Translate any DNA sequence into its corresponding protein using either the standard genetic code or vertebrate mitochondrial code. Select reading frame, reverse complement, and visualize each codon's amino acid property. Includes GC content calculation and ORF detection.
The DNA translation tool simulates the biological process by which ribosomes decode messenger RNA (derived from DNA) into polypeptide chains. Each triplet of nucleotides, called a codon, specifies a single amino acid or a stop signal. This tool uses the standard genetic code (NCBI translation table 1) and optionally the vertebrate mitochondrial code (NCBI table 2), which differs in several codon assignments.
5′‑DNA → 3′‑mRNA → Protein (N‑terminus to C‑terminus)
ATG (start) → Methionine (M) Stop codons vary by table.
Given a DNA sequence, the tool:
The codon‑amino acid mappings are derived from the NCBI taxonomy database, ensuring accuracy and consistency with current biological knowledge.
Use the dropdown above to switch between standard and mitochondrial code. Stop codons shown as *.
Human insulin is synthesized as preproinsulin. A short fragment coding for part of the B‑chain: ATGGCCCTGTGGATGCGC translates to M A L W M R in the standard code. The tool correctly identifies the start codon (ATG) and translates each triplet. Researchers use such translations to verify synthetic gene sequences before ordering oligos. The interactive bar chart reveals the alternating hydrophobic (leucine, methionine) and polar (arginine) residues, aiding in secondary structure prediction.