Structure of PDB 6a00 Chain A Binding Site BS02
Receptor Information
>6a00 Chain A (length=334) Species:
31958
(Amycolatopsis orientalis) [
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TYVSLADLERAARDVLPGEIFDFLAGGSGTEASLVANRTALERVFVIPRM
LRDLTDVTTEIDIFGRRAALPMAVAPVAYQRLFHPEGELAVARAARDAGV
PYTICTLSSVSLEEIAAVGGRPWFQLYWLRDEKRSLDLVRRAEDAGCEAI
VFTVDVPWMGRRLRDMRNGFALPEWVTAANFDFAPATWESVEAVRAHTDL
PVVLKGILAVEDARRAVDAGAGGIVVSNHGGRQLDGAVPGIEMLGEIVAA
VSGGCEVLVDGGIRSGGDVLKATALGASAVLVGRPVMWALAAAGQDGVRQ
LLELLAEEVRDAMGLAGCESVGAARRLNTKLGVV
Ligand information
Ligand ID
FMN
InChI
InChI=1S/C17H21N4O9P/c1-7-3-9-10(4-8(7)2)21(15-13(18-9)16(25)20-17(26)19-15)5-11(22)14(24)12(23)6-30-31(27,28)29/h3-4,11-12,14,22-24H,5-6H2,1-2H3,(H,20,25,26)(H2,27,28,29)/t11-,12+,14-/m0/s1
InChIKey
FVTCRASFADXXNN-SCRDCRAPSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.6
Cc1cc2c(cc1C)N(C3=NC(=O)NC(=O)C3=N2)CC(C(C(COP(=O)(O)O)O)O)O
OpenEye OEToolkits 1.7.6
Cc1cc2c(cc1C)N(C3=NC(=O)NC(=O)C3=N2)C[C@@H]([C@@H]([C@@H](COP(=O)(O)O)O)O)O
ACDLabs 12.01
N=2C(=O)NC(=O)C3=Nc1cc(C)c(C)cc1N(C=23)CC(O)C(O)C(O)COP(=O)(O)O
CACTVS 3.385
Cc1cc2N=C3C(=O)NC(=O)N=C3N(C[CH](O)[CH](O)[CH](O)CO[P](O)(O)=O)c2cc1C
CACTVS 3.385
Cc1cc2N=C3C(=O)NC(=O)N=C3N(C[C@H](O)[C@H](O)[C@H](O)CO[P](O)(O)=O)c2cc1C
Formula
C17 H21 N4 O9 P
Name
FLAVIN MONONUCLEOTIDE;
RIBOFLAVIN MONOPHOSPHATE
ChEMBL
CHEMBL1201794
DrugBank
DB03247
ZINC
ZINC000003831425
PDB chain
6a00 Chain A Residue 402 [
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Receptor-Ligand Complex Structure
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PDB
6a00
Biochemical and structural explorations of alpha-hydroxyacid oxidases reveal a four-electron oxidative decarboxylation reaction.
Resolution
1.59 Å
Binding residue
(original residue number in PDB)
P77 V78 A79 Q126 Y128 T154 K228 H252 R255 D283 G285 R287 G306 R307
Binding residue
(residue number reindexed from 1)
P76 V77 A78 Q125 Y127 T153 K205 H229 R232 D260 G262 R264 G283 R284
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
Y128 D156 H252
Catalytic site (residue number reindexed from 1)
Y127 D155 H229
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:6a00
,
PDBe:6a00
,
PDBj:6a00
PDBsum
6a00
PubMed
31373572
UniProt
O52792
|HMO_AMYOR 4-hydroxymandelate oxidase (Gene Name=hmo)
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