Zobrazeno 1 - 10
of 121
pro vyhledávání: '"G. M. BLACKBURN"'
Autor:
George W. Mobbs, Adli A. Aziz, Samuel R. Dix, G. M. Blackburn, Sveta E. Sedelnikova, Thomas C. Minshull, Mark J. Dickman, Patrick J. Baker, Sheila Nathan, Mohd Firdaus Raih, David W. Rice
Publikováno v:
Communications Biology, Vol 5, Iss 1, Pp 1-11 (2022)
The crystal structure of the toxin from the pathogenic bacterium Burkholderia pseudomallei in complex with its target, human eIF4A, provides insights into substrate specificity and may facilitate the design of inhibitors for the treatment of melioido
Externí odkaz:
https://doaj.org/article/e58c27ff57b144fda8009caa288cd49d
Publikováno v:
Nucleic Acids in Chemistry and Biology ISBN: 9781788019040
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6fa3c157528f7d2dd41d2b85754b8cef
https://doi.org/10.1039/9781837671328-00627
https://doi.org/10.1039/9781837671328-00627
Autor:
George W, Mobbs, Adli A, Aziz, Samuel R, Dix, G M, Blackburn, Sveta E, Sedelnikova, Thomas C, Minshull, Mark J, Dickman, Patrick J, Baker, Sheila, Nathan, Mohd Firdaus, Raih, David W, Rice
Publikováno v:
Communications biology. 5(1)
Burkholderia pseudomallei lethal factor 1 (BLF1) exhibits site-specific glutamine deamidase activity against the eukaryotic RNA helicase, eIF4A, thereby blocking mammalian protein synthesis. The structure of a complex between BLF1 C94S and human eIF4
Metal fluoride complexes mimic the transferring phosphoryl group in many enzyme-catalyzed reactions. We here employ the trifluoromagnesate transition state analog (TSA) to study a Zika virus NS3h helicase, which uses energy from ATP hydrolysis to reo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62efeb62df8e143d72fedc830ed5454c
https://doi.org/10.26434/chemrxiv.11908401.v1
https://doi.org/10.26434/chemrxiv.11908401.v1
Publikováno v:
Phosphorus, Sulfur, and Silicon and the Related Elements. 191:367-372
Tetraalkyl 1,1,3,3-tetrafluoro-2,2-dihydroxypropane-1,3-bisphosphonates were prepared. The complex 31P{1H}- and 19F-NMR spectra were analyzed as [[A]2X]2 and related systems. Modern methods of auto...
Publikováno v:
Biochemistry (Moscow). 77:1083-1096
Early studies on chemical synthesis of biological molecules can be seen to progress to preparation and biological evaluation of phosphonates as analogues of biological phosphates, with emphasis on their isosteric and isopolar character. Work with suc
Bisphosphonates Are Incorporated into Adenine Nucleotides by Human Aminoacyl-tRNA Synthetase Enzymes
Publikováno v:
Biochemical and Biophysical Research Communications. 224:863-869
Bisphosphonates are synthetic pyrophosphate analogues and are therapeutic inhibitors of bone resorption, although their exact mechanisms of action are unclear. Some bisphosphonates can be metabolised into non-hydrolysable ATP analogues by Dictyosteli
Publikováno v:
Collection of Czechoslovak Chemical Communications. 61:88-91
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 4:2573-2578
Phosphonate analogues of 1,3- bis phosphoglyceric acid, several incorporating non-scissile α-difluoro phosphonates, have been synthesised and their binding to phosphoglycerate kinase measured by NMR analysis. The tetrafluoroamide analogue ( 4 ) of 1
Publikováno v:
Biochemistry. 33:235-240
The different patterns of enzymatic cleavage of diadenosine polyphosphates, ApnAs, where n = 3-5, have been established by fast atom bombardment mass spectrometry, FAB MS, of the nucleotide products formed in the presence of H2(18)O. The three specif