Structure of PDB 6a0d Chain A Binding Site BS03
Receptor Information
>6a0d Chain A (length=327) Species:
31958
(Amycolatopsis orientalis) [
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LADLERAARDVLPGEIFDFLAGGSGTEASLVANRTALERVFVIPRMLRDL
TDVTTEIDIFGRRAALPMAVAPVAYQRLFHPEGELAVARAARDAGVPYTI
CTLSSVSLEEIAAVGGRPWFQLFWLRDEKRSLDLVRRAEDAGCEAIVFTV
DVPWMGRRLRDMRNGFALPEWVTAANFFAPATWESVEAVRAHTDLPVVLK
GILAVEDARRAVDAGAGGIVVSNHGGRQLDGAVPGIEMLGEIVAAVSGGC
EVLVDGGIRSGGDVLKATALGASAVLVGRPVMWALAAAGQDGVRQLLELL
AEEVRDAMGLAGCESVGAARRLNTKLG
Ligand information
Ligand ID
9RW
InChI
InChI=1S/C9H10O2/c1-7(9(10)11)8-5-3-2-4-6-8/h2-7H,1H3,(H,10,11)/t7-/m0/s1
InChIKey
YPGCWEMNNLXISK-ZETCQYMHSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 2.0.6
CC(c1ccccc1)C(=O)O
OpenEye OEToolkits 2.0.6
C[C@@H](c1ccccc1)C(=O)O
CACTVS 3.385
C[CH](C(O)=O)c1ccccc1
CACTVS 3.385
C[C@H](C(O)=O)c1ccccc1
Formula
C9 H10 O2
Name
(2~{S})-2-phenylpropanoic acid
ChEMBL
DrugBank
ZINC
ZINC000000391877
PDB chain
6a0d Chain A Residue 403 [
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Receptor-Ligand Complex Structure
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PDB
6a0d
Biochemical and structural explorations of alpha-hydroxyacid oxidases reveal a four-electron oxidative decarboxylation reaction.
Resolution
1.65 Å
Binding residue
(original residue number in PDB)
F46 L354 G355
Binding residue
(residue number reindexed from 1)
F41 L326 G327
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
F128 D156 H252
Catalytic site (residue number reindexed from 1)
F123 D151 H224
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
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:6a0d
,
PDBe:6a0d
,
PDBj:6a0d
PDBsum
6a0d
PubMed
31373572
UniProt
O52792
|HMO_AMYOR 4-hydroxymandelate oxidase (Gene Name=hmo)
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