ASCII Chemical Map of Amino Acids


  • Central alpha-carbon (Cα) connected to:
    • Amino group (H₂N–)
    • Carboxyl group (–COOH)
    • Side chain (R group) unique to each amino acid
    • Hydrogen atom

Key:
NH₂ = amino group
COOH = carboxyl group
R = side chain (described explicitly)
Bonds shown as “–” (single) or “=” (double)


1. Alanine (Ala, A) — C₃H₇NO₂

     H
     |
NH2–C–COOH
     |
    CH3

2. Arginine (Arg, R) — C₆H₁₄N₄O₂

     H
     |
NH2–C–COOH
     |
   CH2–CH2–CH2–NH–C(=NH)–NH2

3. Asparagine (Asn, N) — C₄H₈N₂O₃

     H
     |
NH2–C–COOH
     |
   CH2–C(=O)–NH2

4. Aspartic Acid (Asp, D) — C₄H₇NO₄

     H
     |
NH2–C–COOH
     |
   CH2–COOH

5. Cysteine (Cys, C) — C₃H₇NO₂S

     H
     |
NH2–C–COOH
     |
   CH2–SH

6. Glutamic Acid (Glu, E) — C₅H₉NO₄

     H
     |
NH2–C–COOH
     |
  CH2–CH2–COOH

7. Glutamine (Gln, Q) — C₅H₁₀N₂O₃

     H
     |
NH2–C–COOH
     |
  CH2–CH2–C(=O)–NH2

8. Glycine (Gly, G) — C₂H₅NO₂

     H
     |
NH2–C–COOH
     |
     H

9. Histidine (His, H) — C₆H₉N₃O₂

     H
     |
NH2–C–COOH
     |
   CH2–(imidazole ring)
        /N\
       |   |
       C   C–NH
       \\ //
         N

10. Isoleucine (Ile, I) — C₆H₁₃NO₂

     H
     |
NH2–C–COOH
     |
   CH–CH3
   |
 CH2–CH3

11. Leucine (Leu, L) — C₆H₁₃NO₂

     H
     |
NH2–C–COOH
     |
   CH2–CH–CH3
         |
        CH3

12. Lysine (Lys, K) — C₆H₁₄N₂O₂

     H
     |
NH2–C–COOH
     |
  CH2–CH2–CH2–CH2–NH2

13. Methionine (Met, M) — C₅H₁₁NO₂S

     H
     |
NH2–C–COOH
     |
  CH2–CH2–S–CH3

14. Phenylalanine (Phe, F) — C₉H₁₁NO₂

     H
     |
NH2–C–COOH
     |
   CH2–(benzene ring)

15. Proline (Pro, P) — C₅H₉NO₂

     H
     |
NH–C–COOH
 \  |
  CH2–CH2–CH2
   \________/

16. Serine (Ser, S) — C₃H₇NO₃

     H
     |
NH2–C–COOH
     |
   CH2–OH

17. Threonine (Thr, T) — C₄H₉NO₃

     H
     |
NH2–C–COOH
     |
   CH(OH)–CH3

18. Tryptophan (Trp, W) — C₁₁H₁₂N₂O₂

     H
     |
NH2–C–COOH
     |
   CH2–(indole ring)
        /N\
       |   |
       C   C
       \\ //
        C

19. Tyrosine (Tyr, Y) — C₉H₁₁NO₃

     H
     |
NH2–C–COOH
     |
   CH2–(benzene ring–OH)

20. Valine (Val, V) — C₅H₁₁NO₂

     H
     |
NH2–C–COOH
     |
   CH–CH3
    |
   CH3

Non-standard Amino Acids Found in Nature

21. Selenocysteine (Sec, U) — C₃H₇NO₂Se

     H
     |
NH2–C–COOH
     |
   CH2–SeH
  • Incorporated at UGA codons with SECIS element.
  • “21st amino acid” — similar to cysteine but with selenium instead of sulfur.

22. Pyrrolysine (Pyl, O) — C₁₂H₂₁N₃O₃

     H
     |
NH2–C–COOH
     |
   CH2–(pyrroline ring with lysine chain)
  • Found in certain methanogenic archaea and bacteria.
  • Encoded by UAG stop codon in special contexts.

Amino Acids – SolveForce Communications


Key terms in plain language

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A provider’s written commitment covering service targets such as availability, response time, repair time, and sometimes financial credits when commitments are missed.