specimen
#0401
status: complete
- sequence
- QFFPLMGPKMIAVDVTERNQLGYVNATYNYKFQPKWETCLSRALHPQESKGEMMDPIMQKSTSA
- from wallet
- 7MwD77ZYhYzKLZ2cC3AKjEzCVFkHzbGuCzR4PsNAU3AV
- amount paid
- 0 SOL
- transaction
- YhN5bxVEQziCY68CZc9HnZM1hgSMCHmKxjVXCcNX9SPjFd7tEpPrWqe7uS4F3u2vQXy8VAd7crPD4ivc4gLjdW6 ↗
- structure
- 0% helix · 0% sheet · 100% loop
- actionable triage
- fold confidence47%confidence 52% · band 35-59%ESMFold esmatlas-esmfold-v1disorder estimate100%confidence 52% · band 88-100%PEPFOLD structure heuristic pepfold-triage-v1aggregation risk34%confidence 56% · band 23-45%PEPFOLD developability heuristic pepfold-triage-v1hydrophobic burden39%confidence 84% · band 35-43%PEPFOLD sequence analyzer pepfold-triage-v1charge distribution risk2%confidence 84% · band 0-6%PEPFOLD sequence analyzer pepfold-triage-v1solubility risk28%confidence 56% · band 18-40%PEPFOLD developability heuristic pepfold-triage-v1
- developability flags
- medium: structure confidence is limitedmedium: predicted disorder is elevated
- synthesis hints
- - sequence length >45 aa may reduce synthesis yield
- audit trail
- run: run_a610a99b453d4add82c6c70d1945725dseq sha256: e2a18f729547ec984e67e307cc79915fbc5411376759ea6fb1bbd16b3795fdedreport sha256: ccccfbe57c83f3da3177df45d05fc0b75f50520a1527982c4dfa107c89dbf6d5pepfold-triage-v1 · esmatlas-esmfold-v1
- pep
- “64 residues of pure loop. no helix, no sheet, just a long noodle drifting through space with nothing to commit to. composition is all over the place too, like it was assembled by someone changing their mind mid-sentence.”
- device photo

- created
- Wed, 17 Jun 2026 21:10:27 GMT
- completed
- Wed, 17 Jun 2026 21:29:29 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. LIABILITY REDESIGN ROUNDin silico only · 0–1d
redesign to remove the flagged motif(s) before going wet-lab: contains methionine; oxidation sensitivity possible. minimal substitutions usually suffice (e.g. N→Q for deamidation hotspots, M→L for met oxidation).
trigger: 1 motif liability flag(s) in the sequence - 2. 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 47% (model is uncertain) - 3. 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.