Sandbox Reserved 1546
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='''5H86: HUMAN GCN-5 BOUND TO BUTYRYL-COA'''= | ='''5H86: HUMAN GCN-5 BOUND TO BUTYRYL-COA'''= | ||
This project was completed by Marianne Javier, Karima MuhummadPoe, and Makayla Yang for Dr. Gluick's Spring 2019 BIOL4100K-01 class at Georgia Gwinnett College. | This project was completed by Marianne Javier, Karima MuhummadPoe, and Makayla Yang for Dr. Gluick's Spring 2019 BIOL4100K-01 class at Georgia Gwinnett College. | ||
| - | <p>'''Project Purpose:''' We chose this molecule due to its role as a histone acetyltransferase and its role in transcription regulation <ref name = "Structural basis for acyl-group discrimination by human Gcn5L2">doi: 10.1107/S2059798316007907</ref>. It has a harder time having successful enzymatic activity if the acyl-chain is too long which is the purpose of studying the molecule <ref name = " Structural basis for acyl-group discrimination by human Gcn5L2/>. These researchers made two different acyl-CoA molecules, propionyl-CoA and butyryl-CoA <ref name = " Structural basis for acyl-group discrimination by human Gcn5L2/>. We are looking at the butyryl-CoA which has a conformation that obstructs the lysine from binding. We chose this molecule to see how Gcn5L2 chooses which acyl-chain donor to have the highest enzymatic activity.</p> | + | <p>'''Project Purpose:''' We chose this molecule due to its role as a histone acetyltransferase and its role in transcription regulation <ref name = "Structural basis for acyl-group discrimination by human Gcn5L2">doi: 10.1107/S2059798316007907</ref>. It has a harder time having successful enzymatic activity if the acyl-chain is too long which is the purpose of studying the molecule <ref name = "Structural basis for acyl-group discrimination by human Gcn5L2"/>. These researchers made two different acyl-CoA molecules, propionyl-CoA and butyryl-CoA <ref name = "Structural basis for acyl-group discrimination by human Gcn5L2"/>. We are looking at the butyryl-CoA which has a conformation that obstructs the lysine from binding. We chose this molecule to see how Gcn5L2 chooses which acyl-chain donor to have the highest enzymatic activity.</p> |
==Function== | ==Function== | ||
Revision as of 14:51, 5 May 2019
| This Sandbox is Reserved from May 28 through July 01, 2019 for use in the course Advanced Biochemistry BCHM 4100 taught by Tom Gluick at the Georgia Gwinnett College. This reservation includes Sandbox Reserved 1544 through Sandbox Reserved 1555. |
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Contents |
5H86: HUMAN GCN-5 BOUND TO BUTYRYL-COA
This project was completed by Marianne Javier, Karima MuhummadPoe, and Makayla Yang for Dr. Gluick's Spring 2019 BIOL4100K-01 class at Georgia Gwinnett College.
Project Purpose: We chose this molecule due to its role as a histone acetyltransferase and its role in transcription regulation [1]. It has a harder time having successful enzymatic activity if the acyl-chain is too long which is the purpose of studying the molecule [1]. These researchers made two different acyl-CoA molecules, propionyl-CoA and butyryl-CoA [1]. We are looking at the butyryl-CoA which has a conformation that obstructs the lysine from binding. We chose this molecule to see how Gcn5L2 chooses which acyl-chain donor to have the highest enzymatic activity.
Function
In order to better understand the function of this 5H86 enzyme, we have to understand the basic processes of Fatty Acid Degradation. Fatty Acid Degradation is the procedure that fatty acids go through to be broken down into their metabolites and it takes place in the mitochondrial matrix. Intermediates in fatty acid breakdown are covalently attached to the sulfhydryl group of coenzyme A.
Fatty Acid Degradation happens in three steps:
1. Lipolysis and release from adipose tissue: In the initial steps of degradation, fatty acids are stored in adipocytes. The breakdown of adipocytes is called lipolysis (They are released into blood stream to circulate through body.)
2. Activation and transport into the mitochondria: The mitochondria is where fatty acid oxidation occurs which activates fatty acids to be carried to the mitochondria. The enzyme responsible for the catalysis of this step is Fatty-Acyl Coa Synthetase. Malonyl ACP is the activated donor of two carbon units in the elongation step which is operated by the release of CO2.
3. Β-oxidation: Once inside mitochodria, five steps occur: 1) Activation by ATP, 2) Oxydation by FAD, 3) Hydration, 4) Oxydation by NAD+, and 5) Thyolysis. The final product is Acetyl-Coa which is now able to be able to enter the TCA cycle [2].
Structural Highlights
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Relevance
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References
- ↑ 1.0 1.1 1.2 Ringel AE, Wolberger C. Structural basis for acyl-group discrimination by human Gcn5L2. Acta Crystallogr D Struct Biol. 2016 Jul 1;72(Pt 7):841-8. doi:, 10.1107/S2059798316007907. Epub 2016 Jun 23. PMID:27377381 doi:http://dx.doi.org/10.1107/S2059798316007907
- ↑ Berg JM, Tymoczko JL, Stryer L. Biochemistry. 5th edition. New York: W H Freeman; 2002. Section 22.4, Fatty Acids Are Synthesized and Degraded by Different Pathways. Available from: https://www.ncbi.nlm.nih.gov/books/NBK22554/
