Structure of PDB 5l4n Chain B Binding Site BS02
Receptor Information
>5l4n Chain B (length=254) Species:
5664
(Leishmania major) [
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TVPVALVTGAAKRLGRSIAEGLHAEGYAVCLHYHRSAAEANALSATLNAR
RPNSAITVQADLSNVATAPAPVTLFTRCAELVAACYTHWGRCDVLVNNAS
SFYPTPLLREAMETATADLFGSNAIAPYFLIKAFAHRVAGTPAKHRGTNY
SIINMVDAMTNQPLLGYTIYTMAKGALEGLTRSAALELAPLQIRVNGVGP
GLSVLVHRSKVPLYQRDSSAAEVSDVVIFLCSSKAKYITGTCVKVDGGYS
LTRA
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
5l4n Chain B Residue 602 [
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Receptor-Ligand Complex Structure
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PDB
5l4n
Chroman-4-One Derivatives Targeting Pteridine Reductase 1 and Showing Anti-Parasitic Activity.
Resolution
2.35 Å
Binding residue
(original residue number in PDB)
R17 L18 Y37 H38 R39 S40 L66 N109 A110 S111 S112 M179 D181 Y194 K198 P224 S227
Binding residue
(residue number reindexed from 1)
R13 L14 Y33 H34 R35 S36 L62 N98 A99 S100 S101 M155 D157 Y170 K174 P200 S203
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
R17 D181 Y194
Catalytic site (residue number reindexed from 1)
R13 D157 Y170
Enzyme Commision number
1.5.1.33
: pteridine reductase.
Gene Ontology
Molecular Function
GO:0004155
6,7-dihydropteridine reductase activity
GO:0016491
oxidoreductase activity
GO:0047040
pteridine reductase activity
Biological Process
GO:0006729
tetrahydrobiopterin biosynthetic process
GO:0031427
response to methotrexate
Cellular Component
GO:0005829
cytosol
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:5l4n
,
PDBe:5l4n
,
PDBj:5l4n
PDBsum
5l4n
PubMed
28282886
UniProt
Q01782
|PTR1_LEIMA Pteridine reductase 1 (Gene Name=PTR1)
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