5MZC
Pseudomonas fluorescens kynurenine 3-monooxygenase (KMO) in complex with 3-(5-chloro-6-ethoxy-2-oxo-2,3-dihydro-1,3-benzoxazol-3-yl)propanoic acid
Functional Information from GO Data
Chain | GOid | namespace | contents |
A | 0003824 | molecular_function | catalytic activity |
A | 0004497 | molecular_function | monooxygenase activity |
A | 0004502 | molecular_function | kynurenine 3-monooxygenase activity |
A | 0006569 | biological_process | L-tryptophan catabolic process |
A | 0009435 | biological_process | NAD+ biosynthetic process |
A | 0016174 | molecular_function | NAD(P)H oxidase H2O2-forming activity |
A | 0016491 | molecular_function | oxidoreductase activity |
A | 0019363 | biological_process | pyridine nucleotide biosynthetic process |
A | 0019674 | biological_process | NAD+ metabolic process |
A | 0019805 | biological_process | quinolinate biosynthetic process |
A | 0043420 | biological_process | anthranilate metabolic process |
A | 0050660 | molecular_function | flavin adenine dinucleotide binding |
A | 0070189 | biological_process | kynurenine metabolic process |
A | 0071949 | molecular_function | FAD binding |
B | 0003824 | molecular_function | catalytic activity |
B | 0004497 | molecular_function | monooxygenase activity |
B | 0004502 | molecular_function | kynurenine 3-monooxygenase activity |
B | 0006569 | biological_process | L-tryptophan catabolic process |
B | 0009435 | biological_process | NAD+ biosynthetic process |
B | 0016174 | molecular_function | NAD(P)H oxidase H2O2-forming activity |
B | 0016491 | molecular_function | oxidoreductase activity |
B | 0019363 | biological_process | pyridine nucleotide biosynthetic process |
B | 0019674 | biological_process | NAD+ metabolic process |
B | 0019805 | biological_process | quinolinate biosynthetic process |
B | 0043420 | biological_process | anthranilate metabolic process |
B | 0050660 | molecular_function | flavin adenine dinucleotide binding |
B | 0070189 | biological_process | kynurenine metabolic process |
B | 0071949 | molecular_function | FAD binding |
Functional Information from PDB Data
site_id | AC1 |
Number of Residues | 37 |
Details | binding site for residue FAD A 501 |
Chain | Residue |
A | ILE13 |
A | ALA56 |
A | ARG111 |
A | GLY134 |
A | LEU135 |
A | ALA165 |
A | ASP166 |
A | GLY167 |
A | ALA171 |
A | GLY310 |
A | ASP311 |
A | GLY14 |
A | PRO318 |
A | GLY321 |
A | GLN322 |
A | GLY323 |
A | MET324 |
A | ASN325 |
A | CL502 |
A | 8EQ503 |
A | 8EQ504 |
A | GOL506 |
A | GLY16 |
A | HOH615 |
A | HOH627 |
A | HOH638 |
A | HOH639 |
A | HOH670 |
A | HOH729 |
A | HOH748 |
A | HOH847 |
A | LEU17 |
A | ALA18 |
A | GLU37 |
A | ARG38 |
A | ARG39 |
A | LEU55 |
site_id | AC2 |
Number of Residues | 5 |
Details | binding site for residue CL A 502 |
Chain | Residue |
A | PRO318 |
A | GLN322 |
A | GLY323 |
A | FAD501 |
A | HOH811 |
site_id | AC3 |
Number of Residues | 15 |
Details | binding site for residue 8EQ A 503 |
Chain | Residue |
A | ALA56 |
A | ARG84 |
A | TYR98 |
A | ILE106 |
A | LEU213 |
A | ILE224 |
A | PHE238 |
A | PRO318 |
A | PHE319 |
A | HIS320 |
A | GLY321 |
A | ASN369 |
A | MET373 |
A | TYR404 |
A | FAD501 |
site_id | AC4 |
Number of Residues | 10 |
Details | binding site for residue 8EQ A 504 |
Chain | Residue |
A | ALA15 |
A | ARG39 |
A | PRO42 |
A | ARG111 |
A | ASP112 |
A | ASN115 |
A | FAD501 |
A | HOH638 |
A | HOH729 |
A | HOH819 |
site_id | AC5 |
Number of Residues | 11 |
Details | binding site for residue 8EQ A 505 |
Chain | Residue |
A | LEU427 |
A | PHE430 |
A | ALA431 |
A | HIS435 |
A | ALA445 |
A | GLU449 |
A | HOH644 |
A | HOH888 |
B | HIS185 |
B | ARG296 |
B | HOH629 |
site_id | AC6 |
Number of Residues | 7 |
Details | binding site for residue GOL A 506 |
Chain | Residue |
A | LEU292 |
A | ALA293 |
A | PRO315 |
A | MET316 |
A | FAD501 |
A | HOH614 |
A | HOH743 |
site_id | AC7 |
Number of Residues | 37 |
Details | binding site for residue FAD B 501 |
Chain | Residue |
B | ASP166 |
B | GLY167 |
B | ALA171 |
B | GLY310 |
B | ASP311 |
B | GLY321 |
B | GLN322 |
B | GLY323 |
B | MET324 |
B | ASN325 |
B | CL502 |
B | 8EQ503 |
B | 8EQ504 |
B | GOL505 |
B | HOH605 |
B | HOH612 |
B | HOH621 |
B | HOH641 |
B | HOH651 |
B | HOH730 |
B | HOH763 |
B | HOH798 |
B | HOH801 |
B | ILE13 |
B | GLY14 |
B | GLY16 |
B | LEU17 |
B | ALA18 |
B | GLU37 |
B | ARG38 |
B | ARG39 |
B | LEU55 |
B | ALA56 |
B | ARG111 |
B | GLY134 |
B | LEU135 |
B | ALA165 |
site_id | AC8 |
Number of Residues | 5 |
Details | binding site for residue CL B 502 |
Chain | Residue |
B | PRO318 |
B | GLN322 |
B | GLY323 |
B | FAD501 |
B | HOH790 |
site_id | AC9 |
Number of Residues | 18 |
Details | binding site for residue 8EQ B 503 |
Chain | Residue |
B | ALA56 |
B | ARG84 |
B | ILE215 |
B | ILE224 |
B | THR236 |
B | PHE238 |
B | PRO318 |
B | PHE319 |
B | HIS320 |
B | GLY321 |
B | ASN369 |
B | MET373 |
B | TYR404 |
B | FAD501 |
B | HOH603 |
B | HOH651 |
B | HOH660 |
B | HOH777 |
site_id | AD1 |
Number of Residues | 9 |
Details | binding site for residue 8EQ B 504 |
Chain | Residue |
B | ALA15 |
B | ARG39 |
B | PRO42 |
B | ARG111 |
B | ASP112 |
B | ASN115 |
B | FAD501 |
B | HOH708 |
B | HOH730 |
site_id | AD2 |
Number of Residues | 7 |
Details | binding site for residue GOL B 505 |
Chain | Residue |
B | CYS168 |
B | LEU292 |
B | ALA293 |
B | PRO315 |
B | MET316 |
B | FAD501 |
B | HOH671 |
Functional Information from SwissProt/UniProt
site_id | SWS_FT_FI1 |
Number of Residues | 14 |
Details | BINDING: BINDING => ECO:0000269|PubMed:28336141, ECO:0000269|PubMed:28398044, ECO:0000269|PubMed:28604669, ECO:0000269|PubMed:29208702, ECO:0000269|PubMed:29429898, ECO:0007744|PDB:5FN0, ECO:0007744|PDB:5MZC, ECO:0007744|PDB:5MZI, ECO:0007744|PDB:5MZK, ECO:0007744|PDB:5N7T, ECO:0007744|PDB:5NA5, ECO:0007744|PDB:5NAB, ECO:0007744|PDB:5NAE, ECO:0007744|PDB:5NAG, ECO:0007744|PDB:5NAH, ECO:0007744|PDB:5NAK, ECO:0007744|PDB:5X6P, ECO:0007744|PDB:5X6Q, ECO:0007744|PDB:5Y66, ECO:0007744|PDB:5Y77, ECO:0007744|PDB:5Y7A |
Chain | Residue | Details |
A | LEU17 | |
B | ALA56 | |
B | ARG111 | |
B | LEU135 | |
B | ASP311 | |
B | MET324 | |
A | GLU37 | |
A | ALA56 | |
A | ARG111 | |
A | LEU135 | |
A | ASP311 | |
A | MET324 | |
B | LEU17 | |
B | GLU37 |
site_id | SWS_FT_FI2 |
Number of Residues | 2 |
Details | BINDING: BINDING => ECO:0000269|PubMed:29208702, ECO:0007744|PDB:5Y66, ECO:0007744|PDB:5Y77 |
Chain | Residue | Details |
A | ARG84 | |
B | ARG84 |
site_id | SWS_FT_FI3 |
Number of Residues | 2 |
Details | BINDING: BINDING => ECO:0000269|PubMed:29208702, ECO:0007744|PDB:5Y77 |
Chain | Residue | Details |
A | TYR98 | |
B | TYR98 |
site_id | SWS_FT_FI4 |
Number of Residues | 4 |
Details | BINDING: BINDING => ECO:0000269|PubMed:29208702, ECO:0007744|PDB:5Y66, ECO:0007744|PDB:5Y77, ECO:0007744|PDB:5Y7A |
Chain | Residue | Details |
A | ASN369 | |
A | TYR404 | |
B | ASN369 | |
B | TYR404 |