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4ca4
From Proteopedia
(Difference between revisions)
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| - | ''' | + | ==Crystal structure of FimH lectin domain with the Tyr48Ala mutation, in complex with heptyl alpha-D-mannopyrannoside== |
| - | + | <StructureSection load='4ca4' size='340' side='right' caption='[[4ca4]], [[Resolution|resolution]] 2.84Å' scene=''> | |
| - | + | == Structural highlights == | |
| - | + | <table><tr><td colspan='2'>[[4ca4]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4CA4 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4CA4 FirstGlance]. <br> | |
| - | + | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=KGM:HEPTYL+ALPHA-D-MANNOPYRANNOSIDE'>KGM</scene></td></tr> | |
| - | + | <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=4ca4 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4ca4 OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4ca4 RCSB], [http://www.ebi.ac.uk/pdbsum/4ca4 PDBsum]</span></td></tr> | |
| - | + | </table> | |
| + | __TOC__ | ||
| + | </StructureSection> | ||
| + | [[Category: Bouckaert, J.]] | ||
| + | [[Category: Eid, S.]] | ||
| + | [[Category: Ernst, B.]] | ||
| + | [[Category: Glockshuber, R.]] | ||
| + | [[Category: Preston, R.]] | ||
| + | [[Category: Puorger, C.]] | ||
| + | [[Category: Rabbani, S.]] | ||
| + | [[Category: Thompson, A.]] | ||
| + | [[Category: Zalewski, A.]] | ||
| + | [[Category: Bacterial adhesin]] | ||
| + | [[Category: Cell adhesion]] | ||
| + | [[Category: Fimh antagonist]] | ||
| + | [[Category: Heptyl mannose]] | ||
| + | [[Category: Type 1 fimbriae]] | ||
| + | [[Category: Urinary tract infection]] | ||
| + | [[Category: Variable immunoglobulin fold]] | ||
Revision as of 11:24, 29 October 2014
Crystal structure of FimH lectin domain with the Tyr48Ala mutation, in complex with heptyl alpha-D-mannopyrannoside
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