Ailtozin: Discovery of FGF21-p44, a Human-Specific +1 Frameshifted Microprotein with Stable Alpha-Helical Structure and FGF21-Mimetic Potential

Ailton Douglas de Souza Moreno

doi:10.5281/zenodo.20398834

May 26, 2026Open Access

Ailtozin: Discovery of FGF21-p44, a Human-Specific +1 Frameshifted Microprotein with Stable Alpha-Helical Structure and FGF21-Mimetic Potential

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Key Points

This research focuses on the identification of FGF21-p44, a novel microprotein linked to metabolic health.
Utilized AlphaFold2 to predict the structural stability of the microprotein.
Identified the microprotein through a +1 frameshift mutation in the human FGF21 gene.
FGF21-p44 is a 44-amino acid microprotein with a predicted stable alpha-helical structure.
Establishes Ailtozin as a previously undescribed molecule with potential applications in treating metabolic diseases.

Implication

Preprint reveals FGF21-p44 as a potential FGF21 pathway mimetic in obesity and metabolic disease.

Abstract

We report the discovery of FGF21-p44, named Ailtozin, a novel 44-amino acid microprotein encoded by a +1 frameshift in the human FGF21 gene. AlphaFold2 predicts a stable alpha-helical structure with pLDDT 75. FGF21-p44 represents a previously undescribed human microprotein with potential as an FGF21 pathway mimetic for obesity and metabolic disease. This preprint establishes priority for the Ailtozin sequence and structure. BioRxiv submission ID: BIORXIV/2026/727744

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Cite This Study

Ailton Douglas de Souza Moreno (2026) studied this question.

synapsesocial.com/papers/6a17dd4e3fad632b0f9d9fbf https://doi.org/10.5281/zenodo.20398834

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