scholarly journals Role of Subunit D in Ubiquinone-Binding Site of Vibrio cholerae NQR: Pocket Flexibility and Inhibitor Resistance

ACS Omega ◽  
2019 ◽  
Vol 4 (21) ◽  
pp. 19324-19331 ◽  
Author(s):  
Daniel A. Raba ◽  
Ming Yuan ◽  
Xuan Fang ◽  
William M. Menzer ◽  
Bing Xie ◽  
...  
Keyword(s):  
Binding Site ◽  
Vibrio Cholerae ◽  
Inhibitor Resistance ◽  
Ubiquinone Binding

scholarly journals The Role of Glycine Residues 140 and 141 of Subunit B in the Functional Ubiquinone Binding Site of the Na+-pumping NADH:quinone Oxidoreductase fromVibrio cholerae

2012 ◽  
Vol 287 (30) ◽  
pp. 25678-25685 ◽  
Author(s):  
Oscar Juárez ◽  
Yashvin Neehaul ◽  
Erin Turk ◽  
Najat Chahboun ◽  
Jessica M. DeMicco ◽  
...  
Keyword(s):  
Binding Site ◽  
Nadh:Quinone Oxidoreductase ◽  
Subunit B ◽  
Ubiquinone Binding

scholarly journals Ubiquinone-binding site mutagenesis reveals the role of mitochondrial complex II in cell death initiation

2015 ◽  
Vol 6 (5) ◽  
pp. e1749-e1749 ◽  
Author(s):  
K Kluckova ◽  
M Sticha ◽  
J Cerny ◽  
T Mracek ◽  
L Dong ◽  
...  
Keyword(s):  
Cell Death ◽  
Binding Site ◽  
Mitochondrial Complex ◽  
Complex Ii ◽  
Site Mutagenesis ◽  
Ubiquinone Binding

Cell-specific regulation of IRS-1 gene expression: role of E box and C/EBP binding site in HepG2 cells and CHO cells

Diabetes ◽  
1997 ◽  
Vol 46 (3) ◽  
pp. 354-362 ◽  
Author(s):  
K. Matsuda ◽  
E. Araki ◽  
R. Yoshimura ◽  
K. Tsuruzoe ◽  
N. Furukawa ◽  
...  
Keyword(s):  
Gene Expression ◽  
Binding Site ◽  
Cho Cells ◽  
Hepg2 Cells ◽  
E Box ◽  
Specific Regulation

scholarly journals Excision and transposition of Tn5 as an SOS activity in Escherichia coli.

Genetics ◽  
1991 ◽  
Vol 128 (1) ◽  
pp. 45-57 ◽  
Author(s):  
C T Kuan ◽  
S K Liu ◽  
I Tessman
Keyword(s):  
Escherichia Coli ◽  
Binding Site ◽  
Reca Protein ◽  
Precursor Molecule ◽  
Functional Integrity ◽  
Lexa Protein ◽  
Lexa Binding ◽  
Additional Role ◽  
Stimulation Of

Abstract Excision and transposition of the Tn5 element in Escherichia coli ordinarily appear to occur by recA-independent mechanisms. However, recA(Prtc) genes, which encode RecA proteins that are constitutively activated to the protease state, greatly enhanced excision and transposition; both events appeared to occur concomitantly and without destruction of the donor DNA. The recombinase function of the RecA protein was not required. Transposition was accompanied by partial, and occasionally full, restoration of the functional integrity of the gene vacated by the excised Tn5. The stimulation of transposition was inhibited by an uncleavable LexA protein and was strongly enhanced by an additional role of the RecA(Prtc) protein besides its mediation of LexA cleavage. To account for the enhanced transposition, we suggest that (i) there may be a LexA binding site within the promoter for the IS50 transposase, (ii) activated RecA may cleave the IS50 transposition inhibitor, and (iii) the transposase may be formed by RecA cleavage of a precursor molecule.

The role of Glu196 in the environment around the substrate binding site of leucine aminopeptidase fromStreptomyces griseus

FEBS Letters ◽  
2006 ◽  
Vol 580 (3) ◽  
pp. 912-917 ◽  
Author(s):  
Jiro Arima ◽  
Yoshiko Uesugi ◽  
Misugi Uraji ◽  
Masaki Iwabuchi ◽  
Tadashi Hatanaka
Keyword(s):  
Binding Site ◽  
Leucine Aminopeptidase ◽  
Substrate Binding ◽  
Substrate Binding Site
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