REVIEW 2 cited by
Generative De Novo Protein Design with Global Context
Not yet reviewed by Pith; the record is open.
This paper has not been read by Pith yet. Machine review is queued; the pith claim, tier, and objections will appear here once it completes.
SPECIMEN: schema-true, not a live event
T0 review · schema-true
One-sentence machine reading of the paper's core claim.
pith:XXXXXXXX · record.json · timestamp
read the original abstract
The linear sequence of amino acids determines protein structure and function. Protein design, known as the inverse of protein structure prediction, aims to obtain a novel protein sequence that will fold into the defined structure. Recent works on computational protein design have studied designing sequences for the desired backbone structure with local positional information and achieved competitive performance. However, similar local environments in different backbone structures may result in different amino acids, indicating that protein structure's global context matters. Thus, we propose the Global-Context Aware generative de novo protein design method (GCA), consisting of local and global modules. While local modules focus on relationships between neighbor amino acids, global modules explicitly capture non-local contexts. Experimental results demonstrate that the proposed GCA method outperforms state-of-the-arts on de novo protein design. Our code and pretrained model will be released.
Forward citations
Cited by 2 Pith papers
-
ProtInvTree: Deliberate Protein Inverse Folding with Reward-guided Tree Search
A reward-guided tree search over a frozen protein language model designs diverse sequences that score higher on ESMFold-based self-consistency benchmarks than existing inverse folding methods.
-
EnerBridge-DPO: Energy-Guided Protein Inverse Folding with Markov Bridges and Direct Preference Optimization
A Markov-bridge inverse folding model fine-tuned with energy-based preference pairs and an explicit ΔΔG loss designs lower-energy protein complex sequences while keeping sequence recovery close to state-of-the-art.
Discussion (0). Sign in to comment.