4cfk: Difference between revisions
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{{STRUCTURE_4cfk| PDB=4cfk | SCENE= }} | {{STRUCTURE_4cfk| PDB=4cfk | SCENE= }} | ||
===N-TERMINAL BROMODOMAIN OF HUMAN BRD4 WITH LY294002=== | ===N-TERMINAL BROMODOMAIN OF HUMAN BRD4 WITH LY294002=== | ||
{{ABSTRACT_PUBMED_24533473}} | |||
==About this Structure== | ==About this Structure== | ||
[[4cfk]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4CFK OCA]. | [[4cfk]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4CFK OCA]. | ||
==Reference== | |||
<ref group="xtra">PMID:024533473</ref><references group="xtra"/><references/> | |||
[[Category: Chung, C.]] | [[Category: Chung, C.]] | ||
[[Category: Dittmann, A.]] | [[Category: Dittmann, A.]] | ||
Revision as of 15:15, 3 March 2014
N-TERMINAL BROMODOMAIN OF HUMAN BRD4 WITH LY294002
Template:ABSTRACT PUBMED 24533473
About this Structure
4cfk is a 1 chain structure. Full crystallographic information is available from OCA.
Reference
- Dittmann A, Werner T, Chung CW, Savitski MM, Falth Savitski M, Grandi P, Hopf C, Lindon M, Neubauer G, Prinjha RK, Bantscheff M, Drewes G. The Commonly Used PI3-Kinase Probe LY294002 Is an Inhibitor of BET Bromodomains. ACS Chem Biol. 2014 Feb 21;9(2):495-502. doi: 10.1021/cb400789e. Epub 2013 Dec, 10. PMID:24533473 doi:https://dx.doi.org/10.1021/cb400789e
