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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