Valine Essays

  • Branched Chain Amino Acids On Sports Performance

    1197 Words  | 3 Pages

    vitamins. I. What are Branched chain amino acids? Branched chain amino acids (BCAA) are amino acids whose molecular structure is made up of branched aliphatic side chains. Three amino acids occurring in humans, viz. valine, leucine and isoleucine, are essential BCAAs. They are essential because they are not synthesized by the body and have to be supplied through diet. Amino acids are the building blocks of proteins, which in turn

  • Genetics: The Catechol-O-methyltransferase (COMT) Gene

    616 Words  | 2 Pages

    In the field of genetics, the study of the effect of various genes is imperative in translation and interpretation. As genetic coding influences phenotypic expression, the analysis of specific genes and any polymorphisms are relevant in a clinical setting. One such example is that of personality traits, which are believed to be influenced by specific neurotransmitters, known as catecholamines. Catecholamines are chemicals released by the adrenal glands in response to stress, and operate dually as

  • Essential Amino Acids as Ergogenic Aids

    1477 Words  | 3 Pages

    weightlifting and training. httg:///www.kaiwan.com/-fitnessalaacid.html (hftp://www.thelinx.com/healthy/aminoacd.htm#valine) (hftp://www.getbig.com/articies/protein.htm) The Essential Amino Acids Of 22 amino acids, 8 or 9, are considered essential because our bodies can't manufacture them. These are tryptophan, lysine, methione, phenylalaine, threonine, valine, leucine, isoleucine, and histadine. Leucine "serves as a substrate for muscle metabolism during periods of cellular energy

  • Understanding Inborn Errors of Metabolism

    634 Words  | 2 Pages

    can be synthesized from metabolic precursors, whereas essential cannot and must be taken from the diet. Essential are the ones that have more steps in the production process, so they required more ATP. Essential amino acid includes phenylalanine, valine, threonine, tryptophan, methionine, leucine, isoleucine, lysine, and histidine. And non-essential amino acids are arginine, alanine, asparagine, aspartate, cysteine, glutamate, glutamine, glycine, proline, serine, and tyrosine. Inborn errors of metabolism

  • The Four Stages Of Meiosis

    628 Words  | 2 Pages

    is a potentially fatal disease that disables the body from breaking down valine, leucine and isoleucine. These three amino acids are used to build proteins and are eventually broken down by branched –chain alpha ketoacid dehydrogenase (BCKD). Individuals who are affected by MSUD have a mutation that lack one of the six proteins that assist in the breakdown of the three amino acids. As a result, increased levels of valine, leucine and isoleucine end up in the blood stream and cause degradation of

  • Cassava Case Study

    872 Words  | 2 Pages

    varietal issue. The fat content of cassava is determined by age of plant when harvested, variety and environmental factors. For cassava root, r2 for predicting individual AA from CP content was generally low and was greater than 20% only for TAA and valine. Also, r2 for predicting individual AA from leaf was 25% for TAA while that of peel was above 70% for histidine and threonine. Weak relationship observed among the CP, TAA and TIAA in this study might be due to their percentage proportion and changes

  • Importance Of Amino Acids

    1601 Words  | 4 Pages

    disease due to the keto acids released into the urine, causing it to have a maple syrup-like smell. This condition can result in neurological damage and requires a special diet, including a synthetic infant formula that excludes leucine, isoleucine, and valine.

  • Protein Synthesis Lab Report

    975 Words  | 2 Pages

    Ash Kothare Professor Hanke Honors Biology 19 September 2015 Paper 5 The paper, Function of Aggregated Reticulocyte Ribosomes in Protein Synthesis by A. Gierer, details the findings about a study to answer the question whether multiple ribosomes can operate on one molecule of messenger RNA simultaneously. Firstly, background information is necessary for understanding this paper. Ribosomes, the organelle where protein synthesis occurs, require a messenger RNA to be attached to it to be labelled active

  • Sickle Cell Anemia: A Curse and a Blessing

    585 Words  | 2 Pages

    responsible for delivering oxygen throughout our bodies. Normal hemoglobin is found as a round shape, and is composed of four proteins – two alpha chains and two beta chains. The change that causes Sickle Cell Anemia occurs when an amino acid called valine is substituted for glutamic acid in both of the beta chains. This change in the composure of hemoglobin causes the shape to change when under certain conditions. Two of these conditions are low oxygen and dehydration. The hemoglobin of a person

  • Blue Test Lab Report

    549 Words  | 2 Pages

    of a phosphate group making it a phosphatase. Therefore, answer C is correct. 21) General formula for an amino acid includes: an amino group, a hydrogen, a carboxyl group and a side chain a) A methyl group can only be found in threonine, alanine, valine, leucine, isoleucine,

  • The Importance Of Leucine Protein Synthesis

    1738 Words  | 4 Pages

    What are Leucine and BCAA’S ? Leucine, also known as 2-amino-4-methylpentanoic acid, along with isoleucine and valine are the three branched chained amino acids (BCAA’S). (Homes HC,et al(1995),(Yeh YY(1984) These three amino acids are essential amino acids (EAA’S) meaning that they do not self produce and these must be got from our diet from protein sources or through supplementation. BCAA’s contribute 35% of EAA’S in muscle protein and 40% of the preformed Amino Acids required by mammals and they

  • Protein Powders: A Comprehensive Evaluation

    560 Words  | 2 Pages

    livestrong.com). Since most of us don’t have a steak dinner on hand right after a workout, protein shakes make it easy and quick to get the protein needed to rebuild muscle. Also your body needs essential amino acids that include: Phenylalanine, Valine, Threonine, Tryptophan, Isoleucine, Methionine, Leucine, Lysine, Histidine (your body can manufacture histidine, but usually not in sufficient amounts) (nutribodyprotein.com) If your diet lacks any of these essential amino acids over time your body

  • Acetic Acid Lab Report

    1395 Words  | 3 Pages

    to dissociate all three of the groups found in arginine where as in acetic and boric acid there are only two groups and therefore only need two NaOH equivalents. Valine is similar where it has two groups that can be ionized with pKas of 2.3 for the alpha carboxyl group and 9.7 for the alpha amino group (Plumber, 2004). For 1 mol of valine the required the volume of 0.20M NaOH needed is pH=pKa+log (〖[A〗^-])/[HA] 〖[A〗^-]=〖10〗^((9.8-9.7) )*1=1.3mol so 1.3 mol of NaOH is required D3. The two forms

  • Maple Import Urine Disease Research Paper

    1686 Words  | 4 Pages

    Maple syrup urine disease (MSUD) is a metabolic disorder due to deficiency of branched-chain alpha keto acid dehydrogenase enzyme resulting in accumulation of branched-chain amino acids (BCAAs) (leucine, isoleucine, and valine). Prolonged accumulation of leucine and its metabolites may lead to cerebral edema and its lethal complication like cerebral herniation and severe permanent neuronal damage causing psychomotor developmental delay. Lowering the concentration of these metabolic byproducts can

  • Sweat Residue Lab Report

    656 Words  | 2 Pages

    Perspiration discharges through the sweat glands of our fingertips is mainly made up of water, amino acids (Table 1), sebum (Table 2) and various minerals (Table 3). Amino Acid Value of Abundance Serine 100 Ornithine-Lysine 45 Alanine 30 Threonine 15 Valine 10 Glutamic acid 8 Phenylalanine 6 Tyrosine 5 Table 1. Relative abundance of amino acids in sweat. Lipid Percentage Glycerides 33 Fatty acids 30 Wax esters 22 Cholesterol esters 2 Cholesterol 2 Squalene 10 Table 2. Percentage of lipids in sweat.

  • Exploring Sickle Cell Anemia in Individuals X, Y, Z

    878 Words  | 2 Pages

    Cell or carry the Sickle Cell trait. Sickle cell Anemia is a disease of the red blood cells that is inherited from your parents. Sickle Cell is caused by point mutation in which a single base in the ꞵ-globin gene that results in the substitution of valine instead of glutamate in the amino acid chain. The acid change aggravates the blood cells and make them take a sickle shape and lose elasticity. The main purpose of Hemoglobin is to carry oxygen from the lungs to the body’s tissues. To carry out this

  • Great Achievements of the 20th Century: Antibiotics

    725 Words  | 2 Pages

    One of the greatest achievements in the 20th century was the invention and mass production of antibiotics. Antibiotics or antimicrobials are chemical drugs that are used to treat a variety of different infectious bacterial diseases by destroying or slowing the growth of the bacteria. Antibiotics are toxic to the target cell but do not harm the host. They are designed to attack various kinds of parasites, fungus, and bacteria. Contrary to popular belief antibiotics do not work against viruses like

  • Essay On Amino Acids

    751 Words  | 2 Pages

    Amino acids are the building blocks of the body that make up proteins. Proteins substances are built of twenty amino acids that form the muscle, organs, glands, tendons, nails and hair. On the other hand, amino acids are classified into two groups; these groups are essential and non-essential amino acids. Amino acids that are obtained from food are called essential amino acids, and amino acids that our bodies produce from other sources are called non-essential amino acids. Also the key elements of

  • Sickle Cell Anemia In Sub-Saharan Africa

    872 Words  | 2 Pages

    Hemoglobin A, an oxygen-carrying protein in blood cells, becomes abnormal once a point mutation occurs on chromosome 11. The mutation causes the sixth amino acid of the protein to change from glutamine to valine, resulting in the abnormal hemoglobin S. An autosomal disease known as sickle cell anemia is caused by having homozygous recessive alleles of hemoglobin S. Hemoglobin S form stiff strands within the blood cell which results in the sickle, or crescent

  • Cystic Fibrosis Research Paper

    987 Words  | 2 Pages

    Cystic Fibrosis is an autosomal recessive condition with roughly 1 in 30 Americans being carriers and 30,000 having the disease itself [1]. Its cause, generally speaking, is a mutation with a protein known as Cystic Fibrosis Transmembrane Conductance Regulator (CFTR.) Normally the CFTR protein is folded with the help of chaperone proteins, checked for mutaions by the endoplasmic reticulum and then moved to the apical surface of epithetical cells where it channels chloride ions out of epithelial