PPIPT00731

Target Protein Information
Protein_Name Beta-2-microglobulin
Protein_Sequence MSRSVALAVLALLSLSGLEAIQRTPKIQVYSRHPAENGKSNFLNCYVSGFHPSDIEVDLLKNGERIEKVEHSDLSFSKDWSFYLLYYTEFTPTEKDEYACRVNHVTLSQPKIVKWDRDM
Organism_Source Homo sapiens
Functional_Classification MHC class I light chain
Cellular_Localization Extracellular
Gene_Names B2M
UniProt_ID P61769
Protein-Protein Interaction Networks
Peptide Basic Information
Peptide_Name V1
Peptide_Sequence PPPPPPPPPPPLHHHHHHCW
Peptide_Length 20
Peptide_SMILES CC(C)C[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@@H](CS)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)O
Chemical_Modification None
Cyclization_Method None
Linear/Cyclic Cyclic
N-terminal_Modification Free
C-terminal_Modification Free
Amino_Acid_Distribution
Peptide Physicochemical
Molecular_Weight 2311.66
Aliphatic_Index 19.50000
Aromaticity 0.05000
Average_Rotatable_Bonds 2.30000
Charge_at_pH_7 0.48146
Isoelectric_point 7.78631
Number_of_Hydrogen_Bond_Acceptors 28
Number_of_Hydrogen_Bond_Donors 19
Topological_Polar_Surface_Area 702.20000
X_logP_energy -2.40910
Interaction Information
Affinity KD=1.07 nM
Affinity_Assay ELISA
PDB_ID None
Type Agonist
Structure
Reference Information
Document_Type Patent
Title NOVEL PEPTIDES AND USES THEREOF
Release_Year 2013
Patent_ID US20130331297A1