Trypsin, lipase, chymotrypsin, pancreatic amylase, steapsin, elastases, carboxypeptidase, and nucleases. ~answered by FightingLucario
amylase
Trypsin, lipase, chymotrypsin, pancreatic amylase, steapsin, elastases, carboxypeptidase, and nucleases. ~answered by FightingLucario
Trypsin, lipase, chymotrypsin, pancreatic amylase, steapsin, elastases, carboxypeptidase, and nucleases. ~answered by FightingLucario
Trypsin, lipase, chymotrypsin, pancreatic amylase, steapsin, elastases, carboxypeptidase, and nucleases. ~answered by FightingLucario
The small intestine is the site of work of some digestive enzymes that are secreted there. It is not an ideal site for the continued work of enzymes from the stomach, as the pH is not hospitable for the work of those gastric enzymes.
Trypsin, lipase, chymotrypsin, pancreatic amylase, steapsin, elastases, carboxypeptidase, and nucleases. ~answered by FightingLucario
Trypsin, lipase, chymotrypsin, pancreatic amylase, steapsin, elastases, carboxypeptidase, and nucleases. ~answered by FightingLucario
There are many different types of enzymes because each type have a differently shaped active site (the place where the reaction takes place) and the reaction can only happen if the active site is the right shape for the food molecule. eg. Protease enzymes break down proteins.
No, uncompetitive inhibitors do not bind to the active site of enzymes. They bind to a different site on the enzyme, causing a conformational change that prevents the substrate from binding to the active site.
DNA from two different people may have different sequences in the non-coding regions of their DNA. These differences may result in one person having a particular restriction site and the other person not having it. Different numbers and types of restriction sites will cause different fragments to be produced.
Two different DNA sequences
Allosteric enzymes have an additional regulatory site (allosteric site) distinct from the active site that can bind to specific molecules, affecting enzyme activity. Non-allosteric enzymes lack this additional regulatory site and their activity is primarily controlled by substrate binding to the active site. Allosteric enzymes show sigmoidal kinetics in response to substrate concentration due to cooperativity, while non-allosteric enzymes exhibit hyperbolic kinetics.