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Configuration
Reverse Complement
Length 0 aa
Mass 0 Da
GC Content 0%
Nucleotide Sequence (DNA/RNA)
0 bases Ready
Protein Chain Visualization
Start Stop Hydrophobic
Enter a DNA/RNA sequence to generate polypeptide chain
Raw String Output
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About

The Amino Acid Translator is a specialized bioinformatics utility designed to convert nucleic acid sequences (DNA or RNA) into their corresponding polypeptide chains. This process, known as translation in molecular biology, is governed by the standard genetic code.

Accuracy in translation is critical for determining Open Reading Frames (ORFs) and predicting protein structure. This tool mitigates common errors by automatically sanitizing inputs (removing non-coding characters), handling both Thymine (T) and Uracil (U), and providing instant calculations for molecular properties.

Key constraints addressed include frame shifts and partial codons. The translator processes sequences in strictly defined triplets. Any trailing nucleotides that do not form a complete codon are excluded from the translation but preserved in the frame logic. The tool assumes the Standard Genetic Code (NCBI Table 1) and calculates molecular weight based on average isotopic masses.

bioinformatics genetics dna-translator protein-synthesis molecular-weight

Formulas

The translation process relies on mapping trinucleotide sequences (codons) to specific amino acids. The total molecular weight (MW) of the polypeptide chain is estimated by summing the weight of each amino acid minus the weight of water molecules lost during peptide bond formation.

MWprotein Ni=1 (MWaai) (N 1) × 18.015

Where:

  • N = Total number of amino acids in the sequence.
  • MWaa = Average isotopic mass of the individual amino acid residue.
  • 18.015 = Molecular weight of water (H2O) in Daltons, removed per peptide bond.

For Reverse Complement logic, the input DNA sequence is reversed, and bases are swapped according to Chargaff's rules:

{
A T (or U)C G

Reference Data

Amino Acid3-Letter1-LetterCodons (DNA)Avg Mass (Da)Hydropathy
AlanineAlaAGCT, GCC, GCA, GCG89.091.8
ArginineArgRCGT, CGC, CGA, CGG, AGA, AGG174.20-4.5
AsparagineAsnNAAT, AAC132.12-3.5
Aspartic AcidAspDGAT, GAC133.10-3.5
CysteineCysCTGT, TGC121.162.5
Glutamic AcidGluEGAA, GAG147.13-3.5
GlutamineGlnQCAA, CAG146.15-3.5
GlycineGlyGGGT, GGC, GGA, GGG75.07-0.4
HistidineHisHCAT, CAC155.16-3.2
IsoleucineIleIATT, ATC, ATA131.184.5
LeucineLeuLTTA, TTG, CTT, CTC, CTA, CTG131.183.8
LysineLysKAAA, AAG146.19-3.9
MethionineMetMATG149.211.9
PhenylalaninePheFTTT, TTC165.192.8
ProlineProPCCT, CCC, CCA, CCG115.13-1.6
SerineSerSTCT, TCC, TCA, TCG, AGT, AGC105.09-0.8
ThreonineThrTACT, ACC, ACA, ACG119.12-0.7
TryptophanTrpWTGG204.23-0.9
TyrosineTyrYTAT, TAC181.19-1.3
ValineValVGTT, GTC, GTA, GTG117.154.2
StopTERM*TAA, TAG, TGA0.00N/A

Frequently Asked Questions

Currently, this tool uses a strict Standard Genetic Code. Ambiguous characters like "N" (any base) do not map to a specific amino acid and will be rendered as "X" (Unknown) in the output sequence to maintain alignment without making false assumptions.
Yes. The tool calculates the weight of the residues. It sums the individual amino acid masses and subtracts 18.015 Da for every peptide bond formed (Sequence Length - 1), providing the weight of the dehydrated polypeptide chain.
The genetic code is read in triplets. Shifting the starting position by just 1 or 2 bases (Frame +1 or +2) completely alters the grouping of nucleotides, resulting in an entirely different amino acid sequence. This is critical for finding the correct Open Reading Frame (ORF).
Yes. The tool automatically detects "U" (Uracil) and treats it equivalently to "T" (Thymine) for translation purposes. You can paste mixed DNA/RNA, and the sanitizer will normalize it based on your settings.