Detailed Peptide Information


This page shows detailed information of individual peptides present in PlantPepDB database. The page is majorly divided into 3 sections. The first sections contains primary information like peptide activity, source, sequence, etc. In the secondary information section user can access the tertiary structure as well as the physico-chemical properties by clicking the respective links. Further there is also link of the source database and research article from which the peptide data is retrieved. Download the information by clicking



Primary Information
PPepDB IDPPepDB_2125
Peptide NameCyclotide chassatide C7, Uncyclotide ChaC7
PMID(s)22467870
Plant Source (Scientific Name)Chassalia chartacea
Plant Source (Common Name)--NA--
Plant FamilyRubiaceae
Peptide FamilyCyclotide
Peptide FunctionAntibacterial, Anticancer, Cytotoxic, Hemolytic
Peptide Function DescriptionTarget site: lipid bilayer; shows 50% Hemolysis against Human erythrocytes at 11.6 µM ; Shown to possess antimicrobial, cytotoxic, and hemolytic activities and the oxidation of two Met residue causes loss of bioactivities, strengthening the importance of the hydrophobic patch for membrane interaction.
Activity AgainstEscherichia coli (MIC: 6.4 µM), Staphylococcus aureus (MIC: >80 µM), Staphylococcus epidermidis (MIC: >80 µM), Human cervical carcinoma HeLa (IC50: 1.2 µM)
IC50 value1.2 µM
SequenceIPCGESCVWIPCITAIAGCSCKNKVCYT
Sequence Length28
ValidationExperimental evidence at protein level
Average Molecular Weight (Da)2963.57
Monoisotopic Molecular Weight (Da)2961.34
Isoelectric Point (pI)7.77
Method / ExtractionPcR, MS


Secondary Information
Tertiary Structure and DSSP ReportClick to View Structure
Physico-Chemical Properties of peptidesClick to View Physico-Chemical Details of PPepDB_2125


External links (Uniprot, PDB and Source Information Database)
UniprotI0B6F4
NCBI--NA--
EMBL--NA--
Link to Source DatabasesDBAASP_4286, Cybase_866, CAMPSQ3676, APD_01989
Addtional InformationSynthesis Type : Ribosomal; The compound, however, is also quite toxic (50% hemolysis of human type A blood cells: HL50 11.6 uM). TOXIC TO HeLa cells (IC50 1.2 uM). This is an acyclic peptide. Compared to cyclotides, the C-terminal D/N critical for cyclization is lacking. Surprisingly, this linear form is not only more abundant but also more active than the circular peptides identified in the same plant. APD updated 4/2015.