PPIRE18081

Target Protein Information
Protein_Name Cysteine-rich protein 1
Protein_Sequence MPKCPKCNKEVYFAERVTSLGKDWHRPCLKCEKCGKTLTSGGHAEHEGKPYCNHPCYAAMFGPKGFGRGGAESHTFK
Organism_Source Homo sapiens
Functional_Classification LIM double zinc finger proteins
Cellular_Localization Cytoplasm
Gene_Names CRIP1
UniProt_ID P50238
Protein-Protein Interaction Networks
Peptide Basic Information
Peptide_Name B5
Peptide_Sequence CYDPIWRTCGGGSK
Peptide_Length 14
Peptide_SMILES CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(=O)O)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](N)CS)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](CS)C(=O)NCC(=O)NCC(=O)NCC(=O)N[C@@H](CO)C(=O)N[C@@H](CCCCN)C(=O)O)[C@@H](C)O
Chemical_Modification None
Cyclization_Method side chain-side chain cyclization; C1<-->C9; disulfide bond
Linear/Cyclic Cyclic
N-terminal_Modification Free
C-terminal_Modification Amide
Amino_Acid_Distribution
Peptide Physicochemical
Molecular_Weight 1542.75
Aliphatic_Index 27.85714
Aromaticity 0.14286
Average_Rotatable_Bonds 3.28571
Charge_at_pH_7 0.87333
Isoelectric_Point 8.22116
Hydrogen_Bond_Acceptors 23
Hydrogen_Bond_Donors 25
Topological_Polar_Surface_Area 634.53000
X_logP_energy -7.08083
Interaction Information
Affinity KD=62.5 uM
Affinity_Assay fluorescence-based saturation binding assay
PDB_ID None
Type Affinity ligand
Structure
Reference Information
Document_Type Research Articles
Title Identification and Rational Redesign of Peptide Ligands to CRIP1 A Novel Biomarker for Cancers
Release_Year 2008
PMID 18670594
DOI 10.1371/journal.pcbi.1000138