Structure of PDB 6x3b Chain C Binding Site BS01
Receptor Information
>6x3b Chain C (length=289) Species:
287
(Pseudomonas aeruginosa) [
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QRLFVTGLSGFVGKHLQAYLAAAHTPWALLPVPHRYDLLEPDSLGDLWPE
LPDAVIHLAGQTYVPEAFRDPARTLQINLLGTLNLLQALKARGFSGTFLY
ISSGDVYGQVAEAALPIHEELIPHPRNPYAVSKLAAESLCLQWGITEGWR
VLVARPFNHIGPGQKDSFVIASAARQIARMKQGLQANRLEVGDIDVSRDF
LDVQDVLSAYLRLLSHGEAGAVYNVCSGQEQKIRELIELLADIAQVELEI
VQEQRRVRGSHARLHDATGWKPEITIKQSLRAILSDWES
Ligand information
Ligand ID
NDP
InChI
InChI=1S/C21H30N7O17P3/c22-17-12-19(25-7-24-17)28(8-26-12)21-16(44-46(33,34)35)14(30)11(43-21)6-41-48(38,39)45-47(36,37)40-5-10-13(29)15(31)20(42-10)27-3-1-2-9(4-27)18(23)32/h1,3-4,7-8,10-11,13-16,20-21,29-31H,2,5-6H2,(H2,23,32)(H,36,37)(H,38,39)(H2,22,24,25)(H2,33,34,35)/t10-,11-,13-,14-,15-,16-,20-,21-/m1/s1
InChIKey
ACFIXJIJDZMPPO-NNYOXOHSSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@](=O)(O)O[P@@](=O)(O)OC[C@@H]4[C@H]([C@H]([C@@H](O4)N5C=CCC(=C5)C(=O)N)O)O)O)OP(=O)(O)O)N
CACTVS 3.341
NC(=O)C1=CN(C=CC1)[CH]2O[CH](CO[P](O)(=O)O[P](O)(=O)OC[CH]3O[CH]([CH](O[P](O)(O)=O)[CH]3O)n4cnc5c(N)ncnc45)[CH](O)[CH]2O
CACTVS 3.341
NC(=O)C1=CN(C=CC1)[C@@H]2O[C@H](CO[P@@](O)(=O)O[P@](O)(=O)OC[C@H]3O[C@H]([C@H](O[P](O)(O)=O)[C@@H]3O)n4cnc5c(N)ncnc45)[C@@H](O)[C@H]2O
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)OP(=O)(O)OCC4C(C(C(O4)N5C=CCC(=C5)C(=O)N)O)O)O)OP(=O)(O)O)N
Formula
C21 H30 N7 O17 P3
Name
NADPH DIHYDRO-NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE
ChEMBL
CHEMBL407009
DrugBank
DB02338
ZINC
ZINC000008215411
PDB chain
6x3b Chain C Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
6x3b
X-ray crystallographic structure of RMD, the reductase involved in GDP-d-rhamnose production
Resolution
1.91 Å
Binding residue
(original residue number in PDB)
G9 S11 G12 F13 V14 D39 L40 L60 A61 G62 T64 Y131 K135 P158 H161
Binding residue
(residue number reindexed from 1)
G7 S9 G10 F11 V12 D37 L38 L58 A59 G60 T62 Y129 K133 P156 H159
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
S105 G106 D107 Y131 K135
Catalytic site (residue number reindexed from 1)
S103 G104 D105 Y129 K133
Enzyme Commision number
1.1.1.281
: GDP-4-dehydro-6-deoxy-D-mannose reductase.
Gene Ontology
Molecular Function
GO:0016491
oxidoreductase activity
GO:0033705
GDP-4-dehydro-6-deoxy-D-mannose reductase activity
GO:0070402
NADPH binding
Biological Process
GO:0009103
lipopolysaccharide biosynthetic process
GO:0009243
O antigen biosynthetic process
GO:0019306
GDP-D-rhamnose biosynthetic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:6x3b
,
PDBe:6x3b
,
PDBj:6x3b
PDBsum
6x3b
PubMed
UniProt
Q9HTB6
|RMD_PSEAE GDP-6-deoxy-D-mannose reductase (Gene Name=rmd)
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