Ontology highlight
ABSTRACT:
SUBMITTER: Maciejewska B
PROVIDER: S-EPMC5674055 | biostudies-literature | 2017 Nov
REPOSITORIES: biostudies-literature
Maciejewska Barbara B Źrubek Karol K Espaillat Akbar A Wiśniewska Magdalena M Rembacz Krzysztof P KP Cava Felipe F Dubin Grzegorz G Drulis-Kawa Zuzanna Z
Scientific reports 20171106 1
Endolysins are peptidoglycan-degrading enzymes utilized by bacteriophages to release the progeny from bacterial cells. The lytic properties of phage endolysins make them potential antibacterial agents for medical and industrial applications. Here, we present a comprehensive characterization of phage AP3 modular endolysin (AP3gp15) containing cell wall binding domain and an enzymatic domain (DUF3380 by BLASTP), both widespread and conservative. Our structural analysis demonstrates the low similar ...[more]