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Welcome to the Pubget Medical Subject Headings (MESH) browser. Click on a topic or subtopic below to explore related papers. In the gold box is the most recent paper about the current MESH term, and below are 20 related papers.
Locomotion (1):
Recent article
Locomotion
Molecular Microbiology (77)1 2010
Abstract
We performed mutational analysis of the predicted J-domain, central acidic and proline-rich (APR) domain, and C-terminal domain of TopJ and assessed the phenotypic consequences when introduced into an M. pneumoniae topJ mutant. A TopJ derivative with amino acid substitutions in the canonical J-domai...
|
PMID: 20487283
PDF is available here.
PDF is available here.
| < More recent | Older article > |
Molecular Microbiology (77)1 2010
Abstract
We identify and characterize a phosphodiesterase (BB0363). BB0363 specifically hydrolyzed cyclic-di-GMP with a K(m) of 0.054 microM, confirming it is a functional cyclic-di-GMP phosphodiesterase. A targeted mutation in bb0363 was constructed using a newly developed promoterless antibiotic cassette t...
|
PMID: 20444101
PDF is available here.
PDF is available here.
Molecular Microbiology (77)1 2010
Abstract
We performed mutational analysis of the predicted J-domain, central acidic and proline-rich (APR) domain, and C-terminal domain of TopJ and assessed the phenotypic consequences when introduced into an M. pneumoniae topJ mutant. A TopJ derivative with amino acid substitutions in the canonical J-domai...
|
PMID: 20487283
PDF is available here.
PDF is available here.
Molecular Microbiology (77)1 2010
Abstract
We identify and characterize a phosphodiesterase (BB0363). BB0363 specifically hydrolyzed cyclic-di-GMP with a K(m) of 0.054 microM, confirming it is a functional cyclic-di-GMP phosphodiesterase. A targeted mutation in bb0363 was constructed using a newly developed promoterless antibiotic cassette t...
|
PMID: 20444101
PDF is available here.
PDF is available here.
Molecular Microbiology (77)1 2010
Abstract
We performed mutational analysis of the predicted J-domain, central acidic and proline-rich (APR) domain, and C-terminal domain of TopJ and assessed the phenotypic consequences when introduced into an M. pneumoniae topJ mutant. A TopJ derivative with amino acid substitutions in the canonical J-domai...
|
PMID: 20487283
PDF is available here.
PDF is available here.
Molecular Microbiology (77)1 2010
Abstract
We identify and characterize a phosphodiesterase (BB0363). BB0363 specifically hydrolyzed cyclic-di-GMP with a K(m) of 0.054 microM, confirming it is a functional cyclic-di-GMP phosphodiesterase. A targeted mutation in bb0363 was constructed using a newly developed promoterless antibiotic cassette t...
|
PMID: 20444101
PDF is available here.
PDF is available here.
Molecular Microbiology (77)1 2010
Abstract
We performed mutational analysis of the predicted J-domain, central acidic and proline-rich (APR) domain, and C-terminal domain of TopJ and assessed the phenotypic consequences when introduced into an M. pneumoniae topJ mutant. A TopJ derivative with amino acid substitutions in the canonical J-domai...
|
PMID: 20487283
PDF is available here.
PDF is available here.
Molecular Microbiology (77)1 2010
Abstract
We identify and characterize a phosphodiesterase (BB0363). BB0363 specifically hydrolyzed cyclic-di-GMP with a K(m) of 0.054 microM, confirming it is a functional cyclic-di-GMP phosphodiesterase. A targeted mutation in bb0363 was constructed using a newly developed promoterless antibiotic cassette t...
|
PMID: 20444101
PDF is available here.
PDF is available here.
Molecular Microbiology (77)1 2010
Abstract
We performed mutational analysis of the predicted J-domain, central acidic and proline-rich (APR) domain, and C-terminal domain of TopJ and assessed the phenotypic consequences when introduced into an M. pneumoniae topJ mutant. A TopJ derivative with amino acid substitutions in the canonical J-domai...
|
PMID: 20487283
PDF is available here.
PDF is available here.
Molecular Microbiology (77)1 2010
Abstract
We identify and characterize a phosphodiesterase (BB0363). BB0363 specifically hydrolyzed cyclic-di-GMP with a K(m) of 0.054 microM, confirming it is a functional cyclic-di-GMP phosphodiesterase. A targeted mutation in bb0363 was constructed using a newly developed promoterless antibiotic cassette t...
|
PMID: 20444101
PDF is available here.
PDF is available here.
Molecular Microbiology (77)1 2010
Abstract
We performed mutational analysis of the predicted J-domain, central acidic and proline-rich (APR) domain, and C-terminal domain of TopJ and assessed the phenotypic consequences when introduced into an M. pneumoniae topJ mutant. A TopJ derivative with amino acid substitutions in the canonical J-domai...
|
PMID: 20487283
PDF is available here.
PDF is available here.
Molecular Microbiology (77)1 2010
Abstract
We identify and characterize a phosphodiesterase (BB0363). BB0363 specifically hydrolyzed cyclic-di-GMP with a K(m) of 0.054 microM, confirming it is a functional cyclic-di-GMP phosphodiesterase. A targeted mutation in bb0363 was constructed using a newly developed promoterless antibiotic cassette t...
|
PMID: 20444101
PDF is available here.
PDF is available here.
Molecular Microbiology (77)1 2010
Abstract
We performed mutational analysis of the predicted J-domain, central acidic and proline-rich (APR) domain, and C-terminal domain of TopJ and assessed the phenotypic consequences when introduced into an M. pneumoniae topJ mutant. A TopJ derivative with amino acid substitutions in the canonical J-domai...
|
PMID: 20487283
PDF is available here.
PDF is available here.
Molecular Microbiology (77)1 2010
Abstract
We identify and characterize a phosphodiesterase (BB0363). BB0363 specifically hydrolyzed cyclic-di-GMP with a K(m) of 0.054 microM, confirming it is a functional cyclic-di-GMP phosphodiesterase. A targeted mutation in bb0363 was constructed using a newly developed promoterless antibiotic cassette t...
|
PMID: 20444101
PDF is available here.
PDF is available here.
Molecular Microbiology (77)1 2010
Abstract
We performed mutational analysis of the predicted J-domain, central acidic and proline-rich (APR) domain, and C-terminal domain of TopJ and assessed the phenotypic consequences when introduced into an M. pneumoniae topJ mutant. A TopJ derivative with amino acid substitutions in the canonical J-domai...
|
PMID: 20487283
PDF is available here.
PDF is available here.
Molecular Microbiology (77)1 2010
Abstract
We identify and characterize a phosphodiesterase (BB0363). BB0363 specifically hydrolyzed cyclic-di-GMP with a K(m) of 0.054 microM, confirming it is a functional cyclic-di-GMP phosphodiesterase. A targeted mutation in bb0363 was constructed using a newly developed promoterless antibiotic cassette t...
|
PMID: 20444101
PDF is available here.
PDF is available here.
Molecular Microbiology (77)1 2010
Abstract
We identify and characterize a phosphodiesterase (BB0363). BB0363 specifically hydrolyzed cyclic-di-GMP with a K(m) of 0.054 microM, confirming it is a functional cyclic-di-GMP phosphodiesterase. A targeted mutation in bb0363 was constructed using a newly developed promoterless antibiotic cassette t...
|
PMID: 20444101
PDF is available here.
PDF is available here.
Molecular Microbiology (77)1 2010
Abstract
We performed mutational analysis of the predicted J-domain, central acidic and proline-rich (APR) domain, and C-terminal domain of TopJ and assessed the phenotypic consequences when introduced into an M. pneumoniae topJ mutant. A TopJ derivative with amino acid substitutions in the canonical J-domai...
|
PMID: 20487283
PDF is available here.
PDF is available here.
Molecular Microbiology (77)1 2010
Abstract
We performed mutational analysis of the predicted J-domain, central acidic and proline-rich (APR) domain, and C-terminal domain of TopJ and assessed the phenotypic consequences when introduced into an M. pneumoniae topJ mutant. A TopJ derivative with amino acid substitutions in the canonical J-domai...
|
PMID: 20487283
PDF is available here.
PDF is available here.
Molecular Microbiology (77)1 2010
Abstract
We identify and characterize a phosphodiesterase (BB0363). BB0363 specifically hydrolyzed cyclic-di-GMP with a K(m) of 0.054 microM, confirming it is a functional cyclic-di-GMP phosphodiesterase. A targeted mutation in bb0363 was constructed using a newly developed promoterless antibiotic cassette t...
|
PMID: 20444101
PDF is available here.
PDF is available here.
Molecular Microbiology (77)1 2010
Abstract
We performed mutational analysis of the predicted J-domain, central acidic and proline-rich (APR) domain, and C-terminal domain of TopJ and assessed the phenotypic consequences when introduced into an M. pneumoniae topJ mutant. A TopJ derivative with amino acid substitutions in the canonical J-domai...
|
PMID: 20487283
PDF is available here.
PDF is available here.
Molecular Microbiology (77)1 2010
Abstract
We identify and characterize a phosphodiesterase (BB0363). BB0363 specifically hydrolyzed cyclic-di-GMP with a K(m) of 0.054 microM, confirming it is a functional cyclic-di-GMP phosphodiesterase. A targeted mutation in bb0363 was constructed using a newly developed promoterless antibiotic cassette t...
|
PMID: 20444101
PDF is available here.
PDF is available here.
Molecular Microbiology (77)1 2010
Abstract
We performed mutational analysis of the predicted J-domain, central acidic and proline-rich (APR) domain, and C-terminal domain of TopJ and assessed the phenotypic consequences when introduced into an M. pneumoniae topJ mutant. A TopJ derivative with amino acid substitutions in the canonical J-domai...
|
PMID: 20487283
PDF is available here.
PDF is available here.
Molecular Microbiology (77)1 2010
Abstract
We identify and characterize a phosphodiesterase (BB0363). BB0363 specifically hydrolyzed cyclic-di-GMP with a K(m) of 0.054 microM, confirming it is a functional cyclic-di-GMP phosphodiesterase. A targeted mutation in bb0363 was constructed using a newly developed promoterless antibiotic cassette t...
|
PMID: 20444101
PDF is available here.
PDF is available here.
Molecular Microbiology (77)1 2010
Abstract
We performed mutational analysis of the predicted J-domain, central acidic and proline-rich (APR) domain, and C-terminal domain of TopJ and assessed the phenotypic consequences when introduced into an M. pneumoniae topJ mutant. A TopJ derivative with amino acid substitutions in the canonical J-domai...
|
PMID: 20487283
PDF is available here.
PDF is available here.