enhancement: The X‐ray crystal structure of an arylmalonatedecarboxylase (AMDase) with a mechanism‐based inhibitor bound to an active‐site dioxyanion hole provides insight into the mechanism of this intriguing enzyme. The structure also guided the extension of the AMDase biocatalytic repertoire to include a wide range of α‐alkenyl as well as α‐arylmalonates.
[EN] MACROCYCLIC INHIBITORS OF FLAVIVIRIDAE VIRUSES<br/>[FR] INHIBITEURS MACROCYCLIQUES DES VIRUS FLAVIVIRIDAE
申请人:GILEAD SCIENCES INC
公开号:WO2013185103A1
公开(公告)日:2013-12-12
Provided are compounds of Formula I: and pharmaceutically acceptable salts and esters thereof. The compounds, compositions, and methods provided are useful for the treatment of virus infections, particularly hepatitis C infections.
Provided are compounds of Formula I:
and pharmaceutically acceptable salts and esters thereof. The compounds, compositions, and methods provided are useful for the treatment of virus infections, particularly hepatitis C infections.
GRIECO, PAUL A.;HON, YUNG SON;PEREZ-MEDRANO, ARTURO, J. AMER. CHEM. SOC., 110,(1988) N 5, 1630-1631
作者:GRIECO, PAUL A.、HON, YUNG SON、PEREZ-MEDRANO, ARTURO
DOI:——
日期:——
MALONATE DECARBOXYLASES FOR INDUSTRIAL APPLICATIONS
申请人:BASF SE
公开号:US20150147800A1
公开(公告)日:2015-05-28
The present invention relates to a method for the enzymatic decarboxylation of malonic acid (propanedioic acid) derivatives catalyzed by enzymes structurally and/or functionally related to arylmalonate decarboxylase (AMDase) as isolated from microorganisms of the genus
Bordetella
. The present invention also relates to novel enzymes with a decarboxylase activity, useful for performing the claimed method, mutants thereof, corresponding coding sequences and expression systems, methods of preparing said novel enzymes, and screening methods for obtaining further suitable enzymes also having said decarboxylase activity.