Structure of PDB 2onm Chain B Binding Site BS01
Receptor Information
>2onm Chain B (length=494) Species:
9606
(Homo sapiens) [
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AVPAPNQQPEVFCNQIFINNEWHDAVSRKTFPTVNPSTGEVICQVAEGDK
EDVDKAVKAARAAFQLGSPWRRMDASHRGRLLNRLADLIERDRTYLAALE
TLDNGKPYVISYLVDLDMVLKCLRYYAGWADKYHGKTIPIDGDFFSYTRH
EPVGVCGQIIPWNFPLLMQAWKLGPALATGNVVVMKVAEQTPLTALYVAN
LIKEAGFPPGVVNIVPGFGPTAGAAIASHEDVDKVAFTGSTEIGRVIQVA
AGSSNLKRVTLELGGKSPNIIMSDADMDWAVEQAHFALFFNQGQCCCAGS
RTFVQEDIYDEFVERSVARAKSRVVGNPFDSKTEQGPQVDETQFKKILGY
INTGKQEGAKLLCGGGIAADRGYFIQPTVFGDVQDGMTIAKEEIFGPVMQ
ILKFKTIEEVVGRANNSTYGLAAAVFTKDLDKANYLSQALQAGTVWVNCY
DVFGAQSPFGGYKMSGSGRELGEYGLQAYTKVKTVTVKVPQKNS
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
2onm Chain B Residue 502 [
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Receptor-Ligand Complex Structure
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PDB
2onm
Structural and functional consequences of coenzyme binding to the inactive asian variant of mitochondrial aldehyde dehydrogenase: roles of residues 475 and 487.
Resolution
2.5 Å
Binding residue
(original residue number in PDB)
I165 P167 N169 K192 G225 G229 A230 F243 T244 G245 S246 I249 G270 C302 Q349 E399 F401
Binding residue
(residue number reindexed from 1)
I159 P161 N163 K186 G219 G223 A224 F237 T238 G239 S240 I243 G264 C296 Q343 E393 F395
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
N169 K192 E268 C302 E399 E476
Catalytic site (residue number reindexed from 1)
N163 K186 E262 C296 E393 E470
Enzyme Commision number
1.2.1.3
: aldehyde dehydrogenase (NAD(+)).
Gene Ontology
Molecular Function
GO:0004029
aldehyde dehydrogenase (NAD+) activity
GO:0004030
aldehyde dehydrogenase [NAD(P)+] activity
GO:0008957
phenylacetaldehyde dehydrogenase (NAD+) activity
GO:0009055
electron transfer activity
GO:0016491
oxidoreductase activity
GO:0016620
oxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor
GO:0051287
NAD binding
GO:0106435
carboxylesterase activity
Biological Process
GO:0005975
carbohydrate metabolic process
GO:0006066
alcohol metabolic process
GO:0006068
ethanol catabolic process
GO:0018937
nitroglycerin metabolic process
GO:0046185
aldehyde catabolic process
GO:1903179
regulation of dopamine biosynthetic process
GO:1905627
regulation of serotonin biosynthetic process
Cellular Component
GO:0005739
mitochondrion
GO:0005759
mitochondrial matrix
GO:0070062
extracellular exosome
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Molecular Function
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Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:2onm
,
PDBe:2onm
,
PDBj:2onm
PDBsum
2onm
PubMed
17327228
UniProt
P05091
|ALDH2_HUMAN Aldehyde dehydrogenase, mitochondrial (Gene Name=ALDH2)
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