The structural biology of enzymes involved in natural product glycosylation

S Singh, GN Phillips Jr, JS Thorson - Natural Product Reports, 2012 - pubs.rsc.org
Covering: up to 2012 The glycosylation of microbial natural products often dramatically
influences the biological and/or pharmacological activities of the parental metabolite. Over …

Structure, mechanism, and dynamics of UDP-galactopyranose mutase

JJ Tanner, L Boechi, JA McCammon… - Archives of biochemistry …, 2014 - Elsevier
The flavoenzyme UDP-galactopyranose mutase (UGM) is a key enzyme in galactofuranose
biosynthesis. The enzyme catalyzes the 6-to-5 ring contraction of UDP-galactopyranose to …

Structural Basis of Ligand Binding to UDP-Galactopyranose Mutase from Mycobacterium tuberculosis Using Substrate and Tetrafluorinated Substrate Analogues

KE Van Straaten, JRA Kuttiyatveetil… - Journal of the …, 2015 - ACS Publications
UDP-Galactopyranose mutase (UGM) is a flavin-containing enzyme that catalyzes the
reversible conversion of UDP-galactopyranose (UDP-Gal p) to UDP-galactofuranose (UDP …

Cell-free synthetic glycobiology: designing and engineering glycomolecules outside of living cells

T Jaroentomeechai, MN Taw, M Li, A Aquino… - Frontiers in …, 2020 - frontiersin.org
Glycans and glycosylated biomolecules are directly involved in almost every biological
process as well as the etiology of most major diseases. Hence, glycoscience knowledge is …

Recent advances in the enzymatic synthesis of sugar-nucleotides using nucleotidylyltransferases and glycosyltransferases

S Ahmadipour, L Beswick, GJ Miller - Carbohydrate Research, 2018 - Elsevier
Sugar-nucleotides are imperative to carbohydrate metabolism and glycoconjugate
biosynthesis. Enzymatic methods to access these key materials offer a powerful alternative …

Natural and Synthetic Flavonoids as Potent Mycobacterium tuberculosis UGM Inhibitors

SA Villaume, J Fu, I N'Go, H Liang… - … A European Journal, 2017 - Wiley Online Library
This study reports a novel class of inhibitors of uridine 5′‐diphosphate (UDP)
galactopyranose mutase (UGM) derived from a screening of natural products. This enzyme …

[HTML][HTML] Identification of the furanose ring conformations and the factors driving their adoption

D Walczak, A Sikorski, D Grzywacz, A Nowacki… - Carbohydrate …, 2023 - Elsevier
Three groups of furanoses with restricted freedom of rotation on the C3–C4, C2–C3, and C1–
C2 bonds, respectively, are presented. Conformational analysis of these furanoses is …

Virtual screening for UDP-galactopyranose mutase ligands identifies a new class of antimycobacterial agents

VA Kincaid, N London, K Wangkanont… - ACS chemical …, 2015 - ACS Publications
Galactofuranose (Gal f) is present in glycans critical for the virulence and viability of several
pathogenic microbes, including Mycobacterium tuberculosis, yet the monosaccharide is …

N5 is the new C4a: biochemical functionalization of reduced flavins at the N5 position

BA Beaupre, GR Moran - Frontiers in Molecular Biosciences, 2020 - frontiersin.org
For three decades the C4a-position of reduced flavins was the known site for covalency
within flavoenzymes. The reactivity of this position of the reduced isoalloxazine ring with the …

Identification of novel inhibitors against UDP‐galactopyranose mutase to combat leishmaniasis

M Kashif, S Tabrez, A Husein, M Arish… - Journal of Cellular …, 2018 - Wiley Online Library
Leishmania, a protozoan parasite that causes leishmaniasis, affects 1‐2 million people
every year worldwide. Leishmaniasis is a vector born disease and characterized by a …