Structure of PDB 6dum Chain A Binding Site BS02
Receptor Information
>6dum Chain A (length=494) Species:
9606
(Homo sapiens) [
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DLPVLLTDLKIQYTKIFINNEWHDSVSGKKFPVFNPATEEELCQVEEGDK
EDVDKAVKAARQAFQIGSPWRTMDASERGRLLYKLADLIERDRLLLATME
SMNGGKLYSNAYLSDLAGCIKTLRYCAGWADKIQGRTIPIDGNFFTYTRH
EPIGVCGQIIPWNFPLVMLIWKIGPALSCGNTVVVKPAEQTPLTALHVAS
LIKEAGFPPGVVNIVPGYGPTAGAAISSHMDIDKVAFTGSTEVGKLIKEA
AGKSNLKRVTLELGGKSPCIVLADADLDNAVEFAHHGVFYHQGQCCIAAS
RIFVEESIYDEFVRRSVERAKKYILGNPLTPGVTQGPQIDKEQYDKILDL
IESGKKEGAKLECGGGPWGNKGYFVQPTVFSNVTDEMRIAKEEIFGPVQQ
IMKFKSLDDVIKRANNTFYGLSAGVFTKDIDKAITISSALQAGTVWVNCY
GVVSAQCPFGGFKMSGNGRELGEYGFHEYTEVKTVTVKISQKNS
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
6dum Chain A Residue 604 [
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Receptor-Ligand Complex Structure
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PDB
6dum
Structure-Based Optimization of a Novel Class of Aldehyde Dehydrogenase 1A (ALDH1A) Subfamily-Selective Inhibitors as Potential Adjuncts to Ovarian Cancer Chemotherapy.
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
I166 I167 P168 W169 N170 K193 E196 G226 P227 G230 A231 F244 T245 G246 S247 V250 L270 C303 Q350 K353 E400 F402
Binding residue
(residue number reindexed from 1)
I159 I160 P161 W162 N163 K186 E189 G219 P220 G223 A224 F237 T238 G239 S240 V243 L263 C296 Q343 K346 E393 F395
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
N170 K193 E269 C303 E400 E477
Catalytic site (residue number reindexed from 1)
N163 K186 E262 C296 E393 E470
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:6dum
,
PDBe:6dum
,
PDBj:6dum
PDBsum
6dum
PubMed
30221940
UniProt
P00352
|AL1A1_HUMAN Aldehyde dehydrogenase 1A1 (Gene Name=ALDH1A1)
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