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# PALM

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  1. bioRxiv

    PALM learns overlapping domain and site labels together, reaching 0.941 domain-occurrence F1 on 2.3 million held-out proteins

    Protein sequence databases are growing far faster than curated annotation, and existing language models learn only from sequence likelihood, so InterPro domain and functional-site knowledge stays indirect. PALM builds on ESM2 with LoRA adaptation, learned layer aggregation and a bidirectional LSTM encoder, and uses a soft-target loss that lets one residue keep several valid labels. On 2,309,606 held-out proteins it reached domain- and site-occurrence F1 of 0.941 and 0.877, and still 0.857 and 0.828 in the subset below 20% sequence identity.

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