sickle cell disease will result
In sickle cell anemia, glutamic acid is replaced by valine due to a single base change in the gene that codes for hemoglobin. This substitution causes the hemoglobin protein to form abnormal sickle-shaped red blood cells, leading to the symptoms of the disease.
GUA codes for the amino acid glycine.
The mutation that results in the replacement of glutamate with valine in sickle cell anemia is a missense mutation. This type of mutation occurs when a single nucleotide change in the DNA sequence leads to the substitution of one amino acid for another in the resulting protein. In this case, the specific change involves the codon for glutamic acid being altered to code for valine, which affects the hemoglobin structure and function.
Glutamate is substituted for a valine at position 6. But this is not an amino acid problem, it's the construction of hemoglobin that's in error.
glutamic acid is replaced by valine in the beta chain
it can have effects on your memory
L-Valine is an aminoacid.
Anticodons for valine (Val) are: CAA, CAG, CAU, CAC
The disease sickle cell anaemia occurs due to a mutation. This causes the amino acid glutamic acid (which is hydrophilic) in haemoglobin to be replaced by valine (which is hydrophobic).
The chemical formula for valine is C5H11NO2.
Monosodium glutamate is not harmful. Monosodium glutamate is put in most foods.
Monosodium Glutamate is a compound.