Carbohydrate-binding modules: fine-tuning polysaccharide recognition.

By A. Boraston, D. N. Bolam, H. Gilbert, G. Davies. Biochemical Journal, 2004

1,933 citations recorded by the source corpus.

Subfields: Molecular Biology, Organic Chemistry

View Paper: https://www.semanticscholar.org/paper/85da0fdfdade79da26358b85408fc05e7978ccdf

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In Molecular Biology

In Organic Chemistry

V. Seidl

Citations in the corpus

Comprehending crystalline β-carotene accumulation by comparing engineered cell models and the natural carotenoid-rich system of citrus (2011, neutral): “fr/CAZy), showing notable variations in substrate specificity (Boraston et al., 2004).”
Extracellular enzymes in terrestrial, freshwater, and marine environments: perspectives on system variability and common research needs (2013, background): “Such proxies cannot accommodate extracellular enzymes that contain substrate-binding modules that position macromolecules appropriately for hydrolysis (Boraston et al. 2004).”
Novel enzymes for the degradation of cellulose (2012, background): “Variation in affinity for the various forms of cellulose may in part be a consequence of variation in the presence of CarbohydrateBinding Modules (CBMs) that are covalently attached to the catalytic domains of the enzymes in question [44,46,47].”
Chitinases of filamentous fungi: a large group of diverse proteins with multiple physiological functions (2008, methodology): “However, they seem to have a broader polysaccharide binding spectrum and have also already been reported to bind to chitin (Boraston et al. 2004).”
Access to cellulose limits the efficiency of enzymatic hydrolysis: the role of amorphogenesis (2010, background): “Despite some similarities in functions to that of CBMs, no substantial research has subsequently been conducted to investigate the exact means by which the yellow substance enhances cellulose saccharification.”
Recognition of cellooligosaccharides by a family 28 carbohydrate‐binding module (2010, background): “To date, more than 50 CBM families have been identified [1], and their binding modes have been classified into three types [2]: type A CBMs have a flat hydrophobic surface that interacts with crystalline surfaces; type B CBMs have a cleft to accommodate single glycan chains, and type C CBMs have poc”