Evidence map›Paper›PMID 39964789›Full record

ArticleJournal of synchrotron radiation2025

Macromolecular crystallography at SPring-8 and SACLA.

Masaki Yamamoto, Takashi Kumasaka

Abstract read
In one paragraph

Article in Journal of synchrotron radiation, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
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

2 authors.

Masaki YamamotoRIKEN SPring-8 Center, 1-1-1 Kouto, Sayo, Hyogo 679-5148, Japan.ORCID 0000-0002-1311-1768
Takashi KumasakaJapan Synchrotron Radiation Research Institute (JASRI), 1-1-1 Kouto, Sayo, Hyogo 679-5198, Japan.ORCID 0000-0001-9289-1557

Funding

AMED/BINDS JP21am0101070AMED/BINDS JP22ama121001MEXT/Grant-in-Aid for Scientific Research in the New Academic Area 19H05783
6 · The paper itself

Abstract

Since the groundbreaking determination of the first protein crystal structure by J. C. Kendrew in 1959, macromolecular crystallography (MX) has remained at the forefront of structural biology, driven by continuous technological advancements. The advent of synchrotron radiation in the 1990s revolutionized the field, enhancing data quality, introducing novel phasing methods, and broadening the scope of target samples to include membrane proteins and supramolecular complexes. In 1997, Japan inaugurated SPring-8, one of the world's largest third-generation synchrotron radiation facilities. With its high-brilliance radiation from insertion devices, SPring-8 has dramatically increased the capability of MX. This paper describes MX's evolution, current developments, and prospects at SPring-8 and SACLA.

Indexed as

macromolecular crystallographySACLASPring-8synchrotron radiationXFELsX-ray free electron lasers

Identifiers

PMID39964789
PMCPMC11892910

What OpenQuestion holds

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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.