Structure of PDB 1xrr Chain A Binding Site BS02
Receptor Information
>1xrr Chain A (length=290) Species:
2303
(Thermoplasma acidophilum) [
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ECIENYAKVNGIYIYYKLCKAPEEKAKLMTMHGGPGMSHDYLLSLRDMTK
EGITVLFYDQFGCGRSEEPDQSKFTIDYGVEEAEALRSKLFGNEKVFLMG
SSYGGALALAYAVKYQDHLKGLIVSGGLSSVPLTVKEMNRLIDELPAKYR
DAIKKYGSSGSYENPEYQEAVNYFYHQHLLRSEDWPPEVLKSLEYAERRN
VYRIMNGPNEFTITGTIKDWDITDKISAIKIPTLITVGEYDQVTPNVARV
IHEKIAGSELHVFRDCSHLTMWEDREGYNKLLSDFILKHL
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
1xrr Chain A Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
1xrr
X-ray snapshots of peptide processing in mutants of tricorn-interacting factor F1 from Thermoplasma acidophilum
Resolution
2.4 Å
Binding residue
(original residue number in PDB)
Y205 N212
Binding residue
(residue number reindexed from 1)
Y202 N209
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
G37 S105 Y106 D244 H271
Catalytic site (residue number reindexed from 1)
G34 S102 Y103 D241 H268
Enzyme Commision number
3.4.11.5
: prolyl aminopeptidase.
Gene Ontology
Molecular Function
GO:0004177
aminopeptidase activity
GO:0008233
peptidase activity
Biological Process
GO:0006508
proteolysis
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:1xrr
,
PDBe:1xrr
,
PDBj:1xrr
PDBsum
1xrr
PubMed
15994304
UniProt
P96084
|PIP_THEAC Proline iminopeptidase (Gene Name=pip)
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