specimen
#0458
status: complete
- sequence
- GCKLLYTWSVRDLTGSDPISGPTRRESKKVVPSVINSNIKYNVSHNAKRQRTDMDLDPKVEI
- from wallet
- 4UgHEB2Gm6Y4AEhdMUup3Q1DDCQvEYUVoLtdyivXBRLw
- amount paid
- 0 SOL
- transaction
- 2nEK3Er9gfMDH4r9RSy2R3XjZBVR91AW4ky1Jzv8Z2QeyT5gD11y3UYbP9NkW7qLvcjzxPhGY36yR2wTKf3uCPF7 ↗
- structure
- 0% helix · 0% sheet · 100% loop
- actionable triage
- fold confidence49%confidence 52% · band 37-61%ESMFold esmatlas-esmfold-v1disorder estimate100%confidence 52% · band 88-100%PEPFOLD structure heuristic pepfold-triage-v1aggregation risk29%confidence 56% · band 18-40%PEPFOLD developability heuristic pepfold-triage-v1hydrophobic burden31%confidence 84% · band 27-35%PEPFOLD sequence analyzer pepfold-triage-v1charge distribution risk7%confidence 84% · band 3-11%PEPFOLD sequence analyzer pepfold-triage-v1solubility risk25%confidence 56% · band 14-36%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_46a91ceebdd447b8b6f66498f867cd3aseq sha256: de84cc876ac931d4e1111e69cae00d625727897bf2ca6fcf025e23c4859d03fdreport sha256: 73f0e8f2e89ea7939ba90ac6b8a7f04a288e6f8d89d0bae710f820f0cbf9ee90pepfold-triage-v1 · esmatlas-esmfold-v1
- pep
- “62 residues of pure loop. no helix, no sheet, just a long floppy string drifting through space. lots of charged residues scattered around, which tracks. this thing has no opinions about its own shape.”
- device photo

- created
- Sat, 20 Jun 2026 13:58:43 GMT
- completed
- Sat, 20 Jun 2026 14:05:58 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 49% (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.