4m90

From Proteopedia

Revision as of 09:34, 26 March 2014 by OCA (Talk | contribs)
Jump to: navigation, search

Template:STRUCTURE 4m90

Contents

crystal structure of oxidized hN33/Tusc3

Disease

[TUSC3_HUMAN] Autosomal recessive nonsyndromic intellectual deficit. The disease is caused by mutations affecting the gene represented in this entry.

Function

[TUSC3_HUMAN] Magnesium transporter. May be involved in N-glycosylation through its association with N-oligosaccharyl transferase.[1]

About this Structure

4m90 is a 1 chain structure. Full crystallographic information is available from OCA.

Reference

  1. Zhou H, Clapham DE. Mammalian MagT1 and TUSC3 are required for cellular magnesium uptake and vertebrate embryonic development. Proc Natl Acad Sci U S A. 2009 Sep 15;106(37):15750-5. Epub 2009 Aug 26. PMID:19717468 doi:http://dx.doi.org/0908332106

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools