(Q41206809)

28 September 2017

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title

Design and synthesis of carbohydrate-based inhibitors of protein-carbohydrate interactions (English)

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28 September 2017

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von Itzstein M

1

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28 September 2017

Colman P

series ordinal

2

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28 September 2017

publication date

1 October 1996

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Current Opinion in Structural Biology

28 September 2017

published in

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28 September 2017

volume

6

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28 September 2017

issue

5

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28 September 2017

page(s)

703-709

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Structural aspects of the allosteric inhibition of fructose-1,6-bisphosphatase by AMP: the binding of both the substrate analogue 2,5-anhydro-D-glucitol 1,6-bisphosphate and catalytic metal ions monitored by X-ray crystallography

28 September 2017

cites work

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7 January 2021

Crystal structure of spinach chloroplast fructose-1,6-bisphosphatase at 2.8 A resolution

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7 January 2021

An unlikely sugar substrate site in the 1.65 A structure of the human aldose reductase holoenzyme implicated in diabetic complications

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7 January 2021

An anion binding site in human aldose reductase: mechanistic implications for the binding of citrate, cacodylate, and glucose 6-phosphate

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7 January 2021

Tyrosine-48 is the proton donor and histidine-110 directs substrate stereochemical selectivity in the reduction reaction of human aldose reductase: enzyme kinetics and crystal structure of the Y48H mutant enzyme

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7 January 2021

Structures of human and porcine aldehyde reductase: an enzyme implicated in diabetic complications

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7 January 2021

Crystallization and preliminary structure of porcine aldehyde reductase-NADPH binary complex

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7 January 2021

Aldose reductase as a target for drug design: molecular modeling calculations on the binding of acyclic sugar substrates to the enzyme

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7 January 2021

Mechanism of aldose reductase inhibition: binding of NADP+/NADPH and alrestatin-like inhibitors

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7 January 2021

Synthesis of pyrrolo[3,4-c]pyridine derivatives possessing an acid group and their in vitro and in vivo evaluation as aldose reductase inhibitors

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7 January 2021

The selectins and their ligands

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7 January 2021

Selectin-carbohydrate interactions and the initiation of the inflammatory response

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7 January 2021

Insight into E-selectin/ligand interaction from the crystal structure and mutagenesis of the lec/EGF domains

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7 January 2021

Multivalent sialyl-LeX: potent inhibitors of E-selectin-mediated cell adhesion; reagent for staining activated endothelial cells

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7 January 2021

Sulfated disaccharide inhibitors of L-selectin: deriving structural leads from a physiological selectin ligand

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7 January 2021

Synthesis of a divalent sialyl Lewis x O-glycan, a potent inhibitor of lymphocyte-endothelium adhesion. Evidence that multivalency enhances the saccharide binding to L-selectin

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7 January 2021

Synthesis of a Sialyl Lewis x Mimic with Fixed Carboxylic Acid Group: Chemical Approach toward the Elucidation of the Bioactive Conformation of Sialyl Lewis x

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7 January 2021

Synthesis of deoxygalactose-containing sialyl Le(X) ganglioside analogues to elucidate the structure necessary for selectin recognition

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7 January 2021

A sialic acid-derived phosphonate analog inhibits different strains of influenza virus neuraminidase with different efficiencies

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7 January 2021

Structure-based inhibitors of influenza virus sialidase. A benzoic acid lead with novel interaction

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7 January 2021

Hemagglutinins from two influenza virus variants bind to sialic acid derivatives with millimolar dissociation constants: a 500-MHz proton nuclear magnetic resonance study

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7 January 2021

Carbohydrate materials bearing neuraminidase-resistant C-glycosides of sialic acid strongly inhibit the in vitro infectivity of influenza virus

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7 January 2021

Effective inhibitors of hemagglutination by influenza virus synthesized from polymers having active ester groups. Insight into mechanism of inhibition

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7 January 2021

Structure of murine polyomavirus complexed with an oligosaccharide receptor fragment

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7 January 2021

Structure of the influenza virus haemagglutinin complexed with its receptor, sialic acid

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7 January 2021

Glycosylation inhibitors in biology and medicine

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7 January 2021

Structure of the 70-kDa soluble lytic transglycosylase complexed with bulgecin A. Implications for the enzymatic mechanism

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7 January 2021

The catalytic domain of a bacterial lytic transglycosylase defines a novel class of lysozymes

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7 January 2021

https://api.crossref.org/works/10.1016%2FS0959-440X%2896%2980038-8

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7 January 2021

Lactose binding to heat-labile enterotoxin revealed by X-ray crystallography

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7 January 2021

Crystal structure of cholera toxin B-pentamer bound to receptor GM1 pentasaccharide

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7 January 2021

Thermodynamics of intersubunit interactions in cholera toxin upon binding to the oligosaccharide portion of its cell surface receptor, ganglioside GM1.

1 reference

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7 January 2021

Purification, crystallization and preliminary crystallographic study of neuraminidase from Vibrio cholerae and Salmonella typhimurium LT2.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-440X%2896%2980038-8

7 January 2021

Crystal structure of a bacterial sialidase (from Salmonella typhimurium LT2) shows the same fold as an influenza virus neuraminidase

1 reference

https://api.crossref.org/works/10.1016%2FS0959-440X%2896%2980038-8

7 January 2021

Crystal structure of Vibrio cholerae neuraminidase reveals dual lectin-like domains in addition to the catalytic domain

1 reference

https://api.crossref.org/works/10.1016%2FS0959-440X%2896%2980038-8

7 January 2021

The three domains of a bacterial sialidase: a beta-propeller, an immunoglobulin module and a galactose-binding jelly-roll

1 reference

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7 January 2021

10.1016/S0959-440X(96)80038-8

Identifiers

DOI

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28 September 2017

1 reference