Structure of PDB 3kb6 Chain C Binding Site BS02
Receptor Information
>3kb6 Chain C (length=334) Species:
63363
(Aquifex aeolicus) [
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MNVLFTSVPQEDVPFYQEALKDLSLKIYTTDVSKVPENELKKAELISVFV
YDKLTEELLSKMPRLKLIHTRSVGFDHIDLDYCKKKGILVTHIPAYSPES
VAEHTFAMILTLVKRLKRIEDRVKKLNFSQDSEILARELNRLTLGVIGTG
RIGSRVAMYGLAFGMKVLCYDVVKREDLKEKGCVYTSLDELLKESDVISL
HVPYTKETHHMINEERISLMKDGVYLINTARGKVVDTDALYRAYQRGKFS
GLGLDVFEDEEILILKKYTEGKATDKNLKILELACKDNVIITPHIAYYTD
KSLERIREETVKVVKAFVKGDLEQIKGNFVVGPS
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
3kb6 Chain C Residue 400 [
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Receptor-Ligand Complex Structure
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PDB
3kb6
Structure of D-lactate dehydrogenase from Aquifex aeolicus complexed with NAD(+) and lactic acid (or pyruvate).
Resolution
2.12 Å
Binding residue
(original residue number in PDB)
Y96 V101 G150 R151 I152 D171 H201 P203 T229 A230 R231 H294 A296 Y297
Binding residue
(residue number reindexed from 1)
Y96 V101 G150 R151 I152 D171 H201 P203 T229 A230 R231 H294 A296 Y297
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
S97 R231 D255 E260 H294
Catalytic site (residue number reindexed from 1)
S97 R231 D255 E260 H294
Enzyme Commision number
1.1.1.28
: D-lactate dehydrogenase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0008720
D-lactate dehydrogenase activity
GO:0016491
oxidoreductase activity
GO:0016614
oxidoreductase activity, acting on CH-OH group of donors
GO:0016616
oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
GO:0051287
NAD binding
View graph for
Molecular Function
External links
PDB
RCSB:3kb6
,
PDBe:3kb6
,
PDBj:3kb6
PDBsum
3kb6
PubMed
20054113
UniProt
O66939
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