Structure of PDB 1e8h Chain B Binding Site BS01
Receptor Information
>1e8h Chain B (length=545) Species:
69488
(Penicillium simplicissimum) [
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EFRPLTLPPKLSLSDFNEFIQDIIRIVGSENVEVISMKPTHTHDPTHVMD
QDYFLASAIVAPRNVADVQSIVGLANKFSFPLWPISIGRNSGYGGAAPRV
SGSVVLDMGKNMNRVLEVNVEGAYCVVEPGVTYHDLHNYLEANNLRDKLW
LDVPDLGGGSVLGNAVERGVGYTPYGDHWMMHSGMEVVLANGELLRTGMG
ALPDPKRPETMGLKPEDQPWSKIAHLFPYGFGPYIDGLFSQSNMGIVTKI
GIWLMPNPGGYQSYLITLPKDGDLKQAVDIIRPLRLGMALQNVPTIRHIL
LDAAVLGDKRSYSSRTEPLSDEELDKIAKQLNLGRWNFYGALYGPEPIRR
VLWETIKDAFSAIPGVKFYFPEDTPENSVLRVRDKTMQGIPTYDELKWID
WLPNGAHLFFSPIAKVSGEDAMMQYAVTKKRCQEAGLDFIGTFTVGMREM
HHIVCIVFNKKDLIQKRKVQWLMRTLIDDCAANGWGEYRTHLAFMDQIME
TYNWNNSSFLRFNEVLKNAVDPNGIIAPGKSGVWPSQYSHVTWKL
Ligand information
Ligand ID
ADP
InChI
InChI=1S/C10H15N5O10P2/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(17)6(16)4(24-10)1-23-27(21,22)25-26(18,19)20/h2-4,6-7,10,16-17H,1H2,(H,21,22)(H2,11,12,13)(H2,18,19,20)/t4-,6-,7-,10-/m1/s1
InChIKey
XTWYTFMLZFPYCI-KQYNXXCUSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@](=O)(O)OP(=O)(O)O)O)O)N
CACTVS 3.341
Nc1ncnc2n(cnc12)[CH]3O[CH](CO[P](O)(=O)O[P](O)(O)=O)[CH](O)[CH]3O
ACDLabs 10.04
O=P(O)(O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3O
CACTVS 3.341
Nc1ncnc2n(cnc12)[C@@H]3O[C@H](CO[P@@](O)(=O)O[P](O)(O)=O)[C@@H](O)[C@H]3O
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)OP(=O)(O)O)O)O)N
Formula
C10 H15 N5 O10 P2
Name
ADENOSINE-5'-DIPHOSPHATE
ChEMBL
CHEMBL14830
DrugBank
DB16833
ZINC
ZINC000012360703
PDB chain
1e8h Chain B Residue 600 [
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Receptor-Ligand Complex Structure
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PDB
1e8h
Structural Analysis of Flavinylation in Vanillyl-Alcohol Oxidase
Resolution
2.6 Å
Binding residue
(original residue number in PDB)
S101 I102 G103 R104 S175 E182 I261 V262 K545
Binding residue
(residue number reindexed from 1)
S86 I87 G88 R89 S160 E167 I246 V247 K530
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
Y108 D170 E182 D192 D317 V397 E410 I414 H422 H466 Y503 R504 K545
Catalytic site (residue number reindexed from 1)
Y93 D155 E167 D177 D302 V382 E395 I399 H407 H451 Y488 R489 K530
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:1e8h
,
PDBe:1e8h
,
PDBj:1e8h
PDBsum
1e8h
PubMed
10984479
UniProt
P56216
|VAOX_PENSI Vanillyl-alcohol oxidase (Gene Name=VAOA)
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