48 MHR • Unit 1 Metabolic Processes
from this venom, contains enzyme inhibitors that
prevent blood clots from forming. In 1999,
pharmaceutical researchers found that more than
40% of stroke patients who received ANCROD
recovered all of their mental faculties. Other
venom, such as scorpion venom, is being used
to treat autoimmune disorders.
Figure 2.9Venom from this Malayan pit viper can be used
to treat patients who have had a stroke.
There are two kinds of inhibition that can affect
the activity of enzymes. In non-competitive
inhibition, an inhibitor molecule binds to the
enzyme at a site known as the allosteric site. As a
result, the three-dimensional structure of the enzyme
is altered, which prevents the substrate from binding
to the active site (see Figure 2.10). Most metabolic
pathways are regulated by feedback inhibition. This
is a type of non-competitive inhibition in which the
end product of the pathway binds at an allosteric
site on the first enzyme of the pathway. In this way,
non-competitive inhibitors can play a key role in
the normal functioning and regulation of metabolic
pathways. Study Figure 2.11 to learn how a metabolic
pathway is regulated by feedback inhibition.
Figure 2.10Non-competitive inhibition
Figure 2.11This hypothetical metabolic pathway is
regulated by feedback inhibition.
Molecules that promote the action of enzymes
can also bind to the allosteric site. These molecules
are known as activators. The activity of any
enzyme can change, depending on the number of
activators and inhibitors in its environment. The
regulation of enzyme activity by inhibitors and
activators is known as allosteric regulation.
Competitive inhibitioninvolves chemical
compounds that bind to the active site of the
enzyme and inhibit enzymatic reactions. The
compounds compete with the true substrate for
access to the active site. This competition is
possible because competitive inhibitors are very
similar in shape and structure to the enzyme’s
View of active pathway
View of inhibited pathway
stop
first
reactant
A
end
product
F
end
product
F
EDCB
first
reactant
A
A
E 1
E 1
E 1
E 1
Overall view of pathway
EDCB
first
reactant
A
end
product
F
E 1 E 2 E 3 E 4 E 5
E 1
E 2 E 3 E 4 E 5
substrate
active site
enzyme
allosteric site
inhibitor
molecule
Inhibitor binds to the
enzyme at the allosteric site
A
Shape of
the active
site is
altered
B
Substrate
can no
longer fit
into the
active site
C
The substrate binds to the
active site of the enzyme.
The pathway is now active.
A
Overall view of pathwayOnce enough end product
has been produced, it binds to the allosteric site of
the enzyme. The pathway is no longer active and the
end product is no longer produced.
D
View of active pathway
The pathway remains
active as long as there is
insufficient end product.
B
View of inhibited
pathwayOnce there is
sufficient end product,
the product binds with
the enzyme, changing
the shape of the active
site. This prevents the
enzyme from binding
with additional
substrate and inhibits
the pathway.