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6gwr

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m (Protected "6gwr" [edit=sysop:move=sysop])
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'''Unreleased structure'''
 
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The entry 6gwr is ON HOLD
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==Structure of the kinase domain of human DDR1 in complex with a potent and selective inhibitor of DDR1 and DDR2==
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<StructureSection load='6gwr' size='340' side='right' caption='[[6gwr]], [[Resolution|resolution]] 2.07&Aring;' scene=''>
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Authors: Pinkas, D.M., Fox, A.E., Kupinska, K., Burgess-Brown, N.A., von Delft, F., Arrowsmith, C.H., Edwards, A.M., Bountra, C., Bullock, A.N.
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== Structural highlights ==
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<table><tr><td colspan='2'>[[6gwr]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6GWR OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6GWR FirstGlance]. <br>
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Description: Structure of the kinase domain of human DDR1 in complex with a potent and selective inhibitor of DDR1 and DDR2
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</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=EDO:1,2-ETHANEDIOL'>EDO</scene>, <scene name='pdbligand=FEW:3-(2-imidazo[1,2-a]pyrazin-3-ylethynyl)-~{N}-[3-[(4-methylpiperazin-1-yl)methyl]-5-(trifluoromethyl)phenyl]-4-propan-2-yl-benzamide'>FEW</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene></td></tr>
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[[Category: Unreleased Structures]]
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<tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Receptor_protein-tyrosine_kinase Receptor protein-tyrosine kinase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.10.1 2.7.10.1] </span></td></tr>
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[[Category: Fox, A.E]]
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<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=6gwr FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6gwr OCA], [http://pdbe.org/6gwr PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6gwr RCSB], [http://www.ebi.ac.uk/pdbsum/6gwr PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6gwr ProSAT]</span></td></tr>
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[[Category: Arrowsmith, C.H]]
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</table>
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[[Category: Burgess-Brown, N.A]]
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__TOC__
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[[Category: Von Delft, F]]
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</StructureSection>
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[[Category: Bullock, A.N]]
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[[Category: Receptor protein-tyrosine kinase]]
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[[Category: Pinkas, D.M]]
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[[Category: Arrowsmith, C H]]
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[[Category: Edwards, A.M]]
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[[Category: Bountra, C]]
[[Category: Bountra, C]]
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[[Category: Bullock, A N]]
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[[Category: Burgess-Brown, N A]]
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[[Category: Delft, F von]]
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[[Category: Edwards, A M]]
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[[Category: Fox, A E]]
[[Category: Kupinska, K]]
[[Category: Kupinska, K]]
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[[Category: Pinkas, D M]]
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[[Category: Ai domain]]
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[[Category: Cct domain]]
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[[Category: Peptide binding protein]]
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[[Category: Rfxv motif binding]]
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[[Category: Wnk2]]

Revision as of 21:58, 9 August 2018

Structure of the kinase domain of human DDR1 in complex with a potent and selective inhibitor of DDR1 and DDR2

6gwr, resolution 2.07Å

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