Structure of PDB 2ol4 Chain B Binding Site BS01
Receptor Information
>2ol4 Chain B (length=280) Species:
5833
(Plasmodium falciparum) [
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DICFIAGIGDTNGYGWGIAKELSKRNVKIIFGIWPPVYNIFMKNYKNGKF
DNDMIKMNILDMLPFDASFDTANDIDEETKNNKRYNMLQNYTIEDVANLI
HQKYGKINMLVHSLANAKEVQKDLLNTSRKGYLDALSKSSYSLISLCKYF
VNIMKPQSSIISLTYHASQKVVPGYGGGMSSAKAALESDTRVLAYHLGRN
YNIRINTISAGPLKSRAATAINTFIDYAIEYSEKYAPLRQKLLSTDIGSV
ASFLLSRESRAITGQTIYVDNGLNIMFLPD
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
2ol4 Chain B Residue 451 [
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Receptor-Ligand Complex Structure
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PDB
2ol4
X-ray structural analysis of Plasmodium falciparum enoyl acyl carrier protein reductase as a pathway toward the optimization of triclosan antimalarial efficacy
Resolution
2.26 Å
Binding residue
(original residue number in PDB)
G104 G106 G110 Y111 W131 D168 A169 S215 L216 A217 N218 L265 T266 Y267 K285 A312 G313 P314 L315 S317 A319
Binding residue
(residue number reindexed from 1)
G7 G9 G13 Y14 W34 D66 A67 S113 L114 A115 N116 L163 T164 Y165 K183 A210 G211 P212 L213 S215 A217
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
Y277 K285
Catalytic site (residue number reindexed from 1)
Y175 K183
Enzyme Commision number
1.3.1.9
: enoyl-[acyl-carrier-protein] reductase (NADH).
Gene Ontology
Molecular Function
GO:0004318
enoyl-[acyl-carrier-protein] reductase (NADH) activity
Biological Process
GO:0006633
fatty acid biosynthetic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:2ol4
,
PDBe:2ol4
,
PDBj:2ol4
PDBsum
2ol4
PubMed
17567585
UniProt
Q9BJJ9
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