Structure of PDB 4j58 Chain A Binding Site BS01
Receptor Information
>4j58 Chain A (length=164) Species:
9606
(Homo sapiens) [
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GNPLVYLDVDANGKPLGRVVLELKADVVPKTAENFRALCTGEKGFGYKGS
TFHRVIPSFMCQAGDFTNHNGTGGKSIYGSRFPDENFTLKHVGPGVLSMA
NAGPNTNGSQFFICTIKTDWLDGKHVVFGHVIEGMDVVKKIESFGSKSGR
TSKKIVITDCGQLS
Ligand information
Ligand ID
53Z
InChI
InChI=1S/C14H20N4O2/c15-12-5-3-11(4-6-12)9-16-14(20)17-10-13(19)18-7-1-2-8-18/h3-6H,1-2,7-10,15H2,(H2,16,17,20)
InChIKey
QDOWQYVYSCTSGP-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.370
Nc1ccc(CNC(=O)NCC(=O)N2CCCC2)cc1
ACDLabs 12.01
O=C(N1CCCC1)CNC(=O)NCc2ccc(N)cc2
OpenEye OEToolkits 1.7.6
c1cc(ccc1CNC(=O)NCC(=O)N2CCCC2)N
Formula
C14 H20 N4 O2
Name
1-(4-aminobenzyl)-3-[2-oxo-2-(pyrrolidin-1-yl)ethyl]urea
ChEMBL
CHEMBL3797905
DrugBank
ZINC
ZINC000098208504
PDB chain
4j58 Chain A Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
4j58
Fragment-based discovery of a new family of non-peptidic small-molecule cyclophilin inhibitors with potent antiviral activities.
Resolution
1.28 Å
Binding residue
(original residue number in PDB)
F102 M103 Q105 R124 A143 N144 Q153 F155 H168
Binding residue
(residue number reindexed from 1)
F59 M60 Q62 R81 A100 N101 Q110 F112 H125
Annotation score
1
Binding affinity
PDBbind-CN
: -logKd/Ki=3.30,IC50>500uM
Enzymatic activity
Catalytic site (original residue number in PDB)
R97 F102 Q105 N144 F155 L164 H168
Catalytic site (residue number reindexed from 1)
R54 F59 Q62 N101 F112 L121 H125
Enzyme Commision number
5.2.1.8
: peptidylprolyl isomerase.
Gene Ontology
Molecular Function
GO:0003755
peptidyl-prolyl cis-trans isomerase activity
Biological Process
GO:0000413
protein peptidyl-prolyl isomerization
GO:0006457
protein folding
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:4j58
,
PDBe:4j58
,
PDBj:4j58
PDBsum
4j58
PubMed
27652979
UniProt
P30405
|PPIF_HUMAN Peptidyl-prolyl cis-trans isomerase F, mitochondrial (Gene Name=PPIF)
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