PPIRE15658

Target Protein Information
Protein_Name Putative histone H1.9
Protein_Sequence MLHASTIWHLRSTPPRRKQWGHCDPHRILVASEVTTEITSPTPAPRAQVCGGQPWVTVLDPLSGHTGREAERHFATVSISAVELKYCHGWRPAGQRVPSKTATGQRTCAKPCQKPSTSKVILRAVADKGTCKYVSLATLKKAVSTTGYDMARNAYHFKRVLKGLVDKGSAGSFTLGKKQASKSKLKVKRQRQQRWRSGQRPFGQHRSLLGSKQGHKRLIKGVRRVAKCHCN
Organism_Source Homo sapiens
Functional_Classification histones
Cellular_Localization Nucleus
Gene_Names H1-9P
UniProt_ID P60008
Protein-Protein Interaction Networks
Peptide Basic Information
Peptide_Name G4 linker-assisted heterodimer peptide
Peptide_Sequence CQRPPRGGGGHSPQAY
Peptide_Length 16
Peptide_SMILES C[C@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CO)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)CNC(=O)CNC(=O)CNC(=O)CNC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](N)CS)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)O
Chemical_Modification None
Cyclization_Method None
Linear/Cyclic Linear
N-terminal_Modification Free
C-terminal_Modification Free
Amino_Acid_Distribution
Peptide Physicochemical
Molecular_Weight 1667.82
Aliphatic_Index 6.25000
Aromaticity 0.06250
Average_Rotatable_Bonds 3.00000
Charge_at_pH_7 2.02606
Isoelectric_Point 9.50122
Number_of_Hydrogen_Bond_Acceptors 25
Number_of_Hydrogen_Bond_Donors 26
Topological_Polar_Surface_Area 752.57000
X_logP_energy -11.37186
Interaction Information
Affinity KD=16 mM
Affinity_Assay Surface Plasmon Resonance
PDB_ID None
Type Affinity ligand
Structure
Reference Information
Document_Type Research Articles
Title Conversion of Low-Affinity Peptides to High-Affinity Peptide Binders by Using a b-Hairpin Scaffold-Assisted Approach
Release_Year 2014
PMID 25371172
DOI 10.1002/cbic.201402450