1. Periodate-oxidized NADP+ inhibits the catalytic activity of glucose 6-phosphate dehydrogenase from Candida utilis, competing with NADP+. 2. Incubation of the enzyme with the coenzyme analogue causes partial reversible inactivation of the enzyme as a result of affinity labelling of the coenzyme-binding site. 3. Some kinetic values of the reaction were calculated. 4. The inactivation can be made irreversible by treatment with NaBH4, which reduces a Schiff base formed between an aldehyde group on the coenzyme analogue and a lysine residue on the enzyme. 5. Complete inactivation can be correlated with the binding of only one inhibitor to each enzyme subunit. 6. The lysine residue involved in the binding of the inhibitor is present at the coe...
Initial velocity studies obtained with alternative dinucleotide substrates for the 6-phosphogluconat...
Protein stabilities can be influenced by interactions with low molecular weight compounds, Using glu...
Glucose-6-phosphate dehydrogenase (G6PDH) catalyzes the first and rate-limiting step of the pentose ...
6-Phosphogluconate dehydrogenase from Candida utilis is a dimeric enzyme with apparently identical s...
The mechanism of the inactivation of 6-phosphogluconate dehydrogenase from Candida utilis with two c...
Abstract – Glucose 6- phosphate dehydrogenase from streptomyces aureofaciens was purified and inacti...
The environment of a cysteine residue in the active site of 6-phosphogluconate dehydrogenase from Ca...
Abstract – Some kinetic properties of NAD+- and NADP+- dependent glucose 6-phosphate dehydrogenase (...
The treatement of 6-phosphogluconate dehydrogenase from Candida utilis with Dansyl chloride causes t...
Incubation of 6-phosphogluconate dehydrogenase from Candida utilis with either acetyl phosphate, 1,3...
When an unstable enzyme is incubated with its substrate(s), catalysis may cease before chemical equi...
A complete initial velocity study of the 6-phosphogluconate dehydrogenase from Candida utilis at pH ...
Glucose 6-phosphate dehydrogenase (EC 1.1.1.49) was purified from Aspergillus aculeatus, a filament...
o-phthalaldehyde inactivates homodimeric, NADP+ dependent, 6-phosphogluconate dehydrogenase from she...
6-Phosphogluconate dehydrogenase from human erythrocytes was purified by an improved procedure. Bind...
Initial velocity studies obtained with alternative dinucleotide substrates for the 6-phosphogluconat...
Protein stabilities can be influenced by interactions with low molecular weight compounds, Using glu...
Glucose-6-phosphate dehydrogenase (G6PDH) catalyzes the first and rate-limiting step of the pentose ...
6-Phosphogluconate dehydrogenase from Candida utilis is a dimeric enzyme with apparently identical s...
The mechanism of the inactivation of 6-phosphogluconate dehydrogenase from Candida utilis with two c...
Abstract – Glucose 6- phosphate dehydrogenase from streptomyces aureofaciens was purified and inacti...
The environment of a cysteine residue in the active site of 6-phosphogluconate dehydrogenase from Ca...
Abstract – Some kinetic properties of NAD+- and NADP+- dependent glucose 6-phosphate dehydrogenase (...
The treatement of 6-phosphogluconate dehydrogenase from Candida utilis with Dansyl chloride causes t...
Incubation of 6-phosphogluconate dehydrogenase from Candida utilis with either acetyl phosphate, 1,3...
When an unstable enzyme is incubated with its substrate(s), catalysis may cease before chemical equi...
A complete initial velocity study of the 6-phosphogluconate dehydrogenase from Candida utilis at pH ...
Glucose 6-phosphate dehydrogenase (EC 1.1.1.49) was purified from Aspergillus aculeatus, a filament...
o-phthalaldehyde inactivates homodimeric, NADP+ dependent, 6-phosphogluconate dehydrogenase from she...
6-Phosphogluconate dehydrogenase from human erythrocytes was purified by an improved procedure. Bind...
Initial velocity studies obtained with alternative dinucleotide substrates for the 6-phosphogluconat...
Protein stabilities can be influenced by interactions with low molecular weight compounds, Using glu...
Glucose-6-phosphate dehydrogenase (G6PDH) catalyzes the first and rate-limiting step of the pentose ...