Related references
Note: Only part of the references are listed.Altered Enthalpy-Entropy Compensation in Picomolar Transition State Analogues of Human Purine Nucleoside Phosphorylase
Achelle A. Edwards et al.
BIOCHEMISTRY (2009)
Transition States of Plasmodium falciparum and Human Orotate Phosphoribosyltransferases
Yong Zhang et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2009)
Role for α-L-fucosidase in the control of Helicobacter pylori-infected gastric cancer cells
Ta-Wei Liu et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2009)
Structural analysis of Golgi α-mannosidase II inhibitors identified from a focused glycosidase inhibitor screen
Douglas A. Kuntz et al.
BIOCHEMISTRY (2008)
Glycosidase inhibition: An assessment of the binding of 18 putative transition-state mimics
Tracey M. Gloster et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2007)
The structural basis of glycosidase inhibition by five-membered iminocyclitols:: The clan a glycoside hydrolase endoglycoceramidase as a model system
Matthew E. C. Caines et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2007)
Structural, kinetic, and thermodynamic analysis of glucoimidazole-derived glycosidase inhibitors
Tracey M. Gloster et al.
BIOCHEMISTRY (2006)
Restrained molecular dynamics simulations of HIV-1 protease: The first step in validating a new target for drug design
AL Perryman et al.
BIOPOLYMERS (2006)
Discovery of different types of inhibition between the human and Thermotoga maritima α-fucosidases by fuconojirimycin-based derivatives
Ching-Wen Ho et al.
BIOCHEMISTRY (2006)
Expanding the thioglycoligase strategy to the synthesis of α-linked thioglycosides allows structural investigation of the parent enzyme/substrate complex
YW Kim et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2006)
Femtomolar transition state analogue inhibitors of 5′-methylthioadenosine/S-adenosylhomocysteine nucleosidase from Escherichia coli
V Singh et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2005)
3C-like proteinase from SARS coronavirus catalyzes substrate hydrolysis by a general base mechanism
CK Huang et al.
BIOCHEMISTRY (2004)
Crystal structure of Thermotoga maritima α-L-fucosidase -: Insights into the catalytic mechanism and the molecular basis for fucosidosis
G Sulzenbacher et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2004)
Discovery of picomolar slow tight-binding inhibitors of α-fucosidase
CF Chang et al.
CHEMISTRY & BIOLOGY (2004)
Atomic resolution analyses of the binding of xylobiose-derived deoxynojirimycin and isofagomine to xylanase Xyn10A
TM Gloster et al.
CHEMICAL COMMUNICATIONS (2004)
Glycosidase inhibitors: update and perspectives on practical use
N Asano
GLYCOBIOLOGY (2003)
Direct observation of the protonation state of an imino sugar glycosidase inhibitor upon binding
A Varrot et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2003)
Thermodynamic characterization of ligand-induced conformational changes in UDP-N-acetylglucosamine enolpyruvyl transferase
AK Samland et al.
BIOCHEMISTRY (2001)
Activity of fucosyltransferases and altered glycosylation in cystic fibrosis airway epithelial cells
MC Glick et al.
BIOCHIMIE (2001)
Glycans as legislators of host-microbial interactions: spanning the spectrum from symbiosis to pathogenicity
LV Hooper et al.
GLYCOBIOLOGY (2001)
Detailed structural analysis of glycosidase/inhibitor interactions:: Complexes of Cex from Cellulomonas fimi with xylobiose-derived aza-sugars
V Notenboom et al.
BIOCHEMISTRY (2000)
Discovery and development of GS 4104 (oseltamivir): An orally active influenza neuraminidase inhibitor
W Lew et al.
CURRENT MEDICINAL CHEMISTRY (2000)
Value of the serum alpha-L-fucosidase activity in the diagnosis of colorectal cancer
D Ayude et al.
ONCOLOGY (2000)
Share Paper
