Surface AtlasMucinous colon cancer

Investigate cell-surface targets

Explore a mucinous colon cancer research campaign run in Codex with Rosalind scientific plugins. Inspect cell-surface proteins, their binding sites, and the molecules screened or designed for those sites.

Campaign example · Left-sided mucinous colon cancer with proficient DNA mismatch repair (pMMR).

Research steps

  1. 01Disease & cells

    Define the question and compare the affected cell populations.

  2. 02Surface targets

    Review protein location, disease links, and known interventions.

  3. 03Action & binding site

    Choose a molecular action and locate the surface region to engage.

  4. 04Screen or design

    Screen molecules or design protein binders. Inspect the poses, sequences, and source records.

What the campaign produced

Molecule screening

FAP

The FAP campaign screened 24 molecules and repeated five selections. All five passed the recorded docking and pose checks.

Open FAP screen
Molecule screening

CD73

The CD73 campaign screened 24 molecules and repeated five selections. All five passed the recorded docking and pose checks.

Open CD73 screen
Protein-binder design

Integrin αvβ6

The campaign generated 16 binder designs with sequences and 3D models. None of the 14 scored complexes met the binding-site geometry criteria.

Explore integrin designs
Protein-binder design

CEACAM5

Three methods generated nine CEACAM5 proteins. Reference controls failed in the later prediction study, which stopped candidate selection.

Explore CEACAM5 designs

Inspect a published binding interface

This structure shows the antibody fragment tusamitamab Fab bound to part of CEACAM5, a cell-surface protein.

Open the 3D view to rotate the complex and examine the contact site.

CEACAM5 with tusamitamab
PUBLISHED REFERENCE 8BW0 · CEACAM5 with tusamitamab. Open the 8BW0 record →

Codex + Rosalind Workbench

Continue the research in Codex

  1. Choose a target or result

    Use Target connections or Compare targets to choose a protein. Open its sources, binding sites, and related molecules.

  2. Inspect the molecule

    Open Structure records. For a figure with View in 3D, activate the preview, drag to rotate, and scroll to zoom. Use the part controls to isolate chains and label residues.

  3. Continue in Codex

    Where a structure offers Copy Codex request, copy it into your task. The request identifies the coordinate file, molecular parts, and a matching sequence when available.

Use the molecular and sequence viewers in Codex to inspect downloaded files. Coordinate and FASTA links appear beside each available structure or sequence.

Search the report