4ly1: Difference between revisions
From Proteopedia
Jump to navigationJump to search
m Protected "4ly1" [edit=sysop:move=sysop] |
No edit summary |
||
| Line 1: | Line 1: | ||
{{STRUCTURE_4ly1| PDB=4ly1 | SCENE= }} | |||
===Structure of Human HDAC2 in complex with inhibitor 4-(acetylamino)-N-[2-amino-5-(thiophen-2-yl)phenyl]benzamide=== | |||
{{ABSTRACT_PUBMED_23897821}} | |||
==Function== | |||
[[http://www.uniprot.org/uniprot/HDAC2_HUMAN HDAC2_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. Forms transcriptional repressor complexes by associating with MAD, SIN3, YY1 and N-COR. Interacts in the late S-phase of DNA-replication with DNMT1 in the other transcriptional repressor complex composed of DNMT1, DMAP1, PCNA, CAF1. Deacetylates TSHZ3 and regulates its transcriptional repressor activity. Component of a RCOR/GFI/KDM1A/HDAC complex that suppresses, via histone deacetylase (HDAC) recruitment, a number of genes implicated in multilineage blood cell development.<ref>PMID:19343227</ref> | |||
==About this Structure== | |||
[[4ly1]] 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=4LY1 OCA]. | |||
==Reference== | |||
<ref group="xtra">PMID:023897821</ref><references group="xtra"/><references/> | |||
[[Category: Histone deacetylase]] | |||
[[Category: Homo sapiens]] | |||
[[Category: Fong, R.]] | |||
[[Category: Lupardus, P J.]] | |||
[[Category: Deacetylase]] | |||
[[Category: Histone]] | |||
[[Category: Hydrolase-hydrolase inhibitor complex]] | |||
