Structure of PDB 4g5d Chain A Binding Site BS01
Receptor Information
>4g5d Chain A (length=283) Species:
347515
(Leishmania major strain Friedlin) [
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AGVDKAMVTLSNGVKMPQFGLGVWQSPAGEVTENAVKWALCAGYRHIDTA
AIYKNEESVGAGLRASGVPREDVFITTKLWNTEQGYESTLAAFEESRQKL
GVDYIDLYLIHWPRGKDILSKEGKKYLDSWRAFEQLYKEKKVRAIGVSNF
HIHHLEDVLAMCTVTPMVNQVELHPLNNQADLRAFCDAKQIKVEAWSPLG
QGKLLSNPILSAIGAKYNKTAAQVILRWNIQKNLITIPKSVHRERIEENA
DIFDFELGAEDVMSIDALNTNSRYGPDPDEAQF
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
4g5d Chain A Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
4g5d
Structures of prostaglandin F synthase from the protozoa Leishmania major and Trypanosoma cruzi with NADP.
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
G23 V24 W25 D49 Y54 H112 S149 N150 Q171 W197 S198 P199 L200 Q202 G203 L206 I238 P239 K240 S241 V242 H243 R246 E249 N250
Binding residue
(residue number reindexed from 1)
G22 V23 W24 D48 Y53 H111 S148 N149 Q170 W196 S197 P198 L199 Q201 G202 L205 I237 P238 K239 S240 V241 H242 R245 E248 N249
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
D49 Y54 K79 H112
Catalytic site (residue number reindexed from 1)
D48 Y53 K78 H111
Enzyme Commision number
1.1.1.-
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0004033
aldo-keto reductase (NADPH) activity
GO:0016491
oxidoreductase activity
GO:0016616
oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
GO:0036130
prostaglandin H2 endoperoxidase reductase activity
Biological Process
GO:0001516
prostaglandin biosynthetic process
Cellular Component
GO:0005737
cytoplasm
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:4g5d
,
PDBe:4g5d
,
PDBj:4g5d
PDBsum
4g5d
PubMed
25945716
UniProt
P22045
|PGFS_LEIMA 9,11-endoperoxide prostaglandin H2 reductase (Gene Name=P100/11E)
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