specimen
#0370
status: complete
- sequence
- ASACEQQAGEPSYKIGAPKSDIALETLLEDFVLF
- from wallet
- 4UgHEB2Gm6Y4AEhdMUup3Q1DDCQvEYUVoLtdyivXBRLw
- amount paid
- 0 SOL
- transaction
- P2xVzi99du6sHTpeSoXAChiQ4w8HNePcpVrds8fqGn359r941AeLzgDaUBWPd3x5G77q2zMM6CAtSUdbJNUJ7RF ↗
- structure
- 0% helix · 0% sheet · 100% loop
- actionable triage
- fold confidence57%confidence 52% · band 45-69%ESMFold esmatlas-esmfold-v1disorder estimate100%confidence 52% · band 88-100%PEPFOLD structure heuristic pepfold-triage-v1aggregation risk38%confidence 56% · band 27-49%PEPFOLD developability heuristic pepfold-triage-v1hydrophobic burden44%confidence 84% · band 40-48%PEPFOLD sequence analyzer pepfold-triage-v1charge distribution risk12%confidence 84% · band 8-16%PEPFOLD sequence analyzer pepfold-triage-v1solubility risk34%confidence 56% · band 23-45%PEPFOLD developability heuristic pepfold-triage-v1
- developability flags
- medium: structure confidence is limitedmedium: predicted disorder is elevated
- audit trail
- run: run_f7330a617e1c43c885969f22d21edabeseq sha256: bfb9c064ef307ec929dcdbd0556187629d596c6246accc8f27fd0270d1493b29report sha256: f689cee5e6aaba8ddd6f0c589ebe595439685cc4e2c3410fae00272cb130bf0epepfold-triage-v1 · esmatlas-esmfold-v1
- pep
- “100% loop. no helix, no sheet, just 34 residues of pure indecision. composition is all over the place too, charged residues bumping into hydrophobics with no plan. structurally this is a shrug.”
- device photo
- created
- Wed, 17 Jun 2026 20:02:30 GMT
- completed
- Wed, 17 Jun 2026 20:10:59 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 57% (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.