Evidence map›Paper›PMID 35519399›Full record

ArticleRSC advances2019

Computational elucidation of the binding mechanisms of curcumin analogues as bacterial RecA inhibitors.

Zi-Yuan Zhou, Jing Yuan, Qing Pan, Xiao-Mei Mo, Yong-Li Xie, Feng Yin, Zigang Li, Nai-Kei Wong

Open access · goldAbstract read
In one paragraph

Article in RSC advances, 2019. 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
0.4field-weighted citation impact, top 38% of its field
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, 9 citations in OpenAlex.

  1. Multimodal Inhibition ofJournal of agricultural and food chemistry · 2025
    Article
  2. 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

8 authors at 3 institutions in 1 country.

Zi-Yuan ZhouDepartment of Infectious Diseases, Shenzhen Third People's Hospital, The Second Hospital Affiliated to Southern University of Science and Technology Shenzhen 518112 China wongnksz@163.com.
Jing YuanDepartment of Infectious Diseases, Shenzhen Third People's Hospital, The Second Hospital Affiliated to Southern University of Science and Technology Shenzhen 518112 China wongnksz@163.com.
Qing PanShenzhen Key Laboratory of Microbial Genetic Engineering, College of Life Sciences and Oceanology, Shenzhen University Shenzhen 518055 China.
Xiao-Mei MoDepartment of Infectious Diseases, Shenzhen Third People's Hospital, The Second Hospital Affiliated to Southern University of Science and Technology Shenzhen 518112 China wongnksz@163.com.
Yong-Li XieDepartment of Infectious Diseases, Shenzhen Third People's Hospital, The Second Hospital Affiliated to Southern University of Science and Technology Shenzhen 518112 China wongnksz@163.com.
Feng YinDepartment of Chemical Biology, School of Chemical Biology and Biotechnology, Shenzhen Graduate School of Peking University Shenzhen 518055 China lizg@pkusz.edu.cn.ORCID https://orcid.org/0000-0001-7407-9047
Zigang LiDepartment of Chemical Biology, School of Chemical Biology and Biotechnology, Shenzhen Graduate School of Peking University Shenzhen 518055 China lizg@pkusz.edu.cn.ORCID https://orcid.org/0000-0002-4649-1592
Nai-Kei WongDepartment of Infectious Diseases, Shenzhen Third People's Hospital, The Second Hospital Affiliated to Southern University of Science and Technology Shenzhen 518112 China wongnksz@163.com.
Southern University of Science and Technology · CNPeking University · CNShenzhen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antimicrobial resistance (AMR) presents as a serious threat to global public health, which urgently demands action to develop alternative antimicrobial strategies with minimized selective pressure. The bacterial SOS response regulator RecA has emerged as a promising target in the exploration of new classes of antibiotic adjuvants, as RecA has been implicated in bacterial mutagenesis and thus AMR development through its critical roles in error-prone DNA repair. The natural product curcumin has been reported to be an effective RecA inhibitor in several Gram-negative bacteria, but details on the underlying mechanisms are wanting. In order to bridge the gap in how curcumin operates as a RecA inhibitor, we used computational approaches to model interactions between RecA protein and curcumin analogues. We first identified potential binding sites on

Identifiers

PMID35519399
PMCPMC9065326
OpenAlexW2955327244

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.