315 related articles for article (PubMed ID: 7574720)
1. Identification of a topology control domain in the tetracycline resistance protein.
Miller KW; Jewell JE
Arch Biochem Biophys; 1995 Oct; 322(2):445-52. PubMed ID: 7574720
[TBL] [Abstract][Full Text] [Related]
2. Membrane protein topology determination by proteolysis of maltose binding protein fusions.
Miller KW; Konen PL; Olson J; Ratanavanich KM
Anal Biochem; 1993 Nov; 215(1):118-28. PubMed ID: 8297003
[TBL] [Abstract][Full Text] [Related]
3. Topological characterization of the essential Escherichia coli cell division protein FtsN.
Dai K; Xu Y; Lutkenhaus J
J Bacteriol; 1996 Mar; 178(5):1328-34. PubMed ID: 8631709
[TBL] [Abstract][Full Text] [Related]
4. Overexpression of bacterio-opsin in Escherichia coli as a water-soluble fusion to maltose binding protein: efficient regeneration of the fusion protein and selective cleavage with trypsin.
Chen GQ; Gouaux JE
Protein Sci; 1996 Mar; 5(3):456-67. PubMed ID: 8868482
[TBL] [Abstract][Full Text] [Related]
5. Activity of protein MalE (maltose-binding protein) fused to cytoplasmic and periplasmic regions of an Escherichia coli inner membrane protein.
Dassa E; Lambert P
Res Microbiol; 1997 Jun; 148(5):389-95. PubMed ID: 9765817
[TBL] [Abstract][Full Text] [Related]
6. Twelve-transmembrane-segment (TMS) version (DeltaTMS VII-VIII) of the 14-TMS Tet(L) antibiotic resistance protein retains monovalent cation transport modes but lacks tetracycline efflux capacity.
Jin J; Guffanti AA; Beck C; Krulwich TA
J Bacteriol; 2001 Apr; 183(8):2667-71. PubMed ID: 11274128
[TBL] [Abstract][Full Text] [Related]
7. Use of phoA and lacZ fusions to study the membrane topology of ProW, a component of the osmoregulated ProU transport system of Escherichia coli.
Haardt M; Bremer E
J Bacteriol; 1996 Sep; 178(18):5370-81. PubMed ID: 8808924
[TBL] [Abstract][Full Text] [Related]
8. Expression of active streptolysin O in Escherichia coli as a maltose-binding-protein--streptolysin-O fusion protein. The N-terminal 70 amino acids are not required for hemolytic activity.
Weller U; Müller L; Messner M; Palmer M; Valeva A; Tranum-Jensen J; Agrawal P; Biermann C; Döbereiner A; Kehoe MA; Bhakdi S
Eur J Biochem; 1996 Feb; 236(1):34-9. PubMed ID: 8617283
[TBL] [Abstract][Full Text] [Related]
9. Membrane topology of the staphylococcal tetracycline efflux protein Tet(K) determined by antibacterial resistance gene fusion.
Hirata T; Fujihira E; Kimura-Someya T; Yamaguchi A
J Biochem; 1998 Dec; 124(6):1206-11. PubMed ID: 9832626
[TBL] [Abstract][Full Text] [Related]
10. Alterations in the hydrophilic segment of the maltose-binding protein (MBP) signal peptide that affect either export or translation of MBP.
Puziss JW; Harvey RJ; Bassford PJ
J Bacteriol; 1992 Oct; 174(20):6488-97. PubMed ID: 1400201
[TBL] [Abstract][Full Text] [Related]
11. Gene fusion approaches to membrane protein topology.
Boyd D; Traxler B; Jander G; Prinz W; Beckwith J
Soc Gen Physiol Ser; 1993; 48():23-37. PubMed ID: 8503047
[No Abstract] [Full Text] [Related]
12. Gene fusion analysis of membrane protein topology: a direct comparison of alkaline phosphatase and beta-lactamase fusions.
Prinz WA; Beckwith J
J Bacteriol; 1994 Oct; 176(20):6410-3. PubMed ID: 7929016
[TBL] [Abstract][Full Text] [Related]
13. Transmembrane topology of the two FhuB domains representing the hydrophobic components of bacterial ABC transporters involved in the uptake of siderophores, haem and vitamin B12.
Groeger W; KOstert W
Microbiology (Reading); 1998 Oct; 144 ( Pt 10)():2759-2769. PubMed ID: 9802017
[TBL] [Abstract][Full Text] [Related]
14. Construction of a tagging system for subcellular localization of proteins encoded by open reading frames.
Chuang CH; Hsu SC; Hsu CL; Hsu TC; Syu WJ
J Biomed Sci; 2001; 8(2):170-5. PubMed ID: 11287747
[TBL] [Abstract][Full Text] [Related]
15. Analysis of the topology of a membrane protein by using a minimum number of alkaline phosphatase fusions.
Boyd D; Traxler B; Beckwith J
J Bacteriol; 1993 Jan; 175(2):553-6. PubMed ID: 8419303
[TBL] [Abstract][Full Text] [Related]
16. Model of maltose-binding protein/chemoreceptor complex supports intrasubunit signaling mechanism.
Zhang Y; Gardina PJ; Kuebler AS; Kang HS; Christopher JA; Manson MD
Proc Natl Acad Sci U S A; 1999 Feb; 96(3):939-44. PubMed ID: 9927672
[TBL] [Abstract][Full Text] [Related]
17. Export of maltose-binding protein species with altered charge distribution surrounding the signal peptide hydrophobic core in Escherichia coli cells harboring prl suppressor mutations.
Puziss JW; Strobel SM; Bassford PJ
J Bacteriol; 1992 Jan; 174(1):92-101. PubMed ID: 1729228
[TBL] [Abstract][Full Text] [Related]
18. Genetic analysis of periplasmic binding protein dependent transport in Escherichia coli. Each lobe of maltose-binding protein interacts with a different subunit of the MalFGK2 membrane transport complex.
Hor LI; Shuman HA
J Mol Biol; 1993 Oct; 233(4):659-70. PubMed ID: 8411172
[TBL] [Abstract][Full Text] [Related]
19. Vectors to facilitate the creation of translational fusions to the maltose-binding protein of Escherichia coli.
Aitken R; Gilchrist J; Sinclair MC
Gene; 1994 Jun; 144(1):69-73. PubMed ID: 8026760
[TBL] [Abstract][Full Text] [Related]
20. Second transmembrane segment of FtsH plays a role in its proteolytic activity and homo-oligomerization.
Makino S; Makino T; Abe K; Hashimoto J; Tatsuta T; Kitagawa M; Mori H; Ogura T; Fujii T; Fushinobu S; Wakagi T; Matsuzawa H
FEBS Lett; 1999 Nov; 460(3):554-8. PubMed ID: 10556534
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
