Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM041978-07
Application #
2181165
Study Section
Microbial Physiology and Genetics Subcommittee 2 (MBC)
Project Start
1989-04-01
Project End
1997-03-31
Budget Start
1995-04-01
Budget End
1997-03-31
Support Year
7
Fiscal Year
1995
Total Cost
Indirect Cost
Name
University of Connecticut
Department
Microbiology/Immun/Virology
Type
Schools of Dentistry
DUNS #
City
Farmington
State
CT
Country
United States
Zip Code
06030
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Justice, S S; Garcia-Lara, J; Rothfield, L I (2000) Cell division inhibitors SulA and MinC/MinD block septum formation at different steps in the assembly of the Escherichia coli division machinery. Mol Microbiol 37:410-23
Rowland, S L; Fu, X; Sayed, M A et al. (2000) Membrane redistribution of the Escherichia coli MinD protein induced by MinE. J Bacteriol 182:613-9
King, G F; Rowland, S L; Pan, B et al. (1999) The dimerization and topological specificity functions of MinE reside in a structurally autonomous C-terminal domain. Mol Microbiol 31:1161-9
King, G F; Pan, B; Maciejewski, M W et al. (1999) Backbone and side-chain 1H, 15N, and 13C assignments for the topological specificity domain of the MinE cell division protein. J Biomol NMR 13:395-6
Zhang, Y; Rowland, S; King, G et al. (1998) The relationship between hetero-oligomer formation and function of the topological specificity domain of the Escherichia coli MinE protein. Mol Microbiol 30:265-73
Zhao, C R; de Boer, P A; Rothfield, L I (1995) Proper placement of the Escherichia coli division site requires two functions that are associated with different domains of the MinE protein. Proc Natl Acad Sci U S A 92:4313-7
Wang, X D; de Boer, P A; Rothfield, L I (1991) A factor that positively regulates cell division by activating transcription of the major cluster of essential cell division genes of Escherichia coli. EMBO J 10:3363-72