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Hydrolase

Known as: EC 3, Hydrolases, Hydrolases [Chemical/Ingredient] 
Any member of the class of enzymes that catalyze the cleavage of the substrate and the addition of water to the resulting molecules, e.g., ESTERASES… 
National Institutes of Health

Related topics

Related topics

50 relations
3'-5'-ExonucleasesABHD12 protein, humanALPP protein, humanAPEX1 protein, human

Narrower (14)

3-hydroxykynureninase4-chlorobenzoate dehalogenase4-chlorobenzoyl-CoA dehalogenaseArginine deiminase

Broader (1)

Enzymes

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2012
Review
2012
Industrial biotransformations in the synthesis of building blocks leading to enantiopure drugs.
Review
2011
Review
2011
The lipases from Yarrowia lipolytica: genetics, production, regulation, biochemical characterization and biotechnological applications.
Highly Cited
2008
Highly Cited
2008
Maturity assessment of compost from municipal solid waste through the study of enzyme activities and water-soluble fractions.
Highly Cited
2008
Highly Cited
2008
A diacylglycerol lipase-CB2 cannabinoid pathway regulates adult subventricular zone neurogenesis in an age-dependent manner
Review
2001
Review
2001
Biosensors for direct determination of organophosphate pesticides.
Highly Cited
1999
Highly Cited
1999
Structural basis for the specificity of ubiquitin C‐terminal hydrolases
The release of ubiquitin from attachment to other proteins and adducts is critical for ubiquitin biosynthesis, proteasomal… 
Highly Cited
1991
Highly Cited
1991
Regulated Chlorophyll Degradation in Spinach Leaves during Storage
Degradation of chlorophyll in spinach (Spinacia olearacea L. cv. Hybrid 612) appeared to be regulated through the peroxidase… 
Highly Cited
1984
Highly Cited
1984
In vivo and in vitro evidence for the involvement of cysteine proteinases in bone resorption.
Highly Cited
1980
Highly Cited
1980
Structural studies of phosphorylated high mannose-type oligosaccharides.
Highly Cited
1980
Highly Cited
1980
A lysosomal storage disorder in mice characterized by a dual deficiency of sphingomyelinase and glucocerebrosidase.
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