Structure of PDB 1e0y Chain A Binding Site BS01
Receptor Information
>1e0y Chain A (length=550) Species:
69488
(Penicillium simplicissimum) [
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EFRPLTLPPKLSLSDFNEFIQDIIRIVGSENVEVISVDGSYMKPTHTHDP
HHVMDQDYFLASAIVAPRNVADVQSIVGLANKFSFPLWPISIGRNSGYGG
AAPRVSGSVVLDMGKNMNRVLEVNVEGAYCVVEPGVTYHDLHNYLEANNL
RDKLWLDVPSLGGGSVLGNAVERGVGYTPYGDHWMMHSGMEVVLANGELL
RTGMGALPDPKRPETMGLKPEDQPWSKIAHLFPYGFGPYIDGLFSQSNMG
IVTKIGIWLMPNPGGYQSYLITLPKDGDLKQAVDIIRPLRLGMALQNVPT
IRHILLDAAVLGDKRSYSSRTEPLSDEELDKIAKQLNLGRWNFYGALYGP
EPIRRVLWETIKDAFSAIPGVKFYFPEDTPENSVLRVRDKTMQGIPTYDE
LKWIDWLPNGAHLFFSPIAKVSGEDAMMQYAVTKKRCQEAGLDFIGEFTV
GMREMHHIVCIVFNKKDLIQKRKVQWLMRTLIDDCAANGWGEYRTHLAFM
DQIMETYNWNNSSFLRFNEVLKNAVDPNGIIAPGKSGVWPSQYSHVTWKL
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
1e0y Chain A Residue 600 [
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Receptor-Ligand Complex Structure
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PDB
1e0y
Inversion of Stereospecificity in Vanillyl-Alcohol Oxidase
Resolution
2.75 Å
Binding residue
(original residue number in PDB)
S101 I102 G103 R104 N105 P169 S170 L171 G174 N179 E182 V185 Y187 V262 W413 I414 H422 F424 R504 K545
Binding residue
(residue number reindexed from 1)
S91 I92 G93 R94 N95 P159 S160 L161 G164 N169 E172 V175 Y177 V252 W403 I404 H412 F414 R494 K535
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
Y108 S170 E182 D192 D317 V397 E410 I414 H422 H466 Y503 R504 K545
Catalytic site (residue number reindexed from 1)
Y98 S160 E172 D182 D307 V387 E400 I404 H412 H456 Y493 R494 K535
Enzyme Commision number
1.1.3.38
: vanillyl-alcohol oxidase.
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:0018465
vanillyl-alcohol oxidase activity
GO:0050660
flavin adenine dinucleotide binding
GO:0071949
FAD binding
Biological Process
GO:0015945
methanol metabolic process
GO:1903457
lactate catabolic process
Cellular Component
GO:0005737
cytoplasm
GO:0005739
mitochondrion
GO:0005777
peroxisome
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1e0y
,
PDBe:1e0y
,
PDBj:1e0y
PDBsum
1e0y
PubMed
10920192
UniProt
P56216
|VAOX_PENSI Vanillyl-alcohol oxidase (Gene Name=VAOA)
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