Structure of PDB 1kaq Chain D Binding Site BS01
Receptor Information
>1kaq Chain D (length=186) Species:
1423
(Bacillus subtilis) [
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KKIGIFGGTFDPPHNGHLLMANEVLYQAGLDEIWFMPNQIPPHKQNEDYT
DSFHRVEMLKLAIQSNPSFKLELVEMEREGPSYTFDTVSLLKQRYPNDQL
FFIIGADMIEYLPKWYKLDELLNLIQFIGVKRPGFHVETPYPLLFADVPE
FEVSSTMIRERFKSKKPTDYLIPDKVKKYVEENGLY
Ligand information
Ligand ID
DND
InChI
InChI=1S/C21H26N6O15P2/c22-17-12-18(24-7-23-17)27(8-25-12)20-16(31)14(29)11(41-20)6-39-44(36,37)42-43(34,35)38-5-10-13(28)15(30)19(40-10)26-3-1-2-9(4-26)21(32)33/h1-4,7-8,10-11,13-16,19-20,28-31H,5-6H2,(H4-,22,23,24,32,33,34,35,36,37)/p+1/t10-,11-,13-,14-,15-,16-,19-,20-/m1/s1
InChIKey
SENPVEZBRZQVST-HISDBWNOSA-O
SMILES
Software
SMILES
CACTVS 3.385
Nc1ncnc2n(cnc12)[C@@H]3O[C@H](CO[P](O)(=O)O[P](O)(=O)OC[C@H]4O[C@H]([C@H](O)[C@@H]4O)[n+]5cccc(c5)C(O)=O)[C@@H](O)[C@H]3O
OpenEye OEToolkits 1.7.6
c1cc(c[n+](c1)[C@H]2[C@@H]([C@@H]([C@H](O2)COP(=O)(O)OP(=O)(O)OC[C@@H]3[C@H]([C@H]([C@@H](O3)n4cnc5c4ncnc5N)O)O)O)O)C(=O)O
CACTVS 3.385
Nc1ncnc2n(cnc12)[CH]3O[CH](CO[P](O)(=O)O[P](O)(=O)OC[CH]4O[CH]([CH](O)[CH]4O)[n+]5cccc(c5)C(O)=O)[CH](O)[CH]3O
OpenEye OEToolkits 1.7.6
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)O
Formula
C21 H27 N6 O15 P2
Name
NICOTINIC ACID ADENINE DINUCLEOTIDE;
DEAMIDO-NAD+
ChEMBL
DrugBank
DB04099
ZINC
ZINC000008216447
PDB chain
1kaq Chain D Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
1kaq
Identification, characterization, and crystal structure of Bacillus subtilis nicotinic acid mononucleotide adenylyltransferase.
Resolution
3.2 Å
Binding residue
(original residue number in PDB)
F7 G8 G9 T10 H15 H18 M21 P43 H44 T85 G106 M109 W116 Y117 R133 V154
Binding residue
(residue number reindexed from 1)
F6 G7 G8 T9 H14 H17 M20 P42 H43 T84 G105 M108 W115 Y116 R132 V153
Annotation score
5
Enzymatic activity
Enzyme Commision number
2.7.7.18
: nicotinate-nucleotide adenylyltransferase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0004515
nicotinate-nucleotide adenylyltransferase activity
GO:0005524
ATP binding
GO:0016779
nucleotidyltransferase activity
GO:0070566
adenylyltransferase activity
Biological Process
GO:0009058
biosynthetic process
GO:0009165
nucleotide biosynthetic process
GO:0009435
NAD biosynthetic process
GO:0019363
pyridine nucleotide biosynthetic process
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Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:1kaq
,
PDBe:1kaq
,
PDBj:1kaq
PDBsum
1kaq
PubMed
11704676
UniProt
P54455
|NADD_BACSU Nicotinate-nucleotide adenylyltransferase (Gene Name=nadD)
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