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- PDB-1a0n: NMR STUDY OF THE SH3 DOMAIN FROM FYN PROTO-ONCOGENE TYROSINE KINA... -
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Basic information
Entry | Database: PDB / ID: 1a0n | ||||||
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Title | NMR STUDY OF THE SH3 DOMAIN FROM FYN PROTO-ONCOGENE TYROSINE KINASE COMPLEXED WITH THE SYNTHETIC PEPTIDE P2L CORRESPONDING TO RESIDUES 91-104 OF THE P85 SUBUNIT OF PI3-KINASE, FAMILY OF 25 STRUCTURES | ||||||
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![]() | COMPLEX (PHOSPHOTRANSFERASE/PEPTIDE) / COMPLEX (PHOSPHOTRANSFERASE-PEPTIDE) / SH3 DOMAIN / POLYPROLINE-BINDING / COMPLEX (PHOSPHOTRANSFERASE-PEPTIDE) complex | ||||||
Function / homology | ![]() negative regulation of hydrogen peroxide biosynthetic process / response to singlet oxygen / Reelin signalling pathway / perinuclear endoplasmic reticulum membrane / perinuclear endoplasmic reticulum / regulation of toll-like receptor 4 signaling pathway / NTRK2 activates RAC1 / growth factor receptor binding / phosphatidylinositol kinase activity / regulation of glutamate receptor signaling pathway ...negative regulation of hydrogen peroxide biosynthetic process / response to singlet oxygen / Reelin signalling pathway / perinuclear endoplasmic reticulum membrane / perinuclear endoplasmic reticulum / regulation of toll-like receptor 4 signaling pathway / NTRK2 activates RAC1 / growth factor receptor binding / phosphatidylinositol kinase activity / regulation of glutamate receptor signaling pathway / heart process / Activated NTRK2 signals through FYN / phosphatidylinositol 3-kinase regulator activity / positive regulation of focal adhesion disassembly / IRS-mediated signalling / phosphatidylinositol 3-kinase activator activity / 1-phosphatidylinositol-3-kinase regulator activity / positive regulation of endoplasmic reticulum unfolded protein response / SEMA3A-Plexin repulsion signaling by inhibiting Integrin adhesion / interleukin-18-mediated signaling pathway / myeloid leukocyte migration / regulation of calcium ion import across plasma membrane / phosphatidylinositol 3-kinase complex / T follicular helper cell differentiation / reelin-mediated signaling pathway / PI3K events in ERBB4 signaling / phosphatidylinositol 3-kinase regulatory subunit binding / neurotrophin TRKA receptor binding / Platelet Adhesion to exposed collagen / positive regulation of protein localization to membrane / cellular response to L-glutamate / Activated NTRK2 signals through PI3K / G protein-coupled glutamate receptor signaling pathway / CRMPs in Sema3A signaling / cis-Golgi network / Activated NTRK3 signals through PI3K / FLT3 signaling through SRC family kinases / ErbB-3 class receptor binding / activated T cell proliferation / transmembrane receptor protein tyrosine kinase adaptor activity / Signaling by cytosolic FGFR1 fusion mutants / type 5 metabotropic glutamate receptor binding / Co-stimulation by ICOS / RHOD GTPase cycle / Nef and signal transduction / negative regulation of dendritic spine maintenance / RHOF GTPase cycle / feeding behavior / phosphatidylinositol 3-kinase complex, class IA / Co-stimulation by CD28 / kinase activator activity / Nephrin family interactions / natural killer cell activation / DCC mediated attractive signaling / EPH-Ephrin signaling / Signaling by LTK in cancer / positive regulation of leukocyte migration / Ephrin signaling / Signaling by LTK / dendritic spine maintenance / CD28 dependent Vav1 pathway / MET activates PI3K/AKT signaling / PI3K/AKT activation / negative regulation of stress fiber assembly / RND1 GTPase cycle / positive regulation of filopodium assembly / RND2 GTPase cycle / RND3 GTPase cycle / insulin binding / dendrite morphogenesis / growth hormone receptor signaling pathway / tau-protein kinase activity / Regulation of KIT signaling / Signaling by ALK / leukocyte migration / phospholipase activator activity / RHOV GTPase cycle / PI-3K cascade:FGFR3 / RHOB GTPase cycle / natural killer cell mediated cytotoxicity / Co-inhibition by CTLA4 / Erythropoietin activates Phosphoinositide-3-kinase (PI3K) / GP1b-IX-V activation signalling / EPHA-mediated growth cone collapse / PI-3K cascade:FGFR2 / PI-3K cascade:FGFR4 / PI-3K cascade:FGFR1 / Dectin-2 family / RHOC GTPase cycle / RHOJ GTPase cycle / stimulatory C-type lectin receptor signaling pathway / intracellular glucose homeostasis / phosphatidylinositol phosphate biosynthetic process / negative regulation of osteoclast differentiation / Fc-gamma receptor signaling pathway involved in phagocytosis / phospholipase binding / Synthesis of PIPs at the plasma membrane / PECAM1 interactions / response to amyloid-beta / RHOU GTPase cycle Similarity search - Function | ||||||
Biological species | ![]() | ||||||
Method | SOLUTION NMR | ||||||
![]() | Renzoni, D.A. / Pugh, D.J.R. / Siligardi, G. / Das, P. / Morton, C.J. / Rossi, C. / Waterfield, M.D. / Campbell, I.D. / Ladbury, J.E. | ||||||
![]() | ![]() Title: Structural and thermodynamic characterization of the interaction of the SH3 domain from Fyn with the proline-rich binding site on the p85 subunit of PI3-kinase. Authors: Renzoni, D.A. / Pugh, D.J. / Siligardi, G. / Das, P. / Morton, C.J. / Rossi, C. / Waterfield, M.D. / Campbell, I.D. / Ladbury, J.E. #1: ![]() Title: Solution Structure and Peptide Binding of the SH3 Domain from Human Fyn Authors: Morton, C.J. / Pugh, D.J. / Brown, E.L. / Kahmann, J.D. / Renzoni, D.A. / Campbell, I.D. | ||||||
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Structure visualization
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PDBx/mmCIF format | ![]() | 544 KB | Display | ![]() |
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PDB format | ![]() | 453.9 KB | Display | ![]() |
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-Validation report
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-Related structure data
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Assembly
Deposited unit | ![]()
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NMR ensembles |
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Components
#1: Protein/peptide | Mass: 1405.640 Da / Num. of mol.: 1 / Fragment: P85 SUBUNIT OF PI3-KINASE, RESIDUES 91 - 104 Source method: isolated from a genetically manipulated source References: UniProt: P27986 |
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#2: Protein | Mass: 7698.238 Da / Num. of mol.: 1 / Fragment: SH3 DOMAIN, RESIDUES 82 - 148 / Mutation: N-TERMINAL GS FROM EXPRESSION SYSTEM Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() ![]() ![]() |
-Experimental details
-Experiment
Experiment | Method: SOLUTION NMR |
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Sample preparation
Crystal grow | *PLUS Method: other / Details: NMR |
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Processing
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NMR software | Name: ![]() | ||||||||||||
NMR ensemble | Conformers calculated total number: 50 / Conformers submitted total number: 25 |