General Information
-
DRAMP ID
- DRAMP30631
-
Peptide Name
- Alloferon (3-13)
-
Source
- Synthetic construct(derived from Alloferon-1)
-
Family
- Herpesviridae, Picornaviridae
-
Gene
- Not found
-
Sequence
- VSGHGQHGVHG
-
Sequence Length
- 11
-
UniProt Entry
- P83412
-
Protein Existence
- Not found
-
SMILES
- CC(C)[C@H](N)C(=O)N[C@@H](CO)C(=O)NCC(=O)N[C@@H](Cc1c[nH]cn1)C(=O)NCC(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)NCC(=O)N[C@H](C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)NCC(=O)O)C(C)C
Activity Information
-
Biological Activity
- Antimicrobial, Antiviral
-
Target Organism
-
- [Ref.22883213]Herpesvirus 1 McIntire (HHV-1MC):
Target Organism Activity inhibition of virus replication in Vero cells(IC50=500 µM); - - HHV-1 clinical strain:
Target Organism Activity inhibition of virus replication in Hep-2 cells(IC50=117 µM); - - Coxsackie virus B2(clinical strain):
Target Organism Activity inhibition of virus replication in Hep-2 cells(IC50=38 µM); - - Coxsackie virus 971 PT B2:
Target Organism Activity inhibition of virus replication in HEp-2 cells(IC50=250 µM);inhibition of virus replication in LLC-MK2 cells IC50=93 µM
- [Ref.22883213]Herpesvirus 1 McIntire (HHV-1MC):
-
Hemolytic Activity
-
- No hemolysis information or data found in the reference(s) presented in this entry
-
Cytotoxicity
-
- [Ref.22883213]No cytotoxic against Vero, Hep-2 and LLC-MK2 cells up to 165 µM.
-
Binding Target
- Not found
Structure Information
Physicochemical Information
-
Formula
Absent Amino Acids
Common Amino Acids
Mass
- 0
PI
- 0
Basic Residues
Acidic Residues
Hydrophobic Residues
Net Charge
-
Boman Index
- 0
Hydrophobicity
- 0
Aliphatic Index
- 0
Half Life
-
- Mammalian:
- Yeast:
- E.coli:
Extinction Coefficient Cystines
Absorbance 280nm
- 0
Polar Residues
DRAMP30631
Comments Information
Comment
- No comments found on DRAMP database
Literature Information
- ·Literature 1
-
Title
- New alloferon analogues: synthesis and antiviral properties.
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Pubmed ID
- 22883213
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Reference
- Chem Biol Drug Des. 2013 Feb;81(2):302-9.
-
Author
- Kuczer M, Majewska A, Zahorska R.
