6V8C
Design, Synthesis, and Mechanism of Fluorine-substituted Cyclohexene Analogues of GAMA-Aminobutyric Acid (GABA) as Selective Ornithine Aminotransferase Inactivators
Functional Information from GO Data
Chain | GOid | namespace | contents |
A | 0004587 | molecular_function | ornithine aminotransferase activity |
A | 0005515 | molecular_function | protein binding |
A | 0005654 | cellular_component | nucleoplasm |
A | 0005737 | cellular_component | cytoplasm |
A | 0005739 | cellular_component | mitochondrion |
A | 0005759 | cellular_component | mitochondrial matrix |
A | 0007601 | biological_process | visual perception |
A | 0008483 | molecular_function | transaminase activity |
A | 0010121 | biological_process | arginine catabolic process to proline via ornithine |
A | 0019544 | biological_process | arginine catabolic process to glutamate |
A | 0030170 | molecular_function | pyridoxal phosphate binding |
A | 0042802 | molecular_function | identical protein binding |
A | 0055129 | biological_process | L-proline biosynthetic process |
B | 0004587 | molecular_function | ornithine aminotransferase activity |
B | 0005515 | molecular_function | protein binding |
B | 0005654 | cellular_component | nucleoplasm |
B | 0005737 | cellular_component | cytoplasm |
B | 0005739 | cellular_component | mitochondrion |
B | 0005759 | cellular_component | mitochondrial matrix |
B | 0007601 | biological_process | visual perception |
B | 0008483 | molecular_function | transaminase activity |
B | 0010121 | biological_process | arginine catabolic process to proline via ornithine |
B | 0019544 | biological_process | arginine catabolic process to glutamate |
B | 0030170 | molecular_function | pyridoxal phosphate binding |
B | 0042802 | molecular_function | identical protein binding |
B | 0055129 | biological_process | L-proline biosynthetic process |
C | 0004587 | molecular_function | ornithine aminotransferase activity |
C | 0005515 | molecular_function | protein binding |
C | 0005654 | cellular_component | nucleoplasm |
C | 0005737 | cellular_component | cytoplasm |
C | 0005739 | cellular_component | mitochondrion |
C | 0005759 | cellular_component | mitochondrial matrix |
C | 0007601 | biological_process | visual perception |
C | 0008483 | molecular_function | transaminase activity |
C | 0010121 | biological_process | arginine catabolic process to proline via ornithine |
C | 0019544 | biological_process | arginine catabolic process to glutamate |
C | 0030170 | molecular_function | pyridoxal phosphate binding |
C | 0042802 | molecular_function | identical protein binding |
C | 0055129 | biological_process | L-proline biosynthetic process |
Functional Information from PROSITE/UniProt
site_id | PS00600 |
Number of Residues | 38 |
Details | AA_TRANSFER_CLASS_3 Aminotransferases class-III pyridoxal-phosphate attachment site. FIaDEIqt.GLaRtGrwlavdyenvrp....DIVllGKalsGG |
Chain | Residue | Details |
A | PHE260-GLY297 |
Functional Information from SwissProt/UniProt
site_id | SWS_FT_FI1 |
Number of Residues | 15 |
Details | MOD_RES: N6-acetyllysine => ECO:0000250|UniProtKB:P29758 |
Chain | Residue | Details |
A | LYS49 | |
B | LYS421 | |
C | LYS49 | |
C | LYS66 | |
C | LYS386 | |
C | LYS392 | |
C | LYS421 | |
A | LYS66 | |
A | LYS386 | |
A | LYS392 | |
A | LYS421 | |
B | LYS49 | |
B | LYS66 | |
B | LYS386 | |
B | LYS392 |
site_id | SWS_FT_FI2 |
Number of Residues | 3 |
Details | MOD_RES: N6-succinyllysine => ECO:0000250|UniProtKB:P29758 |
Chain | Residue | Details |
A | LYS102 | |
B | LYS102 | |
C | LYS102 |
site_id | SWS_FT_FI3 |
Number of Residues | 9 |
Details | MOD_RES: N6-succinyllysine; alternate => ECO:0000250|UniProtKB:P29758 |
Chain | Residue | Details |
A | LYS107 | |
A | LYS362 | |
A | LYS405 | |
B | LYS107 | |
B | LYS362 | |
B | LYS405 | |
C | LYS107 | |
C | LYS362 | |
C | LYS405 |
site_id | SWS_FT_FI4 |
Number of Residues | 3 |
Details | MOD_RES: N6-(pyridoxal phosphate)lysine => ECO:0000269|PubMed:3754226 |
Chain | Residue | Details |
A | LYS292 | |
B | LYS292 | |
C | LYS292 |
Catalytic Information from CSA
site_id | MCSA1 |
Number of Residues | 3 |
Details | M-CSA 929 |
Chain | Residue | Details |
A | PHE177 | steric role |
A | ASP263 | electrostatic stabiliser |
A | LYS292 | covalent catalysis, proton shuttle (general acid/base) |
site_id | MCSA2 |
Number of Residues | 3 |
Details | M-CSA 929 |
Chain | Residue | Details |
B | PHE177 | steric role |
B | ASP263 | electrostatic stabiliser |
B | LYS292 | covalent catalysis, proton shuttle (general acid/base) |
site_id | MCSA3 |
Number of Residues | 3 |
Details | M-CSA 929 |
Chain | Residue | Details |
C | PHE177 | steric role |
C | ASP263 | electrostatic stabiliser |
C | LYS292 | covalent catalysis, proton shuttle (general acid/base) |