Evidence map›Paper›PMID 39965656›Full record

ArticleOpen biology2025

Proximal partners of the organellar N-terminal acetyltransferase NAA60: insights into Golgi structure and transmembrane protein topology.

Sebastian Tanco, Veronique Jonckheere, Arun Kumar Tharkeshwar, Annelies Bogaert, Kris Gevaert, Wim Annaert, Petra Van Damme

Abstract read
In one paragraph

Article in Open biology, 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

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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.

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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

7 authors.

Sebastian Tanco *iRIP Unit, Laboratory of Microbiology, Department of Biochemistry and Microbiology, Ghent University, Ghent, Belgium.ORCID 0000-0003-2130-4401
Veronique JonckheereiRIP Unit, Laboratory of Microbiology, Department of Biochemistry and Microbiology, Ghent University, Ghent, Belgium.ORCID 0000-0001-8876-3261
Arun Kumar TharkeshwarDepartment of Neurosciences, KU Leuven, Leuven, Belgium.ORCID 0000-0002-5529-9754
Annelies BogaertVIB Center for Medical Biotechnology, VIB, Ghent, Belgium.ORCID 0000-0002-4467-4299
Kris GevaertVIB Center for Medical Biotechnology, VIB, Ghent, Belgium.ORCID 0000-0002-4237-0283
Wim AnnaertDepartment of Neurosciences, KU Leuven, Leuven, Belgium.ORCID 0000-0003-0150-9661
Petra Van Damme *iRIP Unit, Laboratory of Microbiology, Department of Biochemistry and Microbiology, Ghent University, Ghent, Belgium.ORCID 0000-0001-9090-027X

Funding

FWOGhent UniversityH2020 European Research CouncilKU LeuvenSMINF
6 · The paper itself

Abstract

Biotin identification (BioID) is an interactomics approach that utilizes proximity labelling to map the local interactome or proxeome of proteins within a cell. This study applies BioID to investigate proteins proximal to NAA60 (N-alpha-acetyltransferase 60), an N-terminal acetyltransferase (NAT) of pathological significance in human disease, characterized by its unique Golgi localization. NAA60 is known to N-terminally acetylate transmembrane proteins that present their N-terminus on the cytosolic face of the membrane, and its involvement in maintaining Golgi structure has previously been established. Using a stable cell-line expressing an NAA60-BirA* fusion protein, we isolated biotinylated proteins through streptavidin affinity purification. Mass spectrometry analysis revealed over 100 proximal partners of NAA60, enriched in proteins localized on the

Indexed as

Golgi ApparatusMembrane ProteinsN-Terminal Acetyltransferase EBiotinylationHeLa CellsHumansProtein BindingMembrane ProteinsN-Terminal Acetyltransferase EGolgi fragmentationNAA60N-terminal acetylationproxeomeproximity-dependent biotin identification (BioID)transmembrane protein topology

Identifiers

PMID39965656
PMCPMC11835485

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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.