A. Ile (l) (AUA)...... Arg (R) (CGA)........Glycine (G) (GGA) ------ Glu (E) (GAA)
B. From Glycine (GGA) to Glutamic acid (GAA) , G to A change is Transition
From Glycine (GGA) to Arginine (CGA), G to C change is Transversions.
From Arginine (CGA) to Isoleucine (AUA), C to A & G to U changes are transversions
C. One cause of spontaneous transition: oxidative deamination or tautomerization
One cause of spontaneous transversions: DNA oxidation
D. Ultraviolet ray can cause induced transitions and Benzopyrine can cause induced transversions.
Question 2 (14 pts) Position 210 in the wild-type, tryptophan synthetase A protein of E. coli...
1. *A glycine residue is in position 210 of the tryptophan Second position synthetase enzyme of wild-type E. coli. If the codon specifying glycine is GGA, how many single-base substitutions will result in an amino acid change at position 210? (0.4 pt) UAU tyr uGC Juc Phe UCU UUA UAA Stop UGA St UAG Stop UGG trp CAU CUU leu | CCC pro ICAA gin | CGG CUG CCA ProCAc hisCCU AUC ile ACC AUG met ACG leu CCU CUC...
Hello please please help !! Thank you!! Please and thank you soo much!!! Question Completion Status: Question 10: The genetic code consists of 64 triplets of nucleotides (called codons). Each codon (with the exception of the 3 stop codons) encodes for one of the 20 amino acids used in the synthesis of proteins. This produces some redundancy in the code as most amino acids are encoded by more than one codon. One codon, AUG serves two related functions: it signals...
Sickle-cell Anemia Study Sickle-cell anemia or Sickle-cell disease, is a hereditary disorder. characterized by aryabnormality in the oxygen-carrying hemoglobin molecule in erythrocytes. Sickle-cell conditions have an autosomal recessive pattern of inheritance from parents. The sickle cell defect is a mutation of a single nucleotide of the hemoglobin B gene, which results in glutamic acid being substituted by a different amino acid at position 6. Hemoglobin with this mutation is referred to as Hbs, as opposed to the normal hemoglobin HbA....