1vkg

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==Overview==
==Overview==
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Modulation of the acetylation state of histones plays a pivotal role in, the regulation of gene expression. Histone deacetylases (HDACs) catalyze, the removal of acetyl groups from lysines near the N termini of histones., This reaction promotes the condensation of chromatin, leading to, repression of transcription. HDAC deregulation has been linked to several, types of cancer, suggesting a potential use for HDAC inhibitors in, oncology. Here we describe the first crystal structures of a human HDAC:, the structures of human HDAC8 complexed with four structurally diverse, hydroxamate inhibitors. This work sheds light on the catalytic mechanism, of the HDACs, and on differences in substrate specificity across the HDAC, family. The structure also suggests how phosphorylation of Ser39 affects, HDAC8 activity.
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Modulation of the acetylation state of histones plays a pivotal role in the regulation of gene expression. Histone deacetylases (HDACs) catalyze the removal of acetyl groups from lysines near the N termini of histones. This reaction promotes the condensation of chromatin, leading to repression of transcription. HDAC deregulation has been linked to several types of cancer, suggesting a potential use for HDAC inhibitors in oncology. Here we describe the first crystal structures of a human HDAC: the structures of human HDAC8 complexed with four structurally diverse hydroxamate inhibitors. This work sheds light on the catalytic mechanism of the HDACs, and on differences in substrate specificity across the HDAC family. The structure also suggests how phosphorylation of Ser39 affects HDAC8 activity.
==About this Structure==
==About this Structure==
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[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Arvai, A.]]
[[Category: Arvai, A.]]
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[[Category: Buggy, J.J.]]
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[[Category: Buggy, J J.]]
[[Category: Chi, E.]]
[[Category: Chi, E.]]
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[[Category: Dougan, D.R.]]
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[[Category: Dougan, D R.]]
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[[Category: Ho, J.D.]]
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[[Category: Ho, J D.]]
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[[Category: Jennings, A.J.]]
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[[Category: Jennings, A J.]]
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[[Category: Katz, B.A.]]
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[[Category: Katz, B A.]]
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[[Category: Knuth, M.W.]]
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[[Category: Knuth, M W.]]
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[[Category: Leahy, E.M.]]
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[[Category: Leahy, E M.]]
[[Category: Luong, C.]]
[[Category: Luong, C.]]
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[[Category: McRee, D.E.]]
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[[Category: McRee, D E.]]
[[Category: Mol, C.]]
[[Category: Mol, C.]]
[[Category: Navre, M.]]
[[Category: Navre, M.]]
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[[Category: Sang, B.C.]]
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[[Category: Sang, B C.]]
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[[Category: Skene, R.J.]]
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[[Category: Skene, R J.]]
[[Category: Snell, G.]]
[[Category: Snell, G.]]
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[[Category: Somoza, J.R.]]
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[[Category: Somoza, J R.]]
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[[Category: Swanson, R.V.]]
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[[Category: Swanson, R V.]]
[[Category: Tang, J.]]
[[Category: Tang, J.]]
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[[Category: Tari, L.W.]]
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[[Category: Tari, L W.]]
[[Category: Verner, E.]]
[[Category: Verner, E.]]
[[Category: Wynands, R.]]
[[Category: Wynands, R.]]
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[[Category: zinc hydrolase]]
[[Category: zinc hydrolase]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri Feb 15 17:05:05 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 15:36:13 2008''

Revision as of 13:36, 21 February 2008


1vkg, resolution 2.20Å

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Crystal Structure of Human HDAC8 complexed with CRA-19156

Overview

Modulation of the acetylation state of histones plays a pivotal role in the regulation of gene expression. Histone deacetylases (HDACs) catalyze the removal of acetyl groups from lysines near the N termini of histones. This reaction promotes the condensation of chromatin, leading to repression of transcription. HDAC deregulation has been linked to several types of cancer, suggesting a potential use for HDAC inhibitors in oncology. Here we describe the first crystal structures of a human HDAC: the structures of human HDAC8 complexed with four structurally diverse hydroxamate inhibitors. This work sheds light on the catalytic mechanism of the HDACs, and on differences in substrate specificity across the HDAC family. The structure also suggests how phosphorylation of Ser39 affects HDAC8 activity.

About this Structure

1VKG is a Single protein structure of sequence from Homo sapiens with , and as ligands. Full crystallographic information is available from OCA.

Reference

Structural snapshots of human HDAC8 provide insights into the class I histone deacetylases., Somoza JR, Skene RJ, Katz BA, Mol C, Ho JD, Jennings AJ, Luong C, Arvai A, Buggy JJ, Chi E, Tang J, Sang BC, Verner E, Wynands R, Leahy EM, Dougan DR, Snell G, Navre M, Knuth MW, Swanson RV, McRee DE, Tari LW, Structure. 2004 Jul;12(7):1325-34. PMID:15242608

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