2i50: Difference between revisions

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[[Image:2i50.png|left|200px]]
{{STRUCTURE_2i50|  PDB=2i50  |  SCENE=  }}  
{{STRUCTURE_2i50|  PDB=2i50  |  SCENE=  }}  
===Solution Structure of Ubp-M Znf-UBP domain===
{{ABSTRACT_PUBMED_17512543}}


===Solution Structure of Ubp-M Znf-UBP domain===
==Disease==
[[http://www.uniprot.org/uniprot/UBP16_HUMAN UBP16_HUMAN]] Note=A chromosomal aberration involving USP16 is a cause of Chronic myelomonocytic leukemia. Inversion inv(21) (q21;q22) with RUNX1/AML1.


{{ABSTRACT_PUBMED_17512543}}
==Function==
[[http://www.uniprot.org/uniprot/UBP16_HUMAN UBP16_HUMAN]] Specifically deubiquitinates histone H2A, a specific tag for epigenetic transcriptional repression, thereby acting as a coactivator. Deubiquitination of histone H2A is a prerequisite for subsequent phosphorylation at 'Ser-10' of histone H3, and is required for chromosome segregation when cells enter into mitosis. Regulates Hox gene expression via histone H2A deubiquitination. Prefers nucleosomal substrates. Does not deubiquitinate histone H2B.<ref>PMID:10077596</ref><ref>PMID:11753566</ref><ref>PMID:17914355</ref>


==About this Structure==
==About this Structure==
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==Reference==
==Reference==
<ref group="xtra">PMID:017512543</ref><references group="xtra"/>
<ref group="xtra">PMID:017512543</ref><references group="xtra"/><references/>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Ubiquitin thiolesterase]]
[[Category: Ubiquitin thiolesterase]]

Revision as of 00:00, 25 March 2013

Template:STRUCTURE 2i50

Solution Structure of Ubp-M Znf-UBP domain

Template:ABSTRACT PUBMED 17512543

Disease

[UBP16_HUMAN] Note=A chromosomal aberration involving USP16 is a cause of Chronic myelomonocytic leukemia. Inversion inv(21) (q21;q22) with RUNX1/AML1.

Function

[UBP16_HUMAN] Specifically deubiquitinates histone H2A, a specific tag for epigenetic transcriptional repression, thereby acting as a coactivator. Deubiquitination of histone H2A is a prerequisite for subsequent phosphorylation at 'Ser-10' of histone H3, and is required for chromosome segregation when cells enter into mitosis. Regulates Hox gene expression via histone H2A deubiquitination. Prefers nucleosomal substrates. Does not deubiquitinate histone H2B.[1][2][3]

About this Structure

2i50 is a 1 chain structure with sequence from Homo sapiens. Full experimental information is available from OCA.

Reference

  1. Pai MT, Tzeng SR, Kovacs JJ, Keaton MA, Li SS, Yao TP, Zhou P. Solution structure of the Ubp-M BUZ domain, a highly specific protein module that recognizes the C-terminal tail of free ubiquitin. J Mol Biol. 2007 Jul 6;370(2):290-302. Epub 2007 Apr 12. PMID:17512543 doi:10.1016/j.jmb.2007.04.015
  1. ↑ Cai SY, Babbitt RW, Marchesi VT. A mutant deubiquitinating enzyme (Ubp-M) associates with mitotic chromosomes and blocks cell division. Proc Natl Acad Sci U S A. 1999 Mar 16;96(6):2828-33. PMID:10077596
  2. ↑ Mimnaugh EG, Kayastha G, McGovern NB, Hwang SG, Marcu MG, Trepel J, Cai SY, Marchesi VT, Neckers L. Caspase-dependent deubiquitination of monoubiquitinated nucleosomal histone H2A induced by diverse apoptogenic stimuli. Cell Death Differ. 2001 Dec;8(12):1182-96. PMID:11753566 doi:10.1038/sj.cdd.4400924
  3. ↑ Joo HY, Zhai L, Yang C, Nie S, Erdjument-Bromage H, Tempst P, Chang C, Wang H. Regulation of cell cycle progression and gene expression by H2A deubiquitination. Nature. 2007 Oct 25;449(7165):1068-72. Epub 2007 Oct 3. PMID:17914355 doi:10.1038/nature06256

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