5fdx
From Proteopedia
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| - | '''Unreleased structure''' | ||
| - | + | ==Structure of DDR1 receptor tyrosine kinase in complex with D2164 inhibitor at 2.65 Angstroms resolution.== | |
| + | <StructureSection load='5fdx' size='340' side='right'caption='[[5fdx]], [[Resolution|resolution]] 2.65Å' scene=''> | ||
| + | == Structural highlights == | ||
| + | <table><tr><td colspan='2'>[[5fdx]] is a 2 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=5FDX OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5FDX 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]] 2.65Å</td></tr> | ||
| + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=5X1:3-[(4-METHYLPIPERAZIN-1-YL)METHYL]-~{N}-[(4~{R})-4-METHYL-2-PYRIMIDIN-5-YL-3,4-DIHYDRO-1~{H}-ISOQUINOLIN-7-YL]-5-(TRIFLUOROMETHYL)BENZAMIDE'>5X1</scene>, <scene name='pdbligand=EDO:1,2-ETHANEDIOL'>EDO</scene>, <scene name='pdbligand=PEG:DI(HYDROXYETHYL)ETHER'>PEG</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=5fdx FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5fdx OCA], [https://pdbe.org/5fdx PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5fdx RCSB], [https://www.ebi.ac.uk/pdbsum/5fdx PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5fdx ProSAT]</span></td></tr> | ||
| + | </table> | ||
| + | == Function == | ||
| + | [https://www.uniprot.org/uniprot/DDR1_HUMAN DDR1_HUMAN] | ||
| - | + | ==See Also== | |
| - | + | *[[Epithelial discoidin domain-containing receptor|Epithelial discoidin domain-containing receptor]] | |
| - | + | __TOC__ | |
| - | [[Category: | + | </StructureSection> |
| - | [[Category: | + | [[Category: Homo sapiens]] |
| - | [[Category: | + | [[Category: Large Structures]] |
| - | [[Category: | + | [[Category: Arrowsmith CH]] |
| - | [[Category: | + | [[Category: Bartual SG]] |
| - | [[Category: | + | [[Category: Borkowska O]] |
| - | [[Category: | + | [[Category: Bountra C]] |
| - | [[Category: | + | [[Category: Bullock A]] |
| - | [[Category: | + | [[Category: Burgess-Brown N]] |
| - | [[Category: | + | [[Category: Chaikuad A]] |
| - | [[Category: | + | [[Category: Chalk R]] |
| - | [[Category: | + | [[Category: Ding K]] |
| - | [[Category: | + | [[Category: Edwards AM]] |
| - | [[Category: Kupinska | + | [[Category: Kopec J]] |
| - | [[Category: | + | [[Category: Kupinska K]] |
| - | [[Category: | + | [[Category: Mahajan P]] |
| - | [[Category: | + | [[Category: Mukhopadhyay S]] |
| - | [[Category: | + | [[Category: Newman J]] |
| - | [[Category: | + | [[Category: Pinkas DM]] |
| - | [[Category: | + | [[Category: Sorell F]] |
| - | [[Category: | + | [[Category: Strain-Damerell C]] |
| - | [[Category: Talon | + | [[Category: Tallant C]] |
| - | [[Category: | + | [[Category: Talon R]] |
| - | [[Category: | + | [[Category: Wang Z]] |
| - | [[Category: | + | [[Category: Williams E]] |
| + | [[Category: Von Delft F]] | ||
Current revision
Structure of DDR1 receptor tyrosine kinase in complex with D2164 inhibitor at 2.65 Angstroms resolution.
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Categories: Homo sapiens | Large Structures | Arrowsmith CH | Bartual SG | Borkowska O | Bountra C | Bullock A | Burgess-Brown N | Chaikuad A | Chalk R | Ding K | Edwards AM | Kopec J | Kupinska K | Mahajan P | Mukhopadhyay S | Newman J | Pinkas DM | Sorell F | Strain-Damerell C | Tallant C | Talon R | Wang Z | Williams E | Von Delft F
