PPIPT00734

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 V14-1
Peptide_Sequence PPPTPPRTPPP
Peptide_Length 11
Peptide_SMILES C[C@@H](O)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1)C(=O)N1CCC[C@H]1C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N1CCC[C@H]1C(=O)N1CCC[C@H]1C(=O)N1CCC[C@H]1C(=O)O)[C@@H](C)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 1153.35
Aliphatic_Index 0.00000
Aromaticity 0.00000
Average_Rotatable_Bonds 1.81818
Charge_at_pH_7 0.99798
Isoelectric_point 10.55000
Number_of_Hydrogen_Bond_Acceptors 15
Number_of_Hydrogen_Bond_Donors 10
Topological_Polar_Surface_Area 381.16000
X_logP_energy -3.76073
Interaction Information
Affinity KD=3.9 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