Structure of PDB 4nbt Chain D Binding Site BS01
Receptor Information
>4nbt Chain D (length=239) Species:
441768
(Acholeplasma laidlawii PG-8A) [
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KKLEGKVAVITGGAKGLGQAIALAYAEEGAKVIAGDLGDLTYSHPNVEGM
YLNVTDVTGVEKFYQSVIDKYGKIDILVNNAGITKDAMTRKMTEAQWDAV
IDVNLKGVFNLTRLVGPQMQTNGYGSIINISSVVGVFGNIGQANYAATKA
GVIGLTMTWAKEFALKGANVRVNAIAPGYIMTDILKTVPQDLLDKFAALT
MLNRLGQPEEIAKVALFLASDDASYVTGQTINVNGGMRL
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
4nbt Chain D Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
4nbt
Biochemical and Structural Studies of NADH-Dependent FabG Used To Increase the Bacterial Production of Fatty Acids under Anaerobic Conditions.
Resolution
1.48 Å
Binding residue
(original residue number in PDB)
G13 K16 G17 L18 D37 L38 L53 N54 V55 N81 A82 G83 I131 S133 Y146 K150 P178 G179 Y180 I181 T183 I185
Binding residue
(residue number reindexed from 1)
G12 K15 G16 L17 D36 L37 L52 N53 V54 N80 A81 G82 I130 S132 Y145 K149 P177 G178 Y179 I180 T182 I184
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
G17 S133 Y146 K150
Catalytic site (residue number reindexed from 1)
G16 S132 Y145 K149
Enzyme Commision number
1.1.1.100
: 3-oxoacyl-[acyl-carrier-protein] reductase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0004316
3-oxoacyl-[acyl-carrier-protein] reductase (NADPH) activity
GO:0016491
oxidoreductase activity
View graph for
Molecular Function
External links
PDB
RCSB:4nbt
,
PDBe:4nbt
,
PDBj:4nbt
PDBsum
4nbt
PubMed
24212572
UniProt
A9NFJ2
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