Evidence map›Paper›PMID 39672676›Full record

ArticleBioinformatics (Oxford, England)2024

DPAM-AI: a domain parser for AlphaFold models powered by artificial intelligence.

Jesse Durham, Jing Zhang, Richard D Schaeffer, Qian Cong

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. A structural atlas of death domain fold proteins reveals their versatile roles in biology and function.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Jesse DurhamEugene McDermott Center for Human Growth and Development, University of Texas Southwestern Medical Center, Dallas, TX 75390, United States.ORCID 0000-0001-6335-1332
Jing ZhangEugene McDermott Center for Human Growth and Development, University of Texas Southwestern Medical Center, Dallas, TX 75390, United States.ORCID 0000-0003-4190-3065
Richard D SchaefferDepartment of Biophysics, University of Texas Southwestern Medical Center, Dallas, TX 75390, United States.
Qian CongEugene McDermott Center for Human Growth and Development, University of Texas Southwestern Medical Center, Dallas, TX 75390, United States.ORCID 0000-0002-8909-0414

Funding

ECOD: Large scale classification of predicted and experimental protein structuresR01GM147367 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI Richard Dustin Schaeffer · 2023 to 2026
$1.4M
Functions of Rapidly-Evolving Proteins and Their Roles in PathogenicityK99AI180984 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI ZHANG, JING · 2024 to 2025
$210k
Targeting hyper-reactive cysteines within PPI interfacesF31GM154464 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI DURHAM, JESSE · 2024 to 2025
$81k
NIAID NIH HHS K99 AI180984NIGMS NIH HHS F31 GM154464NIGMS NIH HHS R01 GM147367Welch Foundation R01GM147367
6 · The paper itself

Abstract

motivationDue to the breakthrough in protein structure prediction by AlphaFold, the scientific community has access to 200 million predicted protein structures with near-atomic accuracy from the AlphaFold protein structure DataBase (AFDB), covering nearly the entire protein universe. Segmenting these models into domains and classifying them into an evolutionary hierarchy hold tremendous potential for unraveling essential insights into protein function.

resultsWe introduce DPAM-AI, a Domain Parser for AlphaFold Models based on Artificial Intelligence. DPAM-AI utilizes a convolutional neural network trained with previously classified domains in the Evolutionary Classification Of protein Domains (ECOD) database. DPAM-AI integrates inter-residue distances, predicted aligned errors, and sequence and structural alignments to previously classified domains detected via sequence (HHsuite) and structural (Dali) similarity searches. DPAM-AI has demonstrated its power through rigorous tests, excelling in several benchmark sets compared to its predecessor, DPAM, and other recently published domain parsers, Merizo and Chainsaw. We applied DPAM-AI to representative AFDB models for proteins classified in Pfam. We obtained representative 3D structures for 18 487 (89%) of the 20 795 Pfam families. The remaining families either (i) belong to viral proteins that were excluded from AFDB or (ii) do not adopt globular 3D structures. Our structure-aware domain delineation uncovered a considerable fraction (15%) of Pfam domains containing multiple structural and evolutionary units and refined the boundaries for over half. AVAILABILITY AND IMPLEMENTATION: Pfam and corresponding DPAM-AI domains are at http://prodata.swmed.edu/DPAM-pfam/. Our code is deposited at https://github.com/Jsauce5p/DPAM/tree/dpam_ai, and updates will be released through https://github.com/CongLabCode/DPAM.

Indexed as

Artificial IntelligenceDatabases, ProteinProteinsAlgorithmsComputational BiologyNeural Networks, ComputerProtein DomainsProtein FoldingSoftwareProteins

Identifiers

PMID39672676
PMCPMC11723527

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.