dbacp06577
General Description
Peptide name : Z44
Source/Organism : African clawed frog
Linear/Cyclic : Linear
Chirality : L
Sequence Information
Sequence : ALSKALSKALSKALSKALSKALSK
Peptide length: 24
C-terminal modification: Linear
N-terminal modification : Amidation
Non-natural peptide information: None
Activity Information
Assay type : Trypan blue assay
Assay time : 72h
Activity : IC50 : 80 µg/ml
Cell line : MLA
Cancer type : Leukemia cancer
Other activity : Anti-microbial activity
Physicochemical Properties
Amino acid composition bar chart :
Molecular mass : 2414.9259 Dalton
Aliphatic index : 1.225
Instability index : 9.5833
Hydrophobicity (GRAVY) : 0.225
Isoelectric point : 10.699
Charge (pH 7) : 5.7899
Aromaticity : 0
Molar extinction coefficient (cysteine, cystine): (0, 0)
Hydrophobic/hydrophilic ratio : 1
hydrophobic moment : -0.767
Missing amino acid : W,T,P,I,M,E,F,D,N,G,C,R,H,Q,Y,V
Most occurring amino acid : A
Most occurring amino acid frequency : 6
Least occurring amino acid : A
Least occurring amino acid frequency : 6
Structural Information
3D structure :
Secondary structure fraction (Helix, Turn, Sheet): (0.7, 0.2, 0.2)
SMILES Notation: CC(C)C[C@H](NC(=O)[C@H](C)N)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCCCN)C(=O)O
Secondary Structure :
| Method | Prediction |
|---|---|
| GOR | HHHHHHHHHHHHHHHHHHHHHHHH |
| Chou-Fasman (CF) | HHHHHHHHHHHHHHHHHHHHHCCC |
| Neural Network (NN) | HHHHHHHHHHHHHHHHHHHHHHCC |
| Joint/Consensus | HHHHHHHHHHHHHHHHHHHHHHCC |
Molecular Descriptors and ADMET Properties
Molecular Descriptors: Click here to download
ADMET Properties: Click here to download
Cross Referencing databases
Reference
1 : Cruciani RA, et al. Antibiotic magainins exert cytolytic activity against transformed cell lines through channel formation. Proc Natl Acad Sci U S A. 1991; 88:3792-6. doi: 10.1073/pnas.88.9.3792
2 : Huang CM, et al. Magainin analogs effective against pathogenic protozoa. Antimicrob Agents Chemother. 1990; 34:1824-6. doi: 10.1128/AAC.34.9.1824
Literature
Paper title : Antibiotic magainins exert cytolytic activity against transformed cell lines through channel formation.
Doi : https://doi.org/10.1073/pnas.88.9.3792
Abstract : Magainins are an ionophoric class of vertebrate peptides with antibiotic activity against various microorganisms. Here we show that magainin 2 and synthetic analogues can rapidly and irreversibly lyse hematopoietic tumor and solid tumor target cells with a relative cytotoxic potency that parallels their antibacterial efficacy and at concentrations that are relatively nontoxic to well-differentiated cells. The cytotoxicity is prevented by cell depolarization. Magainins represent a natural cytolytic agent in vertebrates and may provide another therapeutic strategy for certain tumors.
Paper title : Magainin analogs effective against pathogenic protozoa.
Doi : https://doi.org/10.1128/AAC.34.9.1824
Abstract : The in vitro activities of magainin analogs against Blastocystis hominis, Entamoeba histolytica, and Trypanosoma cruzi were assessed by protozoan morphological integrity and motility. The antiprotozoan activities in descending order were magainin B greater than G greater than H, the same order as the alpha-helix contents of the analogs. Magainin B and G were effective against B. hominis, T. cruzi, and E. histolytica.