Structure of PDB 2nsy Chain A Binding Site BS04
Receptor Information
>2nsy Chain A (length=271) Species:
1423
(Bacillus subtilis) [
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SMQEKIMRELHVKPSIDPKQEIEDRVNFLKQYVKKTGAKGFVLGISGGQD
STLAGRLAQLAVESIREEGGDAQFIAVRLPHGTQQDEDDAQLALKFIKPD
KSWKFDIKSTVSAFSDQYQQETGDQLTDFNKGNVKARTRMIAQYAIGGQE
GLLVLGTDHAAEAVTGFFTKYGDGGADLLPLTGLTKRQGRTLLKELGAPE
RLYLKEPTADLLDEKPQQSDETELGISYDEIDDYLEGKEVSAKVSEALEK
RYSMTEHKRQVPASMFDDWWK
Ligand information
Ligand ID
POP
InChI
InChI=1S/H4O7P2/c1-8(2,3)7-9(4,5)6/h(H2,1,2,3)(H2,4,5,6)/p-2
InChIKey
XPPKVPWEQAFLFU-UHFFFAOYSA-L
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
O[P@@](=O)([O-])O[P@@](=O)(O)[O-]
CACTVS 3.341
O[P]([O-])(=O)O[P](O)([O-])=O
ACDLabs 10.04
[O-]P(=O)(O)OP([O-])(=O)O
OpenEye OEToolkits 1.5.0
OP(=O)([O-])OP(=O)(O)[O-]
Formula
H2 O7 P2
Name
PYROPHOSPHATE 2-
ChEMBL
DrugBank
ZINC
PDB chain
2nsy Chain A Residue 863 [
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Receptor-Ligand Complex Structure
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PDB
2nsy
A novel deamido-NAD+-binding site revealed by the trapped NAD-adenylate intermediate in the NAD+ synthetase structure.
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
S46 G48 D50 S51 K186 P207 T208
Binding residue
(residue number reindexed from 1)
S46 G48 D50 S51 K186 P207 T208
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
D50 E162
Catalytic site (residue number reindexed from 1)
D50 E162
Enzyme Commision number
6.3.1.5
: NAD(+) synthase.
Gene Ontology
Molecular Function
GO:0003952
NAD+ synthase (glutamine-hydrolyzing) activity
GO:0004359
glutaminase activity
GO:0005524
ATP binding
GO:0008795
NAD+ synthase activity
GO:0016874
ligase activity
GO:0046872
metal ion binding
Biological Process
GO:0009435
NAD biosynthetic process
GO:0030435
sporulation resulting in formation of a cellular spore
Cellular Component
GO:0005737
cytoplasm
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2nsy
,
PDBe:2nsy
,
PDBj:2nsy
PDBsum
2nsy
PubMed
9753692
UniProt
P08164
|NADE_BACSU NH(3)-dependent NAD(+) synthetase (Gene Name=nadE)
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