We asked: Does motesanib engage KDR in canine HSA × human angiosarcoma?
Co-fold the target with the ligand to test complex formation + affinity.
Cross-species caveat. Co-folded against human 3VHE (VEGFR2 / KDR). The canine KDR/VEGFR2 ortholog (RefSeq NP_001041489.1 / UniProt A0A8I3NL83, taxid 9615) is 93% identical to human overall, 97% across the kinase domain, and 100% identical at every ATP/TKI-pocket residue — so the human structure is a justified cross-species proxy (the binding pocket is sequence-identical), not an unverified substitution.
Pre-registered tests, each locked to a kill-criterion before it ran. Any single one failing rules the whole idea out.
Survived every test the engine could run. Nothing here is proven — that's the point.
Readout. Boltz-2 co-folded motesanib with KDR: interface iptm 0.98, P(binder)=0.96, affinity_pred -1.94 (log µM, lower=stronger). Signal: supports.
Confidence so far: 85% — never proof.
Every result is hashed so anyone can re-derive it. Clearing these checks is necessary, not sufficient — a human still holds the final call, and nothing is auto-promoted.
See the full experiment record.
The pre-registered kill-criterion, the raw readout, and the signed provenance you can verify yourself — plus every new verdict as it lands. Drop your email and we’ll open it up.
A mailing list for early access, not a login. We’ll email you to set up real sign-in once things are polished.