Evidence map›Paper›PMID 27329856›Full record

ArticleMolecular & cellular proteomics : MCP2016

aKMT Catalyzes Extensive Protein Lysine Methylation in the Hyperthermophilic Archaeon Sulfolobus islandicus but is Dispensable for the Growth of the Organism.

Yindi Chu, Yanping Zhu, Yuling Chen, Wei Li, Zhenfeng Zhang, Di Liu, Tongkun Wang, Juncai Ma, Haiteng Deng, Zhi-Jie Liu and 2 more

Open access · hybridAbstract read
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Article in Molecular & cellular proteomics : MCP, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 20% of its field
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 17 citations in OpenAlex.

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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

12 authors at 7 institutions in 1 country.

Yindi ChuFrom the ‡State Key Laboratory of Microbial Resources, Institute of Microbiology, Chinese Academy of Sciences, Beijing, China;
Yanping Zhu§National Laboratory of Biomacromolecules,Institute of Biophysics, Chinese Academy of Sciences, Beijing, China,;
Yuling Chen¶MOE Key Laboratory of Bioinformatics, School of Life Sciences,Tsinghua University, Beijing, China;
Wei Li‖Network Information Center,Institute of Microbiology,Chinese Academy of Sciences, Beijing, China;
Zhenfeng ZhangFrom the ‡State Key Laboratory of Microbial Resources, Institute of Microbiology, Chinese Academy of Sciences, Beijing, China;
Di Liu‖Network Information Center,Institute of Microbiology,Chinese Academy of Sciences, Beijing, China;
Tongkun WangFrom the ‡State Key Laboratory of Microbial Resources, Institute of Microbiology, Chinese Academy of Sciences, Beijing, China;
Juncai MaFrom the ‡State Key Laboratory of Microbial Resources, Institute of Microbiology, Chinese Academy of Sciences, Beijing, China; ‖Network Information Center,Institute of Microbiology,Chinese Academy of Sciences, Beijing, China;
Haiteng Deng¶MOE Key Laboratory of Bioinformatics, School of Life Sciences,Tsinghua University, Beijing, China;
Zhi-Jie Liu§National Laboratory of Biomacromolecules,Institute of Biophysics, Chinese Academy of Sciences, Beijing, China,; **iHuman Institute,Shanghai Tech University, Shanghai, China.
Songying Ouyang§National Laboratory of Biomacromolecules,Institute of Biophysics, Chinese Academy of Sciences, Beijing, China,; huangl@sun.im.ac.cn ouyangsy@ibp.ac.cn.
Li HuangFrom the ‡State Key Laboratory of Microbial Resources, Institute of Microbiology, Chinese Academy of Sciences, Beijing, China; huangl@sun.im.ac.cn ouyangsy@ibp.ac.cn.
Chinese Academy of Sciences · CNInstitute of Process Engineering · CNTsinghua University · CNComputer Network Information Center · CNInstitute of Biophysics · CNInstitute of Physics · CNMicrobiology Institute of Shaanxi · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Protein methylation is believed to occur extensively in creanarchaea. Recently, aKMT, a highly conserved crenarchaeal protein lysine methyltransferase, was identified and shown to exhibit broad substrate specificity in vitro Here, we have constructed an aKMT deletion mutant of the hyperthermophilic crenarchaeon Sulfolobus islandicus The mutant was viable but showed a moderately slower growth rate than the parental strain under non-optimal growth conditions. Consistent with the moderate effect of the lack of aKMT on the growth of the cell, expression of a small number of genes, which encode putative functions in substrate transportation, energy metabolism, transcriptional regulation, stress response proteins, etc, was differentially regulated by more than twofold in the mutant strain, as compared with that in the parental strain. Analysis of the methylation of total cellular protein by mass spectrometry revealed that methylated proteins accounted for ∼2/3 (1,158/1,751) and ∼1/3 (591/1,757) of the identified proteins in the parental and the mutant strains, respectively, indicating that there is extensive protein methylation in S. islandicus and that aKMT is a major protein methyltransferase in this organism. No significant sequence preference was detected at the sites of methylation by aKMT. Methylated lysine residues, when visible in the structure, are all located on the surface of the proteins. The crystal structure of aKMT in complex with S-adenosyl-l-methionine (SAM) or S-adenosyl homocysteine (SAH) reveals that the protein consists of four α helices and seven β sheets, lacking a substrate recognition domain found in PrmA, a bacterial homolog of aKMT, in agreement with the broad substrate specificity of aKMT. Our results suggest that aKMT may serve a role in maintaining the methylation status of cellular proteins required for the efficient growth of the organism under certain non-optimal conditions.

Indexed as

Archaeal ProteinsCrystallography, X-RayGene DeletionGene Expression Regulation, ArchaealLysineMass SpectrometryMethylationModels, MolecularProtein MethyltransferasesProtein Structure, SecondaryProteomicsS-AdenosylhomocysteineS-AdenosylmethionineSulfolobusArchaeal ProteinsLysineProtein MethyltransferasesS-AdenosylhomocysteineS-Adenosylmethionine

Identifiers

PMID27329856
PMCPMC5013307
OpenAlexW2472073934

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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.