Literature DB >> 2681202

Mannose permease of Escherichia coli. Domain structure and function of the phosphorylating subunit.

B Erni1, B Zanolari, P Graff, H P Kocher.   

Abstract

The mannose permease of Escherichia coli is a component of the phosphotransferase system. It transports mannose and related hexoses by a mechanism that couples sugar transport with sugar phosphorylation. It is a complex consisting of two transmembrane subunits (II-PMan and II-MMan) and a hydrophilic subunit (IIIMan). IIIMan also exists in a soluble form as dimer in the cytoplasm. Each monomer of IIIMan consists of two structurally and functionally distinct domains which are linked by a flexible hinge of the sequence KAAPAPAAAAPKAAPTPAKP. Both domains are transiently phosphorylated. The NH2-terminal domain (P13) is phosphorylated at N-3 of His-10 by the cytoplasmic phosphorylcarrier protein phospho-HPr. The COOH-terminal domain (P20) is phosphorylated by P13 at N-1 of His-175. Phosphoryltransfer occurs not only between P13 and P20 on the same IIIMan subunit but also between isolated domains and between domains on different subunits of the dimer. In the presence of the IIMan subunits, the phosphoryl group is directly transferred from His-175 of P20 to the sugar substrates of the permease. The P13 domain contains the contact sites for dimerization of IIIMan. The P20 domain contains the contact sites for interaction with the IIMan subunits. By reconstructing the ptsL gene, the two domains were expressed as individual polypeptides and the length of the hinge between P13 and P20 was changed. The in vivo and in vitro activities of mutant IIIMan were little affected by these modifications. The hinge is highly sensitive to proteolytic cleavage in vitro and its specificity for proteases can be modified by introducing the appropriate specificity determinants.

Entities:  

Mesh:

Substances:

Year:  1989        PMID: 2681202

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  23 in total

1.  The dihydroxyacetone kinase of Escherichia coli utilizes a phosphoprotein instead of ATP as phosphoryl donor.

Authors:  R Gutknecht; R Beutler; L F Garcia-Alles; U Baumann; B Erni
Journal:  EMBO J       Date:  2001-05-15       Impact factor: 11.598

2.  Proposed uniform nomenclature for the proteins and protein domains of the bacterial phosphoenolpyruvate: sugar phosphotransferase system.

Authors:  M H Saier; J Reizer
Journal:  J Bacteriol       Date:  1992-03       Impact factor: 3.490

3.  Bactericidal activity of both secreted and nonsecreted microcin E492 requires the mannose permease.

Authors:  Sylvain Bieler; Filo Silva; Claudio Soto; Dominique Belin
Journal:  J Bacteriol       Date:  2006-10       Impact factor: 3.490

Review 4.  Domains in microbial beta-1, 4-glycanases: sequence conservation, function, and enzyme families.

Authors:  N R Gilkes; B Henrissat; D G Kilburn; R C Miller; R A Warren
Journal:  Microbiol Rev       Date:  1991-06

5.  Absence of a putative mannose-specific phosphotransferase system enzyme IIAB component in a leucocin A-resistant strain of Listeria monocytogenes, as shown by two-dimensional sodium dodecyl sulfate-polyacrylamide gel electrophoresis.

Authors:  M Ramnath; M Beukes; K Tamura; J W Hastings
Journal:  Appl Environ Microbiol       Date:  2000-07       Impact factor: 4.792

6.  Characterization of soluble enzyme II complexes of the Escherichia coli phosphotransferase system.

Authors:  Mohammad Aboulwafa; Milton H Saier
Journal:  J Bacteriol       Date:  2004-12       Impact factor: 3.490

7.  Molecular analysis of the phosphoenolpyruvate-dependent L-sorbose: phosphotransferase system from Klebsiella pneumoniae and of its multidomain structure.

Authors:  U F Wehmeier; B M Wöhrl; J W Lengeler
Journal:  Mol Gen Genet       Date:  1995-03-10

8.  Protein structural similarities predicted by a sequence-structure compatibility method.

Authors:  Y Matsuo; K Nishikawa
Journal:  Protein Sci       Date:  1994-11       Impact factor: 6.725

9.  Sinorhizobium meliloti mutants lacking phosphotransferase system enzyme HPr or EIIA are altered in diverse processes, including carbon metabolism, cobalt requirements, and succinoglycan production.

Authors:  Catalina Arango Pinedo; Ryan M Bringhurst; Daniel J Gage
Journal:  J Bacteriol       Date:  2008-02-15       Impact factor: 3.490

10.  Altered utilization of N-acetyl-D-galactosamine by Escherichia coli O157:H7 from the 2006 spinach outbreak.

Authors:  Amit Mukherjee; Mark K Mammel; J Eugene LeClerc; Thomas A Cebula
Journal:  J Bacteriol       Date:  2007-12-21       Impact factor: 3.490

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.