General Information
Activity Information
-
Biological Activity
- Antimicrobial, Antibacterial, Antifungal
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Target Organism
-
- Yeast: Candida albicans (100% inhibition at 54 nmol), Cryptococcus neoformans.
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Hemolytic Activity
-
- No hemolysis information or data found in the reference(s) presented in this entry
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Cytotoxicity
-
- Not included yet
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Binding Target
- Metal-binding (Zinc)
Structure Information
-
Linear/Cyclic
- Not included yet
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N-terminal Modification
- Not included yet
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C-terminal Modification
- Not included yet
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Nonterminal Modifications and Unusual Amino Acids
- Not included yet
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Stereochemistry
- Not included yet
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Structure
- Alpha helix
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Structure Description
- Not found
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Helical Wheel Diagram
-
PDB ID
- None
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Predicted Structure
- There is no predicted structure for DRAMP03580.
Physicochemical Information
-
Formula
- C133H195N51O33
Absent Amino Acids
- CILMNPQTVW
Common Amino Acids
- H
Mass
- 3036.33
PI
- 10.28
Basic Residues
- 14
Acidic Residues
- 2
Hydrophobic Residues
- 2
Net Charge
- +12
-
Boman Index
- -115.52
Hydrophobicity
- -2.454
Aliphatic Index
- 4.17
Half Life
-
- Mammalian:1.1 hour
- Yeast:3 min
- E.coli:>10 hour
Extinction Coefficient Cystines
- 2980
Absorbance 280nm
- 129.57
Polar Residues
- 6
DRAMP03580
Comments Information
Histatin 5 is a proteolytic product of histatin 3. The active Domain
- of histitin 5 (Dh-5) corresponding to residues 11-24 showed HIV inhibitory effects. However,the results with the Dh-5 mutants are mixed (Groot et al. 2006 J. Virol. 80
Literature Information
- ·Literature 1
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Title
- Histatins, a novel family of histidine-rich proteins in human parotid secretion. Isolation, characterization, primary structure, and fungistatic effects on Candida albicans.
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Pubmed ID
- 3286634
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Reference
- J Biol Chem. 1988 Jun 5;263(16):7472-7477.
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Author
- Oppenheim FG, Xu T, McMillian FM, Levitz SM, Diamond RD, Offner GD, Troxler RF.