specimen
#0345
status: complete
- sequence
- QLGDETAPPCQETPAIGALRQWGWPWGESQ
- from wallet
- 5yNjktkbVSBbNFS7tCzzDPBbWnEyJbnmbxfapxfj2RsY
- amount paid
- 0 SOL
- transaction
- 55BDsr2APbZ42TzRRZuzWz1GjyK5FcHAdP4Fr2S6BuW8dGrFKYrB35Pcck8JERoJ1Dm55aK2oJbFbPdWBn45zuBg ↗
- structure
- 0% helix · 0% sheet · 100% loop
- actionable triage
- fold confidence56%confidence 52% · band 44-68%ESMFold esmatlas-esmfold-v1disorder estimate100%confidence 52% · band 88-100%PEPFOLD structure heuristic pepfold-triage-v1aggregation risk31%confidence 56% · band 20-42%PEPFOLD developability heuristic pepfold-triage-v1hydrophobic burden30%confidence 84% · band 26-34%PEPFOLD sequence analyzer pepfold-triage-v1charge distribution risk10%confidence 84% · band 6-14%PEPFOLD sequence analyzer pepfold-triage-v1solubility risk26%confidence 56% · band 15-37%PEPFOLD developability heuristic pepfold-triage-v1
- developability flags
- medium: structure confidence is limitedmedium: predicted disorder is elevated
- audit trail
- run: run_11d1e7c91ff4470e859f0d5e86b508baseq sha256: 1783c2d35846902acd5737a049c9865390132215e337c2f00b3e51d821accbcdreport sha256: 1c4bc57de108371f7836b13853dbc1705991fb43bbfd1b4631637636dac19ce5pepfold-triage-v1 · esmatlas-esmfold-v1
- pep
- “all loop, no commitment. 30 residues of pure noodle, not a single hydrogen bond willing to settle down. the double WGWPWG stretch is interesting though, tryptophans clustering like they're trying to start something.”
- device photo
- created
- Wed, 17 Jun 2026 17:34:08 GMT
- completed
- Wed, 17 Jun 2026 17:54:37 GMT
next experiment
what to do next
deterministic suggestions derived from this specimen's triage report. each entry cites the signal that triggered it. ordered cheapest-first.
- 1. CD SPECTROSCOPYbiophysical validation · 1–3d
experimental secondary structure check. confirms whether the predicted helix/sheet content matches a real spectrum before committing to higher-cost assays.
trigger: fold_confidence 56% (model is uncertain) - 2. 1H-15N HSQCbiophysical validation · 2–5d
if disorder is real, peaks will collapse into a narrow proton dispersion. if the peptide is actually folded, peaks will spread out. cheapest way to distinguish IDP from misfold.
trigger: disorder_estimate 100% (high)
engine pepfold-recs-v1 · not medical advice. use as a starting point for protocol design.