Q.44 Given below are two statements : One is labelled as Assertion A and the other is labelled as Reason R.
Assertions A : Protein kinases catalyze the transfer of gamma (y) – phosphoryl group of ATP to proteins.
Serine, threonine or Wrosine are the general amino acids that are phosphorylated.
Reason R : Phosphorylation of proteins by protein kinases makes them aggregated and non-functional with
subsequent degradation.
In the light of the above statements. choose the most appropriate answer from the options given below :
1. Both A and R are correct and R is the conect explanation of A
2. Both A and R are correct but R is NOT the comect explanation of A
3. A is correct but R is not correct
4. A is not correct but R is correct
Correct Answer: 3. A is correct but R is not correct
Protein kinases accurately transfer the γ-phosphate from ATP to Ser, Thr, or Tyr residues, but phosphorylation typically regulates function—activating, inactivating, or altering localization—not causing aggregation, loss of function, and degradation as a general rule.
Assertion (A) Analysis
Assertion A is correct. Protein kinases (e.g., PKA, CDK) catalyze transfer of ATP’s γ-phosphoryl (PO₄³⁻) to hydroxyl groups on serine (Ser), threonine (Thr), or tyrosine (Tyr)—the primary phosphoacceptors (>98% of cases). This reversible PTM uses Mg-ATP; reaction: Protein-OH + ATP → Protein-O-PO₃²⁻ + ADP.
Reason (R) Analysis
Reason R is incorrect. Phosphorylation rarely causes aggregation or universal non-function/degradation. Instead:
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Activates (e.g., phosphorylase kinase).
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Inhibits (e.g., glycogen synthase).
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Creates docking sites (e.g., MAPK cascades).
Ubiquitination/proteasome handles degradation; kinases like Aurora B prevent aggregates in mitosis. Disease-linked hyperphosphorylation (e.g., tau in Alzheimer’s) forms tangles, but this is pathological, not the norm.
Option Breakdown
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Option 1: Both correct, R explains A—False. R wrong.
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Option 2: Both correct, R not explanation—False. R incorrect.
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Option 3: A correct, R incorrect—True. Matches analysis.
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Option 4: A incorrect, R correct—False. A precise.
Protein Kinases Phosphorylation: Assertion Reason Molecular Biology
Protein kinases gamma phosphoryl ATP serine threonine tyrosine phosphorylation drives cell signaling, correctly described in Assertion A but misrepresented in Reason R as causing aggregation—key for molecular biology exams.
Protein Kinase Mechanism
Kinases bind ATP in a conserved cleft; Asp residue deprotonates substrate OH, facilitating γ-P transfer:
Protein-OH+γ-PO3-ATP→Protein-O-PO32−+ADP
Targets: Ser/Thr (80%), Tyr (20%); atypical (His/Asp) exist.
Phosphorylation Effects
Reversible switch via phosphatases:
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Conformational change activates (e.g., PKC).
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Inhibits (e.g., IRS-1 in insulin resistance).
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Cascades (RTK → Raf → MEK → ERK).
Not aggregation/degradation—those link to misfolds/ubiquitin.
| Effect | Example | Outcome |
|---|---|---|
| Activation | Glycogen phosphorylase kinase | Breakdown ↑ |
| Inhibition | Myosin light chain phosphatase | Relaxation |
| Localization | STAT1 nuclear entry | Gene expression |
| Docking | SH2 binding phospho-Tyr | Recruitment |
Exam Strategy
Tests PTM details: A recalls mechanism/amino acids right; R confuses with ubiquitination/aggregation pathologies. Prioritize kinase function for GATE Life Sciences.


