2uxw
From Proteopedia
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CRYSTAL STRUCTURE OF HUMAN VERY LONG CHAIN ACYL-COA DEHYDROGENASE (ACADVL)
Disease
Known diseases associated with this structure: VLCAD deficiency OMIM:[609575]
About this Structure
2UXW is a Single protein structure of sequence from Homo sapiens with , and as ligands. Known structural/functional Site: . Full crystallographic information is available from OCA.
Page seeded by OCA on Sun Feb 3 10:48:13 2008
Categories: Homo sapiens | Single protein | Arrowsmith, C.H. | Berridge, G. | Bunkoczi, G. | Burgess, N. | Delft, F.Von. | Edwards, A. | Hozjan, V. | Oppermann, U. | Pike, A.C.W. | Salah, E. | Smee, C. | Sundstrom, M. | Ugochukwu, E. | Uppenberg, J. | Weigelt, J. | EDO | FAD | TH3 | Acetylation | Alternative splicing | Cardiomyopathy | Coenzyme a dehydrogenase | Disease mutation | Fad | Fatty acid metabolism | Flavoprotein | Lipid metabolism | Mitochondrial fatty acid beta-oxidation | Mitochondrion | Oxidoreductase | Polymorphism | Transit peptide | Very long chain fatty acids
