6vqm

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(New page: '''Unreleased structure''' The entry 6vqm is ON HOLD Authors: Seo, H.-S., Dhe-Paganon, S. Description: Crystal Structure Analysis of human ACK1 Category: Unreleased Structures [[Ca...)
Current revision (08:17, 11 October 2023) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 6vqm is ON HOLD
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==Crystal Structure Analysis of human ACK1==
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<StructureSection load='6vqm' size='340' side='right'caption='[[6vqm]], [[Resolution|resolution]] 2.87&Aring;' scene=''>
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Authors: Seo, H.-S., Dhe-Paganon, S.
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== Structural highlights ==
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<table><tr><td colspan='2'>[[6vqm]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6VQM OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6VQM FirstGlance]. <br>
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Description: Crystal Structure Analysis of human ACK1
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.87&#8491;</td></tr>
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[[Category: Unreleased Structures]]
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=R7P:2-({4-[(3R,5S)-3,5-dimethylpiperazin-1-yl]-2-methoxyphenyl}amino)-9-methyl-5,7-dihydro-6H-pyrimido[5,4-d][1,3]benzodiazepin-6-one'>R7P</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene></td></tr>
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[[Category: Dhe-Paganon, S]]
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=6vqm FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6vqm OCA], [https://pdbe.org/6vqm PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6vqm RCSB], [https://www.ebi.ac.uk/pdbsum/6vqm PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6vqm ProSAT]</span></td></tr>
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[[Category: Seo, H.-S]]
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</table>
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== Function ==
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[https://www.uniprot.org/uniprot/ACK1_HUMAN ACK1_HUMAN] Non-receptor tyrosine-protein and serine/threonine-protein kinase that is implicated in cell spreading and migration, cell survival, cell growth and proliferation. Transduces extracellular signals to cytosolic and nuclear effectors. Phosphorylates AKT1, AR, MCF2, WASL and WWOX. Implicated in trafficking and clathrin-mediated endocytosis through binding to epidermal growth factor receptor (EGFR) and clathrin. Binds to both poly- and mono-ubiquitin and regulates ligand-induced degradation of EGFR, thereby contributing to the accumulation of EGFR at the limiting membrane of early endosomes. Downstream effector of CDC42 which mediates CDC42-dependent cell migration via phosphorylation of BCAR1. May be involved both in adult synaptic function and plasticity and in brain development. Activates AKT1 by phosphorylating it on 'Tyr-176'. Phosphorylates AR on 'Tyr-267' and 'Tyr-363' thereby promoting its recruitment to androgen-responsive enhancers (AREs). Phosphorylates WWOX on 'Tyr-287'. Phosphorylates MCF2, thereby enhancing its activity as a guanine nucleotide exchange factor (GEF) toward Rho family proteins. Contributes to the control of AXL receptor levels. Confers metastatic properties on cancer cells and promotes tumor growth by negatively regulating tumor suppressor such as WWOX and positively regulating pro-survival factors such as AKT1 and AR.<ref>PMID:10652228</ref> <ref>PMID:11278436</ref> <ref>PMID:16257963</ref> <ref>PMID:16247015</ref> <ref>PMID:17038317</ref> <ref>PMID:16472662</ref> <ref>PMID:18435854</ref> <ref>PMID:18262180</ref> <ref>PMID:19815557</ref> <ref>PMID:20383201</ref> <ref>PMID:20333297</ref>
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== References ==
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<references/>
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__TOC__
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</StructureSection>
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[[Category: Homo sapiens]]
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[[Category: Large Structures]]
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[[Category: Dhe-Paganon S]]
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[[Category: Seo H-S]]

Current revision

Crystal Structure Analysis of human ACK1

PDB ID 6vqm

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