1s3a | pdb_00001s3a

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File:1s3a.png

Template:STRUCTURE 1s3a

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

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OCA

[1] 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

1s3a | pdb_00001s3a

Contents

NMR Solution Structure of Subunit B8 from Human NADH-Ubiquinone Oxidoreductase Complex I (CI-B8)

Disease

About this Structure

Reference

Proteopedia Page Contributors and Editors (what is this?)

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