Structure of PDB 5vn2 Chain D Binding Site BS01
Receptor Information
>5vn2 Chain D (length=253) Species:
224914
(Brucella melitensis bv. 1 str. 16M) [
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SRQRPVALVTGGRRGIGLGIARALAAKGFDLAITDRESDEAVIHELRGLG
GKVAFFKSDLAAVKTHEATVFAVLDAFGGIDCLVNNAGMGAVERGDFLAL
KPENFDTIMDVNLRGTVFFTQAVVKAMLAADEVRFPRSIVTISSVSSVMT
SPERLDYCISKAGLTAFVQGLALRLAEARIGVFEVRPGIIRTDMTAKVAA
RYDALIEGGLVPMKRWGEASDVGAIVAGLAGGDFIFATGSAIHADGGLSI
AKL
Ligand information
Ligand ID
NAD
InChI
InChI=1S/C21H27N7O14P2/c22-17-12-19(25-7-24-17)28(8-26-12)21-16(32)14(30)11(41-21)6-39-44(36,37)42-43(34,35)38-5-10-13(29)15(31)20(40-10)27-3-1-2-9(4-27)18(23)33/h1-4,7-8,10-11,13-16,20-21,29-32H,5-6H2,(H5-,22,23,24,25,33,34,35,36,37)/t10-,11-,13-,14-,15-,16-,20-,21-/m1/s1
InChIKey
BAWFJGJZGIEFAR-NNYOXOHSSA-N
SMILES
Software
SMILES
CACTVS 3.341
NC(=O)c1ccc[n+](c1)[C@@H]2O[C@H](CO[P]([O-])(=O)O[P@](O)(=O)OC[C@H]3O[C@H]([C@H](O)[C@@H]3O)n4cnc5c(N)ncnc45)[C@@H](O)[C@H]2O
OpenEye OEToolkits 1.5.0
c1cc(c[n+](c1)C2C(C(C(O2)COP(=O)([O-])OP(=O)(O)OCC3C(C(C(O3)n4cnc5c4ncnc5N)O)O)O)O)C(=O)N
CACTVS 3.341
NC(=O)c1ccc[n+](c1)[CH]2O[CH](CO[P]([O-])(=O)O[P](O)(=O)OC[CH]3O[CH]([CH](O)[CH]3O)n4cnc5c(N)ncnc45)[CH](O)[CH]2O
OpenEye OEToolkits 1.5.0
c1cc(c[n+](c1)[C@H]2[C@@H]([C@@H]([C@H](O2)CO[P@@](=O)([O-])O[P@@](=O)(O)OC[C@@H]3[C@H]([C@H]([C@@H](O3)n4cnc5c4ncnc5N)O)O)O)O)C(=O)N
Formula
C21 H27 N7 O14 P2
Name
NICOTINAMIDE-ADENINE-DINUCLEOTIDE
ChEMBL
CHEMBL1234613
DrugBank
DB14128
ZINC
PDB chain
5vn2 Chain D Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
5vn2
Crystal structure of 3-oxoacyl-[acyl-carrier protein] reductase from Brucella melitensis in complex with NAD
Resolution
1.9 Å
Binding residue
(original residue number in PDB)
G12 R14 R15 G16 I17 D36 R37 S59 D60 L61 N87 G89 S145 K162 P188 G189 I191 T193 M195 T196
Binding residue
(residue number reindexed from 1)
G11 R13 R14 G15 I16 D35 R36 S58 D59 L60 N86 G88 S144 K161 P187 G188 I190 T192 M194 T195
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
S145 Y158 K162
Catalytic site (residue number reindexed from 1)
S144 Y157 K161
Enzyme Commision number
1.1.1.100
: 3-oxoacyl-[acyl-carrier-protein] reductase.
Gene Ontology
Molecular Function
GO:0016491
oxidoreductase activity
View graph for
Molecular Function
External links
PDB
RCSB:5vn2
,
PDBe:5vn2
,
PDBj:5vn2
PDBsum
5vn2
PubMed
UniProt
Q8YJQ6
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