Structure of PDB 1wve Chain B Binding Site BS01
Receptor Information
>1wve Chain B (length=515) Species:
303
(Pseudomonas putida) [
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AVLPKGVTQGEFNKAVQKFRALLGDDNVLVESDQLVPYNKIMMPVENAAH
APSAAVTATTVEQVQGVVKICNEHKIPIWTISTGRNFGYGSAAPVQRGQV
ILDLKKMNKIIKIDPEMCYALVEPGVTFGQMYDYIQENNLPVMLSFSAPS
AIAGPVGNTMDRGVGYTPYGEHFMMQCGMEVVLANGDVYRTGMGGVPGSN
TWQIFKWGYGPTLDGMFTQANYGICTKMGFWLMPKPPVFKPFEVIFEDEA
DIVEIVDALRPLRMSNTIPNSVVIASTLWEAGSAHLTRAQYTTEPGHTPD
SVIKQMQKDTGMGAWNLYAALYGTQEQVDVNWKIVTDVFKKLGKGRIVTQ
EEAGDTQPFKYRAQLMSGVPNLQEFGLYNWRGGGGSMWFAPVSEARGSEC
KKQAAMAKRVLHKYGLDYVAEFIVAPRDMHHVIDVLYDRTNPEETKRADA
CFNELLDEFEKEGYAVYRVNTRFQDRVAQSYGPVKRKLEHAIKRAVDPNN
ILAPGRSGIDLNNDF
Ligand information
Ligand ID
FAD
InChI
InChI=1S/C27H33N9O15P2/c1-10-3-12-13(4-11(10)2)35(24-18(32-12)25(42)34-27(43)33-24)5-14(37)19(39)15(38)6-48-52(44,45)51-53(46,47)49-7-16-20(40)21(41)26(50-16)36-9-31-17-22(28)29-8-30-23(17)36/h3-4,8-9,14-16,19-21,26,37-41H,5-7H2,1-2H3,(H,44,45)(H,46,47)(H2,28,29,30)(H,34,42,43)/t14-,15+,16+,19-,20+,21+,26+/m0/s1
InChIKey
VWWQXMAJTJZDQX-UYBVJOGSSA-N
SMILES
Software
SMILES
CACTVS 3.341
Cc1cc2N=C3C(=O)NC(=O)N=C3N(C[C@H](O)[C@H](O)[C@H](O)CO[P@](O)(=O)O[P@@](O)(=O)OC[C@H]4O[C@H]([C@H](O)[C@@H]4O)n5cnc6c(N)ncnc56)c2cc1C
OpenEye OEToolkits 1.5.0
Cc1cc2c(cc1C)N(C3=NC(=O)NC(=O)C3=N2)CC(C(C(COP(=O)(O)OP(=O)(O)OCC4C(C(C(O4)n5cnc6c5ncnc6N)O)O)O)O)O
OpenEye OEToolkits 1.5.0
Cc1cc2c(cc1C)N(C3=NC(=O)NC(=O)C3=N2)C[C@@H]([C@@H]([C@@H](CO[P@@](=O)(O)O[P@](=O)(O)OC[C@@H]4[C@H]([C@H]([C@@H](O4)n5cnc6c5ncnc6N)O)O)O)O)O
CACTVS 3.341
Cc1cc2N=C3C(=O)NC(=O)N=C3N(C[CH](O)[CH](O)[CH](O)CO[P](O)(=O)O[P](O)(=O)OC[CH]4O[CH]([CH](O)[CH]4O)n5cnc6c(N)ncnc56)c2cc1C
ACDLabs 10.04
O=C2C3=Nc1cc(c(cc1N(C3=NC(=O)N2)CC(O)C(O)C(O)COP(=O)(O)OP(=O)(O)OCC6OC(n5cnc4c(ncnc45)N)C(O)C6O)C)C
Formula
C27 H33 N9 O15 P2
Name
FLAVIN-ADENINE DINUCLEOTIDE
ChEMBL
CHEMBL1232653
DrugBank
DB03147
ZINC
ZINC000008215434
PDB chain
1wve Chain B Residue 599 [
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Receptor-Ligand Complex Structure
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PDB
1wve
p-Cresol Methylhydroxylase: Alteration of the Structure of the Flavoprotein Subunit upon Its Binding to the Cytochrome Subunit
Resolution
1.85 Å
Binding residue
(original residue number in PDB)
W85 T86 S88 T89 G90 R91 N92 F93 S153 A154 P155 A159 G160 G163 N164 M166 G169 V170 Y172 C231 E380 F381 Y384 W394 R474 R512
Binding residue
(residue number reindexed from 1)
W79 T80 S82 T83 G84 R85 N86 F87 S147 A148 P149 A153 G154 G157 N158 M160 G163 V164 Y166 C225 E374 F375 Y378 W388 R468 R506
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
S156 Y473 R474
Catalytic site (residue number reindexed from 1)
S150 Y467 R468
Enzyme Commision number
1.17.9.1
: 4-methylphenol dehydrogenase (hydroxylating).
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0004458
D-lactate dehydrogenase (cytochrome) activity
GO:0008720
D-lactate dehydrogenase activity
GO:0016491
oxidoreductase activity
GO:0018695
4-cresol dehydrogenase (hydroxylating) activity
GO:0050660
flavin adenine dinucleotide binding
GO:0071949
FAD binding
Biological Process
GO:1903457
lactate catabolic process
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:1wve
,
PDBe:1wve
,
PDBj:1wve
PDBsum
1wve
PubMed
15723539
UniProt
P09788
|DH4C_PSEPU 4-cresol dehydrogenase [hydroxylating] flavoprotein subunit (Gene Name=pchF)
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