Structure of PDB 2dld Chain A Binding Site BS01
Receptor Information
>2dld Chain A (length=337) Species:
1587
(Lactobacillus helveticus) [
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MTKVFAYAIRKDEEPFLNEWKEAHKDIDVDYTDKLLTPETAKLAKGADGV
VVYQQLDYTADTLQALADAGVTKMSLRNVGVDNIDMDKAKELGFQITNVP
VYSPNAIAEHAAIQAARVLRQDKRMDEKMAKRDLRWAPTIGREVRDQVVG
VVGTGHIGQVFMRIMEGFGAKVIAYDIFKNPELEKKGYYVDSLDDLYKQA
DVISLHVPDVPANVHMINDKSIAEMKDGVVIVNCSRGRLVDTDAVIRGLD
SGKIFGFVMDTYEDEVGVFNKDWEGKEFPDKRLADLIDRPNVLVTPHTAF
YTTHAVRNMVVKAFNNNLKLINGEKPDSPVALNKNKF
Ligand information
Ligand ID
NAI
InChI
InChI=1S/C21H29N7O14P2/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/h1,3-4,7-8,10-11,13-16,20-21,29-32H,2,5-6H2,(H2,23,33)(H,34,35)(H,36,37)(H2,22,24,25)/t10-,11-,13-,14-,15-,16-,20-,21-/m1/s1
InChIKey
BOPGDPNILDQYTO-NNYOXOHSSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)OP(=O)(O)OCC4C(C(C(O4)N5C=CCC(=C5)C(=O)N)O)O)O)O)N
CACTVS 3.341
NC(=O)C1=CN(C=CC1)[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
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@](=O)(O)O[P@@](=O)(O)OC[C@@H]4[C@H]([C@H]([C@@H](O4)N5C=CCC(=C5)C(=O)N)O)O)O)O)N
CACTVS 3.341
NC(=O)C1=CN(C=CC1)[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
Formula
C21 H29 N7 O14 P2
Name
1,4-DIHYDRONICOTINAMIDE ADENINE DINUCLEOTIDE;
NADH
ChEMBL
CHEMBL1234616
DrugBank
DB00157
ZINC
ZINC000008215403
PDB chain
2dld Chain A Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
2dld
Dehydrogenases Engineering to Correct Substrate Inhibition in a Commercial Dehydrogenase
Resolution
2.7 Å
Binding residue
(original residue number in PDB)
T154 G155 H156 I157 D176 I177 V207 P208 N213 C234 S235 H297 F337
Binding residue
(residue number reindexed from 1)
T154 G155 H156 I157 D176 I177 V207 P208 N213 C234 S235 H297 F337
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
S103 R236 D260 E265 H297
Catalytic site (residue number reindexed from 1)
S103 R236 D260 E265 H297
Enzyme Commision number
1.1.1.28
: D-lactate dehydrogenase.
Gene Ontology
Molecular Function
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:2dld
,
PDBe:2dld
,
PDBj:2dld
PDBsum
2dld
PubMed
UniProt
P30901
|LDHD_LACHE D-lactate dehydrogenase
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