Structure of PDB 5mxj Chain B Binding Site BS01
Receptor Information
>5mxj Chain B (length=553) Species:
69488
(Penicillium simplicissimum) [
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EFRPLTLPPKLSLSDFNEFIQDIIRIVGSENVEVISSKIVDGSYMKPTHT
HDPHHVMDQDYFLASAIVAPRNVADVQSIVGLANKFSFPLWPISIGRNSG
FGGAAPRVSGSVVLDMGKNMNRVLEVNVEGAYCVVEPGVTYHDLHNYLEA
NNLRDKLWLDVPDLGGGSVLGNAVERGVGYTPYGDHWMMHSGMEVVLANG
ELLRTGMGALPDPKRPETMGLKPEDQPWSKIAHLFPYGFGPYIDGLFSQS
NMGIVTKIGIWLMPNPRGYQSYLITLPKDGDLKQAVDIIRPLRLGMALQN
VPTIRHILLDAAVLGDKRSYSSRTEPLSDEELDKIAKQLNLGRWNFYGAL
YGPEPIRRVLWETIKDAFSAIPGVKFYFPEDTPENSVLRVRDKTMQGIPT
YDELKWIDWLPNGAHLFFSPIAKVSGEDAMMQYAVTKKRCQEAGLDFIGT
FTVGMREMHHIVCIVFNKKDLIQKRKVQWLMRTLIDDCAANGWGEYRTHL
AFMDQIMETYNWNNSSFLRFNEVLKNAVDPNGIIAPGKSGVWPSQYSHVT
WKL
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
5mxj Chain B Residue 601 [
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Receptor-Ligand Complex Structure
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PDB
5mxj
Two tyrosine residues, Tyr-108 and Tyr-503, are responsible for the deprotonation of phenolic substrates in vanillyl-alcohol oxidase.
Resolution
2.8 Å
Binding residue
(original residue number in PDB)
P99 S101 I102 G103 R104 N105 P169 D170 L171 G174 S175 N179 E182 G184 V185 Y187 I261 V262 W413 H422 F424 R504 K545
Binding residue
(residue number reindexed from 1)
P92 S94 I95 G96 R97 N98 P162 D163 L164 G167 S168 N172 E175 G177 V178 Y180 I254 V255 W406 H415 F417 R497 K538
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
F108 D170 E182 D192 D317 V397 E410 I414 H422 H466 Y503 R504 K545
Catalytic site (residue number reindexed from 1)
F101 D163 E175 D185 D310 V390 E403 I407 H415 H459 Y496 R497 K538
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:5mxj
,
PDBe:5mxj
,
PDBj:5mxj
PDBsum
5mxj
PubMed
28717004
UniProt
P56216
|VAOX_PENSI Vanillyl-alcohol oxidase (Gene Name=VAOA)
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