Structure of PDB 1teh Chain A Binding Site BS03
Receptor Information
>1teh Chain A (length=373) Species:
9606
(Homo sapiens) [
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ANEVIKCKAAVAWEAGKPLSIEEIEVAPPKAHEVRIKIIATAVCHTDAYT
LSGADPEGCFPVILGHEGAGIVESVGEGVTKLKAGDTVIPLYIPQCGECK
FCLNPKTNLCQKIRVTQGKGLMPDGTSRFTCKGKTILHYMGTSTFSEYTV
VADISVAKIDPLAPLDKVCLLGCGISTGYGAAVNTAKLEPGSVCAVFGLG
GVGLAVIMGCKVAGASRIIGVDINKDKFARAKEFGATECINPQDFSKPIQ
EVLIEMTDGGVDYSFECIGNVKVMRAALEACHKGWGVSVVVGVAASGEEI
ATRPFQLVTGRTWKGTAFGGWKSVESVPKLVSEYMSKKIKVDEFVTHNLS
FDEINKAFELMHSGKSIRTVVKI
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
1teh Chain A Residue 377 [
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Receptor-Ligand Complex Structure
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PDB
1teh
Structure of human chi chi alcohol dehydrogenase: a glutathione-dependent formaldehyde dehydrogenase.
Resolution
2.7 Å
Binding residue
(original residue number in PDB)
T178 V203 D223 I224 C268 I269 V292 G293 V294 T317
Binding residue
(residue number reindexed from 1)
T177 V202 D222 I223 C267 I268 V291 G292 V293 T316
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
C46 H47 T48 Y51 H67 E68 C97 C100 C103 C111 R115 C174 T178 R369
Catalytic site (residue number reindexed from 1)
C44 H45 T46 Y49 H66 E67 C96 C99 C102 C110 R114 C173 T177 R368
Enzyme Commision number
1.1.1.-
1.1.1.1
: alcohol dehydrogenase.
1.1.1.284
: S-(hydroxymethyl)glutathione dehydrogenase.
Gene Ontology
Molecular Function
GO:0004022
alcohol dehydrogenase (NAD+) activity
GO:0005504
fatty acid binding
GO:0008270
zinc ion binding
GO:0009055
electron transfer activity
GO:0016491
oxidoreductase activity
GO:0018467
formaldehyde dehydrogenase (NAD+) activity
GO:0042802
identical protein binding
GO:0046872
metal ion binding
GO:0051903
S-(hydroxymethyl)glutathione dehydrogenase [NAD(P)+] activity
GO:0080007
S-nitrosoglutathione reductase (NADH) activity
GO:0106321
S-(hydroxymethyl)glutathione dehydrogenase (NADP+) activity
GO:0106322
S-(hydroxymethyl)glutathione dehydrogenase (NAD+) activity
Biological Process
GO:0001523
retinoid metabolic process
GO:0003016
respiratory system process
GO:0006629
lipid metabolic process
GO:0010430
fatty acid omega-oxidation
GO:0032496
response to lipopolysaccharide
GO:0044281
small molecule metabolic process
GO:0045777
positive regulation of blood pressure
GO:0046294
formaldehyde catabolic process
GO:0051409
response to nitrosative stress
GO:0051775
response to redox state
Cellular Component
GO:0005737
cytoplasm
GO:0005739
mitochondrion
GO:0005829
cytosol
GO:0070062
extracellular exosome
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1teh
,
PDBe:1teh
,
PDBj:1teh
PDBsum
1teh
PubMed
9018047
UniProt
P11766
|ADHX_HUMAN Alcohol dehydrogenase class-3 (Gene Name=ADH5)
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