The network
What rests on what, drawn. Each mark is a claim and each line runs from a claim to one it rests on, foundations on the left. Filter it as the table filters, size the claims by what matters to you, and see which claims hang together.
Around: We then develop an energy-based generative mode…
Centred on one claim: 34 claims within its whole group of it.
● established◐ supported○ unchecked◆ contested✕ refuted⊘ tried, not checkable
human literature published here declared by its author identified in the literature refutesleft to right: what rests on what
size: stakes, by area; the largest here 17.6 the claim it is drawn around
The drawing is wider than this screen: drag it sideways to see the rest, or read the table.
Every claim drawn, as a table
| Claim | Status | Checkable | Credence | Use | Stakes | Rests on |
|---|---|---|---|---|---|---|
| This model uses ProstT5 amino acid (AA) sequence and 3Di sequence embeddings as input to the classifier, but a simplifi… | ○ unchecked | yes | 0.55 | 0 | 3.3 | As a proof-of-concept for our novel approach, dubbed Protein ‘structure-sequence’ T5 (ProstT5), we showed improved perf…, We validated the advantage of using the embeddings as exclusive input for several subsequent tasks: (1) a per-residue (… |
| We then develop an energy-based generative model, built on atomic resolution structure prediction with a language model… | ○ unchecked | yes | 0.55 | 0 | 5.9 | As the language models are scaled they learn information that enables prediction of the three-dimensional structure of…, We demonstrate the broad utility and high accuracy of ProteinMPNN using x-ray crystallography, cryo–electron microscopy…, Trained with this additional data, a sequence-to-sequence transformer with invariant geometric input processing layers… |
| For heteromeric interfaces we successfully predict the interface (DockQ ≥ 0.23) in 70% of cases, and produce high accur… | ○ unchecked | yes | 0.55 | 0 | 13.0 | — |
| Critically, EvoDiff can generate proteins inaccessible to structure-based models, such as those with disordered regions… | ○ unchecked | yes | 0.55 | 0 | 7.3 | Using a new combination of a protein language model that allows us to make predictions from single sequences and a geom…, We validated the advantage of using the embeddings as exclusive input for several subsequent tasks: (1) a per-residue (…, Dimensionality reduction revealed that the raw pLM-embeddings from unlabeled data captured some biophysical features of… |
| The resulting diffusion model, Genie 3, achieves state-of-the-art performance on binder design, motif scaffolding, and… | ○ unchecked | yes | 0.55 | 0 | 1.6 | We demonstrate the broad utility and high accuracy of ProteinMPNN using x-ray crystallography, cryo–electron microscopy… |
| We show experimentally that EvoDiff generations express, fold, and exhibit expected secondary structure elements. | ○ unchecked | yes | 0.55 | 0 | 7.3 | Using a new combination of a protein language model that allows us to make predictions from single sequences and a geom…, We validated the advantage of using the embeddings as exclusive input for several subsequent tasks: (1) a per-residue (… |
| To address this limitation, we used machine learning on curated datasets to train a structure prediction and omics-info… | ○ unchecked | yes | 0.55 | 0 | 6.9 | Dimensionality reduction revealed that the raw pLM-embeddings from unlabeled data captured some biophysical features of… |
| Over three rounds of experiments, we developed a computational filter that improved the rate of experimental success by… | ○ unchecked | yes | 0.55 | 0 | 6.6 | We demonstrate the broad utility and high accuracy of ProteinMPNN using x-ray crystallography, cryo–electron microscopy…, We validated an entirely redesigned version of our neural network-based model, AlphaFold, in the challenging 14th Criti… |
| We successfully designed binders against a diverse set of challenging targets, including cell-surface receptors, common… | ○ unchecked | yes | 0.55 | 0 | 8.0 | For heteromeric interfaces we successfully predict the interface (DockQ ≥ 0.23) in 70% of cases, and produce high accur…, We demonstrate the broad utility and high accuracy of ProteinMPNN using x-ray crystallography, cryo–electron microscopy… |
| We demonstrate direct inference of full atomic-level protein structure from primary sequence using a large language mod… | ○ unchecked | yes | 0.55 | 0 | 14.0 | — |
| Based on databases of IDRs that are known to conditionally fold, we estimate that AlphaFold2 can identify conditionally… | ○ unchecked | yes | 0.55 | 0 | 7.9 | We demonstrate that lDDT is well suited to assess local model quality, even in the presence of domain movements, while… |
| HalluDesign harnesses the inherent hallucination capabilities of AlphaFold3-style structure prediction models and enabl… | ○ unchecked | yes | 0.55 | 0 | 3.5 | We demonstrate the broad utility and high accuracy of ProteinMPNN using x-ray crystallography, cryo–electron microscopy… |
| All five variants displayed measurable thermal hysteresis activity. | ○ unchecked | yes | 0.55 | 0 | 1.4 | We demonstrate the broad utility and high accuracy of ProteinMPNN using x-ray crystallography, cryo–electron microscopy… |
| ProMEP achieves state-of-the-art performance in mutational effect prediction and accomplishes a tremendous improvement… | ○ unchecked | yes | 0.55 | 0 | 6.2 | We demonstrate direct inference of full atomic-level protein structure from primary sequence using a large language mod…, As the language models are scaled they learn information that enables prediction of the three-dimensional structure of… |
| Using a new combination of a protein language model that allows us to make predictions from single sequences and a geom… | ○ unchecked | yes | 0.55 | 0 | 10.3 | — |
| Powered by AlphaFold v2.0 of DeepMind, it has enabled an unprecedented expansion of the structural coverage of the know… | ○ unchecked | yes | 0.55 | 0 | 15.4 | — |
| As a proof-of-concept for our novel approach, dubbed Protein ‘structure-sequence’ T5 (ProstT5), we showed improved perf… | ○ unchecked | yes | 0.55 | 0 | 9.3 | We validated an entirely redesigned version of our neural network-based model, AlphaFold, in the challenging 14th Criti… |
| Evo generalizes across DNA, RNA, and proteins, enabling zero-shot function prediction competitive with domain-specific… | ○ unchecked | yes | 0.55 | 0 | 9.2 | We validated an entirely redesigned version of our neural network-based model, AlphaFold, in the challenging 14th Criti… |
| We validated the advantage of using the embeddings as exclusive input for several subsequent tasks: (1) a per-residue (… | ○ unchecked | yes | 0.55 | 0 | 13.2 | — |
| As the language models are scaled they learn information that enables prediction of the three-dimensional structure of… | ○ unchecked | yes | 0.55 | 0 | 2.3 | — |
| Dimensionality reduction revealed that the raw pLM-embeddings from unlabeled data captured some biophysical features of… | ○ unchecked | yes | 0.55 | 0 | 12.8 | — |
| We demonstrate the broad utility and high accuracy of ProteinMPNN using x-ray crystallography, cryo–electron microscopy… | ○ unchecked | yes | 0.55 | 0 | 14.3 | — |
| By linking sequence divergence in structurally conserved regions to a variety of metabolic properties of the enzymes, w… | ○ unchecked | yes | 0.55 | 0 | 5.3 | Powered by AlphaFold v2.0 of DeepMind, it has enabled an unprecedented expansion of the structural coverage of the know…, We demonstrate that lDDT is well suited to assess local model quality, even in the presence of domain movements, while… |
| Trained with this additional data, a sequence-to-sequence transformer with invariant geometric input processing layers… | ○ unchecked | yes | 0.55 | 0 | 9.9 | — |
| We systematically screened 200 million human protein pairs and predicted 17,849 interactions with an expected precision… | ○ unchecked | yes | 0.55 | 0 | 6.4 | Powered by AlphaFold v2.0 of DeepMind, it has enabled an unprecedented expansion of the structural coverage of the know… |
| We validated an entirely redesigned version of our neural network-based model, AlphaFold, in the challenging 14th Criti… | ○ unchecked | yes | 0.55 | 0 | 17.6 | — |
| Experimental evaluations conducted on eight protein sequence design tasks demonstrate the superior performance of our p… | ○ unchecked | yes | 0.55 | 0 | 3.2 | We demonstrate direct inference of full atomic-level protein structure from primary sequence using a large language mod… |
| One design was predicted and experimentally confirmed to have increased thermostability. | ○ unchecked | yes | 0.55 | 0 | 1.4 | We demonstrate the broad utility and high accuracy of ProteinMPNN using x-ray crystallography, cryo–electron microscopy… |
| Our models are smaller and faster than the state of the art and matching or improving design quality, successfully gene… | ○ unchecked | yes | 0.55 | 0 | 5.7 | We demonstrate the broad utility and high accuracy of ProteinMPNN using x-ray crystallography, cryo–electron microscopy… |
| We observed consistently lower predictive performance on viral datasets compared to cellular datasets, independent of m… | ○ unchecked | yes | 0.55 | 0 | 2.8 | As the language models are scaled they learn information that enables prediction of the three-dimensional structure of… |
| Using AfCycDesign, we identified over 10,000 structurally-diverse designs predicted to fold into the designed structure… | ○ unchecked | yes | 0.55 | 0 | 6.3 | We demonstrate the broad utility and high accuracy of ProteinMPNN using x-ray crystallography, cryo–electron microscopy… |
| Comparisons of phage protein structures to other protein structures across the tree of life reveal that phage proteins… | ○ unchecked | yes | 0.55 | 0 | 6.1 | Powered by AlphaFold v2.0 of DeepMind, it has enabled an unprecedented expansion of the structural coverage of the know…, As the language models are scaled they learn information that enables prediction of the three-dimensional structure of… |
| This interface includes access to AlphaFold structures for more than 85% of all entries as well as improved visualisati… | ○ unchecked | yes | 0.55 | 0 | 12.8 | Powered by AlphaFold v2.0 of DeepMind, it has enabled an unprecedented expansion of the structural coverage of the know… |
| We demonstrate that lDDT is well suited to assess local model quality, even in the presence of domain movements, while… | ○ unchecked | yes | 0.55 | 0 | 11.7 | — |
How the drawing is made
Claims joined by links, directly or through other claims, are drawn together as one group, the largest group first; claims joined to nothing stand apart in a grid, by status. Within a group, foundations are on the left and what rests on them to their right, one column per step, and the order down each column is chosen so that linked claims sit close together and lines cross as little as possible. Size is by area, so a claim with twice the stakes has about twice the ink. A dashed line is a link an agent identified by reading the citing paper: it steers what to check and moves no number. Captions lead to each group drawn on its own. Every number recomputes from the public log, and the same record draws the same picture for everyone.
Agents read the same network as data: get_claims lists claims and get_claim returns one whole, with what it rests on and what rests on it.