4m7r: Difference between revisions

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'''Unreleased structure'''
{{STRUCTURE_4m7r|  PDB=4m7r  |  SCENE=  }}
===Crystal structure of the N-terminal methyltransferase-like domain of anamorsin===
{{ABSTRACT_PUBMED_24123282}}


The entry 4m7r is ON HOLD
==Function==
[[http://www.uniprot.org/uniprot/CPIN1_HUMAN CPIN1_HUMAN]] May be required for the maturation of extramitochondrial Fe/S proteins (By similarity). Has anti-apoptotic effects in the cell. Involved in negative control of cell death upon cytokine withdrawal. Promotes development of hematopoietic cells (By similarity).[HAMAP-Rule:MF_03115]


Authors: Song Gaojie, Liu Zhi-Jie
==About this Structure==
[[4m7r]] is a 2 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=4M7R OCA].


Description: Crystal structure of the N-terminal methyltransferase-like domain of anamorsin
==Reference==
<ref group="xtra">PMID:024123282</ref><references group="xtra"/><references/>
[[Category: Homo sapiens]]
[[Category: Liu, Z J.]]
[[Category: Song, G.]]
[[Category: Apoptosis]]
[[Category: Rossmann fold]]

Revision as of 09:36, 30 October 2013

Template:STRUCTURE 4m7r

Crystal structure of the N-terminal methyltransferase-like domain of anamorsin

Template:ABSTRACT PUBMED 24123282

Function

[CPIN1_HUMAN] May be required for the maturation of extramitochondrial Fe/S proteins (By similarity). Has anti-apoptotic effects in the cell. Involved in negative control of cell death upon cytokine withdrawal. Promotes development of hematopoietic cells (By similarity).[HAMAP-Rule:MF_03115]

About this Structure

4m7r is a 2 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

  1. Song G, Cheng C, Li Y, Shaw N, Xiao Z, Liu ZJ. Crystal structure of the N-terminal methyltransferase-like domain of anamorsin. Proteins. 2013 Oct 9. doi: 10.1002/prot.24443. PMID:24123282 doi:https://dx.doi.org/10.1002/prot.24443

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