Alanine is deaminated to give pyruvic acid (C3H4O3 )
and Ammonia (NH3)
Pyruvic Acid.
Alanine is the amino acid with a methyl group as its R group.
Analyzing the alanine Ramachandran plot in protein structure prediction can provide insights into the preferred conformational angles of alanine residues in proteins. This information can help in understanding the overall structure and stability of the protein, as well as in predicting potential folding patterns and interactions within the protein molecule.
Anticodons for alanine (Ala) are: CGA, CGG, CGU, CGC
An elevated alanine transaminase (ALT) level can indicate liver damage or disease, such as hepatitis, fatty liver disease, or liver cirrhosis. It is often used as a marker for liver health and function. Further evaluation is needed to determine the specific cause of the elevated ALT level.
The DNA sequence TCAGCCACCTATGGA codes for the mRNA sequence UCAGCCACCUAUGGA, which translates to the amino acids Serine-Alanine-Threonine-Tryptophan. Therefore, this DNA sequence codes for 4 amino acids.
Alanine is the major gluconeogenic amino acid. Plasma alanine is used to make glucose in the liver (Glucose-Alanine Cycle), and thus when this occurs plasma alanine concentration is decreased.
1.0 gram of alanine accounts for the production of approximately 0.681 grams of glucose in the glucose-alanine cycle.
Yes, alanine can be hydrolyzed. Alanine is an amino acid with a carboxylic acid group that can undergo hydrolysis, breaking the peptide bond and producing alanine and other components. This process is commonly carried out by enzymes known as proteases.
Alanine Glycine Phenyl alanine Argenine Histidine Tyrosine
The literature value for the enthalpy of ionization of alanine is approximately 170 kilojoules per mole. This value represents the energy required to remove an electron from a gaseous alanine molecule to form a positively charged ion. It is an important parameter in understanding the chemical properties and reactivity of alanine.
ala
Alanine aminotransferase
The polypeptide alanine is composed of a chain of amino acids where each alanine molecule consists of a central carbon atom bonded to an amino group, a carboxyl group, a hydrogen atom, and a side chain made of a methyl group. The repetitive sequence of alanine molecules linked together forms the polypeptide chain.
The three-letter code for the amino acid alanine is Ala.
The amino acid alanine is non-polar, it has a neutral charge, not positive or negative, and it is hydrophobic.
The "l" should be lower case and in italic, and it can be spelled in full as "levo-". It describes the "handedness" of the amino acid molecule. The prefix "levo-" defines one orientation and "dextro-" the other possible orientation; as "l-Alanine" and "d-Alanine"; or, "dl-Alanine" for the racemic mixture of the two configurations of Alanine.
The R group in alanine is a simple methyl group (CH3). This nonpolar, hydrophobic side chain is small and uncharged, making alanine a neutral, aliphatic amino acid.