4m90 | pdb_00004m90
From Proteopedia
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
- ↑ 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:https://dx.doi.org/0908332106
