Basic Information

IDDRAMP21195
SequenceGATYAKKIIKTITKIATTAW
Length20
NameGW-A5 (De novo synthesis)
SourceSynthetic construct
ActivityAntimicrobial, Antibacterial, Anti-Gram+, Anti-Gram-
Pathogen[Ref.18586467] Gram-positive bacteria : Staphylococcus aureus (BCRC 10780)(MIC=128 μg/ml), Staphylococcus xylosus (BCRC 12930)(MIC=64 μg/ml), Staphylococcus aureus (BCRC 10781)(MIC=128 μg/ml), Listeria monocytogenes (BCRC 14845)(MIC=128 μg/ml), Streptococcus bovis (BCRC 14729)(MIC=128 μg/ml), Streptococcus iniae (laboratory strain)(MIC=128 μg/ml), Lactococcus garvieae (laboratory strain)(MIC=128 μg/ml);##Gram-negative bacteria : Klebsiella oxytoca (BCRC 13985)(MIC=64 μg/ml), Pseudomonas aeruginosa (BCRC 10944)(MIC=64 μg/ml), Escherichia coli (BCRC 10675)(MIC=16 μg/ml), Enterobacter aerogenes (BCRC 10370)(MIC=64 μg/ml), Enterobacter cloacae (BCRC 10401)(MIC=32 μg/ml), Yersinia enterocolitica (BCRC 13999)(MIC=128 μg/ml)
Hemolytic Activity[Ref.18586467] MHC=128 μM against human red blood cells
Cytotoxicity[Ref.18586467] No cytotoxicity information found.
N-terminal ModificationFree
C-terminal ModificationFree
Linear/Cyclic/BranchedLinear
Uniprot
PDB
3D View
PDB DownloadDownload PDB Predicted by Alphafold2
PubMed ID18586467

Physicochemical Properties

Residues20
SequenceGATYAKKIIKTITKIATTAW
Molecular Weight2179.6
Grand Average of Hydropathy0.175
Isoelectric Point10.177
Charge at pH 7.43.545
Secondary StructureHelix: 0.300, Turn: 0.050, Sheet: 0.200
Instability Index4.36
Aromaticity0.1

Similar Structure Search

Candidates based on structure

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