Reversible inhibitors bind to enzymes with non-covalent interactions; hydrogen bonds , hydrophobic interactions and ionic bonds .
http://www.chacha.com/question/which-inhibitor-binds-to...
It should be, in theory. In practice, nearly all of the pharmacological chaperones now under development are active-site ligands. However, tight specific binding anywhere on the surface of a protein ought to confer stabilization as a result...
http://jbiol.com/content/8/9/80
This is where the substrate molecule(s) fits into the enzyme molecule; this is where the enzyme "does its job."
http://answers.yahoo.com/question/index?qid=20090223074...
It is the most important region of a functional enzyme and it has a structure that recognizes the substrates shape.
http://www.blurtit.com/q262032.html
Competitive inhibitors reduce enzyme activity by binding (in competition with the enzyme's substrate) to the active site. These inhibitors may be reversible or irreversible. With reversible inhibitors, which may release the enzyme, concentr...
http://wiki.answers.com/Q/What+blocks+enzyme+activity+b...
This would be a competitive inhibitor. It can be a structural analog of the substrate. This type of inhibition can be out competed by adding more substrate. A competitive inhibitor increases the Km of the enzyme.
http://wiki.answers.com/Q/What+type+of+inhibitor+takes+...
The active site is where a substrate binds. Enzymes have very specific shapes as do their active sites. This means that only molecules with that certain shape can fit in the active site. This is called the lock-and-key theory of enzyme spec...
http://wiki.answers.com/Q/How_is_an_active_site_related...