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6FP1

The crystal structure of P.fluorescens Kynurenine 3-monooxygenase (KMO) in complex with competitive inhibitor No. 1

Functional Information from GO Data
ChainGOidnamespacecontents
A0003824molecular_functioncatalytic activity
A0004497molecular_functionmonooxygenase activity
A0004502molecular_functionkynurenine 3-monooxygenase activity
A0006569biological_processtryptophan catabolic process
A0009435biological_processNAD biosynthetic process
A0016174molecular_functionNAD(P)H oxidase H2O2-forming activity
A0019363biological_processpyridine nucleotide biosynthetic process
A0019674biological_processNAD metabolic process
A0019805biological_processquinolinate biosynthetic process
A0034354biological_process'de novo' NAD biosynthetic process from tryptophan
A0043420biological_processanthranilate metabolic process
A0050660molecular_functionflavin adenine dinucleotide binding
A0070189biological_processkynurenine metabolic process
A0071949molecular_functionFAD binding
B0003824molecular_functioncatalytic activity
B0004497molecular_functionmonooxygenase activity
B0004502molecular_functionkynurenine 3-monooxygenase activity
B0006569biological_processtryptophan catabolic process
B0009435biological_processNAD biosynthetic process
B0016174molecular_functionNAD(P)H oxidase H2O2-forming activity
B0019363biological_processpyridine nucleotide biosynthetic process
B0019674biological_processNAD metabolic process
B0019805biological_processquinolinate biosynthetic process
B0034354biological_process'de novo' NAD biosynthetic process from tryptophan
B0043420biological_processanthranilate metabolic process
B0050660molecular_functionflavin adenine dinucleotide binding
B0070189biological_processkynurenine metabolic process
B0071949molecular_functionFAD binding
Functional Information from PDB Data
site_idAC1
Number of Residues32
Detailsbinding site for residue FAD A 501
ChainResidue
AILE12
AALA55
AARG110
AGLY133
ALEU134
AALA164
AASP165
AGLY309
AASP310
AGLY320
AGLN321
AGLY13
AGLY322
AMET323
AASN324
ACL502
AE0Q504
AHOH614
AHOH650
AHOH651
AHOH662
AHOH682
AGLY15
AHOH686
AHOH706
AHOH734
ALEU16
AALA17
AGLU36
AARG37
AARG38
ALEU54

site_idAC2
Number of Residues5
Detailsbinding site for residue CL A 502
ChainResidue
APRO317
AGLN321
AGLY322
AFAD501
AHOH676

site_idAC3
Number of Residues3
Detailsbinding site for residue PEG A 503
ChainResidue
APHE429
AGLU448
BARG295

site_idAC4
Number of Residues11
Detailsbinding site for residue E0Q A 504
ChainResidue
AALA55
AARG83
ATYR97
AILE223
APRO317
APHE318
AGLY320
AASN368
AMET372
ATYR403
AFAD501

site_idAC5
Number of Residues31
Detailsbinding site for residue FAD B 501
ChainResidue
BILE12
BGLY13
BGLY15
BLEU16
BALA17
BGLU36
BARG37
BARG38
BLEU54
BALA55
BARG110
BGLY133
BLEU134
BALA164
BASP165
BGLY309
BASP310
BGLY320
BGLN321
BGLY322
BMET323
BASN324
BCL502
BE0Q507
BHOH624
BHOH633
BHOH636
BHOH689
BHOH695
BHOH712
BHOH743

site_idAC6
Number of Residues4
Detailsbinding site for residue CL B 502
ChainResidue
BPRO317
BGLN321
BGLY322
BFAD501

site_idAC7
Number of Residues4
Detailsbinding site for residue PEG B 503
ChainResidue
AARG295
BLEU426
BGLU448
BHOH650

site_idAC8
Number of Residues2
Detailsbinding site for residue PEG B 504
ChainResidue
BHIS129
BLYS156

site_idAC9
Number of Residues4
Detailsbinding site for residue PEG B 505
ChainResidue
BARG83
BPRO96
BTYR97
BARG99

site_idAD1
Number of Residues2
Detailsbinding site for residue PEG B 506
ChainResidue
BPRO216
BHIS217

site_idAD2
Number of Residues12
Detailsbinding site for residue E0Q B 507
ChainResidue
BARG83
BTYR97
BLEU212
BILE223
BPRO317
BPHE318
BGLY320
BASN368
BMET372
BTYR403
BFAD501
BALA55

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues14
DetailsBINDING: 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
ChainResidueDetails
ALEU16
BALA55
BARG110
BLEU134
BASP310
BMET323
AGLU36
AALA55
AARG110
ALEU134
AASP310
AMET323
BLEU16
BGLU36

site_idSWS_FT_FI2
Number of Residues2
DetailsBINDING: BINDING => ECO:0000269|PubMed:29208702, ECO:0007744|PDB:5Y66, ECO:0007744|PDB:5Y77
ChainResidueDetails
AARG83
BARG83

site_idSWS_FT_FI3
Number of Residues2
DetailsBINDING: BINDING => ECO:0000269|PubMed:29208702, ECO:0007744|PDB:5Y77
ChainResidueDetails
ATYR97
BTYR97

site_idSWS_FT_FI4
Number of Residues4
DetailsBINDING: BINDING => ECO:0000269|PubMed:29208702, ECO:0007744|PDB:5Y66, ECO:0007744|PDB:5Y77, ECO:0007744|PDB:5Y7A
ChainResidueDetails
AASN368
ATYR403
BASN368
BTYR403

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PDB entries from 2024-07-17

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