Structure of PDB 1keu Chain A Binding Site BS02
Receptor Information
>1keu Chain A (length=361) Species:
90371
(Salmonella enterica subsp. enterica serovar Typhimurium) [
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MKILITGGAGFIGSAVVRHIIKNTQDTVVNIDKLTYAGNLESLSDISESN
RYNFEHADICDSAEITRIFEQYQPDAVMHLAAESHVDRSITGPAAFIETN
IVGTYALLEVARKYWSALGEDKKNNFRFHHISTDEVYGDLPHPDEVENSV
TLPLFTETTAYAPSSPYSASKASSDHLVRAWRRTYGLPTIVTNCSNNYGP
YHFPEKLIPLVILNALEGKPLPIYGKGDQIRDWLYVEDHARALHMVVTEG
KAGETYNIGGHNEKKNLDVVFTICDLLDEIVPKATSYREQITYVADRPGH
DRRYAIDAGKISRELGWKPLETFESGIRKTVEWYLANTQWVNNVKSGAYQ
SWIEQNYEGRQ
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
1keu Chain A Residue 1400 [
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Receptor-Ligand Complex Structure
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PDB
1keu
Toward a structural understanding of the dehydratase mechanism.
Resolution
2.4 Å
Binding residue
(original residue number in PDB)
G10 F11 I12 D32 K33 L34 T35 G38 D58 L80 A81 A82 S84 T99 S132 T133 Y167 K171 C194 N196 N197
Binding residue
(residue number reindexed from 1)
G10 F11 I12 D32 K33 L34 T35 G38 D58 L80 A81 A82 S84 T99 S132 T133 Y167 K171 C194 N196 N197
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
T133 D134 E135 L152 L154 F155 T158 Y167 K171
Catalytic site (residue number reindexed from 1)
T133 D134 E135 L152 L154 F155 T158 Y167 K171
Enzyme Commision number
4.2.1.46
: dTDP-glucose 4,6-dehydratase.
Gene Ontology
Molecular Function
GO:0008460
dTDP-glucose 4,6-dehydratase activity
GO:0016829
lyase activity
GO:0070404
NADH binding
Biological Process
GO:0009103
lipopolysaccharide biosynthetic process
GO:0009225
nucleotide-sugar metabolic process
GO:0009243
O antigen biosynthetic process
GO:0019305
dTDP-rhamnose biosynthetic process
GO:0045226
extracellular polysaccharide biosynthetic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:1keu
,
PDBe:1keu
,
PDBj:1keu
PDBsum
1keu
PubMed
11796113
UniProt
P26391
|RMLB_SALTY dTDP-glucose 4,6-dehydratase (Gene Name=rfbB)
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