2wrh

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Line 3: Line 3:
<StructureSection load='2wrh' size='340' side='right'caption='[[2wrh]], [[Resolution|resolution]] 3.00&Aring;' scene=''>
<StructureSection load='2wrh' size='340' side='right'caption='[[2wrh]], [[Resolution|resolution]] 3.00&Aring;' scene=''>
== Structural highlights ==
== Structural highlights ==
-
<table><tr><td colspan='2'>[[2wrh]] is a 6 chain structure with sequence from [http://en.wikipedia.org/wiki/Influenza_a_virus_(a/mallard/alberta/35/1976(h1n1)) Influenza a virus (a/mallard/alberta/35/1976(h1n1))]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2WRH OCA]. For a <b>guided tour on the structure components</b> use [http://proteopedia.org/fgij/fg.htm?mol=2WRH FirstGlance]. <br>
+
<table><tr><td colspan='2'>[[2wrh]] is a 6 chain structure with sequence from [https://en.wikipedia.org/wiki/Influenza_a_virus_(a/mallard/alberta/35/1976(h1n1)) Influenza a virus (a/mallard/alberta/35/1976(h1n1))]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2WRH OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2WRH FirstGlance]. <br>
</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=SIA:O-SIALIC+ACID'>SIA</scene></td></tr>
</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=SIA:O-SIALIC+ACID'>SIA</scene></td></tr>
-
<tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[2wrg|2wrg]], [[2wr4|2wr4]], [[2wr0|2wr0]], [[2wr3|2wr3]], [[2wrf|2wrf]], [[2wrd|2wrd]], [[2wr1|2wr1]], [[2wr2|2wr2]], [[2wr7|2wr7]], [[2wre|2wre]], [[2wrb|2wrb]], [[2wrc|2wrc]], [[2wr5|2wr5]]</td></tr>
+
<tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat"><div style='overflow: auto; max-height: 3em;'>[[2wrg|2wrg]], [[2wr4|2wr4]], [[2wr0|2wr0]], [[2wr3|2wr3]], [[2wrf|2wrf]], [[2wrd|2wrd]], [[2wr1|2wr1]], [[2wr2|2wr2]], [[2wr7|2wr7]], [[2wre|2wre]], [[2wrb|2wrb]], [[2wrc|2wrc]], [[2wr5|2wr5]]</div></td></tr>
-
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://proteopedia.org/fgij/fg.htm?mol=2wrh FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2wrh OCA], [http://pdbe.org/2wrh PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=2wrh RCSB], [http://www.ebi.ac.uk/pdbsum/2wrh PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=2wrh ProSAT]</span></td></tr>
+
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=2wrh FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2wrh OCA], [https://pdbe.org/2wrh PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2wrh RCSB], [https://www.ebi.ac.uk/pdbsum/2wrh PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2wrh ProSAT]</span></td></tr>
</table>
</table>
== Function ==
== Function ==
-
[[http://www.uniprot.org/uniprot/Q9WCE0_I76A4 Q9WCE0_I76A4]] Binds to sialic acid-containing receptors on the cell surface, bringing about the attachment of the virus particle to the cell. This attachment induces virion internalization of about two third of the virus particles through clathrin-dependent endocytosis and about one third through a clathrin- and caveolin-independent pathway. Plays a major role in the determination of host range restriction and virulence. Class I viral fusion protein. Responsible for penetration of the virus into the cell cytoplasm by mediating the fusion of the membrane of the endocytosed virus particle with the endosomal membrane. Low pH in endosomes induces an irreversible conformational change in HA2, releasing the fusion hydrophobic peptide. Several trimers are required to form a competent fusion pore (By similarity).[RuleBase:RU003324][SAAS:SAAS013829_004_327643]
+
[[https://www.uniprot.org/uniprot/Q9WCE0_I76A4 Q9WCE0_I76A4]] Binds to sialic acid-containing receptors on the cell surface, bringing about the attachment of the virus particle to the cell. This attachment induces virion internalization of about two third of the virus particles through clathrin-dependent endocytosis and about one third through a clathrin- and caveolin-independent pathway. Plays a major role in the determination of host range restriction and virulence. Class I viral fusion protein. Responsible for penetration of the virus into the cell cytoplasm by mediating the fusion of the membrane of the endocytosed virus particle with the endosomal membrane. Low pH in endosomes induces an irreversible conformational change in HA2, releasing the fusion hydrophobic peptide. Several trimers are required to form a competent fusion pore (By similarity).[RuleBase:RU003324][SAAS:SAAS013829_004_327643]
== Evolutionary Conservation ==
== Evolutionary Conservation ==
[[Image:Consurf_key_small.gif|200px|right]]
[[Image:Consurf_key_small.gif|200px|right]]

Revision as of 11:14, 6 April 2022

structure of H1 duck albert hemagglutinin with human receptor

PDB ID 2wrh

Drag the structure with the mouse to rotate

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools