidative Stress Induced Senescence | 1.751026e-02 | 1.757 |
R-HSA-111885 | Opioid Signalling | 1.853848e-02 | 1.732 |
R-HSA-167242 | Abortive elongation of HIV-1 transcript in the absence of Tat | 1.886492e-02 | 1.724 |
R-HSA-9833110 | RSV-host interactions | 1.906637e-02 | 1.720 |
R-HSA-2980766 | Nuclear Envelope Breakdown | 1.954588e-02 | 1.709 |
R-HSA-6791312 | TP53 Regulates Transcription of Cell Cycle Genes | 1.954588e-02 | 1.709 |
R-HSA-1257604 | PIP3 activates AKT signaling | 2.079117e-02 | 1.682 |
R-HSA-8878171 | Transcriptional regulation by RUNX1 | 2.114621e-02 | 1.675 |
R-HSA-210991 | Basigin interactions | 2.189279e-02 | 1.660 |
R-HSA-73856 | RNA Polymerase II Transcription Termination | 2.280733e-02 | 1.642 |
R-HSA-112043 | PLC beta mediated events | 2.280733e-02 | 1.642 |
R-HSA-438066 | Unblocking of NMDA receptors, glutamate binding and activation | 2.347715e-02 | 1.629 |
R-HSA-442982 | Ras activation upon Ca2+ influx through NMDA receptor | 2.347715e-02 | 1.629 |
R-HSA-9617324 | Negative regulation of NMDA receptor-mediated neuronal transmission | 2.347715e-02 | 1.629 |
R-HSA-2995383 | Initiation of Nuclear Envelope (NE) Reformation | 2.347715e-02 | 1.629 |
R-HSA-9825892 | Regulation of MITF-M-dependent genes involved in cell cycle and proliferation | 2.347715e-02 | 1.629 |
R-HSA-9617828 | FOXO-mediated transcription of cell cycle genes | 2.347715e-02 | 1.629 |
R-HSA-166208 | mTORC1-mediated signalling | 2.510725e-02 | 1.600 |
R-HSA-5602571 | TRAF3 deficiency - HSE | 2.574726e-02 | 1.589 |
R-HSA-9648895 | Response of EIF2AK1 (HRI) to heme deficiency | 2.678219e-02 | 1.572 |
R-HSA-909733 | Interferon alpha/beta signaling | 2.678338e-02 | 1.572 |
R-HSA-373760 | L1CAM interactions | 2.744387e-02 | 1.562 |
R-HSA-392499 | Metabolism of proteins | 2.801900e-02 | 1.553 |
R-HSA-112040 | G-protein mediated events | 2.822049e-02 | 1.549 |
R-HSA-5621575 | CD209 (DC-SIGN) signaling | 2.850108e-02 | 1.545 |
R-HSA-68875 | Mitotic Prophase | 3.018290e-02 | 1.520 |
R-HSA-9620244 | Long-term potentiation | 3.026304e-02 | 1.519 |
R-HSA-9635486 | Infection with Mycobacterium tuberculosis | 3.089203e-02 | 1.510 |
R-HSA-212165 | Epigenetic regulation of gene expression | 3.101475e-02 | 1.508 |
R-HSA-212436 | Generic Transcription Pathway | 3.157155e-02 | 1.501 |
R-HSA-9022699 | MECP2 regulates neuronal receptors and channels | 3.206721e-02 | 1.494 |
R-HSA-199991 | Membrane Trafficking | 3.231558e-02 | 1.491 |
R-HSA-4641262 | Disassembly of the destruction complex and recruitment of AXIN to the membrane | 3.391275e-02 | 1.470 |
R-HSA-9006115 | Signaling by NTRK2 (TRKB) | 3.391275e-02 | 1.470 |
R-HSA-3656535 | TGFBR1 LBD Mutants in Cancer | 3.418256e-02 | 1.466 |
R-HSA-75064 | mRNA Editing: A to I Conversion | 3.418256e-02 | 1.466 |
R-HSA-75102 | C6 deamination of adenosine | 3.418256e-02 | 1.466 |
R-HSA-167158 | Formation of the HIV-1 Early Elongation Complex | 3.579881e-02 | 1.446 |
R-HSA-113418 | Formation of the Early Elongation Complex | 3.579881e-02 | 1.446 |
R-HSA-9927432 | Developmental Lineage of Mammary Gland Myoepithelial Cells | 3.772456e-02 | 1.423 |
R-HSA-2995410 | Nuclear Envelope (NE) Reassembly | 4.207190e-02 | 1.376 |
R-HSA-5368598 | Negative regulation of TCF-dependent signaling by DVL-interacting proteins | 4.254534e-02 | 1.371 |
R-HSA-350562 | Regulation of ornithine decarboxylase (ODC) | 4.373183e-02 | 1.359 |
R-HSA-1280218 | Adaptive Immune System | 4.516225e-02 | 1.345 |
R-HSA-159227 | Transport of the SLBP independent Mature mRNA | 4.580828e-02 | 1.339 |
R-HSA-69273 | Cyclin A/B1/B2 associated events during G2/M transition | 4.580828e-02 | 1.339 |
R-HSA-9930044 | Nuclear RNA decay | 4.580828e-02 | 1.339 |
R-HSA-442742 | CREB1 phosphorylation through NMDA receptor-mediated activation of RAS signaling | 4.580828e-02 | 1.339 |
R-HSA-159230 | Transport of the SLBP Dependant Mature mRNA | 4.792044e-02 | 1.319 |
R-HSA-9818027 | NFE2L2 regulating anti-oxidant/detoxification enzymes | 4.792044e-02 | 1.319 |
R-HSA-9658195 | Leishmania infection | 4.861349e-02 | 1.313 |
R-HSA-9824443 | Parasitic Infection Pathways | 4.861349e-02 | 1.313 |
R-HSA-9768919 | NPAS4 regulates expression of target genes | 5.006755e-02 | 1.300 |
R-HSA-9013957 | TLR3-mediated TICAM1-dependent programmed cell death | 5.083622e-02 | 1.294 |
R-HSA-69200 | Phosphorylation of proteins involved in G1/S transition by active Cyclin E:Cdk2 ... | 5.083622e-02 | 1.294 |
R-HSA-9706374 | FLT3 signaling through SRC family kinases | 5.083622e-02 | 1.294 |
R-HSA-3301854 | Nuclear Pore Complex (NPC) Disassembly | 5.224885e-02 | 1.282 |
R-HSA-432720 | Lysosome Vesicle Biogenesis | 5.446361e-02 | 1.264 |
R-HSA-3371511 | HSF1 activation | 5.446361e-02 | 1.264 |
R-HSA-163560 | Triglyceride catabolism | 5.446361e-02 | 1.264 |
R-HSA-8986944 | Transcriptional Regulation by MECP2 | 5.735476e-02 | 1.241 |
R-HSA-166520 | Signaling by NTRKs | 5.776248e-02 | 1.238 |
R-HSA-165054 | Rev-mediated nuclear export of HIV RNA | 5.899054e-02 | 1.229 |
R-HSA-202131 | Metabolism of nitric oxide: NOS3 activation and regulation | 5.899054e-02 | 1.229 |
R-HSA-68911 | G2 Phase | 5.905582e-02 | 1.229 |
R-HSA-9032759 | NTRK2 activates RAC1 | 5.905582e-02 | 1.229 |
R-HSA-203754 | NOSIP mediated eNOS trafficking | 5.905582e-02 | 1.229 |
R-HSA-3656534 | Loss of Function of TGFBR1 in Cancer | 5.905582e-02 | 1.229 |
R-HSA-74713 | IRS activation | 5.905582e-02 | 1.229 |
R-HSA-8866376 | Reelin signalling pathway | 5.905582e-02 | 1.229 |
R-HSA-9931529 | Phosphorylation and nuclear translocation of BMAL1 (ARNTL) and CLOCK | 5.905582e-02 | 1.229 |
R-HSA-2682334 | EPH-Ephrin signaling | 6.012542e-02 | 1.221 |
R-HSA-159231 | Transport of Mature mRNA Derived from an Intronless Transcript | 6.130129e-02 | 1.213 |
R-HSA-167200 | Formation of HIV-1 elongation complex containing HIV-1 Tat | 6.130129e-02 | 1.213 |
R-HSA-1236978 | Cross-presentation of soluble exogenous antigens (endosomes) | 6.130129e-02 | 1.213 |
R-HSA-159234 | Transport of Mature mRNAs Derived from Intronless Transcripts | 6.364261e-02 | 1.196 |
R-HSA-167152 | Formation of HIV elongation complex in the absence of HIV Tat | 6.364261e-02 | 1.196 |
R-HSA-167169 | HIV Transcription Elongation | 6.364261e-02 | 1.196 |
R-HSA-167246 | Tat-mediated elongation of the HIV-1 transcript | 6.364261e-02 | 1.196 |
R-HSA-3371568 | Attenuation phase | 6.364261e-02 | 1.196 |
R-HSA-177243 | Interactions of Rev with host cellular proteins | 6.364261e-02 | 1.196 |
R-HSA-9917777 | Epigenetic regulation by WDR5-containing histone modifying complexes | 6.405193e-02 | 1.193 |
R-HSA-5218920 | VEGFR2 mediated vascular permeability | 6.601382e-02 | 1.180 |
R-HSA-9833576 | CDH11 homotypic and heterotypic interactions | 6.720474e-02 | 1.173 |
R-HSA-8849470 | PTK6 Regulates Cell Cycle | 6.720474e-02 | 1.173 |
R-HSA-176417 | Phosphorylation of Emi1 | 6.720474e-02 | 1.173 |
R-HSA-9764302 | Regulation of CDH19 Expression and Function | 6.720474e-02 | 1.173 |
R-HSA-9609736 | Assembly and cell surface presentation of NMDA receptors | 6.841422e-02 | 1.165 |
R-HSA-165159 | MTOR signalling | 7.084315e-02 | 1.150 |
R-HSA-1433557 | Signaling by SCF-KIT | 7.329994e-02 | 1.135 |
R-HSA-69478 | G2/M DNA replication checkpoint | 7.528358e-02 | 1.123 |
R-HSA-113507 | E2F-enabled inhibition of pre-replication complex formation | 7.528358e-02 | 1.123 |
R-HSA-199920 | CREB phosphorylation | 7.528358e-02 | 1.123 |
R-HSA-2980767 | Activation of NIMA Kinases NEK9, NEK6, NEK7 | 7.528358e-02 | 1.123 |
R-HSA-164944 | Nef and signal transduction | 7.528358e-02 | 1.123 |
R-HSA-3304351 | Signaling by TGF-beta Receptor Complex in Cancer | 7.528358e-02 | 1.123 |
R-HSA-373752 | Netrin-1 signaling | 7.578394e-02 | 1.120 |
R-HSA-3371453 | Regulation of HSF1-mediated heat shock response | 7.644814e-02 | 1.117 |
R-HSA-9824272 | Somitogenesis | 7.829448e-02 | 1.106 |
R-HSA-203641 | NOSTRIN mediated eNOS trafficking | 8.329295e-02 | 1.079 |
R-HSA-2562578 | TRIF-mediated programmed cell death | 8.329295e-02 | 1.079 |
R-HSA-111367 | SLBP independent Processing of Histone Pre-mRNAs | 8.329295e-02 | 1.079 |
R-HSA-9032845 | Activated NTRK2 signals through CDK5 | 8.329295e-02 | 1.079 |
R-HSA-5576890 | Phase 3 - rapid repolarisation | 8.329295e-02 | 1.079 |
R-HSA-447041 | CHL1 interactions | 8.329295e-02 | 1.079 |
R-HSA-6811440 | Retrograde transport at the Trans-Golgi-Network | 8.339271e-02 | 1.079 |
R-HSA-1483191 | Synthesis of PC | 8.339271e-02 | 1.079 |
R-HSA-9734779 | Developmental Cell Lineages of the Integumentary System | 8.774453e-02 | 1.057 |
R-HSA-9032500 | Activated NTRK2 signals through FYN | 9.123344e-02 | 1.040 |
R-HSA-77588 | SLBP Dependent Processing of Replication-Dependent Histone Pre-mRNAs | 9.123344e-02 | 1.040 |
R-HSA-112382 | Formation of RNA Pol II elongation complex | 9.655940e-02 | 1.015 |
R-HSA-9634815 | Transcriptional Regulation by NPAS4 | 9.655940e-02 | 1.015 |
R-HSA-201688 | WNT mediated activation of DVL | 9.910564e-02 | 1.004 |
R-HSA-2025928 | Calcineurin activates NFAT | 9.910564e-02 | 1.004 |
R-HSA-448706 | Interleukin-1 processing | 9.910564e-02 | 1.004 |
R-HSA-75072 | mRNA Editing | 9.910564e-02 | 1.004 |
R-HSA-450520 | HuR (ELAVL1) binds and stabilizes mRNA | 9.910564e-02 | 1.004 |
R-HSA-75955 | RNA Polymerase II Transcription Elongation | 9.926016e-02 | 1.003 |
R-HSA-5250924 | B-WICH complex positively regulates rRNA expression | 9.926016e-02 | 1.003 |
R-HSA-432722 | Golgi Associated Vesicle Biogenesis | 9.926016e-02 | 1.003 |
R-HSA-4420097 | VEGFA-VEGFR2 Pathway | 1.032308e-01 | 0.986 |
R-HSA-9762292 | Regulation of CDH11 function | 1.069101e-01 | 0.971 |
R-HSA-6803544 | Ion influx/efflux at host-pathogen interface | 1.069101e-01 | 0.971 |
R-HSA-110056 | MAPK3 (ERK1) activation | 1.069101e-01 | 0.971 |
R-HSA-74749 | Signal attenuation | 1.069101e-01 | 0.971 |
R-HSA-5653656 | Vesicle-mediated transport | 1.081630e-01 | 0.966 |
R-HSA-6785807 | Interleukin-4 and Interleukin-13 signaling | 1.130361e-01 | 0.947 |
R-HSA-9706019 | RHOBTB3 ATPase cycle | 1.146475e-01 | 0.941 |
R-HSA-210990 | PECAM1 interactions | 1.146475e-01 | 0.941 |
R-HSA-429914 | Deadenylation-dependent mRNA decay | 1.158890e-01 | 0.936 |
R-HSA-191859 | snRNP Assembly | 1.158890e-01 | 0.936 |
R-HSA-194441 | Metabolism of non-coding RNA | 1.158890e-01 | 0.936 |
R-HSA-8979227 | Triglyceride metabolism | 1.158890e-01 | 0.936 |
R-HSA-351202 | Metabolism of polyamines | 1.187261e-01 | 0.925 |
R-HSA-9793380 | Formation of paraxial mesoderm | 1.215806e-01 | 0.915 |
R-HSA-2514853 | Condensation of Prometaphase Chromosomes | 1.223183e-01 | 0.913 |
R-HSA-9851695 | Epigenetic regulation of adipogenesis genes by MLL3 and MLL4 complexes | 1.235033e-01 | 0.908 |
R-HSA-9841922 | MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesi... | 1.235033e-01 | 0.908 |
R-HSA-9818564 | Epigenetic regulation of gene expression by MLL3 and MLL4 complexes | 1.235033e-01 | 0.908 |
R-HSA-194138 | Signaling by VEGF | 1.235033e-01 | 0.908 |
R-HSA-375165 | NCAM signaling for neurite out-growth | 1.244519e-01 | 0.905 |
R-HSA-9616222 | Transcriptional regulation of granulopoiesis | 1.244519e-01 | 0.905 |
R-HSA-373755 | Semaphorin interactions | 1.273396e-01 | 0.895 |
R-HSA-187037 | Signaling by NTRK1 (TRKA) | 1.292678e-01 | 0.889 |
R-HSA-9820865 | Z-decay: degradation of maternal mRNAs by zygotically expressed factors | 1.299231e-01 | 0.886 |
R-HSA-9931530 | Phosphorylation and nuclear translocation of the CRY:PER:kinase complex | 1.299231e-01 | 0.886 |
R-HSA-418890 | Role of second messengers in netrin-1 signaling | 1.299231e-01 | 0.886 |
R-HSA-5576891 | Cardiac conduction | 1.370997e-01 | 0.863 |
R-HSA-170660 | Adenylate cyclase activating pathway | 1.374625e-01 | 0.862 |
R-HSA-9661069 | Defective binding of RB1 mutants to E2F1,(E2F2, E2F3) | 1.374625e-01 | 0.862 |
R-HSA-389359 | CD28 dependent Vav1 pathway | 1.374625e-01 | 0.862 |
R-HSA-9659787 | Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects | 1.374625e-01 | 0.862 |
R-HSA-75892 | Platelet Adhesion to exposed collagen | 1.374625e-01 | 0.862 |
R-HSA-75035 | Chk1/Chk2(Cds1) mediated inactivation of Cyclin B:Cdk1 complex | 1.374625e-01 | 0.862 |
R-HSA-162658 | Golgi Cisternae Pericentriolar Stack Reorganization | 1.374625e-01 | 0.862 |
R-HSA-167172 | Transcription of the HIV genome | 1.420063e-01 | 0.848 |
R-HSA-3371497 | HSP90 chaperone cycle for steroid hormone receptors (SHR) in the presence of lig... | 1.420063e-01 | 0.848 |
R-HSA-177504 | Retrograde neurotrophin signalling | 1.449370e-01 | 0.839 |
R-HSA-9933939 | Formation of the polybromo-BAF (pBAF) complex | 1.449370e-01 | 0.839 |
R-HSA-1433559 | Regulation of KIT signaling | 1.449370e-01 | 0.839 |
R-HSA-5578768 | Physiological factors | 1.449370e-01 | 0.839 |
R-HSA-9828642 | Respiratory syncytial virus genome transcription | 1.449370e-01 | 0.839 |
R-HSA-5250913 | Positive epigenetic regulation of rRNA expression | 1.509721e-01 | 0.821 |
R-HSA-170670 | Adenylate cyclase inhibitory pathway | 1.523472e-01 | 0.817 |
R-HSA-418885 | DCC mediated attractive signaling | 1.523472e-01 | 0.817 |
R-HSA-399954 | Sema3A PAK dependent Axon repulsion | 1.523472e-01 | 0.817 |
R-HSA-1810476 | RIP-mediated NFkB activation via ZBP1 | 1.523472e-01 | 0.817 |
R-HSA-450513 | Tristetraprolin (TTP, ZFP36) binds and destabilizes mRNA | 1.523472e-01 | 0.817 |
R-HSA-9755779 | SARS-CoV-2 targets host intracellular signalling and regulatory pathways | 1.523472e-01 | 0.817 |
R-HSA-450385 | Butyrate Response Factor 1 (BRF1) binds and destabilizes mRNA | 1.523472e-01 | 0.817 |
R-HSA-9735871 | SARS-CoV-1 targets host intracellular signalling and regulatory pathways | 1.523472e-01 | 0.817 |
R-HSA-199992 | trans-Golgi Network Vesicle Budding | 1.539857e-01 | 0.813 |
R-HSA-9924644 | Developmental Lineages of the Mammary Gland | 1.539857e-01 | 0.813 |
R-HSA-198725 | Nuclear Events (kinase and transcription factor activation) | 1.539857e-01 | 0.813 |
R-HSA-9664407 | Parasite infection | 1.573556e-01 | 0.803 |
R-HSA-9664417 | Leishmania phagocytosis | 1.573556e-01 | 0.803 |
R-HSA-9664422 | FCGR3A-mediated phagocytosis | 1.573556e-01 | 0.803 |
R-HSA-399955 | SEMA3A-Plexin repulsion signaling by inhibiting Integrin adhesion | 1.596936e-01 | 0.797 |
R-HSA-9673324 | WNT5:FZD7-mediated leishmania damping | 1.596936e-01 | 0.797 |
R-HSA-9664420 | Killing mechanisms | 1.596936e-01 | 0.797 |
R-HSA-176412 | Phosphorylation of the APC/C | 1.596936e-01 | 0.797 |
R-HSA-450604 | KSRP (KHSRP) binds and destabilizes mRNA | 1.596936e-01 | 0.797 |
R-HSA-6804116 | TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest | 1.596936e-01 | 0.797 |
R-HSA-140534 | Caspase activation via Death Receptors in the presence of ligand | 1.596936e-01 | 0.797 |
R-HSA-9678110 | Attachment and Entry | 1.596936e-01 | 0.797 |
R-HSA-674695 | RNA Polymerase II Pre-transcription Events | 1.600475e-01 | 0.796 |
R-HSA-77595 | Processing of Intronless Pre-mRNAs | 1.669768e-01 | 0.777 |
R-HSA-9024446 | NR1H2 and NR1H3-mediated signaling | 1.692210e-01 | 0.772 |
R-HSA-6783783 | Interleukin-10 signaling | 1.722987e-01 | 0.764 |
R-HSA-9955298 | SLC-mediated transport of organic anions | 1.722987e-01 | 0.764 |
R-HSA-139853 | Elevation of cytosolic Ca2+ levels | 1.741974e-01 | 0.759 |
R-HSA-9856530 | High laminar flow shear stress activates signaling by PIEZO1 and PECAM1:CDH5:KDR... | 1.784816e-01 | 0.748 |
R-HSA-9833482 | PKR-mediated signaling | 1.784816e-01 | 0.748 |
R-HSA-3928664 | Ephrin signaling | 1.813558e-01 | 0.741 |
R-HSA-164378 | PKA activation in glucagon signalling | 1.813558e-01 | 0.741 |
R-HSA-156711 | Polo-like kinase mediated events | 1.813558e-01 | 0.741 |
R-HSA-163615 | PKA activation | 1.813558e-01 | 0.741 |
R-HSA-1606322 | ZBP1(DAI) mediated induction of type I IFNs | 1.813558e-01 | 0.741 |
R-HSA-8851708 | Signaling by FGFR2 IIIa TM | 1.884525e-01 | 0.725 |
R-HSA-429958 | mRNA decay by 3' to 5' exoribonuclease | 1.884525e-01 | 0.725 |
R-HSA-113510 | E2F mediated regulation of DNA replication | 1.884525e-01 | 0.725 |
R-HSA-449836 | Other interleukin signaling | 1.884525e-01 | 0.725 |
R-HSA-1362277 | Transcription of E2F targets under negative control by DREAM complex | 1.954882e-01 | 0.709 |
R-HSA-9609523 | Insertion of tail-anchored proteins into the endoplasmic reticulum membrane | 1.954882e-01 | 0.709 |
R-HSA-373753 | Nephrin family interactions | 1.954882e-01 | 0.709 |
R-HSA-389513 | Co-inhibition by CTLA4 | 1.954882e-01 | 0.709 |
R-HSA-5357786 | TNFR1-induced proapoptotic signaling | 2.024634e-01 | 0.694 |
R-HSA-198753 | ERK/MAPK targets | 2.024634e-01 | 0.694 |
R-HSA-111931 | PKA-mediated phosphorylation of CREB | 2.024634e-01 | 0.694 |
R-HSA-438064 | Post NMDA receptor activation events | 2.035246e-01 | 0.691 |
R-HSA-2022377 | Metabolism of Angiotensinogen to Angiotensins | 2.093785e-01 | 0.679 |
R-HSA-9694614 | Attachment and Entry | 2.093785e-01 | 0.679 |
R-HSA-5620912 | Anchoring of the basal body to the plasma membrane | 2.130187e-01 | 0.672 |
R-HSA-6803529 | FGFR2 alternative splicing | 2.162340e-01 | 0.665 |
R-HSA-9670439 | Signaling by phosphorylated juxtamembrane, extracellular and kinase domain KIT m... | 2.162340e-01 | 0.665 |
R-HSA-9669938 | Signaling by KIT in disease | 2.162340e-01 | 0.665 |
R-HSA-112409 | RAF-independent MAPK1/3 activation | 2.162340e-01 | 0.665 |
R-HSA-164952 | The role of Nef in HIV-1 replication and disease pathogenesis | 2.230305e-01 | 0.652 |
R-HSA-75067 | Processing of Capped Intronless Pre-mRNA | 2.297685e-01 | 0.639 |
R-HSA-429947 | Deadenylation of mRNA | 2.297685e-01 | 0.639 |
R-HSA-8863678 | Neurodegenerative Diseases | 2.297685e-01 | 0.639 |
R-HSA-8862803 | Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer's dis... | 2.297685e-01 | 0.639 |
R-HSA-71387 | Metabolism of carbohydrates and carbohydrate derivatives | 2.347369e-01 | 0.629 |
R-HSA-9932451 | SWI/SNF chromatin remodelers | 2.364485e-01 | 0.626 |
R-HSA-9932444 | ATP-dependent chromatin remodelers | 2.364485e-01 | 0.626 |
R-HSA-2029480 | Fcgamma receptor (FCGR) dependent phagocytosis | 2.364514e-01 | 0.626 |
R-HSA-9615933 | Postmitotic nuclear pore complex (NPC) reformation | 2.430710e-01 | 0.614 |
R-HSA-5357769 | Caspase activation via extrinsic apoptotic signalling pathway | 2.430710e-01 | 0.614 |
R-HSA-9614085 | FOXO-mediated transcription | 2.481294e-01 | 0.605 |
R-HSA-167243 | Tat-mediated HIV elongation arrest and recovery | 2.496364e-01 | 0.603 |
R-HSA-167238 | Pausing and recovery of Tat-mediated HIV elongation | 2.496364e-01 | 0.603 |
R-HSA-3928663 | EPHA-mediated growth cone collapse | 2.496364e-01 | 0.603 |
R-HSA-9734009 | Defective Intrinsic Pathway for Apoptosis | 2.496364e-01 | 0.603 |
R-HSA-389357 | CD28 dependent PI3K/Akt signaling | 2.496364e-01 | 0.603 |
R-HSA-70171 | Glycolysis | 2.513358e-01 | 0.600 |
R-HSA-167287 | HIV elongation arrest and recovery | 2.561453e-01 | 0.592 |
R-HSA-167290 | Pausing and recovery of HIV elongation | 2.561453e-01 | 0.592 |
R-HSA-5576892 | Phase 0 - rapid depolarisation | 2.561453e-01 | 0.592 |
R-HSA-171319 | Telomere Extension By Telomerase | 2.561453e-01 | 0.592 |
R-HSA-380994 | ATF4 activates genes in response to endoplasmic reticulum stress | 2.561453e-01 | 0.592 |
R-HSA-5620971 | Pyroptosis | 2.561453e-01 | 0.592 |
R-HSA-442755 | Activation of NMDA receptors and postsynaptic events | 2.577519e-01 | 0.589 |
R-HSA-209968 | Thyroxine biosynthesis | 2.625982e-01 | 0.581 |
R-HSA-450282 | MAPK targets/ Nuclear events mediated by MAP kinases | 2.625982e-01 | 0.581 |
R-HSA-72086 | mRNA Capping | 2.625982e-01 | 0.581 |
R-HSA-9759475 | Regulation of CDH11 Expression and Function | 2.625982e-01 | 0.581 |
R-HSA-418360 | Platelet calcium homeostasis | 2.625982e-01 | 0.581 |
R-HSA-180024 | DARPP-32 events | 2.625982e-01 | 0.581 |
R-HSA-9860931 | Response of endothelial cells to shear stress | 2.641708e-01 | 0.578 |
R-HSA-5619107 | Defective TPR may confer susceptibility towards thyroid papillary carcinoma (TPC... | 2.689954e-01 | 0.570 |
R-HSA-2424491 | DAP12 signaling | 2.689954e-01 | 0.570 |
R-HSA-68962 | Activation of the pre-replicative complex | 2.689954e-01 | 0.570 |
R-HSA-9687139 | Aberrant regulation of mitotic cell cycle due to RB1 defects | 2.689954e-01 | 0.570 |
R-HSA-888590 | GABA synthesis, release, reuptake and degradation | 2.689954e-01 | 0.570 |
R-HSA-1855196 | IP3 and IP4 transport between cytosol and nucleus | 2.753376e-01 | 0.560 |
R-HSA-1855229 | IP6 and IP7 transport between cytosol and nucleus | 2.753376e-01 | 0.560 |
R-HSA-399719 | Trafficking of AMPA receptors | 2.753376e-01 | 0.560 |
R-HSA-9675126 | Diseases of mitotic cell cycle | 2.816251e-01 | 0.550 |
R-HSA-9824439 | Bacterial Infection Pathways | 2.873833e-01 | 0.542 |
R-HSA-1855170 | IPs transport between nucleus and cytosol | 2.878584e-01 | 0.541 |
R-HSA-176187 | Activation of ATR in response to replication stress | 2.878584e-01 | 0.541 |
R-HSA-6804758 | Regulation of TP53 Activity through Acetylation | 2.878584e-01 | 0.541 |
R-HSA-9764260 | Regulation of Expression and Function of Type II Classical Cadherins | 2.878584e-01 | 0.541 |
R-HSA-399721 | Glutamate binding, activation of AMPA receptors and synaptic plasticity | 2.878584e-01 | 0.541 |
R-HSA-9022692 | Regulation of MECP2 expression and activity | 2.878584e-01 | 0.541 |
R-HSA-9768727 | Regulation of CDH1 posttranslational processing and trafficking to plasma membra... | 2.940380e-01 | 0.532 |
R-HSA-170822 | Regulation of Glucokinase by Glucokinase Regulatory Protein | 2.940380e-01 | 0.532 |
R-HSA-163359 | Glucagon signaling in metabolic regulation | 2.940380e-01 | 0.532 |
R-HSA-114508 | Effects of PIP2 hydrolysis | 2.940380e-01 | 0.532 |
R-HSA-6811442 | Intra-Golgi and retrograde Golgi-to-ER traffic | 2.971752e-01 | 0.527 |
R-HSA-9855142 | Cellular responses to mechanical stimuli | 2.994395e-01 | 0.524 |
R-HSA-180746 | Nuclear import of Rev protein | 3.001644e-01 | 0.523 |
R-HSA-203615 | eNOS activation | 3.001644e-01 | 0.523 |
R-HSA-5673000 | RAF activation | 3.001644e-01 | 0.523 |
R-HSA-381042 | PERK regulates gene expression | 3.062380e-01 | 0.514 |
R-HSA-9772755 | Formation of WDR5-containing histone-modifying complexes | 3.062380e-01 | 0.514 |
R-HSA-114604 | GPVI-mediated activation cascade | 3.122593e-01 | 0.505 |
R-HSA-1839126 | FGFR2 mutant receptor activation | 3.122593e-01 | 0.505 |
R-HSA-8853659 | RET signaling | 3.122593e-01 | 0.505 |
R-HSA-70326 | Glucose metabolism | 3.153984e-01 | 0.501 |
R-HSA-1296072 | Voltage gated Potassium channels | 3.182287e-01 | 0.497 |
R-HSA-180910 | Vpr-mediated nuclear import of PICs | 3.182287e-01 | 0.497 |
R-HSA-112314 | Neurotransmitter receptors and postsynaptic signal transmission | 3.279579e-01 | 0.484 |
R-HSA-397014 | Muscle contraction | 3.279579e-01 | 0.484 |
R-HSA-2500257 | Resolution of Sister Chromatid Cohesion | 3.281090e-01 | 0.484 |
R-HSA-73886 | Chromosome Maintenance | 3.281090e-01 | 0.484 |
R-HSA-9725554 | Differentiation of Keratinocytes in Interfollicular Epidermis in Mammalian Skin | 3.300135e-01 | 0.481 |
R-HSA-168276 | NS1 Mediated Effects on Host Pathways | 3.300135e-01 | 0.481 |
R-HSA-9820965 | Respiratory syncytial virus (RSV) genome replication, transcription and translat... | 3.300135e-01 | 0.481 |
R-HSA-176033 | Interactions of Vpr with host cellular proteins | 3.358299e-01 | 0.474 |
R-HSA-5602358 | Diseases associated with the TLR signaling cascade | 3.358299e-01 | 0.474 |
R-HSA-5260271 | Diseases of Immune System | 3.358299e-01 | 0.474 |
R-HSA-9820841 | M-decay: degradation of maternal mRNAs by maternally stored factors | 3.415961e-01 | 0.466 |
R-HSA-168271 | Transport of Ribonucleoproteins into the Host Nucleus | 3.415961e-01 | 0.466 |
R-HSA-3214841 | PKMTs methylate histone lysines | 3.415961e-01 | 0.466 |
R-HSA-446203 | Asparagine N-linked glycosylation | 3.417501e-01 | 0.466 |
R-HSA-9664323 | FCGR3A-mediated IL10 synthesis | 3.470542e-01 | 0.460 |
R-HSA-9656223 | Signaling by RAF1 mutants | 3.473126e-01 | 0.459 |
R-HSA-112315 | Transmission across Chemical Synapses | 3.486951e-01 | 0.458 |
R-HSA-8957322 | Metabolism of steroids | 3.506638e-01 | 0.455 |
R-HSA-991365 | Activation of GABAB receptors | 3.529799e-01 | 0.452 |
R-HSA-977444 | GABA B receptor activation | 3.529799e-01 | 0.452 |
R-HSA-2172127 | DAP12 interactions | 3.641682e-01 | 0.439 |
R-HSA-606279 | Deposition of new CENPA-containing nucleosomes at the centromere | 3.696901e-01 | 0.432 |
R-HSA-774815 | Nucleosome assembly | 3.696901e-01 | 0.432 |
R-HSA-168333 | NEP/NS2 Interacts with the Cellular Export Machinery | 3.696901e-01 | 0.432 |
R-HSA-9660821 | ADORA2B mediated anti-inflammatory cytokines production | 3.696901e-01 | 0.432 |
R-HSA-432040 | Vasopressin regulates renal water homeostasis via Aquaporins | 3.696901e-01 | 0.432 |
R-HSA-2299718 | Condensation of Prophase Chromosomes | 3.751644e-01 | 0.426 |
R-HSA-168274 | Export of Viral Ribonucleoproteins from Nucleus | 3.751644e-01 | 0.426 |
R-HSA-9649948 | Signaling downstream of RAS mutants | 3.751644e-01 | 0.426 |
R-HSA-6802955 | Paradoxical activation of RAF signaling by kinase inactive BRAF | 3.751644e-01 | 0.426 |
R-HSA-6802946 | Signaling by moderate kinase activity BRAF mutants | 3.751644e-01 | 0.426 |
R-HSA-6802949 | Signaling by RAS mutants | 3.751644e-01 | 0.426 |
R-HSA-9660826 | Purinergic signaling in leishmaniasis infection | 3.751644e-01 | 0.426 |
R-HSA-9664424 | Cell recruitment (pro-inflammatory response) | 3.751644e-01 | 0.426 |
R-HSA-3928665 | EPH-ephrin mediated repulsion of cells | 3.805915e-01 | 0.420 |
R-HSA-1428517 | Aerobic respiration and respiratory electron transport | 3.841194e-01 | 0.416 |
R-HSA-389356 | Co-stimulation by CD28 | 3.859717e-01 | 0.413 |
R-HSA-5693571 | Nonhomologous End-Joining (NHEJ) | 3.859717e-01 | 0.413 |
R-HSA-9634597 | GPER1 signaling | 3.859717e-01 | 0.413 |
R-HSA-70263 | Gluconeogenesis | 3.859717e-01 | 0.413 |
R-HSA-425410 | Metal ion SLC transporters | 3.859717e-01 | 0.413 |
R-HSA-9031628 | NGF-stimulated transcription | 3.859717e-01 | 0.413 |
R-HSA-202733 | Cell surface interactions at the vascular wall | 3.869868e-01 | 0.412 |
R-HSA-597592 | Post-translational protein modification | 3.892386e-01 | 0.410 |
R-HSA-5655253 | Signaling by FGFR2 in disease | 3.965935e-01 | 0.402 |
R-HSA-2029482 | Regulation of actin dynamics for phagocytic cup formation | 3.996789e-01 | 0.398 |
R-HSA-912446 | Meiotic recombination | 4.018358e-01 | 0.396 |
R-HSA-4839726 | Chromatin organization | 4.149456e-01 | 0.382 |
R-HSA-112316 | Neuronal System | 4.208923e-01 | 0.376 |
R-HSA-418597 | G alpha (z) signalling events | 4.223564e-01 | 0.374 |
R-HSA-9758941 | Gastrulation | 4.267502e-01 | 0.370 |
R-HSA-9006931 | Signaling by Nuclear Receptors | 4.271088e-01 | 0.369 |
R-HSA-209776 | Metabolism of amine-derived hormones | 4.273764e-01 | 0.369 |
R-HSA-193648 | NRAGE signals death through JNK | 4.273764e-01 | 0.369 |
R-HSA-9662361 | Sensory processing of sound by outer hair cells of the cochlea | 4.273764e-01 | 0.369 |
R-HSA-5578775 | Ion homeostasis | 4.273764e-01 | 0.369 |
R-HSA-9856651 | MITF-M-dependent gene expression | 4.297196e-01 | 0.367 |
R-HSA-5621480 | Dectin-2 family | 4.323531e-01 | 0.364 |
R-HSA-9772572 | Early SARS-CoV-2 Infection Events | 4.372868e-01 | 0.359 |
R-HSA-180786 | Extension of Telomeres | 4.421780e-01 | 0.354 |
R-HSA-352230 | Amino acid transport across the plasma membrane | 4.421780e-01 | 0.354 |
R-HSA-1989781 | PPARA activates gene expression | 4.444446e-01 | 0.352 |
R-HSA-977443 | GABA receptor activation | 4.470269e-01 | 0.350 |
R-HSA-9734767 | Developmental Cell Lineages | 4.470458e-01 | 0.350 |
R-HSA-9610379 | HCMV Late Events | 4.502761e-01 | 0.347 |
R-HSA-400206 | Regulation of lipid metabolism by PPARalpha | 4.502761e-01 | 0.347 |
R-HSA-168325 | Viral Messenger RNA Synthesis | 4.518340e-01 | 0.345 |
R-HSA-1442490 | Collagen degradation | 4.518340e-01 | 0.345 |
R-HSA-445717 | Aquaporin-mediated transport | 4.518340e-01 | 0.345 |
R-HSA-6784531 | tRNA processing in the nucleus | 4.565996e-01 | 0.340 |
R-HSA-2559586 | DNA Damage/Telomere Stress Induced Senescence | 4.565996e-01 | 0.340 |
R-HSA-380284 | Loss of proteins required for interphase microtubule organization from the centr... | 4.613241e-01 | 0.336 |
R-HSA-380259 | Loss of Nlp from mitotic centrosomes | 4.613241e-01 | 0.336 |
R-HSA-6790901 | rRNA modification in the nucleus and cytosol | 4.613241e-01 | 0.336 |
R-HSA-74751 | Insulin receptor signalling cascade | 4.660077e-01 | 0.332 |
R-HSA-936837 | Ion transport by P-type ATPases | 4.660077e-01 | 0.332 |
R-HSA-6802952 | Signaling by BRAF and RAF1 fusions | 4.706510e-01 | 0.327 |
R-HSA-8854518 | AURKA Activation by TPX2 | 4.752541e-01 | 0.323 |
R-HSA-9958863 | SLC-mediated transport of amino acids | 4.798175e-01 | 0.319 |
R-HSA-9662360 | Sensory processing of sound by inner hair cells of the cochlea | 4.843415e-01 | 0.315 |
R-HSA-75105 | Fatty acyl-CoA biosynthesis | 4.932727e-01 | 0.307 |
R-HSA-425407 | SLC-mediated transmembrane transport | 4.937704e-01 | 0.306 |
R-HSA-427413 | NoRC negatively regulates rRNA expression | 4.976805e-01 | 0.303 |
R-HSA-9664433 | Leishmania parasite growth and survival | 4.984081e-01 | 0.302 |
R-HSA-9662851 | Anti-inflammatory response favouring Leishmania parasite infection | 4.984081e-01 | 0.302 |
R-HSA-5578749 | Transcriptional regulation by small RNAs | 5.020502e-01 | 0.299 |
R-HSA-983231 | Factors involved in megakaryocyte development and platelet production | 5.038941e-01 | 0.298 |
R-HSA-380270 | Recruitment of mitotic centrosome proteins and complexes | 5.063822e-01 | 0.296 |
R-HSA-69473 | G2/M DNA damage checkpoint | 5.106768e-01 | 0.292 |
R-HSA-1222556 | ROS and RNS production in phagocytes | 5.106768e-01 | 0.292 |
R-HSA-1226099 | Signaling by FGFR in disease | 5.106768e-01 | 0.292 |
R-HSA-418594 | G alpha (i) signalling events | 5.122503e-01 | 0.291 |
R-HSA-380287 | Centrosome maturation | 5.149342e-01 | 0.288 |
R-HSA-6796648 | TP53 Regulates Transcription of DNA Repair Genes | 5.274872e-01 | 0.278 |
R-HSA-416482 | G alpha (12/13) signalling events | 5.274872e-01 | 0.278 |
R-HSA-191273 | Cholesterol biosynthesis | 5.274872e-01 | 0.278 |
R-HSA-9659379 | Sensory processing of sound | 5.315994e-01 | 0.274 |
R-HSA-5250941 | Negative epigenetic regulation of rRNA expression | 5.356761e-01 | 0.271 |
R-HSA-5617833 | Cilium Assembly | 5.437938e-01 | 0.265 |
R-HSA-5668914 | Diseases of metabolism | 5.482695e-01 | 0.261 |
R-HSA-68877 | Mitotic Prometaphase | 5.515044e-01 | 0.258 |
R-HSA-6802957 | Oncogenic MAPK signaling | 5.555372e-01 | 0.255 |
R-HSA-1500620 | Meiosis | 5.555372e-01 | 0.255 |
R-HSA-141424 | Amplification of signal from the kinetochores | 5.594070e-01 | 0.252 |
R-HSA-141444 | Amplification of signal from unattached kinetochores via a MAD2 inhibitory si... | 5.594070e-01 | 0.252 |
R-HSA-6807505 | RNA polymerase II transcribes snRNA genes | 5.632433e-01 | 0.249 |
R-HSA-380320 | Recruitment of NuMA to mitotic centrosomes | 5.708168e-01 | 0.244 |
R-HSA-9645723 | Diseases of programmed cell death | 5.708168e-01 | 0.244 |
R-HSA-1483206 | Glycerophospholipid biosynthesis | 5.765454e-01 | 0.239 |
R-HSA-112310 | Neurotransmitter release cycle | 5.782598e-01 | 0.238 |
R-HSA-74752 | Signaling by Insulin receptor | 5.891848e-01 | 0.230 |
R-HSA-2029481 | FCGR activation | 5.927636e-01 | 0.227 |
R-HSA-983695 | Antigen activates B Cell Receptor (BCR) leading to generation of second messenge... | 5.927636e-01 | 0.227 |
R-HSA-2219530 | Constitutive Signaling by Aberrant PI3K in Cancer | 5.963115e-01 | 0.225 |
R-HSA-9730414 | MITF-M-regulated melanocyte development | 6.029054e-01 | 0.220 |
R-HSA-6811434 | COPI-dependent Golgi-to-ER retrograde traffic | 6.067721e-01 | 0.217 |
R-HSA-2730905 | Role of LAT2/NTAL/LAB on calcium mobilization | 6.067721e-01 | 0.217 |
R-HSA-1296071 | Potassium Channels | 6.067721e-01 | 0.217 |
R-HSA-157579 | Telomere Maintenance | 6.101988e-01 | 0.215 |
R-HSA-3214847 | HATs acetylate histones | 6.169635e-01 | 0.210 |
R-HSA-69618 | Mitotic Spindle Checkpoint | 6.203020e-01 | 0.207 |
R-HSA-9009391 | Extra-nuclear estrogen signaling | 6.236116e-01 | 0.205 |
R-HSA-418346 | Platelet homeostasis | 6.428763e-01 | 0.192 |
R-HSA-211000 | Gene Silencing by RNA | 6.459905e-01 | 0.190 |
R-HSA-3247509 | Chromatin modifying enzymes | 6.497748e-01 | 0.187 |
R-HSA-9648025 | EML4 and NUDC in mitotic spindle formation | 6.521383e-01 | 0.186 |
R-HSA-8939211 | ESR-mediated signaling | 6.561031e-01 | 0.183 |
R-HSA-6803157 | Antimicrobial peptides | 6.581800e-01 | 0.182 |
R-HSA-1483249 | Inositol phosphate metabolism | 6.611617e-01 | 0.180 |
R-HSA-2980736 | Peptide hormone metabolism | 6.813226e-01 | 0.167 |
R-HSA-9609646 | HCMV Infection | 6.824826e-01 | 0.166 |
R-HSA-2219528 | PI3K/AKT Signaling in Cancer | 6.841038e-01 | 0.165 |
R-HSA-388396 | GPCR downstream signalling | 6.942258e-01 | 0.158 |
R-HSA-6811558 | PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling | 6.976524e-01 | 0.156 |
R-HSA-9816359 | Maternal to zygotic transition (MZT) | 6.976524e-01 | 0.156 |
R-HSA-2132295 | MHC class II antigen presentation | 6.976524e-01 | 0.156 |
R-HSA-6809371 | Formation of the cornified envelope | 7.002921e-01 | 0.155 |
R-HSA-109582 | Hemostasis | 7.056807e-01 | 0.151 |
R-HSA-199418 | Negative regulation of the PI3K/AKT network | 7.181400e-01 | 0.144 |
R-HSA-1474165 | Reproduction | 7.206020e-01 | 0.142 |
R-HSA-1474228 | Degradation of the extracellular matrix | 7.254622e-01 | 0.139 |
R-HSA-8856688 | Golgi-to-ER retrograde transport | 7.254622e-01 | 0.139 |
R-HSA-76002 | Platelet activation, signaling and aggregation | 7.268513e-01 | 0.139 |
R-HSA-163685 | Integration of energy metabolism | 7.372485e-01 | 0.132 |
R-HSA-381119 | Unfolded Protein Response (UPR) | 7.440777e-01 | 0.128 |
R-HSA-1483257 | Phospholipid metabolism | 7.612968e-01 | 0.118 |
R-HSA-9679191 | Potential therapeutics for SARS | 7.696764e-01 | 0.114 |
R-HSA-372790 | Signaling by GPCR | 7.805222e-01 | 0.108 |
R-HSA-877300 | Interferon gamma signaling | 7.871917e-01 | 0.104 |
R-HSA-1852241 | Organelle biogenesis and maintenance | 7.973771e-01 | 0.098 |
R-HSA-1430728 | Metabolism | 7.991184e-01 | 0.097 |
R-HSA-5619102 | SLC transporter disorders | 8.016469e-01 | 0.096 |
R-HSA-72306 | tRNA processing | 8.085045e-01 | 0.092 |
R-HSA-418555 | G alpha (s) signalling events | 8.101818e-01 | 0.091 |
R-HSA-9609690 | HCMV Early Events | 8.476855e-01 | 0.072 |
R-HSA-6805567 | Keratinization | 8.617608e-01 | 0.065 |
R-HSA-416476 | G alpha (q) signalling events | 9.171843e-01 | 0.038 |
R-HSA-1474244 | Extracellular matrix organization | 9.542862e-01 | 0.020 |
R-HSA-556833 | Metabolism of lipids | 9.568472e-01 | 0.019 |
R-HSA-8978868 | Fatty acid metabolism | 9.769800e-01 | 0.010 |
R-HSA-9709957 | Sensory Perception | 9.999887e-01 | 0.000 |
Download
kinase | JSD_mean | pearson_surrounding | kinase_max_IC_position | max_position_JSD |
---|---|---|---|---|
GAK |
0.863 | 0.234 | 1 | 0.895 |
PKR |
0.846 | 0.054 | 1 | 0.821 |
VRK2 |
0.844 | -0.149 | 1 | 0.877 |
PDHK3_TYR |
0.842 | 0.229 | 4 | 0.900 |
GCK |
0.841 | 0.038 | 1 | 0.796 |
ALK4 |
0.840 | 0.097 | -2 | 0.850 |
BMPR2 |
0.839 | -0.038 | -2 | 0.877 |
EEF2K |
0.839 | 0.042 | 3 | 0.840 |
TAK1 |
0.839 | -0.087 | 1 | 0.810 |
MOS |
0.838 | 0.148 | 1 | 0.838 |
TTK |
0.837 | 0.033 | -2 | 0.842 |
TNIK |
0.837 | 0.027 | 3 | 0.847 |
MINK |
0.837 | -0.009 | 1 | 0.785 |
ALPHAK3 |
0.836 | 0.019 | -1 | 0.775 |
BMPR2_TYR |
0.836 | 0.158 | -1 | 0.890 |
ALK2 |
0.836 | 0.138 | -2 | 0.835 |
TGFBR1 |
0.836 | 0.159 | -2 | 0.834 |
MAP2K6_TYR |
0.836 | 0.131 | -1 | 0.874 |
NIK |
0.835 | -0.024 | -3 | 0.827 |
VRK1 |
0.835 | -0.158 | 2 | 0.803 |
MEKK2 |
0.835 | -0.036 | 2 | 0.772 |
DAPK2 |
0.835 | 0.004 | -3 | 0.812 |
PDHK4_TYR |
0.835 | 0.116 | 2 | 0.881 |
PASK |
0.835 | 0.101 | -3 | 0.812 |
LRRK2 |
0.834 | -0.133 | 2 | 0.832 |
PRPK |
0.834 | -0.002 | -1 | 0.860 |
BMPR1B |
0.834 | 0.199 | 1 | 0.762 |
TAO3 |
0.834 | 0.031 | 1 | 0.798 |
PDHK1_TYR |
0.833 | 0.089 | -1 | 0.893 |
MAP2K4_TYR |
0.833 | 0.043 | -1 | 0.872 |
LATS1 |
0.833 | 0.120 | -3 | 0.824 |
MEK1 |
0.833 | -0.181 | 2 | 0.812 |
ASK1 |
0.832 | -0.141 | 1 | 0.754 |
KHS2 |
0.832 | 0.070 | 1 | 0.785 |
CLK3 |
0.832 | 0.339 | 1 | 0.872 |
MST3 |
0.832 | 0.052 | 2 | 0.818 |
KHS1 |
0.832 | 0.024 | 1 | 0.774 |
NLK |
0.831 | 0.120 | 1 | 0.875 |
BIKE |
0.831 | 0.138 | 1 | 0.815 |
TAO2 |
0.831 | -0.062 | 2 | 0.822 |
CDKL1 |
0.831 | 0.126 | -3 | 0.761 |
GRK7 |
0.831 | 0.191 | 1 | 0.818 |
JNK2 |
0.831 | 0.175 | 1 | 0.699 |
CAMLCK |
0.831 | -0.016 | -2 | 0.812 |
PDK1 |
0.831 | -0.074 | 1 | 0.792 |
EPHA6 |
0.830 | 0.141 | -1 | 0.870 |
P38A |
0.830 | 0.173 | 1 | 0.787 |
PKMYT1_TYR |
0.830 | 0.034 | 3 | 0.837 |
CAMK1B |
0.830 | 0.032 | -3 | 0.817 |
MAP3K15 |
0.830 | -0.081 | 1 | 0.765 |
MPSK1 |
0.829 | 0.112 | 1 | 0.832 |
PRP4 |
0.829 | 0.151 | -3 | 0.745 |
BRAF |
0.829 | -0.140 | -4 | 0.797 |
FYN |
0.829 | 0.264 | -1 | 0.860 |
DLK |
0.829 | -0.125 | 1 | 0.829 |
YES1 |
0.829 | 0.152 | -1 | 0.856 |
NEK5 |
0.829 | -0.100 | 1 | 0.831 |
HPK1 |
0.828 | -0.004 | 1 | 0.775 |
TESK1_TYR |
0.828 | -0.068 | 3 | 0.860 |
JNK3 |
0.828 | 0.148 | 1 | 0.735 |
ANKRD3 |
0.828 | -0.091 | 1 | 0.841 |
NEK1 |
0.828 | -0.147 | 1 | 0.800 |
MAP2K7_TYR |
0.828 | -0.132 | 2 | 0.852 |
MST2 |
0.828 | -0.106 | 1 | 0.803 |
HGK |
0.828 | -0.050 | 3 | 0.847 |
BLK |
0.827 | 0.241 | -1 | 0.870 |
COT |
0.827 | 0.261 | 2 | 0.861 |
OSR1 |
0.827 | -0.058 | 2 | 0.762 |
MEK5 |
0.827 | -0.266 | 2 | 0.795 |
EPHB4 |
0.826 | 0.096 | -1 | 0.828 |
ICK |
0.826 | 0.109 | -3 | 0.787 |
LCK |
0.826 | 0.220 | -1 | 0.862 |
FGR |
0.826 | 0.105 | 1 | 0.883 |
MEKK3 |
0.826 | -0.067 | 1 | 0.799 |
ACVR2B |
0.825 | 0.096 | -2 | 0.817 |
SKMLCK |
0.825 | 0.102 | -2 | 0.848 |
P38B |
0.825 | 0.163 | 1 | 0.726 |
MST1 |
0.825 | -0.146 | 1 | 0.786 |
PINK1_TYR |
0.825 | -0.115 | 1 | 0.850 |
TXK |
0.824 | 0.151 | 1 | 0.808 |
MEKK1 |
0.824 | -0.136 | 1 | 0.803 |
ATR |
0.824 | -0.025 | 1 | 0.818 |
ACVR2A |
0.824 | 0.079 | -2 | 0.799 |
HCK |
0.823 | 0.135 | -1 | 0.852 |
MEKK6 |
0.823 | -0.122 | 1 | 0.797 |
AAK1 |
0.823 | 0.193 | 1 | 0.731 |
DMPK1 |
0.823 | 0.079 | -3 | 0.750 |
DAPK3 |
0.823 | 0.033 | -3 | 0.783 |
ABL2 |
0.822 | 0.063 | -1 | 0.812 |
BMPR1A |
0.822 | 0.163 | 1 | 0.734 |
EPHA4 |
0.822 | 0.077 | 2 | 0.816 |
YSK4 |
0.822 | -0.080 | 1 | 0.771 |
NEK11 |
0.822 | -0.152 | 1 | 0.785 |
RET |
0.821 | -0.067 | 1 | 0.816 |
CSF1R |
0.821 | 0.016 | 3 | 0.785 |
CAMK2G |
0.821 | 0.043 | 2 | 0.846 |
GRK6 |
0.821 | 0.066 | 1 | 0.835 |
MST1R |
0.820 | -0.052 | 3 | 0.809 |
LKB1 |
0.820 | -0.175 | -3 | 0.745 |
LIMK2_TYR |
0.820 | -0.055 | -3 | 0.812 |
MYO3B |
0.820 | -0.057 | 2 | 0.795 |
MYO3A |
0.820 | -0.084 | 1 | 0.763 |
ERK5 |
0.820 | 0.105 | 1 | 0.862 |
SRMS |
0.819 | 0.077 | 1 | 0.842 |
PBK |
0.819 | 0.072 | 1 | 0.832 |
NEK8 |
0.819 | -0.183 | 2 | 0.798 |
FER |
0.819 | -0.003 | 1 | 0.870 |
SMMLCK |
0.818 | -0.027 | -3 | 0.767 |
ZAK |
0.818 | -0.129 | 1 | 0.771 |
PIM1 |
0.818 | 0.162 | -3 | 0.776 |
PLK1 |
0.818 | -0.009 | -2 | 0.818 |
YSK1 |
0.818 | -0.088 | 2 | 0.778 |
CAMKK1 |
0.817 | -0.248 | -2 | 0.732 |
INSRR |
0.817 | 0.010 | 3 | 0.744 |
PIM3 |
0.817 | 0.164 | -3 | 0.816 |
ABL1 |
0.817 | 0.027 | -1 | 0.802 |
TYRO3 |
0.817 | -0.073 | 3 | 0.790 |
TYK2 |
0.817 | -0.129 | 1 | 0.814 |
P38G |
0.816 | 0.156 | 1 | 0.638 |
KIT |
0.816 | 0.003 | 3 | 0.795 |
ROS1 |
0.816 | -0.062 | 3 | 0.758 |
EPHB2 |
0.816 | 0.081 | -1 | 0.809 |
NEK4 |
0.816 | -0.185 | 1 | 0.785 |
ITK |
0.816 | 0.051 | -1 | 0.800 |
MLK1 |
0.816 | -0.028 | 2 | 0.795 |
RAF1 |
0.816 | -0.103 | 1 | 0.827 |
DSTYK |
0.816 | 0.103 | 2 | 0.888 |
HIPK1 |
0.815 | 0.155 | 1 | 0.783 |
FGFR2 |
0.815 | -0.026 | 3 | 0.796 |
JAK2 |
0.815 | -0.100 | 1 | 0.809 |
DDR1 |
0.815 | -0.116 | 4 | 0.842 |
MET |
0.815 | 0.032 | 3 | 0.786 |
CDK1 |
0.815 | 0.188 | 1 | 0.716 |
SRC |
0.815 | 0.146 | -1 | 0.846 |
TLK2 |
0.815 | -0.040 | 1 | 0.779 |
DAPK1 |
0.814 | 0.028 | -3 | 0.763 |
EPHB1 |
0.814 | 0.021 | 1 | 0.828 |
TNK2 |
0.814 | 0.035 | 3 | 0.780 |
EPHB3 |
0.814 | 0.034 | -1 | 0.813 |
WNK1 |
0.814 | 0.056 | -2 | 0.869 |
ROCK2 |
0.813 | 0.020 | -3 | 0.772 |
P38D |
0.813 | 0.169 | 1 | 0.647 |
KDR |
0.813 | -0.018 | 3 | 0.759 |
JAK3 |
0.813 | -0.069 | 1 | 0.793 |
CAMKK2 |
0.813 | -0.285 | -2 | 0.717 |
MAK |
0.813 | 0.195 | -2 | 0.741 |
LIMK1_TYR |
0.813 | -0.219 | 2 | 0.829 |
PTK2 |
0.813 | 0.164 | -1 | 0.818 |
BMX |
0.812 | 0.036 | -1 | 0.744 |
PKN3 |
0.812 | 0.048 | -3 | 0.781 |
MLK2 |
0.812 | -0.153 | 2 | 0.786 |
CDKL5 |
0.812 | 0.134 | -3 | 0.751 |
PERK |
0.811 | -0.146 | -2 | 0.830 |
GRK5 |
0.811 | -0.107 | -3 | 0.797 |
JNK1 |
0.811 | 0.131 | 1 | 0.696 |
EPHA7 |
0.811 | 0.052 | 2 | 0.807 |
FLT3 |
0.811 | -0.053 | 3 | 0.794 |
STLK3 |
0.811 | -0.278 | 1 | 0.741 |
NUAK2 |
0.811 | 0.093 | -3 | 0.815 |
MERTK |
0.811 | -0.001 | 3 | 0.765 |
FRK |
0.811 | 0.062 | -1 | 0.855 |
LYN |
0.810 | 0.089 | 3 | 0.715 |
CDK5 |
0.810 | 0.160 | 1 | 0.771 |
MTOR |
0.810 | 0.047 | 1 | 0.833 |
WNK4 |
0.809 | -0.068 | -2 | 0.868 |
PLK3 |
0.809 | 0.029 | 2 | 0.804 |
MEK2 |
0.809 | -0.344 | 2 | 0.764 |
GRK1 |
0.809 | 0.174 | -2 | 0.778 |
SYK |
0.809 | 0.149 | -1 | 0.811 |
PDHK4 |
0.809 | -0.252 | 1 | 0.855 |
EGFR |
0.809 | 0.066 | 1 | 0.735 |
CHAK2 |
0.809 | -0.056 | -1 | 0.812 |
TLK1 |
0.809 | -0.106 | -2 | 0.859 |
DYRK2 |
0.809 | 0.148 | 1 | 0.761 |
EPHA8 |
0.808 | 0.090 | -1 | 0.826 |
MASTL |
0.808 | -0.238 | -2 | 0.807 |
HRI |
0.808 | -0.183 | -2 | 0.847 |
FLT1 |
0.808 | -0.023 | -1 | 0.829 |
ERK2 |
0.807 | 0.071 | 1 | 0.757 |
TEC |
0.807 | -0.011 | -1 | 0.738 |
NEK9 |
0.807 | -0.163 | 2 | 0.804 |
CLK4 |
0.807 | 0.139 | -3 | 0.761 |
FGFR3 |
0.807 | -0.028 | 3 | 0.772 |
ERBB2 |
0.807 | -0.038 | 1 | 0.805 |
DCAMKL1 |
0.807 | 0.032 | -3 | 0.776 |
MLK3 |
0.807 | 0.027 | 2 | 0.732 |
MST4 |
0.807 | 0.071 | 2 | 0.826 |
FGFR1 |
0.807 | -0.090 | 3 | 0.771 |
PDGFRB |
0.807 | -0.123 | 3 | 0.805 |
PKCD |
0.807 | 0.052 | 2 | 0.769 |
ERK1 |
0.807 | 0.131 | 1 | 0.716 |
RIPK3 |
0.806 | -0.061 | 3 | 0.733 |
LOK |
0.806 | -0.127 | -2 | 0.718 |
PLK2 |
0.806 | 0.123 | -3 | 0.800 |
RIPK1 |
0.806 | -0.166 | 1 | 0.797 |
EPHA3 |
0.806 | -0.030 | 2 | 0.784 |
JAK1 |
0.806 | -0.035 | 1 | 0.753 |
MLK4 |
0.806 | -0.005 | 2 | 0.714 |
PTK2B |
0.806 | 0.044 | -1 | 0.774 |
GSK3A |
0.805 | 0.117 | 4 | 0.512 |
EPHA5 |
0.805 | 0.055 | 2 | 0.801 |
DNAPK |
0.805 | 0.043 | 1 | 0.695 |
PKN2 |
0.805 | 0.043 | -3 | 0.793 |
TEK |
0.805 | -0.090 | 3 | 0.739 |
PIM2 |
0.805 | 0.095 | -3 | 0.727 |
CDC7 |
0.805 | -0.019 | 1 | 0.792 |
BTK |
0.805 | -0.089 | -1 | 0.756 |
GRK2 |
0.804 | -0.023 | -2 | 0.718 |
ERK7 |
0.804 | 0.107 | 2 | 0.577 |
SRPK1 |
0.804 | 0.165 | -3 | 0.732 |
AXL |
0.804 | -0.096 | 3 | 0.768 |
HASPIN |
0.803 | 0.021 | -1 | 0.701 |
TSSK2 |
0.803 | -0.052 | -5 | 0.861 |
PDHK1 |
0.803 | -0.245 | 1 | 0.836 |
LTK |
0.803 | -0.064 | 3 | 0.756 |
ATM |
0.803 | 0.011 | 1 | 0.749 |
CAMK2B |
0.803 | 0.133 | 2 | 0.832 |
MATK |
0.803 | -0.044 | -1 | 0.740 |
FGFR4 |
0.802 | 0.017 | -1 | 0.764 |
CDK14 |
0.802 | 0.135 | 1 | 0.743 |
WEE1_TYR |
0.802 | -0.075 | -1 | 0.738 |
NTRK1 |
0.802 | -0.128 | -1 | 0.799 |
ALK |
0.802 | -0.078 | 3 | 0.738 |
EPHA1 |
0.802 | -0.025 | 3 | 0.771 |
DDR2 |
0.802 | 0.012 | 3 | 0.753 |
TAO1 |
0.802 | -0.113 | 1 | 0.722 |
CLK2 |
0.801 | 0.254 | -3 | 0.760 |
DCAMKL2 |
0.801 | -0.000 | -3 | 0.790 |
DYRK1A |
0.801 | 0.111 | 1 | 0.795 |
CDK3 |
0.801 | 0.197 | 1 | 0.665 |
SRPK3 |
0.801 | 0.108 | -3 | 0.701 |
CHK1 |
0.801 | -0.018 | -3 | 0.796 |
DRAK1 |
0.801 | -0.041 | 1 | 0.746 |
AMPKA1 |
0.801 | -0.043 | -3 | 0.815 |
HUNK |
0.801 | -0.123 | 2 | 0.800 |
CAMK2D |
0.800 | 0.028 | -3 | 0.772 |
ERBB4 |
0.800 | 0.089 | 1 | 0.748 |
IRAK4 |
0.800 | -0.119 | 1 | 0.787 |
TBK1 |
0.800 | -0.063 | 1 | 0.743 |
INSR |
0.800 | -0.102 | 3 | 0.712 |
TGFBR2 |
0.800 | -0.017 | -2 | 0.814 |
GSK3B |
0.800 | 0.041 | 4 | 0.501 |
P70S6KB |
0.800 | 0.005 | -3 | 0.770 |
RSK2 |
0.800 | 0.099 | -3 | 0.753 |
TNK1 |
0.799 | -0.123 | 3 | 0.759 |
MOK |
0.799 | 0.119 | 1 | 0.790 |
CSK |
0.799 | -0.036 | 2 | 0.804 |
SLK |
0.799 | -0.120 | -2 | 0.671 |
TNNI3K_TYR |
0.799 | -0.073 | 1 | 0.809 |
PTK6 |
0.799 | -0.173 | -1 | 0.714 |
HIPK3 |
0.799 | 0.095 | 1 | 0.778 |
HIPK4 |
0.798 | 0.109 | 1 | 0.816 |
NTRK3 |
0.798 | -0.078 | -1 | 0.759 |
CDK2 |
0.798 | 0.108 | 1 | 0.800 |
EPHA2 |
0.798 | 0.066 | -1 | 0.785 |
NEK2 |
0.798 | -0.152 | 2 | 0.783 |
NEK10_TYR |
0.798 | -0.168 | 1 | 0.690 |
DYRK4 |
0.798 | 0.171 | 1 | 0.697 |
NEK7 |
0.798 | -0.129 | -3 | 0.741 |
PDGFRA |
0.798 | -0.204 | 3 | 0.807 |
CLK1 |
0.797 | 0.165 | -3 | 0.734 |
SGK3 |
0.797 | 0.042 | -3 | 0.738 |
FLT4 |
0.797 | -0.141 | 3 | 0.748 |
TSSK1 |
0.796 | -0.004 | -3 | 0.832 |
MARK4 |
0.796 | -0.033 | 4 | 0.808 |
P90RSK |
0.796 | 0.065 | -3 | 0.754 |
DYRK1B |
0.796 | 0.117 | 1 | 0.730 |
CDK18 |
0.796 | 0.159 | 1 | 0.700 |
NTRK2 |
0.796 | -0.164 | 3 | 0.764 |
MYLK4 |
0.795 | -0.011 | -2 | 0.727 |
ROCK1 |
0.795 | -0.018 | -3 | 0.738 |
CAMK2A |
0.795 | 0.093 | 2 | 0.842 |
NEK6 |
0.795 | -0.030 | -2 | 0.878 |
MRCKA |
0.795 | -0.008 | -3 | 0.738 |
TTBK2 |
0.795 | -0.124 | 2 | 0.703 |
HIPK2 |
0.795 | 0.169 | 1 | 0.682 |
CDK17 |
0.794 | 0.128 | 1 | 0.649 |
ULK2 |
0.794 | -0.177 | 2 | 0.762 |
CDK16 |
0.794 | 0.150 | 1 | 0.674 |
PINK1 |
0.794 | -0.178 | 1 | 0.851 |
AKT2 |
0.794 | 0.054 | -3 | 0.685 |
IKKB |
0.793 | -0.037 | -2 | 0.733 |
CRIK |
0.793 | 0.013 | -3 | 0.689 |
IKKE |
0.793 | -0.090 | 1 | 0.728 |
DYRK3 |
0.792 | 0.095 | 1 | 0.772 |
GRK4 |
0.792 | -0.070 | -2 | 0.830 |
CDK8 |
0.792 | 0.110 | 1 | 0.747 |
IRE1 |
0.792 | -0.070 | 1 | 0.779 |
CDK13 |
0.792 | 0.098 | 1 | 0.729 |
MRCKB |
0.792 | -0.006 | -3 | 0.720 |
WNK3 |
0.792 | -0.232 | 1 | 0.810 |
CDK6 |
0.791 | 0.102 | 1 | 0.721 |
PAK1 |
0.791 | -0.032 | -2 | 0.743 |
SMG1 |
0.791 | -0.095 | 1 | 0.770 |
PKCA |
0.790 | 0.031 | 2 | 0.711 |
CHAK1 |
0.790 | -0.181 | 2 | 0.742 |
CDK12 |
0.789 | 0.101 | 1 | 0.703 |
FAM20C |
0.789 | 0.250 | 2 | 0.724 |
SGK1 |
0.789 | 0.053 | -3 | 0.617 |
IGF1R |
0.789 | -0.082 | 3 | 0.657 |
IKKA |
0.788 | 0.023 | -2 | 0.741 |
IRE2 |
0.788 | -0.079 | 2 | 0.727 |
PKCZ |
0.788 | -0.029 | 2 | 0.757 |
AMPKA2 |
0.788 | -0.041 | -3 | 0.793 |
NEK3 |
0.788 | -0.217 | 1 | 0.758 |
RSK4 |
0.788 | 0.086 | -3 | 0.738 |
ZAP70 |
0.788 | 0.075 | -1 | 0.738 |
PKCH |
0.788 | -0.026 | 2 | 0.703 |
NDR1 |
0.788 | -0.010 | -3 | 0.805 |
CDK4 |
0.787 | 0.080 | 1 | 0.695 |
MAPKAPK3 |
0.787 | -0.001 | -3 | 0.739 |
BUB1 |
0.787 | -0.046 | -5 | 0.791 |
PAK2 |
0.787 | -0.114 | -2 | 0.723 |
CK1D |
0.787 | 0.055 | -3 | 0.507 |
PKCB |
0.786 | 0.029 | 2 | 0.716 |
GCN2 |
0.786 | -0.104 | 2 | 0.796 |
RSK3 |
0.786 | 0.046 | -3 | 0.744 |
GRK3 |
0.785 | 0.003 | -2 | 0.682 |
CHK2 |
0.785 | 0.013 | -3 | 0.635 |
CAMK4 |
0.785 | -0.117 | -3 | 0.785 |
PKCG |
0.785 | 0.011 | 2 | 0.729 |
CDK7 |
0.784 | 0.075 | 1 | 0.748 |
MSK1 |
0.784 | 0.032 | -3 | 0.719 |
CDK10 |
0.784 | 0.135 | 1 | 0.725 |
IRAK1 |
0.784 | -0.275 | -1 | 0.726 |
NDR2 |
0.783 | 0.068 | -3 | 0.813 |
MAPKAPK2 |
0.783 | 0.099 | -3 | 0.716 |
PRKD1 |
0.783 | 0.047 | -3 | 0.762 |
MELK |
0.783 | -0.070 | -3 | 0.770 |
MUSK |
0.783 | -0.083 | 1 | 0.730 |
CAMK1D |
0.782 | -0.014 | -3 | 0.685 |
PKACG |
0.781 | -0.020 | -2 | 0.689 |
PLK4 |
0.781 | -0.101 | 2 | 0.616 |
CAMK1G |
0.781 | -0.034 | -3 | 0.727 |
SRPK2 |
0.781 | 0.122 | -3 | 0.664 |
PAK3 |
0.781 | -0.100 | -2 | 0.737 |
LATS2 |
0.781 | 0.012 | -5 | 0.752 |
AKT1 |
0.780 | 0.026 | -3 | 0.701 |
NIM1 |
0.780 | -0.081 | 3 | 0.749 |
CK1A2 |
0.780 | 0.042 | -3 | 0.512 |
CDK19 |
0.780 | 0.116 | 1 | 0.714 |
CDK9 |
0.780 | 0.050 | 1 | 0.738 |
PKCE |
0.779 | 0.027 | 2 | 0.714 |
AURA |
0.779 | -0.011 | -2 | 0.570 |
PRKD3 |
0.779 | -0.006 | -3 | 0.714 |
MARK2 |
0.779 | -0.058 | 4 | 0.709 |
FES |
0.779 | -0.054 | -1 | 0.715 |
QIK |
0.778 | -0.131 | -3 | 0.773 |
AURB |
0.778 | -0.030 | -2 | 0.594 |
KIS |
0.778 | 0.190 | 1 | 0.762 |
MNK1 |
0.778 | -0.008 | -2 | 0.752 |
MSK2 |
0.777 | -0.019 | -3 | 0.711 |
CK1E |
0.776 | 0.047 | -3 | 0.562 |
YANK3 |
0.776 | -0.012 | 2 | 0.454 |
NUAK1 |
0.776 | 0.003 | -3 | 0.770 |
BCKDK |
0.776 | -0.167 | -1 | 0.767 |
PRKD2 |
0.776 | 0.047 | -3 | 0.743 |
ULK1 |
0.775 | -0.241 | -3 | 0.712 |
QSK |
0.775 | -0.038 | 4 | 0.775 |
STK33 |
0.775 | -0.178 | 2 | 0.633 |
MNK2 |
0.775 | -0.022 | -2 | 0.750 |
PKACB |
0.775 | 0.046 | -2 | 0.622 |
MARK3 |
0.774 | -0.035 | 4 | 0.738 |
SBK |
0.773 | 0.042 | -3 | 0.577 |
CK2A2 |
0.773 | 0.070 | 1 | 0.638 |
PKCI |
0.773 | -0.044 | 2 | 0.729 |
PKG2 |
0.773 | -0.029 | -2 | 0.610 |
MARK1 |
0.772 | -0.093 | 4 | 0.756 |
PKCT |
0.772 | -0.043 | 2 | 0.704 |
RIPK2 |
0.772 | -0.330 | 1 | 0.724 |
AURC |
0.770 | 0.012 | -2 | 0.596 |
SSTK |
0.769 | -0.121 | 4 | 0.771 |
PHKG1 |
0.768 | -0.049 | -3 | 0.793 |
TTBK1 |
0.766 | -0.174 | 2 | 0.635 |
SIK |
0.765 | -0.044 | -3 | 0.736 |
P70S6K |
0.765 | -0.044 | -3 | 0.676 |
CK2A1 |
0.765 | 0.054 | 1 | 0.612 |
YANK2 |
0.764 | -0.039 | 2 | 0.469 |
CAMK1A |
0.763 | -0.031 | -3 | 0.646 |
MAPKAPK5 |
0.763 | -0.082 | -3 | 0.666 |
AKT3 |
0.762 | 0.030 | -3 | 0.628 |
PKACA |
0.762 | 0.015 | -2 | 0.559 |
PRKX |
0.760 | 0.085 | -3 | 0.707 |
PKN1 |
0.759 | -0.009 | -3 | 0.693 |
PAK6 |
0.758 | -0.016 | -2 | 0.640 |
BRSK1 |
0.756 | -0.071 | -3 | 0.763 |
SNRK |
0.756 | -0.251 | 2 | 0.665 |
BRSK2 |
0.753 | -0.138 | -3 | 0.772 |
PHKG2 |
0.752 | -0.045 | -3 | 0.768 |
CK1G1 |
0.747 | 0.001 | -3 | 0.567 |
PAK5 |
0.739 | -0.089 | -2 | 0.582 |
CK1G3 |
0.738 | -0.001 | -3 | 0.393 |
PAK4 |
0.731 | -0.077 | -2 | 0.588 |
CK1G2 |
0.727 | 0.032 | -3 | 0.482 |
PKG1 |
0.720 | -0.095 | -2 | 0.511 |
CK1A |
0.717 | 0.005 | -3 | 0.434 |