Results 21 to 30 of about 420,970 (290)

The Role of Carbohydrate in Maintaining Extensin in an Extended Conformation [PDF]

open access: yesPlant Physiology, 1986
Monomers of the plant cell wall glycoprotein extensin are secreted into the wall where they become cross-linked to each other to form a rigid matrix. Expression of the extensin matrix is correlated with the inhibition of further cell elongation during normal development, with increased resistance to virulent pathogens and with other physiological ...
J P, Stafstrom, L A, Staehelin
openaire   +2 more sources

Silyl-protective groups influencing the reactivity and selectivity in glycosylations

open access: yesBeilstein Journal of Organic Chemistry, 2017
Silyl groups such as TBDPS, TBDMS, TIPS or TMS are well-known and widely used alcohol protective groups in organic chemistry. Cyclic silylene protective groups are also becoming increasingly popular. In carbohydrate chemistry silyl protective groups have
Mikael Bols, Christian Marcus Pedersen
doaj   +1 more source

Multicentered hydrogen bonding in 1-[(1-deoxy-β-d-fructopyranos-1-yl)azaniumyl]cyclopentanecarboxylate (`d-fructose-cycloleucine')

open access: yesActa Crystallographica Section E: Crystallographic Communications, 2019
The title compound, C12H21NO7, (I), is conformationally unstable; the predominant form present in its solution is the β-pyranose form (74.3%), followed by the β- and α-furanoses (12.1 and 10.2%, respectively), α-pyranose (3.4%), and traces of the acyclic
Valeri V. Mossine   +2 more
doaj   +1 more source

Conformational studies on the N‐linked carbohydrate chain of bromelain [PDF]

open access: yesEuropean Journal of Biochemistry, 1990
1H‐ and 13C‐NMR assignments for the carbohydrate part of the glycopeptide α‐d‐Man‐(1→6)‐[ß‐d‐Xyl‐(1→2)]‐ß‐d‐Man‐(1→4)‐ß‐d‐GlcNAc‐(1→4)‐[α‐l‐Fuc‐(1→3)]‐ß‐d‐ GlcNAc‐(1→N)‐Asn∼, derived from the proteolytic enzyme bromelain (EC 3.4.22.4), have been obtained using homo‐ and heteronuclear correlation spectroscopy, two‐dimensional homonuclear Hartmann‐Hahn ...
Vliegenthart, J.F.G.   +5 more
openaire   +3 more sources

Carbohydrate–carbohydrate interaction provides adhesion force and specificity for cellular recognition [PDF]

open access: yes, 2004
© 2004 Bucior et al. This article is distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported License. The definitive version was published in Journal of Cell Biology 165 (2004): 529-537, doi:10.1083/jcb ...
Bucior, Iwona   +15 more
core   +1 more source

Roles of adenine methylation in the physiology of Lacticaseibacillus paracasei

open access: yesNature Communications, 2023
Lacticaseibacillus paracasei is an economically important bacterial species, used in the food industry and as a probiotic. Here, we investigate the roles of N6-methyladenine (6mA) modification in L.
Jie Zhao   +9 more
doaj   +1 more source

1-Deoxy-1-(N-methyl-4-fluorophenylamino)-d-arabino-hexulose

open access: yesIUCrData, 2018
The title compound, C13H18FNO5, consists of d-fructose with an aromatic amine. The carbohydrate chain is in the acyclic keto form and has the zigzag conformation, while the solid-state NMR data suggests a conformational dimorphism at the aromatic amine ...
Valeri V. Mossine   +2 more
doaj   +1 more source

Comparative Molecular Modelling of Capsular Polysaccharide Conformations in Streptococcus suis Serotypes 1, 2, 1/2 and 14 Identifies Common Epitopes for Antibody Binding

open access: yesFrontiers in Molecular Biosciences, 2022
Streptococcus suis is an encapsulated, commensal, potentially pathogenic bacterium that infects swine globally and causes sporadic life-threatening zoonotic septicemia and meningitis infections in humans.
Michelle M. Kuttel
doaj   +1 more source

Crystal structure of 4-nitrophenyl 6-O-ethyl-β-d-galactopyranoside monohydrate

open access: yesActa Crystallographica Section E: Crystallographic Communications, 2017
The synthesis and crystal structure of the title compound, C14H19NO8·H2O, prepared in three steps from 6-O-ethyl-1,2;3,4-di-O-isopropylidene-α-d-galactopyranose using protecting-group strategies employed in carbohydrate chemistry, is reported.
Bruno Leonardo Silva   +2 more
doaj   +1 more source

GAG-DB, the New Interface of the Three-Dimensional Landscape of Glycosaminoglycans

open access: yesBiomolecules, 2020
Glycosaminoglycans (GAGs) are complex linear polysaccharides. GAG-DB is a curated database that classifies the three-dimensional features of the six mammalian GAGs (chondroitin sulfate, dermatan sulfate, heparin, heparan sulfate, hyaluronan, and keratan ...
Serge Pérez   +5 more
doaj   +1 more source

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