Molecular Microbiology · 2002 · 31 citations · 43 references
Life SciencesMicrobiologyMolecular BiologyEnzyme MechanismEnzymologyStructural BiologyBacterial Secretion SystemsEnzyme FunctionEnzyme StructureEnzyme-substrate RecognitionProtein MotifsSecretory PathwayBacterial Secretion StructuresEnzyme Secretion PathwaysEnzyme Secretion SystemsPolygalacturonase ActivityPolysaccharide SecretionProtein Secretion SystemsType Ii Secretion System
Intramolecular information specifying protein secretion through the type II (GSP) pathway of Gram-negative bacteria was investigated. Two regions of the polygalacturonase (PehA) of Erwinia carotovora containing residues proposed to be included in a targeting motif were located, one close to the C-terminus between residues 342 and 369 and another between residues 84 and 135 in the large central loops. The regions were required together to promote secretion. Further residues in the middle of the protein were required for proper positioning of the regions, suggesting that they were both involved in interaction with the GSP. To our knowledge, this is the first time that a possible three-dimensional targeting motif has been defined. At least one of the motifs comprises a cluster on the surface of the protein. The two motifs are structurally dissimilar, suggesting that there are two distinct recognition regions in the GSP apparatus. Finally, we propose that the targeting motifs are of a complex conformational nature with some variability accommodated, as illustrated by the observation that many mutations exhibited no clear phenotype individually but, in combination, severely compromised secretion.
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Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4
Ulrich K. Laemmli · Nature · 1970 · 251.6K citations
Molecular Cloning. A Laboratory Manual
EJ Wood · Biochemical Education · 1983 · 30.6K citations