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Building blocks and blueprints for bacterial autolysins
by
Mitchell, Spencer J.
, Bailey-Kellogg, Chris
, Griswold, Karl E.
, Verma, Deeptak
in
Annotations
/ Anti-Bacterial Agents - metabolism
/ Anti-Bacterial Agents - pharmacology
/ Antibiotics
/ Apoptosis
/ Architecture
/ Autolysins
/ Autolysis
/ Bacteria
/ Bacterial Proteins - metabolism
/ Biodegradation
/ Biofilms
/ Biology and Life Sciences
/ Catalysis
/ Cats
/ Cell death
/ Cell division
/ Cell walls
/ Computational Biology - methods
/ Data collection
/ Databases, Protein
/ Domains
/ Drugs
/ Engineering and Technology
/ Enzymes
/ Food safety
/ Gram-Negative Bacteria - enzymology
/ Gram-Positive Bacteria - enzymology
/ Homology
/ Hydrolases
/ Lysins
/ Lytic enzymes
/ Medicine and Health Sciences
/ N-Acetylmuramoyl-L-alanine Amidase - metabolism
/ N-Acetylmuramoyl-L-alanine Amidase - pharmacology
/ Peptidoglycans
/ Physical Sciences
/ Physiological aspects
/ Physiology
/ Proteins
/ Sequences
/ Streptococcus infections
2021
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Building blocks and blueprints for bacterial autolysins
by
Mitchell, Spencer J.
, Bailey-Kellogg, Chris
, Griswold, Karl E.
, Verma, Deeptak
in
Annotations
/ Anti-Bacterial Agents - metabolism
/ Anti-Bacterial Agents - pharmacology
/ Antibiotics
/ Apoptosis
/ Architecture
/ Autolysins
/ Autolysis
/ Bacteria
/ Bacterial Proteins - metabolism
/ Biodegradation
/ Biofilms
/ Biology and Life Sciences
/ Catalysis
/ Cats
/ Cell death
/ Cell division
/ Cell walls
/ Computational Biology - methods
/ Data collection
/ Databases, Protein
/ Domains
/ Drugs
/ Engineering and Technology
/ Enzymes
/ Food safety
/ Gram-Negative Bacteria - enzymology
/ Gram-Positive Bacteria - enzymology
/ Homology
/ Hydrolases
/ Lysins
/ Lytic enzymes
/ Medicine and Health Sciences
/ N-Acetylmuramoyl-L-alanine Amidase - metabolism
/ N-Acetylmuramoyl-L-alanine Amidase - pharmacology
/ Peptidoglycans
/ Physical Sciences
/ Physiological aspects
/ Physiology
/ Proteins
/ Sequences
/ Streptococcus infections
2021
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Do you wish to request the book?
Building blocks and blueprints for bacterial autolysins
by
Mitchell, Spencer J.
, Bailey-Kellogg, Chris
, Griswold, Karl E.
, Verma, Deeptak
in
Annotations
/ Anti-Bacterial Agents - metabolism
/ Anti-Bacterial Agents - pharmacology
/ Antibiotics
/ Apoptosis
/ Architecture
/ Autolysins
/ Autolysis
/ Bacteria
/ Bacterial Proteins - metabolism
/ Biodegradation
/ Biofilms
/ Biology and Life Sciences
/ Catalysis
/ Cats
/ Cell death
/ Cell division
/ Cell walls
/ Computational Biology - methods
/ Data collection
/ Databases, Protein
/ Domains
/ Drugs
/ Engineering and Technology
/ Enzymes
/ Food safety
/ Gram-Negative Bacteria - enzymology
/ Gram-Positive Bacteria - enzymology
/ Homology
/ Hydrolases
/ Lysins
/ Lytic enzymes
/ Medicine and Health Sciences
/ N-Acetylmuramoyl-L-alanine Amidase - metabolism
/ N-Acetylmuramoyl-L-alanine Amidase - pharmacology
/ Peptidoglycans
/ Physical Sciences
/ Physiological aspects
/ Physiology
/ Proteins
/ Sequences
/ Streptococcus infections
2021
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Journal Article
Building blocks and blueprints for bacterial autolysins
2021
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Overview
Bacteria utilize a wide variety of endogenous cell wall hydrolases, or autolysins, to remodel their cell walls during processes including cell division, biofilm formation, and programmed death. We here systematically investigate the composition of these enzymes in order to gain insights into their associated biological processes, potential ways to disrupt them via chemotherapeutics, and strategies by which they might be leveraged as recombinant antibacterial biotherapies. To do so, we developed LEDGOs (lytic enzyme domains grouped by organism), a pipeline to create and analyze databases of autolytic enzyme sequences, constituent domain annotations, and architectural patterns of multi-domain enzymes that integrate peptidoglycan binding and degrading functions. We applied LEDGOs to eight pathogenic bacteria, gram negatives Acinetobacter baumannii , Klebsiella pneumoniae , Neisseria gonorrhoeae , and Pseudomonas aeruginosa ; and gram positives Clostridioides difficile , Enterococcus faecium , Staphylococcus aureus , and Streptococcus pneumoniae . Our analysis of the autolytic enzyme repertoires of these pathogens reveals commonalities and differences in their key domain building blocks and architectures, including correlations and preferred orders among domains in multi-domain enzymes, repetitions of homologous binding domains with potentially complementarity recognition modalities, and sequence similarity patterns indicative of potential divergence of functional specificity among related domains. We have further identified a variety of unannotated sequence regions within the lytic enzymes that may themselves contain new domains with important functions.
Publisher
Public Library of Science,Public Library of Science (PLoS)
Subject
/ Anti-Bacterial Agents - metabolism
/ Anti-Bacterial Agents - pharmacology
/ Bacteria
/ Bacterial Proteins - metabolism
/ Biofilms
/ Cats
/ Computational Biology - methods
/ Domains
/ Drugs
/ Enzymes
/ Gram-Negative Bacteria - enzymology
/ Gram-Positive Bacteria - enzymology
/ Homology
/ Lysins
/ Medicine and Health Sciences
/ N-Acetylmuramoyl-L-alanine Amidase - metabolism
/ N-Acetylmuramoyl-L-alanine Amidase - pharmacology
/ Proteins
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