Evidence map›Paper›PMID 34321660›Full record

ArticleNature2021

Structural basis of ketamine action on human NMDA receptors.

Youyi Zhang, Fei Ye, Tongtong Zhang, Shiyun Lv, Liping Zhou, Daohai Du, He Lin, Fei Guo, Cheng Luo, Shujia Zhu

Erratum issuedAbstract read
PubMed Publisher
In one paragraph

Article in Nature, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 112 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
112citing papers in PubMed, 2 pooled it
8.7field-weighted citation impact, top 1% 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

112 citing papers in PubMed, 2 syntheses or guidelines pooled it, 197 citations in OpenAlex.

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  11. Structural basis of opioid receptor activation by PCP and ketamine.Nature structural & molecular biology · 2026
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52 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 5 institutions in 1 country.

Youyi Zhang *Institute of Neuroscience, State Key Laboratory of Neuroscience, CAS Center for Excellence in Brain Science and Intelligence Technology, Chinese Academy of Sciences, Shanghai, China.ORCID http://orcid.org/0000-0001-7558-6454
Fei Ye *College of Life Sciences and Medicine, Zhejiang Sci-Tech University, Hangzhou, China.ORCID http://orcid.org/0000-0003-4119-3219
Tongtong Zhang *Institute of Neuroscience, State Key Laboratory of Neuroscience, CAS Center for Excellence in Brain Science and Intelligence Technology, Chinese Academy of Sciences, Shanghai, China.ORCID http://orcid.org/0000-0002-2414-8048
Shiyun LvInstitute of Neuroscience, State Key Laboratory of Neuroscience, CAS Center for Excellence in Brain Science and Intelligence Technology, Chinese Academy of Sciences, Shanghai, China.ORCID http://orcid.org/0000-0001-8779-9430
Liping ZhouUniversity of Chinese Academy of Sciences, Beijing, China.
Daohai DuDrug Discovery and Design Center, the Center for Chemical Biology, State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, China.ORCID http://orcid.org/0000-0002-6623-7778
He LinCriminal Investigation Technology Department, The Third Research Institute of Ministry of Public Security, Shanghai, China.
Fei GuoDrug Discovery and Design Center, the Center for Chemical Biology, State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, China.
Cheng LuoUniversity of Chinese Academy of Sciences, Beijing, China. cluo@simm.ac.cn.ORCID http://orcid.org/0000-0003-3864-8382
Shujia ZhuInstitute of Neuroscience, State Key Laboratory of Neuroscience, CAS Center for Excellence in Brain Science and Intelligence Technology, Chinese Academy of Sciences, Shanghai, China. shujiazhu@ion.ac.cn.ORCID http://orcid.org/0000-0001-8358-2859
Chinese Academy of Sciences · CNCenter for Excellence in Brain Science and Intelligence Technology · CNMinistry of Public Security of the People's Republic of China · CNShanghai Institute of Materia Medica · CNZhejiang Sci-Tech University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ketamine is a non-competitive channel blocker of N-methyl-D-aspartate (NMDA) receptors

Indexed as

Cryoelectron MicroscopyAntidepressive AgentsAsparagineBinding SitesGlutamic AcidGlycineHumansHydrogen BondingHydrophobic and Hydrophilic InteractionsKetamineLeucineMolecular Dynamics SimulationNerve Tissue ProteinsReceptors, N-Methyl-D-AspartateAntidepressive AgentsAsparagineGlutamic AcidGlycineGprin1 protein, mouseKetamineLeucineNerve Tissue ProteinsNR2B NMDA receptorReceptors, N-Methyl-D-Aspartate

Identifiers

PMID34321660
OpenAlexW3183790491

What OpenQuestion holds

Textmetadata
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.