# SegDesign: A modular framework for controllable protein segment engineering

**Authors:** Chenjie Feng, Junbo Yin, Chao Zha, Mohammed Saif, Xiaopeng Xu, Xin Gao, Wenjia He

PMC · DOI: 10.1002/pro.70542 · Protein Science : A Publication of the Protein Society · 2026-03-24

## TL;DR

SegDesign is a new framework for precisely modifying specific parts of proteins while keeping the overall structure intact.

## Contribution

SegDesign introduces a modular framework for controllable, region-specific protein structure engineering.

## Key findings

- SegDesign successfully converted a flexible loop in GgTdT into stable α-helix or β-strand without disrupting the global fold.
- The framework was applied to six enzymes, demonstrating its generality and effectiveness.
- SegDesign integrates backbone reconstruction, sequence redesign, and structural evaluation into a unified workflow.

## Abstract

Local protein structure engineering, such as targeted remodeling of loops or flexible regions, is critical for mechanistic studies and protein optimization but remains challenging to perform in a controllable and reproducible manner. Despite advances in protein foundation models and generative structure design, most existing methods emphasize global scaffold generation and offer limited support for precise, region‐specific intervention while preserving the overall fold. Here we present SegDesign, a modular framework for segment‐level protein engineering that integrates backbone reconstruction, sequence redesign, and multi‐stage structural evaluation into a unified workflow. SegDesign enables user‐defined secondary‐structure manipulation of selected regions and produces traceable, experimentally testable variant panels. Applied to Gallus gallus terminal deoxynucleotidyl transferase (GgTdT), SegDesign converts an intrinsically flexible loop into either a stable α‐helix or β‐strand without disrupting the global fold, as supported by AlphaFold3 modeling. Applications to six additional enzymes further demonstrate the generality of the approach. SegDesign establishes an accessible paradigm for controllable local protein structure engineering in both mechanistic and applied settings. The standalone implementation of SegDesign is publicly available at https://github.com/mike114b/Segdesign.

## Linked entities

- **Species:** Gallus gallus (taxon 9031)

## Full-text entities

- **Genes:** DNTT (DNA nucleotidylexotransferase) [NCBI Gene 396351] {aka TDT}, LDHD (lactate dehydrogenase D) [NCBI Gene 415689]
- **Chemicals:** hydrogen (MESH:D006859), 2'-deoxyribonucleoside 5'-triphosphates (-), His (MESH:D006639)
- **Species:** Gallus gallus (bantam, species) [taxon 9031], Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090], Klebsiella pneumoniae (species) [taxon 573]
- **Cell lines:** GgTdT — Homo sapiens (Human), Transformed cell line (CVCL_B2YD)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC13042651/full.md

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13042651/full.md

## References

42 references — full list in the complete paper: https://tomesphere.com/paper/PMC13042651/full.md

---
Source: https://tomesphere.com/paper/PMC13042651