Structure of PDB 2igv Chain A Binding Site BS02
Receptor Information
>2igv Chain A (length=172) Species:
6239
(Caenorhabditis elegans) [
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MSRSKVFFDITIGGKASGRIVMELYDDVVPKTAGNFRALCTGENGIGKSG
KPLHFKGSKFHRIIPNFMIQGGDFTRGNGTGGESIYGEKFPDENFKEKHT
GPGVLSMANAGPNTNGSQFFLCTVKTEWLDGKHVVFGRVVEGLDVVKAVE
SNGSQSGKPVKDCMIADCGQLK
Ligand information
Ligand ID
PRO
InChI
InChI=1S/C5H9NO2/c7-5(8)4-2-1-3-6-4/h4,6H,1-3H2,(H,7,8)/t4-/m0/s1
InChIKey
ONIBWKKTOPOVIA-BYPYZUCNSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
C1C[C@H](NC1)C(=O)O
CACTVS 3.341
OC(=O)[C@@H]1CCCN1
CACTVS 3.341
OC(=O)[CH]1CCCN1
OpenEye OEToolkits 1.5.0
C1CC(NC1)C(=O)O
ACDLabs 10.04
O=C(O)C1NCCC1
Formula
C5 H9 N O2
Name
PROLINE
ChEMBL
CHEMBL54922
DrugBank
DB00172
ZINC
ZINC000000895360
PDB chain
2igv Chain A Residue 202 [
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Receptor-Ligand Complex Structure
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PDB
2igv
Experimental Determination of van der Waals Energies in a Biological System.
Resolution
1.67 Å
Binding residue
(original residue number in PDB)
R62 Q70 F120 H133
Binding residue
(residue number reindexed from 1)
R62 Q70 F120 H133
Annotation score
1
Binding affinity
PDBbind-CN
: -logKd/Ki=2.23,Kd=5.9mM
Enzymatic activity
Catalytic site (original residue number in PDB)
R62 F67 Q70 N109 F120 L129 H133
Catalytic site (residue number reindexed from 1)
R62 F67 Q70 N109 F120 L129 H133
Enzyme Commision number
5.2.1.8
: peptidylprolyl isomerase.
Gene Ontology
Molecular Function
GO:0003755
peptidyl-prolyl cis-trans isomerase activity
GO:0005515
protein binding
GO:0016018
cyclosporin A binding
Biological Process
GO:0000413
protein peptidyl-prolyl isomerization
GO:0006457
protein folding
Cellular Component
GO:0005634
nucleus
GO:0005737
cytoplasm
GO:0005739
mitochondrion
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2igv
,
PDBe:2igv
,
PDBj:2igv
PDBsum
2igv
PubMed
17654646
UniProt
P52011
|CYP3_CAEEL Peptidyl-prolyl cis-trans isomerase 3 (Gene Name=cyn-3)
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