6v8x: Difference between revisions

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-'''Unreleased structure'''
-The entry 6v8x is ON HOLD
+==VRC01 Bound BG505 F14 HIV-1 SOSIP Envelope Trimer Structure==
+<StructureSection load='6v8x' size='340' side='right'caption='[[6v8x]], [[Resolution|resolution]] 3.00&Aring;' scene=''>
-Authors: Acharya, P., Henderson, R.
+== Structural highlights ==
+<table><tr><td colspan='2'>[[6v8x]] is a 12 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6V8X OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6V8X FirstGlance]. <br>
-Description: VRC01 Bound BG505 F14 HIV-1 SOSIP Envelope Trimer Structure
+</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>
-[[Category: Unreleased Structures]]
+<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=6v8x FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6v8x OCA], [http://pdbe.org/6v8x PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6v8x RCSB], [http://www.ebi.ac.uk/pdbsum/6v8x PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6v8x ProSAT]</span></td></tr>
+</table>
+== Function ==
+[[http://www.uniprot.org/uniprot/Q2N0S6_9HIV1 Q2N0S6_9HIV1]] The envelope glyprotein gp160 precursor down-modulates cell surface CD4 antigen by interacting with it in the endoplasmic reticulum and blocking its transport to the cell surface (By similarity).[RuleBase:RU004292][SAAS:SAAS000328_004_020447]  The gp120-gp41 heterodimer allows rapid transcytosis of the virus through CD4 negative cells such as simple epithelial monolayers of the intestinal, rectal and endocervical epithelial barriers. Both gp120 and gp41 specifically recognize glycosphingolipids galactosyl-ceramide (GalCer) or 3' sulfo-galactosyl-ceramide (GalS) present in the lipid rafts structures of epithelial cells. Binding to these alternative receptors allows the rapid transcytosis of the virus through the epithelial cells. This transcytotic vesicle-mediated transport of virions from the apical side to the basolateral side of the epithelial cells does not involve infection of the cells themselves (By similarity).[SAAS:SAAS000328_004_240990]
+__TOC__
+</StructureSection>
+[[Category: Large Structures]]
 [[Category: Acharya, P]]
 [[Category: Henderson, R]]
+[[Category: Complex]]
+[[Category: Hiv-1]]
+[[Category: Immunogen]]
+[[Category: Trimer]]
+[[Category: Viral protein-immune system complex]]