Structure of PDB 5zzt Chain A Binding Site BS01
Receptor Information
>5zzt Chain A (length=331) Species:
31958
(Amycolatopsis orientalis) [
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YVSLADLERAARDVLPGEIFDFLAGGSGTEASLVANRTALERVFVIPRML
RDLTDVTTEIDIFGRRAALPMAVAPVAYQRLFHPEGELAVARAARDAGVP
YTICTLSSVSLEEIAAVGGRPWFQLYWLRDEKRSLDLVRRAEDAGCEAIV
FTVDVPWMGRRLRDMRNGFALPEWVTAANFFAPATWESVEAVRAHTDLPV
VLKGILAVEDARRAVDAGAGGIVVSNHGGRQLDGAVPGIEMLGEIVAAVS
GGCEVLVDGGIRSGGDVLKATALGASAVLVGRPVMWALAAAGQDGVRQLL
ELLAEEVRDAMGLAGCESVGAARRLNTKLGV
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
5zzt Chain A Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
5zzt
Structural and chemical trapping of flavin-oxide intermediates reveals substrate-directed reaction multiplicity.
Resolution
1.35 Å
Binding residue
(original residue number in PDB)
P77 V78 A79 Q126 Y128 T154 K228 H252 G253 R255 D283 G284 G285 R287 G306 R307
Binding residue
(residue number reindexed from 1)
P75 V76 A77 Q124 Y126 T152 K203 H227 G228 R230 D258 G259 G260 R262 G281 R282
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
Y128 D156 H252
Catalytic site (residue number reindexed from 1)
Y126 D154 H227
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:5zzt
,
PDBe:5zzt
,
PDBj:5zzt
PDBsum
5zzt
PubMed
32362037
UniProt
O52792
|HMO_AMYOR 4-hydroxymandelate oxidase (Gene Name=hmo)
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