1n7x
From Proteopedia
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[[Image:1n7x.png|left|200px]] | [[Image:1n7x.png|left|200px]] | ||
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{{STRUCTURE_1n7x| PDB=1n7x | SCENE= }} | {{STRUCTURE_1n7x| PDB=1n7x | SCENE= }} | ||
===HUMAN SERUM TRANSFERRIN, N-LOBE Y45E MUTANT=== | ===HUMAN SERUM TRANSFERRIN, N-LOBE Y45E MUTANT=== | ||
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{{ABSTRACT_PUBMED_12458193}} | {{ABSTRACT_PUBMED_12458193}} | ||
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- | ==Disease== | ||
- | Known disease associated with this structure: Atransferrinemia OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=190000 190000]], Iron deficiency anemia, susceptibility to OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=190000 190000]] | ||
==About this Structure== | ==About this Structure== | ||
- | + | [[1n7x]] is a 1 chain structure of [[Transferrin]] with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1N7X OCA]. | |
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+ | ==See Also== | ||
+ | *[[Transferrin|Transferrin]] | ||
==Reference== | ==Reference== | ||
- | <ref group="xtra">PMID: | + | <ref group="xtra">PMID:012458193</ref><references group="xtra"/> |
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Adams, T E.]] | [[Category: Adams, T E.]] | ||
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[[Category: Smith, V C.]] | [[Category: Smith, V C.]] | ||
[[Category: Iron transport]] | [[Category: Iron transport]] | ||
- | + | [[Category: Transport protein]] | |
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Revision as of 11:19, 25 July 2012
Contents |
HUMAN SERUM TRANSFERRIN, N-LOBE Y45E MUTANT
Template:ABSTRACT PUBMED 12458193
About this Structure
1n7x is a 1 chain structure of Transferrin with sequence from Homo sapiens. Full crystallographic information is available from OCA.
See Also
Reference
- Adams TE, Mason AB, He QY, Halbrooks PJ, Briggs SK, Smith VC, MacGillivray RT, Everse SJ. The position of arginine 124 controls the rate of iron release from the N-lobe of human serum transferrin. A structural study. J Biol Chem. 2003 Feb 21;278(8):6027-33. Epub 2002 Nov 27. PMID:12458193 doi:10.1074/jbc.M210349200