1s3a: Difference between revisions
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{{ABSTRACT_PUBMED_15341729}} | {{ABSTRACT_PUBMED_15341729}} | ||
==Disease== | |||
Known disease associated with this structure: Leigh syndrome due to mitochondrial complex I deficiency OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602137 602137]] | |||
==About this Structure== | ==About this Structure== | ||
1S3A is a | 1S3A is a 1 chain structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1S3A OCA]. | ||
==Reference== | ==Reference== | ||
<ref group="xtra">PMID:15341729</ref><references group="xtra"/> | |||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Brockmann, C.]] | [[Category: Brockmann, C.]] | ||
[[Category: Diehl, A.]] | [[Category: Diehl, A.]] | ||
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[[Category: Nmr]] | [[Category: Nmr]] | ||
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Feb 16 12:56:57 2009'' | ||
Revision as of 10:56, 16 February 2009
NMR Solution Structure of Subunit B8 from Human NADH-Ubiquinone Oxidoreductase Complex I (CI-B8)
Template:ABSTRACT PUBMED 15341729
Disease
Known disease associated with this structure: Leigh syndrome due to mitochondrial complex I deficiency OMIM:[602137]
About this Structure
1S3A is a 1 chain structure of sequence from Homo sapiens. Full experimental information is available from OCA.
Reference
- Brockmann C, Diehl A, Rehbein K, Strauss H, Schmieder P, Korn B, Kuhne R, Oschkinat H. The oxidized subunit B8 from human complex I adopts a thioredoxin fold. Structure. 2004 Sep;12(9):1645-54. PMID:15341729 doi:https://dx.doi.org/10.1016/j.str.2004.06.021
Page seeded by OCA on Mon Feb 16 12:56:57 2009
