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PEPDIA-INT-068532

Silver

Unnamed peptide

65

Quality

4

Source DBs

6

Activities

4

Source refs

2

Literature

0

Patents

Integrated record

Sequence and molecular profile

VTN
Indexed sequence3 aa
1VTN

Length

3

Molecular weight

332.36 Da

Formula

C13H24N4O6

Structure type

Linear

Synthesis

Synthetic

Chirality

-

Family

-

Gene

-

Residue composition

V
1
T
1
N
1

Physicochemical profile

Hydrophobic1

Membrane affinity proxy

Polar2

Solubility proxy

Charged0

Net charge proxy +0

Aromatic0

Binding interaction proxy

Versioned scientific descriptors

Physicochemical properties and standard representations

calculated sequence and structure

Reported properties

Legacy compatibility fields are materialized from the versioned PepDiana computed release; no separate source-reported property is available.

Computed properties

physchem-20260620

Molecular weight

332.3528 Da

Molecular formula

C13H24N4O6

Theoretical pI

5.495

Net charge at pH 7

-0.266

GRAVY

0

Instability index

-71.7333

Aromaticity

0

Topological polar surface area

184.84 Ų

cLogP

-2.7199

Hydrogen-bond donors

6

Hydrogen-bond acceptors

6

Rotatable bonds

9

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

Sequence representations

representations-20260620 · RDKit 2024.09.6

ProForma 2.0

validated simple linear

VTN

HELM 2.0

validated simple linear

PEPTIDE1{V.T.N}$$$$V2.0

Canonical SMILES

validated

CC(C)C(N)C(=O)NC(C(=O)NC(CC(N)=O)C(=O)O)C(C)O

Isomeric SMILES

validated

CC(C)[C@H](N)C(=O)N[C@H](C(=O)N[C@@H](CC(N)=O)C(=O)O)[C@@H](C)O

Follow-up research

External analysis tools

Research workflow

Citation and local history

BibTeX

@misc{PEPDIA-INT-068532,
  title = {Unnamed peptide},
  author = {{PepDiana Consortium}},
  year = {2026},
  howpublished = {PepDiana Multifunctional Peptide Database},
  url = {http://127.0.0.1:3004/peptides/PEPDIA-INT-068532},
  note = {Accessed from local PepDiana development build}
}

APA-style note

Unnamed peptide. (2026). PepDiana record PEPDIA-INT-068532. PepDiana Multifunctional Peptide Database. http://127.0.0.1:3004/peptides/PEPDIA-INT-068532

This record is saved to local recent-view history so it can reappear on the peptide browser page.

Integrated source-database annotations

Biological activity (6 records)

Stable recordActivitySubtypeValueTargetAssay methodSource
CTPDB_P068532_ACT_camp_0001AntimicrobialAnti-Gram+Not available in the current structured importUnknownNot reported by sourceCAMPSQ21483camp / linked
CTPDB_P068532_ACT_camp_0002AntimicrobialAnti-Gram-Not available in the current structured importUnknownNot reported by sourceCAMPSQ21483camp / linked
CTPDB_P068532_ACT_dbaasp_0003Antimicrobial-NAHIV-1Not reported by sourceDBAASPS_6019_chain0dbaasp / linked
CTPDB_P068532_ACT_hipdb_0000AntiviralAnti-HIVLowHIVNot reported by sourceHIPdb_HIP1070hipdb / unavailable
CTPDB_P068532_ACT_satpdb_0004Antiviral-Not available in the current structured importUnknownNot reported by sourcesatpdb18873satpdb / linked
CTPDB_P068532_ACT_satpdb_0005Antimicrobial-Not available in the current structured importUnknownNot reported by sourcesatpdb18873satpdb / linked

Provenance

Source database records (4)

hipdb

HIPdb_HIP1070

Raw sequence

VTN

camp

CAMPSQ21483

Raw sequence

VTN

dbaasp

DBAASPS_6019_chain0

Raw sequence

VTN

satpdb

satpdb18873

Raw sequence

VTN

Citation trail

Literature (2 records)

{"pubmed_id": "9425262.0", "paper": "The p2gag peptide, AEAMSQVTNTATIM, processed from HIV-1 Pr55gag was found to be a suicide inhibitor of HIV-1 protease.", "authors": "Misumi S, Kudo A, Azuma R, Tomonaga M, Furuishi K, Shoji S.", "reference": "Biochem Biophys Res Commun. 1997 Dec 18;241(2):275-80."}

{"pubmed_id": "9425262.0", "paper": "The p2gag peptide, AEAMSQVTNTATIM, processed from HIV-1 Pr55gag was found to be a suicide inhibitor of HIV-1 protease.", "authors": "Misumi S, Kudo A, Azuma R, Tomonaga M, Furuishi K, Shoji S.", "reference": "Biochem Biophys Res Commun. 1997 Dec 18;241(2):275-80."}

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Audit surface

Raw annotations and release metadata

Integrated record last updated: 2026-04-15T00:59:13.602083+00:00

Modification summary

No structured modification annotations are available for this record.

Source metadata
[
  {
    "source_db": "hipdb",
    "organism_name": "Unknown"
  },
  {
    "source_db": "camp",
    "organism_name": "Unknown"
  },
  {
    "source_db": "dbaasp",
    "organism_name": "Unknown"
  },
  {
    "source_db": "satpdb",
    "organism_name": "Unknown"
  }
]
Structure metadata
{
  "source_db": "satpdb",
  "dssp_states": "CCC"
}