ProForma 2.0
validated simple linear
KAPGFGDRR
KAPGFGDRR
Aliases: KAPGFGDRR
Normalized sequence
KAPGFGDRR
9 amino acids
Release PepDiana-V1-20260620
1
Activity records
1
Source papers
1
Positive
0
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
1003.1159 Da
Molecular formula
C43H70N16O12
Theoretical pI
10.835
Net charge at pH 7
1.7602
GRAVY
-1.5778
Instability index
85.5556
Aromaticity
0.1111
Topological polar surface area
474.45 Ų
cLogP
-5.5615
Hydrogen-bond donors
17
Hydrogen-bond acceptors
14
Rotatable bonds
32
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
KAPGFGDRR
HELM 2.0
validated simple linear
PEPTIDE1{K.A.P.G.F.G.D.R.R}$$$$V2.0
Canonical SMILES
validated
CC(NC(=O)C(N)CCCCN)C(=O)N1CCCC1C(=O)NCC(=O)NC(Cc1ccccc1)C(=O)NCC(=O)NC(CC(=O)O)C(=O)NC(CCCNC(=N)N)C(=O)NC(CCCNC(=N)N)C(=O)O
Isomeric SMILES
validated
C[C@H](NC(=O)[C@@H](N)CCCCN)C(=O)N1CCC[C@H]1C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)NCC(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)O
Paper-level observations
Table 2: KAPGFGDRR, PepRank 0.78. Predicted bioactivity score from PeptideRanker.
Citation and release provenance
Cite this identity as PepDiana record PEPDIA-PLP-001418, release PepDiana-V1-20260620. Experimental observations retain their paper, mention, and activity-record identifiers.
Record updated: 2026-06-22T07:14:26.229247+00:00