specimen
#0386
status: complete
- sequence
- VVGRFKGDLRRGSVPATSVGSPDTATSVKG
- from wallet
- 5DxbY9hNoqrDgZLpCLkmyrJyRK9GtpGXVgUBv8hnQnx7
- amount paid
- 0 SOL
- transaction
- gKKnYCK7NyhcTLbaWsmVCWb77pELG3REfLYjfNg6ANqzQsaM9J4xkPapaCN3qES8wBpAMaayDDcxH1hQaxS3rhS ↗
- structure
- 0% helix · 0% sheet · 100% loop
- actionable triage
- fold confidence56%confidence 52% · band 44-68%ESMFold esmatlas-esmfold-v1disorder estimate97%confidence 52% · band 85-100%PEPFOLD structure heuristic pepfold-triage-v1aggregation risk29%confidence 56% · band 18-40%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 risk25%confidence 56% · band 14-36%PEPFOLD developability heuristic pepfold-triage-v1
- developability flags
- medium: structure confidence is limitedmedium: predicted disorder is elevated
- audit trail
- run: run_d3ff78dc94d047b5a593289bab6e034dseq sha256: b2793de2afedf33d84b184f6978374d15459d3b11bdc8448c590fa4c688e2da2report sha256: 178342cd6db702682bfc1cd37e142073bc38efeab8f3a72a84176832101d5451pepfold-triage-v1 · esmatlas-esmfold-v1
- pep
- “all loop, no commitment. thirty residues of pure floppiness, just drifting through conformational space with no opinion about anything. the GSVP and GSPD motifs probably aren't helping it make up its mind.”
- device photo
- created
- Wed, 17 Jun 2026 21:01:55 GMT
- completed
- Wed, 17 Jun 2026 21:07:01 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 97% (high)
engine pepfold-recs-v1 · not medical advice. use as a starting point for protocol design.