2OAT | Aminotransferase | date | May 07, 1998 | ||||||||||||
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title | Ornithine Aminotransferase Complexed With 5-Fluoromethylornithine | ||||||||||||||
authors | P.Storici, G.Capitani, R.Muller, T.Schirmer, J.N.Jansonius | ||||||||||||||
compound | source | ||||||||||||||
Molecule: Ornithine Aminotransferase Chain: A, B, C Ec: 2.6.1.13 Engineered: Yes Biological_unit: Homotetramer |
Organism_scientific: Homo Sapiens Organism_common: Human Organ: Liver Organelle: Mitochondria Cellular_location: Intramitochondria Gene: Oat Expression_system: Escherichia Coli Expression_system_strain: Tb1 Expression_system_plasmid: Pmal-C2 | ||||||||||||||
symmetry | Space Group: P 32 2 1 | R_factor | 0.204 | ||||||||||||
crystal cell |
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method | X-Ray Diffraction | resolution | 1.95 Å | ||||||||||||
ligand | PFM | enzyme | Ornithine-oxo-acid transaminase. Ornithine d-transaminase. L-ornithine. Alpha-ketoglutarate d-aminotransferase. OAT. L-ornithine 5-aminotransferase. L-ornithine aminotransferase. Ornithine 5-aminotransferase. Ornithine transaminase. Ornithine-alpha-ketoglutarate aminotransferase. Ornithine-2-oxoacid aminotransferase. Ornithine-keto acid aminotransferase. Ornithine-keto acid transaminase. Ornithine-ketoglutarate aminotransferase. Ornithine-oxo acid aminotransferase. Ornithine. Alpha-oxoglutarate transaminase. Transferase E.C.2.6.1.13 | ||||||||||||
note | 2OAT is a representative structure | ||||||||||||||
related structures | by homologous chain: 1GBN | ||||||||||||||
similarity | Belongs to class-iii of pyridoxal-phosphate-dependent aminotransferases.[aminotran_3] | ||||||||||||||
subunit | Homotetramer. | ||||||||||||||
catalytic activ. | L-ornithine + a 2-oxo acid = l-glutamate 5- semialdehyde + an l-amino acid. | ||||||||||||||
subcellular loc. | Mitochondrial matrix. | ||||||||||||||
gene | OAT (H. sapiens) | ||||||||||||||
disease | Gyrate atrophy of choroid and retina with ornithinemia,B6responsive or unresponsive Defects in oat are the cause of ornithinemia with gyrate atrophy (ga) of choroid and retina. Ga is a slowly progressive blinding autosomal recessive disorder. |
Data retrieval |
View 2OAT in 3D |
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Visual 3D analysis of 2OAT |
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Structure-derived information |
- Domain d2oata_, region A: [rasmolscript] [script source] - Domain d2oatb_, region B: [rasmolscript] [script source] - Domain d2oatc_, region C: [rasmolscript] [script source] |
Sequence-derived information |
Other resources with information on 2OAT |
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