dbACP: A Comprehensive Database of Anti-Cancer Peptides

dbacp07430

General Description

Peptide name : GP-3

Source/Organism : Ginseng Leaf Peptide

Linear/Cyclic : Linear

Chirality : L

Sequence Information

Sequence : FSHTYV

Peptide length: 6

C-terminal modification: Linear

N-terminal modification : Amidation

Non-natural peptide information:

Activity Information

Assay type : MTT assay

Assay time : 48-h

Activity : IC50 = 162 ± 17.1 µM

Cell line : CaCo-2

Cancer type : Colon Cancer

Other activity : Anticancer

Physicochemical Properties

Amino acid composition bar chart :

Molecular mass : 752.8138 Dalton

Aliphatic index : 0.483

Instability index : -4.2333

Hydrophobicity (GRAVY) : 0.1667

Isoelectric point : 6.7402

Charge (pH 7) : -0.1537

Aromaticity : 33.33

Molar extinction coefficient (cysteine, cystine): (0, 0)

Hydrophobic/hydrophilic ratio : 0.5

hydrophobic moment : 0.2304

Missing amino acid : A,C,D,E,G,I,K,L,M,N,P,Q,R,W

Most occurring amino acid : F

Most occurring amino acid frequency : 1

Least occurring amino acid : F

Least occurring amino acid frequency : 1

Structural Information

3D structure :

Secondary structure fraction (Helix, Turn, Sheet): (0, 16., 66.)

SMILES Notation: CC(C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc1ccccc1)[C@@H](C)O)C(=O)O

Secondary Structure :

Method Prediction
GOR EEEEEE
Chou-Fasman (CF) EEECCC
Neural Network (NN) CCCCEE
Joint/Consensus EEEEEE

Molecular Descriptors and ADMET Properties

Molecular Descriptors: Click here to download

ADMET Properties: Click here to download

Cross Referencing databases

Pubmed Id : 33462944.0

Uniprot : Not available

PDB : Not available

CancerPPD : Not available

ApIAPDB : Not available

CancerPPD2 ID: 6773

Reference

1 : Liu Z, et al. Anti-colon cancer activity tracking isolation of peptide from ginseng leaves and potential mechanisms evaluation in vitro and in vivo. J Pept Sci. 2021; 27:e3297. doi: 10.1002/psc.3297

Literature

Paper title : Anti-colon cancer activity tracking isolation of peptide from ginseng leaves and potential mechanisms evaluation in vitro and in vivo.

Doi : https://doi.org/10.1002/psc.3297

Abstract : The ginseng has been used for over hundred years, in the belief of promoting longevity. However, the anticancer activity of ginseng leaf peptide (GP) has been never explored. In current study, we isolated the GPs and explored the anti-colon cancer activity in vitro and in vivo. MTT results showed that the GP-1 (GP-1~FKEHGY) performed most antiproliferative activity against colon cancer CT-26 cells with an IC<sub>50</sub> of 86.4 ± 9.46 μM (48 h). Further study indicated that GP-1 activated the caspases, regulated the p53/murine double minute 2 (MDM2) state, and induced the CT-26 cells apoptosis in a mitochondrial pathway. Meanwhile, the GP-1 arrested the CT-26 cells in G0/G1 phase accompanied with cyclin expression regulation. In addition, GP-1 significantly suppressed the tumor growth and induced the tumor cells apoptosis in vivo. Notably, the GP-1 would be a potential anti-colon cancer candidate.