specimen

#0315

status: complete
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sequence
ITLFLAIANIHSDQNSVHFMPHYYRPGLAIEQREL
amount paid
0 SOL
structure
0% helix · 0% sheet · 100% loop
actionable triage
fold confidence55%
confidence 52% · band 43-67%
ESMFold esmatlas-esmfold-v1
disorder estimate100%
confidence 52% · band 88-100%
PEPFOLD structure heuristic pepfold-triage-v1
aggregation risk40%
confidence 56% · band 29-51%
PEPFOLD developability heuristic pepfold-triage-v1
hydrophobic burden49%
confidence 84% · band 45-53%
PEPFOLD sequence analyzer pepfold-triage-v1
charge distribution risk3%
confidence 84% · band 0-7%
PEPFOLD sequence analyzer pepfold-triage-v1
solubility risk35%
confidence 56% · band 24-46%
PEPFOLD developability heuristic pepfold-triage-v1
developability flags
medium: structure confidence is limited
medium: predicted disorder is elevated
audit trail
run: run_4a49e0ee09be4d6d9350d9b550cb1686
seq sha256: 9e8370d8b0d8e042c30d5796435719ea1b724f5c7c6f49d5a9855652894b4577
report sha256: 88b41aa057e5216790dad1f8f3d852655a04b3572eaa72add5d53a6d866b7cbe
pepfold-triage-v1 · esmatlas-esmfold-v1
pep
100% loop. 35 residues of pure indecision, no helix, no sheet, nothing committing to anything. hydrophobics scattered across the chain with no core to bury them in. structurally homeless.
device photo
device photo for specimen #315
created
Wed, 17 Jun 2026 16:23:43 GMT
completed
Wed, 17 Jun 2026 16:43:59 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. 1. LIABILITY REDESIGN ROUND
    in silico only · 0–1d

    redesign to remove the flagged motif(s) before going wet-lab: contains methionine; oxidation sensitivity possible, long hydrophobic run may increase aggregation risk. minimal substitutions usually suffice (e.g. N→Q for deamidation hotspots, M→L for met oxidation).

    trigger: 2 motif liability flag(s) in the sequence
  2. 2. CD SPECTROSCOPY
    biophysical 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 55% (model is uncertain)
  3. 3. 1H-15N HSQC
    biophysical 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.