6cs2

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m (Protected "6cs2" [edit=sysop:move=sysop])
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'''Unreleased structure'''
 
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The entry 6cs2 is ON HOLD
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==SARS Spike Glycoprotein - human ACE2 complex, Stabilized variant, all ACE2-bound particles==
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<StructureSection load='6cs2' size='340' side='right' caption='[[6cs2]], [[Resolution|resolution]] 4.40&Aring;' scene=''>
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Authors:
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== Structural highlights ==
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<table><tr><td colspan='2'>[[6cs2]] is a 4 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6CS2 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6CS2 FirstGlance]. <br>
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Description:
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</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=BMA:BETA-D-MANNOSE'>BMA</scene>, <scene name='pdbligand=MAN:ALPHA-D-MANNOSE'>MAN</scene>, <scene name='pdbligand=NAG:N-ACETYL-D-GLUCOSAMINE'>NAG</scene></td></tr>
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[[Category: Unreleased Structures]]
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<tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Angiotensin-converting_enzyme_2 Angiotensin-converting enzyme 2], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.17.23 3.4.17.23] </span></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=6cs2 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6cs2 OCA], [http://pdbe.org/6cs2 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6cs2 RCSB], [http://www.ebi.ac.uk/pdbsum/6cs2 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6cs2 ProSAT]</span></td></tr>
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</table>
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== Function ==
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[[http://www.uniprot.org/uniprot/SPIKE_CVHSA SPIKE_CVHSA]] S1 attaches the virion to the cell membrane by interacting with human ACE2 and CLEC4M/DC-SIGNR, initiating the infection. Binding to the receptor and internalization of the virus into the endosomes of the host cell probably induces conformational changes in the S glycoprotein. Proteolysis by cathepsin CTSL may unmask the fusion peptide of S2 and activate membranes fusion within endosomes. S2 is a class I viral fusion protein. Under the current model, the protein has at least three conformational states: pre-fusion native state, pre-hairpin intermediate state, and post-fusion hairpin state. During viral and target cell membrane fusion, the coiled coil regions (heptad repeats) assume a trimer-of-hairpins structure, positioning the fusion peptide in close proximity to the C-terminal region of the ectodomain. The formation of this structure appears to drive apposition and subsequent fusion of viral and target cell membranes. [[http://www.uniprot.org/uniprot/ACE2_HUMAN ACE2_HUMAN]] Carboxypeptidase which converts angiotensin I to angiotensin 1-9, a peptide of unknown function, and angiotensin II to angiotensin 1-7, a vasodilator. Also able to hydrolyze apelin-13 and dynorphin-13 with high efficiency. May be an important regulator of heart function. In case of human coronaviruses SARS and HCoV-NL63 infections, serve as functional receptor for the spike glycoprotein of both coronaviruses.<ref>PMID:10969042</ref> <ref>PMID:10924499</ref> <ref>PMID:14647384</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: Angiotensin-converting enzyme 2]]
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[[Category: Cottrell, C A]]
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[[Category: Kirchdoerfer, R N]]
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[[Category: McLellan, J S]]
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[[Category: Pallesen, J]]
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[[Category: Turner, H L]]
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[[Category: Wang, N]]
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[[Category: Ward, A B]]
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[[Category: Glycoprotein]]
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[[Category: Membrane fusion]]
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[[Category: Receptor binding]]
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[[Category: Viral protein]]

Revision as of 13:55, 11 April 2018

SARS Spike Glycoprotein - human ACE2 complex, Stabilized variant, all ACE2-bound particles

6cs2, resolution 4.40Å

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