PPIPT00733

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 V16-1
Peptide_Sequence PPPPPPPPPHHHHHH
Peptide_Length 15
Peptide_SMILES O=C(O)[C@H](Cc1c[nH]cn1)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@H](Cc1c[nH]cn1)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]1CCCN1
Chemical_Modification None
Cyclization_Method None
Linear/Cyclic Cyclic
N-terminal_Modification Free
C-terminal_Modification Free
Amino_Acid_Distribution
Peptide Physicochemical
Molecular_Weight 1714.91
Aliphatic_Index 0.00000
Aromaticity 0.00000
Average_Rotatable_Bonds 2.20000
Charge_at_pH_7 0.54344
Isoelectric_point 7.97858
Number_of_Hydrogen_Bond_Acceptors 22
Number_of_Hydrogen_Bond_Donors 14
Topological_Polar_Surface_Area 558.49000
X_logP_energy -3.54540
Interaction Information
Affinity KD=0.74 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