3wuv

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'''Unreleased structure'''
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==Structure basis of inactivating cell abscission with chimera peptide 2==
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<StructureSection load='3wuv' size='340' side='right' caption='[[3wuv]], [[Resolution|resolution]] 2.79&Aring;' scene=''>
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The entry 3wuv is ON HOLD until Jul 15 2016
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== Structural highlights ==
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<table><tr><td colspan='2'>[[3wuv]] is a 18 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3WUV OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=3WUV FirstGlance]. <br>
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Authors: Kim, H.J., Matsuura, A., Lee, H.H.
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</td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[3wut|3wut]], [[3wuu|3wuu]]</td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=3wuv FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3wuv OCA], [http://www.rcsb.org/pdb/explore.do?structureId=3wuv RCSB], [http://www.ebi.ac.uk/pdbsum/3wuv PDBsum]</span></td></tr>
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Description: Structure basis of inactivating cell abscission with chimera peptide 2
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</table>
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[[Category: Unreleased Structures]]
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== Function ==
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[[Category: Lee, H.H]]
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[[http://www.uniprot.org/uniprot/CEP55_HUMAN CEP55_HUMAN]] Plays a role in mitotic exit and cytokinesis. Not required for microtubule nucleation. Recruits PDCD6IP and TSG101 to midbody during cytokinesis.<ref>PMID:16198290</ref> <ref>PMID:17853893</ref> [[http://www.uniprot.org/uniprot/PDC6I_HUMAN PDC6I_HUMAN]] Class E VPS protein involved in concentration and sorting of cargo proteins of the multivesicular body (MVB) for incorporation into intralumenal vesicles (ILVs) that are generated by invagination and scission from the limiting membrane of the endosome. Binds to the phospholipid lysobisphosphatidic acid (LBPA) which is abundant in MVBs internal membranes. The MVB pathway appears to require the sequential function of ESCRT-O, -I,-II and -III complexes. The ESCRT machinery also functions in topologically equivalent membrane fission events, such as the terminal stages of cytokinesis and enveloped virus budding (HIV-1 and other lentiviruses). Appears to be an adapter for a subset of ESCRT-III proteins, such as CHMP4, to function at distinct membranes. Required for completion of cytokinesis. Involved in HIV-1 virus budding. Can replace TSG101 it its role of supporting HIV-1 release; this function implies the interaction with CHMP4B. May play a role in the regulation of both apoptosis and cell proliferation.<ref>PMID:14505569</ref> <ref>PMID:14505570</ref> <ref>PMID:14739459</ref> <ref>PMID:17853893</ref> <ref>PMID:17428861</ref> <ref>PMID:17556548</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: Kim, H J]]
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[[Category: Lee, H H]]
[[Category: Matsuura, A]]
[[Category: Matsuura, A]]
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[[Category: Kim, H.J]]
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[[Category: Cell cycle]]
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[[Category: Coiled-coil]]

Revision as of 13:29, 15 July 2015

Structure basis of inactivating cell abscission with chimera peptide 2

3wuv, resolution 2.79Å

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