Structure of PDB 1ker Chain A Binding Site BS02
Receptor Information
>1ker Chain A (length=346) Species:
1307
(Streptococcus suis) [
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QFKNIIVTGGAGFIGSNFVHYVYNNHPDVHVTVLDKLTYAGNKANLEAIL
GDRVELVVGDIADAELVDKLAAKADAIVHYAAESHNDNSLNDPSPFIHTN
FIGTYTLLEAARKYDIRFHHVSTDEVYGDLPLREDLPGHGEGPGEKFTAE
TNYNPSSPYSSTKAASDLIVKAWVRSFGVKATISNCSNNYGPYQHIEKFI
PRQITNILAGIKPKLYGEGKNVRDWIHTNDHSTGVWAILTKGRMGETYLI
GADGEKNNKEVLELILEKMGQPKDAYDHVTDRAGHDLRYAIDASKLRDEL
GWTPQFTDFSEGLEETIQWYTDNQDWWKAEKEAVEANYAKTQEVIK
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
1ker Chain A Residue 1400 [
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Receptor-Ligand Complex Structure
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PDB
1ker
Toward a structural understanding of the dehydratase mechanism.
Resolution
2.2 Å
Binding residue
(original residue number in PDB)
G14 F15 I16 D37 K38 L39 T40 A42 G43 D62 I63 Y82 A83 A84 S86 T101 V123 S124 T125 Y161 K165 C188 N191
Binding residue
(residue number reindexed from 1)
G12 F13 I14 D35 K36 L37 T38 A40 G41 D60 I61 Y80 A81 A82 S84 T99 V121 S122 T123 Y159 K163 C186 N189
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
T125 D126 E127 Y161 K165
Catalytic site (residue number reindexed from 1)
T123 D124 E125 Y159 K163
Enzyme Commision number
4.2.1.46
: dTDP-glucose 4,6-dehydratase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0008460
dTDP-glucose 4,6-dehydratase activity
GO:0016829
lyase activity
Biological Process
GO:0009225
nucleotide-sugar metabolic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:1ker
,
PDBe:1ker
,
PDBj:1ker
PDBsum
1ker
PubMed
11796113
UniProt
Q8GIP9
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