Results 61 to 70 of about 3,627 (132)

Functional expression of uridine diphospho glucuronosyltransferases in fission yeast [PDF]

, 2011
Uridine diphospho (UDP) glucuronosyltransferases (UGTs) catalyze the transfer of a sugar moiety from UDP-sugar to endogenous or exogenous compounds. The water solubility of these substances is increased thereby and their excretion from the human body is ...
Buchheit, Daniela
core  

Engineering protein prenylation: an emerging tool for selective protein modification. [PDF]

Biochem Soc Trans
Venkatachalapathy S, Lichtenfels C, Wagner CR, Distefano MD.   +3 more
europepmc   +1 more source

Photocrosslinking and capture for the analysis of carbohydrate-dependent interactions. [PDF]

Bioorg Med Chem Lett
Pratt MR.
europepmc   +1 more source

Bimolecular Homolytic Substitution (S_H2) and Radical Ligand Transfer (RLT): Emerging Paradigms in Radical Transformations. [PDF]

ACS Cent Sci
Fernandes AJ, Katayev D.
europepmc   +1 more source

Vinigrol Tricyclic Scaffold Biosynthesis Employs an Atypical Terpene Cyclase and a Multipotent Cyclization Cascade. [PDF]

J Am Chem Soc
Tsukada K, Sato F, Matsuyama T, Matsuda R, Ozaki T, Morishita Y, Furumura S, Homma Y, Sekiya H, Sugawara A, Kubota M, Mitsuhashi T, Yasuno Y, Shinada T, Nagata R, Kuzuyama T, Taniguchi T, Fujita M, Uchiyama M, Asai T.   +19 more
europepmc   +1 more source

Specific and Multi-Product Clade I and Clade IV Sesquiterpene Synthases Contribute to the Psilocybe cubensis Volatilome. [PDF]

Chembiochem
Schober S, Dorfmann L, Walther K, Blei F, Chadeayne AR, Gressler M, Bartram S, O'Connor SE, Hoffmeister D.   +8 more
europepmc   +1 more source

Host metabolic integration enables superior polystyrene degradation in cockroaches. [PDF]

Environ Sci Ecotechnol
Li MX, Wang YQ, Wang JY, Ding MQ, Yang SS, Ding J, Wu WM.   +6 more
europepmc   +1 more source

Introducing Small Rings into Farnesyl Pyrophosphates Paves the Way for the Enzymatic Generation of Unnatural Sesquiterpene Scaffolds. [PDF]

J Am Chem Soc
Taser D, Victoria C, Garrel LV, Droste J, Tabet C, Dräger G, Hassanin A, Davari MD, Kirschning A.   +8 more
europepmc   +1 more source

EFSA Panel on Food Contact Material, Enzymes, Flavourings and Processing Aids (CEF); Scientific Opinion on Flavouring Group Evaluation 47, Revision 1: Bi- and tricyclic secondary, ketones and related esters from chemical groups 7 and 8 [PDF]

, 2012
Anderson, Austin, Azizan, Banerjee, Boutin, Cinti, Clayton, Clayton, Clayton, Clegg, CoE, Cramer, Dean, Denine, EC, EC, EC, EC, EFFA, EFSA, Fishman, Gaunt, Gibson, Gomes‐Carneiro, Hiroi, Hutson, Hämäläinen, IOFI, Jacobziner, Jakoby, Kopelman, Köppel, Leibman, Leuschner, Marzin, Miller, Nelson, Opdyke, Opdyke, Parke, Phelan, Pryde, Quick, Quick, Reinartz, Riggs, Rimini, Robertson, SCF, Scott, Skramlik, Tamura, TNO, TNO, Wagreich, White, Wild, Williams, Yoo   +58 more
core   +1 more source

Uncrossing the 'X': Characterization of alternative alleles for KSLX in Oryza. [PDF]

Phytochemistry
Weers T, Feng Y, Peters RJ.
europepmc   +1 more source