Structure of PDB 3rcf Chain A Binding Site BS01
Receptor Information
>3rcf Chain A (length=164) Species:
9606
(Homo sapiens) [
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GNPLVYLDVDANGKPLGRVVLELKADVVPKTAENFRALCTGEKGFGYKGS
TFHRVIPSFMCQAGDFTNHNGTGGKSIYGSRFPDENFTLKHVGPGVLSMA
NAGPNTNGSQFFICTIKTDWLDGKHVVFGHVIEGMDVVKKIESFGSKSGR
TSKKIVITDCGQLS
Ligand information
Ligand ID
BS4
InChI
InChI=1S/C13H12N2O3S/c14-11-6-8-12(9-7-11)19(17,18)15-13(16)10-4-2-1-3-5-10/h1-9H,14H2,(H,15,16)
InChIKey
PBCZLFBEBARBBI-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.370
Nc1ccc(cc1)[S](=O)(=O)NC(=O)c2ccccc2
OpenEye OEToolkits 1.7.0
c1ccc(cc1)C(=O)NS(=O)(=O)c2ccc(cc2)N
ACDLabs 12.01
O=S(=O)(NC(=O)c1ccccc1)c2ccc(N)cc2
Formula
C13 H12 N2 O3 S
Name
N-[(4-aminophenyl)sulfonyl]benzamide
ChEMBL
CHEMBL1243
DrugBank
DB09355
ZINC
ZINC000005421253
PDB chain
3rcf Chain A Residue 1 [
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Receptor-Ligand Complex Structure
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PDB
3rcf
Fragment-based discovery of a new family of non-peptidic small-molecule cyclophilin inhibitors with potent antiviral activities.
Resolution
1.15 Å
Binding residue
(original residue number in PDB)
F102 F155 W163
Binding residue
(residue number reindexed from 1)
F59 F112 W120
Annotation score
1
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
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Molecular Function
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Biological Process
External links
PDB
RCSB:3rcf
,
PDBe:3rcf
,
PDBj:3rcf
PDBsum
3rcf
PubMed
27652979
UniProt
P30405
|PPIF_HUMAN Peptidyl-prolyl cis-trans isomerase F, mitochondrial (Gene Name=PPIF)
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