Structure of PDB 6r9u Chain A Binding Site BS01
Receptor Information
>6r9u Chain A (length=164) Species:
9606
(Homo sapiens) [
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GNPLVYLDVDANGKPLGRVVLELKADVVPKTAENFRALCTGEKGFGYKGS
TFHRVIPSFMCQAGDFTNHNGTGGKSIYGSRFPDENFTLKHVGPGVLSMA
NAGPNTNGSQFFICTIKTDWLDGKHVVFGHVIEGMDVVKKIESFGSKSGR
TSKKIVITDCGQLS
Ligand information
Ligand ID
JVQ
InChI
InChI=1S/C13H16N2O3/c1-2-15-7-9-5-11-12(18-8-17-11)6-10(9)14-4-3-13(15)16/h5-6,14H,2-4,7-8H2,1H3
InChIKey
LCKKANZPYFOBHG-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 2.0.7
CCN1Cc2cc3c(cc2NCCC1=O)OCO3
CACTVS 3.385
CCN1Cc2cc3OCOc3cc2NCCC1=O
Formula
C13 H16 N2 O3
Name
14-ethyl-4,6-dioxa-10,14-diazatricyclo[7.6.0.0^{3,7}]pentadeca-1(9),2,7-trien-13-one
ChEMBL
CHEMBL3438117
DrugBank
ZINC
ZINC000299851959
PDB chain
6r9u Chain A Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
6r9u
Discovery of novel Cyclophilin D inhibitors starting from three dimensional fragments with millimolar potencies.
Resolution
1.26 Å
Binding residue
(original residue number in PDB)
T115 G116 G117 S123 R124 A143 N144 T149 Q153
Binding residue
(residue number reindexed from 1)
T72 G73 G74 S80 R81 A100 N101 T106 Q110
Annotation score
1
Binding affinity
MOAD
: Kd=7.5mM
PDBbind-CN
: -logKd/Ki=2.12,Kd=7.5mM
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
View graph for
Biological Process
External links
PDB
RCSB:6r9u
,
PDBe:6r9u
,
PDBj:6r9u
PDBsum
6r9u
PubMed
31635932
UniProt
P30405
|PPIF_HUMAN Peptidyl-prolyl cis-trans isomerase F, mitochondrial (Gene Name=PPIF)
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