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Sickle Cell Anemia Research Paper

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Proteins are macromolecules made up of many amino acids that play a lot of important roles in our body. In living organisms proteins have various functions. For example enzymes are proteins that are very important to our body. Enzymes are invovled in thousands of chemical reaction wporking by lowering the activation energy therefore speeding up the reactons. Proteins can also function as a messenger, transporter, and also for storage in the body. Proteins are polymers made up of a lot of amino acid monomers. The amino acid on the protein gives the protein its special function or unique property. A phenotype is an observable trait or characteristics on an organism. For example eye color, height, and a size of a bird's beak are all phenotypes,they …show more content…

Although Sickle cell anemia, a mutation will not be universally looked as a ''positive'' mutation, sickle cell anemia does infact prevent the host from malaria. Sickle cell is protected from diseases like malria because of the shape of the hemoglobin. The sickle shaped hemoglobin indirectly interfeeres, and in a way tolerattes the disease. The sickle shaped hemoglobin makes the person infected in a way tolerant to the effects that malaria provide. There are several types of mutations, Substitution, Insertion, Deletion, and frameshift mutations. First the subsitution mutation is when bases are switched. Sickle cell aniema like mentioned earlier is an example of a result from substitution mutation. Sickle cell anemia is a result of a valine being substituied in instead of the glutamae. Hunnington's disease, a brain disorder that cause loss of body control, and loss of cognition is caused by insertion mutation. Insertion mutation is when a extra base pair is added to the DNA making it longer than it should be. Deletion is the next mutation, and here a segment of the DNA will either be lost or deleted, due to it not being copied during DNA replication. An example deletion mutation is the DiGeroge anomaly which can cause psyhicatric disorders, immune disorders, and congential heart disease. Digeorge anomaly is caused by a deletion in a segment of chromosome 22. The last mutation is frameshift mutation is caused by either insertion or deletion of nucleotides squences not divisble by three. Frameshift mutation are present in diseases like cystic fibrosis which causes poor growth, frequent chest infecitions and many other complications in the

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