178 related articles for article (PubMed ID: 15330757)
1. Arginine mutations within a transmembrane domain of Tar, an Escherichia coli aspartate receptor, can drive homodimer dissociation and heterodimer association in vivo.
Sal-Man N; Shai Y
Biochem J; 2005 Jan; 385(Pt 1):29-36. PubMed ID: 15330757
[TBL] [Abstract][Full Text] [Related]
2. The composition rather than position of polar residues (QxxS) drives aspartate receptor transmembrane domain dimerization in vivo.
Sal-Man N; Gerber D; Shai Y
Biochemistry; 2004 Mar; 43(8):2309-13. PubMed ID: 14979727
[TBL] [Abstract][Full Text] [Related]
3. Hetero-assembly between all-L- and all-D-amino acid transmembrane domains: forces involved and implication for inactivation of membrane proteins.
Sal-Man N; Gerber D; Shai Y
J Mol Biol; 2004 Nov; 344(3):855-64. PubMed ID: 15533450
[TBL] [Abstract][Full Text] [Related]
4. Genetic selection for and molecular dynamic modeling of a protein transmembrane domain multimerization motif from a random Escherichia coli genomic library.
Leeds JA; Boyd D; Huber DR; Sonoda GK; Luu HT; Engelman DM; Beckwith J
J Mol Biol; 2001 Oct; 313(1):181-95. PubMed ID: 11601855
[TBL] [Abstract][Full Text] [Related]
5. Transmembrane domain mediated self-assembly of major coat protein subunits from Ff bacteriophage.
Melnyk RA; Partridge AW; Deber CM
J Mol Biol; 2002 Jan; 315(1):63-72. PubMed ID: 11771966
[TBL] [Abstract][Full Text] [Related]
6. An aspartate residue at the extracellular boundary of TMII and an arginine residue in TMVII of the gastrin-releasing peptide receptor interact to facilitate heterotrimeric G protein coupling.
Donohue PJ; Sainz E; Akeson M; Kroog GS; Mantey SA; Battey JF; Jensen RT; Northup JK
Biochemistry; 1999 Jul; 38(29):9366-72. PubMed ID: 10413511
[TBL] [Abstract][Full Text] [Related]
7. Non-native interhelical hydrogen bonds in the cystic fibrosis transmembrane conductance regulator domain modulated by polar mutations.
Choi MY; Cardarelli L; Therien AG; Deber CM
Biochemistry; 2004 Jun; 43(25):8077-83. PubMed ID: 15209503
[TBL] [Abstract][Full Text] [Related]
8. Lambda repressor N-terminal DNA-binding domain as an assay for protein transmembrane segment interactions in vivo.
Leeds JA; Beckwith J
J Mol Biol; 1998 Jul; 280(5):799-810. PubMed ID: 9671551
[TBL] [Abstract][Full Text] [Related]
9. Hydrophobic helical hairpins: design and packing interactions in membrane environments.
Johnson RM; Heslop CL; Deber CM
Biochemistry; 2004 Nov; 43(45):14361-9. PubMed ID: 15533040
[TBL] [Abstract][Full Text] [Related]
10. Characterization of peptides corresponding to the seven transmembrane domains of human adenosine A2a receptor.
Lazarova T; Brewin KA; Stoeber K; Robinson CR
Biochemistry; 2004 Oct; 43(40):12945-54. PubMed ID: 15461468
[TBL] [Abstract][Full Text] [Related]
11. Activation of membrane fusion by murine leukemia viruses is controlled in cis or in trans by interactions between the receptor-binding domain and a conserved disulfide loop of the carboxy terminus of the surface glycoprotein.
Lavillette D; Boson B; Russell SJ; Cosset FL
J Virol; 2001 Apr; 75(8):3685-95. PubMed ID: 11264358
[TBL] [Abstract][Full Text] [Related]
12. Structural adaptation of the glycophorin A transmembrane homodimer to D-amino acid modifications.
Gerber D; Sal-Man N; Shai Y
J Mol Biol; 2004 May; 339(1):243-50. PubMed ID: 15123435
[TBL] [Abstract][Full Text] [Related]
13. D2 dopamine receptor homodimerization is mediated by multiple sites of interaction, including an intermolecular interaction involving transmembrane domain 4.
Lee SP; O'Dowd BF; Rajaram RD; Nguyen T; George SR
Biochemistry; 2003 Sep; 42(37):11023-31. PubMed ID: 12974638
[TBL] [Abstract][Full Text] [Related]
14. Two motifs within a transmembrane domain, one for homodimerization and the other for heterodimerization.
Gerber D; Sal-Man N; Shai Y
J Biol Chem; 2004 May; 279(20):21177-82. PubMed ID: 14985340
[TBL] [Abstract][Full Text] [Related]
15. Identification and functional characterization of the zeta-chain dimerization motif for TCR surface expression.
Bolliger L; Johansson B
J Immunol; 1999 Oct; 163(7):3867-76. PubMed ID: 10490986
[TBL] [Abstract][Full Text] [Related]
16. An arginine residue (Arg101), which is conserved in many GroEL homologues, is required for interactions between the two heptameric rings.
Jones S; Wallington EJ; George R; Lund PA
J Mol Biol; 1998 Oct; 282(4):789-800. PubMed ID: 9743627
[TBL] [Abstract][Full Text] [Related]
17. Motifs of serine and threonine can drive association of transmembrane helices.
Dawson JP; Weinger JS; Engelman DM
J Mol Biol; 2002 Feb; 316(3):799-805. PubMed ID: 11866532
[TBL] [Abstract][Full Text] [Related]
18. Amino-terminal residues 1-45 of the Escherichia coli pyruvate dehydrogenase complex E1 subunit interact with the E2 subunit and are required for activity of the complex but not for reductive acetylation of the E2 subunit.
Park YH; Wei W; Zhou L; Nemeria N; Jordan F
Biochemistry; 2004 Nov; 43(44):14037-46. PubMed ID: 15518552
[TBL] [Abstract][Full Text] [Related]
19. Conformational changes in the cytoplasmic domain of the Escherichia coli aspartate receptor upon adaptive methylation.
Le Moual H; Quang T; Koshland DE
Biochemistry; 1998 Oct; 37(42):14852-9. PubMed ID: 9778360
[TBL] [Abstract][Full Text] [Related]
20. Interactions between charged amino acid residues within transmembrane helices in the sulfate transporter SHST1.
Shelden MC; Loughlin P; Tierney ML; Howitt SM
Biochemistry; 2003 Nov; 42(44):12941-9. PubMed ID: 14596609
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
