4m90
From Proteopedia
(Difference between revisions)
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- | + | {{STRUCTURE_4m90| PDB=4m90 | SCENE= }} | |
+ | ===crystal structure of oxidized hN33/Tusc3=== | ||
- | The | + | ==Disease== |
+ | [[http://www.uniprot.org/uniprot/TUSC3_HUMAN TUSC3_HUMAN]] Autosomal recessive nonsyndromic intellectual deficit. The disease is caused by mutations affecting the gene represented in this entry. | ||
- | + | ==Function== | |
+ | [[http://www.uniprot.org/uniprot/TUSC3_HUMAN TUSC3_HUMAN]] Magnesium transporter. May be involved in N-glycosylation through its association with N-oligosaccharyl transferase.<ref>PMID:19717468</ref> | ||
- | + | ==About this Structure== | |
+ | [[4m90]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4M90 OCA]. | ||
+ | |||
+ | ==Reference== | ||
+ | <references group="xtra"/><references/> | ||
+ | [[Category: Aebi, M.]] | ||
+ | [[Category: Brozzo, M S.]] | ||
+ | [[Category: Glockshuber, R.]] | ||
+ | [[Category: Malojcic, G.]] | ||
+ | [[Category: Mohorko, E.]] | ||
+ | [[Category: Owen, R L.]] | ||
+ | [[Category: Endoplasmic reticulum]] | ||
+ | [[Category: Oxidoreductase]] | ||
+ | [[Category: Redox active]] | ||
+ | [[Category: Thioredoxin-like fold]] |
Revision as of 09:34, 26 March 2014
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
- ↑ 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