Structure of PDB 5isy Chain C Binding Site BS02
Receptor Information
>5isy Chain C (length=249) Species:
83333
(Escherichia coli K-12) [
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DRIIEKDHGWWVVSHEQKLWLPKGELPYGEAANFDLVGQRALQIGEWQGE
PVWLVQQQRRHDMGSVRQVIDLDVGLFQLAGRGVQLAEFYRSHKYCGYCG
HEMYPSKTEWAMLCSHCRERYYPQIAPCIIVAIRRDDSILLAQHTRHRNG
VHTVLAGFVEVGETLEQAVAREVMEQSGIKVKNLRYVTSQPWPFPQSLMT
AFMAEYDSGDIVIDPKELLEANWYRYDDLPLLPPPGTVARRLIEDTVAM
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
5isy Chain C Residue 302 [
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Receptor-Ligand Complex Structure
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PDB
5isy
Structural basis of prokaryotic NAD-RNA decapping by NudC
Resolution
2.354 Å
Binding residue
(original residue number in PDB)
F160 W194 M201 V240 A241
Binding residue
(residue number reindexed from 1)
F158 W192 M199 V238 A239
Annotation score
4
Enzymatic activity
Enzyme Commision number
3.6.1.-
3.6.1.22
: NAD(+) diphosphatase.
Gene Ontology
Molecular Function
GO:0000210
NAD+ diphosphatase activity
GO:0000287
magnesium ion binding
GO:0008270
zinc ion binding
GO:0016787
hydrolase activity
GO:0030145
manganese ion binding
GO:0035529
NADH pyrophosphatase activity
GO:0042803
protein homodimerization activity
GO:0046872
metal ion binding
GO:0110153
RNA NAD-cap (NMN-forming) hydrolase activity
Biological Process
GO:0006402
mRNA catabolic process
GO:0006734
NADH metabolic process
GO:0006742
NADP catabolic process
GO:0019677
NAD catabolic process
GO:0048255
mRNA stabilization
GO:0110155
NAD-cap decapping
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:5isy
,
PDBe:5isy
,
PDBj:5isy
PDBsum
5isy
PubMed
27561816
UniProt
P32664
|NUDC_ECOLI NAD-capped RNA hydrolase NudC (Gene Name=nudC)
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