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3v7c
From Proteopedia
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| - | [[Image:3v7c.jpg|left|200px]] | ||
| - | + | ==Cystal structure of SaBPL in complex with inhibitor== | |
| - | + | <StructureSection load='3v7c' size='340' side='right'caption='[[3v7c]], [[Resolution|resolution]] 2.70Å' scene=''> | |
| - | + | == Structural highlights == | |
| - | + | <table><tr><td colspan='2'>[[3v7c]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Staphylococcus_aureus_A9781 Staphylococcus aureus A9781]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3V7C OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=3V7C FirstGlance]. <br> | |
| - | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.7Å</td></tr> | |
| - | + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=C77:5-DEOXY-2,3-O-(1-METHYLETHYLIDENE)-5-(4-{5-[(3AS,4S,6AR)-2-OXOHEXAHYDRO-1H-THIENO[3,4-D]IMIDAZOL-4-YL]PENTYL}-1H-1,2,3-TRIAZOL-1-YL)ADENOSINE'>C77</scene></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=3v7c FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3v7c OCA], [https://pdbe.org/3v7c PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=3v7c RCSB], [https://www.ebi.ac.uk/pdbsum/3v7c PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=3v7c ProSAT]</span></td></tr> | |
| - | + | </table> | |
| - | + | __TOC__ | |
| - | + | </StructureSection> | |
| - | + | [[Category: Large Structures]] | |
| - | < | + | [[Category: Staphylococcus aureus A9781]] |
| - | + | [[Category: Pendini NR]] | |
| - | + | [[Category: Yap MY]] | |
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| - | [[3v7c]] is a 1 chain structure with sequence from [ | + | |
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Current revision
Cystal structure of SaBPL in complex with inhibitor
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