2wr7

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Line 3: Line 3:
<StructureSection load='2wr7' size='340' side='right'caption='[[2wr7]], [[Resolution|resolution]] 2.50&Aring;' scene=''>
<StructureSection load='2wr7' size='340' side='right'caption='[[2wr7]], [[Resolution|resolution]] 2.50&Aring;' scene=''>
== Structural highlights ==
== Structural highlights ==
-
<table><tr><td colspan='2'>[[2wr7]] is a 3 chain structure with sequence from [http://en.wikipedia.org/wiki/Influenza_a_virus_(a/singapore/1/1957(h2n2)) Influenza a virus (a/singapore/1/1957(h2n2))]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2WR7 OCA]. For a <b>guided tour on the structure components</b> use [http://proteopedia.org/fgij/fg.htm?mol=2WR7 FirstGlance]. <br>
+
<table><tr><td colspan='2'>[[2wr7]] is a 3 chain structure with sequence from [https://en.wikipedia.org/wiki/Influenza_a_virus_(a/singapore/1/1957(h2n2)) Influenza a virus (a/singapore/1/1957(h2n2))]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2WR7 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2WR7 FirstGlance]. <br>
-
</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=GAL:BETA-D-GALACTOSE'>GAL</scene>, <scene name='pdbligand=NAG:N-ACETYL-D-GLUCOSAMINE'>NAG</scene>, <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=GAL:BETA-D-GALACTOSE'>GAL</scene>, <scene name='pdbligand=NAG:N-ACETYL-D-GLUCOSAMINE'>NAG</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]], [[2wre|2wre]], [[2wrb|2wrb]], [[2wrh|2wrh]], [[2wrc|2wrc]], [[2wr5|2wr5]]</td></tr>
+
<tr id='NonStdRes'><td class="sblockLbl"><b>[[Non-Standard_Residue|NonStd Res:]]</b></td><td class="sblockDat"><scene name='pdbligand=SIA:O-SIALIC+ACID'>SIA</scene></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=2wr7 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2wr7 OCA], [http://pdbe.org/2wr7 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=2wr7 RCSB], [http://www.ebi.ac.uk/pdbsum/2wr7 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=2wr7 ProSAT]</span></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]], [[2wre|2wre]], [[2wrb|2wrb]], [[2wrh|2wrh]], [[2wrc|2wrc]], [[2wr5|2wr5]]</div></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=2wr7 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2wr7 OCA], [https://pdbe.org/2wr7 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2wr7 RCSB], [https://www.ebi.ac.uk/pdbsum/2wr7 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2wr7 ProSAT]</span></td></tr>
</table>
</table>
== Function ==
== Function ==
-
[[http://www.uniprot.org/uniprot/B4UR26_I57A5 B4UR26_I57A5]] 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/B4UR26_I57A5 B4UR26_I57A5]] 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

the structure of influenza H2 human singapore hemagglutinin with human receptor

PDB ID 2wr7

Drag the structure with the mouse to rotate

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools