4umt
From Proteopedia
(Difference between revisions)
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==Structure of MELK in complex with inhibitors== | ==Structure of MELK in complex with inhibitors== | ||
- | <StructureSection load='4umt' size='340' side='right' caption='[[4umt]], [[Resolution|resolution]] 1.98Å' scene=''> | + | <StructureSection load='4umt' size='340' side='right'caption='[[4umt]], [[Resolution|resolution]] 1.98Å' scene=''> |
== Structural highlights == | == Structural highlights == | ||
- | <table><tr><td colspan='2'>[[4umt]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4UMT OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4UMT FirstGlance]. <br> | + | <table><tr><td colspan='2'>[[4umt]] is a 1 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=4UMT OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4UMT FirstGlance]. <br> |
</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=47W:1-(4-{[3-(ISOQUINOLIN-7-YL)PROP-2-YN-1-YL]OXY}-2-METHOXYBENZYL)PIPERAZINEDIIUM'>47W</scene>, <scene name='pdbligand=DMS:DIMETHYL+SULFOXIDE'>DMS</scene></td></tr> | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=47W:1-(4-{[3-(ISOQUINOLIN-7-YL)PROP-2-YN-1-YL]OXY}-2-METHOXYBENZYL)PIPERAZINEDIIUM'>47W</scene>, <scene name='pdbligand=DMS:DIMETHYL+SULFOXIDE'>DMS</scene></td></tr> | ||
<tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[4ump|4ump]], [[4umq|4umq]], [[4umr|4umr]], [[4umu|4umu]]</td></tr> | <tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[4ump|4ump]], [[4umq|4umq]], [[4umr|4umr]], [[4umu|4umu]]</td></tr> | ||
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__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
+ | [[Category: Human]] | ||
+ | [[Category: Large Structures]] | ||
[[Category: Beke, L]] | [[Category: Beke, L]] | ||
[[Category: Berdini, V]] | [[Category: Berdini, V]] |
Revision as of 09:22, 21 May 2019
Structure of MELK in complex with inhibitors
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Categories: Human | Large Structures | Beke, L | Berdini, V | Bonnet, P | Brehmer, D | Coyle, J E | Day, P J | Frederickson, M | Freyne, E J.E | Gilissen, R A.H J | Hamlett, C C.F | Howard, S | Johnson, C N | Linders, J T.M | McMenamin, R | Meerpoel, L | Patel, S | Rees, D C | Sharff, A | Sommen, F | Wu, T | Fragment based drug design | Transferase