2f2s
From Proteopedia
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Human mitochondrial acetoacetyl-CoA thiolase
Disease
Known diseases associated with this structure: Alpha-methylacetoacetic aciduria OMIM:[607809], Hypermethioninemia, persistent, autosomal dominant, due to methionine adenosyltransferase I/III deficiency OMIM:[250850], Methionine adenosyltransferase deficiency, autosomal recessive OMIM:[250850]
About this Structure
2F2S is a Single protein structure of sequence from Homo sapiens with CL and COA as ligands. This structure superseeds the now removed PDB entry 2ES8. Active as Acetyl-CoA C-acetyltransferase, with EC number 2.3.1.9 Full crystallographic information is available from OCA.
Page seeded by OCA on Mon Nov 12 21:59:04 2007
Categories: Acetyl-CoA C-acetyltransferase | Homo sapiens | Single protein | Antoshenko, T. | Arrowsmith, C.H. | Bochkarev, A. | Dombrovski, L. | Edwards, A.M. | Loppnau, P. | Min, J.R. | Plotnikov, A.N. | SGC, Structural.Genomics.Consortium. | Sundstrom, M. | Weigelt, J. | Wu, H. | CL | COA | Acat1; acetyl-coenzyme a acetyltransferase 1; t2; mat; thil | Sgc | Structural genomics | Structural genomics consortium
