Structure of PDB 3h4v Chain E Binding Site BS01
Receptor Information
>3h4v Chain E (length=266) Species:
5664
(Leishmania major) [
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VPVALVTGAAKRLGRSIAEGLHAEGYAVCLHYHRSAAEANALSATLNARR
PNSAITVQADLSNVATAPAPVTLFTRCAELVAACYTHWGRCDVLVNNASS
FYPTPLLRGDREAMETATADLFGSNAIAPYFLIKAFAHRVAGTPAKHRGT
NYSIINMVDAMTNQPLLGYTIYTMAKGALEGLTRSAALELAPLQIRVNGV
GPGLSVLVDDMPPAVWEGHRSKVPLYQRDSSAAEVSDVVIFLCSSKAKYI
TGTCVKVDGGYSLTRA
Ligand information
Ligand ID
NAP
InChI
InChI=1S/C21H28N7O17P3/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/h1-4,7-8,10-11,13-16,20-21,29-31H,5-6H2,(H7-,22,23,24,25,32,33,34,35,36,37,38,39)/t10-,11-,13-,14-,15-,16-,20-,21-/m1/s1
InChIKey
XJLXINKUBYWONI-NNYOXOHSSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1cc(c[n+](c1)C2C(C(C(O2)COP(=O)([O-])OP(=O)(O)OCC3C(C(C(O3)n4cnc5c4ncnc5N)OP(=O)(O)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[P](O)(O)=O)[CH]3O)n4cnc5c(N)ncnc45)[CH](O)[CH]2O
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[P](O)(O)=O)[C@@H]3O)n4cnc5c(N)ncnc45)[C@@H](O)[C@H]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)OP(=O)(O)O)O)O)O)C(=O)N
Formula
C21 H28 N7 O17 P3
Name
NADP NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE;
2'-MONOPHOSPHOADENOSINE 5'-DIPHOSPHORIBOSE
ChEMBL
CHEMBL295069
DrugBank
DB03461
ZINC
PDB chain
3h4v Chain E Residue 300 [
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Receptor-Ligand Complex Structure
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PDB
3h4v
Discovery of potent pteridine reductase inhibitors to guide antiparasite drug development
Resolution
2.4 Å
Binding residue
(original residue number in PDB)
R17 L18 H36 Y37 H38 R39 S40 L66 N109 A110 S111 S112 M179 V180 K198 P224 S227
Binding residue
(residue number reindexed from 1)
R12 L13 H31 Y32 H33 R34 S35 L61 N97 A98 S99 S100 M157 V158 K176 P202 S205
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
R17 D181 Y194
Catalytic site (residue number reindexed from 1)
R12 D159 Y172
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:3h4v
,
PDBe:3h4v
,
PDBj:3h4v
PDBsum
3h4v
PubMed
18245389
UniProt
Q01782
|PTR1_LEIMA Pteridine reductase 1 (Gene Name=PTR1)
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