dbACP: A Comprehensive Database of Anti-Cancer Peptides

dbacp06525

General Description

Peptide name : Viscotoxin B

Source/Organism : European mistletoe

Linear/Cyclic : Not found

Chirality : L

Sequence Information

Sequence : KSCCPNTTGRNIYNTCRLGGGSRERCASLSGCKIISASTCPSDYPK

Peptide length: 46

C-terminal modification: Not found

N-terminal modification : Free

Non-natural peptide information: None

Activity Information

Assay type : Not specified

Assay time : Not found

Activity : Not found

Cell line : Not found

Cancer type : Colorectal cancer

Other activity : Not found

Physicochemical Properties

Amino acid composition bar chart :

Molecular mass : 4857.4906 Dalton

Aliphatic index : 0.467

Instability index : 46.5174

Hydrophobicity (GRAVY) : -0.55

Isoelectric point : 9.1252

Charge (pH 7) : 4.6996

Aromaticity : 0.043

Molar extinction coefficient (cysteine, cystine): (2980, 3355)

Hydrophobic/hydrophilic ratio : 0.84

hydrophobic moment : 0.376

Missing amino acid : W,H,Q,M,F,V

Most occurring amino acid : S

Most occurring amino acid frequency : 7

Least occurring amino acid : E

Least occurring amino acid frequency : 1

Structural Information

3D structure :

Secondary structure fraction (Helix, Turn, Sheet): (0.1, 0.4, 0.2)

SMILES Notation: CC[C@H](C)[C@H](NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CS)NC(=O)[C@H](CS)NC(=O)[C@H](CO)NC(=O)[C@@H](N)CCCCN)[C@@H](C)O)[C@@H](C)O)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@H](C(=O)N[C@@H](CS)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CC(C)C)C(=O)NCC(=O)NCC(=O)NCC(=O)N[C@@H](CO)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CS)C(=O)N[C@@H](C)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CO)C(=O)NCC(=O)N[C@@H](CS)C(=O)N[C@@H](CCCCN)C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@@H](CO)C(=O)N[C@@H](C)C(=O)N[C@@H](CO)C(=O)N[C@H](C(=O)N[C@@H](CS)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCCCN)C(=O)O)[C@@H](C)O)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O

Secondary Structure :

Method Prediction
GOR TTTCTTTCCCEEEEEEETTTCCEEEHTTTTTCEEEEETCCCTCCCT
Chou-Fasman (CF) CCCCCEECEEEEEEEECCCCCHHHHHHCCCEEEEEEECCCCCCCCC
Neural Network (NN) CCCCCCCCCCEEEEEEECCCCCCCEEECCCCCEEEECCCCCCCCCC
Joint/Consensus CCCCCCCCCCEEEEEEECCCCCCCCCCCCCCCEEEEECCCCCCCCC

Molecular Descriptors and ADMET Properties

Molecular Descriptors: Click here to download

ADMET Properties: Click here to download

Cross Referencing databases

Pubmed Id : 1710983

Uniprot : Not available

PDB : 1JMP

CancerPPD : Not available

ApIAPDB : Not available

CancerPPD2 ID : Not available

Reference

1 : Schrader G and Apel K. Isolation and characterization of cDNAs encoding viscotoxins of mistletoe (Viscum album). Eur J Biochem. 1991; 198:549-53. doi: 10.1111/j.1432-1033.1991.tb16049.x

Literature

Paper title : Isolation and characterization of cDNAs encoding viscotoxins of mistletoe (Viscum album).

Doi : https://doi.org/10.1111/j.1432-1033.1991.tb16049.x

Abstract : Viscotoxins have been isolated from leaf homogenates of European mistletoe (Viscum album L.) and purified to apparent homogeneity. Antisera raised against these polypeptides were used to screen a cDNA expression library in lambda gt11. Two positive clones have been isolated, one encoding a full-length preprotein of viscotoxin A3 and the other encoding the precursor of viscotoxin B. Besides the viscotoxin domain the precursor contained a signal sequence and an acidic polypeptide domain. Similar higher molecular mass precursor proteins have been described for thionins of leaves and seeds of barley. Even though the acidic part of the viscotoxin precursor is much shorter than the corresponding domain of the precursors of the leaf and seed thionins of barley, both the negative charge and the number and the relative position of cysteine residues have been conserved within the acidic domain. This result is consistent with our proposal that the acidic domain of the thionin precursor may play an important role in keeping the thionin inactive within the plant cell.