7uad
From Proteopedia
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- | '''Unreleased structure''' | ||
- | + | ==Crystal structure of human PTPN2 with inhibitor ABBV-CLS-484== | |
- | + | <StructureSection load='7uad' size='340' side='right'caption='[[7uad]], [[Resolution|resolution]] 2.04Å' scene=''> | |
- | + | == Structural highlights == | |
- | + | <table><tr><td colspan='2'>[[7uad]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7UAD OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7UAD 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]] 2.044Å</td></tr> | |
- | [[Category: | + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=M5R:5-{(7R)-1-fluoro-3-hydroxy-7-[(3-methylbutyl)amino]-5,6,7,8-tetrahydronaphthalen-2-yl}-1lambda~6~,2,5-thiadiazolidine-1,1,3-trione'>M5R</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=7uad FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7uad OCA], [https://pdbe.org/7uad PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7uad RCSB], [https://www.ebi.ac.uk/pdbsum/7uad PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7uad ProSAT]</span></td></tr> | ||
+ | </table> | ||
+ | == Function == | ||
+ | [https://www.uniprot.org/uniprot/PTN2_HUMAN PTN2_HUMAN] | ||
+ | __TOC__ | ||
+ | </StructureSection> | ||
+ | [[Category: Homo sapiens]] | ||
+ | [[Category: Large Structures]] | ||
+ | [[Category: Frost JM]] | ||
+ | [[Category: Longenecker KL]] | ||
+ | [[Category: Qiu W]] | ||
+ | [[Category: Sun Q]] |
Current revision
Crystal structure of human PTPN2 with inhibitor ABBV-CLS-484
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