Q43.Match List I with List II List I A. Glycine B. Tyrosine C. Tryptophan D. Threonine List II I. Aromatic amino acid II. Amino acid having chiral C-atom in side chain III. Optically inactive IV. Amino acid undergoes phosphorylation Choose the correct answer from the options given below : (1) A-IV, B-III, C-II, D-I (2) A-III, B-II, C-IV, D-I (3) A-III, B-I, C-IV, D-II (4) A-III, B-IV, C-I, D-II

Q43.Match List I with List II

List I
A. Glycine
B. Tyrosine
C. Tryptophan
D. Threonine

List II
I. Aromatic amino acid
II. Amino acid having chiral C-atom in side chain
III. Optically inactive
IV. Amino acid undergoes phosphorylation

Choose the correct answer from the options given below :

(1) A-IV, B-III, C-II, D-I
(2) A-III, B-II, C-IV, D-I
(3) A-III, B-I, C-IV, D-II
(4) A-III, B-IV, C-I, D-II

Correct Answer: (3) A-III, B-I, C-IV, D-II

Amino acids glycine, tyrosine, tryptophan, and threonine have unique structural and biochemical properties that match specific descriptions in List II.

Definitions

  • Glycine (A): Simplest amino acid with H as side chain (-H), making its alpha carbon achiral and optically inactive (III).

  • Tyrosine (B): Aromatic amino acid with phenol ring in side chain (I); also has -OH group that undergoes phosphorylation (IV).

  • Tryptophan (C): Aromatic amino acid with indole ring (I); undergoes phosphorylation on nitrogen in some contexts.

  • Threonine (D): Has chiral carbon in side chain (-CH(OH)CH₃), making both alpha and beta carbons chiral (II).

Option Analysis

Option A B C D Correct?
(1) A-IV, B-III, C-II, D-I IV(phospho) III(inactive) II(chiral side) I(aromatic) No: Glycine can’t phosphorylate
(2) A-III, B-II, C-IV, D-I III(inactive) ✓ II(chiral side) IV(phospho) I(aromatic) No: Tyrosine aromatic (I), not chiral side chain
(3) A-III, B-I, C-IV, D-II III(inactive) ✓ I(aromatic) ✓ IV(phospho) ✓ II(chiral side) ✓ Yes: Perfect match
(4) A-III, B-IV, C-I, D-II III(inactive) ✓ IV(phospho) I(aromatic) ✓ II(chiral side) ✓ Partial: B should be I (aromatic), not IV

Master glycine tyrosine tryptophan threonine amino acid matching for biochemistry exams. Correct option (3) pairs optically inactive glycine (III), aromatic tyrosine (I), phosphorylatable tryptophan (IV), and chiral-side-chain threonine (II).

Key Properties Explained

Glycine lacks side chain chirality, making it optically inactive (III)—unique among standard amino acids.
Tyrosine features aromatic phenol ring (I) and phosphorylatable -OH group.
Tryptophan is aromatic (indole ring) and undergoes kinase-mediated phosphorylation (IV).
Threonine has chiral β-carbon in side chain (II), creating two chiral centers.

Why Option 3 Wins

Perfect alignment: glycine’s H-side chain → achiral (III); tyrosine/tryptophan’s rings → aromatic (I/IV); threonine’s -CH(OH)CH₃ → chiral side chain (II). Others confuse aromaticity with phosphorylation.

Exam Memory Aid

“Glycine = No optics (III), Tyr/Trp = Rings + phosphate (I/IV), Thr = Two chirals (II).” Visualize structures: glycine flat, tyrosine phenolic, tryptophan bulky indole, threonine branched.

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