Results 151 to 160 of about 48,869 (270)

Structural studies on the sialidases from Streptococcus pneumoniae and Pseudomonas aeruginosa

open access: yes, 2009
The sialidases are a group of glycosyl hydrolases that specifically remove terminal sialic acid (Neu5Ac) residues from various glycans. In the two common human pathogenic bacteria Streptococcus pneumoniae and Pseudomonas aeruginosa, these enzymes have
Xu, Guogang
core  

SOME PHYSICOCHEMICAL PROPERTIES OF VIBRIO NEURAMINIDASE

open access: yes, 2020
Some physico-chemical properties of commercially available neuraminidase preparations from non-choleraic vibrio were studied. The neuraminidase was shown to be weakly acid glycoprotein with molecular mass 90 +/- 5 kDa, sedimentation constant 5.37 S and ...
BERESOV T.T., LAVROVSKY S.N.
core  

Computational antiviral drug design

open access: yes, 2010
This study designed and computational docked a group of ligands intended to find potent inhibitors for Neuraminidase 4 which would have strong interactions with 8 conserved amino acids in the active site. Several trials of ligands were designed based on
Liu, Lishan
core  

Antiviral Activity of Polyene Macrolides Against Newcastle Disease Virus: Computational and Experimental Insights. [PDF]

open access: yesMolecules
Mukhametkaliyev A   +10 more
europepmc   +1 more source

Oseltamivir aziridines are potent influenza neuraminidase inhibitors and imaging agents. [PDF]

open access: yesProc Natl Acad Sci U S A
Vriends MBL   +22 more
europepmc   +1 more source

Cross-reactive human antibody responses to H9N2 influenza virus, New York, United States, 2025. [PDF]

open access: yesEuro Surveill
Singh G   +9 more
europepmc   +1 more source

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