2uxw | pdb_00002uxw
From Proteopedia
CRYSTAL STRUCTURE OF HUMAN VERY LONG CHAIN ACYL-COA DEHYDROGENASE (ACADVL)
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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 EDO, FAD and TH3 as ligands. Known structural/functional Site: AC1. Full crystallographic information is available from OCA.
Page seeded by OCA on Tue Dec 18 20:21:25 2007
Proteopedia Page Contributors and Editors (what is this?)
Categories:
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- 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
