PPIPT00735

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 6
Peptide_Sequence PPPVPPPLLLLLLLL
Peptide_Length 15
Peptide_SMILES CC(C)C[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1)C(C)C)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 1605.12
Aliphatic_Index 227.33333
Aromaticity 0.00000
Average_Rotatable_Bonds 2.73333
Charge_at_pH_7 -0.00202
Isoelectric_point 6.10000
Number_of_Hydrogen_Bond_Acceptors 16
Number_of_Hydrogen_Bond_Donors 11
Topological_Polar_Surface_Area 412.78000
X_logP_energy 4.16600
Interaction Information
Affinity KD=11 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