Motif 212 (n=183)
Position-wise Probabilities
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uniprot | genes | site | source | protein | function |
---|---|---|---|---|---|
A1A5D9 | BICDL2 | S330 | ochoa | BICD family-like cargo adapter 2 (Bicaudal D-related protein 2) (BICD-related protein 2) (BICDR-2) (Coiled-coil domain-containing protein 64B) | None |
A6NDB9 | PALM3 | S124 | ochoa | Paralemmin-3 | ATP-binding protein, which may act as a adapter in the Toll-like receptor (TLR) signaling. {ECO:0000269|PubMed:21187075}. |
A6NJU9 | NPIPB13 | S1099 | ochoa | Nuclear pore complex-interacting protein family member B13 | None |
A8MRT5 | NPIPB5 | S1065 | ochoa | Nuclear pore complex-interacting protein family member B5 | None |
C9JG80 | NPIPB4 | S1070 | ochoa | Nuclear pore complex-interacting protein family member B4 | None |
E5RHQ5 | NPIPB11 | S1122 | ochoa | Nuclear pore complex-interacting protein family member B11 | None |
O00506 | STK25 | S231 | ochoa | Serine/threonine-protein kinase 25 (EC 2.7.11.1) (Ste20-like kinase) (Sterile 20/oxidant stress-response kinase 1) (SOK-1) (Ste20/oxidant stress response kinase 1) | Oxidant stress-activated serine/threonine kinase that may play a role in the response to environmental stress. Targets to the Golgi apparatus where it appears to regulate protein transport events, cell adhesion, and polarity complexes important for cell migration. Part of the striatin-interacting phosphatase and kinase (STRIPAK) complexes. STRIPAK complexes have critical roles in protein (de)phosphorylation and are regulators of multiple signaling pathways including Hippo, MAPK, nuclear receptor and cytoskeleton remodeling. Different types of STRIPAK complexes are involved in a variety of biological processes such as cell growth, differentiation, apoptosis, metabolism and immune regulation (PubMed:18782753). {ECO:0000269|PubMed:15037601, ECO:0000269|PubMed:18782753}. |
O14939 | PLD2 | S146 | psp | Phospholipase D2 (PLD 2) (hPLD2) (EC 3.1.4.4) (Choline phosphatase 2) (PLD1C) (Phosphatidylcholine-hydrolyzing phospholipase D2) | Function as phospholipase selective for phosphatidylcholine (PubMed:9582313). May have a role in signal-induced cytoskeletal regulation and/or endocytosis (By similarity). {ECO:0000250|UniProtKB:P97813, ECO:0000269|PubMed:9582313}. |
O14981 | BTAF1 | S91 | ochoa | TATA-binding protein-associated factor 172 (EC 3.6.4.-) (ATP-dependent helicase BTAF1) (B-TFIID transcription factor-associated 170 kDa subunit) (TAF(II)170) (TBP-associated factor 172) (TAF-172) | Regulates transcription in association with TATA binding protein (TBP). Removes TBP from the TATA box in an ATP-dependent manner. |
O15258 | RER1 | S100 | ochoa | Protein RER1 | Involved in the retrieval of endoplasmic reticulum membrane proteins from the early Golgi compartment. {ECO:0000250}. |
O43303 | CCP110 | S337 | ochoa | Centriolar coiled-coil protein of 110 kDa (Centrosomal protein of 110 kDa) (CP110) (Cep110) | Necessary for centrosome duplication at different stages of procentriole formation. Acts as a key negative regulator of ciliogenesis in collaboration with CEP97 by capping the mother centriole thereby preventing cilia formation (PubMed:17681131, PubMed:17719545, PubMed:23486064, PubMed:30375385, PubMed:35301795). Also involved in promoting ciliogenesis. May play a role in the assembly of the mother centriole subdistal appendages (SDA) thereby effecting the fusion of recycling endosomes to basal bodies during cilia formation (By similarity). Required for correct spindle formation and has a role in regulating cytokinesis and genome stability via cooperation with CALM1 and CETN2 (PubMed:16760425). {ECO:0000250|UniProtKB:Q7TSH4, ECO:0000269|PubMed:12361598, ECO:0000269|PubMed:16760425, ECO:0000269|PubMed:17681131, ECO:0000269|PubMed:17719545, ECO:0000269|PubMed:23486064, ECO:0000269|PubMed:30375385, ECO:0000269|PubMed:35301795}. |
O43303 | CCP110 | S384 | ochoa | Centriolar coiled-coil protein of 110 kDa (Centrosomal protein of 110 kDa) (CP110) (Cep110) | Necessary for centrosome duplication at different stages of procentriole formation. Acts as a key negative regulator of ciliogenesis in collaboration with CEP97 by capping the mother centriole thereby preventing cilia formation (PubMed:17681131, PubMed:17719545, PubMed:23486064, PubMed:30375385, PubMed:35301795). Also involved in promoting ciliogenesis. May play a role in the assembly of the mother centriole subdistal appendages (SDA) thereby effecting the fusion of recycling endosomes to basal bodies during cilia formation (By similarity). Required for correct spindle formation and has a role in regulating cytokinesis and genome stability via cooperation with CALM1 and CETN2 (PubMed:16760425). {ECO:0000250|UniProtKB:Q7TSH4, ECO:0000269|PubMed:12361598, ECO:0000269|PubMed:16760425, ECO:0000269|PubMed:17681131, ECO:0000269|PubMed:17719545, ECO:0000269|PubMed:23486064, ECO:0000269|PubMed:30375385, ECO:0000269|PubMed:35301795}. |
O43426 | SYNJ1 | S1391 | ochoa | Synaptojanin-1 (EC 3.1.3.36) (Synaptic inositol 1,4,5-trisphosphate 5-phosphatase 1) | Phosphatase that acts on various phosphoinositides, including phosphatidylinositol 4-phosphate, phosphatidylinositol (4,5)-bisphosphate and phosphatidylinositol (3,4,5)-trisphosphate (PubMed:23804563, PubMed:27435091). Has a role in clathrin-mediated endocytosis (By similarity). Hydrolyzes PIP2 bound to actin regulatory proteins resulting in the rearrangement of actin filaments downstream of tyrosine kinase and ASH/GRB2 (By similarity). {ECO:0000250|UniProtKB:O18964, ECO:0000250|UniProtKB:Q62910, ECO:0000269|PubMed:23804563, ECO:0000269|PubMed:27435091}. |
O43896 | KIF1C | S983 | ochoa | Kinesin-like protein KIF1C | Motor required for the retrograde transport of Golgi vesicles to the endoplasmic reticulum. Has a microtubule plus end-directed motility. {ECO:0000269|PubMed:9685376}. |
O60333 | KIF1B | S1468 | ochoa | Kinesin-like protein KIF1B (Klp) (EC 5.6.1.3) | Has a plus-end-directed microtubule motor activity and functions as a motor for transport of vesicles and organelles along microtubules. {ECO:0000269|PubMed:16225668}.; FUNCTION: [Isoform 2]: Has a plus-end-directed microtubule motor activity and functions as a motor for anterograde synaptic vesicle transport along axonal microtubules from the cell body to the presynapse in neuronal cells (By similarity). Functions as a downstream effector in a developmental apoptotic pathway that is activated when nerve growth factor (NGF) becomes limiting for neuronal progenitor cells (PubMed:18334619). {ECO:0000250|UniProtKB:Q60575, ECO:0000269|PubMed:18334619}.; FUNCTION: [Isoform 3]: Has a plus-end-directed microtubule motor activity and functions as a motor for anterograde transport of mitochondria. {ECO:0000269|PubMed:16225668}. |
O75363 | BCAS1 | S115 | ochoa | Breast carcinoma-amplified sequence 1 (Amplified and overexpressed in breast cancer) (Novel amplified in breast cancer 1) | Required for myelination. {ECO:0000250|UniProtKB:Q80YN3}. |
O75385 | ULK1 | S556 | ochoa|psp | Serine/threonine-protein kinase ULK1 (EC 2.7.11.1) (Autophagy-related protein 1 homolog) (ATG1) (hATG1) (Unc-51-like kinase 1) | Serine/threonine-protein kinase involved in autophagy in response to starvation (PubMed:18936157, PubMed:21460634, PubMed:21795849, PubMed:23524951, PubMed:25040165, PubMed:29487085, PubMed:31123703). Acts upstream of phosphatidylinositol 3-kinase PIK3C3 to regulate the formation of autophagophores, the precursors of autophagosomes (PubMed:18936157, PubMed:21460634, PubMed:21795849, PubMed:25040165). Part of regulatory feedback loops in autophagy: acts both as a downstream effector and negative regulator of mammalian target of rapamycin complex 1 (mTORC1) via interaction with RPTOR (PubMed:21795849). Activated via phosphorylation by AMPK and also acts as a regulator of AMPK by mediating phosphorylation of AMPK subunits PRKAA1, PRKAB2 and PRKAG1, leading to negatively regulate AMPK activity (PubMed:21460634). May phosphorylate ATG13/KIAA0652 and RPTOR; however such data need additional evidences (PubMed:18936157). Plays a role early in neuronal differentiation and is required for granule cell axon formation (PubMed:11146101). Also phosphorylates SESN2 and SQSTM1 to regulate autophagy (PubMed:25040165, PubMed:37306101). Phosphorylates FLCN, promoting autophagy (PubMed:25126726). Phosphorylates AMBRA1 in response to autophagy induction, releasing AMBRA1 from the cytoskeletal docking site to induce autophagosome nucleation (PubMed:20921139). Phosphorylates ATG4B, leading to inhibit autophagy by decreasing both proteolytic activation and delipidation activities of ATG4B (PubMed:28821708). {ECO:0000269|PubMed:11146101, ECO:0000269|PubMed:18936157, ECO:0000269|PubMed:20921139, ECO:0000269|PubMed:21460634, ECO:0000269|PubMed:21795849, ECO:0000269|PubMed:23524951, ECO:0000269|PubMed:25040165, ECO:0000269|PubMed:25126726, ECO:0000269|PubMed:28821708, ECO:0000269|PubMed:29487085, ECO:0000269|PubMed:31123703, ECO:0000269|PubMed:37306101}. |
O75385 | ULK1 | S588 | ochoa | Serine/threonine-protein kinase ULK1 (EC 2.7.11.1) (Autophagy-related protein 1 homolog) (ATG1) (hATG1) (Unc-51-like kinase 1) | Serine/threonine-protein kinase involved in autophagy in response to starvation (PubMed:18936157, PubMed:21460634, PubMed:21795849, PubMed:23524951, PubMed:25040165, PubMed:29487085, PubMed:31123703). Acts upstream of phosphatidylinositol 3-kinase PIK3C3 to regulate the formation of autophagophores, the precursors of autophagosomes (PubMed:18936157, PubMed:21460634, PubMed:21795849, PubMed:25040165). Part of regulatory feedback loops in autophagy: acts both as a downstream effector and negative regulator of mammalian target of rapamycin complex 1 (mTORC1) via interaction with RPTOR (PubMed:21795849). Activated via phosphorylation by AMPK and also acts as a regulator of AMPK by mediating phosphorylation of AMPK subunits PRKAA1, PRKAB2 and PRKAG1, leading to negatively regulate AMPK activity (PubMed:21460634). May phosphorylate ATG13/KIAA0652 and RPTOR; however such data need additional evidences (PubMed:18936157). Plays a role early in neuronal differentiation and is required for granule cell axon formation (PubMed:11146101). Also phosphorylates SESN2 and SQSTM1 to regulate autophagy (PubMed:25040165, PubMed:37306101). Phosphorylates FLCN, promoting autophagy (PubMed:25126726). Phosphorylates AMBRA1 in response to autophagy induction, releasing AMBRA1 from the cytoskeletal docking site to induce autophagosome nucleation (PubMed:20921139). Phosphorylates ATG4B, leading to inhibit autophagy by decreasing both proteolytic activation and delipidation activities of ATG4B (PubMed:28821708). {ECO:0000269|PubMed:11146101, ECO:0000269|PubMed:18936157, ECO:0000269|PubMed:20921139, ECO:0000269|PubMed:21460634, ECO:0000269|PubMed:21795849, ECO:0000269|PubMed:23524951, ECO:0000269|PubMed:25040165, ECO:0000269|PubMed:25126726, ECO:0000269|PubMed:28821708, ECO:0000269|PubMed:29487085, ECO:0000269|PubMed:31123703, ECO:0000269|PubMed:37306101}. |
O75815 | BCAR3 | S269 | ochoa | Breast cancer anti-estrogen resistance protein 3 (Novel SH2-containing protein 2) (SH2 domain-containing protein 3B) | Acts as an adapter protein downstream of several growth factor receptors to promote cell proliferation, migration, and redistribution of actin fibers (PubMed:24216110). Specifically involved in INS/insulin signaling pathway by mediating MAPK1/ERK2-MAPK3/ERK1 activation and DNA synthesis (PubMed:24216110). Promotes insulin-mediated membrane ruffling (By similarity). In response to vasoconstrictor peptide EDN1, involved in the activation of RAP1 downstream of PTK2B via interaction with phosphorylated BCAR1 (PubMed:19086031). Inhibits cell migration and invasion via regulation of TGFB-mediated matrix digestion, actin filament rearrangement, and inhibition of invadopodia activity (By similarity). May inhibit TGFB-SMAD signaling, via facilitating BCAR1 and SMAD2 and/or SMAD3 interaction (By similarity). Regulates EGF-induced DNA synthesis (PubMed:18722344). Required for the maintenance of ocular lens morphology and structural integrity, potentially via regulation of focal adhesion complex signaling (By similarity). Acts upstream of PTPRA to regulate the localization of BCAR1 and PTPRA to focal adhesions, via regulation of SRC-mediated phosphorylation of PTPRA (By similarity). Positively regulates integrin-induced tyrosine phosphorylation of BCAR1 (By similarity). Acts as a guanine nucleotide exchange factor (GEF) for small GTPases RALA, RAP1A and RRAS (By similarity). However, in a contrasting study, lacks GEF activity towards RAP1 (PubMed:22081014). {ECO:0000250|UniProtKB:D3ZAZ5, ECO:0000250|UniProtKB:Q9QZK2, ECO:0000269|PubMed:18722344, ECO:0000269|PubMed:19086031, ECO:0000269|PubMed:22081014, ECO:0000269|PubMed:24216110}. |
O76024 | WFS1 | S32 | ochoa | Wolframin | Participates in the regulation of cellular Ca(2+) homeostasis, at least partly, by modulating the filling state of the endoplasmic reticulum Ca(2+) store (PubMed:16989814). Negatively regulates the ER stress response and positively regulates the stability of V-ATPase subunits ATP6V1A and ATP1B1 by preventing their degradation through an unknown proteasome-independent mechanism (PubMed:23035048). {ECO:0000269|PubMed:16989814, ECO:0000269|PubMed:23035048}. |
O94761 | RECQL4 | S325 | ochoa | ATP-dependent DNA helicase Q4 (EC 5.6.2.4) (DNA 3'-5' helicase RecQ4) (DNA helicase, RecQ-like type 4) (RecQ4) (RTS) (RecQ protein-like 4) | An ATP-dependent DNA helicase which unwinds dsDNA with a 3'-overhang in a 3'-5' direction (PubMed:28653661). Does not unwind more than 18 bp of dsDNA (PubMed:28653661). May modulate chromosome segregation. The N-terminal domain (residues 1-54) binds DNA Y-shaped DNA better than ss- or dsDNA (PubMed:22730300). The core helicase domain binds ssDNA (PubMed:22730300, PubMed:28653661). {ECO:0000269|PubMed:15317757, ECO:0000269|PubMed:22730300, ECO:0000269|PubMed:28653661}. |
O95180 | CACNA1H | S1099 | ochoa | Voltage-dependent T-type calcium channel subunit alpha-1H (Low-voltage-activated calcium channel alpha1 3.2 subunit) (Voltage-gated calcium channel subunit alpha Cav3.2) | Voltage-sensitive calcium channel that gives rise to T-type calcium currents. T-type calcium channels belong to the 'low-voltage activated (LVA)' group. A particularity of this type of channel is an opening at quite negative potentials, and a voltage-dependent inactivation (PubMed:27149520, PubMed:9670923, PubMed:9930755). T-type channels serve pacemaking functions in both central neurons and cardiac nodal cells and support calcium signaling in secretory cells and vascular smooth muscle (Probable). They may also be involved in the modulation of firing patterns of neurons (PubMed:15048902). In the adrenal zona glomerulosa, participates in the signaling pathway leading to aldosterone production in response to either AGT/angiotensin II, or hyperkalemia (PubMed:25907736, PubMed:27729216). {ECO:0000269|PubMed:24277868, ECO:0000269|PubMed:25907736, ECO:0000269|PubMed:27149520, ECO:0000269|PubMed:27729216, ECO:0000269|PubMed:9670923, ECO:0000269|PubMed:9930755, ECO:0000305, ECO:0000305|PubMed:15048902}. |
O95466 | FMNL1 | S1044 | ochoa | Formin-like protein 1 (CLL-associated antigen KW-13) (Leukocyte formin) | May play a role in the control of cell motility and survival of macrophages (By similarity). Plays a role in the regulation of cell morphology and cytoskeletal organization. Required in the cortical actin filament dynamics and cell shape. {ECO:0000250, ECO:0000269|PubMed:21834987}. |
O95613 | PCNT | S2433 | ochoa | Pericentrin (Kendrin) (Pericentrin-B) | Integral component of the filamentous matrix of the centrosome involved in the initial establishment of organized microtubule arrays in both mitosis and meiosis. Plays a role, together with DISC1, in the microtubule network formation. Is an integral component of the pericentriolar material (PCM). May play an important role in preventing premature centrosome splitting during interphase by inhibiting NEK2 kinase activity at the centrosome. {ECO:0000269|PubMed:10823944, ECO:0000269|PubMed:11171385, ECO:0000269|PubMed:18955030, ECO:0000269|PubMed:20599736, ECO:0000269|PubMed:30420784}. |
O95639 | CPSF4 | S230 | ochoa | Cleavage and polyadenylation specificity factor subunit 4 (Cleavage and polyadenylation specificity factor 30 kDa subunit) (CPSF 30 kDa subunit) (NS1 effector domain-binding protein 1) (Neb-1) (No arches homolog) | Component of the cleavage and polyadenylation specificity factor (CPSF) complex that play a key role in pre-mRNA 3'-end formation, recognizing the AAUAAA signal sequence and interacting with poly(A) polymerase and other factors to bring about cleavage and poly(A) addition. CPSF4 binds RNA polymers with a preference for poly(U). {ECO:0000269|PubMed:14749727, ECO:0000269|PubMed:9224719}. |
O95685 | PPP1R3D | S77 | ochoa | Protein phosphatase 1 regulatory subunit 3D (Protein phosphatase 1 regulatory subunit 6) (PP1 subunit R6) (Protein phosphatase 1-binding subunit R6) | Seems to act as a glycogen-targeting subunit for PP1. PP1 is essential for cell division, and participates in the regulation of glycogen metabolism, muscle contractility and protein synthesis. |
O95835 | LATS1 | S1107 | ochoa | Serine/threonine-protein kinase LATS1 (EC 2.7.11.1) (Large tumor suppressor homolog 1) (WARTS protein kinase) (h-warts) | Negative regulator of YAP1 in the Hippo signaling pathway that plays a pivotal role in organ size control and tumor suppression by restricting proliferation and promoting apoptosis (PubMed:10518011, PubMed:10831611, PubMed:18158288, PubMed:26437443, PubMed:28068668). The core of this pathway is composed of a kinase cascade wherein STK3/MST2 and STK4/MST1, in complex with its regulatory protein SAV1, phosphorylates and activates LATS1/2 in complex with its regulatory protein MOB1, which in turn phosphorylates and inactivates YAP1 oncoprotein and WWTR1/TAZ (PubMed:18158288, PubMed:26437443, PubMed:28068668). Phosphorylation of YAP1 by LATS1 inhibits its translocation into the nucleus to regulate cellular genes important for cell proliferation, cell death, and cell migration (PubMed:18158288, PubMed:26437443, PubMed:28068668). Acts as a tumor suppressor which plays a critical role in maintenance of ploidy through its actions in both mitotic progression and the G1 tetraploidy checkpoint (PubMed:15122335, PubMed:19927127). Negatively regulates G2/M transition by down-regulating CDK1 kinase activity (PubMed:9988268). Involved in the control of p53 expression (PubMed:15122335). Affects cytokinesis by regulating actin polymerization through negative modulation of LIMK1 (PubMed:15220930). May also play a role in endocrine function. Plays a role in mammary gland epithelial cell differentiation, both through the Hippo signaling pathway and the intracellular estrogen receptor signaling pathway by promoting the degradation of ESR1 (PubMed:28068668). Acts as an activator of the NLRP3 inflammasome by mediating phosphorylation of 'Ser-265' of NLRP3 following NLRP3 palmitoylation, promoting NLRP3 activation by NEK7 (PubMed:39173637). {ECO:0000269|PubMed:10518011, ECO:0000269|PubMed:10831611, ECO:0000269|PubMed:15122335, ECO:0000269|PubMed:15220930, ECO:0000269|PubMed:18158288, ECO:0000269|PubMed:19927127, ECO:0000269|PubMed:26437443, ECO:0000269|PubMed:28068668, ECO:0000269|PubMed:39173637, ECO:0000269|PubMed:9988268}. |
O95866 | MPIG6B | S208 | ochoa | Megakaryocyte and platelet inhibitory receptor G6b (Protein G6b) | Inhibitory receptor that acts as a critical regulator of hematopoietic lineage differentiation, megakaryocyte function and platelet production (PubMed:12665801, PubMed:17311996, PubMed:27743390). Inhibits platelet aggregation and activation by agonists such as ADP and collagen-related peptide (PubMed:12665801). This regulation of megakaryocate function as well as platelet production ann activation is done through the inhibition (via the 2 ITIM motifs) of the receptors CLEC1B and GP6:FcRgamma signaling (PubMed:17311996). Appears to operate in a calcium-independent manner (PubMed:12665801). {ECO:0000269|PubMed:12665801, ECO:0000269|PubMed:17311996, ECO:0000269|PubMed:27743390}.; FUNCTION: Isoform B, displayed in this entry, is the only isoform to contain both a transmembrane region and 2 immunoreceptor tyrosine-based inhibitor motifs (ITIMs) and, thus, the only one which probably has a role of inhibitory receptor. Isoform A may be the activating counterpart of isoform B. {ECO:0000305|PubMed:11544253}. |
P00519 | ABL1 | S828 | ochoa | Tyrosine-protein kinase ABL1 (EC 2.7.10.2) (Abelson murine leukemia viral oncogene homolog 1) (Abelson tyrosine-protein kinase 1) (Proto-oncogene c-Abl) (p150) | Non-receptor tyrosine-protein kinase that plays a role in many key processes linked to cell growth and survival such as cytoskeleton remodeling in response to extracellular stimuli, cell motility and adhesion, receptor endocytosis, autophagy, DNA damage response and apoptosis. Coordinates actin remodeling through tyrosine phosphorylation of proteins controlling cytoskeleton dynamics like WASF3 (involved in branch formation); ANXA1 (involved in membrane anchoring); DBN1, DBNL, CTTN, RAPH1 and ENAH (involved in signaling); or MAPT and PXN (microtubule-binding proteins). Phosphorylation of WASF3 is critical for the stimulation of lamellipodia formation and cell migration. Involved in the regulation of cell adhesion and motility through phosphorylation of key regulators of these processes such as BCAR1, CRK, CRKL, DOK1, EFS or NEDD9 (PubMed:22810897). Phosphorylates multiple receptor tyrosine kinases and more particularly promotes endocytosis of EGFR, facilitates the formation of neuromuscular synapses through MUSK, inhibits PDGFRB-mediated chemotaxis and modulates the endocytosis of activated B-cell receptor complexes. Other substrates which are involved in endocytosis regulation are the caveolin (CAV1) and RIN1. Moreover, ABL1 regulates the CBL family of ubiquitin ligases that drive receptor down-regulation and actin remodeling. Phosphorylation of CBL leads to increased EGFR stability. Involved in late-stage autophagy by regulating positively the trafficking and function of lysosomal components. ABL1 targets to mitochondria in response to oxidative stress and thereby mediates mitochondrial dysfunction and cell death. In response to oxidative stress, phosphorylates serine/threonine kinase PRKD2 at 'Tyr-717' (PubMed:28428613). ABL1 is also translocated in the nucleus where it has DNA-binding activity and is involved in DNA-damage response and apoptosis. Many substrates are known mediators of DNA repair: DDB1, DDB2, ERCC3, ERCC6, RAD9A, RAD51, RAD52 or WRN. Activates the proapoptotic pathway when the DNA damage is too severe to be repaired. Phosphorylates TP73, a primary regulator for this type of damage-induced apoptosis. Phosphorylates the caspase CASP9 on 'Tyr-153' and regulates its processing in the apoptotic response to DNA damage. Phosphorylates PSMA7 that leads to an inhibition of proteasomal activity and cell cycle transition blocks. ABL1 also acts as a regulator of multiple pathological signaling cascades during infection. Several known tyrosine-phosphorylated microbial proteins have been identified as ABL1 substrates. This is the case of A36R of Vaccinia virus, Tir (translocated intimin receptor) of pathogenic E.coli and possibly Citrobacter, CagA (cytotoxin-associated gene A) of H.pylori, or AnkA (ankyrin repeat-containing protein A) of A.phagocytophilum. Pathogens can highjack ABL1 kinase signaling to reorganize the host actin cytoskeleton for multiple purposes, like facilitating intracellular movement and host cell exit. Finally, functions as its own regulator through autocatalytic activity as well as through phosphorylation of its inhibitor, ABI1. Regulates T-cell differentiation in a TBX21-dependent manner (By similarity). Positively regulates chemokine-mediated T-cell migration, polarization, and homing to lymph nodes and immune-challenged tissues, potentially via activation of NEDD9/HEF1 and RAP1 (By similarity). Phosphorylates TBX21 on tyrosine residues leading to an enhancement of its transcriptional activator activity (By similarity). {ECO:0000250|UniProtKB:P00520, ECO:0000269|PubMed:10391250, ECO:0000269|PubMed:11971963, ECO:0000269|PubMed:12379650, ECO:0000269|PubMed:12531427, ECO:0000269|PubMed:12672821, ECO:0000269|PubMed:15031292, ECO:0000269|PubMed:15556646, ECO:0000269|PubMed:15657060, ECO:0000269|PubMed:15886098, ECO:0000269|PubMed:16424036, ECO:0000269|PubMed:16678104, ECO:0000269|PubMed:16943190, ECO:0000269|PubMed:17306540, ECO:0000269|PubMed:17623672, ECO:0000269|PubMed:18328268, ECO:0000269|PubMed:18945674, ECO:0000269|PubMed:19891780, ECO:0000269|PubMed:20357770, ECO:0000269|PubMed:20417104, ECO:0000269|PubMed:22810897, ECO:0000269|PubMed:28428613, ECO:0000269|PubMed:9037071, ECO:0000269|PubMed:9144171, ECO:0000269|PubMed:9461559}. |
P05023 | ATP1A1 | S668 | ochoa | Sodium/potassium-transporting ATPase subunit alpha-1 (Na(+)/K(+) ATPase alpha-1 subunit) (EC 7.2.2.13) (Sodium pump subunit alpha-1) | This is the catalytic component of the active enzyme, which catalyzes the hydrolysis of ATP coupled with the exchange of sodium and potassium ions across the plasma membrane. This action creates the electrochemical gradient of sodium and potassium ions, providing the energy for active transport of various nutrients (PubMed:29499166, PubMed:30388404). Could also be part of an osmosensory signaling pathway that senses body-fluid sodium levels and controls salt intake behavior as well as voluntary water intake to regulate sodium homeostasis (By similarity). {ECO:0000250|UniProtKB:Q8VDN2, ECO:0000269|PubMed:29499166, ECO:0000269|PubMed:30388404}. |
P06213 | INSR | S1216 | psp | Insulin receptor (IR) (EC 2.7.10.1) (CD antigen CD220) [Cleaved into: Insulin receptor subunit alpha; Insulin receptor subunit beta] | Receptor tyrosine kinase which mediates the pleiotropic actions of insulin. Binding of insulin leads to phosphorylation of several intracellular substrates, including, insulin receptor substrates (IRS1, 2, 3, 4), SHC, GAB1, CBL and other signaling intermediates. Each of these phosphorylated proteins serve as docking proteins for other signaling proteins that contain Src-homology-2 domains (SH2 domain) that specifically recognize different phosphotyrosine residues, including the p85 regulatory subunit of PI3K and SHP2. Phosphorylation of IRSs proteins lead to the activation of two main signaling pathways: the PI3K-AKT/PKB pathway, which is responsible for most of the metabolic actions of insulin, and the Ras-MAPK pathway, which regulates expression of some genes and cooperates with the PI3K pathway to control cell growth and differentiation. Binding of the SH2 domains of PI3K to phosphotyrosines on IRS1 leads to the activation of PI3K and the generation of phosphatidylinositol-(3, 4, 5)-triphosphate (PIP3), a lipid second messenger, which activates several PIP3-dependent serine/threonine kinases, such as PDPK1 and subsequently AKT/PKB. The net effect of this pathway is to produce a translocation of the glucose transporter SLC2A4/GLUT4 from cytoplasmic vesicles to the cell membrane to facilitate glucose transport. Moreover, upon insulin stimulation, activated AKT/PKB is responsible for: anti-apoptotic effect of insulin by inducing phosphorylation of BAD; regulates the expression of gluconeogenic and lipogenic enzymes by controlling the activity of the winged helix or forkhead (FOX) class of transcription factors. Another pathway regulated by PI3K-AKT/PKB activation is mTORC1 signaling pathway which regulates cell growth and metabolism and integrates signals from insulin. AKT mediates insulin-stimulated protein synthesis by phosphorylating TSC2 thereby activating mTORC1 pathway. The Ras/RAF/MAP2K/MAPK pathway is mainly involved in mediating cell growth, survival and cellular differentiation of insulin. Phosphorylated IRS1 recruits GRB2/SOS complex, which triggers the activation of the Ras/RAF/MAP2K/MAPK pathway. In addition to binding insulin, the insulin receptor can bind insulin-like growth factors (IGFI and IGFII). Isoform Short has a higher affinity for IGFII binding. When present in a hybrid receptor with IGF1R, binds IGF1. PubMed:12138094 shows that hybrid receptors composed of IGF1R and INSR isoform Long are activated with a high affinity by IGF1, with low affinity by IGF2 and not significantly activated by insulin, and that hybrid receptors composed of IGF1R and INSR isoform Short are activated by IGF1, IGF2 and insulin. In contrast, PubMed:16831875 shows that hybrid receptors composed of IGF1R and INSR isoform Long and hybrid receptors composed of IGF1R and INSR isoform Short have similar binding characteristics, both bind IGF1 and have a low affinity for insulin. In adipocytes, inhibits lipolysis (By similarity). {ECO:0000250|UniProtKB:P15208, ECO:0000269|PubMed:12138094, ECO:0000269|PubMed:16314505, ECO:0000269|PubMed:16831875, ECO:0000269|PubMed:8257688, ECO:0000269|PubMed:8276809, ECO:0000269|PubMed:8452530, ECO:0000269|PubMed:9428692}. |
P06400 | RB1 | S794 | ochoa | Retinoblastoma-associated protein (p105-Rb) (p110-RB1) (pRb) (Rb) (pp110) | Tumor suppressor that is a key regulator of the G1/S transition of the cell cycle (PubMed:10499802). The hypophosphorylated form binds transcription regulators of the E2F family, preventing transcription of E2F-responsive genes (PubMed:10499802). Both physically blocks E2Fs transactivating domain and recruits chromatin-modifying enzymes that actively repress transcription (PubMed:10499802). Cyclin and CDK-dependent phosphorylation of RB1 induces its dissociation from E2Fs, thereby activating transcription of E2F responsive genes and triggering entry into S phase (PubMed:10499802). RB1 also promotes the G0-G1 transition upon phosphorylation and activation by CDK3/cyclin-C (PubMed:15084261). Directly involved in heterochromatin formation by maintaining overall chromatin structure and, in particular, that of constitutive heterochromatin by stabilizing histone methylation. Recruits and targets histone methyltransferases SUV39H1, KMT5B and KMT5C, leading to epigenetic transcriptional repression. Controls histone H4 'Lys-20' trimethylation. Inhibits the intrinsic kinase activity of TAF1. Mediates transcriptional repression by SMARCA4/BRG1 by recruiting a histone deacetylase (HDAC) complex to the c-FOS promoter. In resting neurons, transcription of the c-FOS promoter is inhibited by BRG1-dependent recruitment of a phospho-RB1-HDAC1 repressor complex. Upon calcium influx, RB1 is dephosphorylated by calcineurin, which leads to release of the repressor complex (By similarity). {ECO:0000250|UniProtKB:P13405, ECO:0000250|UniProtKB:P33568, ECO:0000269|PubMed:10499802, ECO:0000269|PubMed:15084261}.; FUNCTION: (Microbial infection) In case of viral infections, interactions with SV40 large T antigen, HPV E7 protein or adenovirus E1A protein induce the disassembly of RB1-E2F1 complex thereby disrupting RB1's activity. {ECO:0000269|PubMed:1316611, ECO:0000269|PubMed:17974914, ECO:0000269|PubMed:18701596, ECO:0000269|PubMed:2839300, ECO:0000269|PubMed:8892909}. |
P07359 | GP1BA | S632 | ochoa|psp | Platelet glycoprotein Ib alpha chain (GP-Ib alpha) (GPIb-alpha) (GPIbA) (Glycoprotein Ibalpha) (Antigen CD42b-alpha) (CD antigen CD42b) [Cleaved into: Glycocalicin] | GP-Ib, a surface membrane protein of platelets, participates in the formation of platelet plugs by binding to the A1 domain of vWF, which is already bound to the subendothelium. |
P07451 | CA3 | S100 | ochoa | Carbonic anhydrase 3 (EC 4.2.1.1) (Carbonate dehydratase III) (Carbonic anhydrase III) (CA-III) | Reversible hydration of carbon dioxide. {ECO:0000269|PubMed:17427958, ECO:0000269|PubMed:18618712}. |
P10070 | GLI2 | S135 | ochoa | Zinc finger protein GLI2 (GLI family zinc finger protein 2) (Tax helper protein) | Functions as a transcription regulator in the hedgehog (Hh) pathway (PubMed:18455992, PubMed:26565916). Functions as a transcriptional activator (PubMed:19878745, PubMed:24311597, PubMed:9557682). May also function as transcriptional repressor (By similarity). Requires STK36 for full transcriptional activator activity. Required for normal embryonic development (PubMed:15994174, PubMed:20685856). {ECO:0000250|UniProtKB:Q0VGT2, ECO:0000269|PubMed:15994174, ECO:0000269|PubMed:18455992, ECO:0000269|PubMed:19878745, ECO:0000269|PubMed:24311597, ECO:0000269|PubMed:26565916, ECO:0000269|PubMed:9557682, ECO:0000305|PubMed:20685856}.; FUNCTION: [Isoform 1]: Involved in the smoothened (SHH) signaling pathway. {ECO:0000269|PubMed:18455992}.; FUNCTION: [Isoform 2]: Involved in the smoothened (SHH) signaling pathway. {ECO:0000269|PubMed:18455992}.; FUNCTION: [Isoform 3]: Involved in the smoothened (SHH) signaling pathway. {ECO:0000269|PubMed:18455992}.; FUNCTION: [Isoform 4]: Involved in the smoothened (SHH) signaling pathway. {ECO:0000269|PubMed:18455992}.; FUNCTION: [Isoform 1]: Acts as a transcriptional activator in T-cell leukemia virus type 1 (HTLV-1)-infected cells in a Tax-dependent manner. Binds to the DNA sequence 5'-GAACCACCCA-3' which is part of the Tax-responsive element (TRE-2S) regulatory element that augments the Tax-dependent enhancer of HTLV-1 (PubMed:9557682). {ECO:0000269|PubMed:15994174, ECO:0000269|PubMed:9557682}.; FUNCTION: [Isoform 2]: (Microbial infection) Acts as a transcriptional activators in T-cell leukemia virus type 1 (HTLV-1)-infected cells in a Tax-dependent manner. Binds to the DNA sequence 5'-GAACCACCCA-3' which is part of the Tax-responsive element (TRE-2S) regulatory element that augments the Tax-dependent enhancer of HTLV-1 (PubMed:9557682). {ECO:0000269|PubMed:15994174, ECO:0000269|PubMed:9557682}.; FUNCTION: [Isoform 3]: (Microbial infection) Acts as a transcriptional activators in T-cell leukemia virus type 1 (HTLV-1)-infected cells in a Tax-dependent manner. Binds to the DNA sequence 5'-GAACCACCCA-3' which is part of the Tax-responsive element (TRE-2S) regulatory element that augments the Tax-dependent enhancer of HTLV-1 (PubMed:9557682). {ECO:0000269|PubMed:15994174, ECO:0000269|PubMed:9557682}.; FUNCTION: [Isoform 4]: (Microbial infection) Acts as a transcriptional activators in T-cell leukemia virus type 1 (HTLV-1)-infected cells in a Tax-dependent manner. Binds to the DNA sequence 5'-GAACCACCCA-3' which is part of the Tax-responsive element (TRE-2S) regulatory element that augments the Tax-dependent enhancer of HTLV-1 (PubMed:9557682). {ECO:0000269|PubMed:15994174, ECO:0000269|PubMed:9557682}.; FUNCTION: [Isoform 5]: Acts as a transcriptional repressor. {ECO:0000269|PubMed:15994174}. |
P10636 | MAPT | S171 | ochoa | Microtubule-associated protein tau (Neurofibrillary tangle protein) (Paired helical filament-tau) (PHF-tau) | Promotes microtubule assembly and stability, and might be involved in the establishment and maintenance of neuronal polarity (PubMed:21985311). The C-terminus binds axonal microtubules while the N-terminus binds neural plasma membrane components, suggesting that tau functions as a linker protein between both (PubMed:21985311, PubMed:32961270). Axonal polarity is predetermined by TAU/MAPT localization (in the neuronal cell) in the domain of the cell body defined by the centrosome. The short isoforms allow plasticity of the cytoskeleton whereas the longer isoforms may preferentially play a role in its stabilization. {ECO:0000269|PubMed:21985311, ECO:0000269|PubMed:32961270}. |
P11137 | MAP2 | S1640 | ochoa | Microtubule-associated protein 2 (MAP-2) | The exact function of MAP2 is unknown but MAPs may stabilize the microtubules against depolymerization. They also seem to have a stiffening effect on microtubules. |
P13498 | CYBA | S153 | ochoa|psp | Cytochrome b-245 light chain (Cytochrome b(558) alpha chain) (Cytochrome b558 subunit alpha) (Neutrophil cytochrome b 22 kDa polypeptide) (Superoxide-generating NADPH oxidase light chain subunit) (p22 phagocyte B-cytochrome) (p22-phox) (p22phox) | Subunit of NADPH oxidase complexes that is required for the NADPH oxidase activity that generates, in various cell types, superoxide from molecular oxygen utilizing NADPH as an electron donor (PubMed:15824103, PubMed:17140397, PubMed:38355798). Subunit of the phagocyte NADPH oxidase complex that mediates the transfer of electrons from cytosolic NADPH to O2 to produce the superoxide anion (O2(-)) (PubMed:38355798). In the activated complex, electrons are first transferred from NADPH to flavin adenine dinucleotide (FAD) and subsequently transferred via two heme molecules to molecular oxygen, producing superoxide through an outer-sphere reaction (PubMed:38355798). Activation of the NADPH oxidase complex is initiated by the assembly of cytosolic subunits of the NADPH oxidase complex with the core NADPH oxidase complex to form a complex at the plasma membrane or phagosomal membrane (PubMed:38355798). This activation process is initiated by phosphorylation dependent binding of the cytosolic NCF1/p47-phox subunit to the C-terminus of CYBA/p22-phox (PubMed:19948736). Aassociates with NOX3 to form a functional NADPH oxidase constitutively generating superoxide (PubMed:15824103, PubMed:17140397). {ECO:0000269|PubMed:15824103, ECO:0000269|PubMed:17140397, ECO:0000269|PubMed:19948736, ECO:0000269|PubMed:38355798}. |
P20810 | CAST | S236 | ochoa | Calpastatin (Calpain inhibitor) (Sperm BS-17 component) | Specific inhibition of calpain (calcium-dependent cysteine protease). Plays a key role in postmortem tenderization of meat and have been proposed to be involved in muscle protein degradation in living tissue. |
P26358 | DNMT1 | T166 | ochoa | DNA (cytosine-5)-methyltransferase 1 (Dnmt1) (EC 2.1.1.37) (CXXC-type zinc finger protein 9) (DNA methyltransferase HsaI) (DNA MTase HsaI) (M.HsaI) (MCMT) | Methylates CpG residues. Preferentially methylates hemimethylated DNA. Associates with DNA replication sites in S phase maintaining the methylation pattern in the newly synthesized strand, that is essential for epigenetic inheritance. Associates with chromatin during G2 and M phases to maintain DNA methylation independently of replication. It is responsible for maintaining methylation patterns established in development. DNA methylation is coordinated with methylation of histones. Mediates transcriptional repression by direct binding to HDAC2. In association with DNMT3B and via the recruitment of CTCFL/BORIS, involved in activation of BAG1 gene expression by modulating dimethylation of promoter histone H3 at H3K4 and H3K9. Probably forms a corepressor complex required for activated KRAS-mediated promoter hypermethylation and transcriptional silencing of tumor suppressor genes (TSGs) or other tumor-related genes in colorectal cancer (CRC) cells (PubMed:24623306). Also required to maintain a transcriptionally repressive state of genes in undifferentiated embryonic stem cells (ESCs) (PubMed:24623306). Associates at promoter regions of tumor suppressor genes (TSGs) leading to their gene silencing (PubMed:24623306). Promotes tumor growth (PubMed:24623306). {ECO:0000269|PubMed:16357870, ECO:0000269|PubMed:18413740, ECO:0000269|PubMed:18754681, ECO:0000269|PubMed:24623306}. |
P28290 | ITPRID2 | S1152 | ochoa | Protein ITPRID2 (Cleavage signal-1 protein) (CS-1) (ITPR-interacting domain-containing protein 2) (Ki-ras-induced actin-interacting protein) (Sperm-specific antigen 2) | None |
P30260 | CDC27 | S192 | ochoa | Cell division cycle protein 27 homolog (Anaphase-promoting complex subunit 3) (APC3) (CDC27 homolog) (CDC27Hs) (H-NUC) | Component of the anaphase promoting complex/cyclosome (APC/C), a cell cycle-regulated E3 ubiquitin ligase that controls progression through mitosis and the G1 phase of the cell cycle (PubMed:18485873). The APC/C complex acts by mediating ubiquitination and subsequent degradation of target proteins: it mainly mediates the formation of 'Lys-11'-linked polyubiquitin chains and, to a lower extent, the formation of 'Lys-48'- and 'Lys-63'-linked polyubiquitin chains (PubMed:18485873). The APC/C complex catalyzes assembly of branched 'Lys-11'-/'Lys-48'-linked branched ubiquitin chains on target proteins (PubMed:29033132). {ECO:0000269|PubMed:18485873, ECO:0000269|PubMed:29033132}. |
P38159 | RBMX | S165 | ochoa | RNA-binding motif protein, X chromosome (Glycoprotein p43) (Heterogeneous nuclear ribonucleoprotein G) (hnRNP G) [Cleaved into: RNA-binding motif protein, X chromosome, N-terminally processed] | RNA-binding protein that plays several role in the regulation of pre- and post-transcriptional processes. Implicated in tissue-specific regulation of gene transcription and alternative splicing of several pre-mRNAs. Binds to and stimulates transcription from the tumor suppressor TXNIP gene promoter; may thus be involved in tumor suppression. When associated with SAFB, binds to and stimulates transcription from the SREBF1 promoter. Associates with nascent mRNAs transcribed by RNA polymerase II. Component of the supraspliceosome complex that regulates pre-mRNA alternative splice site selection. Can either activate or suppress exon inclusion; acts additively with TRA2B to promote exon 7 inclusion of the survival motor neuron SMN2. Represses the splicing of MAPT/Tau exon 10. Binds preferentially to single-stranded 5'-CC[A/C]-rich RNA sequence motifs localized in a single-stranded conformation; probably binds RNA as a homodimer. Binds non-specifically to pre-mRNAs. Also plays a role in the cytoplasmic TNFR1 trafficking pathways; promotes both the IL-1-beta-mediated inducible proteolytic cleavage of TNFR1 ectodomains and the release of TNFR1 exosome-like vesicles to the extracellular compartment. {ECO:0000269|PubMed:12165565, ECO:0000269|PubMed:12761049, ECO:0000269|PubMed:16707624, ECO:0000269|PubMed:18445477, ECO:0000269|PubMed:18541147, ECO:0000269|PubMed:19282290, ECO:0000269|PubMed:21327109}. |
P41145 | OPRK1 | S358 | psp | Kappa-type opioid receptor (K-OR-1) (KOR-1) | G-protein coupled opioid receptor that functions as a receptor for endogenous alpha-neoendorphins and dynorphins, but has low affinity for beta-endorphins. Also functions as a receptor for various synthetic opioids and for the psychoactive diterpene salvinorin A. Ligand binding causes a conformation change that triggers signaling via guanine nucleotide-binding proteins (G proteins) and modulates the activity of down-stream effectors, such as adenylate cyclase. Signaling leads to the inhibition of adenylate cyclase activity. Inhibits neurotransmitter release by reducing calcium ion currents and increasing potassium ion conductance. Plays a role in the perception of pain. Plays a role in mediating reduced physical activity upon treatment with synthetic opioids. Plays a role in the regulation of salivation in response to synthetic opioids. May play a role in arousal and regulation of autonomic and neuroendocrine functions. {ECO:0000269|PubMed:12004055, ECO:0000269|PubMed:22437504, ECO:0000269|PubMed:7624359, ECO:0000269|PubMed:8060324}. |
P43403 | ZAP70 | S106 | ochoa | Tyrosine-protein kinase ZAP-70 (EC 2.7.10.2) (70 kDa zeta-chain associated protein) (Syk-related tyrosine kinase) | Tyrosine kinase that plays an essential role in regulation of the adaptive immune response. Regulates motility, adhesion and cytokine expression of mature T-cells, as well as thymocyte development. Also contributes to the development and activation of primary B-lymphocytes. When antigen presenting cells (APC) activate T-cell receptor (TCR), a serie of phosphorylations lead to the recruitment of ZAP70 to the doubly phosphorylated TCR component CD247/CD3Z through ITAM motif at the plasma membrane. This recruitment serves to localization to the stimulated TCR and to relieve its autoinhibited conformation. Release of ZAP70 active conformation is further stabilized by phosphorylation mediated by LCK. Subsequently, ZAP70 phosphorylates at least 2 essential adapter proteins: LAT and LCP2. In turn, a large number of signaling molecules are recruited and ultimately lead to lymphokine production, T-cell proliferation and differentiation. Furthermore, ZAP70 controls cytoskeleton modifications, adhesion and mobility of T-lymphocytes, thus ensuring correct delivery of effectors to the APC. ZAP70 is also required for TCR-CD247/CD3Z internalization and degradation through interaction with the E3 ubiquitin-protein ligase CBL and adapter proteins SLA and SLA2. Thus, ZAP70 regulates both T-cell activation switch on and switch off by modulating TCR expression at the T-cell surface. During thymocyte development, ZAP70 promotes survival and cell-cycle progression of developing thymocytes before positive selection (when cells are still CD4/CD8 double negative). Additionally, ZAP70-dependent signaling pathway may also contribute to primary B-cells formation and activation through B-cell receptor (BCR). {ECO:0000269|PubMed:11353765, ECO:0000269|PubMed:12051764, ECO:0000269|PubMed:1423621, ECO:0000269|PubMed:20135127, ECO:0000269|PubMed:26903241, ECO:0000269|PubMed:38614099, ECO:0000269|PubMed:8124727, ECO:0000269|PubMed:8702662, ECO:0000269|PubMed:9489702}. |
P46013 | MKI67 | S2686 | ochoa | Proliferation marker protein Ki-67 (Antigen identified by monoclonal antibody Ki-67) (Antigen KI-67) (Antigen Ki67) | Protein that associates with the surface of mitotic chromosomes and acts both as a chromosome repellent during early mitosis and chromosome attractant during late mitosis (PubMed:27362226, PubMed:32879492, PubMed:35513709, PubMed:39153474). Required to maintain individual mitotic chromosomes dispersed in the cytoplasm following nuclear envelope disassembly (PubMed:27362226). During early mitosis, relocalizes from nucleoli to the chromosome surface where it forms extended brush structures that cover a substantial fraction of the chromosome surface (PubMed:27362226). The MKI67 brush structure prevents chromosomes from collapsing into a single chromatin mass by forming a steric and electrostatic charge barrier: the protein has a high net electrical charge and acts as a surfactant, dispersing chromosomes and enabling independent chromosome motility (PubMed:27362226). During mitotic anaphase, the MKI67 brush structure collapses and MKI67 switches from a chromosome repellent to a chromosome attractant to promote chromosome clustering and facilitate the exclusion of large cytoplasmic particles from the future nuclear space (PubMed:32879492, PubMed:39153474). Mechanistically, dephosphorylation during mitotic exit and simultaneous exposure of a conserved basic patch induce the RNA-dependent formation of a liquid-like condensed phase on the chromosome surface, promoting coalescence of neighboring chromosome surfaces and clustering of chromosomes (PubMed:39153474). Binds premature ribosomal RNAs during anaphase; promoting liquid-liquid phase separation (PubMed:28935370, PubMed:39153474). Binds DNA, with a preference for supercoiled DNA and AT-rich DNA (PubMed:10878551). Does not contribute to the internal structure of mitotic chromosomes (By similarity). May play a role in chromatin organization; it is however unclear whether it plays a direct role in chromatin organization or whether it is an indirect consequence of its function in mitotic chromosome (PubMed:24867636). {ECO:0000250|UniProtKB:E9PVX6, ECO:0000269|PubMed:10878551, ECO:0000269|PubMed:24867636, ECO:0000269|PubMed:27362226, ECO:0000269|PubMed:28935370, ECO:0000269|PubMed:32879492, ECO:0000269|PubMed:35513709, ECO:0000269|PubMed:39153474}. |
P49450 | CENPA | S37 | ochoa | Histone H3-like centromeric protein A (Centromere autoantigen A) (Centromere protein A) (CENP-A) | Histone H3-like nucleosomal protein that is specifically found in centromeric nucleosomes (PubMed:11756469, PubMed:14667408, PubMed:15282608, PubMed:15475964, PubMed:15702419, PubMed:17651496, PubMed:19114591, PubMed:20739937, PubMed:27499292, PubMed:7962047, PubMed:9024683). Replaces conventional H3 in the nucleosome core of centromeric chromatin that serves as an assembly site for the inner kinetochore (PubMed:18072184). The presence of CENPA subtly modifies the nucleosome structure and the way DNA is wrapped around the nucleosome and gives rise to protruding DNA ends that are less well-ordered and rigid compared to nucleosomes containing histone H3 (PubMed:26878239, PubMed:27499292). May serve as an epigenetic mark that propagates centromere identity through replication and cell division (PubMed:15282608, PubMed:15475964, PubMed:20739937, PubMed:21478274, PubMed:26878239). Required for recruitment and assembly of kinetochore proteins, and as a consequence required for progress through mitosis, chromosome segregation and cytokinesis (PubMed:11756469, PubMed:14667408, PubMed:18072184, PubMed:23818633, PubMed:25556658, PubMed:27499292). {ECO:0000269|PubMed:11756469, ECO:0000269|PubMed:14667408, ECO:0000269|PubMed:15282608, ECO:0000269|PubMed:15475964, ECO:0000269|PubMed:15702419, ECO:0000269|PubMed:17651496, ECO:0000269|PubMed:18072184, ECO:0000269|PubMed:19114591, ECO:0000269|PubMed:21478274, ECO:0000269|PubMed:23818633, ECO:0000269|PubMed:25556658, ECO:0000269|PubMed:26878239, ECO:0000269|PubMed:27499292, ECO:0000269|PubMed:7962047, ECO:0000269|PubMed:9024683, ECO:0000305|PubMed:20739937}. |
P51587 | BRCA2 | S76 | ochoa|psp | Breast cancer type 2 susceptibility protein (Fanconi anemia group D1 protein) | Involved in double-strand break repair and/or homologous recombination. Binds RAD51 and potentiates recombinational DNA repair by promoting assembly of RAD51 onto single-stranded DNA (ssDNA). Acts by targeting RAD51 to ssDNA over double-stranded DNA, enabling RAD51 to displace replication protein-A (RPA) from ssDNA and stabilizing RAD51-ssDNA filaments by blocking ATP hydrolysis. Part of a PALB2-scaffolded HR complex containing RAD51C and which is thought to play a role in DNA repair by HR. May participate in S phase checkpoint activation. Binds selectively to ssDNA, and to ssDNA in tailed duplexes and replication fork structures. May play a role in the extension step after strand invasion at replication-dependent DNA double-strand breaks; together with PALB2 is involved in both POLH localization at collapsed replication forks and DNA polymerization activity. In concert with NPM1, regulates centrosome duplication. Interacts with the TREX-2 complex (transcription and export complex 2) subunits PCID2 and SEM1, and is required to prevent R-loop-associated DNA damage and thus transcription-associated genomic instability. Silencing of BRCA2 promotes R-loop accumulation at actively transcribed genes in replicating and non-replicating cells, suggesting that BRCA2 mediates the control of R-loop associated genomic instability, independently of its known role in homologous recombination (PubMed:24896180). {ECO:0000269|PubMed:15115758, ECO:0000269|PubMed:15199141, ECO:0000269|PubMed:15671039, ECO:0000269|PubMed:18317453, ECO:0000269|PubMed:20729832, ECO:0000269|PubMed:20729858, ECO:0000269|PubMed:20729859, ECO:0000269|PubMed:21084279, ECO:0000269|PubMed:21719596, ECO:0000269|PubMed:24485656, ECO:0000269|PubMed:24896180}. |
P51957 | NEK4 | S665 | ochoa | Serine/threonine-protein kinase Nek4 (EC 2.7.11.1) (Never in mitosis A-related kinase 4) (NimA-related protein kinase 4) (Serine/threonine-protein kinase 2) (Serine/threonine-protein kinase NRK2) | Protein kinase that seems to act exclusively upon threonine residues (By similarity). Required for normal entry into proliferative arrest after a limited number of cell divisions, also called replicative senescence. Required for normal cell cycle arrest in response to double-stranded DNA damage. {ECO:0000250|UniProtKB:Q9Z1J2, ECO:0000269|PubMed:22851694}. |
P52179 | MYOM1 | S618 | psp | Myomesin-1 (190 kDa connectin-associated protein) (190 kDa titin-associated protein) (Myomesin family member 1) | Major component of the vertebrate myofibrillar M band. Binds myosin, titin, and light meromyosin. This binding is dose dependent. |
P56945 | BCAR1 | S407 | ochoa | Breast cancer anti-estrogen resistance protein 1 (CRK-associated substrate) (Cas scaffolding protein family member 1) (p130cas) | Docking protein which plays a central coordinating role for tyrosine kinase-based signaling related to cell adhesion (PubMed:12432078, PubMed:12832404). Implicated in induction of cell migration and cell branching (PubMed:12432078, PubMed:12832404, PubMed:17038317). Involved in the BCAR3-mediated inhibition of TGFB signaling (By similarity). {ECO:0000250|UniProtKB:Q61140, ECO:0000269|PubMed:12432078, ECO:0000269|PubMed:12832404, ECO:0000269|PubMed:17038317}. |
P82094 | TMF1 | S136 | ochoa | TATA element modulatory factor (TMF) (Androgen receptor coactivator 160 kDa protein) (Androgen receptor-associated protein of 160 kDa) | Potential coactivator of the androgen receptor. Mediates STAT3 degradation. May play critical roles in two RAB6-dependent retrograde transport processes: one from endosomes to the Golgi and the other from the Golgi to the ER. This protein binds the HIV-1 TATA element and inhibits transcriptional activation by the TATA-binding protein (TBP). {ECO:0000269|PubMed:10428808, ECO:0000269|PubMed:1409643, ECO:0000269|PubMed:15467733, ECO:0000269|PubMed:17698061}. |
Q01780 | EXOSC10 | S217 | ochoa | Exosome complex component 10 (EC 3.1.13.-) (Autoantigen PM/Scl 2) (P100 polymyositis-scleroderma overlap syndrome-associated autoantigen) (Polymyositis/scleroderma autoantigen 100 kDa) (PM/Scl-100) (Polymyositis/scleroderma autoantigen 2) | 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. 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). 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. EXOSC10 is required for nucleolar localization of C1D and probably mediates the association of MTREX, C1D and MPHOSPH6 with the RNA exosome involved in the maturation of 5.8S rRNA. Plays a role in the recruitment of replication protein A complex (RPA) and RAD51 to DNA double-strand breaks caused by irradiation, contributing to DNA repair by homologous recombination (PubMed:25632158, PubMed:31086179). Regulates levels of damage-induced RNAs in order to prevent DNA-RNA hybrid formation at DNA double-strand breaks and limit DNA end resection after damage (PubMed:31086179). Plays a role in oocyte development, maturation and survival (By similarity). Required for normal testis development and mitotic division of spermatogonia (By similarity). Plays a role in proper embryo development (By similarity). Required for global protein translation (PubMed:26857222, PubMed:36912080). Required for cell proliferation (PubMed:36912080). Regulates metabolism of C9orf72-derived repeat RNA that can be translated into toxic dipeptide repeat proteins (PubMed:32830871). {ECO:0000250|UniProtKB:P56960, ECO:0000269|PubMed:14527413, ECO:0000269|PubMed:16455498, ECO:0000269|PubMed:17412707, ECO:0000269|PubMed:17545563, ECO:0000269|PubMed:18172165, ECO:0000269|PubMed:19056938, ECO:0000269|PubMed:20368444, ECO:0000269|PubMed:20699273, ECO:0000269|PubMed:25632158, ECO:0000269|PubMed:26857222, ECO:0000269|PubMed:31086179, ECO:0000269|PubMed:32830871, ECO:0000269|PubMed:34516797, ECO:0000269|PubMed:36912080}. |
Q02218 | OGDH | S870 | ochoa | 2-oxoglutarate dehydrogenase complex component E1 (E1o) (HsOGDH) (OGDC-E1) (OGDH-E1) (EC 1.2.4.2) (2-oxoglutarate dehydrogenase, mitochondrial) (Alpha-ketoglutarate dehydrogenase) (Alpha-KGDH-E1) (Thiamine diphosphate (ThDP)-dependent 2-oxoglutarate dehydrogenase) | 2-oxoglutarate dehydrogenase (E1o) component of the 2-oxoglutarate dehydrogenase complex (OGDHC) (PubMed:24495017, PubMed:25210035, PubMed:28435050). Participates in the first step, rate limiting for the overall conversion of 2-oxoglutarate to succinyl-CoA and CO(2) catalyzed by the whole OGDHC (PubMed:24495017, PubMed:25210035, PubMed:28435050). Catalyzes the irreversible decarboxylation of 2-oxoglutarate (alpha-ketoglutarate) via the thiamine diphosphate (ThDP) cofactor and subsequent transfer of the decarboxylated acyl intermediate on an oxidized dihydrolipoyl group that is covalently amidated to the E2 enzyme (dihydrolipoyllysine-residue succinyltransferase or DLST) (PubMed:24495017, PubMed:25210035, PubMed:28435050, PubMed:35272141). Plays a key role in the Krebs (citric acid) cycle, which is a common pathway for oxidation of fuel molecules, including carbohydrates, fatty acids, and amino acids (PubMed:25210035). Can catalyze the decarboxylation of 2-oxoadipate in vitro, but at a much lower rate than 2-oxoglutarate (PubMed:28435050). Mainly active in the mitochondrion (PubMed:29211711). A fraction of the 2-oxoglutarate dehydrogenase complex also localizes in the nucleus and is required for lysine succinylation of histones: associates with KAT2A on chromatin and provides succinyl-CoA to histone succinyltransferase KAT2A (PubMed:29211711). {ECO:0000269|PubMed:24495017, ECO:0000269|PubMed:25210035, ECO:0000269|PubMed:28435050, ECO:0000269|PubMed:29211711, ECO:0000303|PubMed:25210035}. |
Q04721 | NOTCH2 | S2388 | ochoa | Neurogenic locus notch homolog protein 2 (Notch 2) (hN2) [Cleaved into: Notch 2 extracellular truncation (N2ECD); Notch 2 intracellular domain (N2ICD)] | Functions as a receptor for membrane-bound ligands Jagged-1 (JAG1), Jagged-2 (JAG2) and Delta-1 (DLL1) to regulate cell-fate determination. Upon ligand activation through the released notch intracellular domain (NICD) it forms a transcriptional activator complex with RBPJ/RBPSUH and activates genes of the enhancer of split locus (PubMed:21378985, PubMed:21378989). Affects the implementation of differentiation, proliferation and apoptotic programs (By similarity). Involved in bone remodeling and homeostasis. In collaboration with RELA/p65 enhances NFATc1 promoter activity and positively regulates RANKL-induced osteoclast differentiation (PubMed:29149593). Positively regulates self-renewal of liver cancer cells (PubMed:25985737). {ECO:0000250|UniProtKB:O35516, ECO:0000269|PubMed:21378985, ECO:0000269|PubMed:21378989, ECO:0000269|PubMed:25985737, ECO:0000269|PubMed:29149593}. |
Q07157 | TJP1 | S1196 | ochoa | Tight junction protein 1 (Tight junction protein ZO-1) (Zona occludens protein 1) (Zonula occludens protein 1) | TJP1, TJP2, and TJP3 are closely related scaffolding proteins that link tight junction (TJ) transmembrane proteins such as claudins, junctional adhesion molecules, and occludin to the actin cytoskeleton (PubMed:7798316, PubMed:9792688). Forms a multistranded TJP1/ZO1 condensate which elongates to form a tight junction belt, the belt is anchored at the apical cell membrane via interaction with PATJ (By similarity). The tight junction acts to limit movement of substances through the paracellular space and as a boundary between the compositionally distinct apical and basolateral plasma membrane domains of epithelial and endothelial cells. Necessary for lumenogenesis, and particularly efficient epithelial polarization and barrier formation (By similarity). Plays a role in the regulation of cell migration by targeting CDC42BPB to the leading edge of migrating cells (PubMed:21240187). Plays an important role in podosome formation and associated function, thus regulating cell adhesion and matrix remodeling (PubMed:20930113). With TJP2 and TJP3, participates in the junctional retention and stability of the transcription factor DBPA, but is not involved in its shuttling to the nucleus (By similarity). May play a role in mediating cell morphology changes during ameloblast differentiation via its role in tight junctions (By similarity). {ECO:0000250|UniProtKB:O97758, ECO:0000250|UniProtKB:P39447, ECO:0000269|PubMed:20930113, ECO:0000269|PubMed:21240187}. |
Q10586 | DBP | S165 | ochoa | D site-binding protein (Albumin D box-binding protein) (Albumin D-element-binding protein) (Tax-responsive enhancer element-binding protein 302) (TaxREB302) | This transcriptional activator recognizes and binds to the sequence 5'-RTTAYGTAAY-3' found in the promoter of genes such as albumin, CYP2A4 and CYP2A5. It is not essential for circadian rhythm generation, but modulates important clock output genes. May be a direct target for regulation by the circadian pacemaker component clock. May affect circadian period and sleep regulation. |
Q12789 | GTF3C1 | S1868 | ochoa | General transcription factor 3C polypeptide 1 (TF3C-alpha) (TFIIIC box B-binding subunit) (Transcription factor IIIC 220 kDa subunit) (TFIIIC 220 kDa subunit) (TFIIIC220) (Transcription factor IIIC subunit alpha) | Required for RNA polymerase III-mediated transcription. Component of TFIIIC that initiates transcription complex assembly on tRNA and is required for transcription of 5S rRNA and other stable nuclear and cytoplasmic RNAs. Binds to the box B promoter element. |
Q13191 | CBLB | S856 | ochoa | E3 ubiquitin-protein ligase CBL-B (EC 2.3.2.27) (Casitas B-lineage lymphoma proto-oncogene b) (RING finger protein 56) (RING-type E3 ubiquitin transferase CBL-B) (SH3-binding protein CBL-B) (Signal transduction protein CBL-B) | E3 ubiquitin-protein ligase which accepts ubiquitin from specific E2 ubiquitin-conjugating enzymes, and transfers it to substrates, generally promoting their degradation by the proteasome. Negatively regulates TCR (T-cell receptor), BCR (B-cell receptor) and FCER1 (high affinity immunoglobulin epsilon receptor) signal transduction pathways. In naive T-cells, inhibits VAV1 activation upon TCR engagement and imposes a requirement for CD28 costimulation for proliferation and IL-2 production. Also acts by promoting PIK3R1/p85 ubiquitination, which impairs its recruitment to the TCR and subsequent activation. In activated T-cells, inhibits PLCG1 activation and calcium mobilization upon restimulation and promotes anergy. In B-cells, acts by ubiquitinating SYK and promoting its proteasomal degradation. Slightly promotes SRC ubiquitination. May be involved in EGFR ubiquitination and internalization. May be functionally coupled with the E2 ubiquitin-protein ligase UB2D3. In association with CBL, required for proper feedback inhibition of ciliary platelet-derived growth factor receptor-alpha (PDGFRA) signaling pathway via ubiquitination and internalization of PDGFRA (By similarity). {ECO:0000250|UniProtKB:Q3TTA7, ECO:0000269|PubMed:10022120, ECO:0000269|PubMed:10086340, ECO:0000269|PubMed:11087752, ECO:0000269|PubMed:11526404, ECO:0000269|PubMed:14661060, ECO:0000269|PubMed:20525694}. |
Q13459 | MYO9B | S2049 | ochoa | Unconventional myosin-IXb (Unconventional myosin-9b) | Myosins are actin-based motor molecules with ATPase activity. Unconventional myosins serve in intracellular movements. Binds actin with high affinity both in the absence and presence of ATP and its mechanochemical activity is inhibited by calcium ions (PubMed:9490638). Also acts as a GTPase activator for RHOA (PubMed:26529257, PubMed:9490638). Plays a role in the regulation of cell migration via its role as RHOA GTPase activator. This is regulated by its interaction with the SLIT2 receptor ROBO1; interaction with ROBO1 impairs interaction with RHOA and subsequent activation of RHOA GTPase activity, and thereby leads to increased levels of active, GTP-bound RHOA (PubMed:26529257). {ECO:0000269|PubMed:26529257, ECO:0000269|PubMed:9490638}. |
Q13946 | PDE7A | S28 | ochoa | High affinity 3',5'-cyclic-AMP phosphodiesterase 7A (EC 3.1.4.53) (HCP1) (TM22) (cAMP-specific phosphodiesterase 7A) | Hydrolyzes the second messenger cAMP, which is a key regulator of many important physiological processes (PubMed:19350606, PubMed:8389765, PubMed:9195912). May have a role in muscle signal transduction (PubMed:9195912). {ECO:0000269|PubMed:19350606, ECO:0000269|PubMed:8389765, ECO:0000269|PubMed:9195912}. |
Q13950 | RUNX2 | S347 | psp | Runt-related transcription factor 2 (Acute myeloid leukemia 3 protein) (Core-binding factor subunit alpha-1) (CBF-alpha-1) (Oncogene AML-3) (Osteoblast-specific transcription factor 2) (OSF-2) (Polyomavirus enhancer-binding protein 2 alpha A subunit) (PEA2-alpha A) (PEBP2-alpha A) (SL3-3 enhancer factor 1 alpha A subunit) (SL3/AKV core-binding factor alpha A subunit) | Transcription factor involved in osteoblastic differentiation and skeletal morphogenesis (PubMed:28505335, PubMed:28703881, PubMed:28738062). Essential for the maturation of osteoblasts and both intramembranous and endochondral ossification. CBF binds to the core site, 5'-PYGPYGGT-3', of a number of enhancers and promoters, including murine leukemia virus, polyomavirus enhancer, T-cell receptor enhancers, osteocalcin, osteopontin, bone sialoprotein, alpha 1(I) collagen, LCK, IL-3 and GM-CSF promoters. In osteoblasts, supports transcription activation: synergizes with SPEN/MINT to enhance FGFR2-mediated activation of the osteocalcin FGF-responsive element (OCFRE) (By similarity). Inhibits KAT6B-dependent transcriptional activation. {ECO:0000250, ECO:0000269|PubMed:11965546, ECO:0000269|PubMed:28505335, ECO:0000269|PubMed:28703881, ECO:0000269|PubMed:28738062}. |
Q13950 | RUNX2 | S388 | psp | Runt-related transcription factor 2 (Acute myeloid leukemia 3 protein) (Core-binding factor subunit alpha-1) (CBF-alpha-1) (Oncogene AML-3) (Osteoblast-specific transcription factor 2) (OSF-2) (Polyomavirus enhancer-binding protein 2 alpha A subunit) (PEA2-alpha A) (PEBP2-alpha A) (SL3-3 enhancer factor 1 alpha A subunit) (SL3/AKV core-binding factor alpha A subunit) | Transcription factor involved in osteoblastic differentiation and skeletal morphogenesis (PubMed:28505335, PubMed:28703881, PubMed:28738062). Essential for the maturation of osteoblasts and both intramembranous and endochondral ossification. CBF binds to the core site, 5'-PYGPYGGT-3', of a number of enhancers and promoters, including murine leukemia virus, polyomavirus enhancer, T-cell receptor enhancers, osteocalcin, osteopontin, bone sialoprotein, alpha 1(I) collagen, LCK, IL-3 and GM-CSF promoters. In osteoblasts, supports transcription activation: synergizes with SPEN/MINT to enhance FGFR2-mediated activation of the osteocalcin FGF-responsive element (OCFRE) (By similarity). Inhibits KAT6B-dependent transcriptional activation. {ECO:0000250, ECO:0000269|PubMed:11965546, ECO:0000269|PubMed:28505335, ECO:0000269|PubMed:28703881, ECO:0000269|PubMed:28738062}. |
Q14157 | UBAP2L | S859 | ochoa | Ubiquitin-associated protein 2-like (Protein NICE-4) (RNA polymerase II degradation factor UBAP2L) | Recruits the ubiquitination machinery to RNA polymerase II for polyubiquitination, removal and degradation, when the transcription-coupled nucleotide excision repair (TC-NER) machinery fails to resolve DNA damage (PubMed:35633597). Plays an important role in the activity of long-term repopulating hematopoietic stem cells (LT-HSCs) (By similarity). Is a regulator of stress granule assembly, required for their efficient formation (PubMed:29395067, PubMed:35977029). Required for proper brain development and neocortex lamination (By similarity). {ECO:0000250|UniProtKB:Q80X50, ECO:0000269|PubMed:29395067, ECO:0000269|PubMed:35633597}. |
Q14517 | FAT1 | S4476 | ochoa | Protocadherin Fat 1 (Cadherin family member 7) (Cadherin-related tumor suppressor homolog) (Protein fat homolog) [Cleaved into: Protocadherin Fat 1, nuclear form] | [Protocadherin Fat 1]: Plays an essential role for cellular polarization, directed cell migration and modulating cell-cell contact. {ECO:0000250}. |
Q14526 | HIC1 | S304 | ochoa | Hypermethylated in cancer 1 protein (Hic-1) (Zinc finger and BTB domain-containing protein 29) | Transcriptional repressor (PubMed:12052894, PubMed:15231840). Recognizes and binds to the consensus sequence '5-[CG]NG[CG]GGGCA[CA]CC-3' (PubMed:15231840). May act as a tumor suppressor (PubMed:20154726). Involved in development of head, face, limbs and ventral body wall (By similarity). Involved in down-regulation of SIRT1 and thereby is involved in regulation of p53/TP53-dependent apoptotic DNA-damage responses (PubMed:16269335). The specific target gene promoter association seems to be depend on corepressors, such as CTBP1 or CTBP2 and MTA1 (PubMed:12052894, PubMed:20547755). In cooperation with MTA1 (indicative for an association with the NuRD complex) represses transcription from CCND1/cyclin-D1 and CDKN1C/p57Kip2 specifically in quiescent cells (PubMed:20547755). Involved in regulation of the Wnt signaling pathway probably by association with TCF7L2 and preventing TCF7L2 and CTNNB1 association with promoters of TCF-responsive genes (PubMed:16724116). Seems to repress transcription from E2F1 and ATOH1 which involves ARID1A, indicative for the participation of a distinct SWI/SNF-type chromatin-remodeling complex (PubMed:18347096, PubMed:19486893). Probably represses transcription of ACKR3, FGFBP1 and EFNA1 (PubMed:16690027, PubMed:19525223, PubMed:20154726). {ECO:0000250|UniProtKB:Q9R1Y5, ECO:0000269|PubMed:12052894, ECO:0000269|PubMed:15231840, ECO:0000269|PubMed:16269335, ECO:0000269|PubMed:16690027, ECO:0000269|PubMed:16724116, ECO:0000269|PubMed:18347096, ECO:0000269|PubMed:19486893, ECO:0000269|PubMed:19525223, ECO:0000269|PubMed:20154726, ECO:0000269|PubMed:20547755}. |
Q14699 | RFTN1 | S238 | ochoa | Raftlin (Cell migration-inducing gene 2 protein) (Raft-linking protein) | Involved in protein trafficking via association with clathrin and AP2 complex (PubMed:21266579, PubMed:27022195). Upon bacterial lipopolysaccharide stimulation, mediates internalization of TLR4 to endosomes in dendritic cells and macrophages; and internalization of poly(I:C) to TLR3-positive endosomes in myeloid dendritic cells and epithelial cells; resulting in activation of TICAM1-mediated signaling and subsequent IFNB1 production (PubMed:21266579, PubMed:27022195). Involved in T-cell antigen receptor-mediated signaling by regulating tyrosine kinase LCK localization, T-cell dependent antibody production and cytokine secretion (By similarity). May regulate B-cell antigen receptor-mediated signaling (PubMed:12805216). May play a pivotal role in the formation and/or maintenance of lipid rafts (PubMed:12805216). {ECO:0000250|UniProtKB:Q6A0D4, ECO:0000269|PubMed:12805216, ECO:0000269|PubMed:21266579, ECO:0000269|PubMed:27022195}. |
Q15648 | MED1 | S770 | ochoa | Mediator of RNA polymerase II transcription subunit 1 (Activator-recruited cofactor 205 kDa component) (ARC205) (Mediator complex subunit 1) (Peroxisome proliferator-activated receptor-binding protein) (PBP) (PPAR-binding protein) (Thyroid hormone receptor-associated protein complex 220 kDa component) (Trap220) (Thyroid receptor-interacting protein 2) (TR-interacting protein 2) (TRIP-2) (Vitamin D receptor-interacting protein complex component DRIP205) (p53 regulatory protein RB18A) | Component of the Mediator complex, a coactivator involved in the regulated transcription of nearly all RNA polymerase II-dependent genes. Mediator functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery. Mediator is recruited to promoters by direct interactions with regulatory proteins and serves as a scaffold for the assembly of a functional preinitiation complex with RNA polymerase II and the general transcription factors (PubMed:10406464, PubMed:11867769, PubMed:12037571, PubMed:12218053, PubMed:12556447, PubMed:14636573, PubMed:15340084, PubMed:15471764, PubMed:15989967, PubMed:16574658, PubMed:9653119). Acts as a coactivator for GATA1-mediated transcriptional activation during erythroid differentiation of K562 erythroleukemia cells (PubMed:24245781). {ECO:0000269|PubMed:10406464, ECO:0000269|PubMed:11867769, ECO:0000269|PubMed:12037571, ECO:0000269|PubMed:12218053, ECO:0000269|PubMed:12556447, ECO:0000269|PubMed:14636573, ECO:0000269|PubMed:15340084, ECO:0000269|PubMed:15471764, ECO:0000269|PubMed:15989967, ECO:0000269|PubMed:16574658, ECO:0000269|PubMed:24245781, ECO:0000269|PubMed:9653119}. |
Q15648 | MED1 | S772 | ochoa | Mediator of RNA polymerase II transcription subunit 1 (Activator-recruited cofactor 205 kDa component) (ARC205) (Mediator complex subunit 1) (Peroxisome proliferator-activated receptor-binding protein) (PBP) (PPAR-binding protein) (Thyroid hormone receptor-associated protein complex 220 kDa component) (Trap220) (Thyroid receptor-interacting protein 2) (TR-interacting protein 2) (TRIP-2) (Vitamin D receptor-interacting protein complex component DRIP205) (p53 regulatory protein RB18A) | Component of the Mediator complex, a coactivator involved in the regulated transcription of nearly all RNA polymerase II-dependent genes. Mediator functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery. Mediator is recruited to promoters by direct interactions with regulatory proteins and serves as a scaffold for the assembly of a functional preinitiation complex with RNA polymerase II and the general transcription factors (PubMed:10406464, PubMed:11867769, PubMed:12037571, PubMed:12218053, PubMed:12556447, PubMed:14636573, PubMed:15340084, PubMed:15471764, PubMed:15989967, PubMed:16574658, PubMed:9653119). Acts as a coactivator for GATA1-mediated transcriptional activation during erythroid differentiation of K562 erythroleukemia cells (PubMed:24245781). {ECO:0000269|PubMed:10406464, ECO:0000269|PubMed:11867769, ECO:0000269|PubMed:12037571, ECO:0000269|PubMed:12218053, ECO:0000269|PubMed:12556447, ECO:0000269|PubMed:14636573, ECO:0000269|PubMed:15340084, ECO:0000269|PubMed:15471764, ECO:0000269|PubMed:15989967, ECO:0000269|PubMed:16574658, ECO:0000269|PubMed:24245781, ECO:0000269|PubMed:9653119}. |
Q15751 | HERC1 | S2706 | ochoa | Probable E3 ubiquitin-protein ligase HERC1 (EC 2.3.2.26) (HECT domain and RCC1-like domain-containing protein 1) (HECT-type E3 ubiquitin transferase HERC1) (p532) (p619) | Involved in membrane trafficking via some guanine nucleotide exchange factor (GEF) activity and its ability to bind clathrin. Acts as a GEF for Arf and Rab, by exchanging bound GDP for free GTP. Binds phosphatidylinositol 4,5-bisphosphate, which is required for GEF activity. May also act as a E3 ubiquitin-protein ligase which accepts ubiquitin from an E2 ubiquitin-conjugating enzyme in the form of a thioester and then directly transfers the ubiquitin to targeted substrates. {ECO:0000269|PubMed:15642342, ECO:0000269|PubMed:8861955, ECO:0000269|PubMed:9233772}. |
Q16825 | PTPN21 | S538 | ochoa | Tyrosine-protein phosphatase non-receptor type 21 (EC 3.1.3.48) (Protein-tyrosine phosphatase D1) | None |
Q2M3V2 | SOWAHA | S264 | ochoa | Ankyrin repeat domain-containing protein SOWAHA (Ankyrin repeat domain-containing protein 43) (Protein sosondowah homolog A) | None |
Q2TAL8 | QRICH1 | S240 | ochoa | Transcriptional regulator QRICH1 (Glutamine-rich protein 1) | Transcriptional regulator that acts as a mediator of the integrated stress response (ISR) through transcriptional control of protein homeostasis under conditions of ER stress (PubMed:33384352). Controls the outcome of the unfolded protein response (UPR) which is an ER-stress response pathway (PubMed:33384352). ER stress induces QRICH1 translation by a ribosome translation re-initiation mechanism in response to EIF2S1/eIF-2-alpha phosphorylation, and stress-induced QRICH1 regulates a transcriptional program associated with protein translation, protein secretion-mediated proteotoxicity and cell death during the terminal UPR (PubMed:33384352). May cooperate with ATF4 transcription factor signaling to regulate ER homeostasis which is critical for cell viability (PubMed:33384352). Up-regulates CASP3/caspase-3 activity in epithelial cells under ER stress. Central regulator of proteotoxicity associated with ER stress-mediated inflammatory diseases in the intestines and liver (PubMed:33384352). Involved in chondrocyte hypertrophy, a process required for normal longitudinal bone growth (PubMed:30281152). {ECO:0000269|PubMed:30281152, ECO:0000269|PubMed:33384352}. |
Q2TAZ0 | ATG2A | S866 | ochoa | Autophagy-related protein 2 homolog A | Lipid transfer protein involved in autophagosome assembly (PubMed:28561066, PubMed:30952800, PubMed:31271352). Tethers the edge of the isolation membrane (IM) to the endoplasmic reticulum (ER) and mediates direct lipid transfer from ER to IM for IM expansion (PubMed:30952800, PubMed:31271352). Binds to the ER exit site (ERES), which is the membrane source for autophagosome formation, and extracts phospholipids from the membrane source and transfers them to ATG9 (ATG9A or ATG9B) to the IM for membrane expansion (PubMed:30952800, PubMed:31271352). Lipid transfer activity is enhanced by WIPI1 and WDR45/WIPI4, which promote ATG2A-association with phosphatidylinositol 3-monophosphate (PI3P)-containing membranes (PubMed:31271352). Also regulates lipid droplets morphology and distribution within the cell (PubMed:22219374, PubMed:28561066). {ECO:0000269|PubMed:22219374, ECO:0000269|PubMed:28561066, ECO:0000269|PubMed:30952800, ECO:0000269|PubMed:31271352}. |
Q58A45 | PAN3 | S368 | ochoa | PAN2-PAN3 deadenylation complex subunit PAN3 (PAB1P-dependent poly(A)-specific ribonuclease) (Poly(A)-nuclease deadenylation complex subunit 3) (PAN deadenylation complex subunit 3) | Regulatory subunit of the poly(A)-nuclease (PAN) deadenylation complex, one of two cytoplasmic mRNA deadenylases involved in general and miRNA-mediated mRNA turnover. PAN specifically shortens poly(A) tails of RNA and the activity is stimulated by poly(A)-binding protein (PABP). PAN deadenylation is followed by rapid degradation of the shortened mRNA tails by the CCR4-NOT complex. Deadenylated mRNAs are then degraded by two alternative mechanisms, namely exosome-mediated 3'-5' exonucleolytic degradation, or deadenylation-dependent mRNA decapping and subsequent 5'-3' exonucleolytic degradation by XRN1. PAN3 acts as a regulator for PAN activity, recruiting the catalytic subunit PAN2 to mRNA via its interaction with RNA and PABP, and to miRNA targets via its interaction with GW182 family proteins. {ECO:0000255|HAMAP-Rule:MF_03181, ECO:0000269|PubMed:14583602, ECO:0000269|PubMed:23932717}.; FUNCTION: [Isoform 1]: Decreases PAN2-mediated deadenylation, possibly by preventing progression into the second CCR4-NOT mediated stage of biphasic deadenylation. Has a significant effect on mRNA stability, generally stabilizing a subset of the transcriptome. Stabilizes mRNAs degraded by the AU-rich element (ARE)-mediated mRNA decay pathway but promotes degradation of mRNAs by the microRNA-mediated pathway (PubMed:28559491). Its activity influences mRNP remodeling, specifically reducing formation of a subset of P-bodies containing GW220, an isoform of TNRC6A (PubMed:28559491). {ECO:0000269|PubMed:28559491}.; FUNCTION: [Isoform 3]: Enhances PAN2 deadenylase activity and has an extensive effect on mRNA stability, generally enhancing mRNA decay across the transcriptome by multiple pathways, including the AU-rich element (ARE)-mediated pathway, microRNA-mediated pathway and the nonsense-mediated pathway (NMD) (PubMed:28559491). Its activity is required for efficient P-body formation (PubMed:28559491). May be involved in regulating mRNAs of genes involved in cell cycle progression and cell proliferation (PubMed:28559491). {ECO:0000269|PubMed:28559491}. |
Q5JTV8 | TOR1AIP1 | S60 | ochoa | Torsin-1A-interacting protein 1 (Lamin-associated protein 1B) (LAP1B) | Required for nuclear membrane integrity. Induces TOR1A and TOR1B ATPase activity and is required for their location on the nuclear membrane. Binds to A- and B-type lamins. Possible role in membrane attachment and assembly of the nuclear lamina. {ECO:0000269|PubMed:23569223}. |
Q5SYE7 | NHSL1 | S328 | ochoa | NHS-like protein 1 | None |
Q5T6F2 | UBAP2 | S946 | ochoa | Ubiquitin-associated protein 2 (UBAP-2) (RNA polymerase II degradation factor UBAP2) | Recruits the ubiquitination machinery to RNA polymerase II for polyubiquitination, removal and degradation, when the transcription-coupled nucleotide excision repair (TC-NER) machinery fails to resolve DNA damage (PubMed:35633597). May promote the degradation of ANXA2 (PubMed:27121050). {ECO:0000269|PubMed:27121050, ECO:0000269|PubMed:35633597}. |
Q5T8P6 | RBM26 | S487 | ochoa | RNA-binding protein 26 (CTCL tumor antigen se70-2) (RNA-binding motif protein 26) | May be involved in the turnover of nuclear polyadenylated (pA+) RNA. {ECO:0000269|PubMed:31950173}. |
Q5TEJ8 | THEMIS2 | S606 | ochoa | Protein THEMIS2 (Induced by contact to basement membrane 1 protein) (Protein ICB-1) (Thymocyte-expressed molecule involved in selection protein 2) | May constitute a control point in macrophage inflammatory response, promoting LPS-induced TLR4-mediated TNF production (PubMed:20644716). Determines the threshold for activation of B cells by low-affinity and low-avidity ligands via PLCG2 activation and its downstream pathways (By similarity). {ECO:0000250|UniProtKB:Q91YX0, ECO:0000269|PubMed:20644716}. |
Q5VT52 | RPRD2 | S491 | ochoa | Regulation of nuclear pre-mRNA domain-containing protein 2 | None |
Q658P3 | STEAP3 | S19 | ochoa | Metalloreductase STEAP3 (EC 1.16.1.-) (Dudulin-2) (Six-transmembrane epithelial antigen of prostate 3) (Tumor suppressor-activated pathway protein 6) (hTSAP6) (pHyde) (hpHyde) | Integral membrane protein that functions as a NADPH-dependent ferric-chelate reductase, using NADPH from one side of the membrane to reduce a Fe(3+) chelate that is bound on the other side of the membrane (PubMed:26205815). Mediates sequential transmembrane electron transfer from NADPH to FAD and onto heme, and finally to the Fe(3+) chelate (By similarity). Can also reduce Cu(2+) to Cu(1+) (By similarity). Mediates efficient transferrin-dependent iron uptake in erythroid cells (By similarity). May play a role downstream of p53/TP53 to interface apoptosis and cell cycle progression (By similarity). Indirectly involved in exosome secretion by facilitating the secretion of proteins such as TCTP (PubMed:15319436, PubMed:16651434). {ECO:0000250|UniProtKB:Q5RKL5, ECO:0000250|UniProtKB:Q687X5, ECO:0000250|UniProtKB:Q8CI59, ECO:0000269|PubMed:15319436, ECO:0000269|PubMed:16651434, ECO:0000269|PubMed:26205815}. |
Q68CZ2 | TNS3 | S1292 | ochoa | Tensin-3 (EC 3.1.3.-) (Tensin-like SH2 domain-containing protein 1) (Tumor endothelial marker 6) | May act as a protein phosphatase and/or a lipid phosphatase (Probable). Involved in the dissociation of the integrin-tensin-actin complex (PubMed:17643115). EGF activates TNS4 and down-regulates TNS3 which results in capping the tail of ITGB1 (PubMed:17643115). Increases DOCK5 guanine nucleotide exchange activity towards Rac and plays a role in osteoclast podosome organization (By similarity). Enhances RHOA activation in the presence of DLC1 (PubMed:26427649). Required for growth factor-induced epithelial cell migration; growth factor stimulation induces TNS3 phosphorylation which changes its binding preference from DLC1 to the p85 regulatory subunit of the PI3K kinase complex, displacing PI3K inhibitor PTEN and resulting in translocation of the TNS3-p85 complex to the leading edge of migrating cells to promote RAC1 activation (PubMed:26166433). Meanwhile, PTEN switches binding preference from p85 to DLC1 and the PTEN-DLC1 complex translocates to the posterior of migrating cells to activate RHOA (PubMed:26166433). Acts as an adapter protein by bridging the association of scaffolding protein PEAK1 with integrins ITGB1, ITGB3 and ITGB5 which contributes to the promotion of cell migration (PubMed:35687021). Controls tonsil-derived mesenchymal stem cell proliferation and differentiation by regulating the activity of integrin ITGB1 (PubMed:31905841). {ECO:0000250|UniProtKB:Q5SSZ5, ECO:0000269|PubMed:17643115, ECO:0000269|PubMed:26166433, ECO:0000269|PubMed:26427649, ECO:0000269|PubMed:31905841, ECO:0000269|PubMed:35687021, ECO:0000305}. |
Q6IAA8 | LAMTOR1 | S55 | ochoa | Ragulator complex protein LAMTOR1 (Late endosomal/lysosomal adaptor and MAPK and MTOR activator 1) (Lipid raft adaptor protein p18) (Protein associated with DRMs and endosomes) (p27Kip1-releasing factor from RhoA) (p27RF-Rho) | Key component of the Ragulator complex, a multiprotein complex involved in amino acid sensing and activation of mTORC1, a signaling complex promoting cell growth in response to growth factors, energy levels, and amino acids (PubMed:20381137, PubMed:22980980, PubMed:29158492). Activated by amino acids through a mechanism involving the lysosomal V-ATPase, the Ragulator plays a dual role for the small GTPases Rag (RagA/RRAGA, RagB/RRAGB, RagC/RRAGC and/or RagD/RRAGD): it (1) acts as a guanine nucleotide exchange factor (GEF), activating the small GTPases Rag and (2) mediates recruitment of Rag GTPases to the lysosome membrane (PubMed:22980980, PubMed:28935770, PubMed:29158492, PubMed:30181260, PubMed:31001086, PubMed:32686708, PubMed:36476874). Activated Ragulator and Rag GTPases function as a scaffold recruiting mTORC1 to lysosomes where it is in turn activated (PubMed:20381137, PubMed:22980980, PubMed:29158492). LAMTOR1 is directly responsible for anchoring the Ragulator complex to the lysosomal membrane (PubMed:31001086, PubMed:32686708). LAMTOR1 wraps around the other subunits of the Ragulator complex to hold them in place and interacts with the Rag GTPases, thereby playing a key role in the recruitment of the mTORC1 complex to lysosomes (PubMed:28935770, PubMed:29107538, PubMed:29123114, PubMed:29285400). Also involved in the control of embryonic stem cells differentiation via non-canonical RagC/RRAGC and RagD/RRAGD activation: together with FLCN, it is necessary to recruit and activate RagC/RRAGC and RagD/RRAGD at the lysosomes, and to induce exit of embryonic stem cells from pluripotency via non-canonical, mTOR-independent TFE3 inactivation (By similarity). Also required for late endosomes/lysosomes biogenesis it may regulate both the recycling of receptors through endosomes and the MAPK signaling pathway through recruitment of some of its components to late endosomes (PubMed:20381137, PubMed:22980980). May be involved in cholesterol homeostasis regulating LDL uptake and cholesterol release from late endosomes/lysosomes (PubMed:20544018). May also play a role in RHOA activation (PubMed:19654316). {ECO:0000250|UniProtKB:Q9CQ22, ECO:0000269|PubMed:19654316, ECO:0000269|PubMed:20381137, ECO:0000269|PubMed:20544018, ECO:0000269|PubMed:22980980, ECO:0000269|PubMed:28935770, ECO:0000269|PubMed:29107538, ECO:0000269|PubMed:29123114, ECO:0000269|PubMed:29158492, ECO:0000269|PubMed:29285400, ECO:0000269|PubMed:30181260, ECO:0000269|PubMed:31001086, ECO:0000269|PubMed:32686708, ECO:0000269|PubMed:36476874}. |
Q6KC79 | NIPBL | S305 | ochoa | Nipped-B-like protein (Delangin) (SCC2 homolog) | Plays an important role in the loading of the cohesin complex on to DNA. Forms a heterodimeric complex (also known as cohesin loading complex) with MAU2/SCC4 which mediates the loading of the cohesin complex onto chromatin (PubMed:22628566, PubMed:28914604). Plays a role in cohesin loading at sites of DNA damage. Its recruitment to double-strand breaks (DSBs) sites occurs in a CBX3-, RNF8- and RNF168-dependent manner whereas its recruitment to UV irradiation-induced DNA damage sites occurs in a ATM-, ATR-, RNF8- and RNF168-dependent manner (PubMed:28167679). Along with ZNF609, promotes cortical neuron migration during brain development by regulating the transcription of crucial genes in this process. Preferentially binds promoters containing paused RNA polymerase II. Up-regulates the expression of SEMA3A, NRP1, PLXND1 and GABBR2 genes, among others (By similarity). {ECO:0000250|UniProtKB:Q6KCD5, ECO:0000269|PubMed:22628566, ECO:0000269|PubMed:28167679, ECO:0000269|PubMed:28914604}. |
Q6NTF9 | RHBDD2 | S266 | ochoa | Rhomboid domain-containing protein 2 | None |
Q6P0N0 | MIS18BP1 | S365 | ochoa | Mis18-binding protein 1 (Kinetochore-associated protein KNL-2 homolog) (HsKNL-2) (P243) | Required for recruitment of CENPA to centromeres and normal chromosome segregation during mitosis. {ECO:0000269|PubMed:17199038, ECO:0000269|PubMed:17339379}. |
Q6PJI9 | WDR59 | S834 | ochoa | GATOR2 complex protein WDR59 (WD repeat-containing protein 59) | As a component of the GATOR2 complex, functions as an activator of the amino acid-sensing branch of the mTORC1 signaling pathway (PubMed:23723238, PubMed:25457612, PubMed:27487210, PubMed:35831510, PubMed:36528027, PubMed:36577058). The GATOR2 complex indirectly activates mTORC1 through the inhibition of the GATOR1 subcomplex (PubMed:23723238, PubMed:27487210, PubMed:35831510, PubMed:36528027). GATOR2 probably acts as an E3 ubiquitin-protein ligase toward GATOR1 (PubMed:36528027). In the presence of abundant amino acids, the GATOR2 complex mediates ubiquitination of the NPRL2 core component of the GATOR1 complex, leading to GATOR1 inactivation (PubMed:36528027). In the absence of amino acids, GATOR2 is inhibited, activating the GATOR1 complex (PubMed:25457612, PubMed:27487210). {ECO:0000269|PubMed:23723238, ECO:0000269|PubMed:25457612, ECO:0000269|PubMed:27487210, ECO:0000269|PubMed:35831510, ECO:0000269|PubMed:36528027, ECO:0000269|PubMed:36577058}. |
Q6ZMT1 | STAC2 | S112 | ochoa | SH3 and cysteine-rich domain-containing protein 2 (24b2/STAC2) (Src homology 3 and cysteine-rich domain-containing protein 2) | Plays a redundant role in promoting the expression of calcium channel CACNA1S at the cell membrane, and thereby contributes to increased channel activity. Slows down the inactivation rate of the calcium channel CACNA1C. {ECO:0000250|UniProtKB:Q8R1B0}. |
Q6ZNJ1 | NBEAL2 | S1836 | ochoa | Neurobeachin-like protein 2 | Probably involved in thrombopoiesis. Plays a role in the development or secretion of alpha-granules, that contain several growth factors important for platelet biogenesis. {ECO:0000269|PubMed:21765411, ECO:0000269|PubMed:21765412}. |
Q7KZ85 | SUPT6H | S1535 | ochoa | Transcription elongation factor SPT6 (hSPT6) (Histone chaperone suppressor of Ty6) (Tat-cotransactivator 2 protein) (Tat-CT2 protein) | Histone H3-H4 chaperone that plays a key role in the regulation of transcription elongation and mRNA processing. Enhances the transcription elongation by RNA polymerase II (RNAPII) and is also required for the efficient activation of transcriptional elongation by the HIV-1 nuclear transcriptional activator, Tat. Besides chaperoning histones in transcription, acts to transport and splice mRNA by forming a complex with IWS1 and the C-terminal domain (CTD) of the RNAPII subunit RPB1 (POLR2A). The SUPT6H:IWS1:CTD complex recruits mRNA export factors (ALYREF/THOC4, EXOSC10) as well as histone modifying enzymes (such as SETD2), to ensure proper mRNA splicing, efficient mRNA export and elongation-coupled H3K36 methylation, a signature chromatin mark of active transcription. SUPT6H via its association with SETD1A, regulates both class-switch recombination and somatic hypermutation through formation of H3K4me3 epigenetic marks on activation-induced cytidine deaminase (AICDA) target loci. Promotes the activation of the myogenic gene program by entailing erasure of the repressive H3K27me3 epigenetic mark through stabilization of the chromatin interaction of the H3K27 demethylase KDM6A. {ECO:0000269|PubMed:15060154, ECO:0000269|PubMed:17234882, ECO:0000269|PubMed:22316138, ECO:0000269|PubMed:23503590, ECO:0000269|PubMed:9514752}. |
Q7L4E1 | MIGA2 | S220 | ochoa | Mitoguardin 2 (Protein FAM73B) | Regulator of mitochondrial fusion: acts by forming homo- and heterodimers at the mitochondrial outer membrane and facilitating the formation of PLD6/MitoPLD dimers. May act by regulating phospholipid metabolism via PLD6/MitoPLD. {ECO:0000269|PubMed:26711011}. |
Q7RTP6 | MICAL3 | S1290 | ochoa | [F-actin]-monooxygenase MICAL3 (EC 1.14.13.225) (Molecule interacting with CasL protein 3) (MICAL-3) | Monooxygenase that promotes depolymerization of F-actin by mediating oxidation of specific methionine residues on actin to form methionine-sulfoxide, resulting in actin filament disassembly and preventing repolymerization. In the absence of actin, it also functions as a NADPH oxidase producing H(2)O(2). Seems to act as Rab effector protein and plays a role in vesicle trafficking. Involved in exocytic vesicles tethering and fusion: the monooxygenase activity is required for this process and implicates RAB8A associated with exocytotic vesicles. Required for cytokinesis. Contributes to stabilization and/or maturation of the intercellular bridge independently of its monooxygenase activity. Promotes recruitment of Rab8 and ERC1 to the intercellular bridge, and together these proteins are proposed to function in timely abscission. {ECO:0000269|PubMed:21596566, ECO:0000269|PubMed:24440334}. |
Q7Z3B3 | KANSL1 | S1021 | ochoa | KAT8 regulatory NSL complex subunit 1 (MLL1/MLL complex subunit KANSL1) (MSL1 homolog 1) (hMSL1v1) (NSL complex protein NSL1) (Non-specific lethal 1 homolog) | Non-catalytic component of the NSL histone acetyltransferase complex, a multiprotein complex that mediates histone H4 acetylation at 'Lys-5'- and 'Lys-8' (H4K5ac and H4K8ac) at transcription start sites and promotes transcription initiation (PubMed:20018852, PubMed:22547026, PubMed:33657400). The NSL complex also acts as a regulator of gene expression in mitochondria (PubMed:27768893). In addition to its role in transcription, KANSL1 also plays an essential role in spindle assembly during mitosis (PubMed:26243146). Associates with microtubule ends and contributes to microtubule stability (PubMed:26243146). {ECO:0000269|PubMed:20018852, ECO:0000269|PubMed:22547026, ECO:0000269|PubMed:26243146, ECO:0000269|PubMed:27768893, ECO:0000269|PubMed:33657400}. |
Q7Z5J4 | RAI1 | S1064 | ochoa | Retinoic acid-induced protein 1 | Transcriptional regulator of the circadian clock components: CLOCK, BMAL1, BMAL2, PER1/3, CRY1/2, NR1D1/2 and RORA/C. Positively regulates the transcriptional activity of CLOCK a core component of the circadian clock. Regulates transcription through chromatin remodeling by interacting with other proteins in chromatin as well as proteins in the basic transcriptional machinery. May be important for embryonic and postnatal development. May be involved in neuronal differentiation. {ECO:0000269|PubMed:22578325}. |
Q7Z6Z7 | HUWE1 | S2931 | ochoa | E3 ubiquitin-protein ligase HUWE1 (EC 2.3.2.26) (ARF-binding protein 1) (ARF-BP1) (HECT, UBA and WWE domain-containing protein 1) (HECT-type E3 ubiquitin transferase HUWE1) (Homologous to E6AP carboxyl terminus homologous protein 9) (HectH9) (Large structure of UREB1) (LASU1) (Mcl-1 ubiquitin ligase E3) (Mule) (Upstream regulatory element-binding protein 1) (URE-B1) (URE-binding protein 1) | E3 ubiquitin-protein ligase which mediates ubiquitination and subsequent proteasomal degradation of target proteins (PubMed:15567145, PubMed:15767685, PubMed:15989957, PubMed:17567951, PubMed:18488021, PubMed:19037095, PubMed:19713937, PubMed:20534529, PubMed:30217973). Regulates apoptosis by catalyzing the polyubiquitination and degradation of MCL1 (PubMed:15989957). Mediates monoubiquitination of DNA polymerase beta (POLB) at 'Lys-41', 'Lys-61' and 'Lys-81', thereby playing a role in base-excision repair (PubMed:19713937). Also ubiquitinates the p53/TP53 tumor suppressor and core histones including H1, H2A, H2B, H3 and H4 (PubMed:15567145, PubMed:15767685, PubMed:15989956). Ubiquitinates MFN2 to negatively regulate mitochondrial fusion in response to decreased stearoylation of TFRC (PubMed:26214738). Ubiquitination of MFN2 also takes place following induction of mitophagy; AMBRA1 acts as a cofactor for HUWE1-mediated ubiquitination (PubMed:30217973). Regulates neural differentiation and proliferation by catalyzing the polyubiquitination and degradation of MYCN (PubMed:18488021). May regulate abundance of CDC6 after DNA damage by polyubiquitinating and targeting CDC6 to degradation (PubMed:17567951). Mediates polyubiquitination of isoform 2 of PA2G4 (PubMed:19037095). Acts in concert with MYCBP2 to regulate the circadian clock gene expression by promoting the lithium-induced ubiquination and degradation of NR1D1 (PubMed:20534529). Binds to an upstream initiator-like sequence in the preprodynorphin gene (By similarity). Mediates HAPSTR1 degradation, but is also a required cofactor in the pathway by which HAPSTR1 governs stress signaling (PubMed:35776542). Acts as a regulator of the JNK and NF-kappa-B signaling pathways by mediating assembly of heterotypic 'Lys-63'-/'Lys-48'-linked branched ubiquitin chains that are then recognized by TAB2: HUWE1 mediates branching of 'Lys-48'-linked chains of substrates initially modified with 'Lys-63'-linked conjugates by TRAF6 (PubMed:27746020). 'Lys-63'-/'Lys-48'-linked branched ubiquitin chains protect 'Lys-63'-linkages from CYLD deubiquitination (PubMed:27746020). Ubiquitinates PPARA in hepatocytes (By similarity). {ECO:0000250|UniProtKB:P51593, ECO:0000250|UniProtKB:Q7TMY8, ECO:0000269|PubMed:15567145, ECO:0000269|PubMed:15767685, ECO:0000269|PubMed:15989956, ECO:0000269|PubMed:15989957, ECO:0000269|PubMed:17567951, ECO:0000269|PubMed:18488021, ECO:0000269|PubMed:19037095, ECO:0000269|PubMed:19713937, ECO:0000269|PubMed:20534529, ECO:0000269|PubMed:26214738, ECO:0000269|PubMed:27746020, ECO:0000269|PubMed:30217973, ECO:0000269|PubMed:35776542}. |
Q86TC9 | MYPN | S1051 | ochoa | Myopalladin (145 kDa sarcomeric protein) | Component of the sarcomere that tethers together nebulin (skeletal muscle) and nebulette (cardiac muscle) to alpha-actinin, at the Z lines. {ECO:0000269|PubMed:11309420}. |
Q86VI3 | IQGAP3 | S1429 | ochoa | Ras GTPase-activating-like protein IQGAP3 | None |
Q86X10 | RALGAPB | S1022 | ochoa | Ral GTPase-activating protein subunit beta (p170) | Non-catalytic subunit of the heterodimeric RalGAP1 and RalGAP2 complexes which act as GTPase activators for the Ras-like small GTPases RALA and RALB. {ECO:0000250}. |
Q8IWR0 | ZC3H7A | S780 | ochoa | Zinc finger CCCH domain-containing protein 7A | May be a specific regulator of miRNA biogenesis. Binds to microRNAs MIR7-1, MIR16-2 and MIR29A hairpins recognizing the 3'-ATA(A/T)-5' motif in the apical loop. {ECO:0000269|PubMed:28431233}. |
Q8IX21 | SLF2 | S653 | ochoa | SMC5-SMC6 complex localization factor protein 2 (Smc5/6 localization factor 1) | Plays a role in the DNA damage response (DDR) pathway by regulating postreplication repair of UV-damaged DNA and genomic stability maintenance (PubMed:25931565). The SLF1-SLF2 complex acts to link RAD18 with the SMC5-SMC6 complex at replication-coupled interstrand cross-links (ICL) and DNA double-strand breaks (DSBs) sites on chromatin during DNA repair in response to stalled replication forks (PubMed:25931565). Promotes the recruitment of the SMC5-SMC6 complex to DNA lesions (PubMed:25931565). Plays a role in SMC5-SMC6 complex recruitment for viral restriction. Forms a complex with SIMC1 and this complex is required to recruit SMC5-SMC6 complex to PML nuclear bodies and sites of viral replication (PubMed:36373674). {ECO:0000269|PubMed:25931565, ECO:0000269|PubMed:36373674}. |
Q8IY92 | SLX4 | S1452 | ochoa | Structure-specific endonuclease subunit SLX4 (BTB/POZ domain-containing protein 12) | Regulatory subunit that interacts with and increases the activity of different structure-specific endonucleases. Has several distinct roles in protecting genome stability by resolving diverse forms of deleterious DNA structures originating from replication and recombination intermediates and from DNA damage. Component of the SLX1-SLX4 structure-specific endonuclease that resolves DNA secondary structures generated during DNA repair and recombination. Has endonuclease activity towards branched DNA substrates, introducing single-strand cuts in duplex DNA close to junctions with ss-DNA. Has a preference for 5'-flap structures, and promotes symmetrical cleavage of static and migrating Holliday junctions (HJs). Resolves HJs by generating two pairs of ligatable, nicked duplex products. Interacts with the structure-specific ERCC4-ERCC1 endonuclease and promotes the cleavage of bubble structures. Interacts with the structure-specific MUS81-EME1 endonuclease and promotes the cleavage of 3'-flap and replication fork-like structures. SLX4 is required for recovery from alkylation-induced DNA damage and is involved in the resolution of DNA double-strand breaks. {ECO:0000269|PubMed:19595721, ECO:0000269|PubMed:19595722, ECO:0000269|PubMed:19596235, ECO:0000269|PubMed:19596236}. |
Q8IYD8 | FANCM | S52 | ochoa | Fanconi anemia group M protein (Protein FACM) (EC 3.6.4.13) (ATP-dependent RNA helicase FANCM) (Fanconi anemia-associated polypeptide of 250 kDa) (FAAP250) (Protein Hef ortholog) | DNA-dependent ATPase component of the Fanconi anemia (FA) core complex (PubMed:16116422). Required for the normal activation of the FA pathway, leading to monoubiquitination of the FANCI-FANCD2 complex in response to DNA damage, cellular resistance to DNA cross-linking drugs, and prevention of chromosomal breakage (PubMed:16116422, PubMed:19423727, PubMed:20347428, PubMed:20347429, PubMed:29231814). In complex with CENPS and CENPX, binds double-stranded DNA (dsDNA), fork-structured DNA (fsDNA) and Holliday junction substrates (PubMed:20347428, PubMed:20347429). Its ATP-dependent DNA branch migration activity can process branched DNA structures such as a movable replication fork. This activity is strongly stimulated in the presence of CENPS and CENPX (PubMed:20347429). In complex with FAAP24, efficiently binds to single-strand DNA (ssDNA), splayed-arm DNA, and 3'-flap substrates (PubMed:17289582). In vitro, on its own, strongly binds ssDNA oligomers and weakly fsDNA, but does not bind to dsDNA (PubMed:16116434). {ECO:0000269|PubMed:16116422, ECO:0000269|PubMed:16116434, ECO:0000269|PubMed:17289582, ECO:0000269|PubMed:19423727, ECO:0000269|PubMed:20347428, ECO:0000269|PubMed:20347429, ECO:0000269|PubMed:29231814}. |
Q8N350 | CBARP | S503 | ochoa | Voltage-dependent calcium channel beta subunit-associated regulatory protein | Negatively regulates voltage-gated calcium channels by preventing the interaction between their alpha and beta subunits. Thereby, negatively regulates calcium channels activity at the plasma membrane and indirectly inhibits calcium-regulated exocytosis. {ECO:0000250|UniProtKB:Q66L44}. |
Q8N3K9 | CMYA5 | S2854 | ochoa | Cardiomyopathy-associated protein 5 (Dystrobrevin-binding protein 2) (Genethonin-3) (Myospryn) (SPRY domain-containing protein 2) (Tripartite motif-containing protein 76) | May serve as an anchoring protein that mediates the subcellular compartmentation of protein kinase A (PKA) via binding to PRKAR2A (By similarity). May function as a repressor of calcineurin-mediated transcriptional activity. May attenuate calcineurin ability to induce slow-fiber gene program in muscle and may negatively modulate skeletal muscle regeneration (By similarity). Plays a role in the assembly of ryanodine receptor (RYR2) clusters in striated muscle (By similarity). {ECO:0000250, ECO:0000250|UniProtKB:Q70KF4}. |
Q8N4C8 | MINK1 | S641 | ochoa | Misshapen-like kinase 1 (EC 2.7.11.1) (GCK family kinase MiNK) (MAPK/ERK kinase kinase kinase 6) (MEK kinase kinase 6) (MEKKK 6) (Misshapen/NIK-related kinase) (Mitogen-activated protein kinase kinase kinase kinase 6) | Serine/threonine kinase which acts as a negative regulator of Ras-related Rap2-mediated signal transduction to control neuronal structure and AMPA receptor trafficking (PubMed:10708748, PubMed:16337592). Required for normal synaptic density, dendrite complexity, as well as surface AMPA receptor expression in hippocampal neurons (By similarity). Can activate the JNK and MAPK14/p38 pathways and mediates stimulation of the stress-activated protein kinase MAPK14/p38 MAPK downstream of the Raf/ERK pathway. Phosphorylates TANC1 upon stimulation by RAP2A, MBP and SMAD1 (PubMed:18930710, PubMed:21690388). Has an essential function in negative selection of thymocytes, perhaps by coupling NCK1 to activation of JNK1 (By similarity). Activator of the Hippo signaling pathway which plays a pivotal role in organ size control and tumor suppression by restricting proliferation and promoting apoptosis. MAP4Ks act in parallel to and are partially redundant with STK3/MST2 and STK4/MST2 in the phosphorylation and activation of LATS1/2, and establish MAP4Ks as components of the expanded Hippo pathway (PubMed:26437443). {ECO:0000250|UniProtKB:F1LP90, ECO:0000250|UniProtKB:Q9JM52, ECO:0000269|PubMed:10708748, ECO:0000269|PubMed:16337592, ECO:0000269|PubMed:18930710, ECO:0000269|PubMed:21690388, ECO:0000269|PubMed:26437443}.; FUNCTION: Isoform 4 can activate the JNK pathway. Involved in the regulation of actin cytoskeleton reorganization, cell-matrix adhesion, cell-cell adhesion and cell migration. |
Q8N884 | CGAS | S64 | ochoa | Cyclic GMP-AMP synthase (cGAMP synthase) (cGAS) (h-cGAS) (EC 2.7.7.86) (2'3'-cGAMP synthase) (Mab-21 domain-containing protein 1) | Nucleotidyltransferase that catalyzes the formation of cyclic GMP-AMP (2',3'-cGAMP) from ATP and GTP and plays a key role in innate immunity (PubMed:21478870, PubMed:23258413, PubMed:23707061, PubMed:23707065, PubMed:23722159, PubMed:24077100, PubMed:24116191, PubMed:24462292, PubMed:25131990, PubMed:26300263, PubMed:29976794, PubMed:30799039, PubMed:31142647, PubMed:32814054, PubMed:33273464, PubMed:33542149, PubMed:37217469, PubMed:37802025). Catalysis involves both the formation of a 2',5' phosphodiester linkage at the GpA step and the formation of a 3',5' phosphodiester linkage at the ApG step, producing c[G(2',5')pA(3',5')p] (PubMed:28214358, PubMed:28363908). Acts as a key DNA sensor: directly binds double-stranded DNA (dsDNA), inducing the formation of liquid-like droplets in which CGAS is activated, leading to synthesis of 2',3'-cGAMP, a second messenger that binds to and activates STING1, thereby triggering type-I interferon production (PubMed:28314590, PubMed:28363908, PubMed:29976794, PubMed:32817552, PubMed:33230297, PubMed:33606975, PubMed:35322803, PubMed:35438208, PubMed:35460603, PubMed:35503863). Preferentially recognizes and binds curved long dsDNAs of a minimal length of 40 bp (PubMed:30007416). Acts as a key foreign DNA sensor, the presence of double-stranded DNA (dsDNA) in the cytoplasm being a danger signal that triggers the immune responses (PubMed:28363908). Has antiviral activity by sensing the presence of dsDNA from DNA viruses in the cytoplasm (PubMed:28363908, PubMed:35613581). Also acts as an innate immune sensor of infection by retroviruses, such as HIV-2, by detecting the presence of reverse-transcribed DNA in the cytosol (PubMed:23929945, PubMed:24269171, PubMed:30270045, PubMed:32852081). In contrast, HIV-1 is poorly sensed by CGAS, due to its capsid that cloaks viral DNA from CGAS detection (PubMed:24269171, PubMed:30270045, PubMed:32852081). Detection of retroviral reverse-transcribed DNA in the cytosol may be indirect and be mediated via interaction with PQBP1, which directly binds reverse-transcribed retroviral DNA (PubMed:26046437). Also detects the presence of DNA from bacteria, such as M.tuberculosis (PubMed:26048138). 2',3'-cGAMP can be transferred from producing cells to neighboring cells through gap junctions, leading to promote STING1 activation and convey immune response to connecting cells (PubMed:24077100). 2',3'-cGAMP can also be transferred between cells by virtue of packaging within viral particles contributing to IFN-induction in newly infected cells in a cGAS-independent but STING1-dependent manner (PubMed:26229115). Also senses the presence of neutrophil extracellular traps (NETs) that are translocated to the cytosol following phagocytosis, leading to synthesis of 2',3'-cGAMP (PubMed:33688080). In addition to foreign DNA, can also be activated by endogenous nuclear or mitochondrial DNA (PubMed:28738408, PubMed:28759889, PubMed:31299200, PubMed:33031745, PubMed:33230297). When self-DNA leaks into the cytosol during cellular stress (such as mitochondrial stress, SARS-CoV-2 infection causing severe COVID-19 disease, DNA damage, mitotic arrest or senescence), or is present in form of cytosolic micronuclei, CGAS is activated leading to a state of sterile inflammation (PubMed:28738408, PubMed:28759889, PubMed:31299200, PubMed:33031745, PubMed:33230297, PubMed:35045565). Acts as a regulator of cellular senescence by binding to cytosolic chromatin fragments that are present in senescent cells, leading to trigger type-I interferon production via STING1 and promote cellular senescence (By similarity). Also involved in the inflammatory response to genome instability and double-stranded DNA breaks: acts by localizing to micronuclei arising from genome instability (PubMed:28738408, PubMed:28759889). Micronuclei, which are frequently found in cancer cells, consist of chromatin surrounded by their own nuclear membrane: following breakdown of the micronuclear envelope, a process associated with chromothripsis, CGAS binds self-DNA exposed to the cytosol, leading to 2',3'-cGAMP synthesis and subsequent activation of STING1 and type-I interferon production (PubMed:28738408, PubMed:28759889). Activated in response to prolonged mitotic arrest, promoting mitotic cell death (PubMed:31299200). In a healthy cell, CGAS is however kept inactive even in cellular events that directly expose it to self-DNA, such as mitosis, when cGAS associates with chromatin directly after nuclear envelope breakdown or remains in the form of postmitotic persistent nuclear cGAS pools bound to chromatin (PubMed:31299200, PubMed:33542149). Nuclear CGAS is inactivated by chromatin via direct interaction with nucleosomes, which block CGAS from DNA binding and thus prevent CGAS-induced autoimmunity (PubMed:31299200, PubMed:32911482, PubMed:32912999, PubMed:33051594, PubMed:33542149). Also acts as a suppressor of DNA repair in response to DNA damage: inhibits homologous recombination repair by interacting with PARP1, the CGAS-PARP1 interaction leading to impede the formation of the PARP1-TIMELESS complex (PubMed:30356214, PubMed:31544964). In addition to DNA, also sense translation stress: in response to translation stress, translocates to the cytosol and associates with collided ribosomes, promoting its activation and triggering type-I interferon production (PubMed:34111399). In contrast to other mammals, human CGAS displays species-specific mechanisms of DNA recognition and produces less 2',3'-cGAMP, allowing a more fine-tuned response to pathogens (PubMed:30007416). {ECO:0000250|UniProtKB:Q8C6L5, ECO:0000269|PubMed:21478870, ECO:0000269|PubMed:23258413, ECO:0000269|PubMed:23707061, ECO:0000269|PubMed:23707065, ECO:0000269|PubMed:23722159, ECO:0000269|PubMed:23929945, ECO:0000269|PubMed:24077100, ECO:0000269|PubMed:24116191, ECO:0000269|PubMed:24269171, ECO:0000269|PubMed:24462292, ECO:0000269|PubMed:25131990, ECO:0000269|PubMed:26046437, ECO:0000269|PubMed:26048138, ECO:0000269|PubMed:26229115, ECO:0000269|PubMed:26300263, ECO:0000269|PubMed:28214358, ECO:0000269|PubMed:28314590, ECO:0000269|PubMed:28363908, ECO:0000269|PubMed:28738408, ECO:0000269|PubMed:28759889, ECO:0000269|PubMed:29976794, ECO:0000269|PubMed:30007416, ECO:0000269|PubMed:30270045, ECO:0000269|PubMed:30356214, ECO:0000269|PubMed:30799039, ECO:0000269|PubMed:31142647, ECO:0000269|PubMed:31299200, ECO:0000269|PubMed:31544964, ECO:0000269|PubMed:32814054, ECO:0000269|PubMed:32817552, ECO:0000269|PubMed:32852081, ECO:0000269|PubMed:32911482, ECO:0000269|PubMed:32912999, ECO:0000269|PubMed:33031745, ECO:0000269|PubMed:33051594, ECO:0000269|PubMed:33230297, ECO:0000269|PubMed:33273464, ECO:0000269|PubMed:33542149, ECO:0000269|PubMed:33606975, ECO:0000269|PubMed:33688080, ECO:0000269|PubMed:34111399, ECO:0000269|PubMed:35045565, ECO:0000269|PubMed:35322803, ECO:0000269|PubMed:35438208, ECO:0000269|PubMed:35460603, ECO:0000269|PubMed:35503863, ECO:0000269|PubMed:35613581, ECO:0000269|PubMed:37217469, ECO:0000269|PubMed:37802025}. |
Q8NAX2 | KDF1 | S208 | ochoa | Keratinocyte differentiation factor 1 | Plays a role in the regulation of the epidermis formation during early development. Required both as an inhibitor of basal cell proliferation and a promoter of differentiation of basal progenitor cell progeny (By similarity). {ECO:0000250|UniProtKB:A2A9F4}. |
Q8NBV4 | PLPP7 | S46 | ochoa | Inactive phospholipid phosphatase 7 (Phosphatidic acid phosphatase type 2 domain-containing protein 3) | Plays a role as negative regulator of myoblast differentiation, in part through effects on MTOR signaling. Has no detectable enzymatic activity (By similarity). {ECO:0000250}. |
Q8ND83 | SLAIN1 | S403 | ochoa | SLAIN motif-containing protein 1 | Microtubule plus-end tracking protein that might be involved in the regulation of cytoplasmic microtubule dynamics, microtubule organization and microtubule elongation. {ECO:0000269|PubMed:21646404}. |
Q8NFC6 | BOD1L1 | S1989 | ochoa | Biorientation of chromosomes in cell division protein 1-like 1 | Component of the fork protection machinery required to protect stalled/damaged replication forks from uncontrolled DNA2-dependent resection. Acts by stabilizing RAD51 at stalled replication forks and protecting RAD51 nucleofilaments from the antirecombinogenic activities of FBH1 and BLM (PubMed:26166705, PubMed:29937342). Does not regulate spindle orientation (PubMed:26166705). {ECO:0000269|PubMed:26166705, ECO:0000269|PubMed:29937342}. |
Q8NFH8 | REPS2 | S218 | ochoa | RalBP1-associated Eps domain-containing protein 2 (Partner of RalBP1) (RalBP1-interacting protein 2) | Involved in ligand-dependent receptor mediated endocytosis of the EGF and insulin receptors as part of the Ral signaling pathway (PubMed:10393179, PubMed:12771942, PubMed:9422736). By controlling growth factor receptors endocytosis may regulate cell survival (PubMed:12771942). Through ASAP1 may regulate cell adhesion and migration (PubMed:12149250). {ECO:0000269|PubMed:10393179, ECO:0000269|PubMed:12149250, ECO:0000269|PubMed:12771942, ECO:0000269|PubMed:9422736}. |
Q8NG48 | LINS1 | S591 | ochoa | Protein Lines homolog 1 (Wnt-signaling molecule Lines homolog 1) | None |
Q8TDM6 | DLG5 | Y1077 | ochoa | Disks large homolog 5 (Discs large protein P-dlg) (Placenta and prostate DLG) | Acts as a regulator of the Hippo signaling pathway (PubMed:28087714, PubMed:28169360). Negatively regulates the Hippo signaling pathway by mediating the interaction of MARK3 with STK3/4, bringing them together to promote MARK3-dependent hyperphosphorylation and inactivation of STK3 kinase activity toward LATS1 (PubMed:28087714). Positively regulates the Hippo signaling pathway by mediating the interaction of SCRIB with STK4/MST1 and LATS1 which is important for the activation of the Hippo signaling pathway. Involved in regulating cell proliferation, maintenance of epithelial polarity, epithelial-mesenchymal transition (EMT), cell migration and invasion (PubMed:28169360). Plays an important role in dendritic spine formation and synaptogenesis in cortical neurons; regulates synaptogenesis by enhancing the cell surface localization of N-cadherin. Acts as a positive regulator of hedgehog (Hh) signaling pathway. Plays a critical role in the early point of the SMO activity cycle by interacting with SMO at the ciliary base to induce the accumulation of KIF7 and GLI2 at the ciliary tip for GLI2 activation (By similarity). {ECO:0000250|UniProtKB:E9Q9R9, ECO:0000269|PubMed:28087714, ECO:0000269|PubMed:28169360}. |
Q8TEQ0 | SNX29 | S444 | ochoa | Sorting nexin-29 (RUN domain-containing protein 2A) | None |
Q8TEW0 | PARD3 | S924 | ochoa | Partitioning defective 3 homolog (PAR-3) (PARD-3) (Atypical PKC isotype-specific-interacting protein) (ASIP) (CTCL tumor antigen se2-5) (PAR3-alpha) | Adapter protein involved in asymmetrical cell division and cell polarization processes (PubMed:10954424, PubMed:27925688). Seems to play a central role in the formation of epithelial tight junctions (PubMed:27925688). Targets the phosphatase PTEN to cell junctions (By similarity). Involved in Schwann cell peripheral myelination (By similarity). Association with PARD6B may prevent the interaction of PARD3 with F11R/JAM1, thereby preventing tight junction assembly (By similarity). The PARD6-PARD3 complex links GTP-bound Rho small GTPases to atypical protein kinase C proteins (PubMed:10934474). Required for establishment of neuronal polarity and normal axon formation in cultured hippocampal neurons (PubMed:19812038, PubMed:27925688). {ECO:0000250|UniProtKB:Q99NH2, ECO:0000250|UniProtKB:Q9Z340, ECO:0000269|PubMed:10934474, ECO:0000269|PubMed:10954424, ECO:0000269|PubMed:19812038, ECO:0000269|PubMed:27925688}. |
Q8TEW8 | PARD3B | S780 | ochoa | Partitioning defective 3 homolog B (Amyotrophic lateral sclerosis 2 chromosomal region candidate gene 19 protein) (PAR3-beta) (Partitioning defective 3-like protein) (PAR3-L protein) | Putative adapter protein involved in asymmetrical cell division and cell polarization processes. May play a role in the formation of epithelial tight junctions. |
Q8WUX9 | CHMP7 | S410 | ochoa | Charged multivesicular body protein 7 (Chromatin-modifying protein 7) | ESCRT-III-like protein required to recruit the ESCRT-III complex to the nuclear envelope (NE) during late anaphase (PubMed:26040712). Together with SPAST, the ESCRT-III complex promotes NE sealing and mitotic spindle disassembly during late anaphase (PubMed:26040712, PubMed:28242692). Recruited to the reforming NE during anaphase by LEMD2 (PubMed:28242692). Plays a role in the endosomal sorting pathway (PubMed:16856878). {ECO:0000269|PubMed:16856878, ECO:0000269|PubMed:26040712, ECO:0000269|PubMed:28242692}. |
Q8WY36 | BBX | S177 | ochoa | HMG box transcription factor BBX (Bobby sox homolog) (HMG box-containing protein 2) | Transcription factor that is necessary for cell cycle progression from G1 to S phase. {ECO:0000269|PubMed:11680820}. |
Q92617 | NPIPB3 | S982 | ochoa | Nuclear pore complex-interacting protein family member B3 (Nuclear pore complex-interacting protein-like 3) (Protein pps22-1) | None |
Q92766 | RREB1 | S522 | ochoa | Ras-responsive element-binding protein 1 (RREB-1) (Finger protein in nuclear bodies) (Raf-responsive zinc finger protein LZ321) (Zinc finger motif enhancer-binding protein 1) (Zep-1) | Transcription factor that binds specifically to the RAS-responsive elements (RRE) of gene promoters (PubMed:10390538, PubMed:15067362, PubMed:17550981, PubMed:8816445, PubMed:9305772). Represses the angiotensinogen gene (PubMed:15067362). Negatively regulates the transcriptional activity of AR (PubMed:17550981). Potentiates the transcriptional activity of NEUROD1 (PubMed:12482979). Promotes brown adipocyte differentiation (By similarity). May be involved in Ras/Raf-mediated cell differentiation by enhancing calcitonin expression (PubMed:8816445). {ECO:0000250|UniProtKB:Q3UH06, ECO:0000269|PubMed:10390538, ECO:0000269|PubMed:12482979, ECO:0000269|PubMed:15067362, ECO:0000269|PubMed:17550981, ECO:0000269|PubMed:8816445, ECO:0000269|PubMed:9305772}. |
Q969G9 | NKD1 | S317 | ochoa | Protein naked cuticle homolog 1 (Naked-1) (hNkd) (hNkd1) | Cell autonomous antagonist of the canonical Wnt signaling pathway. May activate a second Wnt signaling pathway that controls planar cell polarity. {ECO:0000269|PubMed:11752446, ECO:0000269|PubMed:15687260, ECO:0000269|PubMed:16567647}. |
Q969W3 | VCF1 | S144 | ochoa | Protein VCF1 (VCP nuclear cofactor family member 1) | None |
Q96AY4 | TTC28 | S28 | ochoa | Tetratricopeptide repeat protein 28 (TPR repeat protein 28) (TPR repeat-containing big gene cloned at Keio) | During mitosis, may be involved in the condensation of spindle midzone microtubules, leading to the formation of midbody. {ECO:0000269|PubMed:23036704}. |
Q96E09 | PABIR1 | S189 | ochoa | PPP2R1A-PPP2R2A-interacting phosphatase regulator 1 (PABIR family member 1) | Acts as an inhibitor of serine/threonine-protein phosphatase 2A (PP2A) activity (PubMed:27588481, PubMed:33108758, PubMed:38123684). Inhibits PP2A activity by blocking the substrate binding site on PPP2R2A and the active site of PPP2CA (PubMed:38123684). Potentiates ubiquitin-mediated proteasomal degradation of serine/threonine-protein phosphatase 2A catalytic subunit alpha (PPP2CA) (PubMed:27588481). Inhibits PP2A-mediated dephosphorylation of WEE1, promoting ubiquitin-mediated proteolysis of WEE1, thereby releasing G2/M checkpoint (PubMed:33108758). {ECO:0000269|PubMed:27588481, ECO:0000269|PubMed:33108758, ECO:0000269|PubMed:38123684}. |
Q96EY5 | MVB12A | S170 | ochoa|psp | Multivesicular body subunit 12A (CIN85/CD2AP family-binding protein) (ESCRT-I complex subunit MVB12A) (Protein FAM125A) | Component of the ESCRT-I complex, a regulator of vesicular trafficking process. Required for the sorting of endocytic ubiquitinated cargos into multivesicular bodies. May be involved in the ligand-mediated internalization and down-regulation of EGF receptor. {ECO:0000269|PubMed:16895919}. |
Q96ID5 | IGSF21 | S389 | ochoa | Immunoglobulin superfamily member 21 (IgSF21) | Involved in synaptic inhibition in the brain. Selectively regulates inhibitory presynaptic differentiation through interacting with presynaptic NRXN2. {ECO:0000250|UniProtKB:Q7TNR6}. |
Q96JK2 | DCAF5 | S496 | ochoa | DDB1- and CUL4-associated factor 5 (Breakpoint cluster region protein 2) (BCRP2) (WD repeat-containing protein 22) | Is a substrate receptor for the CUL4-DDB1 E3 ubiquitin-protein ligase complex (CRL4) (PubMed:29691401, PubMed:30442713). The complex CRL4-DCAF5 is involved in the ubiquitination of a set of methylated non-histone proteins, including SOX2, DNMT1 and E2F1 (PubMed:29691401, PubMed:30442713). {ECO:0000269|PubMed:16949367, ECO:0000269|PubMed:16964240, ECO:0000269|PubMed:29691401, ECO:0000269|PubMed:30442713}. |
Q96PE2 | ARHGEF17 | S1002 | ochoa | Rho guanine nucleotide exchange factor 17 (164 kDa Rho-specific guanine-nucleotide exchange factor) (p164-RhoGEF) (p164RhoGEF) (Tumor endothelial marker 4) | Acts as a guanine nucleotide exchange factor (GEF) for RhoA GTPases. {ECO:0000269|PubMed:12071859}. |
Q96PE2 | ARHGEF17 | S2005 | ochoa | Rho guanine nucleotide exchange factor 17 (164 kDa Rho-specific guanine-nucleotide exchange factor) (p164-RhoGEF) (p164RhoGEF) (Tumor endothelial marker 4) | Acts as a guanine nucleotide exchange factor (GEF) for RhoA GTPases. {ECO:0000269|PubMed:12071859}. |
Q96SB4 | SRPK1 | S333 | ochoa | SRSF protein kinase 1 (EC 2.7.11.1) (SFRS protein kinase 1) (Serine/arginine-rich protein-specific kinase 1) (SR-protein-specific kinase 1) | Serine/arginine-rich protein-specific kinase which specifically phosphorylates its substrates at serine residues located in regions rich in arginine/serine dipeptides, known as RS domains and is involved in the phosphorylation of SR splicing factors and the regulation of splicing. Plays a central role in the regulatory network for splicing, controlling the intranuclear distribution of splicing factors in interphase cells and the reorganization of nuclear speckles during mitosis. Can influence additional steps of mRNA maturation, as well as other cellular activities, such as chromatin reorganization in somatic and sperm cells and cell cycle progression. Isoform 2 phosphorylates SFRS2, ZRSR2, LBR and PRM1. Isoform 2 phosphorylates SRSF1 using a directional (C-terminal to N-terminal) and a dual-track mechanism incorporating both processive phosphorylation (in which the kinase stays attached to the substrate after each round of phosphorylation) and distributive phosphorylation steps (in which the kinase and substrate dissociate after each phosphorylation event). The RS domain of SRSF1 binds first to a docking groove in the large lobe of the kinase domain of SRPK1. This induces certain structural changes in SRPK1 and/or RRM2 domain of SRSF1, allowing RRM2 to bind the kinase and initiate phosphorylation. The cycles continue for several phosphorylation steps in a processive manner (steps 1-8) until the last few phosphorylation steps (approximately steps 9-12). During that time, a mechanical stress induces the unfolding of the beta-4 motif in RRM2, which then docks at the docking groove of SRPK1. This also signals RRM2 to begin to dissociate, which facilitates SRSF1 dissociation after phosphorylation is completed. Isoform 2 can mediate hepatitis B virus (HBV) core protein phosphorylation. It plays a negative role in the regulation of HBV replication through a mechanism not involving the phosphorylation of the core protein but by reducing the packaging efficiency of the pregenomic RNA (pgRNA) without affecting the formation of the viral core particles. Isoform 1 and isoform 2 can induce splicing of exon 10 in MAPT/TAU. The ratio of isoform 1/isoform 2 plays a decisive role in determining cell fate in K-562 leukaemic cell line: isoform 2 favors proliferation where as isoform 1 favors differentiation. {ECO:0000269|PubMed:10049757, ECO:0000269|PubMed:10390541, ECO:0000269|PubMed:11509566, ECO:0000269|PubMed:12134018, ECO:0000269|PubMed:14555757, ECO:0000269|PubMed:15034300, ECO:0000269|PubMed:16122776, ECO:0000269|PubMed:16209947, ECO:0000269|PubMed:18155240, ECO:0000269|PubMed:18687337, ECO:0000269|PubMed:19240134, ECO:0000269|PubMed:19477182, ECO:0000269|PubMed:19886675, ECO:0000269|PubMed:20708644, ECO:0000269|PubMed:8208298, ECO:0000269|PubMed:9237760}. |
Q99081 | TCF12 | S163 | ochoa | Transcription factor 12 (TCF-12) (Class B basic helix-loop-helix protein 20) (bHLHb20) (DNA-binding protein HTF4) (E-box-binding protein) (Transcription factor HTF-4) | Transcriptional regulator. Involved in the initiation of neuronal differentiation. Activates transcription by binding to the E box (5'-CANNTG-3') (By similarity). May be involved in the functional network that regulates the development of the GnRH axis (PubMed:32620954). {ECO:0000250|UniProtKB:Q61286, ECO:0000269|PubMed:32620954}. |
Q99550 | MPHOSPH9 | S1006 | ochoa | M-phase phosphoprotein 9 | Negatively regulates cilia formation by recruiting the CP110-CEP97 complex (a negative regulator of ciliogenesis) at the distal end of the mother centriole in ciliary cells (PubMed:30375385). At the beginning of cilia formation, MPHOSPH9 undergoes TTBK2-mediated phosphorylation and degradation via the ubiquitin-proteasome system and removes itself and the CP110-CEP97 complex from the distal end of the mother centriole, which subsequently promotes cilia formation (PubMed:30375385). {ECO:0000269|PubMed:30375385}. |
Q99569 | PKP4 | S1153 | ochoa | Plakophilin-4 (p0071) | Plays a role as a regulator of Rho activity during cytokinesis. May play a role in junctional plaques. {ECO:0000269|PubMed:17115030}. |
Q99640 | PKMYT1 | S473 | ochoa | Membrane-associated tyrosine- and threonine-specific cdc2-inhibitory kinase (EC 2.7.11.1) (Myt1 kinase) | Acts as a negative regulator of entry into mitosis (G2 to M transition) by phosphorylation of the CDK1 kinase specifically when CDK1 is complexed to cyclins (PubMed:10373560, PubMed:10504341, PubMed:9001210, PubMed:9268380). Mediates phosphorylation of CDK1 predominantly on 'Thr-14'. Also involved in Golgi fragmentation (PubMed:9001210, PubMed:9268380). May be involved in phosphorylation of CDK1 on 'Tyr-15' to a lesser degree, however tyrosine kinase activity is unclear and may be indirect (PubMed:9001210, PubMed:9268380). {ECO:0000269|PubMed:10373560, ECO:0000269|PubMed:10504341, ECO:0000269|PubMed:9001210, ECO:0000269|PubMed:9268380}. |
Q99755 | PIP5K1A | S71 | ochoa | Phosphatidylinositol 4-phosphate 5-kinase type-1 alpha (PIP5K1-alpha) (PtdIns(4)P-5-kinase 1 alpha) (EC 2.7.1.68) (68 kDa type I phosphatidylinositol 4-phosphate 5-kinase alpha) (Phosphatidylinositol 4-phosphate 5-kinase type I alpha) (PIP5KIalpha) | Catalyzes the phosphorylation of phosphatidylinositol 4-phosphate (PtdIns(4)P/PI4P) to form phosphatidylinositol 4,5-bisphosphate (PtdIns(4,5)P2/PIP2), a lipid second messenger that regulates several cellular processes such as signal transduction, vesicle trafficking, actin cytoskeleton dynamics, cell adhesion, and cell motility (PubMed:21477596, PubMed:22942276, PubMed:8955136). PtdIns(4,5)P2 can directly act as a second messenger or can be utilized as a precursor to generate other second messengers: inositol 1,4,5-trisphosphate (IP3), diacylglycerol (DAG) or phosphatidylinositol-3,4,5-trisphosphate (PtdIns(3,4,5)P3/PIP3) (PubMed:19158393, PubMed:20660631). PIP5K1A-mediated phosphorylation of PtdIns(4)P is the predominant pathway for PtdIns(4,5)P2 synthesis (By similarity). Can also use phosphatidylinositol (PtdIns) as substrate in vitro (PubMed:22942276). Together with PIP5K1C, is required for phagocytosis, both enzymes regulating different types of actin remodeling at sequential steps (By similarity). Promotes particle ingestion by activating the WAS GTPase-binding protein that induces Arp2/3 dependent actin polymerization at the nascent phagocytic cup (By similarity). Together with PIP5K1B, is required, after stimulation by G-protein coupled receptors, for the synthesis of IP3 that will induce stable platelet adhesion (By similarity). Recruited to the plasma membrane by the E-cadherin/beta-catenin complex where it provides the substrate PtdIns(4,5)P2 for the production of PtdIns(3,4,5)P3, IP3 and DAG, that will mobilize internal calcium and drive keratinocyte differentiation (PubMed:19158393). Positively regulates insulin-induced translocation of SLC2A4 to the cell membrane in adipocytes (By similarity). Together with PIP5K1C has a role during embryogenesis (By similarity). Independently of its catalytic activity, is required for membrane ruffling formation, actin organization and focal adhesion formation during directional cell migration by controlling integrin-induced translocation of the small GTPase RAC1 to the plasma membrane (PubMed:20660631). Also functions in the nucleus where it acts as an activator of TUT1 adenylyltransferase activity in nuclear speckles, thereby regulating mRNA polyadenylation of a select set of mRNAs (PubMed:18288197). {ECO:0000250|UniProtKB:P70182, ECO:0000269|PubMed:18288197, ECO:0000269|PubMed:19158393, ECO:0000269|PubMed:20660631, ECO:0000269|PubMed:21477596, ECO:0000269|PubMed:22942276, ECO:0000269|PubMed:8955136}. |
Q9BRD0 | BUD13 | S175 | ochoa | BUD13 homolog | Involved in pre-mRNA splicing as component of the activated spliceosome. As a component of the minor spliceosome, involved in the splicing of U12-type introns in pre-mRNAs (Probable). {ECO:0000269|PubMed:29360106, ECO:0000269|PubMed:29361316, ECO:0000305|PubMed:33509932}. |
Q9BVT8 | TMUB1 | S113 | ochoa | Transmembrane and ubiquitin-like domain-containing protein 1 (Dendritic cell-derived ubiquitin-like protein) (DULP) (Hepatocyte odd protein shuttling protein) (Ubiquitin-like protein SB144) [Cleaved into: iHOPS] | Involved in sterol-regulated ubiquitination and degradation of HMG-CoA reductase HMGCR (PubMed:21343306). Involved in positive regulation of AMPA-selective glutamate receptor GRIA2 recycling to the cell surface (By similarity). Acts as a negative regulator of hepatocyte growth during regeneration (By similarity). {ECO:0000250|UniProtKB:Q53AQ4, ECO:0000250|UniProtKB:Q9JMG3, ECO:0000269|PubMed:21343306}.; FUNCTION: [iHOPS]: May contribute to the regulation of translation during cell-cycle progression. May contribute to the regulation of cell proliferation (By similarity). May be involved in centrosome assembly. Modulates stabilization and nucleolar localization of tumor suppressor CDKN2A and enhances association between CDKN2A and NPM1 (By similarity). {ECO:0000250|UniProtKB:Q9JMG3}. |
Q9BW04 | SARG | S281 | ochoa | Specifically androgen-regulated gene protein | Putative androgen-specific receptor. {ECO:0000269|PubMed:15525603}. |
Q9BW71 | HIRIP3 | S100 | ochoa | HIRA-interacting protein 3 | Histone chaperone that carries a H2A-H2B histone complex and facilitates its deposition onto chromatin. {ECO:0000269|PubMed:38334665, ECO:0000269|PubMed:9710638}. |
Q9H0W5 | CCDC8 | S273 | ochoa | Coiled-coil domain-containing protein 8 | Core component of the 3M complex, a complex required to regulate microtubule dynamics and genome integrity. It is unclear how the 3M complex regulates microtubules, it could act by controlling the level of a microtubule stabilizer (PubMed:24793695, PubMed:24793696). Required for localization of CUL7 to the centrosome (PubMed:24793695). {ECO:0000269|PubMed:24793695, ECO:0000269|PubMed:24793696}. |
Q9H1B7 | IRF2BPL | S219 | ochoa | Probable E3 ubiquitin-protein ligase IRF2BPL (EC 2.3.2.27) (Enhanced at puberty protein 1) (Interferon regulatory factor 2-binding protein-like) | Probable E3 ubiquitin protein ligase involved in the proteasome-mediated ubiquitin-dependent degradation of target proteins (PubMed:29374064). Through the degradation of CTNNB1, functions downstream of FOXF2 to negatively regulate the Wnt signaling pathway (PubMed:29374064). Probably plays a role in the development of the central nervous system and in neuronal maintenance (Probable). Also acts as a transcriptional regulator of genes controlling female reproductive function. May play a role in gene transcription by transactivating GNRH1 promoter and repressing PENK promoter (By similarity). {ECO:0000250|UniProtKB:Q5EIC4, ECO:0000269|PubMed:29374064, ECO:0000305|PubMed:17334524, ECO:0000305|PubMed:29374064, ECO:0000305|PubMed:30057031}. |
Q9H4L5 | OSBPL3 | S309 | ochoa | Oxysterol-binding protein-related protein 3 (ORP-3) (OSBP-related protein 3) | Phosphoinositide-binding protein which associates with both cell and endoplasmic reticulum (ER) membranes (PubMed:16143324). Can bind to the ER membrane protein VAPA and recruit VAPA to plasma membrane sites, thus linking these intracellular compartments (PubMed:25447204). The ORP3-VAPA complex stimulates RRAS signaling which in turn attenuates integrin beta-1 (ITGB1) activation at the cell surface (PubMed:18270267, PubMed:25447204). With VAPA, may regulate ER morphology (PubMed:16143324). Has a role in regulation of the actin cytoskeleton, cell polarity and cell adhesion (PubMed:18270267). Binds to phosphoinositides with preference for PI(3,4)P2 and PI(3,4,5)P3 (PubMed:16143324). Also binds 25-hydroxycholesterol and cholesterol (PubMed:17428193). {ECO:0000269|PubMed:16143324, ECO:0000269|PubMed:17428193, ECO:0000269|PubMed:18270267, ECO:0000269|PubMed:25447204}. |
Q9H7E2 | TDRD3 | S345 | ochoa | Tudor domain-containing protein 3 | Scaffolding protein that specifically recognizes and binds dimethylarginine-containing proteins (PubMed:15955813). Plays a role in the regulation of translation of target mRNAs by binding Arg/Gly-rich motifs (GAR) in dimethylarginine-containing proteins. In nucleus, acts as a coactivator: recognizes and binds asymmetric dimethylation on the core histone tails associated with transcriptional activation (H3R17me2a and H4R3me2a) and recruits proteins at these arginine-methylated loci (PubMed:21172665). In cytoplasm, acts as an antiviral factor that participates in the assembly of stress granules together with G3BP1 (PubMed:35085371). {ECO:0000269|PubMed:15955813, ECO:0000269|PubMed:18632687, ECO:0000269|PubMed:21172665, ECO:0000269|PubMed:35085371}. |
Q9H910 | JPT2 | S75 | ochoa | Jupiter microtubule associated homolog 2 (Hematological and neurological expressed 1-like protein) (HN1-like protein) | Nicotinic acid adenine dinucleotide phosphate (NAADP) binding protein required for NAADP-evoked intracellular calcium release (PubMed:33758061, PubMed:33758062). Confers NAADP-sensitivity to the two pore channels (TPCs) complex (PubMed:33758061). Enables NAADP to activate Ca(2+) release from the endoplasmic reticulum through ryanodine receptors (PubMed:33758062). {ECO:0000269|PubMed:33758061, ECO:0000269|PubMed:33758062}.; FUNCTION: (Microbial infection) Involved in the endolysosomal trafficking of human coronavirus SARS-CoV-2. {ECO:0000269|PubMed:33758061}. |
Q9NSY1 | BMP2K | S1111 | ochoa | BMP-2-inducible protein kinase (BIKe) (EC 2.7.11.1) | May be involved in osteoblast differentiation. {ECO:0000250|UniProtKB:Q91Z96}. |
Q9NUL3 | STAU2 | S93 | ochoa | Double-stranded RNA-binding protein Staufen homolog 2 | RNA-binding protein required for the microtubule-dependent transport of neuronal RNA from the cell body to the dendrite. As protein synthesis occurs within the dendrite, the localization of specific mRNAs to dendrites may be a prerequisite for neurite outgrowth and plasticity at sites distant from the cell body (By similarity). {ECO:0000250|UniProtKB:Q68SB1}. |
Q9P0V3 | SH3BP4 | S122 | ochoa | SH3 domain-binding protein 4 (EH-binding protein 10) (Transferrin receptor-trafficking protein) | May function in transferrin receptor internalization at the plasma membrane through a cargo-specific control of clathrin-mediated endocytosis. Alternatively, may act as a negative regulator of the amino acid-induced TOR signaling by inhibiting the formation of active Rag GTPase complexes. Preferentially binds inactive Rag GTPase complexes and prevents their interaction with the mTORC1 complex inhibiting its relocalization to lysosomes and its activation. Thereby, may indirectly regulate cell growth, proliferation and autophagy. {ECO:0000269|PubMed:16325581, ECO:0000269|PubMed:22575674}. |
Q9P206 | NHSL3 | S314 | ochoa | NHS-like protein 3 | Able to directly activate the TNF-NFkappaB signaling pathway. {ECO:0000269|PubMed:32854746}. |
Q9P242 | NYAP2 | S154 | ochoa | Neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adapter 2 | Activates PI3K and concomitantly recruits the WAVE1 complex to the close vicinity of PI3K and regulates neuronal morphogenesis. {ECO:0000250}. |
Q9P244 | LRFN1 | S731 | ochoa | Leucine-rich repeat and fibronectin type III domain-containing protein 1 (Synaptic adhesion-like molecule 2) | Promotes neurite outgrowth in hippocampal neurons. Involved in the regulation and maintenance of excitatory synapses. Induces the clustering of excitatory postsynaptic proteins, including DLG4, DLGAP1, GRIA1 and GRIN1 (By similarity). {ECO:0000250}. |
Q9UBY5 | LPAR3 | S331 | ochoa | Lysophosphatidic acid receptor 3 (LPA receptor 3) (LPA-3) (Lysophosphatidic acid receptor Edg-7) | Receptor for lysophosphatidic acid (LPA), a mediator of diverse cellular activities. May play a role in the development of ovarian cancer. Seems to be coupled to the G(i)/G(o) and G(q) families of heteromeric G proteins. |
Q9UEE9 | CFDP1 | S221 | ochoa | Craniofacial development protein 1 (Bucentaur) | May play a role during embryogenesis. {ECO:0000250}. |
Q9UHD8 | SEPTIN9 | S247 | ochoa | Septin-9 (MLL septin-like fusion protein MSF-A) (MLL septin-like fusion protein) (Ovarian/Breast septin) (Ov/Br septin) (Septin D1) | Filament-forming cytoskeletal GTPase (By similarity). May play a role in cytokinesis (Potential). May play a role in the internalization of 2 intracellular microbial pathogens, Listeria monocytogenes and Shigella flexneri. {ECO:0000250, ECO:0000305}. |
Q9UHI6 | DDX20 | S47 | ochoa | Probable ATP-dependent RNA helicase DDX20 (EC 3.6.1.15) (EC 3.6.4.13) (Component of gems 3) (DEAD box protein 20) (DEAD box protein DP 103) (Gemin-3) | The SMN complex catalyzes the assembly of small nuclear ribonucleoproteins (snRNPs), the building blocks of the spliceosome, and thereby plays an important role in the splicing of cellular pre-mRNAs. Most spliceosomal snRNPs contain a common set of Sm proteins SNRPB, SNRPD1, SNRPD2, SNRPD3, SNRPE, SNRPF and SNRPG that assemble in a heptameric protein ring on the Sm site of the small nuclear RNA to form the core snRNP (Sm core). In the cytosol, the Sm proteins SNRPD1, SNRPD2, SNRPE, SNRPF and SNRPG are trapped in an inactive 6S pICln-Sm complex by the chaperone CLNS1A that controls the assembly of the core snRNP. To assemble core snRNPs, the SMN complex accepts the trapped 5Sm proteins from CLNS1A forming an intermediate. Binding of snRNA inside 5Sm triggers eviction of the SMN complex, thereby allowing binding of SNRPD3 and SNRPB to complete assembly of the core snRNP. May also play a role in the metabolism of small nucleolar ribonucleoprotein (snoRNPs). {ECO:0000269|PubMed:18984161}. |
Q9UHY8 | FEZ2 | S65 | ochoa | Fasciculation and elongation protein zeta-2 (Zygin II) (Zygin-2) | Involved in axonal outgrowth and fasciculation. {ECO:0000250}. |
Q9UJY1 | HSPB8 | S24 | ochoa|psp | Heat shock protein beta-8 (HspB8) (Alpha-crystallin C chain) (E2-induced gene 1 protein) (Heat shock protein family B member 8) (Protein kinase H11) (Small stress protein-like protein HSP22) | Involved in the chaperone-assisted selective autophagy (CASA), a crucial process for protein quality control, particularly in mechanical strained cells and tissues such as muscle. Displays temperature-dependent chaperone activity. {ECO:0000250|UniProtKB:Q9JK92}. |
Q9UKD1 | GMEB2 | S366 | ochoa | Glucocorticoid modulatory element-binding protein 2 (GMEB-2) (DNA-binding protein p79PIF) (Parvovirus initiation factor p79) (PIF p79) | Trans-acting factor that binds to glucocorticoid modulatory elements (GME) present in the TAT (tyrosine aminotransferase) promoter and increases sensitivity to low concentrations of glucocorticoids. Also binds to the transferrin receptor promoter. Essential auxiliary factor for the replication of parvoviruses. |
Q9UKE5 | TNIK | S659 | ochoa | TRAF2 and NCK-interacting protein kinase (EC 2.7.11.1) | Serine/threonine kinase that acts as an essential activator of the Wnt signaling pathway. Recruited to promoters of Wnt target genes and required to activate their expression. May act by phosphorylating TCF4/TCF7L2. Appears to act upstream of the JUN N-terminal pathway. May play a role in the response to environmental stress. Part of a signaling complex composed of NEDD4, RAP2A and TNIK which regulates neuronal dendrite extension and arborization during development. More generally, it may play a role in cytoskeletal rearrangements and regulate cell spreading. Phosphorylates SMAD1 on Thr-322. Activator of the Hippo signaling pathway which plays a pivotal role in organ size control and tumor suppression by restricting proliferation and promoting apoptosis. MAP4Ks act in parallel to and are partially redundant with STK3/MST2 and STK4/MST2 in the phosphorylation and activation of LATS1/2, and establish MAP4Ks as components of the expanded Hippo pathway (PubMed:26437443). {ECO:0000269|PubMed:10521462, ECO:0000269|PubMed:15342639, ECO:0000269|PubMed:19061864, ECO:0000269|PubMed:19816403, ECO:0000269|PubMed:20159449, ECO:0000269|PubMed:21690388, ECO:0000269|PubMed:26437443}. |
Q9ULH7 | MRTFB | S395 | ochoa | Myocardin-related transcription factor B (MRTF-B) (MKL/myocardin-like protein 2) (Megakaryoblastic leukemia 2) | Acts as a transcriptional coactivator of serum response factor (SRF). Required for skeletal myogenic differentiation. {ECO:0000269|PubMed:14565952}. |
Q9UQC2 | GAB2 | S404 | ochoa | GRB2-associated-binding protein 2 (GRB2-associated binder 2) (Growth factor receptor bound protein 2-associated protein 2) (pp100) | Adapter protein which acts downstream of several membrane receptors including cytokine, antigen, hormone, cell matrix and growth factor receptors to regulate multiple signaling pathways. Regulates osteoclast differentiation mediating the TNFRSF11A/RANK signaling. In allergic response, it plays a role in mast cells activation and degranulation through PI-3-kinase regulation. Also involved in the regulation of cell proliferation and hematopoiesis. {ECO:0000269|PubMed:15750601, ECO:0000269|PubMed:19172738}. |
Q9Y2B5 | VPS9D1 | S116 | ochoa | VPS9 domain-containing protein 1 (Protein ATP-BL) | None |
Q9Y2K7 | KDM2A | S562 | ochoa | Lysine-specific demethylase 2A (EC 1.14.11.27) (CXXC-type zinc finger protein 8) (F-box and leucine-rich repeat protein 11) (F-box protein FBL7) (F-box protein Lilina) (F-box/LRR-repeat protein 11) (JmjC domain-containing histone demethylation protein 1A) ([Histone-H3]-lysine-36 demethylase 1A) | Histone demethylase that specifically demethylates 'Lys-36' of histone H3, thereby playing a central role in histone code. Preferentially demethylates dimethylated H3 'Lys-36' residue while it has weak or no activity for mono- and tri-methylated H3 'Lys-36'. May also recognize and bind to some phosphorylated proteins and promote their ubiquitination and degradation. Required to maintain the heterochromatic state. Associates with centromeres and represses transcription of small non-coding RNAs that are encoded by the clusters of satellite repeats at the centromere. Required to sustain centromeric integrity and genomic stability, particularly during mitosis. Regulates circadian gene expression by repressing the transcriptional activator activity of CLOCK-BMAL1 heterodimer and RORA in a catalytically-independent manner (PubMed:26037310). {ECO:0000269|PubMed:16362057, ECO:0000269|PubMed:19001877, ECO:0000269|PubMed:26037310, ECO:0000269|PubMed:28262558}. |
Q9Y3S1 | WNK2 | S49 | ochoa | Serine/threonine-protein kinase WNK2 (EC 2.7.11.1) (Antigen NY-CO-43) (Protein kinase lysine-deficient 2) (Protein kinase with no lysine 2) (Serologically defined colon cancer antigen 43) | Serine/threonine-protein kinase component of the WNK2-SPAK/OSR1 kinase cascade, which plays an important role in the regulation of electrolyte homeostasis, cell signaling, survival, and proliferation (PubMed:17667937, PubMed:18593598, PubMed:21733846). The WNK2-SPAK/OSR1 kinase cascade is composed of WNK2, which mediates phosphorylation and activation of downstream kinases OXSR1/OSR1 and STK39/SPAK (By similarity). Following activation, OXSR1/OSR1 and STK39/SPAK catalyze phosphorylation of ion cotransporters, regulating their activity (By similarity). Acts as an activator and inhibitor of sodium-coupled chloride cotransporters and potassium-coupled chloride cotransporters respectively (PubMed:21733846). Activates SLC12A2, SCNN1A, SCNN1B, SCNN1D and SGK1 and inhibits SLC12A5 (PubMed:21733846). Negatively regulates the EGF-induced activation of the ERK/MAPK-pathway and the downstream cell cycle progression (PubMed:17667937, PubMed:18593598). Affects MAPK3/MAPK1 activity by modulating the activity of MAP2K1 and this modulation depends on phosphorylation of MAP2K1 by PAK1 (PubMed:17667937, PubMed:18593598). WNK2 acts by interfering with the activity of PAK1 by controlling the balance of the activity of upstream regulators of PAK1 activity, RHOA and RAC1, which display reciprocal activity (PubMed:17667937, PubMed:18593598). {ECO:0000250|UniProtKB:Q9H4A3, ECO:0000269|PubMed:17667937, ECO:0000269|PubMed:18593598, ECO:0000269|PubMed:21733846}. |
Q9Y4H2 | IRS2 | S805 | ochoa | Insulin receptor substrate 2 (IRS-2) | Signaling adapter protein that participates in the signal transduction from two prominent receptor tyrosine kinases, insulin receptor/INSR and insulin-like growth factor I receptor/IGF1R (PubMed:25879670). Plays therefore an important role in development, growth, glucose homeostasis as well as lipid metabolism (PubMed:24616100). Upon phosphorylation by the insulin receptor, functions as a signaling scaffold that propagates insulin action through binding to SH2 domain-containing proteins including the p85 regulatory subunit of PI3K, NCK1, NCK2, GRB2 or SHP2 (PubMed:15316008, PubMed:19109239). Recruitment of GRB2 leads to the activation of the guanine nucleotide exchange factor SOS1 which in turn triggers the Ras/Raf/MEK/MAPK signaling cascade (By similarity). Activation of the PI3K/AKT pathway is responsible for most of insulin metabolic effects in the cell, and the Ras/Raf/MEK/MAPK is involved in the regulation of gene expression and in cooperation with the PI3K pathway regulates cell growth and differentiation. Acts a positive regulator of the Wnt/beta-catenin signaling pathway through suppression of DVL2 autophagy-mediated degradation leading to cell proliferation (PubMed:24616100). Plays a role in cell cycle progression by promoting a robust spindle assembly checkpoint (SAC) during M-phase (PubMed:32554797). In macrophages, IL4-induced tyrosine phosphorylation of IRS2 leads to the recruitment and activation of phosphoinositide 3-kinase (PI3K) (PubMed:19109239). {ECO:0000250|UniProtKB:P35570, ECO:0000269|PubMed:15316008, ECO:0000269|PubMed:19109239, ECO:0000269|PubMed:24616100, ECO:0000269|PubMed:25879670, ECO:0000269|PubMed:32554797}. |
Q9Y520 | PRRC2C | S834 | ochoa | Protein PRRC2C (BAT2 domain-containing protein 1) (HBV X-transactivated gene 2 protein) (HBV XAg-transactivated protein 2) (HLA-B-associated transcript 2-like 2) (Proline-rich and coiled-coil-containing protein 2C) | Required for efficient formation of stress granules. {ECO:0000269|PubMed:29395067}. |
Q9Y6X6 | MYO16 | S1362 | ochoa | Unconventional myosin-XVI (Neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adapter 3) (Unconventional myosin-16) | Myosins are actin-based motor molecules with ATPase activity. Unconventional myosins serve in intracellular movements. Their highly divergent tails are presumed to bind to membranous compartments, which would be moved relative to actin filaments. May be involved in targeting of the catalytic subunit of protein phosphatase 1 during brain development. Activates PI3K and concomitantly recruits the WAVE1 complex to the close vicinity of PI3K and regulates neuronal morphogenesis (By similarity). {ECO:0000250}. |
P00491 | PNP | S163 | Sugiyama | Purine nucleoside phosphorylase (PNP) (EC 2.4.2.1) (Inosine phosphorylase) (Inosine-guanosine phosphorylase) | Catalyzes the phosphorolytic breakdown of the N-glycosidic bond in the beta-(deoxy)ribonucleoside molecules, with the formation of the corresponding free purine bases and pentose-1-phosphate (PubMed:23438750, PubMed:9305964). Preferentially acts on 6-oxopurine nucleosides including inosine and guanosine (PubMed:9305964). {ECO:0000269|PubMed:23438750, ECO:0000269|PubMed:9305964}. |
P29401 | TKT | S305 | Sugiyama | Transketolase (TK) (EC 2.2.1.1) | Catalyzes the transfer of a two-carbon ketol group from a ketose donor to an aldose acceptor, via a covalent intermediate with the cofactor thiamine pyrophosphate. {ECO:0000269|PubMed:27259054}. |
Q9H4F8 | SMOC1 | S65 | Sugiyama | SPARC-related modular calcium-binding protein 1 (Secreted modular calcium-binding protein 1) (SMOC-1) | Plays essential roles in both eye and limb development. Probable regulator of osteoblast differentiation. {ECO:0000269|PubMed:20359165, ECO:0000269|PubMed:21194678, ECO:0000269|PubMed:21194680}. |
P46060 | RANGAP1 | S454 | Sugiyama | Ran GTPase-activating protein 1 (RanGAP1) | GTPase activator for RAN (PubMed:16428860, PubMed:8146159, PubMed:8896452). Converts cytoplasmic GTP-bound RAN to GDP-bound RAN, which is essential for RAN-mediated nuclear import and export (PubMed:27160050, PubMed:8896452). Mediates dissociation of cargo from nuclear export complexes containing XPO1, RAN and RANBP2 after nuclear export (PubMed:27160050). {ECO:0000269|PubMed:16428860, ECO:0000269|PubMed:27160050, ECO:0000269|PubMed:8146159, ECO:0000269|PubMed:8896452}. |
Q92888 | ARHGEF1 | S545 | Sugiyama | Rho guanine nucleotide exchange factor 1 (115 kDa guanine nucleotide exchange factor) (p115-RhoGEF) (p115RhoGEF) (Sub1.5) | Seems to play a role in the regulation of RhoA GTPase by guanine nucleotide-binding alpha-12 (GNA12) and alpha-13 (GNA13) subunits (PubMed:9641915, PubMed:9641916). Acts as a GTPase-activating protein (GAP) for GNA12 and GNA13, and as guanine nucleotide exchange factor (GEF) for RhoA GTPase (PubMed:30521495, PubMed:8810315, PubMed:9641915, PubMed:9641916). Activated G alpha 13/GNA13 stimulates the RhoGEF activity through interaction with the RGS-like domain (PubMed:9641916). This GEF activity is inhibited by binding to activated GNA12 (PubMed:9641916). Mediates angiotensin-2-induced RhoA activation (PubMed:20098430). In lymphoid follicles, may trigger activation of GNA13 as part of S1PR2-dependent signaling pathway that leads to inhibition of germinal center (GC) B cell growth and migration outside the GC niche. {ECO:0000250|UniProtKB:Q61210, ECO:0000269|PubMed:20098430, ECO:0000269|PubMed:30521495, ECO:0000269|PubMed:8810315, ECO:0000269|PubMed:9641915, ECO:0000269|PubMed:9641916}. |
Q14204 | DYNC1H1 | S4162 | Sugiyama | Cytoplasmic dynein 1 heavy chain 1 (Cytoplasmic dynein heavy chain 1) (Dynein heavy chain, cytosolic) | Cytoplasmic dynein 1 acts as a motor for the intracellular retrograde motility of vesicles and organelles along microtubules. Dynein has ATPase activity; the force-producing power stroke is thought to occur on release of ADP. Plays a role in mitotic spindle assembly and metaphase plate congression (PubMed:27462074). {ECO:0000269|PubMed:27462074}. |
Q8NAF0 | ZNF579 | S455 | Sugiyama | Zinc finger protein 579 | May be involved in transcriptional regulation. |
Q08289 | CACNB2 | S483 | EPSD | Voltage-dependent L-type calcium channel subunit beta-2 (CAB2) (Calcium channel voltage-dependent subunit beta 2) (Lambert-Eaton myasthenic syndrome antigen B) (MYSB) | Beta subunit of voltage-dependent calcium channels which contributes to the function of the calcium channel by increasing peak calcium current (By similarity). Plays a role in shifting voltage dependencies of activation and inactivation of the channel (By similarity). May modulate G protein inhibition (By similarity). May contribute to beta-adrenergic augmentation of Ca(2+) influx in cardiomyocytes, thereby regulating increases in heart rate and contractile force (PubMed:36424916). Involved in membrane targeting of the alpha-1 subunit CACNA1C (PubMed:17525370). {ECO:0000250|UniProtKB:Q8CC27, ECO:0000250|UniProtKB:Q8VGC3, ECO:0000269|PubMed:17525370, ECO:0000269|PubMed:36424916}. |
Q9NZQ3 | NCKIPSD | S256 | Sugiyama | NCK-interacting protein with SH3 domain (54 kDa VacA-interacting protein) (54 kDa vimentin-interacting protein) (VIP54) (90 kDa SH3 protein interacting with Nck) (AF3p21) (Dia-interacting protein 1) (DIP-1) (Diaphanous protein-interacting protein) (SH3 adapter protein SPIN90) (WASP-interacting SH3-domain protein) (WISH) (Wiskott-Aldrich syndrome protein-interacting protein) | Has an important role in stress fiber formation induced by active diaphanous protein homolog 1 (DRF1). Induces microspike formation, in vivo (By similarity). In vitro, stimulates N-WASP-induced ARP2/3 complex activation in the absence of CDC42 (By similarity). May play an important role in the maintenance of sarcomeres and/or in the assembly of myofibrils into sarcomeres. Implicated in regulation of actin polymerization and cell adhesion. Plays a role in angiogenesis. {ECO:0000250, ECO:0000269|PubMed:22419821}. |
Q12959 | DLG1 | S733 | Sugiyama | Disks large homolog 1 (Synapse-associated protein 97) (SAP-97) (SAP97) (hDlg) | Essential multidomain scaffolding protein required for normal development (By similarity). Recruits channels, receptors and signaling molecules to discrete plasma membrane domains in polarized cells. Promotes epithelial cell layer barrier function via maintaining cell-cell adhesion (By similarity). May also play a role in adherens junction assembly, signal transduction, cell proliferation, synaptogenesis and lymphocyte activation. Regulates the excitability of cardiac myocytes by modulating the functional expression of Kv4 channels. Functional regulator of Kv1.5 channel. During long-term depression in hippocampal neurons, it recruits ADAM10 to the plasma membrane (PubMed:23676497). {ECO:0000250|UniProtKB:A0A8C0TYJ0, ECO:0000250|UniProtKB:Q811D0, ECO:0000269|PubMed:10656683, ECO:0000269|PubMed:12445884, ECO:0000269|PubMed:14699157, ECO:0000269|PubMed:15263016, ECO:0000269|PubMed:19213956, ECO:0000269|PubMed:20605917, ECO:0000269|PubMed:23676497}. |
Q15700 | DLG2 | S699 | Sugiyama | Disks large homolog 2 (Channel-associated protein of synapse-110) (Chapsyn-110) (Postsynaptic density protein PSD-93) | Required for perception of chronic pain through NMDA receptor signaling. Regulates surface expression of NMDA receptors in dorsal horn neurons of the spinal cord. Interacts with the cytoplasmic tail of NMDA receptor subunits as well as inward rectifying potassium channels. Involved in regulation of synaptic stability at cholinergic synapses. Part of the postsynaptic protein scaffold of excitatory synapses (By similarity). {ECO:0000250}. |
P30305 | CDC25B | S219 | SIGNOR | M-phase inducer phosphatase 2 (EC 3.1.3.48) (Dual specificity phosphatase Cdc25B) | Tyrosine protein phosphatase which functions as a dosage-dependent inducer of mitotic progression (PubMed:1836978, PubMed:20360007). Directly dephosphorylates CDK1 and stimulates its kinase activity (PubMed:20360007). Required for G2/M phases of the cell cycle progression and abscission during cytokinesis in a ECT2-dependent manner (PubMed:17332740). The three isoforms seem to have a different level of activity (PubMed:1836978). {ECO:0000269|PubMed:17332740, ECO:0000269|PubMed:1836978, ECO:0000269|PubMed:20360007}. |
P00966 | ASS1 | S189 | Sugiyama | Argininosuccinate synthase (EC 6.3.4.5) (Citrulline--aspartate ligase) | One of the enzymes of the urea cycle, the metabolic pathway transforming neurotoxic amonia produced by protein catabolism into inocuous urea in the liver of ureotelic animals. Catalyzes the formation of arginosuccinate from aspartate, citrulline and ATP and together with ASL it is responsible for the biosynthesis of arginine in most body tissues. {ECO:0000305|PubMed:18473344, ECO:0000305|PubMed:27287393, ECO:0000305|PubMed:8792870}. |
Q16512 | PKN1 | S296 | Sugiyama | Serine/threonine-protein kinase N1 (EC 2.7.11.13) (Protease-activated kinase 1) (PAK-1) (Protein kinase C-like 1) (Protein kinase C-like PKN) (Protein kinase PKN-alpha) (Protein-kinase C-related kinase 1) (Serine-threonine protein kinase N) | PKC-related serine/threonine-protein kinase involved in various processes such as regulation of the intermediate filaments of the actin cytoskeleton, cell migration, tumor cell invasion and transcription regulation. Part of a signaling cascade that begins with the activation of the adrenergic receptor ADRA1B and leads to the activation of MAPK14. Regulates the cytoskeletal network by phosphorylating proteins such as VIM and neurofilament proteins NEFH, NEFL and NEFM, leading to inhibit their polymerization. Phosphorylates 'Ser-575', 'Ser-637' and 'Ser-669' of MAPT/Tau, lowering its ability to bind to microtubules, resulting in disruption of tubulin assembly. Acts as a key coactivator of androgen receptor (AR)-dependent transcription, by being recruited to AR target genes and specifically mediating phosphorylation of 'Thr-11' of histone H3 (H3T11ph), a specific tag for epigenetic transcriptional activation that promotes demethylation of histone H3 'Lys-9' (H3K9me) by KDM4C/JMJD2C. Phosphorylates HDAC5, HDAC7 and HDAC9, leading to impair their import in the nucleus. Phosphorylates 'Thr-38' of PPP1R14A, 'Ser-159', 'Ser-163' and 'Ser-170' of MARCKS, and GFAP. Able to phosphorylate RPS6 in vitro. {ECO:0000269|PubMed:11104762, ECO:0000269|PubMed:12514133, ECO:0000269|PubMed:17332740, ECO:0000269|PubMed:18066052, ECO:0000269|PubMed:20188095, ECO:0000269|PubMed:21224381, ECO:0000269|PubMed:21754995, ECO:0000269|PubMed:24248594, ECO:0000269|PubMed:8557118, ECO:0000269|PubMed:8621664, ECO:0000269|PubMed:9175763}. |
Q96PE3 | INPP4A | S788 | Sugiyama | Inositol polyphosphate-4-phosphatase type I A (Inositol polyphosphate 4-phosphatase type I) (Type I inositol 3,4-bisphosphate 4-phosphatase) (EC 3.1.3.66) | Catalyzes the hydrolysis of the 4-position phosphate of phosphatidylinositol 3,4-bisphosphate (PtdIns(3,4)P2) (PubMed:15716355, PubMed:20463662). Also catalyzes inositol 1,3,4-trisphosphate and inositol 1,4-bisphosphate (By similarity). Antagonizes the PI3K-AKT/PKB signaling pathway by dephosphorylating phosphoinositides and thereby modulating cell cycle progression and cell survival (By similarity) (PubMed:30071275). May protect neurons from excitotoxic cell death by regulating the synaptic localization of cell surface N-methyl-D-aspartate-type glutamate receptors (NMDARs) and NMDAR-mediated excitatory postsynaptic current (By similarity). {ECO:0000250|UniProtKB:Q62784, ECO:0000250|UniProtKB:Q9EPW0, ECO:0000269|PubMed:15716355, ECO:0000269|PubMed:20463662, ECO:0000269|PubMed:30071275}.; FUNCTION: [Isoform 4]: Displays no 4-phosphatase activity for PtdIns(3,4)P2, Ins(3,4)P2, or Ins(1,3,4)P3. {ECO:0000269|PubMed:9295334}. |
Q9Y4K4 | MAP4K5 | S413 | Sugiyama | Mitogen-activated protein kinase kinase kinase kinase 5 (EC 2.7.11.1) (Kinase homologous to SPS1/STE20) (KHS) (MAPK/ERK kinase kinase kinase 5) (MEK kinase kinase 5) (MEKKK 5) | May play a role in the response to environmental stress. Appears to act upstream of the JUN N-terminal pathway. {ECO:0000269|PubMed:9038372}. |
Download
reactome_id | name | p | -log10_p |
---|---|---|---|
R-HSA-8941284 | RUNX2 regulates chondrocyte maturation | 0.000110 | 3.957 |
R-HSA-9725371 | Nuclear events stimulated by ALK signaling in cancer | 0.000096 | 4.016 |
R-HSA-8941326 | RUNX2 regulates bone development | 0.000256 | 3.591 |
R-HSA-8940973 | RUNX2 regulates osteoblast differentiation | 0.001032 | 2.986 |
R-HSA-8941333 | RUNX2 regulates genes involved in differentiation of myeloid cells | 0.002787 | 2.555 |
R-HSA-74713 | IRS activation | 0.003762 | 2.425 |
R-HSA-438066 | Unblocking of NMDA receptors, glutamate binding and activation | 0.005254 | 2.280 |
R-HSA-442982 | Ras activation upon Ca2+ influx through NMDA receptor | 0.005254 | 2.280 |
R-HSA-8849932 | Synaptic adhesion-like molecules | 0.003371 | 2.472 |
R-HSA-8935964 | RUNX1 regulates expression of components of tight junctions | 0.004872 | 2.312 |
R-HSA-447038 | NrCAM interactions | 0.003762 | 2.425 |
R-HSA-9617324 | Negative regulation of NMDA receptor-mediated neuronal transmission | 0.005254 | 2.280 |
R-HSA-9725370 | Signaling by ALK fusions and activated point mutants | 0.004590 | 2.338 |
R-HSA-9700206 | Signaling by ALK in cancer | 0.004590 | 2.338 |
R-HSA-8878166 | Transcriptional regulation by RUNX2 | 0.007736 | 2.111 |
R-HSA-9620244 | Long-term potentiation | 0.007662 | 2.116 |
R-HSA-8939246 | RUNX1 regulates transcription of genes involved in differentiation of myeloid ce... | 0.008983 | 2.047 |
R-HSA-9661070 | Defective translocation of RB1 mutants to the nucleus | 0.012712 | 1.896 |
R-HSA-451308 | Activation of Ca-permeable Kainate Receptor | 0.012339 | 1.909 |
R-HSA-8941332 | RUNX2 regulates genes involved in cell migration | 0.014192 | 1.848 |
R-HSA-9615710 | Late endosomal microautophagy | 0.010626 | 1.974 |
R-HSA-74749 | Signal attenuation | 0.012339 | 1.909 |
R-HSA-451306 | Ionotropic activity of kainate receptors | 0.014192 | 1.848 |
R-HSA-442742 | CREB1 phosphorylation through NMDA receptor-mediated activation of RAS signaling | 0.014168 | 1.849 |
R-HSA-69273 | Cyclin A/B1/B2 associated events during G2/M transition | 0.014168 | 1.849 |
R-HSA-8878171 | Transcriptional regulation by RUNX1 | 0.014638 | 1.835 |
R-HSA-9818028 | NFE2L2 regulates pentose phosphate pathway genes | 0.016157 | 1.792 |
R-HSA-69278 | Cell Cycle, Mitotic | 0.019647 | 1.707 |
R-HSA-9709275 | Impaired BRCA2 translocation to the nucleus | 0.025262 | 1.598 |
R-HSA-9763198 | Impaired BRCA2 binding to SEM1 (DSS1) | 0.025262 | 1.598 |
R-HSA-9735763 | Defective PNP disrupts phosphorolysis of (deoxy)guanosine and (deoxy)inosine | 0.073897 | 1.131 |
R-HSA-9735786 | Nucleotide catabolism defects | 0.073897 | 1.131 |
R-HSA-69200 | Phosphorylation of proteins involved in G1/S transition by active Cyclin E:Cdk2 ... | 0.073897 | 1.131 |
R-HSA-5083630 | Defective LFNG causes SCDO3 | 0.073897 | 1.131 |
R-HSA-9845620 | Enhanced binding of GP1BA variant to VWF multimer:collagen | 0.085674 | 1.067 |
R-HSA-9846298 | Defective binding of VWF variant to GPIb:IX:V | 0.085674 | 1.067 |
R-HSA-9673221 | Defective F9 activation | 0.085674 | 1.067 |
R-HSA-8985586 | SLIT2:ROBO1 increases RHOA activity | 0.097301 | 1.012 |
R-HSA-9027283 | Erythropoietin activates STAT5 | 0.108782 | 0.963 |
R-HSA-9645135 | STAT5 Activation | 0.108782 | 0.963 |
R-HSA-9687136 | Aberrant regulation of mitotic exit in cancer due to RB1 defects | 0.027557 | 1.560 |
R-HSA-428890 | Role of ABL in ROBO-SLIT signaling | 0.120117 | 0.920 |
R-HSA-1912399 | Pre-NOTCH Processing in the Endoplasmic Reticulum | 0.120117 | 0.920 |
R-HSA-112412 | SOS-mediated signalling | 0.120117 | 0.920 |
R-HSA-9027277 | Erythropoietin activates Phospholipase C gamma (PLCG) | 0.153268 | 0.815 |
R-HSA-112308 | Presynaptic depolarization and calcium channel opening | 0.164040 | 0.785 |
R-HSA-2197563 | NOTCH2 intracellular domain regulates transcription | 0.185177 | 0.732 |
R-HSA-9027276 | Erythropoietin activates Phosphoinositide-3-kinase (PI3K) | 0.185177 | 0.732 |
R-HSA-9853506 | OGDH complex synthesizes succinyl-CoA from 2-OG | 0.195545 | 0.709 |
R-HSA-9659787 | Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects | 0.195545 | 0.709 |
R-HSA-9661069 | Defective binding of RB1 mutants to E2F1,(E2F2, E2F3) | 0.195545 | 0.709 |
R-HSA-917729 | Endosomal Sorting Complex Required For Transport (ESCRT) | 0.074620 | 1.127 |
R-HSA-9687139 | Aberrant regulation of mitotic cell cycle due to RB1 defects | 0.078306 | 1.106 |
R-HSA-69166 | Removal of the Flap Intermediate | 0.205781 | 0.687 |
R-HSA-9027284 | Erythropoietin activates RAS | 0.215888 | 0.666 |
R-HSA-2173791 | TGF-beta receptor signaling in EMT (epithelial to mesenchymal transition) | 0.215888 | 0.666 |
R-HSA-176412 | Phosphorylation of the APC/C | 0.225867 | 0.646 |
R-HSA-77595 | Processing of Intronless Pre-mRNAs | 0.235720 | 0.628 |
R-HSA-174437 | Removal of the Flap Intermediate from the C-strand | 0.245448 | 0.610 |
R-HSA-372708 | p130Cas linkage to MAPK signaling for integrins | 0.245448 | 0.610 |
R-HSA-8939902 | Regulation of RUNX2 expression and activity | 0.059650 | 1.224 |
R-HSA-5651801 | PCNA-Dependent Long Patch Base Excision Repair | 0.255052 | 0.593 |
R-HSA-380284 | Loss of proteins required for interphase microtubule organization from the centr... | 0.063825 | 1.195 |
R-HSA-380259 | Loss of Nlp from mitotic centrosomes | 0.063825 | 1.195 |
R-HSA-1912420 | Pre-NOTCH Processing in Golgi | 0.264535 | 0.578 |
R-HSA-174048 | APC/C:Cdc20 mediated degradation of Cyclin B | 0.264535 | 0.578 |
R-HSA-9709603 | Impaired BRCA2 binding to PALB2 | 0.264535 | 0.578 |
R-HSA-8854518 | AURKA Activation by TPX2 | 0.070333 | 1.153 |
R-HSA-9701193 | Defective homologous recombination repair (HRR) due to PALB2 loss of function | 0.273898 | 0.562 |
R-HSA-9701192 | Defective homologous recombination repair (HRR) due to BRCA1 loss of function | 0.273898 | 0.562 |
R-HSA-9704331 | Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of... | 0.273898 | 0.562 |
R-HSA-9704646 | Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of... | 0.273898 | 0.562 |
R-HSA-179409 | APC-Cdc20 mediated degradation of Nek2A | 0.283142 | 0.548 |
R-HSA-606279 | Deposition of new CENPA-containing nucleosomes at the centromere | 0.148015 | 0.830 |
R-HSA-774815 | Nucleosome assembly | 0.148015 | 0.830 |
R-HSA-380270 | Recruitment of mitotic centrosome proteins and complexes | 0.086616 | 1.062 |
R-HSA-76066 | RNA Polymerase III Transcription Initiation From Type 2 Promoter | 0.292269 | 0.534 |
R-HSA-5696397 | Gap-filling DNA repair synthesis and ligation in GG-NER | 0.292269 | 0.534 |
R-HSA-380287 | Centrosome maturation | 0.091537 | 1.038 |
R-HSA-202430 | Translocation of ZAP-70 to Immunological synapse | 0.318962 | 0.496 |
R-HSA-174178 | APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins ... | 0.184013 | 0.735 |
R-HSA-5693554 | Resolution of D-loop Structures through Synthesis-Dependent Strand Annealing (SD... | 0.327635 | 0.485 |
R-HSA-141424 | Amplification of signal from the kinetochores | 0.120549 | 0.919 |
R-HSA-141444 | Amplification of signal from unattached kinetochores via a MAD2 inhibitory si... | 0.120549 | 0.919 |
R-HSA-380320 | Recruitment of NuMA to mitotic centrosomes | 0.128986 | 0.889 |
R-HSA-174414 | Processive synthesis on the C-strand of the telomere | 0.344653 | 0.463 |
R-HSA-9006335 | Signaling by Erythropoietin | 0.361242 | 0.442 |
R-HSA-9709570 | Impaired BRCA2 binding to RAD51 | 0.361242 | 0.442 |
R-HSA-2979096 | NOTCH2 Activation and Transmission of Signal to the Nucleus | 0.283142 | 0.548 |
R-HSA-9639288 | Amino acids regulate mTORC1 | 0.044316 | 1.353 |
R-HSA-5620912 | Anchoring of the basal body to the plasma membrane | 0.134724 | 0.871 |
R-HSA-9646399 | Aggrephagy | 0.122122 | 0.913 |
R-HSA-69183 | Processive synthesis on the lagging strand | 0.215888 | 0.666 |
R-HSA-9851695 | Epigenetic regulation of adipogenesis genes by MLL3 and MLL4 complexes | 0.266716 | 0.574 |
R-HSA-9841922 | MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesi... | 0.266716 | 0.574 |
R-HSA-198203 | PI3K/AKT activation | 0.153268 | 0.815 |
R-HSA-6783310 | Fanconi Anemia Pathway | 0.148015 | 0.830 |
R-HSA-76061 | RNA Polymerase III Transcription Initiation From Type 1 Promoter | 0.301280 | 0.521 |
R-HSA-9818564 | Epigenetic regulation of gene expression by MLL3 and MLL4 complexes | 0.266716 | 0.574 |
R-HSA-191650 | Regulation of gap junction activity | 0.073897 | 1.131 |
R-HSA-5635851 | GLI proteins bind promoters of Hh responsive genes to promote transcription | 0.097301 | 1.012 |
R-HSA-73863 | RNA Polymerase I Transcription Termination | 0.344653 | 0.463 |
R-HSA-453276 | Regulation of mitotic cell cycle | 0.268156 | 0.572 |
R-HSA-174143 | APC/C-mediated degradation of cell cycle proteins | 0.268156 | 0.572 |
R-HSA-69618 | Mitotic Spindle Checkpoint | 0.055374 | 1.257 |
R-HSA-5685942 | HDR through Homologous Recombination (HRR) | 0.072567 | 1.139 |
R-HSA-5693537 | Resolution of D-Loop Structures | 0.093588 | 1.029 |
R-HSA-163754 | Insulin effects increased synthesis of Xylulose-5-Phosphate | 0.120117 | 0.920 |
R-HSA-430116 | GP1b-IX-V activation signalling | 0.142358 | 0.847 |
R-HSA-113501 | Inhibition of replication initiation of damaged DNA by RB1/E2F1 | 0.174676 | 0.758 |
R-HSA-5693568 | Resolution of D-loop Structures through Holliday Junction Intermediates | 0.089690 | 1.047 |
R-HSA-5576893 | Phase 2 - plateau phase | 0.235720 | 0.628 |
R-HSA-176407 | Conversion from APC/C:Cdc20 to APC/C:Cdh1 in late anaphase | 0.245448 | 0.610 |
R-HSA-9619483 | Activation of AMPK downstream of NMDARs | 0.353001 | 0.452 |
R-HSA-69186 | Lagging Strand Synthesis | 0.283142 | 0.548 |
R-HSA-2467813 | Separation of Sister Chromatids | 0.205636 | 0.687 |
R-HSA-76046 | RNA Polymerase III Transcription Initiation | 0.369379 | 0.433 |
R-HSA-9675126 | Diseases of mitotic cell cycle | 0.085843 | 1.066 |
R-HSA-9930044 | Nuclear RNA decay | 0.089690 | 1.047 |
R-HSA-74752 | Signaling by Insulin receptor | 0.143494 | 0.843 |
R-HSA-427413 | NoRC negatively regulates rRNA expression | 0.268156 | 0.572 |
R-HSA-74751 | Insulin receptor signalling cascade | 0.065962 | 1.181 |
R-HSA-168315 | Inhibition of Host mRNA Processing and RNA Silencing | 0.037654 | 1.424 |
R-HSA-8875513 | MET interacts with TNS proteins | 0.061970 | 1.208 |
R-HSA-9705677 | SARS-CoV-2 targets PDZ proteins in cell-cell junction | 0.073897 | 1.131 |
R-HSA-69478 | G2/M DNA replication checkpoint | 0.108782 | 0.963 |
R-HSA-2470946 | Cohesin Loading onto Chromatin | 0.120117 | 0.920 |
R-HSA-174490 | Membrane binding and targetting of GAG proteins | 0.195545 | 0.709 |
R-HSA-2559584 | Formation of Senescence-Associated Heterochromatin Foci (SAHF) | 0.195545 | 0.709 |
R-HSA-162588 | Budding and maturation of HIV virion | 0.082047 | 1.086 |
R-HSA-141430 | Inactivation of APC/C via direct inhibition of the APC/C complex | 0.235720 | 0.628 |
R-HSA-113510 | E2F mediated regulation of DNA replication | 0.264535 | 0.578 |
R-HSA-350054 | Notch-HLH transcription pathway | 0.301280 | 0.521 |
R-HSA-912526 | Interleukin receptor SHC signaling | 0.310178 | 0.508 |
R-HSA-75067 | Processing of Capped Intronless Pre-mRNA | 0.318962 | 0.496 |
R-HSA-110314 | Recognition of DNA damage by PCNA-containing replication complex | 0.318962 | 0.496 |
R-HSA-77387 | Insulin receptor recycling | 0.353001 | 0.452 |
R-HSA-5576892 | Phase 0 - rapid depolarisation | 0.353001 | 0.452 |
R-HSA-9917777 | Epigenetic regulation by WDR5-containing histone modifying complexes | 0.071486 | 1.146 |
R-HSA-2428928 | IRS-related events triggered by IGF1R | 0.221098 | 0.655 |
R-HSA-9613829 | Chaperone Mediated Autophagy | 0.255052 | 0.593 |
R-HSA-6794361 | Neurexins and neuroligins | 0.179442 | 0.746 |
R-HSA-112399 | IRS-mediated signalling | 0.202457 | 0.694 |
R-HSA-983168 | Antigen processing: Ubiquitination & Proteasome degradation | 0.344234 | 0.463 |
R-HSA-68882 | Mitotic Anaphase | 0.186718 | 0.729 |
R-HSA-525793 | Myogenesis | 0.063920 | 1.194 |
R-HSA-6811558 | PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling | 0.100382 | 0.998 |
R-HSA-2555396 | Mitotic Metaphase and Anaphase | 0.188892 | 0.724 |
R-HSA-9823587 | Defects of platelet adhesion to exposed collagen | 0.097301 | 1.012 |
R-HSA-9735804 | Diseases of nucleotide metabolism | 0.195545 | 0.709 |
R-HSA-174495 | Synthesis And Processing Of GAG, GAGPOL Polyproteins | 0.205781 | 0.687 |
R-HSA-6794362 | Protein-protein interactions at synapses | 0.032436 | 1.489 |
R-HSA-5693567 | HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA) | 0.079698 | 1.099 |
R-HSA-212165 | Epigenetic regulation of gene expression | 0.152708 | 0.816 |
R-HSA-9703648 | Signaling by FLT3 ITD and TKD mutants | 0.318962 | 0.496 |
R-HSA-2995410 | Nuclear Envelope (NE) Reassembly | 0.310514 | 0.508 |
R-HSA-1839117 | Signaling by cytosolic FGFR1 fusion mutants | 0.255052 | 0.593 |
R-HSA-2428924 | IGF1R signaling cascade | 0.235170 | 0.629 |
R-HSA-5693538 | Homology Directed Repair | 0.090694 | 1.042 |
R-HSA-73886 | Chromosome Maintenance | 0.249615 | 0.603 |
R-HSA-9612973 | Autophagy | 0.025426 | 1.595 |
R-HSA-2028269 | Signaling by Hippo | 0.032797 | 1.484 |
R-HSA-1236973 | Cross-presentation of particulate exogenous antigens (phagosomes) | 0.153268 | 0.815 |
R-HSA-451326 | Activation of kainate receptors upon glutamate binding | 0.070993 | 1.149 |
R-HSA-141405 | Inhibition of the proteolytic activity of APC/C required for the onset of anapha... | 0.235720 | 0.628 |
R-HSA-6783984 | Glycine degradation | 0.235720 | 0.628 |
R-HSA-1660499 | Synthesis of PIPs at the plasma membrane | 0.061721 | 1.210 |
R-HSA-9821993 | Replacement of protamines by nucleosomes in the male pronucleus | 0.318962 | 0.496 |
R-HSA-2565942 | Regulation of PLK1 Activity at G2/M Transition | 0.115043 | 0.939 |
R-HSA-420029 | Tight junction interactions | 0.327635 | 0.485 |
R-HSA-5250941 | Negative epigenetic regulation of rRNA expression | 0.310514 | 0.508 |
R-HSA-8939236 | RUNX1 regulates transcription of genes involved in differentiation of HSCs | 0.329200 | 0.483 |
R-HSA-68877 | Mitotic Prometaphase | 0.137606 | 0.861 |
R-HSA-110373 | Resolution of AP sites via the multiple-nucleotide patch replacement pathway | 0.336198 | 0.473 |
R-HSA-2404192 | Signaling by Type 1 Insulin-like Growth Factor 1 Receptor (IGF1R) | 0.239873 | 0.620 |
R-HSA-2500257 | Resolution of Sister Chromatid Cohesion | 0.249615 | 0.603 |
R-HSA-9609736 | Assembly and cell surface presentation of NMDA receptors | 0.025630 | 1.591 |
R-HSA-1632852 | Macroautophagy | 0.053691 | 1.270 |
R-HSA-199418 | Negative regulation of the PI3K/AKT network | 0.116829 | 0.932 |
R-HSA-2029482 | Regulation of actin dynamics for phagocytic cup formation | 0.329098 | 0.483 |
R-HSA-8934903 | Receptor Mediated Mitophagy | 0.153268 | 0.815 |
R-HSA-9702518 | STAT5 activation downstream of FLT3 ITD mutants | 0.235720 | 0.628 |
R-HSA-5334118 | DNA methylation | 0.361242 | 0.442 |
R-HSA-380972 | Energy dependent regulation of mTOR by LKB1-AMPK | 0.369379 | 0.433 |
R-HSA-442755 | Activation of NMDA receptors and postsynaptic events | 0.058348 | 1.234 |
R-HSA-1912422 | Pre-NOTCH Expression and Processing | 0.215998 | 0.666 |
R-HSA-9663891 | Selective autophagy | 0.128986 | 0.889 |
R-HSA-68886 | M Phase | 0.076142 | 1.118 |
R-HSA-9664422 | FCGR3A-mediated phagocytosis | 0.325619 | 0.487 |
R-HSA-9664417 | Leishmania phagocytosis | 0.325619 | 0.487 |
R-HSA-9664407 | Parasite infection | 0.325619 | 0.487 |
R-HSA-9668250 | Defective factor IX causes hemophilia B | 0.153268 | 0.815 |
R-HSA-68884 | Mitotic Telophase/Cytokinesis | 0.174676 | 0.758 |
R-HSA-69109 | Leading Strand Synthesis | 0.185177 | 0.732 |
R-HSA-69091 | Polymerase switching | 0.185177 | 0.732 |
R-HSA-1475029 | Reversible hydration of carbon dioxide | 0.195545 | 0.709 |
R-HSA-166208 | mTORC1-mediated signalling | 0.301280 | 0.521 |
R-HSA-429947 | Deadenylation of mRNA | 0.318962 | 0.496 |
R-HSA-9839394 | TGFBR3 expression | 0.327635 | 0.485 |
R-HSA-69275 | G2/M Transition | 0.049566 | 1.305 |
R-HSA-69231 | Cyclin D associated events in G1 | 0.143623 | 0.843 |
R-HSA-69236 | G1 Phase | 0.143623 | 0.843 |
R-HSA-1640170 | Cell Cycle | 0.048881 | 1.311 |
R-HSA-453274 | Mitotic G2-G2/M phases | 0.051484 | 1.288 |
R-HSA-9673324 | WNT5:FZD7-mediated leishmania damping | 0.225867 | 0.646 |
R-HSA-9664420 | Killing mechanisms | 0.225867 | 0.646 |
R-HSA-9703465 | Signaling by FLT3 fusion proteins | 0.336198 | 0.473 |
R-HSA-5656169 | Termination of translesion DNA synthesis | 0.361242 | 0.442 |
R-HSA-8856688 | Golgi-to-ER retrograde transport | 0.294339 | 0.531 |
R-HSA-1855183 | Synthesis of IP2, IP, and Ins in the cytosol | 0.063920 | 1.194 |
R-HSA-112314 | Neurotransmitter receptors and postsynaptic signal transmission | 0.345519 | 0.462 |
R-HSA-8853659 | RET signaling | 0.105563 | 0.976 |
R-HSA-419408 | Lysosphingolipid and LPA receptors | 0.215888 | 0.666 |
R-HSA-1483148 | Synthesis of PG | 0.235720 | 0.628 |
R-HSA-9931509 | Expression of BMAL (ARNTL), CLOCK, and NPAS2 | 0.117924 | 0.928 |
R-HSA-9615933 | Postmitotic nuclear pore complex (NPC) reformation | 0.336198 | 0.473 |
R-HSA-9648025 | EML4 and NUDC in mitotic spindle formation | 0.202835 | 0.693 |
R-HSA-416482 | G alpha (12/13) signalling events | 0.301130 | 0.521 |
R-HSA-2029480 | Fcgamma receptor (FCGR) dependent phagocytosis | 0.235129 | 0.629 |
R-HSA-9701898 | STAT3 nuclear events downstream of ALK signaling | 0.215888 | 0.666 |
R-HSA-69242 | S Phase | 0.164965 | 0.783 |
R-HSA-438064 | Post NMDA receptor activation events | 0.035779 | 1.446 |
R-HSA-5693532 | DNA Double-Strand Break Repair | 0.177350 | 0.751 |
R-HSA-140837 | Intrinsic Pathway of Fibrin Clot Formation | 0.283142 | 0.548 |
R-HSA-109704 | PI3K Cascade | 0.170354 | 0.769 |
R-HSA-174411 | Polymerase switching on the C-strand of the telomere | 0.327635 | 0.485 |
R-HSA-400042 | Adrenaline,noradrenaline inhibits insulin secretion | 0.336198 | 0.473 |
R-HSA-73894 | DNA Repair | 0.359401 | 0.444 |
R-HSA-199991 | Membrane Trafficking | 0.239645 | 0.620 |
R-HSA-73933 | Resolution of Abasic Sites (AP sites) | 0.126356 | 0.898 |
R-HSA-8936459 | RUNX1 regulates genes involved in megakaryocyte differentiation and platelet fun... | 0.254006 | 0.595 |
R-HSA-76009 | Platelet Aggregation (Plug Formation) | 0.148015 | 0.830 |
R-HSA-6811442 | Intra-Golgi and retrograde Golgi-to-ER traffic | 0.308109 | 0.511 |
R-HSA-9764790 | Positive Regulation of CDH1 Gene Transcription | 0.153268 | 0.815 |
R-HSA-193648 | NRAGE signals death through JNK | 0.197825 | 0.704 |
R-HSA-983189 | Kinesins | 0.216423 | 0.665 |
R-HSA-8863678 | Neurodegenerative Diseases | 0.057106 | 1.243 |
R-HSA-8862803 | Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer's dis... | 0.057106 | 1.243 |
R-HSA-1483255 | PI Metabolism | 0.177136 | 0.752 |
R-HSA-9671793 | Diseases of hemostasis | 0.264535 | 0.578 |
R-HSA-110357 | Displacement of DNA glycosylase by APEX1 | 0.120117 | 0.920 |
R-HSA-9734009 | Defective Intrinsic Pathway for Apoptosis | 0.067425 | 1.171 |
R-HSA-75892 | Platelet Adhesion to exposed collagen | 0.195545 | 0.709 |
R-HSA-5685939 | HDR through MMEJ (alt-NHEJ) | 0.195545 | 0.709 |
R-HSA-175474 | Assembly Of The HIV Virion | 0.292269 | 0.534 |
R-HSA-70635 | Urea cycle | 0.336198 | 0.473 |
R-HSA-6803204 | TP53 Regulates Transcription of Genes Involved in Cytochrome C Release | 0.067425 | 1.171 |
R-HSA-8983432 | Interleukin-15 signaling | 0.185177 | 0.732 |
R-HSA-3214842 | HDMs demethylate histones | 0.327635 | 0.485 |
R-HSA-1483166 | Synthesis of PA | 0.202457 | 0.694 |
R-HSA-2032785 | YAP1- and WWTR1 (TAZ)-stimulated gene expression | 0.022694 | 1.644 |
R-HSA-9931510 | Phosphorylated BMAL1:CLOCK (ARNTL:CLOCK) activates expression of core clock gene... | 0.063920 | 1.194 |
R-HSA-5358606 | Mismatch repair (MMR) directed by MSH2:MSH3 (MutSbeta) | 0.245448 | 0.610 |
R-HSA-9013695 | NOTCH4 Intracellular Domain Regulates Transcription | 0.283142 | 0.548 |
R-HSA-2559583 | Cellular Senescence | 0.044082 | 1.356 |
R-HSA-9933387 | RORA,B,C and NR1D1 (REV-ERBA) regulate gene expression | 0.369379 | 0.433 |
R-HSA-9645723 | Diseases of programmed cell death | 0.128986 | 0.889 |
R-HSA-2586552 | Signaling by Leptin | 0.153268 | 0.815 |
R-HSA-1834941 | STING mediated induction of host immune responses | 0.264535 | 0.578 |
R-HSA-69656 | Cyclin A:Cdk2-associated events at S phase entry | 0.272874 | 0.564 |
R-HSA-73884 | Base Excision Repair | 0.361546 | 0.442 |
R-HSA-162582 | Signal Transduction | 0.125082 | 0.903 |
R-HSA-351906 | Apoptotic cleavage of cell adhesion proteins | 0.131308 | 0.882 |
R-HSA-264870 | Caspase-mediated cleavage of cytoskeletal proteins | 0.142358 | 0.847 |
R-HSA-9825892 | Regulation of MITF-M-dependent genes involved in cell cycle and proliferation | 0.047407 | 1.324 |
R-HSA-419037 | NCAM1 interactions | 0.109643 | 0.960 |
R-HSA-5358565 | Mismatch repair (MMR) directed by MSH2:MSH6 (MutSalpha) | 0.245448 | 0.610 |
R-HSA-9674555 | Signaling by CSF3 (G-CSF) | 0.361242 | 0.442 |
R-HSA-69620 | Cell Cycle Checkpoints | 0.284493 | 0.546 |
R-HSA-9856532 | Mechanical load activates signaling by PIEZO1 and integrins in osteocytes | 0.038393 | 1.416 |
R-HSA-9755088 | Ribavirin ADME | 0.292269 | 0.534 |
R-HSA-1912408 | Pre-NOTCH Transcription and Translation | 0.137626 | 0.861 |
R-HSA-9707616 | Heme signaling | 0.225782 | 0.646 |
R-HSA-9022699 | MECP2 regulates neuronal receptors and channels | 0.063920 | 1.194 |
R-HSA-1660516 | Synthesis of PIPs at the early endosome membrane | 0.327635 | 0.485 |
R-HSA-9909396 | Circadian clock | 0.123283 | 0.909 |
R-HSA-9833482 | PKR-mediated signaling | 0.310514 | 0.508 |
R-HSA-9694631 | Maturation of nucleoprotein | 0.264535 | 0.578 |
R-HSA-9764560 | Regulation of CDH1 Gene Transcription | 0.263439 | 0.579 |
R-HSA-9772755 | Formation of WDR5-containing histone-modifying complexes | 0.101526 | 0.993 |
R-HSA-156711 | Polo-like kinase mediated events | 0.255052 | 0.593 |
R-HSA-162599 | Late Phase of HIV Life Cycle | 0.336056 | 0.474 |
R-HSA-2262752 | Cellular responses to stress | 0.118842 | 0.925 |
R-HSA-5358508 | Mismatch Repair | 0.255052 | 0.593 |
R-HSA-204998 | Cell death signalling via NRAGE, NRIF and NADE | 0.277590 | 0.557 |
R-HSA-9651496 | Defects of contact activation system (CAS) and kallikrein/kinin system (KKS) | 0.235720 | 0.628 |
R-HSA-8953897 | Cellular responses to stimuli | 0.071823 | 1.144 |
R-HSA-111465 | Apoptotic cleavage of cellular proteins | 0.085843 | 1.066 |
R-HSA-2559580 | Oxidative Stress Induced Senescence | 0.058348 | 1.234 |
R-HSA-9855142 | Cellular responses to mechanical stimuli | 0.219317 | 0.659 |
R-HSA-9682706 | Replication of the SARS-CoV-1 genome | 0.195545 | 0.709 |
R-HSA-9694686 | Replication of the SARS-CoV-2 genome | 0.245448 | 0.610 |
R-HSA-5633008 | TP53 Regulates Transcription of Cell Death Genes | 0.287016 | 0.542 |
R-HSA-375165 | NCAM signaling for neurite out-growth | 0.225782 | 0.646 |
R-HSA-5620971 | Pyroptosis | 0.353001 | 0.452 |
R-HSA-9679514 | SARS-CoV-1 Genome Replication and Transcription | 0.205781 | 0.687 |
R-HSA-1266695 | Interleukin-7 signaling | 0.327635 | 0.485 |
R-HSA-9694682 | SARS-CoV-2 Genome Replication and Transcription | 0.264535 | 0.578 |
R-HSA-982772 | Growth hormone receptor signaling | 0.310178 | 0.508 |
R-HSA-75153 | Apoptotic execution phase | 0.152434 | 0.817 |
R-HSA-9679504 | Translation of Replicase and Assembly of the Replication Transcription Complex | 0.255052 | 0.593 |
R-HSA-9694676 | Translation of Replicase and Assembly of the Replication Transcription Complex | 0.301280 | 0.521 |
R-HSA-9772572 | Early SARS-CoV-2 Infection Events | 0.207101 | 0.684 |
R-HSA-8986944 | Transcriptional Regulation by MECP2 | 0.366122 | 0.436 |
R-HSA-381038 | XBP1(S) activates chaperone genes | 0.343125 | 0.465 |
R-HSA-381070 | IRE1alpha activates chaperones | 0.370686 | 0.431 |
R-HSA-1483257 | Phospholipid metabolism | 0.377013 | 0.424 |
R-HSA-1257604 | PIP3 activates AKT signaling | 0.377013 | 0.424 |
R-HSA-399719 | Trafficking of AMPA receptors | 0.377413 | 0.423 |
R-HSA-186763 | Downstream signal transduction | 0.377413 | 0.423 |
R-HSA-73887 | Death Receptor Signaling | 0.377663 | 0.423 |
R-HSA-5663202 | Diseases of signal transduction by growth factor receptors and second messengers | 0.379590 | 0.421 |
R-HSA-2219530 | Constitutive Signaling by Aberrant PI3K in Cancer | 0.384297 | 0.415 |
R-HSA-69190 | DNA strand elongation | 0.385346 | 0.414 |
R-HSA-9610379 | HCMV Late Events | 0.387995 | 0.411 |
R-HSA-162587 | HIV Life Cycle | 0.387995 | 0.411 |
R-HSA-9711097 | Cellular response to starvation | 0.391430 | 0.407 |
R-HSA-9668328 | Sealing of the nuclear envelope (NE) by ESCRT-III | 0.393177 | 0.405 |
R-HSA-1839124 | FGFR1 mutant receptor activation | 0.393177 | 0.405 |
R-HSA-5685938 | HDR through Single Strand Annealing (SSA) | 0.393177 | 0.405 |
R-HSA-354192 | Integrin signaling | 0.393177 | 0.405 |
R-HSA-399721 | Glutamate binding, activation of AMPA receptors and synaptic plasticity | 0.393177 | 0.405 |
R-HSA-1855204 | Synthesis of IP3 and IP4 in the cytosol | 0.393177 | 0.405 |
R-HSA-6811434 | COPI-dependent Golgi-to-ER retrograde traffic | 0.397781 | 0.400 |
R-HSA-74160 | Gene expression (Transcription) | 0.402874 | 0.395 |
R-HSA-9701190 | Defective homologous recombination repair (HRR) due to BRCA2 loss of function | 0.408544 | 0.389 |
R-HSA-1980145 | Signaling by NOTCH2 | 0.408544 | 0.389 |
R-HSA-9675136 | Diseases of DNA Double-Strand Break Repair | 0.408544 | 0.389 |
R-HSA-5696400 | Dual Incision in GG-NER | 0.408544 | 0.389 |
R-HSA-9680350 | Signaling by CSF1 (M-CSF) in myeloid cells | 0.408544 | 0.389 |
R-HSA-110328 | Recognition and association of DNA glycosylase with site containing an affected ... | 0.408544 | 0.389 |
R-HSA-5205647 | Mitophagy | 0.408544 | 0.389 |
R-HSA-1368108 | BMAL1:CLOCK,NPAS2 activates circadian expression | 0.408544 | 0.389 |
R-HSA-193704 | p75 NTR receptor-mediated signalling | 0.411128 | 0.386 |
R-HSA-983169 | Class I MHC mediated antigen processing & presentation | 0.413898 | 0.383 |
R-HSA-5610787 | Hedgehog 'off' state | 0.415545 | 0.381 |
R-HSA-5693616 | Presynaptic phase of homologous DNA pairing and strand exchange | 0.416081 | 0.381 |
R-HSA-917977 | Transferrin endocytosis and recycling | 0.416081 | 0.381 |
R-HSA-9860927 | Turbulent (oscillatory, disturbed) flow shear stress activates signaling by PIEZ... | 0.416081 | 0.381 |
R-HSA-2559585 | Oncogene Induced Senescence | 0.416081 | 0.381 |
R-HSA-212300 | PRC2 methylates histones and DNA | 0.423523 | 0.373 |
R-HSA-74158 | RNA Polymerase III Transcription | 0.423523 | 0.373 |
R-HSA-749476 | RNA Polymerase III Abortive And Retractive Initiation | 0.423523 | 0.373 |
R-HSA-9682385 | FLT3 signaling in disease | 0.423523 | 0.373 |
R-HSA-114604 | GPVI-mediated activation cascade | 0.423523 | 0.373 |
R-HSA-140877 | Formation of Fibrin Clot (Clotting Cascade) | 0.423523 | 0.373 |
R-HSA-422475 | Axon guidance | 0.437723 | 0.359 |
R-HSA-5693579 | Homologous DNA Pairing and Strand Exchange | 0.438125 | 0.358 |
R-HSA-74217 | Purine salvage | 0.438125 | 0.358 |
R-HSA-165054 | Rev-mediated nuclear export of HIV RNA | 0.438125 | 0.358 |
R-HSA-8875878 | MET promotes cell motility | 0.438125 | 0.358 |
R-HSA-159231 | Transport of Mature mRNA Derived from an Intronless Transcript | 0.445287 | 0.351 |
R-HSA-71336 | Pentose phosphate pathway | 0.445287 | 0.351 |
R-HSA-168276 | NS1 Mediated Effects on Host Pathways | 0.445287 | 0.351 |
R-HSA-201556 | Signaling by ALK | 0.445287 | 0.351 |
R-HSA-112315 | Transmission across Chemical Synapses | 0.447289 | 0.349 |
R-HSA-69239 | Synthesis of DNA | 0.450262 | 0.347 |
R-HSA-983231 | Factors involved in megakaryocyte development and platelet production | 0.452254 | 0.345 |
R-HSA-9678108 | SARS-CoV-1 Infection | 0.452254 | 0.345 |
R-HSA-202433 | Generation of second messenger molecules | 0.452358 | 0.345 |
R-HSA-159234 | Transport of Mature mRNAs Derived from Intronless Transcripts | 0.452358 | 0.345 |
R-HSA-451927 | Interleukin-2 family signaling | 0.452358 | 0.345 |
R-HSA-177243 | Interactions of Rev with host cellular proteins | 0.452358 | 0.345 |
R-HSA-9609646 | HCMV Infection | 0.454245 | 0.343 |
R-HSA-5625886 | Activated PKN1 stimulates transcription of AR (androgen receptor) regulated gene... | 0.459340 | 0.338 |
R-HSA-9607240 | FLT3 Signaling | 0.459340 | 0.338 |
R-HSA-8853884 | Transcriptional Regulation by VENTX | 0.459340 | 0.338 |
R-HSA-110313 | Translesion synthesis by Y family DNA polymerases bypasses lesions on DNA templa... | 0.459340 | 0.338 |
R-HSA-5610783 | Degradation of GLI2 by the proteasome | 0.466233 | 0.331 |
R-HSA-174417 | Telomere C-strand (Lagging Strand) Synthesis | 0.466233 | 0.331 |
R-HSA-5655302 | Signaling by FGFR1 in disease | 0.466233 | 0.331 |
R-HSA-1483249 | Inositol phosphate metabolism | 0.471364 | 0.327 |
R-HSA-73762 | RNA Polymerase I Transcription Initiation | 0.473038 | 0.325 |
R-HSA-165159 | MTOR signalling | 0.473038 | 0.325 |
R-HSA-110329 | Cleavage of the damaged pyrimidine | 0.473038 | 0.325 |
R-HSA-73928 | Depyrimidination | 0.473038 | 0.325 |
R-HSA-512988 | Interleukin-3, Interleukin-5 and GM-CSF signaling | 0.473038 | 0.325 |
R-HSA-9710421 | Defective pyroptosis | 0.479758 | 0.319 |
R-HSA-1433557 | Signaling by SCF-KIT | 0.479758 | 0.319 |
R-HSA-8854214 | TBC/RABGAPs | 0.479758 | 0.319 |
R-HSA-4420097 | VEGFA-VEGFR2 Pathway | 0.491976 | 0.308 |
R-HSA-9006925 | Intracellular signaling by second messengers | 0.493895 | 0.306 |
R-HSA-5653656 | Vesicle-mediated transport | 0.494182 | 0.306 |
R-HSA-373760 | L1CAM interactions | 0.496038 | 0.304 |
R-HSA-174084 | Autodegradation of Cdh1 by Cdh1:APC/C | 0.499408 | 0.302 |
R-HSA-72695 | Formation of the ternary complex, and subsequently, the 43S complex | 0.499408 | 0.302 |
R-HSA-9675135 | Diseases of DNA repair | 0.499408 | 0.302 |
R-HSA-2299718 | Condensation of Prophase Chromosomes | 0.499408 | 0.302 |
R-HSA-9839373 | Signaling by TGFBR3 | 0.499408 | 0.302 |
R-HSA-5357905 | Regulation of TNFR1 signaling | 0.499408 | 0.302 |
R-HSA-5617833 | Cilium Assembly | 0.500987 | 0.300 |
R-HSA-9711123 | Cellular response to chemical stress | 0.503854 | 0.298 |
R-HSA-2219528 | PI3K/AKT Signaling in Cancer | 0.504099 | 0.297 |
R-HSA-174154 | APC/C:Cdc20 mediated degradation of Securin | 0.505793 | 0.296 |
R-HSA-6811440 | Retrograde transport at the Trans-Golgi-Network | 0.505793 | 0.296 |
R-HSA-9675108 | Nervous system development | 0.508416 | 0.294 |
R-HSA-9694516 | SARS-CoV-2 Infection | 0.510714 | 0.292 |
R-HSA-9031628 | NGF-stimulated transcription | 0.512096 | 0.291 |
R-HSA-9759194 | Nuclear events mediated by NFE2L2 | 0.516035 | 0.287 |
R-HSA-73893 | DNA Damage Bypass | 0.518320 | 0.285 |
R-HSA-157858 | Gap junction trafficking and regulation | 0.518320 | 0.285 |
R-HSA-389661 | Glyoxylate metabolism and glycine degradation | 0.518320 | 0.285 |
R-HSA-73857 | RNA Polymerase II Transcription | 0.527745 | 0.278 |
R-HSA-912446 | Meiotic recombination | 0.530531 | 0.275 |
R-HSA-3371571 | HSF1-dependent transactivation | 0.530531 | 0.275 |
R-HSA-194138 | Signaling by VEGF | 0.535503 | 0.271 |
R-HSA-174184 | Cdc20:Phospho-APC/C mediated degradation of Cyclin A | 0.536520 | 0.270 |
R-HSA-72187 | mRNA 3'-end processing | 0.536520 | 0.270 |
R-HSA-73772 | RNA Polymerase I Promoter Escape | 0.536520 | 0.270 |
R-HSA-112382 | Formation of RNA Pol II elongation complex | 0.536520 | 0.270 |
R-HSA-9692916 | SARS-CoV-1 activates/modulates innate immune responses | 0.536520 | 0.270 |
R-HSA-9658195 | Leishmania infection | 0.538434 | 0.269 |
R-HSA-9824443 | Parasitic Infection Pathways | 0.538434 | 0.269 |
R-HSA-179419 | APC:Cdc20 mediated degradation of cell cycle proteins prior to satisfation of th... | 0.542434 | 0.266 |
R-HSA-5250924 | B-WICH complex positively regulates rRNA expression | 0.542434 | 0.266 |
R-HSA-75955 | RNA Polymerase II Transcription Elongation | 0.542434 | 0.266 |
R-HSA-445355 | Smooth Muscle Contraction | 0.542434 | 0.266 |
R-HSA-187037 | Signaling by NTRK1 (TRKA) | 0.546925 | 0.262 |
R-HSA-72649 | Translation initiation complex formation | 0.548272 | 0.261 |
R-HSA-69017 | CDK-mediated phosphorylation and removal of Cdc6 | 0.548272 | 0.261 |
R-HSA-9754678 | SARS-CoV-2 modulates host translation machinery | 0.548272 | 0.261 |
R-HSA-73929 | Base-Excision Repair, AP Site Formation | 0.548272 | 0.261 |
R-HSA-5357801 | Programmed Cell Death | 0.550450 | 0.259 |
R-HSA-176409 | APC/C:Cdc20 mediated degradation of mitotic proteins | 0.554036 | 0.256 |
R-HSA-6811436 | COPI-independent Golgi-to-ER retrograde traffic | 0.554036 | 0.256 |
R-HSA-5673001 | RAF/MAP kinase cascade | 0.559106 | 0.253 |
R-HSA-176814 | Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins | 0.559727 | 0.252 |
R-HSA-6782210 | Gap-filling DNA repair synthesis and ligation in TC-NER | 0.559727 | 0.252 |
R-HSA-72702 | Ribosomal scanning and start codon recognition | 0.559727 | 0.252 |
R-HSA-5578775 | Ion homeostasis | 0.559727 | 0.252 |
R-HSA-3299685 | Detoxification of Reactive Oxygen Species | 0.559727 | 0.252 |
R-HSA-75893 | TNF signaling | 0.559727 | 0.252 |
R-HSA-5576891 | Cardiac conduction | 0.561847 | 0.250 |
R-HSA-9006934 | Signaling by Receptor Tyrosine Kinases | 0.565437 | 0.248 |
R-HSA-72662 | Activation of the mRNA upon binding of the cap-binding complex and eIFs, and sub... | 0.570893 | 0.243 |
R-HSA-6782135 | Dual incision in TC-NER | 0.570893 | 0.243 |
R-HSA-397014 | Muscle contraction | 0.571169 | 0.243 |
R-HSA-6798695 | Neutrophil degranulation | 0.575242 | 0.240 |
R-HSA-194441 | Metabolism of non-coding RNA | 0.576370 | 0.239 |
R-HSA-191859 | snRNP Assembly | 0.576370 | 0.239 |
R-HSA-180786 | Extension of Telomeres | 0.576370 | 0.239 |
R-HSA-429914 | Deadenylation-dependent mRNA decay | 0.576370 | 0.239 |
R-HSA-5693565 | Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at... | 0.576370 | 0.239 |
R-HSA-5684996 | MAPK1/MAPK3 signaling | 0.576782 | 0.239 |
R-HSA-8943724 | Regulation of PTEN gene transcription | 0.581778 | 0.235 |
R-HSA-9764725 | Negative Regulation of CDH1 Gene Transcription | 0.581778 | 0.235 |
R-HSA-163685 | Integration of energy metabolism | 0.583570 | 0.234 |
R-HSA-73856 | RNA Polymerase II Transcription Termination | 0.587116 | 0.231 |
R-HSA-8956321 | Nucleotide salvage | 0.587116 | 0.231 |
R-HSA-5358351 | Signaling by Hedgehog | 0.590633 | 0.229 |
R-HSA-176408 | Regulation of APC/C activators between G1/S and early anaphase | 0.592387 | 0.227 |
R-HSA-6784531 | tRNA processing in the nucleus | 0.592387 | 0.227 |
R-HSA-2559586 | DNA Damage/Telomere Stress Induced Senescence | 0.592387 | 0.227 |
R-HSA-186797 | Signaling by PDGF | 0.592387 | 0.227 |
R-HSA-381119 | Unfolded Protein Response (UPR) | 0.594131 | 0.226 |
R-HSA-112316 | Neuronal System | 0.597428 | 0.224 |
R-HSA-2426168 | Activation of gene expression by SREBF (SREBP) | 0.597591 | 0.224 |
R-HSA-8848021 | Signaling by PTK6 | 0.597591 | 0.224 |
R-HSA-9006927 | Signaling by Non-Receptor Tyrosine Kinases | 0.597591 | 0.224 |
R-HSA-936837 | Ion transport by P-type ATPases | 0.602729 | 0.220 |
R-HSA-9679506 | SARS-CoV Infections | 0.607148 | 0.217 |
R-HSA-8856828 | Clathrin-mediated endocytosis | 0.611288 | 0.214 |
R-HSA-162906 | HIV Infection | 0.613539 | 0.212 |
R-HSA-5693606 | DNA Double Strand Break Response | 0.617754 | 0.209 |
R-HSA-453279 | Mitotic G1 phase and G1/S transition | 0.621316 | 0.207 |
R-HSA-9662360 | Sensory processing of sound by inner hair cells of the cochlea | 0.622635 | 0.206 |
R-HSA-3371497 | HSP90 chaperone cycle for steroid hormone receptors (SHR) in the presence of lig... | 0.622635 | 0.206 |
R-HSA-5218859 | Regulated Necrosis | 0.622635 | 0.206 |
R-HSA-166520 | Signaling by NTRKs | 0.627890 | 0.202 |
R-HSA-69202 | Cyclin E associated events during G1/S transition | 0.632213 | 0.199 |
R-HSA-1834949 | Cytosolic sensors of pathogen-associated DNA | 0.632213 | 0.199 |
R-HSA-1852241 | Organelle biogenesis and maintenance | 0.634231 | 0.198 |
R-HSA-9856651 | MITF-M-dependent gene expression | 0.634375 | 0.198 |
R-HSA-5250913 | Positive epigenetic regulation of rRNA expression | 0.636911 | 0.196 |
R-HSA-5632684 | Hedgehog 'on' state | 0.636911 | 0.196 |
R-HSA-3906995 | Diseases associated with O-glycosylation of proteins | 0.636911 | 0.196 |
R-HSA-9755511 | KEAP1-NFE2L2 pathway | 0.637585 | 0.195 |
R-HSA-212436 | Generic Transcription Pathway | 0.638081 | 0.195 |
R-HSA-74259 | Purine catabolism | 0.641549 | 0.193 |
R-HSA-198725 | Nuclear Events (kinase and transcription factor activation) | 0.641549 | 0.193 |
R-HSA-69306 | DNA Replication | 0.643938 | 0.191 |
R-HSA-1445148 | Translocation of SLC2A4 (GLUT4) to the plasma membrane | 0.646128 | 0.190 |
R-HSA-69052 | Switching of origins to a post-replicative state | 0.646128 | 0.190 |
R-HSA-1169410 | Antiviral mechanism by IFN-stimulated genes | 0.647082 | 0.189 |
R-HSA-157118 | Signaling by NOTCH | 0.647931 | 0.188 |
R-HSA-674695 | RNA Polymerase II Pre-transcription Events | 0.650649 | 0.187 |
R-HSA-1226099 | Signaling by FGFR in disease | 0.650649 | 0.187 |
R-HSA-9013694 | Signaling by NOTCH4 | 0.650649 | 0.187 |
R-HSA-1222556 | ROS and RNS production in phagocytes | 0.650649 | 0.187 |
R-HSA-6781827 | Transcription-Coupled Nucleotide Excision Repair (TC-NER) | 0.655112 | 0.184 |
R-HSA-71403 | Citric acid cycle (TCA cycle) | 0.655112 | 0.184 |
R-HSA-917937 | Iron uptake and transport | 0.655112 | 0.184 |
R-HSA-3000171 | Non-integrin membrane-ECM interactions | 0.655112 | 0.184 |
R-HSA-73854 | RNA Polymerase I Promoter Clearance | 0.659519 | 0.181 |
R-HSA-9694635 | Translation of Structural Proteins | 0.663869 | 0.178 |
R-HSA-9006936 | Signaling by TGFB family members | 0.665486 | 0.177 |
R-HSA-73864 | RNA Polymerase I Transcription | 0.668165 | 0.175 |
R-HSA-383280 | Nuclear Receptor transcription pathway | 0.668165 | 0.175 |
R-HSA-109581 | Apoptosis | 0.671448 | 0.173 |
R-HSA-9659379 | Sensory processing of sound | 0.672405 | 0.172 |
R-HSA-1655829 | Regulation of cholesterol biosynthesis by SREBP (SREBF) | 0.672405 | 0.172 |
R-HSA-421270 | Cell-cell junction organization | 0.675305 | 0.171 |
R-HSA-6806834 | Signaling by MET | 0.676592 | 0.170 |
R-HSA-2151201 | Transcriptional activation of mitochondrial biogenesis | 0.680725 | 0.167 |
R-HSA-2559582 | Senescence-Associated Secretory Phenotype (SASP) | 0.684806 | 0.164 |
R-HSA-72202 | Transport of Mature Transcript to Cytoplasm | 0.684806 | 0.164 |
R-HSA-9707564 | Cytoprotection by HMOX1 | 0.688835 | 0.162 |
R-HSA-5683057 | MAPK family signaling cascades | 0.692594 | 0.160 |
R-HSA-5696399 | Global Genome Nucleotide Excision Repair (GG-NER) | 0.692813 | 0.159 |
R-HSA-1500620 | Meiosis | 0.696740 | 0.157 |
R-HSA-8876198 | RAB GEFs exchange GTP for GDP on RABs | 0.700617 | 0.155 |
R-HSA-6807505 | RNA polymerase II transcribes snRNA genes | 0.704445 | 0.152 |
R-HSA-9764265 | Regulation of CDH1 Expression and Function | 0.705431 | 0.152 |
R-HSA-9764274 | Regulation of Expression and Function of Type I Classical Cadherins | 0.705431 | 0.152 |
R-HSA-9824446 | Viral Infection Pathways | 0.714336 | 0.146 |
R-HSA-76002 | Platelet activation, signaling and aggregation | 0.727419 | 0.138 |
R-HSA-9772573 | Late SARS-CoV-2 Infection Events | 0.729910 | 0.137 |
R-HSA-68867 | Assembly of the pre-replicative complex | 0.733365 | 0.135 |
R-HSA-446728 | Cell junction organization | 0.735785 | 0.133 |
R-HSA-9837999 | Mitochondrial protein degradation | 0.736776 | 0.133 |
R-HSA-72203 | Processing of Capped Intron-Containing Pre-mRNA | 0.737844 | 0.132 |
R-HSA-375276 | Peptide ligand-binding receptors | 0.738906 | 0.131 |
R-HSA-72689 | Formation of a pool of free 40S subunits | 0.743468 | 0.129 |
R-HSA-983712 | Ion channel transport | 0.746157 | 0.127 |
R-HSA-2730905 | Role of LAT2/NTAL/LAB on calcium mobilization | 0.746751 | 0.127 |
R-HSA-381340 | Transcriptional regulation of white adipocyte differentiation | 0.746751 | 0.127 |
R-HSA-6807878 | COPI-mediated anterograde transport | 0.746751 | 0.127 |
R-HSA-157579 | Telomere Maintenance | 0.749991 | 0.125 |
R-HSA-170834 | Signaling by TGF-beta Receptor Complex | 0.749991 | 0.125 |
R-HSA-8957275 | Post-translational protein phosphorylation | 0.753191 | 0.123 |
R-HSA-422356 | Regulation of insulin secretion | 0.753191 | 0.123 |
R-HSA-3214847 | HATs acetylate histones | 0.756349 | 0.121 |
R-HSA-192105 | Synthesis of bile acids and bile salts | 0.756349 | 0.121 |
R-HSA-72163 | mRNA Splicing - Major Pathway | 0.757859 | 0.120 |
R-HSA-9609690 | HCMV Early Events | 0.762409 | 0.118 |
R-HSA-9759476 | Regulation of Homotypic Cell-Cell Adhesion | 0.762409 | 0.118 |
R-HSA-8856825 | Cargo recognition for clathrin-mediated endocytosis | 0.771549 | 0.113 |
R-HSA-9860931 | Response of endothelial cells to shear stress | 0.771549 | 0.113 |
R-HSA-9833110 | RSV-host interactions | 0.774474 | 0.111 |
R-HSA-5696398 | Nucleotide Excision Repair | 0.777361 | 0.109 |
R-HSA-376176 | Signaling by ROBO receptors | 0.777755 | 0.109 |
R-HSA-1483206 | Glycerophospholipid biosynthesis | 0.777755 | 0.109 |
R-HSA-9692914 | SARS-CoV-1-host interactions | 0.780212 | 0.108 |
R-HSA-72172 | mRNA Splicing | 0.781979 | 0.107 |
R-HSA-72706 | GTP hydrolysis and joining of the 60S ribosomal subunit | 0.785804 | 0.105 |
R-HSA-156827 | L13a-mediated translational silencing of Ceruloplasmin expression | 0.785804 | 0.105 |
R-HSA-1236975 | Antigen processing-Cross presentation | 0.785804 | 0.105 |
R-HSA-2672351 | Stimuli-sensing channels | 0.785804 | 0.105 |
R-HSA-69002 | DNA Replication Pre-Initiation | 0.788548 | 0.103 |
R-HSA-202403 | TCR signaling | 0.791256 | 0.102 |
R-HSA-194068 | Bile acid and bile salt metabolism | 0.791256 | 0.102 |
R-HSA-9730414 | MITF-M-regulated melanocyte development | 0.800127 | 0.097 |
R-HSA-381426 | Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-l... | 0.804287 | 0.095 |
R-HSA-1500931 | Cell-Cell communication | 0.805469 | 0.094 |
R-HSA-5628897 | TP53 Regulates Metabolic Genes | 0.806795 | 0.093 |
R-HSA-2029485 | Role of phospholipids in phagocytosis | 0.809270 | 0.092 |
R-HSA-418990 | Adherens junctions interactions | 0.809623 | 0.092 |
R-HSA-72737 | Cap-dependent Translation Initiation | 0.811714 | 0.091 |
R-HSA-72613 | Eukaryotic Translation Initiation | 0.811714 | 0.091 |
R-HSA-9007101 | Rab regulation of trafficking | 0.814127 | 0.089 |
R-HSA-1592230 | Mitochondrial biogenesis | 0.814127 | 0.089 |
R-HSA-8951664 | Neddylation | 0.815127 | 0.089 |
R-HSA-68875 | Mitotic Prophase | 0.821182 | 0.086 |
R-HSA-3371556 | Cellular response to heat stress | 0.823474 | 0.084 |
R-HSA-9705683 | SARS-CoV-2-host interactions | 0.827422 | 0.082 |
R-HSA-9816359 | Maternal to zygotic transition (MZT) | 0.827971 | 0.082 |
R-HSA-2132295 | MHC class II antigen presentation | 0.827971 | 0.082 |
R-HSA-6809371 | Formation of the cornified envelope | 0.830176 | 0.081 |
R-HSA-162909 | Host Interactions of HIV factors | 0.830176 | 0.081 |
R-HSA-69206 | G1/S Transition | 0.834503 | 0.079 |
R-HSA-3247509 | Chromatin modifying enzymes | 0.837372 | 0.077 |
R-HSA-69481 | G2/M Checkpoints | 0.838720 | 0.076 |
R-HSA-8956319 | Nucleotide catabolism | 0.842830 | 0.074 |
R-HSA-1474165 | Reproduction | 0.846836 | 0.072 |
R-HSA-9843745 | Adipogenesis | 0.848801 | 0.071 |
R-HSA-1474228 | Degradation of the extracellular matrix | 0.850740 | 0.070 |
R-HSA-4839726 | Chromatin organization | 0.860024 | 0.065 |
R-HSA-9018519 | Estrogen-dependent gene expression | 0.860073 | 0.065 |
R-HSA-9820952 | Respiratory Syncytial Virus Infection Pathway | 0.861868 | 0.065 |
R-HSA-1643685 | Disease | 0.864667 | 0.063 |
R-HSA-6807070 | PTEN Regulation | 0.865391 | 0.063 |
R-HSA-199977 | ER to Golgi Anterograde Transport | 0.880169 | 0.055 |
R-HSA-9679191 | Potential therapeutics for SARS | 0.884727 | 0.053 |
R-HSA-1989781 | PPARA activates gene expression | 0.891944 | 0.050 |
R-HSA-5663205 | Infectious disease | 0.892302 | 0.049 |
R-HSA-400206 | Regulation of lipid metabolism by PPARalpha | 0.894703 | 0.048 |
R-HSA-373076 | Class A/1 (Rhodopsin-like receptors) | 0.902057 | 0.045 |
R-HSA-6791226 | Major pathway of rRNA processing in the nucleolus and cytosol | 0.912149 | 0.040 |
R-HSA-72306 | tRNA processing | 0.912149 | 0.040 |
R-HSA-418594 | G alpha (i) signalling events | 0.912992 | 0.040 |
R-HSA-418555 | G alpha (s) signalling events | 0.913279 | 0.039 |
R-HSA-5689880 | Ub-specific processing proteases | 0.915495 | 0.038 |
R-HSA-168255 | Influenza Infection | 0.921812 | 0.035 |
R-HSA-8953854 | Metabolism of RNA | 0.924897 | 0.034 |
R-HSA-3781865 | Diseases of glycosylation | 0.926716 | 0.033 |
R-HSA-8868773 | rRNA processing in the nucleus and cytosol | 0.930418 | 0.031 |
R-HSA-168249 | Innate Immune System | 0.933053 | 0.030 |
R-HSA-8957322 | Metabolism of steroids | 0.935700 | 0.029 |
R-HSA-1474244 | Extracellular matrix organization | 0.940326 | 0.027 |
R-HSA-948021 | Transport to the Golgi and subsequent modification | 0.941968 | 0.026 |
R-HSA-2454202 | Fc epsilon receptor (FCERI) signaling | 0.942716 | 0.026 |
R-HSA-388396 | GPCR downstream signalling | 0.943521 | 0.025 |
R-HSA-6805567 | Keratinization | 0.945612 | 0.024 |
R-HSA-109582 | Hemostasis | 0.947692 | 0.023 |
R-HSA-3700989 | Transcriptional Regulation by TP53 | 0.949501 | 0.023 |
R-HSA-9748784 | Drug ADME | 0.953457 | 0.021 |
R-HSA-72312 | rRNA processing | 0.961196 | 0.017 |
R-HSA-15869 | Metabolism of nucleotides | 0.963162 | 0.016 |
R-HSA-8939211 | ESR-mediated signaling | 0.963638 | 0.016 |
R-HSA-1280218 | Adaptive Immune System | 0.966244 | 0.015 |
R-HSA-913531 | Interferon Signaling | 0.966406 | 0.015 |
R-HSA-372790 | Signaling by GPCR | 0.970680 | 0.013 |
R-HSA-5688426 | Deubiquitination | 0.971228 | 0.013 |
R-HSA-416476 | G alpha (q) signalling events | 0.974409 | 0.011 |
R-HSA-5668914 | Diseases of metabolism | 0.979381 | 0.009 |
R-HSA-500792 | GPCR ligand binding | 0.985319 | 0.006 |
R-HSA-1428517 | Aerobic respiration and respiratory electron transport | 0.990634 | 0.004 |
R-HSA-9006931 | Signaling by Nuclear Receptors | 0.992979 | 0.003 |
R-HSA-1266738 | Developmental Biology | 0.996145 | 0.002 |
R-HSA-446203 | Asparagine N-linked glycosylation | 0.996806 | 0.001 |
R-HSA-72766 | Translation | 0.997087 | 0.001 |
R-HSA-71291 | Metabolism of amino acids and derivatives | 0.997731 | 0.001 |
R-HSA-449147 | Signaling by Interleukins | 0.997912 | 0.001 |
R-HSA-71387 | Metabolism of carbohydrates and carbohydrate derivatives | 0.997932 | 0.001 |
R-HSA-168256 | Immune System | 0.999295 | 0.000 |
R-HSA-1280215 | Cytokine Signaling in Immune system | 0.999656 | 0.000 |
R-HSA-556833 | Metabolism of lipids | 0.999739 | 0.000 |
R-HSA-382551 | Transport of small molecules | 0.999808 | 0.000 |
R-HSA-597592 | Post-translational protein modification | 0.999841 | 0.000 |
R-HSA-392499 | Metabolism of proteins | 0.999999 | 0.000 |
R-HSA-9709957 | Sensory Perception | 1.000000 | 0.000 |
R-HSA-1430728 | Metabolism | 1.000000 | 0.000 |
Download
kinase | JSD_mean | pearson_surrounding | kinase_max_IC_position | max_position_JSD |
---|---|---|---|---|
CDC7 |
0.882 | 0.249 | 1 | 0.890 |
COT |
0.877 | 0.067 | 2 | 0.765 |
PIM3 |
0.875 | 0.192 | -3 | 0.840 |
CLK3 |
0.875 | 0.236 | 1 | 0.796 |
MOS |
0.872 | 0.174 | 1 | 0.884 |
NDR2 |
0.868 | 0.104 | -3 | 0.832 |
PRKD1 |
0.867 | 0.210 | -3 | 0.827 |
RSK2 |
0.867 | 0.185 | -3 | 0.785 |
HIPK4 |
0.867 | 0.210 | 1 | 0.732 |
PRPK |
0.866 | -0.059 | -1 | 0.860 |
CAMK1B |
0.865 | 0.091 | -3 | 0.862 |
SRPK1 |
0.864 | 0.194 | -3 | 0.777 |
NLK |
0.864 | 0.063 | 1 | 0.801 |
IKKB |
0.863 | -0.046 | -2 | 0.766 |
RAF1 |
0.862 | -0.016 | 1 | 0.834 |
CDKL1 |
0.862 | 0.107 | -3 | 0.828 |
P90RSK |
0.862 | 0.147 | -3 | 0.790 |
PIM1 |
0.861 | 0.172 | -3 | 0.791 |
MTOR |
0.861 | -0.058 | 1 | 0.774 |
TBK1 |
0.861 | -0.057 | 1 | 0.729 |
PRKD2 |
0.861 | 0.173 | -3 | 0.773 |
GRK1 |
0.860 | 0.103 | -2 | 0.791 |
CDKL5 |
0.859 | 0.118 | -3 | 0.821 |
ERK5 |
0.859 | 0.035 | 1 | 0.771 |
ATR |
0.859 | 0.002 | 1 | 0.769 |
DAPK2 |
0.859 | 0.159 | -3 | 0.864 |
NDR1 |
0.859 | 0.064 | -3 | 0.826 |
DSTYK |
0.859 | -0.041 | 2 | 0.778 |
IKKE |
0.859 | -0.062 | 1 | 0.727 |
PKN3 |
0.859 | 0.054 | -3 | 0.826 |
SKMLCK |
0.858 | 0.107 | -2 | 0.903 |
RSK3 |
0.858 | 0.123 | -3 | 0.777 |
BMPR2 |
0.858 | -0.093 | -2 | 0.898 |
CAMK2G |
0.858 | -0.071 | 2 | 0.735 |
CAMLCK |
0.858 | 0.104 | -2 | 0.901 |
PDHK4 |
0.857 | -0.226 | 1 | 0.832 |
GCN2 |
0.857 | -0.176 | 2 | 0.724 |
BMPR1B |
0.857 | 0.226 | 1 | 0.881 |
CHAK2 |
0.857 | 0.086 | -1 | 0.818 |
AURC |
0.856 | 0.159 | -2 | 0.726 |
KIS |
0.856 | 0.088 | 1 | 0.658 |
GRK5 |
0.855 | -0.037 | -3 | 0.851 |
ULK2 |
0.855 | -0.154 | 2 | 0.720 |
LATS2 |
0.855 | 0.061 | -5 | 0.784 |
ICK |
0.855 | 0.118 | -3 | 0.855 |
MAPKAPK2 |
0.855 | 0.135 | -3 | 0.744 |
NUAK2 |
0.855 | 0.064 | -3 | 0.831 |
P70S6KB |
0.855 | 0.106 | -3 | 0.800 |
AMPKA1 |
0.855 | 0.098 | -3 | 0.837 |
TGFBR2 |
0.855 | 0.009 | -2 | 0.800 |
NIK |
0.855 | 0.023 | -3 | 0.867 |
SRPK2 |
0.855 | 0.170 | -3 | 0.708 |
NEK6 |
0.854 | -0.020 | -2 | 0.867 |
MAPKAPK3 |
0.854 | 0.095 | -3 | 0.776 |
GRK6 |
0.854 | 0.040 | 1 | 0.859 |
PDHK1 |
0.854 | -0.167 | 1 | 0.808 |
TSSK2 |
0.853 | 0.098 | -5 | 0.846 |
PKACG |
0.853 | 0.095 | -2 | 0.804 |
RSK4 |
0.853 | 0.178 | -3 | 0.757 |
CAMK2D |
0.852 | 0.024 | -3 | 0.838 |
MARK4 |
0.852 | 0.018 | 4 | 0.846 |
PKN2 |
0.852 | 0.045 | -3 | 0.824 |
SRPK3 |
0.851 | 0.162 | -3 | 0.757 |
MST4 |
0.851 | 0.009 | 2 | 0.761 |
AMPKA2 |
0.851 | 0.108 | -3 | 0.808 |
LATS1 |
0.850 | 0.152 | -3 | 0.839 |
WNK1 |
0.850 | -0.031 | -2 | 0.902 |
IKKA |
0.850 | -0.020 | -2 | 0.749 |
NEK7 |
0.849 | -0.134 | -3 | 0.860 |
TGFBR1 |
0.849 | 0.106 | -2 | 0.805 |
CLK2 |
0.849 | 0.223 | -3 | 0.757 |
TSSK1 |
0.849 | 0.092 | -3 | 0.850 |
DYRK2 |
0.849 | 0.094 | 1 | 0.660 |
RIPK3 |
0.848 | -0.105 | 3 | 0.764 |
ALK4 |
0.848 | 0.086 | -2 | 0.837 |
CAMK2A |
0.848 | 0.094 | 2 | 0.710 |
PKCD |
0.848 | 0.043 | 2 | 0.706 |
MLK1 |
0.848 | -0.129 | 2 | 0.718 |
CAMK2B |
0.848 | 0.063 | 2 | 0.698 |
FAM20C |
0.847 | 0.041 | 2 | 0.560 |
HUNK |
0.847 | -0.128 | 2 | 0.708 |
PIM2 |
0.846 | 0.172 | -3 | 0.759 |
PKACB |
0.846 | 0.154 | -2 | 0.742 |
CDK8 |
0.846 | 0.022 | 1 | 0.640 |
MSK1 |
0.846 | 0.124 | -3 | 0.762 |
PRKD3 |
0.846 | 0.111 | -3 | 0.753 |
MSK2 |
0.846 | 0.064 | -3 | 0.768 |
CLK4 |
0.845 | 0.136 | -3 | 0.773 |
ULK1 |
0.845 | -0.192 | -3 | 0.822 |
PLK1 |
0.845 | 0.002 | -2 | 0.818 |
BCKDK |
0.845 | -0.172 | -1 | 0.784 |
MASTL |
0.845 | -0.203 | -2 | 0.840 |
GRK7 |
0.844 | 0.101 | 1 | 0.784 |
AURB |
0.844 | 0.114 | -2 | 0.724 |
ACVR2B |
0.844 | 0.124 | -2 | 0.804 |
PAK1 |
0.844 | 0.041 | -2 | 0.842 |
CDK19 |
0.843 | 0.039 | 1 | 0.604 |
CLK1 |
0.843 | 0.144 | -3 | 0.749 |
HIPK2 |
0.843 | 0.138 | 1 | 0.581 |
ACVR2A |
0.843 | 0.098 | -2 | 0.791 |
DLK |
0.843 | -0.126 | 1 | 0.818 |
NIM1 |
0.843 | -0.064 | 3 | 0.811 |
CAMK4 |
0.842 | -0.016 | -3 | 0.806 |
QSK |
0.842 | 0.071 | 4 | 0.827 |
HIPK1 |
0.842 | 0.139 | 1 | 0.677 |
WNK3 |
0.842 | -0.227 | 1 | 0.771 |
NEK9 |
0.842 | -0.149 | 2 | 0.749 |
GRK4 |
0.841 | -0.130 | -2 | 0.826 |
PAK3 |
0.841 | 0.010 | -2 | 0.843 |
AURA |
0.841 | 0.102 | -2 | 0.694 |
PKG2 |
0.841 | 0.111 | -2 | 0.744 |
CDK7 |
0.841 | 0.033 | 1 | 0.656 |
PRKX |
0.841 | 0.170 | -3 | 0.674 |
MLK2 |
0.840 | -0.117 | 2 | 0.745 |
MELK |
0.840 | 0.015 | -3 | 0.794 |
ATM |
0.840 | -0.065 | 1 | 0.710 |
AKT2 |
0.840 | 0.132 | -3 | 0.706 |
SGK3 |
0.840 | 0.110 | -3 | 0.758 |
BRSK1 |
0.840 | 0.036 | -3 | 0.786 |
IRE1 |
0.840 | -0.073 | 1 | 0.723 |
ANKRD3 |
0.839 | -0.165 | 1 | 0.816 |
MYLK4 |
0.839 | 0.080 | -2 | 0.832 |
JNK2 |
0.839 | 0.068 | 1 | 0.608 |
ALK2 |
0.839 | 0.068 | -2 | 0.813 |
CDK13 |
0.839 | 0.027 | 1 | 0.629 |
RIPK1 |
0.839 | -0.180 | 1 | 0.765 |
MLK3 |
0.839 | -0.063 | 2 | 0.659 |
JNK3 |
0.838 | 0.044 | 1 | 0.637 |
BMPR1A |
0.838 | 0.159 | 1 | 0.861 |
PKCA |
0.838 | 0.033 | 2 | 0.651 |
MEK1 |
0.838 | -0.090 | 2 | 0.771 |
CDK5 |
0.838 | 0.056 | 1 | 0.669 |
IRE2 |
0.837 | -0.029 | 2 | 0.687 |
DYRK1A |
0.837 | 0.104 | 1 | 0.698 |
PAK2 |
0.837 | 0.015 | -2 | 0.826 |
PKCB |
0.837 | 0.004 | 2 | 0.652 |
PKCG |
0.837 | -0.001 | 2 | 0.654 |
PAK6 |
0.837 | 0.059 | -2 | 0.773 |
CDK1 |
0.837 | 0.049 | 1 | 0.628 |
TTBK2 |
0.837 | -0.195 | 2 | 0.643 |
HIPK3 |
0.836 | 0.110 | 1 | 0.671 |
NUAK1 |
0.836 | 0.003 | -3 | 0.785 |
MNK1 |
0.836 | 0.038 | -2 | 0.859 |
QIK |
0.836 | -0.052 | -3 | 0.827 |
SIK |
0.836 | 0.038 | -3 | 0.763 |
PKR |
0.836 | -0.060 | 1 | 0.782 |
CDK18 |
0.836 | 0.052 | 1 | 0.587 |
VRK2 |
0.836 | -0.152 | 1 | 0.819 |
PHKG1 |
0.836 | -0.022 | -3 | 0.814 |
MNK2 |
0.835 | -0.000 | -2 | 0.848 |
CHAK1 |
0.835 | -0.053 | 2 | 0.752 |
MARK3 |
0.835 | 0.044 | 4 | 0.781 |
NEK2 |
0.835 | -0.058 | 2 | 0.750 |
DRAK1 |
0.834 | 0.029 | 1 | 0.829 |
YSK4 |
0.834 | -0.110 | 1 | 0.765 |
P38A |
0.834 | 0.035 | 1 | 0.675 |
PLK3 |
0.834 | -0.069 | 2 | 0.693 |
GRK2 |
0.834 | 0.023 | -2 | 0.715 |
P38B |
0.833 | 0.052 | 1 | 0.612 |
MARK2 |
0.833 | 0.012 | 4 | 0.753 |
MLK4 |
0.832 | -0.090 | 2 | 0.644 |
PKCH |
0.832 | -0.019 | 2 | 0.642 |
CDK12 |
0.832 | 0.026 | 1 | 0.602 |
CHK1 |
0.832 | 0.015 | -3 | 0.801 |
BRSK2 |
0.832 | -0.039 | -3 | 0.802 |
DNAPK |
0.832 | -0.029 | 1 | 0.652 |
DYRK4 |
0.832 | 0.073 | 1 | 0.600 |
CDK9 |
0.832 | 0.004 | 1 | 0.634 |
P70S6K |
0.832 | 0.090 | -3 | 0.723 |
ERK1 |
0.831 | 0.026 | 1 | 0.603 |
PKACA |
0.831 | 0.129 | -2 | 0.697 |
DYRK1B |
0.831 | 0.087 | 1 | 0.630 |
PASK |
0.831 | 0.107 | -3 | 0.857 |
PKCZ |
0.830 | -0.045 | 2 | 0.709 |
SSTK |
0.830 | 0.056 | 4 | 0.807 |
TLK2 |
0.830 | -0.088 | 1 | 0.736 |
P38G |
0.830 | 0.033 | 1 | 0.539 |
DCAMKL1 |
0.830 | 0.022 | -3 | 0.771 |
SNRK |
0.830 | -0.123 | 2 | 0.655 |
SMG1 |
0.829 | -0.083 | 1 | 0.708 |
CDK14 |
0.829 | 0.057 | 1 | 0.632 |
DYRK3 |
0.829 | 0.103 | 1 | 0.672 |
CDK17 |
0.828 | 0.022 | 1 | 0.543 |
MPSK1 |
0.828 | 0.102 | 1 | 0.736 |
CAMK1G |
0.828 | 0.006 | -3 | 0.773 |
CK2A2 |
0.828 | 0.158 | 1 | 0.819 |
BRAF |
0.827 | -0.081 | -4 | 0.829 |
AKT1 |
0.827 | 0.116 | -3 | 0.714 |
SMMLCK |
0.827 | 0.059 | -3 | 0.824 |
DAPK3 |
0.827 | 0.131 | -3 | 0.797 |
MARK1 |
0.827 | -0.011 | 4 | 0.795 |
MAPKAPK5 |
0.826 | -0.049 | -3 | 0.740 |
CDK10 |
0.826 | 0.091 | 1 | 0.618 |
ERK2 |
0.826 | -0.026 | 1 | 0.645 |
CK1E |
0.826 | -0.000 | -3 | 0.561 |
P38D |
0.826 | 0.067 | 1 | 0.537 |
PRP4 |
0.825 | -0.019 | -3 | 0.717 |
PLK4 |
0.824 | -0.150 | 2 | 0.598 |
PERK |
0.824 | -0.145 | -2 | 0.840 |
CAMK1D |
0.824 | 0.070 | -3 | 0.697 |
CDK3 |
0.824 | 0.042 | 1 | 0.563 |
DAPK1 |
0.823 | 0.133 | -3 | 0.785 |
PINK1 |
0.823 | -0.101 | 1 | 0.768 |
MST3 |
0.823 | -0.014 | 2 | 0.745 |
MEK5 |
0.823 | -0.224 | 2 | 0.751 |
WNK4 |
0.822 | -0.116 | -2 | 0.892 |
MEKK1 |
0.822 | -0.176 | 1 | 0.763 |
GSK3B |
0.822 | 0.030 | 4 | 0.518 |
TLK1 |
0.822 | -0.112 | -2 | 0.831 |
ZAK |
0.822 | -0.162 | 1 | 0.755 |
HRI |
0.822 | -0.176 | -2 | 0.860 |
GRK3 |
0.822 | 0.014 | -2 | 0.664 |
CDK16 |
0.821 | 0.040 | 1 | 0.557 |
NEK5 |
0.821 | -0.117 | 1 | 0.772 |
PKCT |
0.821 | -0.011 | 2 | 0.654 |
CDK2 |
0.821 | -0.054 | 1 | 0.706 |
SGK1 |
0.821 | 0.139 | -3 | 0.634 |
MAK |
0.821 | 0.162 | -2 | 0.788 |
CK1D |
0.820 | 0.017 | -3 | 0.515 |
DCAMKL2 |
0.820 | -0.040 | -3 | 0.795 |
AKT3 |
0.820 | 0.134 | -3 | 0.652 |
GSK3A |
0.820 | 0.049 | 4 | 0.523 |
MEKK3 |
0.820 | -0.211 | 1 | 0.783 |
PHKG2 |
0.819 | -0.036 | -3 | 0.776 |
CK2A1 |
0.819 | 0.145 | 1 | 0.806 |
MEKK2 |
0.819 | -0.168 | 2 | 0.725 |
IRAK4 |
0.819 | -0.130 | 1 | 0.726 |
TAO3 |
0.818 | -0.053 | 1 | 0.774 |
PKCI |
0.818 | -0.004 | 2 | 0.676 |
GAK |
0.817 | 0.013 | 1 | 0.828 |
BUB1 |
0.817 | 0.185 | -5 | 0.821 |
ERK7 |
0.817 | 0.009 | 2 | 0.503 |
PKCE |
0.816 | 0.045 | 2 | 0.641 |
CK1A2 |
0.816 | 0.004 | -3 | 0.514 |
LKB1 |
0.816 | 0.003 | -3 | 0.817 |
PDK1 |
0.816 | -0.042 | 1 | 0.764 |
JNK1 |
0.816 | 0.020 | 1 | 0.604 |
CK1G1 |
0.815 | -0.044 | -3 | 0.556 |
CAMKK1 |
0.815 | -0.122 | -2 | 0.785 |
PAK5 |
0.815 | 0.018 | -2 | 0.708 |
MOK |
0.815 | 0.139 | 1 | 0.678 |
PKN1 |
0.814 | 0.039 | -3 | 0.732 |
EEF2K |
0.814 | 0.010 | 3 | 0.888 |
GCK |
0.814 | 0.030 | 1 | 0.804 |
PAK4 |
0.813 | 0.023 | -2 | 0.715 |
NEK8 |
0.813 | -0.159 | 2 | 0.740 |
TAO2 |
0.812 | -0.087 | 2 | 0.766 |
CHK2 |
0.812 | 0.073 | -3 | 0.649 |
CDK6 |
0.812 | 0.043 | 1 | 0.607 |
CAMKK2 |
0.812 | -0.089 | -2 | 0.788 |
TNIK |
0.812 | 0.044 | 3 | 0.908 |
MINK |
0.812 | 0.011 | 1 | 0.769 |
MRCKA |
0.812 | 0.092 | -3 | 0.753 |
HGK |
0.811 | 0.010 | 3 | 0.907 |
CDK4 |
0.811 | 0.038 | 1 | 0.587 |
NEK11 |
0.811 | -0.179 | 1 | 0.779 |
ROCK2 |
0.811 | 0.103 | -3 | 0.776 |
MRCKB |
0.811 | 0.089 | -3 | 0.738 |
HPK1 |
0.810 | 0.038 | 1 | 0.789 |
CAMK1A |
0.810 | 0.068 | -3 | 0.671 |
NEK4 |
0.810 | -0.090 | 1 | 0.744 |
PLK2 |
0.809 | -0.044 | -3 | 0.776 |
IRAK1 |
0.809 | -0.252 | -1 | 0.733 |
TTBK1 |
0.809 | -0.211 | 2 | 0.570 |
MEKK6 |
0.808 | -0.095 | 1 | 0.758 |
PBK |
0.808 | 0.069 | 1 | 0.743 |
SBK |
0.808 | 0.093 | -3 | 0.599 |
KHS1 |
0.808 | 0.074 | 1 | 0.760 |
MST2 |
0.808 | -0.109 | 1 | 0.794 |
TAK1 |
0.807 | -0.094 | 1 | 0.800 |
MAP3K15 |
0.807 | -0.100 | 1 | 0.737 |
NEK1 |
0.806 | -0.060 | 1 | 0.748 |
KHS2 |
0.806 | 0.087 | 1 | 0.780 |
LOK |
0.806 | -0.035 | -2 | 0.812 |
LRRK2 |
0.805 | -0.125 | 2 | 0.774 |
DMPK1 |
0.804 | 0.124 | -3 | 0.758 |
CRIK |
0.802 | 0.137 | -3 | 0.725 |
VRK1 |
0.802 | -0.188 | 2 | 0.755 |
PDHK3_TYR |
0.802 | 0.221 | 4 | 0.903 |
MEK2 |
0.801 | -0.183 | 2 | 0.755 |
MST1 |
0.800 | -0.110 | 1 | 0.768 |
STK33 |
0.798 | -0.169 | 2 | 0.565 |
SLK |
0.798 | -0.087 | -2 | 0.742 |
YSK1 |
0.797 | -0.092 | 2 | 0.727 |
PKG1 |
0.797 | 0.042 | -2 | 0.667 |
RIPK2 |
0.796 | -0.252 | 1 | 0.713 |
ROCK1 |
0.796 | 0.074 | -3 | 0.746 |
MAP2K4_TYR |
0.794 | 0.093 | -1 | 0.872 |
TESK1_TYR |
0.792 | 0.041 | 3 | 0.915 |
MAP2K6_TYR |
0.791 | 0.034 | -1 | 0.875 |
OSR1 |
0.791 | -0.073 | 2 | 0.728 |
PDHK4_TYR |
0.790 | 0.042 | 2 | 0.801 |
NEK3 |
0.790 | -0.148 | 1 | 0.706 |
TTK |
0.790 | -0.061 | -2 | 0.822 |
HASPIN |
0.790 | -0.019 | -1 | 0.679 |
BIKE |
0.790 | 0.032 | 1 | 0.710 |
LIMK2_TYR |
0.789 | 0.096 | -3 | 0.876 |
PKMYT1_TYR |
0.789 | -0.003 | 3 | 0.882 |
BMPR2_TYR |
0.788 | 0.021 | -1 | 0.860 |
PDHK1_TYR |
0.788 | 0.016 | -1 | 0.882 |
MYO3B |
0.787 | -0.027 | 2 | 0.762 |
MAP2K7_TYR |
0.787 | -0.166 | 2 | 0.785 |
ASK1 |
0.787 | -0.135 | 1 | 0.729 |
CK1A |
0.787 | 0.006 | -3 | 0.427 |
EPHA6 |
0.787 | 0.047 | -1 | 0.859 |
YANK3 |
0.787 | -0.072 | 2 | 0.366 |
PINK1_TYR |
0.785 | -0.114 | 1 | 0.811 |
ALPHAK3 |
0.785 | -0.068 | -1 | 0.781 |
TXK |
0.783 | 0.137 | 1 | 0.879 |
EPHB4 |
0.783 | 0.007 | -1 | 0.839 |
MYO3A |
0.783 | -0.074 | 1 | 0.738 |
TAO1 |
0.779 | -0.115 | 1 | 0.694 |
RET |
0.779 | -0.103 | 1 | 0.755 |
ROS1 |
0.779 | -0.029 | 3 | 0.810 |
LIMK1_TYR |
0.778 | -0.127 | 2 | 0.788 |
ABL2 |
0.778 | 0.001 | -1 | 0.818 |
TYRO3 |
0.778 | -0.092 | 3 | 0.839 |
AAK1 |
0.777 | 0.083 | 1 | 0.609 |
TYK2 |
0.777 | -0.126 | 1 | 0.751 |
FGR |
0.776 | -0.009 | 1 | 0.831 |
INSRR |
0.776 | -0.037 | 3 | 0.775 |
MST1R |
0.775 | -0.136 | 3 | 0.845 |
YES1 |
0.775 | -0.039 | -1 | 0.849 |
FER |
0.775 | -0.065 | 1 | 0.859 |
CSF1R |
0.775 | -0.087 | 3 | 0.818 |
LCK |
0.774 | 0.047 | -1 | 0.840 |
JAK2 |
0.774 | -0.122 | 1 | 0.748 |
EPHA4 |
0.773 | -0.035 | 2 | 0.689 |
HCK |
0.773 | -0.038 | -1 | 0.836 |
ABL1 |
0.772 | -0.038 | -1 | 0.807 |
EPHB1 |
0.772 | -0.038 | 1 | 0.841 |
SRMS |
0.772 | -0.047 | 1 | 0.858 |
BLK |
0.772 | 0.048 | -1 | 0.840 |
ITK |
0.772 | -0.025 | -1 | 0.802 |
TNK2 |
0.772 | -0.022 | 3 | 0.770 |
JAK3 |
0.772 | -0.105 | 1 | 0.751 |
DDR1 |
0.772 | -0.171 | 4 | 0.817 |
EPHB3 |
0.770 | -0.056 | -1 | 0.825 |
NEK10_TYR |
0.770 | -0.023 | 1 | 0.664 |
STLK3 |
0.770 | -0.212 | 1 | 0.717 |
EPHB2 |
0.770 | -0.042 | -1 | 0.815 |
JAK1 |
0.768 | 0.010 | 1 | 0.709 |
BMX |
0.768 | -0.007 | -1 | 0.734 |
MERTK |
0.768 | -0.058 | 3 | 0.795 |
TNNI3K_TYR |
0.767 | -0.014 | 1 | 0.735 |
PDGFRB |
0.766 | -0.155 | 3 | 0.835 |
KIT |
0.765 | -0.138 | 3 | 0.819 |
TEC |
0.765 | -0.047 | -1 | 0.739 |
FGFR2 |
0.764 | -0.188 | 3 | 0.805 |
TNK1 |
0.764 | -0.088 | 3 | 0.818 |
AXL |
0.764 | -0.118 | 3 | 0.797 |
FLT3 |
0.764 | -0.156 | 3 | 0.833 |
ALK |
0.763 | -0.085 | 3 | 0.746 |
EPHA7 |
0.763 | -0.058 | 2 | 0.695 |
FYN |
0.762 | -0.016 | -1 | 0.822 |
KDR |
0.761 | -0.150 | 3 | 0.769 |
PTK6 |
0.761 | -0.138 | -1 | 0.749 |
TEK |
0.761 | -0.178 | 3 | 0.764 |
BTK |
0.760 | -0.163 | -1 | 0.767 |
PDGFRA |
0.760 | -0.184 | 3 | 0.831 |
LTK |
0.760 | -0.122 | 3 | 0.761 |
FGFR1 |
0.760 | -0.195 | 3 | 0.789 |
PTK2B |
0.760 | -0.016 | -1 | 0.771 |
MET |
0.759 | -0.132 | 3 | 0.809 |
WEE1_TYR |
0.759 | -0.090 | -1 | 0.747 |
NTRK1 |
0.758 | -0.186 | -1 | 0.826 |
EPHA3 |
0.758 | -0.133 | 2 | 0.672 |
EPHA1 |
0.758 | -0.112 | 3 | 0.792 |
INSR |
0.758 | -0.132 | 3 | 0.764 |
FRK |
0.756 | -0.109 | -1 | 0.840 |
EPHA5 |
0.756 | -0.081 | 2 | 0.676 |
LYN |
0.755 | -0.093 | 3 | 0.751 |
CK1G3 |
0.755 | -0.053 | -3 | 0.382 |
ERBB2 |
0.755 | -0.181 | 1 | 0.745 |
NTRK3 |
0.755 | -0.119 | -1 | 0.790 |
FLT1 |
0.755 | -0.160 | -1 | 0.839 |
DDR2 |
0.754 | -0.061 | 3 | 0.746 |
NTRK2 |
0.753 | -0.205 | 3 | 0.777 |
PTK2 |
0.753 | 0.020 | -1 | 0.786 |
EPHA8 |
0.753 | -0.086 | -1 | 0.814 |
FGFR3 |
0.753 | -0.205 | 3 | 0.776 |
SRC |
0.752 | -0.086 | -1 | 0.817 |
YANK2 |
0.750 | -0.110 | 2 | 0.375 |
FLT4 |
0.749 | -0.233 | 3 | 0.763 |
SYK |
0.749 | -0.009 | -1 | 0.793 |
EGFR |
0.748 | -0.119 | 1 | 0.660 |
MATK |
0.748 | -0.142 | -1 | 0.738 |
EPHA2 |
0.745 | -0.090 | -1 | 0.785 |
CSK |
0.744 | -0.185 | 2 | 0.698 |
IGF1R |
0.743 | -0.131 | 3 | 0.701 |
FGFR4 |
0.741 | -0.162 | -1 | 0.782 |
MUSK |
0.740 | -0.151 | 1 | 0.647 |
ERBB4 |
0.737 | -0.094 | 1 | 0.699 |
CK1G2 |
0.737 | -0.059 | -3 | 0.473 |
FES |
0.731 | -0.114 | -1 | 0.710 |
ZAP70 |
0.722 | -0.078 | -1 | 0.712 |