139 results on '"Pugsley, Anthony P."'
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102. A second prepilin peptidase gene inEscherichia coliK-12
103. Recent progress and future directions in studies of the main terminal branch of the general secretory pathway in Gram-negative bacteria – a review
104. The conserved tetracysteine motif in the general secretory pathway component PulE is required for efficient pullulanase secretion
105. Identification of two regions of Klebsiella oxytoca pullulanase that together are capable of promoting ?-lactamase secretion by the general secretory pathway
106. Molecular characterization of PulE, a protein required for pullulanase secretion
107. The general secretory pathway of Klebsiella oxytoca: no evidence for relocalization or assembly of pilin‐like PulG protein into a multiprotein complex
108. The role of the lipoprotein sorting signal (aspartate +2) in pullulanase secretion
109. Processing and methylation of PulG, a pilin-like component of the general secretory pathway of Klebsiella oxytoca
110. PuIO, a component of the pullulanase secretion pathway of Klebsiella oxytoca, correctly and efficiently processes gonococcal type IV prepilin in Escherichia coli
111. An enzyme with type IV prepilin peptidase activity is required to process components of the general extracellular protein secretion pathway ofKlebsiella oxytoca
112. MicroMeeting Getting out: protein traffic in prokaryotes.
113. Expression of the endogenous type II secretion pathway in Escherichia coli leads to chitinase secretion.
114. The ChiA (YheB) protein of Escherichia coli K-12 is an endochitinase whose gene is negatively controlled by the nucleoid-structuring protein H-NS.
115. The C-terminal domain of the secretin PulD contains the binding site for its cognate chaperone, PulS, and confers PulS dependence on plVf1 function.
116. Export and secretion of proteins by bacteria.
117. Regulated OmpF porin synthesis in Escherichia coli K-12.
118. On the effect of ompR on colicin E2 production.
119. OmpF porin synthesis in Escherichia coli strains B and K-12 carrying heterologous ompB and/or ompF loci.
120. An enzyme with type IV prepilin peptidase activity is required to process components of the general extracellular protein secretion pathway of Klebsiella oxytoca.
121. Mode of action of diptericin A, a bactericidal peptide induced in the hemolymph of Phormia terranovae larvae.
122. Correlation Between the Expression of an Escherichia coliCell Surface Protein and the Ability of the Protein to Bind to Lipopolysaccharide
123. The BtuB Group Col Plasmids and Homology Between the Colicins They Encode
124. Comparison of Colicins B-K260 and D-CA23: Purification and Characterization of the Colicins and Examination of Colicin Immunity in the Producing Strains
125. Outer Membrane Proteins of Escherichia coliVII. Evidence That Bacteriophage-Directed Protein 2 Functions as a Pore
126. Map location of the cbr gene coding for production of the outer membrane receptor for ferrienterochelin and colicins B and D in Escherichia coli K-12.
127. In vivo effects of local anesthetics on the production of major outer membrane proteins by Escherichia coli
128. On the effect ofompRon colicin E2 production
129. Regulated OmpF porin synthesis inEscherichia coliK-12
130. Outer Membrane Proteins of Escherichia coli VII. Evidence That Bacteriophage-Directed Protein 2 Functions as a Pore
131. Defective growth functions in mutants of Escherichia coli K12 lacking a major outer membrane protein
132. OmpF porin synthesis inEscherichia colistrains B and K-12 carrying heterologousompBand/orompFloci
133. Map location of thecbrgene coding for production of the outer membrane receptor for ferrienterochelin and colicins B and D inEscherichia coliK-12
134. Factors affecting the electrophoretic mobility of the major outer membrane proteins of Escherichia coli in polyacrylamide gels
135. Outer Membrane Targeting of Pseudomonas aeruginosaProteins Shows Variable Dependence on the Components of Bam and Lol Machineries
136. Gram -ve bacteria secrete proteins via an extended general export pathway
137. Prepore Stability Controls Productive Folding of the BAMindependent Multimeric Outer Membrane Secretin PulD.
138. Bacterial Secretins Form Constitutively Open Pores Akin to General Porins.
139. Minor pseudopilin self-assembly primes type II secretion pseudopilus elongation.
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