PPIRE04367

Target Protein Information
Protein_Name Calpain-2 catalytic subunit
Protein_Sequence MAGIAMKLAKDREAAEGLGSHERAIKYLNQDYETLRNECLEAGALFQDPSFPALPSSLGFKELGPYSSKTRGIEWKRPTEICADPQFIIGGATRTDICQGALGDCWLLAAIASLTLNEEILARVVPLDQSFQENYAGIFHFQFWQYGEWVEVVVDDRLPTKDGELLFVHSAEGSEFWSALLEKAYAKINGCYEALSGGATTEGFEDFTGGIAEWYELRKPPPNLFKIIQKALEKGSLLGCSIDITSAADSEAVTYQKLVKGHAYSVTGAEEVESSGSLQKLIRIRNPWGQVEWTGKWNDNCPSWNTVDPEVRANLTERQEDGEFWMSFSDFLRHYSRLEICNLTPDTLTCDSYKKWKLTKMDGNWRRGSTAGGCRNYPNTFWMNPQYLIKLEEEDEDDEDGERGCTFLVGLIQKHRRRQRKMGEDMHTIGFGIYEVPEELTGQTNIHLSKNFFLTTRARERSDTFINLREVLNRFKLPPGEYVLVPSTFEPHKNGDFCIRVFSEKKADYQTVDDEIEANIEEIEANEEDIGDGFRRLFAQLAGEDAEISAFELQTILRRVLAKREDIKSDGFSIETCKIMVDMLDEDGSGKLGLKEFYILWTKIQKYQKIYREIDVDRSGTMNSYEMRKALEEAGFKLPCQLHQVIVARFADDELIIDFDNFVRCLVRLEILFKIFKQLDPENTGTIQLDLISWLSFSVL
Organism_Source Rattus norvegicus
Functional_Classification cysteine proteases
Cellular_Localization Cytoplasm
Gene_Names Capn2
UniProt_ID Q07009
Protein-Protein Interaction Networks
Peptide Basic Information
Peptide_Name Leupeptin
Peptide_Sequence LLR
Peptide_Length 3
Peptide_SMILES CC(C)C[C@H](NC(=O)[C@@H](N)CC(C)C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)O
Chemical_Modification None
Cyclization_Method None
Linear/Cyclic Linear
N-terminal_Modification Acetyl
C-terminal_Modification aldehyde
Amino_Acid_Distribution
Peptide Physicochemical
Molecular_Weight 400.52
Aliphatic_Index 260.00000
Aromaticity 0.00000
Average_Rotatable_Bonds 4.33333
Charge_at_pH_7 0.99798
Isoelectric_Point 10.55000
Number_of_Hydrogen_Bond_Acceptors 5
Number_of_Hydrogen_Bond_Donors 7
Topological_Polar_Surface_Area 183.42000
X_logP_energy -0.27663
Interaction Information
Affinity IC50=3 mM
Affinity_Assay Enzyme Inhibition Kinetics
PDB_ID 1TL9
Type Inhibitor
Structure
Reference Information
Document_Type Research Articles
Title Crystal structures of calpain-E64 and -leupeptin inhibitor complexes reveal mobile loops gating the active site.
Release_Year 2004
PMID 15491615
DOI 10.1016/j.jmb.2004.09.016