pe
pep-10002 v1 CC-BY-SA-4.0

Test fork prod

A lab-made fragment of human growth hormone designed to burn fat without raising blood sugar or triggering unwanted growth effects; experimental, not an approved drug.

statuscomputed targetFAT-METABOLISM length12 aa refs0
reclassified-feb-2026hgh-fragmentlipolyticgrowth-hormoneweight-lossfda-not-approvedreference-scaffold
EARLY ENTRY This candidate is newly indexed — supporting evidence is still being added. Have a paper or data point? Contribute below.
status 2 / 5
prediction metrics openfold3-mlx 0.3.1
ipTM0.769
pTM0.710
avg pLDDT41.0
ranking score0.832
STRUCTURE · PEP-10002 × FAT-METABOLISM
ranking0.832
target interface 4.5Å peptide drag rotate · ctrl+scroll zoom · right-click pan
openfold3-mlx 0.3.1 · mmCIF ↓ download
sequence12 aa
151012
YLRIVQCRSVEG
details expand to inspect
full evidence table2 metrics
metricvaluetool
ipTM 0.7693435549736023 openfold3-mlx
ranking score 0.8319073915481567 openfold3-mlx
structural qualityopenfold3
0
metricvaluenote
gpde0.721global PDE — lower = better
disorder0.149fraction disordered
chain pair ipTM (A, B)0.769interface quality
3-letter notation
Tyr-Leu-Arg-Ile-Val-Gln-Cys-Arg-Ser-Val-Glu-Gly
recipeopenfold3-mlx 0.3.1
parametervalue
modelopenfold3-mlx 0.3.1
weightsaedd8f3eb814e392…
hardwareapple_m4_base_16gb
mlx version0.31.1
python3.14.3
random seed42
msa strategycolabfold
diffusion samples1
runtime383s
predicted bymlx@peptide
predicted at2026-04-19
python3 openfold3/run_openfold.py predict --query_json {query.json} --runner_yaml examples/example_runner_yamls/mlx_runner.yml --output_dir {output_dir} --num_diffusion_samples 1
lineage 1 parent
▶ pep-10002 YLRIVQCRSVEG [this]
citationbibtex
peptidemodel (2026). Test fork prod (pep-10002, v1). PeptideModel. https://peptidemodel.com/card/pep-10002
@peptide{pep10002,
  sequence = {YLRIVQCRSVEG},
  target   = {fat-metabolism},
  author   = {peptidemodel},
  year     = {2026},
  status   = {computed}
}
references 0 papers
0
no peer-reviewed references this sequence isn't grounded in any published literature.
discussion no comments
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