TCID | Name | Domain | Kingdom/Phylum | Protein(s) |
---|---|---|---|---|
*1.C.85.1.1 | β-defensin-1 | Eukaryota |
Metazoa | β-defensin-1 of Homo sapiens (P60022) |
*1.C.85.1.2 | β-defensin-2 | Eukaryota |
Metazoa | β-defensin 2 of Homo sapiens (O15263) |
*1.C.85.1.3 | β-defensin-3 of 67 aas and 1 N-terminal TMS. Canine BD103 (van Damme et al. 2009) is 79% identical. | Eukaryota |
Metazoa | β-defensin-3 of Homo sapiens (P81534) |
*1.C.85.1.4 | β-defensin-14 | Eukaryota |
Metazoa | β-defensin-14 of Mus musculus (Q7TNV9) |
*1.C.85.1.5 | Epididymus sperm-associated antigen (EP2E) | Eukaryota |
Metazoa | EP2E of Homo sapiens (Q9H4P9) |
*1.C.85.1.6 | β-defensin-2 of 71 aas and 1 TMS | Eukaryota |
Metazoa | Defensin β2 of Mus musculus |
*1.C.85.1.7 | β-defensin 11 of 69 aas and 1 TMS | Eukaryota |
Metazoa | Defb11 of Rattus norvegicus |
*1.C.85.1.8 | beta-Defensin 3 of 63 aas and 1 TMS (Colavita et al. 2015). Sass et al. have proposed that interference with the organisation of membrane-bound multienzyme complexes such as the electron transport chain and the cell wall biosynthetic complex rather than on formation of defined transmembrane pores is responsible for death of Staphylococcus aureus (Sass et al. 2008). | Eukaryota |
Metazoa | BD3 pf Mus musculus |
*1.C.85.1.9 | Canine β-defensin-1, cBD1, of 41 aas and 1 N-terminal TMS. Production of beta-defensins constitutes an important role in skin defense, and variable expression of three cBDs in different organ systems of the dog has been observed. In skin, three beta-defensins, cBD1, cBD103 and cBD107, were extensively expressed (van Damme et al. 2009). There is a possible defect in the innate immune response of dogs with atopic dermatitis. cDB1 may be a marker for Leishmania infantum infection in dogs (da Silva et al. 2017). | Eukaryota |
Metazoa | Defensin 1 of Canis lupus familiaris (Dog) (Canis familiaris) |
*1.C.85.1.10 | Canine β-defensin 107, cBD107, of 70 aas and 1 N-terminal TMS (van Damme et al. 2009). | Eukaryota |
Metazoa | cBD107 of Canis lupus familiaris (Dog) (Canis familiaris) |
*1.C.85.2.1 | Myotoxin-4 or Crotamine-4. Specifically modifies voltage-sensitive Na+ channels and exhibits analgesic effects. Belongs to the snake myotoxin family. | Eukaryota |
Metazoa | Myotoxin-4 of Crotalus durissus terrificus (P24334) |
*1.C.85.2.2 | Crotamine-IV-2 toxin of 42 aas and 0 TMSs | Eukaryota |
Metazoa | Croamine-IV-2 of Crotalus durissus cumanensis |
*1.C.85.2.3 | β-defensin-like protein of 63 aas and 1 TMS | Eukaryota |
Metazoa | defensin-like protein of Bothrops matogrossensis (Pitviper) (Bothrops neuwiedi matogrossensis) |
*1.C.85.2.4 | Crotamine-like precursor of 76 aas and 1 TMS. | Eukaryota |
Metazoa | Crotamine-like peptide of Thamnodynastes strigatus (Coastal house snake) |
*1.C.85.3.1 | Epithelial Gallinacin-1α. The full length antimicrobial peptide precursor is CHP2. Attacks bacteria and fungi. | Eukaryota |
Metazoa | Gallinacin 1α of Gallus gallus (P46157) |
*1.C.85.3.2 | β-defensin prepropeptide of 59 aas and 2 TMSs. | Eukaryota |
Metazoa | β-defensin of Meleagris gallopavo (turkey) |
*1.C.85.3.3 | Avian beta-defensin, 5beta of 66 aas and 1 TMS.
| Eukaryota |
Metazoa | Beta-defensin of Columba livia (domestic pigeon) |
*1.C.85.4.1 | Helofensin-1 lethal toxin of 183 aas (PMID 19837656). This toxin possesses an inhibitory effect on electrical stimulation of the isolated hemi-diaphragm of mice. Neither hemorrhagic nor hemolytic activities were detected, but Huang et al. 2016 reported it to be a membrane active protein.
| Eukaryota |
Metazoa | Helofensin-1 of Heloderma suspectum cinctum (Banded Gila monster) |
*1.C.85.4.2 | Helofensin-3 (90% identical to helofensin-1) of 182 aas. A lethal toxin. | Eukaryota |
Metazoa | Helofensin-3 of Heloderma suspectum cinctum (Banded Gila monster) |
*1.C.85.4.3 | Uncharacterized protein of 172 aas | Eukaryota |
Metazoa | UP of Nematostella vectensis (Starlet sea anemone) |