Structure of PDB 1pl8 Chain C Binding Site BS02
Receptor Information
>1pl8 Chain C (length=356) Species:
9606
(Homo sapiens) [
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AAAAKPNNLSLVVHGPGDLRLENYPIPEPGPNEVLLRMHSVGICGSDVHY
WEYGRIGNFIVKKPMVLGHEASGTVEKVGSSVKHLKPGDRVAIEPGAPRE
NDEFCKMGRYNLSPSIFFCATPPDDGNLCRFYKHNAAFCYKLPDNVTFEE
GALIEPLSVGIHACRRGGVTLGHKVLVCGAGPIGMVTLLVAKAMGAAQVV
VTDLSATRLSKAKEIGADLVLQISKESPQEIARKVEGQLGCKPEVTIECT
GAEASIQAGIYATRSGGTLVLVGLGSEMTTVPLLHAAIREVDIKGVFRYC
NTWPVAISMLASKSVNVKPLVTHRFPLEKALEAFETFKKGLGLKIMLKCD
PSDQNP
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
1pl8 Chain C Residue 400 [
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Receptor-Ligand Complex Structure
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PDB
1pl8
X-ray crystallographic and kinetic studies of human sorbitol dehydrogenase.
Resolution
1.9 Å
Binding residue
(original residue number in PDB)
G181 P182 I183 D203 L204 R208 C249 T250 V272 G273 L274 V296 R298
Binding residue
(residue number reindexed from 1)
G181 P182 I183 D203 L204 R208 C249 T250 V272 G273 L274 V296 R298
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
C44 G45 S46 H49 H69 E70 R99 D102 C105 S113 F117 P156 G160 K344
Catalytic site (residue number reindexed from 1)
C44 G45 S46 H49 H69 E70 R99 D102 C105 S113 F117 P156 G160 K344
Enzyme Commision number
1.1.1.-
1.1.1.14
: L-iditol 2-dehydrogenase.
1.1.1.4
: (R,R)-butanediol dehydrogenase.
1.1.1.56
: ribitol 2-dehydrogenase.
1.1.1.9
: D-xylulose reductase.
Gene Ontology
Molecular Function
GO:0000721
(R,R)-butanediol dehydrogenase activity
GO:0003824
catalytic activity
GO:0003939
L-iditol 2-dehydrogenase (NAD+) activity
GO:0008270
zinc ion binding
GO:0016491
oxidoreductase activity
GO:0016616
oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
GO:0030246
carbohydrate binding
GO:0042802
identical protein binding
GO:0046526
D-xylulose reductase activity
GO:0046872
metal ion binding
GO:0047833
D-sorbitol dehydrogenase (acceptor) activity
GO:0050255
ribitol 2-dehydrogenase (NAD+) activity
GO:0051287
NAD binding
Biological Process
GO:0006006
glucose metabolic process
GO:0006060
sorbitol metabolic process
GO:0006062
sorbitol catabolic process
GO:0019640
D-glucuronate catabolic process to D-xylulose 5-phosphate
GO:0030317
flagellated sperm motility
GO:0046370
fructose biosynthetic process
GO:0051160
xylitol catabolic process
GO:0051164
xylitol metabolic process
Cellular Component
GO:0005615
extracellular space
GO:0005739
mitochondrion
GO:0005829
cytosol
GO:0016020
membrane
GO:0031514
motile cilium
GO:0031966
mitochondrial membrane
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:1pl8
,
PDBe:1pl8
,
PDBj:1pl8
PDBsum
1pl8
PubMed
12962626
UniProt
Q00796
|DHSO_HUMAN Sorbitol dehydrogenase (Gene Name=SORD)
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