3abu

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'''Unreleased structure'''
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{{Seed}}
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[[Image:3abu.jpg|left|200px]]
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The entry 3abu is ON HOLD until Paper Publication
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{{STRUCTURE_3abu| PDB=3abu | SCENE= }}
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Authors: Mimasu, S., Umezawa, N., Sato, S., Higuchi, T., Umehara, T., Yokoyama, S., RIKEN Structural Genomics/Proteomics Initiative (RSGI)
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===Crystal Structure of LSD1 in complex with a 2-PCPA derivative, S1201===
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Description:
 
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Feb 3 09:13:50 2010''
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The line below this paragraph, {{ABSTRACT_PUBMED_20568732}}, adds the Publication Abstract to the page
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{{ABSTRACT_PUBMED_20568732}}
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==About this Structure==
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3ABU 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=3ABU OCA].
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==Reference==
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<ref group="xtra">PMID:20568732</ref><references group="xtra"/>
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[[Category: Homo sapiens]]
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[[Category: Higuchi, T.]]
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[[Category: Mimasu, S.]]
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[[Category: RSGI, RIKEN Structural Genomics/Proteomics Initiative.]]
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[[Category: Sato, S.]]
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[[Category: Umehara, T.]]
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[[Category: Umezawa, N.]]
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[[Category: Yokoyama, S.]]
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[[Category: Amine oxidase]]
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[[Category: Chromatin regulator]]
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[[Category: Developmental protein]]
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[[Category: Fad]]
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[[Category: H3k4]]
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[[Category: Histone demethylase]]
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[[Category: National project on protein structural and functional analyse]]
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[[Category: Nppsfa]]
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[[Category: Nucleus]]
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[[Category: Oxidoreductase]]
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[[Category: Phosphoprotein]]
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[[Category: Repressor]]
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[[Category: Riken structural genomics/proteomics initiative]]
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[[Category: Rsgi]]
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[[Category: Structural genomic]]
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[[Category: Tower domain]]
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[[Category: Transcription]]
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[[Category: Transcription regulation]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Jul 7 08:39:16 2010''

Revision as of 04:33, 7 July 2010

Image:3abu.jpg

Template:STRUCTURE 3abu

Crystal Structure of LSD1 in complex with a 2-PCPA derivative, S1201

Template:ABSTRACT PUBMED 20568732

About this Structure

3ABU is a 1 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

  • Mimasu S, Umezawa N, Sato S, Higuchi T, Umehara T, Yokoyama S. Structurally Designed Trans-2-phenylcyclopropylamine Derivatives Potently Inhibit Histone Demethylase LSD1/KDM1. Biochemistry. 2010 Jun 22. PMID:20568732 doi:10.1021/bi100299r

Page seeded by OCA on Wed Jul 7 08:39:16 2010

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