Zobrazeno 1 - 10
of 53
pro vyhledávání: '"Leonid L., Danilov"'
Autor:
Leonid L. Danilov, Vladimir I. Torgov, Inka Brockhausen, Alexander Kocev, Vladimir V. Veselovsky, Jacob Melamed
Publikováno v:
Glycobiology. 30:9003-9014
The O antigen of enterotoxigenic Escherichia coli serotype O117 consists of repeating units with the structure [-D-GalNAcβ1-3-L-Rhaα1-4-D-Glcα1-4-D-Galβ1-3-D-GalNAcα1-4]n. A related structure is found in E. coli O107 where Glc is replaced by a G
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a91c5458402fb969ce8e4c277278b3c4
https://doi.org/10.1093/glycob/cwaa045
https://doi.org/10.1093/glycob/cwaa045
Autor:
Elaine Adair, Helge C. Dorfmueller, Azul Zorzoli, Vladimir I. Torgov, Benjamin H. Meyer, Vladimir V. Veselovsky, Leonid L. Danilov, Dušan Uhrín
Publikováno v:
Journal of Biological Chemistry. 294:15237-15256
Group A carbohydrate (GAC) is a bacterial peptidoglycan-anchored surface rhamnose polysaccharide (RhaPS) that is essential for growth of Streptococcus pyogenes and contributes to its ability to infect the human host. In this study, using molecular an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e22340a74f17ec7ef47124bfdb5d759
https://doi.org/10.1074/jbc.ra119.009894
https://doi.org/10.1074/jbc.ra119.009894
Autor:
Leonid L. Danilov, Inka Brockhausen, Vladimir V. Veselovsky, N. S. Utkina, Vladimir I. Torgov
Publikováno v:
Carbohydrate Research. :19-25
Two new phenoxyundecyl diphosphate sugars were synthesized for the first time: P1-(11-phenoxyundecyl)-P2- (2-acetamido-2-deoxy-3-O-α-D-rhamnopyranosyl-α-D-glucopyranosyl) diphosphate and P1-(11-phenoxyundecyl)-P2-(2-acetamido-2-deoxy-3-O-β-D-galac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d11918ff4ad5cb9cd546f49a2570a9d1
https://doi.org/10.1016/j.carres.2017.10.016
https://doi.org/10.1016/j.carres.2017.10.016
Autor:
Azul, Zorzoli, Benjamin H, Meyer, Elaine, Adair, Vladimir I, Torgov, Vladimir V, Veselovsky, Leonid L, Danilov, Dusan, Uhrin, Helge C, Dorfmueller
Publikováno v:
The Journal of Biological Chemistry
Group A carbohydrate (GAC) is a bacterial peptidoglycan-anchored surface rhamnose polysaccharide (RhaPS) that is essential for growth of Streptococcus pyogenes and contributes to its ability to infect the human host. In this study, using molecular an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f13b8cbb4f37e7666c563ec9ae00a13f
https://pubmed.ncbi.nlm.nih.gov/31506299
https://pubmed.ncbi.nlm.nih.gov/31506299
Autor:
Inka Brockhausen, Vladimir I. Torgov, N. S. Utkina, Vladimir V. Veselovsky, Alexander Kocev, Leonid L. Danilov
Publikováno v:
Methods in Molecular Biology ISBN: 9781493991532
The biosynthesis of O antigenic polysaccharides in enteric bacteria from nucleoside diphosphate sugars (donor substrates) is catalyzed by the corresponding glycosyltransferases and proceeds through the intermediate formation of undecaprenyl diphospha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bf6b3c61da241deb6f57c6e733fc332c
https://doi.org/10.1007/978-1-4939-9154-9_13
https://doi.org/10.1007/978-1-4939-9154-9_13
Autor:
Dawei Zhou, Leonid L. Danilov, Xi Hou, Vladimir I. Torgov, Lu Feng, Chao Chen, Bin Liu, N. S. Utkina, Vladimir V. Veselovsky
Publikováno v:
Carbohydrate research.
Glycosyltransferases (GTs) catalyze the formation of regio- and stereospecific glycosidic linkages between specific sugar donors and recipients. In this study, the function of the wfcD gene from the Escherichia coli O141 O-antigen gene cluster encodi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21866f32e53ae9d9f1c2982c3a4e9753
https://pubmed.ncbi.nlm.nih.gov/28402841
https://pubmed.ncbi.nlm.nih.gov/28402841
Autor:
Leonid L. Danilov, N. S. Utkina, Vladimir I. Torgov, Vladimir V. Veselovsky, N. M. Balagurova, N. A. Kalinchuk, A. N. Vinnikova, Druzhinina Tn
Publikováno v:
Russian Journal of Bioorganic Chemistry. 40:89-96
11-[(2-Pyridyl)amino]undecyl phosphate and 11-[(9-anthracenylcarbonyl)amino]undecyl phosphate were chemically synthesized. The abiliy of these new fluorescent derivatives of undecyl phosphate to serve as acceptor substrate of galactosyl phosphate res
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::502159b81f93399b19d2a12a218b64d0
https://doi.org/10.1134/s1068162014010038
https://doi.org/10.1134/s1068162014010038
Publikováno v:
Journal of Separation Science. 39:525-527
A reversed-phase ion-pair high-performance liquid chromatography procedure was developed for the separation of polyprenyl diphosphate oligomer homologues obtained chemically from plant polyprenols. Tetrabutylammonium phosphate was used as the ion-pai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fb495fd7aad8ce50bd9c366be55fde93
https://doi.org/10.1002/jssc.201501098
https://doi.org/10.1002/jssc.201501098
Publikováno v:
Archivum Immunologiae et Therapiae Experimentalis
The ability of plant polyisoprenoids (polyprenols and polyprenyl phosphates) to diminish the levels of serum cholesterol affecting its biosynthetic pathway are highlighted here. Possible mechanism of such process is discussed. It is also noted that p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07fcf6d001e153851969c6e0ea38a61c
https://doi.org/10.1007/s00005-013-0253-y
https://doi.org/10.1007/s00005-013-0253-y
Autor:
Lei Wang, Inka Brockhausen, Vladimir I. Torgov, Druzhinina Tn, N. S. Utkina, Vladimir V. Veselovsky, Leonid L. Danilov, Bin Liu, A. N. Vinnikova, Shuo Wang
Publikováno v:
Carbohydrate Research. 366:17-24
The assembly of the repeating units of O-antigens in Gram negative bacteria is catalyzed by specific glycosyltransferases. Previously we used GlcNAc/GalNAcα-diphosphate-phenoxyundecyl as natural acceptor substrate analogs in assays of the transfer o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81a8ff147f81c7322b3b8a87cf8719e4
https://doi.org/10.1016/j.carres.2012.11.009
https://doi.org/10.1016/j.carres.2012.11.009