Structure of PDB 1dqs Chain B Binding Site BS02
Receptor Information
>1dqs Chain B (length=380) Species:
162425
(Aspergillus nidulans) [
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NPTKISILGRESIIADFGLWRNYVAKDLISDCSSTTYVLVTDTNIGSIYT
PSFEEAFRKRAAEITPSPRLLIYNRPPGEVSKSRQTKADIEDWMLSQNPP
CGRDTVVIALGGGVIGDLTGFVASTYMRGVRYVQVPTTLLAMVDSSIGGK
TAIDTPLGKNLIGAIWQPTKIYIDLEFLETLPVREFINGMAEVIKTAAIS
SEEEFTALEENAETILKAVRRTEEILKARILASARHKAYVVSADEREGGL
RNLLNWGHSIGHAIEAILTPQILHGECVAIGMVKEAELARHLGILKGVAV
SRIVKCLAAYGLPTSLKDARIRKLTAGKHCSVDQLMFNMALDKKNDGPKK
KIVLLSAIGTPYETRASVVANEDIRVVLAP
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
1dqs Chain B Residue 400 [
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Receptor-Ligand Complex Structure
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PDB
1dqs
Structure of dehydroquinate synthase reveals an active site capable of multistep catalysis.
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
D44 N46 I47 E81 K84 G114 G115 V116 D119 T139 T140 L142 D146 S147 K161 T182 L183 P184 E187 H287
Binding residue
(residue number reindexed from 1)
D42 N44 I45 E79 K82 G112 G113 V114 D117 T137 T138 L140 D144 S145 K159 T180 L181 P182 E185 H274
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
R130 K152 E194 K250 E260 R264 N268 H271 H275 H287
Catalytic site (residue number reindexed from 1)
R128 K150 E192 K237 E247 R251 N255 H258 H262 H274
Enzyme Commision number
1.1.1.25
: shikimate dehydrogenase (NADP(+)).
2.5.1.19
: 3-phosphoshikimate 1-carboxyvinyltransferase.
2.7.1.71
: shikimate kinase.
4.2.1.10
: 3-dehydroquinate dehydratase.
4.2.3.4
: 3-dehydroquinate synthase.
Gene Ontology
Molecular Function
GO:0003856
3-dehydroquinate synthase activity
GO:0016838
carbon-oxygen lyase activity, acting on phosphates
Biological Process
GO:0009073
aromatic amino acid family biosynthetic process
Cellular Component
GO:0005737
cytoplasm
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1dqs
,
PDBe:1dqs
,
PDBj:1dqs
PDBsum
1dqs
PubMed
9685163
UniProt
P07547
|ARO1_EMENI Pentafunctional AROM polypeptide (Gene Name=aromA)
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