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KAS1_KASSE
ID   KAS1_KASSE              Reviewed;          21 AA.
AC   P0C010;
DT   07-JUN-2005, integrated into UniProtKB/Swiss-Prot.
DT   07-JUN-2005, sequence version 1.
DT   25-MAY-2022, entry version 33.
DE   RecName: Full=Kassinatuerin-1;
OS   Kassina senegalensis (Senegal running frog).
OC   Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Amphibia;
OC   Batrachia; Anura; Neobatrachia; Microhyloidea; Hyperoliidae; Kassina.
OX   NCBI_TaxID=8415;
RN   [1]
RP   PROTEIN SEQUENCE, SYNTHESIS, FUNCTION, MASS SPECTROMETRY, AND AMIDATION AT
RP   ILE-21.
RC   TISSUE=Skin;
RX   PubMed=10679222; DOI=10.1006/bbrc.2000.2136;
RA   Mattute B., Knoop F.C., Conlon J.M.;
RT   "Kassinatuerin-1: a peptide with broad-spectrum antimicrobial activity
RT   isolated from the skin of the hyperoliid frog, Kassina senegalensis.";
RL   Biochem. Biophys. Res. Commun. 268:433-436(2000).
RN   [2]
RP   SYNTHESIS, FUNCTION, MINIMAL INHIBITORY CONCENTRATION, AND MUTAGENESIS OF
RP   GLY-7; ALA-13; SER-18 AND ASP-19.
RX   PubMed=15885852; DOI=10.1016/j.peptides.2005.04.003;
RA   Conlon J.M., Abraham B., Galadari S., Knoop F.C., Sonnevend A., Pal T.;
RT   "Antimicrobial and cytolytic properties of the frog skin peptide,
RT   kassinatuerin-1 and its L- and D-lysine-substituted derivatives.";
RL   Peptides 26:2104-2110(2005).
CC   -!- FUNCTION: Shows broad-spectrum antimicrobial activity against the Gram-
CC       negative bacterium E.coli (MIC=6.25 uM), K.pneumoniae (MIC=25 uM),
CC       E.cloacae (MIC=6.25 uM), P.aeruginosa (MIC=25 uM), the Gram-positive
CC       bacterium S.aureus (MIC=6.25 uM), S.epidermidis (MIC=6.25 uM),
CC       E.faecalis (MIC=12.5 uM), and the fungus C.albicans (MIC=100 uM). Has
CC       no antimicrobial effect against P.mirabilis (MIC>100 uM). Has
CC       relatively high cytolytic and hemolytic activities. Its alpha-helix has
CC       considerable amphipathic character. {ECO:0000269|PubMed:10679222,
CC       ECO:0000269|PubMed:15885852}.
CC   -!- SUBCELLULAR LOCATION: Secreted.
CC   -!- TISSUE SPECIFICITY: Expressed by the skin dorsal glands.
CC   -!- MASS SPECTROMETRY: Mass=2282.5; Method=Electrospray;
CC       Evidence={ECO:0000269|PubMed:10679222};
CC   -!- MISCELLANEOUS: This peptide was also synthesized without its N-terminal
CC       amidation. This modification decreases its antimicrobial and hemolytic
CC       activities.
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DR   AlphaFoldDB; P0C010; -.
DR   GO; GO:0005576; C:extracellular region; IEA:UniProtKB-SubCell.
DR   GO; GO:0042742; P:defense response to bacterium; IEA:UniProtKB-KW.
DR   GO; GO:0050832; P:defense response to fungus; IEA:UniProtKB-KW.
DR   GO; GO:0044179; P:hemolysis in another organism; IEA:UniProtKB-KW.
PE   1: Evidence at protein level;
KW   Amidation; Antibiotic; Antimicrobial; Cytolysis; Direct protein sequencing;
KW   Fungicide; Hemolysis; Secreted.
FT   PEPTIDE         1..21
FT                   /note="Kassinatuerin-1"
FT                   /id="PRO_0000043808"
FT   MOD_RES         21
FT                   /note="Isoleucine amide"
FT                   /evidence="ECO:0000269|PubMed:10679222"
FT   MUTAGEN         7
FT                   /note="G->K: When associated with K-19, no change in
FT                   antibacterial activity against E.coli and S.aureus, 2-fold
FT                   increase in antimicrobial activity against C.albicans,
FT                   little increase in hemolytic activity. When associated with
FT                   K-18 and K-19, no change in antibacterial activity against
FT                   E.coli and S.aureus, 4-fold increase in antimicrobial
FT                   activity against C.albicans, little increase in hemolytic
FT                   activity."
FT                   /evidence="ECO:0000269|PubMed:15885852"
FT   MUTAGEN         13
FT                   /note="A->K: Loss of antimicrobial activity, loss of
FT                   hemolytic activity."
FT                   /evidence="ECO:0000269|PubMed:15885852"
FT   MUTAGEN         18
FT                   /note="S->K: When associated with K-19, no change in
FT                   antibacterial activity against E.coli, 2-fold increase in
FT                   antibacterial activity against S.aureus, 4-fold increase in
FT                   antimicrobial activity against C.albicans, 2.6-fold
FT                   increase in hemolytic activity. When associated with K-7
FT                   and K-19, no change in antibacterial activity against
FT                   E.coli and S.aureus, 4-fold increase in antimicrobial
FT                   activity against C.albicans, little increase in hemolytic
FT                   activity."
FT                   /evidence="ECO:0000269|PubMed:15885852"
FT   MUTAGEN         19
FT                   /note="D->K: No change in antibacterial activity against
FT                   E.coli, 2-fold increase in antibacterial activity against
FT                   S.aureus, 2-fold increase in antimicrobial activity against
FT                   C.albicans, little increase in hemolytic activity. When
FT                   associated with K-18, no change in antibacterial activity
FT                   against E.coli, 2-fold increase in antibacterial activity
FT                   against S.aureus, 4-fold increase in antimicrobial activity
FT                   against C.albicans, 2.6-fold increase in hemolytic
FT                   activity. When associated with K-7, no change in
FT                   antibacterial activity against E.coli and S.aureus, 2-fold
FT                   increase in antimicrobial activity against C.albicans,
FT                   little increase in hemolytic activity. When associated with
FT                   K-18 and K-7, no change in antibacterial activity against
FT                   E.coli and S.aureus, 4-fold increase in antimicrobial
FT                   activity against C.albicans, little increase in hemolytic
FT                   activity."
FT                   /evidence="ECO:0000269|PubMed:15885852"
SQ   SEQUENCE   21 AA;  2284 MW;  86E8E32C8798C4E3 CRC64;
     GFMKYIGPLI PHAVKAISDL I
 
 
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