Think of a protein as a super‑strong LEGO® set made from tiny blocks called amino acids. Each block has a unique shape and colour, and when you snap them together in a specific order, you build a functional machine – the protein. 🧩
There are 20 standard amino acids. Each has a central carbon (the α‑carbon) bonded to:
The side chain determines the amino acid’s properties – hydrophobic, polar, acidic, or basic.
When two amino acids link, a peptide bond forms between the carboxyl carbon of one and the amino nitrogen of the next, releasing a water molecule (a condensation reaction):
\$\ce{H2N-CHR-COOH + H2N-CHR'-COOH -> H2N-CHR-CO-NH-CHR'-COOH + H2O}\$
The resulting chain is called a polypeptide.
1️⃣ Write the sequence of amino acids using their one‑letter codes (e.g., M for methionine).
2️⃣ Connect the α‑carbons with a straight line to represent the backbone.
3️⃣ Attach side chains to each α‑carbon – use different shapes or colours for each R group.
4️⃣ Show peptide bonds as short lines between the carbonyl carbon and the nitrogen.
5️⃣ Indicate secondary structure by shading α‑helices (spiral) or β‑sheets (zig‑zag).
6️⃣ Label key functional sites (e.g., active site, binding pocket) if relevant.
| One‑Letter Code | Full Name | Side Chain (R) |
|---|---|---|
| A | Alanine | –CH₃ |
| C | Cysteine | –CH₂–SH |
| D | Aspartic acid | –CH₂–COOH |
Good luck – you’ve got this! 🚀