The following are major free radical scavengers except: A Superoxide dismutase B Catalase C Glutathione D Glutamine
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A: Answer - Autoclave
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A:
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A:
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- please show DETAILED mechanism and I will upvote: biotin carboxylase Ö— NH N-carboxyblotin O-C-OH + ATP bicarbonateUnbranched homopolymer of N-acetyl glucosamine is : 1.Cellulose 2.Chitin 3.Curcumin 4.Concanavalin ACertain microorganisms with a modified citric acid cycle decarboxylate α-ketoglutarate to produce succinate semialdehyde:
- Which of the following is a non-reducing sugar? 2,3-di-O-methyl B-D-galactopyranoside 2-0-methyl-a-D-mannopyranoside Fructose 1-0-methyl-ß-D-glucopyranoside dextrinIn this step of purine biosynthesis, which functional group gets activated by ATP Pribose NH, ATP Carboxyaminolmidazole ribonedeotide Asp AD Fumarate Pribose NH, S-Aminolmidazole- 4(N-succinylcarboxamide) ribonucleotide O Carboxyaminoimidazole ribonucleotide COOH O Carboxyaminoimidazole ribonucleotide NH2 O Asp side chain COOH O Asp main chain NH2 O Asp main chain COOHWhich of the structures below is that of О-а-D-glucopyranosy-(1->1)- а-D-glucoругanoside CH2OH CH2OH O. H H. он H. он H OH ÓH CH2OH HOH2 H. CH2OH CH2OH O. H H. он он H OH он CH2OH H. о, он он H он он
- There is a cysteine protease, which uses a similar chemical mechanism to chymotrypsin except for using cysteine instead of serine during catalysis. Please draw the stepwise chemical mechanism for the cysteine protease.Consider this mechanism of enzyme action: Urease can catalyze the hydrolysis of Urea, H,N – C – NH, II but not H H the hydrolysis of diethyl urea N -C - C;H5 C2H5 Explain this action.Draw the Fischer projection for L-glucose. Drag the appropriate labels to their respective targets. H as OH H =0 C CH₂OH Reset Help
- The following reaction is catalyzed by this type of enzyme? Coo COO™ I HIC-H H-C-H COO™ succinate isomerase hydrolase O ligase transferase oxidoreductase succinate dehydrogenase FAD FADH2 H-C || C-H COO fumarateDescribe the function implied by the name of each of the following enzymes Citrate decarboxylase Adenine diphosphate phosphorylase Oxalate reductase Nitrite oxidase cis-trans isomeraseThe following are known substrates for ALP (Alkaline Phosphotase); nucleotide tri, di and monophosphate, deoxynucleotides, phosphoglycerate, 2-naphthyl phosphate, 4-nitrophenyl phosphate, cysteamine S-phosphate, fructose-6-phosphate, fructose-1-phosphate, glucose-6-phosphate, phosphoserine, phosphothreonine, pyridoxyl phosphate, pyrophosphate. From looking at the structure can you offer an explanation for how ALP can accommodate such different substrates?