Zobrazeno 1 - 10
of 24
pro vyhledávání: '"T M, Makarova"'
Autor:
T. M. Makarova
Publikováno v:
Science and Education a New Dimension. :36-40
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fb0f46a9a11b63695d8e64eee8f9bd7b
https://doi.org/10.31174/send-ph2021-260ix76-08
https://doi.org/10.31174/send-ph2021-260ix76-08
Autor:
T. M. Makarova, G. I. Makarov
Publikováno v:
Journal of Computer-Aided Molecular Design. 34:281-291
Linezolid, an antibiotic of oxazolidinone family, is a translation inhibitor. The mechanism of its action that consists in preventing the binding of aminoacyl-tRNA to the A-site of the large subunit of a ribosome was embraced on the basis of the X-ra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a328c1939dc9b6d6607fea0fb3ab5186
https://doi.org/10.1007/s10822-019-00269-x
https://doi.org/10.1007/s10822-019-00269-x
Autor:
T. M. Makarova
Publikováno v:
Humanities science current issues. 2:52-57
Макарова, Т. М. Фреймова модель англійськомовної протестантської проповіді / Т. М. Макарова // Актуальні питання гуманітарних наук. - Дрого
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ad6aa171c5c7b4307e7b807947610749
https://doi.org/10.24919/2308-4863.2/24.176800
https://doi.org/10.24919/2308-4863.2/24.176800
Autor:
T. M. Makarova, G. I. Makarov
Publikováno v:
Biochemistry. Biokhimiia. 85(11)
Ribosome is a molecular machine that synthesizes all cellular proteins. It also is a target of about half of the clinically used antibiotics. Adaptive chemical modification of ribosomal RNAs residues is one of the ways to provide resistance to certai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59cb17833d3ae1b4763ae1ee17f95656
https://pubmed.ncbi.nlm.nih.gov/33280585
https://pubmed.ncbi.nlm.nih.gov/33280585
Autor:
T. M. Makarova, Alexey A. Bogdanov
Publikováno v:
Biochimie. 167
The A site of the ribosome, which determines binding and orientation of a new amino acid residue for the peptidyl transferase reaction, was found to occupy two different conformational states upon the molecular dynamics (MD) simulations study of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b4352e1d7342d279db6038e1c8babf8
https://pubmed.ncbi.nlm.nih.gov/31605738
https://pubmed.ncbi.nlm.nih.gov/31605738
Publikováno v:
Biochemistry (Moscow). 81:1579-1588
The ribosome as a complex molecular machine undergoes significant conformational changes while synthesizing a protein molecule. Molecular dynamics simulations have been used as complementary approaches to X-ray crystallography and cryoelectron micros
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::274354fd52b90dbe623116d63c8925b7
https://doi.org/10.1134/s0006297916130010
https://doi.org/10.1134/s0006297916130010
Autor:
T. M. Makarova, Alexey A. Bogdanov
Publikováno v:
Biochemistry. Biokhimiia. 82(13)
The ribosome as a complex molecular machine undergoes significant conformational rearrangements during the synthesis of polypeptide chains of proteins. In this review, information obtained using various experimental methods on the internal consistenc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19e5ebe0ffa549d9849976672eee495c
https://pubmed.ncbi.nlm.nih.gov/29523059
https://pubmed.ncbi.nlm.nih.gov/29523059
Autor:
T. M. Makarova, G. I. Makarov
Publikováno v:
Biochimica et biophysica acta. General subjects. 1862(12)
Chloramphenicol, an antibiotic belonging to the family of amphenicols, is an inhibitor of translation. On the basis of X-ray structural analysis of the binding of chloramphenicol to free bacterial ribosomes, the chloramphenicol action mechanism that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e336ec7c54fdba38566bae24382e4ddd
https://pubmed.ncbi.nlm.nih.gov/30248377
https://pubmed.ncbi.nlm.nih.gov/30248377
Autor:
G. I. Makarov, Alexey A. Bogdanov, T. M. Makarova, Galina A. Korshunova, A. V. Shishkina, Andrey G Tereshchenkov
Publikováno v:
Biochemistry (Moscow). 80:1500-1507
Using a method of static simulation, a series of erythromycin A analogs was designed with aldehyde functions introduced instead of one of the methyl substituents in the 3'-N-position of the antibiotic that was potentially capable of forming a covalen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32d2a549e59923cabd3217b6683e4b90
https://doi.org/10.1134/s0006297915110127
https://doi.org/10.1134/s0006297915110127
Publikováno v:
Gigiena i sanitariia. (6)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::aac43715a2a361aa547aa2b46d9b1dfb
https://pubmed.ncbi.nlm.nih.gov/16404890
https://pubmed.ncbi.nlm.nih.gov/16404890