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4m90

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'''Unreleased structure'''
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{{STRUCTURE_4m90| PDB=4m90 | SCENE= }}
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===crystal structure of oxidized hN33/Tusc3===
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The entry 4m90 is ON HOLD until Paper Publication
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==Disease==
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[[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.
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Authors: Mohorko, E., Owen, R.L., Malojcic, G., Brozzo, M.S., Aebi, M., Glockshuber, R.
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==Function==
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[[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>
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Description: crystal structure of oxidized hN33/Tusc3
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==About this Structure==
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[[4m90]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4M90 OCA].
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==Reference==
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<references group="xtra"/><references/>
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[[Category: Aebi, M.]]
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[[Category: Brozzo, M S.]]
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[[Category: Glockshuber, R.]]
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[[Category: Malojcic, G.]]
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[[Category: Mohorko, E.]]
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[[Category: Owen, R L.]]
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[[Category: Endoplasmic reticulum]]
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[[Category: Oxidoreductase]]
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[[Category: Redox active]]
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[[Category: Thioredoxin-like fold]]

Revision as of 09:34, 26 March 2014

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

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