PPIRE19440

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 2
Peptide_Sequence DXFXKYCV
Peptide_Length 8
Peptide_SMILES CC(C)[C@H](NC(=O)[C@H](CS)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCCN)NC(=O)CNC(=O)[C@H](Cc1ccccc1)NC(=O)CNC(=O)[C@@H](N)CC(=O)O)C(=O)O
Chemical_Modification X2=2-2-dimethylcysteine; X4=D-Tpi
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 888.01
Aliphatic_Index 36.25000
Aromaticity 0.25000
Average_Rotatable_Bonds 3.37500
Charge_at_pH_7 -0.06469
Isoelectric_Point 6.15753
Hydrogen_Bond_Acceptors 13
Hydrogen_Bond_Donors 13
Topological_Polar_Surface_Area 350.57000
X_logP_energy -2.56480
Interaction Information
Affinity Ki=6.92 nM
Affinity_Assay Radioligand binding assay
PDB_ID None
Type Agonist
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