Structure of PDB 3qw2 Chain B Binding Site BS02
Receptor Information
>3qw2 Chain B (length=392) Species:
2234
(Archaeoglobus fulgidus) [
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MKVWLVGAYGIVSTTAMVGARAIERGIAPKIGLVSELPHFEGIEKYAPFS
FEFGGHEIRLLSNAYEAAKEHWELNRHFDREILEAVKSDLEGIVARKGTA
LNCGSGIKELGDIKTLEGEGLSLAEMVSRIEEDIKSFADDETVVINVAST
EPLPNYSEEYHGSLEGFERMIDEDRKEYASASMLYAYAALKLGLPYANFT
PSPGSAIPALKELAEKKGVPHAGNDGKTGETLVKTTLAPMFAYRNMEVVG
WMSYAILGDYDGKVLSARDNKESKVLSKDKVLEKMLGYSPYSITEIQYFP
SLVDNKTAFDFVHFKGFLGKLMKFYFIWDAIDAIVAAPLILDIARFLLFA
KKKGVKGVVKEMAFFFKSPMDTNVINTHEQFVVLKEWYSNLK
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
3qw2 Chain B Residue 396 [
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Receptor-Ligand Complex Structure
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PDB
3qw2
Crystal structure of a trapped catalytic intermediate suggests that forced atomic proximity drives the catalysis of mIPS.
Resolution
2.59 Å
Binding residue
(original residue number in PDB)
G7 G10 I11 V12 E57 I58 R59 T99 L110 V147 A148 S149 T150 Y185 F199 D225 G226 T228 D261 D332 A336
Binding residue
(residue number reindexed from 1)
G7 G10 I11 V12 E57 I58 R59 T99 L110 V147 A148 S149 T150 Y185 F199 D225 G226 T228 D261 D332 A336
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
D225 K274 K306 K367
Catalytic site (residue number reindexed from 1)
D225 K274 K306 K367
Enzyme Commision number
5.5.1.4
: inositol-3-phosphate synthase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0004512
inositol-3-phosphate synthase activity
Biological Process
GO:0006021
inositol biosynthetic process
GO:0006629
lipid metabolic process
GO:0008654
phospholipid biosynthetic process
Cellular Component
GO:0005737
cytoplasm
GO:0016020
membrane
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:3qw2
,
PDBe:3qw2
,
PDBj:3qw2
PDBsum
3qw2
PubMed
22261071
UniProt
O28480
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