Structure of PDB 6a23 Chain A Binding Site BS02
Receptor Information
>6a23 Chain A (length=333) Species:
31958
(Amycolatopsis orientalis) [
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YVSLADLERAARDVLPGEIFDFLAGGSGTEASLVANRTALERVFVIPRML
RDLTDVTTEIDIFGRRAALPMAVAPVAYQRLFHPEGELAVARAARDAGVP
YTICTLSSVSLEEIAAVGGRPWFQLFWLRDEKRSLDLVRRAEDAGCEAIV
FTVDVPWMGRRLRDMRNGFALPEWVTAANFDFAPATWESVEAVRAHTDLP
VVLKGILAVEDARRAVDAGAGGIVVSNHGGRQLDGAVPGIEMLGEIVAAV
SGGCEVLVDGGIRSGGDVLKATALGASAVLVGRPVMWALAAAGQDGVRQL
LELLAEEVRDAMGLAGCESVGAARRLNTKLGVV
Ligand information
Ligand ID
MG
InChI
InChI=1S/Mg/q+2
InChIKey
JLVVSXFLKOJNIY-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mg+2]
CACTVS 3.341
[Mg++]
Formula
Mg
Name
MAGNESIUM ION
ChEMBL
DrugBank
DB01378
ZINC
PDB chain
6a23 Chain A Residue 402 [
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Receptor-Ligand Complex Structure
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PDB
6a23
The flavin mononucleotide cofactor in alpha-hydroxyacid oxidases exerts its electrophilic/nucleophilic duality in control of the substrate-oxidation level.
Resolution
1.65 Å
Binding residue
(original residue number in PDB)
D283 G284 I286
Binding residue
(residue number reindexed from 1)
D259 G260 I262
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
F128 D156 H252
Catalytic site (residue number reindexed from 1)
F126 D154 H228
Enzyme Commision number
1.1.3.46
: 4-hydroxymandelate oxidase.
Gene Ontology
Molecular Function
GO:0004459
L-lactate dehydrogenase activity
GO:0010181
FMN binding
GO:0016491
oxidoreductase activity
GO:0016899
oxidoreductase activity, acting on the CH-OH group of donors, oxygen as acceptor
Biological Process
GO:0017000
antibiotic biosynthetic process
GO:0033072
vancomycin biosynthetic process
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Molecular Function
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Biological Process
External links
PDB
RCSB:6a23
,
PDBe:6a23
,
PDBj:6a23
PDBsum
6a23
PubMed
31588923
UniProt
O52792
|HMO_AMYOR 4-hydroxymandelate oxidase (Gene Name=hmo)
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