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P53 protein

Introduction

	Cancer is one of the most popular diseases occurring today. Research has been done on this issue for an extended amount of years to figure out how this devastating case works and what factors are contributing to this devastating illness. Throughout time there have been some successful answers while some things still remain in question during this existent investigation. One of the most interesting roles in the fight with cancer happens to be a protein quite phenomenal to cell life. This protein is none other than the unique p53 protein. P53 protein is an extremely important system in cell cycle control and the area of cancer. This protein was researched by Bert Vogelstein, David Lane, and Arnold Levine. The p53 protein is also called the guardian of the genome because of the role it has in checkpoint pathways of the cell cycle. This protein is located on chromosome 17 on the short arm which is where the open reading frames occur for proteins. The p53 protein was discovered through co-purification with a large T antigen in SV40 virus transformed cells.

Structure The structure of the p53 protein is pretty interesting. This protein has a single polypeptide chain divided into three discrete domains, which show a structure that has facilitated study in the absence of the rest of the protein. These domains have been found to be a concern with tetramerization, transcriptional activation, and DNA binding. In the p53 protein a N-terminal transactivation domain extends from residues 1-99 and is followed by the central core region, the largest domain, which contains residues 100-300 that bind specific DNA sequences. The third region of this protein is the C-terminal domain from residues 301-393, which includes a regulatory region and a tetramerization domain. These are the main three domains described for this protein, it has been disputed that there are four domains instead of three. Discrete domains are linked by flexible linkers creating a molecule with dynamic conformation. The p53 protein has been found to be difficult to crystallize when in the form of its full length. The p53 protein is a β sandwich formed by the interaction of antiparallel four and five stranded elements of the β sheet.