PPIRE19441

Target Protein Information
Protein_Name Urotensin-2 receptor
Protein_Sequence MALTPESPSSFPGLAATGSSVPEPPGGPNATLNSSWASPTEPSSLEDLVATGTIGTLLSAMGVVGVVGNAYTLVVTCRSLRAVASMYVYVVNLALADLLYLLSIPFIVATYVTKEWHFGDVGCRVLFGLDFLTMHASIFTLTVMSSERYAAVLRPLDTVQRPKGYRKLLALGTWLLALLLTLPVMLAMRLVRRGPKSLCLPAWGPRAHRAYLTLLFATSIAGPGLLIGLLYARLARAYRRSQRASFKRARRPGARALRLVLGIVLLFWACFLPFWLWQLLAQYHQAPLAPRTARIVNYLTTCLTYGNSCANPFLYTLLTRNYRDHLRGRVRGPGSGGGRGPVPSLQPRARFQRCSGRSLSSCSPQPTDSLVLAPAAPARPAPEGPRAPA
Organism_Source Homo sapiens
Functional_Classification G protein-coupled receptor
Cellular_Localization Plasma membrane
Gene_Names UTS2R
UniProt_ID Q9UKP6
Protein-Protein Interaction Networks
Peptide Basic Information
Peptide_Name Compound 3
Peptide_Sequence DXFWXYCV
Peptide_Length 8
Peptide_SMILES CC(C)[C@H](NC(=O)[C@H](CS)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)CNC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1ccccc1)NC(=O)CNC(=O)[C@@H](N)CC(=O)O)C(=O)O
Chemical_Modification X2=2-2-dimethylcysteine; X5=ornithine
Cyclization_Method Side chain-side chain cyclization; X2<-->C7; disulfide bond
Linear/Cyclic Cyclic
N-terminal_Modification Free
C-terminal_Modification Free
Amino_Acid_Distribution
Peptide Physicochemical
Molecular_Weight 946.04
Aliphatic_Index 36.25000
Aromaticity 0.37500
Average_Rotatable_Bonds 3.12500
Charge_at_pH_7 -1.06439
Isoelectric_Point 3.74997
Hydrogen_Bond_Acceptors 12
Hydrogen_Bond_Donors 13
Topological_Polar_Surface_Area 340.34000
X_logP_energy -0.96980
Interaction Information
Affinity Ki=24.5 nM
Affinity_Assay Radioligand binding assay
PDB_ID None
Type Antagonist
Structure
Reference Information
Document_Type Research Articles
Title New insight into the binding mode of peptides at urotensin-II receptor by Trp-constrained analogues of P5U and urantide
Release_Year 2013
PMID 23526702
DOI 10.1002/psc.2498