Add ProtTucker from "Contrastive learning on protein embeddings enlightens midnight zone"

Description of feature

https://academic.oup.com/nargab/article/4/2/lqac043/6605840?login=false

Experimental structures are leveraged through multiple sequence alignments, or more generally through homology-based inference (HBI), facilitating the transfer of information from a protein with known annotation to a query without any annotation. A recent alternative expands the concept of HBI from sequence-distance lookup to embedding-based annotation transfer (EAT). These embeddings are derived from protein Language Models (pLMs). Here, we introduce using single protein representations from pLMs for contrastive learning. This learning procedure creates a new set of embeddings that optimizes constraints captured by hierarchical classifications of protein 3D structures defined by the CATH resource. The approach, dubbed ProtTucker, has an improved ability to recognize distant homologous relationships than more traditional techniques such as threading or fold recognition. Thus, these embeddings have allowed sequence comparison to step into the ‘midnight zone’ of protein similarity, i.e. the region in which distantly related sequences have a seemingly random pairwise sequence similarity. The novelty of this work is in the particular combination of tools and sampling techniques that ascertained good performance comparable or better to existing state-of-the-art sequence comparison methods. Additionally, since this method does not need to generate alignments it is also orders of magnitudes faster. The code is available at https://github.com/Rostlab/EAT.

Start by reading the linked ProtTucker paper and the referenced Rostlab/EAT repository, then inspect the proteinannotator pipeline entry points to determine how a new annotation method is integrated. Done means ProtTucker is supported in the workflow with documented inputs, outputs, and validation against the project's existing annotation behavior.