Dunathan stereoelectronic hypothesis
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Dunathan stereoelectronic hypothesis is a concept in chemistry to explain the stereospecefic cleavage of bonds using pyridoxal phosphate. This occurs because stereoelectronic effects controls the actions of the enzyme.[1]
History
Before the correlation between fold type and reaction correlation of proteins were understood, Harmon C. Dunathan, a chemist at Haverford College[2] proposed that the bond that is cleaved using pyridoxal is perpendicular to the system.[3] Though an important concept in bioorganic chemistry, it is now known that enzyme conformations play a critical role in the final chemical reaction.
Mode of action
The transition state is stabilized by the extended pi bond network (formation of anion).[4] Furthermore hyperconjugation caused by the extended network draws electrons from the bond to be cleaved, thus weakening the chemical bond and making it labile[5] The sigma bond that is parallel to the pi bond network will break.[6] The bond that has the highest chance of being cleaved is one with the largest HOMO-LUMO overlap.[7] This effect might be effected by electrostatic effects within the enzyme.[8]
Applications
This was seen in transferase and future interests lie in decarboxylation in various catalytic cycles.[9]
References
- ↑ Lua error in package.lua at line 80: module 'strict' not found.
- ↑ http://www.haverford.edu/chem/mackay/ColinWeb/MacKay_Web.html
- ↑ http://chemgroups.ucdavis.edu/~toney/Stereoelectronic.html
- ↑ http://chem.uaf.edu/keller/Courses/654Fa11/PDF/654-10-6-11.pdf
- ↑ http://chemgroups.ucdavis.edu/~toney/Publications/BBA%20-%20Proteins%20and%20Proteomics%202011%20Toney.pdf
- ↑ http://faculty.washington.edu/gelb/Chp9.ppt
- ↑ Lua error in package.lua at line 80: module 'strict' not found.
- ↑ http://www.chem.wisc.edu/areas/organic/studsemin/steinkruger/steinkruger-sem.pdf
- ↑ http://www.life.illinois.edu/biochem/455/Lab%20exercises/5GOT/PLP%20enzyme%20review.pdf
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