Results 11 to 20 of about 9,178 (231)

Surface AMP deaminase 2 as a novel regulator modifying extracellular adenine nucleotide metabolism [PDF]

open access: bronzeThe FASEB Journal, 2021
Abstract Adenine nucleotides represent crucial immunomodulators in the extracellular environment. The ectonucleotidases CD39 and CD73 are responsible for the sequential catabolism of ATP to adenosine via AMP, thus promoting an anti‐inflammatory milieu induced by the “adenosine halo”.
Lisa Ehlers   +8 more
openalex   +4 more sources

Single nucleotide editing without DNA cleavage using CRISPR/Cas9‐deaminase in the sea urchin embryo [PDF]

open access: bronzeDevelopmental Dynamics, 2017
Background: A single base pair mutation in the genome can result in many congenital disorders in humans. The recent gene editing approach using CRISPR/Cas9 has rapidly become a powerful tool to replicate or repair such mutations in the genome. These approaches rely on cleaving DNA, while presenting unexpected risks.
Saba Shevidi   +4 more
openalex   +3 more sources

Nucleotide Activation of Threonine Deaminase from Escherichia coli

open access: hybridJournal of Biological Chemistry, 1965
Masaharu Hirata   +3 more
openalex   +3 more sources

Adenine Nucleotide Pool Perturbation Is a Metabolic Trigger for AMP Deaminase Inhibitor-Based Herbicide Toxicity [PDF]

open access: hybridPlant Physiology, 2007
AMP deaminase (AMPD) is essential for plant life, but the underlying mechanisms responsible for lethality caused by genetic and herbicide-based limitations in catalytic activity are unknown. Deaminoformycin (DF) is a synthetic modified nucleoside that is taken up by plant cells and 5'-phosphorylated into a potent transition state-type inhibitor of AMPD.
Richard L. Sabina   +4 more
openalex   +4 more sources

Nucleotide sequence of the gene for threonine deaminase (ILV1) of Saccharomyces cerevisiae [PDF]

open access: bronzeCarlsberg Research Communications, 1984
The 1,728 base pair coding region of theILV1 gene and the adjacent 777 base pair upstream and 261 base pair downstream regions were sequenced. The size of the polypeptide deduced from the coding region is larger than previously determined values for the molecular weight of threonine deaminase, suggesting that a peptide with a molecular weight of about ...
Morten C. Kielland‐Brandt   +3 more
openalex   +3 more sources

Correction: A cytidine deaminase-like protein modulates pyrimidine nucleotide homeostasis in Trypanosoma brucei [PDF]

open access: goldScientific Reports
Ana Moro-Bulnes   +7 more
openalex   +2 more sources

Nucleotide Weight Matrices Reveal Ubiquitous Mutational Footprints of AID/APOBEC Deaminases in Human Cancer Genomes [PDF]

open access: goldCancers, 2019
Cancer genomes accumulate nucleotide sequence variations that number in the tens of thousands per genome. A prominent fraction of these mutations is thought to arise as a consequence of the off-target activity of DNA/RNA editing cytosine deaminases.
Igor B. Rogozin   +8 more
openalex   +7 more sources

Bisulfite-free and single-nucleotide resolution sequencing of DNA epigenetic modification of 5-hydroxymethylcytosine using engineered deaminase

open access: diamondChemical Science, 2022
In EDM-seq, the original C and 5mC in DNA are deaminated by eA3A to form U and T, both of which are read as T during sequencing. While the 5hmC is resistant to deamination by eA3A and is still read as C during sequencing.
Neng‐Bin Xie   +6 more
openalex   +4 more sources

AMP Deaminase Inhibitors. 2. Initial Discovery of a Non-Nucleotide Transition-State Inhibitor Series

open access: greenJournal of Medicinal Chemistry, 2000
A series of N3-substituted coformycin aglycon analogues are described that inhibit adenosine 5'-monophosphate deaminase (AMPDA) or adenosine deaminase (ADA). The key steps involved in the preparation of these compounds are (1) treating the sodium salt of 6, 7-dihydroimidazo[4,5-d][1,3]diazepin-8(3H)-one (4) with an alkyl bromide or an alkyl mesylate to
Brett C. Bookser   +3 more
openalex   +3 more sources

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