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Searched for: data_source:NCI_NATURE [All Organisms, All Data Sources]

Your search has found 935 relevant records:

Molecules (935)
Showing Results 1 - 10 of 935  | Next 10
99%99%
Protein: P53_HUMAN [Homo sapiens]  from IntAct, MINT, BioGRID, Reactome, Cancer Cell Map, NCI / Nature Pathway Interaction Database  [15 pathways, 6 interactions]
Cellular tumor antigen p53

Summary:  FUNCTION: Acts as a tumor suppressor in many tumor types; induces growth arrest or apoptosis depending on the physiological circumstances and cell type. Involved in cell cycle regulation as a trans-activator that acts to negatively regulate cell division by controlling a set of genes required for this process. One of the activated genes is an inhibitor of cyclin-dependent kinases. Apoptosis induction seems to be mediated either by stimulation of BAX and FAS antigen expression, or by repression of Bcl-2 expression. Implicated in Notch signaling cross-over. Isoform 2 enhances the transactivation activity of isoform 1 from some but not all TP53-inducible promoters. Isoform 4 suppresses transactivation activity and impairs growth suppression mediated by isoform 1. Isoform 7 inhibits isoform 1-mediated apoptosis. COFACTOR: Binds 1 zinc ion per subunit.

74%74%
Protein: HDAC1_HUMAN [Homo sapiens]  from IntAct, MINT, BioGRID, Reactome, Cancer Cell Map, NCI / Nature Pathway Interaction Database  [5 pathways, 2 interactions]
Histone deacetylase 1

Summary:  FUNCTION: Responsible for the deacetylation of lysine residues on the N-terminal part of the core histones (H2A, H2B, H3 and H4). Histone deacetylation gives a tag for epigenetic repression and plays an important role in transcriptional regulation, cell cycle progression and developmental events. Histone deacetylases act via the formation of large multiprotein complexes. Deacetylates SP proteins, SP1 and SP3, and regulates their function. Component of the BRG1-RB1-HDAC1 complex, which negatively regulates the CREST- mediated transcription in resting neurons. Upon calcium stimulation, HDAC1 is released from the complex and CREBBP is recruited, which facilitates transcriptional activation. Deacetylates TSHZ3 and regulates its transcriptional repressor activity. Deacetylates 'Lys-310' in RELA and thereby inhibits the transcriptional activity of NF-kappa-B. CATALYTIC ACTIVITY: Hydrolysis of an N(6)-acetyl-lysine residue of a histone to yield a deacetylated histone.

63%63%
Protein: EP300_HUMAN [Homo sapiens]  from IntAct, MINT, HPRD, BioGRID, Reactome, Cancer Cell Map, NCI / Nature Pathway Interaction Database  [4 pathways, 1 interaction]
Histone acetyltransferase p300

Summary:  FUNCTION: Functions as histone acetyltransferase and regulates transcription via chromatin remodeling. Acetylates all four core histones in nucleosomes. Histone acetylation gives an epigenetic tag for transcriptional activation. Binds to and may be involved in the transforming capacity of the adenovirus E1A protein. Mediates cAMP-gene regulation by binding specifically to phosphorylated CREB protein. In case of HIV-1 infection, it is recruited by the viral protein Tat. Regulates Tat's transactivating activity and may help inducing chromatin remodeling of proviral genes. Acetylates the 'Lys-131' residue of ALX1 and acts as its coactivator in the presence of CREBBP. Acts as a TFAP2A-mediated transcriptional coactivator in presence of CITED2. Plays a role as a coactivator of NEUROD1-dependent transcription of the secretin and p21 genes and controls terminal differentiation of cells in the intestinal epithelium. CATALYTIC ACTIVITY: Acetyl-CoA + [histone] = CoA + acetyl- [histone].

51%51%
Protein: EGFR_HUMAN [Homo sapiens]  from IntAct, MINT, HumanCyc, HPRD, BioGRID, Reactome, Cancer Cell Map, IMID, NCI / Nature Pathway Interaction Database  [16 pathways, 2 interactions]
Epidermal growth factor receptor

Summary:  FUNCTION: Cell surface receptor for EGF, but also for other members of the EGF family, such as TGF-alpha, BTC/betacellulin, AREGAREGB/amphiregulin, HBEGF, GP30 and vaccinia virus growth factor. Ligand binding triggers a conformation change, leading to activation of the kinase and subsequent phosphorylation of down- stream protein kinases. Is involved in the control of cell growth, proliferation and differentiation. Phosphorylates MUC1 in breast cancer cells and increases the interaction of MUC1 with SRC and CTNNB1/beta-catenin.

51%51%
Protein: 1433Z_HUMAN [Homo sapiens]  from IntAct, MINT, HPRD, BioGRID, Reactome, Cancer Cell Map, NCI / Nature Pathway Interaction Database  [12 pathways, 2 interactions]
14-3-3 protein zeta/delta

Summary:  FUNCTION: Adapter protein implicated in the regulation of a large spectrum of both general and specialized signaling pathways. Binds to a large number of partners, usually by recognition of a phosphoserine or phosphothreonine motif. Binding generally results in the modulation of the activity of the binding partner.

49%49%
Protein: CBP_HUMAN [Homo sapiens]  from IntAct, MINT, HPRD, BioGRID, Reactome, Cancer Cell Map, IMID, NCI / Nature Pathway Interaction Database  [2 pathways, 1 interaction]
CREB-binding protein

Summary:  FUNCTION: Acetylates histones, giving a specific tag for transcriptional activation. Also acetylates non-histone proteins, like NCOA3 coactivator. Binds specifically to phosphorylated CREB and enhances its transcriptional activity toward cAMP-responsive genes. Acts as a coactivator of ALX1 in the presence of EP300. CATALYTIC ACTIVITY: Acetyl-CoA + [histone] = CoA + acetyl- [histone].

49%49%
Protein: CBL_HUMAN [Homo sapiens]  from IntAct, MINT, HPRD, BioGRID, Reactome, Cancer Cell Map, NCI / Nature Pathway Interaction Database  [14 pathways, 12 interactions]
E3 ubiquitin-protein ligase CBL

Summary:  FUNCTION: Participates in signal transduction in hematopoietic cells. Adapter protein that functions as a negative regulator of many signaling pathways that start from receptors at the cell surface. Acts as an E3 ubiquitin-protein ligase, which accepts ubiquitin from specific E2 ubiquitin-conjugating enzymes, and then transfers it to substrates promoting their degradation by the proteasome. Recognizes activated receptor tyrosine kinases, including PDGFA, EGF and CSF1, and terminates signaling. Essential for osteoclastic bone resorption. The Tyr-731 phosphorylated form induces the activation and recruitment of phosphatidylinositol 3- kinase to the cell membrane in a signaling pathway that is critical for osteoclast function.

48%48%
Protein: TAT protein [nucleoplasm] [Human immunodeficiency virus 1]  from BioGRID, Reactome, NCI / Nature Pathway Interaction Database  [1 interaction]

Summary:  Converted from EntitySet in Reactome. Each synonym is a name of a PhysicalEntity, and each XREF points to one PhysicalEntity

44%44%
Protein: AKT1_HUMAN [Homo sapiens]  from IntAct, MINT, HPRD, BioGRID, Reactome, Cancer Cell Map, IMID, NCI / Nature Pathway Interaction Database  [14 pathways, 3 interactions]
RAC-alpha serine/threonine-protein kinase

Summary:  FUNCTION: Plays a role as a key modulator of the AKT-mTOR signaling pathway controlling the tempo of the process of newborn neurons integration during adult neurogenesis, including correct neuron positioning, dendritic development and synapse formation (By similarity). General protein kinase capable of phosphorylating several known proteins. Phosphorylates TBC1D4. Signals downstream of phosphatidylinositol 3-kinase (PI(3)K) to mediate the effects of various growth factors such as platelet-derived growth factor (PDGF), epidermal growth factor (EGF), insulin and insulin-like growth factor I (IGF-I). Plays a role in glucose transport by mediating insulin-induced translocation of the GLUT4 glucose transporter to the cell surface. Mediates the antiapoptotic effects of IGF-I. Mediates insulin-stimulated protein synthesis by phosphorylating TSC2 at 'Ser-939' and 'Thr-1462', thereby activating mTORC1 signaling and leading to both phosphorylation of 4E-BP1 and in activation of RPS6KB1. Promotes glycogen synthesis by mediating the insulin-induced activation of glycogen synthase. The activated form can suppress FoxO gene transcription and promote cell cycle progression. Essential for the SPATA13-mediated regulation of cell migration and adhesion assembly and disassembly. May be involved in the regulation of the placental development. CATALYTIC ACTIVITY: ATP + a protein = ADP + a phosphoprotein.

44%44%
Protein: TRAF2_HUMAN [Homo sapiens]  from IntAct, MINT, HPRD, BioGRID, Reactome, Cancer Cell Map, NCI / Nature Pathway Interaction Database  [6 pathways, 1 interaction]
TNF receptor-associated factor 2

Summary:  FUNCTION: Regulates activation of NF-kappa-B and JNK and plays a central role in the regulation of cell survival and apoptosis. Required for normal antibody isotype switching from IgM to IgG. Has E3 ubiquitin-protein ligase activity and promotes 'Lys-63'- linked ubiquitination of target proteins, such as BIRC3, RIPK1 and TICAM1. Is an essential constituent of several E3 ubiquitin- protein ligase complexes, where it promotes the ubiquitination of target proteins by bringing them into contact with other E3 ubiquitin ligases. Regulates BIRC2 and BIRC3 protein levels by inhibiting their autoubiquitination and subsequent degradation; this does not depend on the TRAF2 RING-type zinc finger domain.