ProForma 2.0
validated simple linear
FKCRRWQWRMKKLGAPSITCVRRAFGGGSSVDGKEDLIWKLLSKAQEKFGKNKSR
LFCA
Aliases: LFCA
Normalized sequence
FKCRRWQWRMKKLGAPSITCVRRAFGGGSSVDGKEDLIWKLLSKAQEKFGKNKSR
55 amino acids
Release PepDiana-V1-20260620
18
Activity records
1
Source papers
18
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
6371.4316 Da
Molecular formula
C284H460N88O73S3
Theoretical pI
10.772
Net charge at pH 7
10.7391
GRAVY
-0.8127
Instability index
56.3109
Aromaticity
0.1091
Topological polar surface area
2678.73 Ų
cLogP
-25.7985
Hydrogen-bond donors
100
Hydrogen-bond acceptors
87
Rotatable bonds
223
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
FKCRRWQWRMKKLGAPSITCVRRAFGGGSSVDGKEDLIWKLLSKAQEKFGKNKSR
HELM 2.0
validated simple linear
PEPTIDE1{F.K.C.R.R.W.Q.W.R.M.K.K.L.G.A.P.S.I.T.C.V.R.R.A.F.G.G.G.S.S.V.D.G.K.E.D.L.I.W.K.L.L.S.K.A.Q.E.K.F.G.K.N.K.S.R}$$$$V2.0
Canonical SMILES
validated
CCC(C)C(NC(=O)C(CC(C)C)NC(=O)C(CC(=O)O)NC(=O)C(CCC(=O)O)NC(=O)C(CCCCN)NC(=O)CNC(=O)C(CC(=O)O)NC(=O)C(NC(=O)C(CO)NC(=O)C(CO)NC(=O)CNC(=O)CNC(=O)CNC(=O)C(Cc1ccccc1)NC(=O)C(C)NC(=O)C(CCCNC(=N)N)NC(=O)C(CCCNC(=N)N)NC(=O)C(NC(=O)C(CS)NC(=O)C(NC(=O)C(NC(=O)C(CO)NC(=O)C1CCCN1C(=O)C(C)NC(=O)CNC(=O)C(CC(C)C)NC(=O)C(CCCCN)NC(=O)C(CCCCN)NC(=O)C(CCSC)NC(=O)C(CCCNC(=N)N)NC(=O)C(Cc1c[nH]c2ccccc12)NC(=O)C(CCC(N)=O)NC(=O)C(Cc1c[nH]c2ccccc12)NC(=O)C(CCCNC(=N)N)NC(=O)C(CCCNC(=N)N)NC(=O)C(CS)NC(=O)C(CCCCN)NC(=O)C(N)Cc1ccccc1)C(C)CC)C(C)O)C(C)C)C(C)C)C(=O)NC(Cc1c[nH]c2ccccc12)C(=O)NC(CCCCN)C(=O)NC(CC(C)C)C(=O)NC(CC(C)C)C(=O)NC(CO)C(=O)NC(CCCCN)C(=O)NC(C)C(=O)NC(CCC(N)=O)C(=O)NC(CCC(=O)O)C(=O)NC(CCCCN)C(=O)NC(Cc1ccccc1)C(=O)NCC(=O)NC(CCCCN)C(=O)NC(CC(N)=O)C(=O)NC(CCCCN)C(=O)NC(CO)C(=O)NC(CCCNC(=N)N)C(=O)O
Isomeric SMILES
validated
CC[C@H](C)[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)CNC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@H](CO)NC(=O)CNC(=O)CNC(=O)CNC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](NC(=O)[C@H](CS)NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H]1CCCN1C(=O)[C@H](C)NC(=O)CNC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CS)NC(=O)[C@H](CCCCN)NC(=O)[C@@H](N)Cc1ccccc1)[C@@H](C)CC)[C@@H](C)O)C(C)C)C(C)C)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](Cc1ccccc1)C(=O)NCC(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCCNC(=N)N)C(=O)O
Paper-level observations
The inhibition rate could reach 94.9% after pretreatment before SVA infection.
The inhibition rates of the virus in the stages of adsorption, invasion, and replication were 91.2%, 75.6%, and 65.9%, respectively.
The inhibition rates of the virus in the stages of adsorption, invasion, and replication were 91.2%, 75.6%, and 65.9%, respectively.
The inhibition rates of the virus in the stages of adsorption, invasion, and replication were 91.2%, 75.6%, and 65.9%, respectively.
The highest inhibition rate of FMDV replication was observed in LFCA-treated cells (74.3%).
The inhibition effect of the adsorption stage was second only to that of the replication stage, and the inhibition rate was 63.4%.
The 50% inhibitory concentration of LFCA against SVA was determined to be 8.96 μg/mL.
Data analysis revealed that the 50% inhibitory concentration (IC50) of LFCA against FMDV was 203.9 μg/mL.
The inhibition rates of SVA by LFCA were 41.8%, 57.3%, 80.3%, 89.6%, 94.5%, and 96.1%.
The inhibition rates of SVA by LFCA were 41.8%, 57.3%, 80.3%, 89.6%, 94.5%, and 96.1%.
The inhibition rates of SVA by LFCA were 41.8%, 57.3%, 80.3%, 89.6%, 94.5%, and 96.1%.
The inhibition rates of SVA by LFCA were 41.8%, 57.3%, 80.3%, 89.6%, 94.5%, and 96.1%.
The inhibition rates of SVA by LFCA were 41.8%, 57.3%, 80.3%, 89.6%, 94.5%, and 96.1%.
The inhibition rates of SVA by LFCA were 41.8%, 57.3%, 80.3%, 89.6%, 94.5%, and 96.1%.
LFCA demonstrated an inhibition rate of 66.3% against FMDV at 400 μg/mL; this rate decreased with lower concentrations and was absent at 50 μg/mL.
LFCA demonstrated an inhibition rate of 66.3% against FMDV at 400 μg/mL; this rate decreased with lower concentrations and was absent at 50 μg/mL.
After treatment with LFCA of different dilutions, the cell survival rate was about 100% (Figure 1), and LFCA at concentrations of less than 400 μg/mL had no toxicity to cells.
After treatment with LFCA of different dilutions, the cell survival rate was about 100% (Figure 1), and LFCA at concentrations of less than 400 μg/mL had no toxicity to cells.
Citation and release provenance
Cite this identity as PepDiana record PEPDIA-PLP-000726, release PepDiana-V1-20260620. Experimental observations retain their paper, mention, and activity-record identifiers.
Record updated: 2026-06-22T07:14:26.229247+00:00