dbACP: A Comprehensive Database of Anti-Cancer Peptides

dbacp08052

General Description

Peptide name : Poca A

Source/Organism : Pombalia calceolaria

Linear/Cyclic : Cyclic

Chirality : L

Sequence Information

Sequence : GLPCAESCVFIPCTITAILGCSCRDRVCYD

Peptide length: 30

C-terminal modification: Cyclic

N-terminal modification : Cyclized

Non-natural peptide information:

Activity Information

Assay type : MTS assay

Assay time : 24-h

Activity : IC50 = 1.8 μM

Cell line : MDA-MB-231

Cancer type : Breast Cancer

Other activity : Antimicrobial,Cytotoxic

Physicochemical Properties

Amino acid composition bar chart :

Molecular mass : 3209.7811 Dalton

Aliphatic index : 0.91

Instability index : 58.4067

Hydrophobicity (GRAVY) : 0.77

Isoelectric point : 4.7806

Charge (pH 7) : -1.2921

Aromaticity : 6.666

Molar extinction coefficient (cysteine, cystine): (6, 3)

Hydrophobic/hydrophilic ratio : 2

hydrophobic moment : 0.1446

Missing amino acid : H,K,M,N,Q,W

Most occurring amino acid : C

Most occurring amino acid frequency : 6

Least occurring amino acid : E

Least occurring amino acid frequency : 1

Structural Information

3D structure :

Secondary structure fraction (Helix, Turn, Sheet): (16., 26., 36.)

SMILES Notation: CC[C@H](C)[C@H](NC(=O)[C@H](C)NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@H](CS)NC(=O)[C@@H]1CCCN1C(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)[C@H](CS)NC(=O)[C@H](CO)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CS)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(C)C)NC(=O)CN)C(C)C)[C@@H](C)CC)[C@@H](C)O)[C@@H](C)CC)[C@@H](C)O)C(=O)N[C@@H](CC(C)C)C(=O)NCC(=O)N[C@@H](CS)C(=O)N[C@@H](CO)C(=O)N[C@@H](CS)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@H](C(=O)N[C@@H](CS)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CC(=O)O)C(=O)O)C(C)C

Secondary Structure :

Method Prediction
GOR CCCTTTTEEECCCCECEEETCCTTTTTEET
Chou-Fasman (CF) CHHHHEEEEEEEEEEEEEECCCCEEEECCC
Neural Network (NN) CCCCCCCCCECCCCCEEEEECCCCCCCECC
Joint/Consensus CCCCCCCEEECCCCEEEEECCCCCCCCCCC

Molecular Descriptors and ADMET Properties

Molecular Descriptors: Click here to download

ADMET Properties: Click here to download

Cross Referencing databases

Pubmed Id : 29757646.0

Uniprot : Not available

PDB : Not available

CancerPPD : Not available

ApIAPDB : Not available

CancerPPD2 ID: 5972

Reference

1 : Pinto MEF, et al. Inhibition of Breast Cancer Cell Migration by Cyclotides Isolated from Pombalia calceolaria. J Nat Prod. 2018; 81:1203-1208. doi: 10.1021/acs.jnatprod.7b00969

Literature

Paper title : Inhibition of Breast Cancer Cell Migration by Cyclotides Isolated from Pombalia calceolaria.

Doi : https://doi.org/10.1021/acs.jnatprod.7b00969

Abstract : Two new bracelet cyclotides from roots of Pombalia calceolaria with potential anticancer activity have been characterized in this work. The cyclotides Poca A and B (1 and 2) and the previously known CyO4 (3) were de novo sequenced by MALDI-TOF/TOF mass spectrometry (MS). The MS2 spectra were examined and the amino acid sequences were determined. The purified peptides were tested for their cytotoxicity and effects on cell migration of MDA-MB-231, a triple-negative breast cancer cell line. The isolated cyclotides reduced the number of cancer cells by more than 80% at 20 μM, and the concentration-related cytotoxic responses were observed with IC<sub>50</sub> values of 1.8, 2.7, and 9.8 μM for Poca A (1), Poca B (2), and CyO4 (3), respectively. Additionally, the inhibition of cell migration (wound-healing assay) exhibited that CyO4 (3) presents an interesting activity profile, in being able to inhibit cell migration (50%) at a subtoxic concentration (2 μM). The distribution of these cyclotides in the roots was analyzed by MALDI imaging, demonstrating that all three compounds are present in the phloem and cortical parenchyma regions.