Structure of PDB 5w9g Chain A Binding Site BS03
Receptor Information
>5w9g Chain A (length=178) Species:
641501
(Influenza A virus (A/California/04/2009(H1N1))) [
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RGSHMEDFVRQCFNPMIVELAEKAMKEYGEDPKIETNKFAAICTHLEVCF
MYSDGGSKHRFEIIEGRDRIMAWTVVNSICNTTGVEKPKFLPDLYDYKEN
RFIEIGVTRREVHIYYLEKANKIKKTHIHIFSFTGEEMATKADYTLDEES
RARIKTRLFTIRQEMASRSLWDSFRQSE
Ligand information
Ligand ID
KU2
InChI
InChI=1S/C25H25ClN4O5S/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
SAJTUABEFGSMCM-SFHVURJKSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 2.0.6
c1ccc(cc1)OCCNC(=O)C2=C(C(=O)NC(=N2)[C@@H]3CCCN3C(=O)CSc4ccccc4Cl)O
CACTVS 3.385
OC1=C(N=C(NC1=O)[C@@H]2CCCN2C(=O)CSc3ccccc3Cl)C(=O)NCCOc4ccccc4
ACDLabs 12.01
C(CSc1c(cccc1)Cl)(N4C(C=3NC(C(=C(C(=O)NCCOc2ccccc2)N=3)O)=O)CCC4)=O
OpenEye OEToolkits 2.0.6
c1ccc(cc1)OCCNC(=O)C2=C(C(=O)NC(=N2)C3CCCN3C(=O)CSc4ccccc4Cl)O
CACTVS 3.385
OC1=C(N=C(NC1=O)[CH]2CCCN2C(=O)CSc3ccccc3Cl)C(=O)NCCOc4ccccc4
Formula
C25 H25 Cl N4 O5 S
Name
2-[(2S)-1-{[(2-chlorophenyl)sulfanyl]acetyl}pyrrolidin-2-yl]-5-hydroxy-6-oxo-N-(2-phenoxyethyl)-1,6-dihydropyrimidine-4 -carboxamide;
SRI-30023
ChEMBL
DrugBank
ZINC
PDB chain
5w9g Chain A Residue 204 [
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Receptor-Ligand Complex Structure
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PDB
5w9g
Protein-Structure Assisted Optimization of 4,5-Dihydroxypyrimidine-6-Carboxamide Inhibitors of Influenza Virus Endonuclease.
Resolution
2.1 Å
Binding residue
(original residue number in PDB)
Y24 I38 H41 E80 D108 E119 Y130
Binding residue
(residue number reindexed from 1)
Y28 I42 H45 E65 D93 E104 Y115
Annotation score
1
Binding affinity
MOAD
: Ki=0.15uM
PDBbind-CN
: -logKd/Ki=6.82,Ki=0.15uM
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:5w9g
,
PDBe:5w9g
,
PDBj:5w9g
PDBsum
5w9g
PubMed
29215062
UniProt
C3W5S0
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