Structure of PDB 3ak4 Chain C Binding Site BS01
Receptor Information
>3ak4 Chain C (length=258) Species:
358
(Agrobacterium tumefaciens) [
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GIFDLSGRKAIVTGGSKGIGAAIARALDKAGATVAIADLDVMAAQAVVAG
LENGGFAVEVDVTKRASVDAAMQKAIDALGGFDLLCANAGVSTMRPAVDI
TDEEWDFNFDVNARGVFLANQIACRHFLASNTKGVIVNTASLAAKVGAPL
LAHYSASKFAVFGWTQALAREMAPKNIRVNCVCPGFVKTAMQEREIIWEA
ELRGMTPEAVRAEYVSLTPLGRIEEPEDVADVVVFLASDAARFMTGQGIN
VTGGVRMD
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
3ak4 Chain C Residue 903 [
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Receptor-Ligand Complex Structure
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PDB
3ak4
Crystal structure of NADH-dependent quinuclidinone reductase from Agrobacterium tumefaciens
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
G16 K19 G20 I21 D40 L41 V62 D63 V64 N90 A91 G92 T141 S143 Y156 K160 P186 G187 V189 T191 M193
Binding residue
(residue number reindexed from 1)
G14 K17 G18 I19 D38 L39 V60 D61 V62 N88 A89 G90 T139 S141 Y154 K158 P184 G185 V187 T189 M191
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
G20 S143 L153 Y156 K160 E201
Catalytic site (residue number reindexed from 1)
G18 S141 L151 Y154 K158 E199
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0016491
oxidoreductase activity
GO:0016616
oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
View graph for
Molecular Function
External links
PDB
RCSB:3ak4
,
PDBe:3ak4
,
PDBj:3ak4
PDBsum
3ak4
PubMed
UniProt
G1K3P5
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