2f2s | pdb_00002f2s
From Proteopedia
Human mitochondrial acetoacetyl-CoA thiolase
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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
Proteopedia Page Contributors and Editors (what is this?)
Categories:
- Pages with broken file links
- 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
