ProForma 2.0
validated simple linear
DVGRG
DVGRG
Aliases: DVGRG
Normalized sequence
DVGRG
5 amino acids
Release PepDiana-V1-20260620
12
Activity records
1
Source papers
11
Positive
1
Negative / threshold
Versioned scientific descriptors
No separate physicochemical property was reported in the primary-literature identity record. PepDiana release values are shown as computed properties.
Molecular weight
502.522 Da
Molecular formula
C19H34N8O8
Theoretical pI
5.8364
Net charge at pH 7
-0.2388
GRAVY
-0.92
Instability index
-25.96
Aromaticity
0
Topological polar surface area
278.92 Ų
cLogP
-4.0057
Hydrogen-bond donors
10
Hydrogen-bond acceptors
8
Rotatable bonds
16
Method: PepDiana sequence/structure descriptor pipeline
Tool: Biopython+RDKit · Biopython 1.85; RDKit 2024.09.6
Calculated: 2026-06-20T11:01:38.358971+00:00
Assumptions: ph=7; termini=free N-terminus and free C-terminus for simple linear peptides; stereochemistry=standard L-amino acids; smiles_length_limit=200
ProForma 2.0
validated simple linear
DVGRG
HELM 2.0
validated simple linear
PEPTIDE1{D.V.G.R.G}$$$$V2.0
Canonical SMILES
validated
CC(C)C(NC(=O)C(N)CC(=O)O)C(=O)NCC(=O)NC(CCCNC(=N)N)C(=O)NCC(=O)O
Isomeric SMILES
validated
CC(C)[C@H](NC(=O)[C@@H](N)CC(=O)O)C(=O)NCC(=O)N[C@@H](CCCNC(=N)N)C(=O)NCC(=O)O
Paper-level observations
In the CSE-induced injury model (cell viability: 50.89 ± 2.68% vs. control), pretreatment with tuna peptides S1, S5, S6, and S7 significantly restored viability... (Figure 1B).
pretreatment with S1, S5, S6, and S7 significantly reduced ROS levels in a concentration-dependent manner. (Figure 2A,B)
In comparison to the model group, all tuna peptide treatment groups at a concentration of 200 μM demonstrated enhanced cellular antioxidant capacity, characterized by increased CAT and SOD activities, elevated GSH levels, and reduced MDA levels (p < 0.001). (Figure 3)
treatment with tuna peptides S1, S5, S6, and S7, resulted in a significant reduction in green fluorescence and a notable increase in red fluorescence (p < 0.001), suggesting that these peptides effectively restored MMP and inhibited CSE-induced apoptosis. (Figure 6)
pretreatment with 200 μM tuna peptides S1, S5, S6, and S7 significantly increased Nrf2 mRNA expression and decreased Keap1 mRNA expression in MLE-12 cells compared to the model group. (Figure 8)
At a concentration of 200 μM, the nuclear Nrf2 levels in the S1 and S6 peptide-treated groups showed significant higher compared to the model group (p < 0.05). (Figure 9)
At a concentration of 200 μM, the tuna peptide treatment groups (S1, S6, and S7) showed a significant reduction in these inflammatory markers compared to the model group. (Figure 4)
treatment with 200 µM tuna peptides S1, S5, S6, and S7 significantly reduced p65 mRNA expression and increased IκBα mRNA expression (p < 0.001). (Figure 11A,B)
At a concentration of 200 µM, the apoptosis rate in the peptide-treated groups was significantly lower than that in the model group (p < 0.001). (Figure 5)
pretreatment with 200 μM tuna peptides S1, S5, S6, and S7 significantly increased the Bcl-2/Bax mRNA expression ratio compared to the model group, with highly significant differences (p < 0.001). (Figure 11C)
To assess the safety of tuna peptides, cells were treated with 200 µM of peptide S1–8, which maintained viability above 90%, comparable to the blank control (100.00 ± 18.18%) and non-toxic relative to the positive control (134.31 ± 10.75%) (Figure 1B).
tuna peptides S1, S5, S6, and S7 significantly promote the migration of MLE-12 cells and accelerate wound closure in a concentration-dependent manner. (Figure 7)
Citation and release provenance
Cite this identity as PepDiana record PEPDIA-PLP-000492, release PepDiana-V1-20260620. Experimental observations retain their paper, mention, and activity-record identifiers.
Record updated: 2026-06-22T07:14:26.229247+00:00