Evidence map›Paper›PMID 42261074›Full record

ArticleJournal of chemical information and modeling2026

KNexPHENIX: A PHENIX-Based Workflow for Improving Cryo-EM and Crystallographic Structural Models.

Suparno Nandi, Graeme L Conn

Abstract read
In one paragraph

Article in Journal of chemical information and modeling, 2026. 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. Article
  2. Mechanism of 30S subunit recognition and modification by the conserved bacterial ribosomal RNA methyltransferase RsmI.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Suparno NandiDepartment of Biochemistry, Emory University School of Medicine, Atlanta, Georgia30322, United States.ORCID 0000-0002-3534-8002
Graeme L ConnDepartment of Biochemistry, Emory University School of Medicine, Atlanta, Georgia30322, United States.ORCID 0000-0002-2419-380X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

New and improved methods for visualizing complex macromolecules in atomic detail continue to expand structural information in the Protein Data Bank but accurately refining atomic models from experimental maps remains a challenge due to efficiency limitations of current refinement approaches. Standard PHENIX refinement can partially address these limitations with its speed and accessibility but often fails to yield the best model compared to more computationally demanding approaches. To support improved macromolecular model building, we therefore developed "KNexPHENIX", a PHENIX-based workflow that combines staged refinement, geometry minimization, and customized refinement parameters. KNexPHENIX can be used to refine macromolecular structures obtained via cryo-electron microscopy (cryo-EM) or X-ray crystallography, regardless of molecular size or composition. KNexPHENIX was evaluated on deposited structures and

Indexed as

Cryoelectron MicroscopyModels, MolecularSoftwareCrystallography, X-RayProtein ConformationWorkflow

Identifiers

PMID42261074
PMCPMC13292208

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.