Structure of PDB 8ene Chain A Binding Site BS01
Receptor Information
>8ene Chain A (length=493) Species:
9606
(Homo sapiens) [
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LPVLLTDLKIQYTKIFINNEWHDSVSGKKFPVFNPATEEELCQVEEGDKE
DVDKAVKAARQAFQIGSPWRTMDASERGRLLYKLADLIERDRLLLATMES
MNGGKLYSNAYLNDLAGCIKTLRYCAGWADKIQGRTIPIDGNFFTYTRHE
PIGVCGQIIPWNFPLVMLIWKIGPALSCGNTVVVKPAEQTPLTALHVASL
IKEAGFPPGVVNIVPGYGPTAGAAISSHMDIDKVAFTGSTEVGKLIKEAA
GKSNLKRVTLELGGKSPCIVLADADLDNAVEFAHHGVFYHQGQCCIAASR
IFVEESIYDEFVRRSVERAKKYILGNPLTPGVTQGPQIDKEQYDKILDLI
ESGKKEGAKLECGGGPWGNKGYFVQPTVFSNVTDEMRIAKEEIFGPVQQI
MKFKSLDDVIKRANNTFYGLSAGVFTKDIDKAITISSALQAGTVWVNCYG
VVSAQCPFGGFKMSGNGRELGEYGFHEYTEVKTVTVKISQKNS
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
8ene Chain A Residue 601 [
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Receptor-Ligand Complex Structure
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PDB
8ene
Aldehyde dehydrogenase 1 family member A1 from human liver
Resolution
2.64 Å
Binding residue
(original residue number in PDB)
I166 I167 P168 W169 N170 K193 A195 G226 P227 G230 F244 G246 S247 V250 G271 C303 Q350 E400 F402
Binding residue
(residue number reindexed from 1)
I158 I159 P160 W161 N162 K185 A187 G218 P219 G222 F236 G238 S239 V242 G263 C295 Q342 E392 F394
Annotation score
4
Enzymatic activity
Enzyme Commision number
1.2.1.19
: aminobutyraldehyde dehydrogenase.
1.2.1.28
: benzaldehyde dehydrogenase (NAD(+)).
1.2.1.3
: aldehyde dehydrogenase (NAD(+)).
1.2.1.36
: retinal dehydrogenase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0001758
retinal dehydrogenase activity
GO:0004029
aldehyde dehydrogenase (NAD+) activity
GO:0005096
GTPase activator activity
GO:0005497
androgen binding
GO:0005515
protein binding
GO:0016491
oxidoreductase activity
GO:0016620
oxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor
GO:0018479
benzaldehyde dehydrogenase (NAD+) activity
GO:0019145
aminobutyraldehyde dehydrogenase (NAD+) activity
GO:0051287
NAD binding
GO:0106373
3-deoxyglucosone dehydrogenase activity
Biological Process
GO:0001523
retinoid metabolic process
GO:0006081
cellular aldehyde metabolic process
GO:0006629
lipid metabolic process
GO:0009449
gamma-aminobutyric acid biosynthetic process
GO:0030392
fructosamine catabolic process
GO:0036438
maintenance of lens transparency
GO:0042572
retinol metabolic process
GO:0110095
cellular detoxification of aldehyde
GO:0120163
negative regulation of cold-induced thermogenesis
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
GO:0030424
axon
GO:0042995
cell projection
GO:0045202
synapse
GO:0070062
extracellular exosome
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:8ene
,
PDBe:8ene
,
PDBj:8ene
PDBsum
8ene
PubMed
37289586
UniProt
P00352
|AL1A1_HUMAN Aldehyde dehydrogenase 1A1 (Gene Name=ALDH1A1)
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