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_2123
Peptide NameHedyotide B1
PMID(s)21979955, 21776968
Plant Source (Scientific Name)Leptopetalum biflorum, Hedyotis biflora
Plant Source (Common Name)Damanpapra
Plant FamilyRubiaceae
Peptide FamilyCyclotide
Peptide FunctionAntimicrobial, Enzymatic-degradation
Peptide Function DescriptionTarget site- Lipid Bilayer; Shown to possess antimicrobial and enzymatic degradation activity.
Activity AgainstStaphylococcus aureus (MIC: >80 µM), Staphylococcus epidermidis (MIC: >80 µM), Escherichia coli (MIC: 3.4 µM), Streptococcus salivarius (MIC: 5.9 µM)
IC50 value--NA--
SequenceGTRCGETCFVLPCWSAKFGCYCQKGFCYRN
Sequence Length30
ValidationExperimental evidence at transcript level
Average Molecular Weight (Da)3429
Monoisotopic Molecular Weight (Da)3426.47
Isoelectric Point (pI)8.66
Method / ExtractionMS, PcR


Secondary Information
Tertiary Structure and DSSP ReportClick to View Structure
Physico-Chemical Properties of peptidesClick to View Physico-Chemical Details of PPepDB_2123


External links (Uniprot, PDB and Source Information Database)
UniprotG9I0X2
NCBI365824243
EMBL--NA--
Link to Source DatabasesDBAASP_4696, Cybase_613, CAMPSQ3621, APD_01916
Addtional InformationSynthesis Type: Ribosomal; Hedyotide B1 is active against E. coli and S. salivarius. However, hedyotide B2 was found to be inactive against the bacteria tested under the conditions. Its exact functional roles remain to be elucidated. The authors suggested the name "uncyclotides" in this article for uncyclized cyclotides.