Ligases are enzymes that catalyze the formation of new bonds between molecules. A classic example is DNA ligase, an enzyme that synthesizes phosphodiester bonds in the DNA backbone.

Transferases move small molecules from one molecule to another, sometimes altering the functional groups of a compound. Isomerases convert molecules from one isomer to another. Lyases are enzymes that break bonds through a means other than hydrolysis (typically by formation of a double bond). 

Since chymotrypsin uses a water molecule in order to cleave the polymer, it is considered a hydrolase enzyme.

Since the enzyme has changed the shape of the molecule without altering its chemical formula, the enzyme has simply made a new isomer of the molecule. This action is accomplished by isomerase enzymes.

All answer choices fit the description. Epigenetics (above the gene) are heritable modifications of chromatin and DNA that affect gene expression. Pioneer transcription factors are able to bind DNA in heterochromatin and recruit enzymes that promote euchromatin formation which allows other transcription factors to bind and effect gene expression. Histone methyltransferases and acetyltransferases methylate and acetylate histones, respectively, to alter gene expression. DNA methyltransferases are also enzymes that confer epigenetic changes to DNA by methylation, which usually represses gene expression. 

The correct answer is acetylases. DNA can be directly methylated by methylases, mended during DNA repair by ligases, uncoiled by topoisomerases, and replicated by polymerases. However, DNA cannot be acetylated. Epigenetic associated-acetylation occurs only on histones to determine the chromatin state of a specific region. 

Flippases use ATP to permit membrane lipids to reorient themselves in the cellular membrane, specifically in the direction from extracellular to intracellular facing. Floppases catalyze the reverse movement: intracellular to extracellular. Migratases are not a class of enzyme. Phospholipases and kinases catalyze other types of reactions and certainly can act on lipids, but not this particular lipid movement. 

The difference between the binding of cAMP and phosphorylation is that the latter is a covalent modification. Covalent modifications are a different way to regulate proteins, and do not fall under the category of allosteric regulation. Allosteric regulation only occurs outside of the active site, often simply called an allosteric site. The non-covalent binding of cAMP to a region of an enzyme outside of the active site thus qualifies as allosteric regulation.

Because the inhibitor binds at the active site, it is actively competing with the ligand for access to the enzyme. This type of inhibitor displays competitive inhibition. Competitive inhibition can be overcome by adding excessive amounts of substrate. If the amount of substrate greatly out-measures the amount of inhibitor, then the substrate will still bind the enzyme very frequently and allow the reaction to proceed.

Noncompetitive inhibitors bind an enzyme at a spot that is not the active site. Uncompetitive inhibitors bind the enzyme-substrate complex, once the substrate has already entered the active site. Suicide inhibitors "kill" enzymes, typically by making permanent modifications to amino acids in the active site.

The x-intercept on a Lineweaver-Burk plot tells us the negative reciprocal of .

Because the x-intercept is less negative, this tells us that the inhibited reaction has a larger . Having a different x-intercept but the same y-intercept is characteristic of competitive inhibition. The inhibitor and the substrate are competing for the same binding site. 

Plotting the concentration of the inhibitor versus the concentration of the substrate will not give you any useful information because the reaction rate is essential in determining the type of inhibitor present.

Plotting initial reaction rate versus substrate concentration, or plotting the inverses, describes the graphical representation of Michaelis-Menten kinetics and a Lineweaver-Burk plot, respectively. Both of these are excellent methods to visually determine the type of inhibition displayed. On the graph, the line representing the inhibited enzyme will shift in predictable fashions depending on the type of inhibition.