isomerase sentence in Hindi
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- Movement problems typically become apparent by age 2 in people with triosephosphate isomerase deficiency.
- The protein encoded by this gene belongs to the aconitase / IPM isomerase family.
- The deficiency of phosphohexose isomerase can lead to a condition referred to as hemolytic syndrome.
- If it gives off one product, it is solely enoyl Co-Al isomerase.
- It is formed through the conversion of maleylacetoacetate into fumarylacetoacetate by the enzyme maleylacetoacetate isomerase.
- People with triosephosphate isomerase deficiency often do not survive past childhood due to respiratory failure.
- IPP is isomerized to the allylic ester dimethylallyl pyrophosphate ( DMAPP ) by IPP isomerase.
- We chose the article Isomerase for review.
- Methylmalonyl-CoA mutase is a member of the isomerase subfamily of adensylcobalamin-dependent enzymes.
- Prolyl isomerase folding can be autocatalytic and therefore the speed of folding depends on reactant concentration.
- The xylose isomerase from " Streptomyces olivochromogenes " is used in the food industry.
- AGR2 is a protein disulfide isomerase, with CXXC active domain motifs for oxidation and reduction reactions.
- This encoded protein is a cis-trans prolyl isomerase that binds the immunosuppressants FK506 and rapamycin.
- The most common infections in people with triosephosphate isomerase deficiency are bacterial infections of the respiratory tract.
- Phosphoglucose isomerase ( PGI ) is a housekeeping cytosolic enzyme with roles in both glycolysis and gluconeogenesis pathways.
- One of them is FKBP-type peptidyl prolyl isomerase, which appears around 25kDa ( SlyD ).
- Mannose-6-Phosphate Isomerase may also enable the synthesis of GDP-mannose in eukaryotic organisms.
- This gene encodes a member of the peptidyl-prolyl cis-trans isomerase ( PPIase ) family.
- The enzyme is a hexamer, forming the largest structurally known ketol isomerase, and has no residues.
- The systematic name of this enzyme class is "'benzyl-thiocyanate isomerase " '.
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