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 [[Single protein]] 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].  
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==
The oxidized subunit B8 from human complex I adopts a thioredoxin fold., Brockmann C, Diehl A, Rehbein K, Strauss H, Schmieder P, Korn B, Kuhne R, Oschkinat H, Structure. 2004 Sep;12(9):1645-54. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/15341729 15341729]
<ref group="xtra">PMID:15341729</ref><references group="xtra"/>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Single protein]]
[[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 Sun Jul 27 15:15:31 2008''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Feb 16 12:56:57 2009''