Structure of PDB 5w73 Chain A Binding Site BS03
Receptor Information
>5w73 Chain A (length=179) Species:
641501
(Influenza A virus (A/California/04/2009(H1N1))) [
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GSHMEDFVRQCFNPMIVELAEKAMKEYGEDPKIETNKFAAICTHLEVCFM
YSDGGSKHRFEIIEGRDRIMAWTVVNSICNTTGVEKPKFLPDLYDYKENR
FIEIGVTRREVHIYYLEKANKIKSEKTHIHIFSFTGEEMATKADYTLDEE
SRARIKTRLFTIRQEMASRSLWDSFRQSE
Ligand information
Ligand ID
GY9
InChI
InChI=1S/C25H25ClN4O6/c26-17-9-4-5-11-19(17)36-15-20(31)30-13-6-10-18(30)23-28-21(22(32)25(34)29-23)24(33)27-12-14-35-16-7-2-1-3-8-16/h1-5,7-9,11,18,32H,6,10,12-15H2,(H,27,33)(H,28,29,34)/t18-/m0/s1
InChIKey
FJNCSYKYMWITQI-SFHVURJKSA-N
SMILES
Software
SMILES
CACTVS 3.385
OC1=C(N=C(NC1=O)[CH]2CCCN2C(=O)COc3ccccc3Cl)C(=O)NCCOc4ccccc4
CACTVS 3.385
OC1=C(N=C(NC1=O)[C@@H]2CCCN2C(=O)COc3ccccc3Cl)C(=O)NCCOc4ccccc4
ACDLabs 12.01
C=2(NC(C(=C(C(=O)NCCOc1ccccc1)N=2)O)=O)C4CCCN4C(COc3c(cccc3)Cl)=O
OpenEye OEToolkits 2.0.6
c1ccc(cc1)OCCNC(=O)C2=C(C(=O)NC(=N2)C3CCCN3C(=O)COc4ccccc4Cl)O
OpenEye OEToolkits 2.0.6
c1ccc(cc1)OCCNC(=O)C2=C(C(=O)NC(=N2)[C@@H]3CCCN3C(=O)COc4ccccc4Cl)O
Formula
C25 H25 Cl N4 O6
Name
2-{(2S)-1-[(2-chlorophenoxy)acetyl]pyrrolidin-2-yl}-5-hydroxy-6-oxo-N-(2-phenoxyethyl)-1,6-dihydropyrimidine-4-carboxamide;
SRI-29835
ChEMBL
DrugBank
ZINC
PDB chain
5w73 Chain A Residue 205 [
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Receptor-Ligand Complex Structure
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PDB
5w73
Protein-Structure Assisted Optimization of 4,5-Dihydroxypyrimidine-6-Carboxamide Inhibitors of Influenza Virus Endonuclease.
Resolution
2.202 Å
Binding residue
(original residue number in PDB)
Y24 K34 I38 H41 E80 D108 E119 K134 K137
Binding residue
(residue number reindexed from 1)
Y27 K37 I41 H44 E64 D92 E103 K118 K121
Annotation score
1
Binding affinity
MOAD
: Ki=0.5uM
PDBbind-CN
: -logKd/Ki=6.30,Ki=0.5uM
Enzymatic activity
Enzyme Commision number
3.1.-.-
Gene Ontology
Molecular Function
GO:0003723
RNA binding
Biological Process
GO:0039694
viral RNA genome replication
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Molecular Function
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Biological Process
External links
PDB
RCSB:5w73
,
PDBe:5w73
,
PDBj:5w73
PDBsum
5w73
PubMed
29215062
UniProt
C3W5S0
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