3zns

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m (Protected "3zns" [edit=sysop:move=sysop])
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'''Unreleased structure'''
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{{STRUCTURE_3zns| PDB=3zns | SCENE= }}
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===HDAC7 bound with TFMO inhibitor tmp942===
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The entry 3zns is ON HOLD until sometime in the future
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==Function==
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[[http://www.uniprot.org/uniprot/HDAC7_HUMAN HDAC7_HUMAN]] Responsible for the deacetylation of lysine residues on the N-terminal part of the core histones (H2A, H2B, H3 and H4). Histone deacetylation gives a tag for epigenetic repression and plays an important role in transcriptional regulation, cell cycle progression and developmental events. Histone deacetylases act via the formation of large multiprotein complexes. Involved in muscle maturation by repressing transcription of myocyte enhancer factors such as MEF2A, MEF2B and MEF2C. During muscle differentiation, it shuttles into the cytoplasm, allowing the expression of myocyte enhancer factors (By similarity). May be involved in Epstein-Barr virus (EBV) latency, possibly by repressing the viral BZLF1 gene.<ref>PMID:12239305</ref>
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Authors: lobera, m., madauss, k., pohlhaus, d., trump, r., nolan, m.
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==About this Structure==
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[[3zns]] is a 3 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=3ZNS OCA].
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Description: HDAC7 bound with TFMO inhibitor tmp942
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==Reference==
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<references group="xtra"/><references/>
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[[Category: Histone deacetylase]]
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[[Category: Homo sapiens]]
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[[Category: Lobera, M.]]
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[[Category: Madauss, K P.]]
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[[Category: Nolan, M A.]]
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[[Category: Pohlhaus, D T.]]
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[[Category: Trump, R P.]]
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[[Category: Hydrolase]]
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[[Category: Mbg]]
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[[Category: Zbg]]

Revision as of 08:54, 27 March 2013

Template:STRUCTURE 3zns

Contents

HDAC7 bound with TFMO inhibitor tmp942

Function

[HDAC7_HUMAN] Responsible for the deacetylation of lysine residues on the N-terminal part of the core histones (H2A, H2B, H3 and H4). Histone deacetylation gives a tag for epigenetic repression and plays an important role in transcriptional regulation, cell cycle progression and developmental events. Histone deacetylases act via the formation of large multiprotein complexes. Involved in muscle maturation by repressing transcription of myocyte enhancer factors such as MEF2A, MEF2B and MEF2C. During muscle differentiation, it shuttles into the cytoplasm, allowing the expression of myocyte enhancer factors (By similarity). May be involved in Epstein-Barr virus (EBV) latency, possibly by repressing the viral BZLF1 gene.[1]

About this Structure

3zns is a 3 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

  1. ↑ Bryant H, Farrell PJ. Signal Transduction and Transcription Factor Modification during Reactivation of Epstein-Barr Virus from Latency. J Virol. 2002 Oct;76(20):10290-8. PMID:12239305

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