4wcd
From Proteopedia
(Difference between revisions)
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| - | ''' | + | ==Trypanosoma brucei PTR1 in complex with inhibitor 10== |
| - | + | <StructureSection load='4wcd' size='340' side='right' caption='[[4wcd]], [[Resolution|resolution]] 1.68Å' scene=''> | |
| - | + | == Structural highlights == | |
| - | + | <table><tr><td colspan='2'>[[4wcd]] is a 4 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4WCD OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4WCD FirstGlance]. <br> | |
| - | + | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=3KH:5-(1H-BENZOTRIAZOL-6-YL)-1,3,4-THIADIAZOL-2-AMINE'>3KH</scene>, <scene name='pdbligand=ACT:ACETATE+ION'>ACT</scene>, <scene name='pdbligand=GOL:GLYCEROL'>GOL</scene>, <scene name='pdbligand=NAP:NADP+NICOTINAMIDE-ADENINE-DINUCLEOTIDE+PHOSPHATE'>NAP</scene></td></tr> | |
| - | + | <tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[2yhi|2yhi]], [[2yhu|2yhu]]</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=4wcd FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4wcd OCA], [http://pdbe.org/4wcd PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=4wcd RCSB], [http://www.ebi.ac.uk/pdbsum/4wcd PDBsum]</span></td></tr> | |
| - | [[ | + | </table> |
| - | [[ | + | __TOC__ |
| + | </StructureSection> | ||
[[Category: Mangani, S]] | [[Category: Mangani, S]] | ||
| - | [[Category: | + | [[Category: Pisa, F Di]] |
| + | [[Category: Pozzi, C]] | ||
| + | [[Category: Oxidoreductase]] | ||
| + | [[Category: Tbptr1]] | ||
| + | [[Category: Thiadiazole derivatives inhibitor]] | ||
| + | [[Category: Trypanosoma brucei ptr1]] | ||
Revision as of 14:39, 30 September 2015
Trypanosoma brucei PTR1 in complex with inhibitor 10
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