Structure of PDB 6bi4 Chain B Binding Site BS02
Receptor Information
>6bi4 Chain B (length=310) Species:
198094
(Bacillus anthracis str. Ames) [
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AMNILVTGGAGFIGSNFVHYMLQSYETYKIINFDALTYSGNLNNVKSIQD
HPNYYFVKGEIQNGELLEHVIKERDVQVIVNFAAESIPFYDTNVIGTVTL
LELVKKYPHIKLVQVSTDEVYGSLGKTGRFTEETPLAPNSPYSSSKASAD
MIALAYYKTYQLPVIVTRCSNNYGPYQYPEKLIPLMVTNALEGKKLPLYG
DGLNVRDWLHVTDHCSAIDVVLHKGRVGEVYNIGGNNEKTNVEVVEQIIT
LLGKTKKDIEYVTGHDRRYAINAEKMKNEFDWEPKYTFEQGLQETVQWYE
KNEEWWKPLK
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
6bi4 Chain B Residue 402 [
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Receptor-Ligand Complex Structure
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PDB
6bi4
Structure of the Bacillus anthracis dTDP-l-rhamnose biosynthetic pathway enzyme: dTDP-alpha-d-glucose 4,6-dehydratase, RfbB.
Resolution
2.91 Å
Binding residue
(original residue number in PDB)
G7 G10 F11 I12 D33 A34 L35 T36 S38 G39 E59 F81 A82 A83 T100 S124 T125 Y150 K154 C177
Binding residue
(residue number reindexed from 1)
G8 G11 F12 I13 D34 A35 L36 T37 S39 G40 E60 F82 A83 A84 T92 S116 T117 Y142 K146 C169
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
T125 D126 E127 Y150 K154
Catalytic site (residue number reindexed from 1)
T117 D118 E119 Y142 K146
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:6bi4
,
PDBe:6bi4
,
PDBj:6bi4
PDBsum
6bi4
PubMed
29331609
UniProt
A0A6L7HMN5
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