6das
From Proteopedia
(Difference between revisions)
Line 1: | Line 1: | ||
==Discovery of Potent 2-Aryl-6,7-Dihydro-5HPyrrolo[ 1,2-a]imidazoles as WDR5 WIN-site Inhibitors Using Fragment-Based Methods and Structure-Based Design== | ==Discovery of Potent 2-Aryl-6,7-Dihydro-5HPyrrolo[ 1,2-a]imidazoles as WDR5 WIN-site Inhibitors Using Fragment-Based Methods and Structure-Based Design== | ||
- | <StructureSection load='6das' size='340' side='right' caption='[[6das]], [[Resolution|resolution]] 1.80Å' scene=''> | + | <StructureSection load='6das' size='340' side='right'caption='[[6das]], [[Resolution|resolution]] 1.80Å' scene=''> |
== Structural highlights == | == Structural highlights == | ||
- | <table><tr><td colspan='2'>[[6das]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6DAS OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6DAS FirstGlance]. <br> | + | <table><tr><td colspan='2'>[[6das]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/Human Human]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6DAS OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6DAS FirstGlance]. <br> |
</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=G2D:N-[(1R)-6-(6,7-dihydro-5H-pyrrolo[1,2-a]imidazol-2-yl)-2,3-dihydro-1H-inden-1-yl]-3-methoxy-4-methylbenzamide'>G2D</scene></td></tr> | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=G2D:N-[(1R)-6-(6,7-dihydro-5H-pyrrolo[1,2-a]imidazol-2-yl)-2,3-dihydro-1H-inden-1-yl]-3-methoxy-4-methylbenzamide'>G2D</scene></td></tr> | ||
+ | <tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">WDR5, BIG3 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 HUMAN])</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=6das FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6das OCA], [http://pdbe.org/6das PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6das RCSB], [http://www.ebi.ac.uk/pdbsum/6das PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6das ProSAT]</span></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=6das FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6das OCA], [http://pdbe.org/6das PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6das RCSB], [http://www.ebi.ac.uk/pdbsum/6das PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6das ProSAT]</span></td></tr> | ||
</table> | </table> | ||
Line 18: | Line 19: | ||
</div> | </div> | ||
<div class="pdbe-citations 6das" style="background-color:#fffaf0;"></div> | <div class="pdbe-citations 6das" style="background-color:#fffaf0;"></div> | ||
+ | |||
+ | ==See Also== | ||
+ | *[[WD repeat-containing protein|WD repeat-containing protein]] | ||
== References == | == References == | ||
<references/> | <references/> | ||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
+ | [[Category: Human]] | ||
+ | [[Category: Large Structures]] | ||
[[Category: Fesik, S W]] | [[Category: Fesik, S W]] | ||
[[Category: Phan, J]] | [[Category: Phan, J]] |
Revision as of 10:02, 18 December 2019
Discovery of Potent 2-Aryl-6,7-Dihydro-5HPyrrolo[ 1,2-a]imidazoles as WDR5 WIN-site Inhibitors Using Fragment-Based Methods and Structure-Based Design
|