Structure of PDB 1xhl Chain B Binding Site BS01
Receptor Information
>1xhl Chain B (length=274) Species:
6239
(Caenorhabditis elegans) [
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RFSGKSVIITGSSNGIGRSAAVIFAKEGAQVTITGRNEDRLEETKQQILK
AGVPAEKINAVVADVTEASGQDDIINTTLAKFGKIDILVNNAGANLADGT
ANTDQPVELYQKTFKLNFQAVIEMTQKTKEHLIKTKGEIVNVSSIVAGPQ
AHSGYPYYACAKAALDQYTRCTAIDLIQHGVRVNSVSPGAVATGFMGAMG
LPETASDKLYSFIGSRKECIPVGHCGKPEEIANIIVFLADRNLSSYIIGQ
SIVADGGSTLVMGMQTHDLMSVLS
Ligand information
Ligand ID
NDP
InChI
InChI=1S/C21H30N7O17P3/c22-17-12-19(25-7-24-17)28(8-26-12)21-16(44-46(33,34)35)14(30)11(43-21)6-41-48(38,39)45-47(36,37)40-5-10-13(29)15(31)20(42-10)27-3-1-2-9(4-27)18(23)32/h1,3-4,7-8,10-11,13-16,20-21,29-31H,2,5-6H2,(H2,23,32)(H,36,37)(H,38,39)(H2,22,24,25)(H2,33,34,35)/t10-,11-,13-,14-,15-,16-,20-,21-/m1/s1
InChIKey
ACFIXJIJDZMPPO-NNYOXOHSSA-N
SMILES
Software
SMILES
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)OP(=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[P](O)(O)=O)[CH]3O)n4cnc5c(N)ncnc45)[CH](O)[CH]2O
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[P](O)(O)=O)[C@@H]3O)n4cnc5c(N)ncnc45)[C@@H](O)[C@H]2O
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)OP(=O)(O)O)N
Formula
C21 H30 N7 O17 P3
Name
NADPH DIHYDRO-NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE
ChEMBL
CHEMBL407009
DrugBank
DB02338
ZINC
ZINC000008215411
PDB chain
1xhl Chain B Residue 2278 [
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Receptor-Ligand Complex Structure
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PDB
1xhl
Crystal Structure of putative Tropinone Reductase-II from Caenorhabditis Elegans with Cofactor and Substrate
Resolution
2.4 Å
Binding residue
(original residue number in PDB)
G13 S15 G17 I18 R38 N39 R42 D66 V67 N93 G95 L118 S146 Y160 K164 P190 G191 A192 V193 T195 G196 F197
Binding residue
(residue number reindexed from 1)
G11 S13 G15 I16 R36 N37 R40 D64 V65 N91 G93 L116 S144 Y158 K162 P188 G189 A190 V191 T193 G194 F195
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
G17 F26 Q32 N92 S146 Q152 Y157 Y160 K164 E205
Catalytic site (residue number reindexed from 1)
G15 F24 Q30 N90 S144 Q150 Y155 Y158 K162 E203
Enzyme Commision number
1.1.1.236
: tropinone reductase II.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0016491
oxidoreductase activity
View graph for
Molecular Function
External links
PDB
RCSB:1xhl
,
PDBe:1xhl
,
PDBj:1xhl
PDBsum
1xhl
PubMed
UniProt
Q19774
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