Structure of PDB 3sjo Chain B Binding Site BS01
Receptor Information
>3sjo Chain B (length=179) Species:
39054
(Enterovirus A71) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
LDFALSLLRRNIRQVQTDQGHFTMLGVRDRLAVLPRHSQPGKTIWIEHKL
VNVLDAVELVDEQGVNLELTLITLDTNEKFRDITKFIPENISTASDATLV
INTEHMPSMFVPVGDVVQYGFLNLSGKPTHRTMMYNFPTKAGQCGGVVTS
VGKVIGIHIGGNGRQGFCAGLKRSYFASE
Ligand information
Ligand ID
AG7
InChI
InChI=1S/C31H41FN4O7/c1-5-42-27(38)11-10-24(16-21-12-13-33-29(21)39)34-30(40)22(15-20-6-8-23(32)9-7-20)17-26(37)28(18(2)3)35-31(41)25-14-19(4)43-36-25/h6-9,14,18,21-22,24,28H,5,10-13,15-17H2,1-4H3,(H,33,39)(H,34,40)(H,35,41)/t21-,22+,24+,28-/m0/s1
InChIKey
LMIUALQNZXJHOG-IFILWLFVSA-N
SMILES
Software
SMILES
ACDLabs 12.01
O=C(NC(C(=O)CC(C(=O)NC(CC1C(=O)NCC1)CCC(=O)OCC)Cc2ccc(F)cc2)C(C)C)c3noc(c3)C
CACTVS 3.370
CCOC(=O)CC[CH](C[CH]1CCNC1=O)NC(=O)[CH](CC(=O)[CH](NC(=O)c2cc(C)on2)C(C)C)Cc3ccc(F)cc3
OpenEye OEToolkits 1.7.2
CCOC(=O)CCC(CC1CCNC1=O)NC(=O)C(Cc2ccc(cc2)F)CC(=O)C(C(C)C)NC(=O)c3cc(on3)C
CACTVS 3.370
CCOC(=O)CC[C@H](C[C@@H]1CCNC1=O)NC(=O)[C@@H](CC(=O)[C@@H](NC(=O)c2cc(C)on2)C(C)C)Cc3ccc(F)cc3
OpenEye OEToolkits 1.7.2
CCOC(=O)CC[C@H](C[C@@H]1CCNC1=O)NC(=O)[C@H](Cc2ccc(cc2)F)CC(=O)[C@H](C(C)C)NC(=O)c3cc(on3)C
Formula
C31 H41 F N4 O7
Name
4-{2-(4-FLUORO-BENZYL)-6-METHYL-5-[(5-METHYL-ISOXAZOLE-3-CARBONYL)-AMINO]-4-OXO-HEPTANOYLAMINO}-5-(2-OXO-PYRROLIDIN-3-YL)-PENTANOIC ACID ETHYL ESTER;
RUPINTRIVIR, bound form
ChEMBL
DrugBank
ZINC
ZINC000014880293
PDB chain
3sjo Chain B Residue 501 [
Download ligand structure
] [
Download structure with residue number starting from 1
] [
View ligand structure
]
Receptor-Ligand Complex Structure
Global view
Local view
Structure summary
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
PDB
3sjo
Enterovirus 71 and Coxsackievirus A16 3C Proteases: Binding to Rupintrivir and Their Substrates and Anti-Hand, Foot, and Mouth Disease Virus Drug Design.
Resolution
1.702 Å
Binding residue
(original residue number in PDB)
R39 H40 E71 L125 L127 S128 K130 T142 K143 A144 C147 H161 I162 G163 G164 N165 F170
Binding residue
(residue number reindexed from 1)
R36 H37 E68 L122 L124 S125 K127 T139 K140 A141 C144 H158 I159 G160 G161 N162 F167
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H40 E71 G145 C147
Catalytic site (residue number reindexed from 1)
H37 E68 G142 C144
Enzyme Commision number
2.7.7.48
: RNA-directed RNA polymerase.
3.4.22.28
: picornain 3C.
3.4.22.29
: picornain 2A.
3.6.1.15
: nucleoside-triphosphate phosphatase.
Gene Ontology
Molecular Function
GO:0004197
cysteine-type endopeptidase activity
Biological Process
GO:0006508
proteolysis
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:3sjo
,
PDBe:3sjo
,
PDBj:3sjo
PDBsum
3sjo
PubMed
21795339
UniProt
E0WWC7
[
Back to BioLiP
]