MYP_102141
Basic Information
Fusaricidin B
Antimicrobial
Antimicrobial Antibacterial
Antimicrobial Antibacterial Anti-Gram-positive
Antimicrobial Antifungal
Standard
6 amino acids
C26H47N7O10
Standard
Sequence
TVVTQA
Physicochemical Analysis
617.69 Da
5.18
-0.60
-0.79
-0.1003
0.88
0.41
0.30
-18.38
113.33
0.0000
0.00
0.00
The radar chart summarizes major physicochemical dimensions for quick comparison, while exact numerical values remain listed on the left.
Residue Composition
Amino Acid Composition
Chemical Descriptors
292.37
-3.82
10.0
10.0
18.0
43.0
0.0
6.0
Structural Visualization
3D PDB MODEL
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2D CHEMICAL STRUCTURE
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Experimental Records
RECORD: Rec_0297194 VERIFIED: YES
Provenance & Taxonomy
Bacillus polymyxa [Bacterium]
Bacteriocin
Structure & Mods
topology not specified [Not included yet]
canonical L-amino-acid peptide [L]
Bio-Activity Profile
Antimicrobial Antibacterial Anti-Gram-positive Antifungal
Gram-positive
RECORD: Rec_0300426 VERIFIED: YES
Provenance & Taxonomy
Bacillus polymyxa [Bacterium]
Structure & Mods
head-to-tail cyclic peptide [Cyclic]
mixed L/D amino-acid peptide [Mixed]
Lipidation
Esterification
The carboxylic end of Ala6 forms an ester bond with the hydroxyl group of T1. Val2, Gln5, Ala6 are D-amino acids and Thr4 is a D-allo-Thr. In addition, the N-terminus NH is lipidated with 15-guanidino-3-hydroxypentadecanoic acid (GHPD). Refer to the article for additional physical properties
Bio-Activity Profile
Antimicrobial Antifungal
Candida albicans IFO 1594, S. cerevisiae HUT 7099
12.5 μg/mL
MIC
Showing 2 records on this page · Page 2 of 2