Structure of PDB 2c59 Chain A Binding Site BS03
Receptor Information
>2c59 Chain A (length=364) Species:
3702
(Arabidopsis thaliana) [
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YTYKELEREQYWPSENLKISITGAGGFIASHIARRLKHEGHYVIASDWKK
NEHMTEDMFCDEFHLVDLRVMENCLKVTEGVDHVFNLAADMGGMGFIQSN
HSVIMYNNTMISFNMIEAARINGIKRFFYASSACIYPEFKQLETTNVSLK
ESDAWPAEPQDAYGLEKLATEELCKHYNKDFGIECRIGRFHNIYGPFGTW
KGGREKAPAAFCRKAQTSTDRFEMWGDGLQTRSFTFIDECVEGVLRLTKS
DFREPVNIGSDEMVSMNEMAEMVLSFEEKKLPIHHIPGPEGVRGRNSDNN
LIKEKLGWAPNMRLKEGLRITYFWIKEQIEKEKAKGSDVSLYGSSKVVGT
QAPVQLGSLRAADG
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
2c59 Chain A Residue 1379 [
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Receptor-Ligand Complex Structure
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PDB
2c59
Structure and Function of Gdp-Mannose-3',5'-Epimerase: An Enzyme which Performs Three Chemical Reactions at the Same Active Site.
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
G34 G37 F38 I39 D58 W59 K60 D78 L79 L98 A100 M102 I122 A141 S143 Y174 K178 F201 N203 I204 K217
Binding residue
(residue number reindexed from 1)
G23 G26 F27 I28 D47 W48 K49 D67 L68 L87 A89 M91 I111 A130 S132 Y163 K167 F190 N192 I193 K206
Annotation score
2
Enzymatic activity
Catalytic site (original residue number in PDB)
S143 A144 C145 Y174 K178 K217
Catalytic site (residue number reindexed from 1)
S132 A133 C134 Y163 K167 K206
Enzyme Commision number
5.1.3.18
: GDP-mannose 3,5-epimerase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0016853
isomerase activity
GO:0047918
GDP-mannose 3,5-epimerase activity
GO:0051287
NAD binding
Biological Process
GO:0019853
L-ascorbic acid biosynthetic process
Cellular Component
GO:0005829
cytosol
GO:0009536
plastid
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2c59
,
PDBe:2c59
,
PDBj:2c59
PDBsum
2c59
PubMed
16366586
UniProt
Q93VR3
|GME_ARATH GDP-mannose 3,5-epimerase (Gene Name=At5g28840)
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