3sff: Difference between revisions
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===Crystal Structure of Human HDAC8 Inhibitor Complex, an Amino Acid Derived Inhibitor=== | |||
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{{ABSTRACT_PUBMED_21723733}} | |||
==About this Structure== | |||
[[3sff]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3SFF OCA]. | |||
==Reference== | |||
<ref group="xtra">PMID:021723733</ref><references group="xtra"/> | |||
[[Category: Histone deacetylase]] | |||
[[Category: Homo sapiens]] | |||
[[Category: Stams, T.]] | |||
[[Category: Vash, B.]] | |||
[[Category: Deacetylase]] | |||
[[Category: Hydrolase-hydrolase inhibitor complex]] | |||
[[Category: Nvp-lci785]] | |||
Revision as of 09:37, 20 July 2011
Crystal Structure of Human HDAC8 Inhibitor Complex, an Amino Acid Derived InhibitorCrystal Structure of Human HDAC8 Inhibitor Complex, an Amino Acid Derived Inhibitor
Template:ABSTRACT PUBMED 21723733
About this StructureAbout this Structure
3sff is a 1 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.
ReferenceReference
- ↑ Whitehead L, Dobler MR, Radetich B, Zhu Y, Atadja PW, Claiborne T, Grob JE, McRiner A, Pancost MR, Patnaik A, Shao W, Shultz M, Tichkule R, Tommasi RA, Vash B, Wang P, Stams T. Human HDAC isoform selectivity achieved via exploitation of the acetate release channel with structurally unique small molecule inhibitors. Bioorg Med Chem. 2011 Aug 1;19(15):4626-34. Epub 2011 Jun 15. PMID:21723733 doi:10.1016/j.bmc.2011.06.030