Evidence map›Paper›PMID 10567215›Full record

ArticleThe Biochemical journal1999

alpha5 subunit in Trypanosoma brucei proteasome can self-assemble to form a cylinder of four stacked heptamer rings.

Y Yao, C R Toth, L Huang, M L Wong, P Dias, A L Burlingame, P Coffino, C C Wang

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in The Biochemical journal, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

13 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Proteasome Structure and Assembly.Journal of molecular biology · 2017
    Review
  5. Article
  6. Review
  7. Assembly of the 20S proteasome.Biochimica et biophysica acta · 2014
    Review
  8. Review
  9. Article
  10. Review
  11. Molecular mechanisms of proteasome assembly.Nature reviews. Molecular cell biology · 2009
    Review
  12. Article
  13. 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 2 institutions in 1 country.

Y YaoDepartment of Pharmaceutical Chemistry, Howard Hughes Medical Institute, University of California at San Francisco, San Francisco, CA 94143-0446, USA.
C R Toth
L Huang
M L Wong
P Dias
A L Burlingame
P Coffino
C C Wang
Howard Hughes Medical Institute · USUniversity of California, San Francisco · US

Funding

Ubiquitin-Independent Proteasome DegradationR01GM045335 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI COFFINO, PHILIP · 1991 to 2012
$4.5M
REGULATION OF THE DEVELOPMENT OF TRYPANOSOMA BRUCEIR01AI021786 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI WANG, CHING CHUNG · 1985 to 2012
$4.2M
NIAID NIH HHS R01 AI-21786NIGMS NIH HHS R01 GM-45335
6 · The paper itself

Abstract

The proteasomes have a central role in catalysing protein degradation among both prokaryotes and eukaryotes. The 20 S proteasome constitutes their catalytic core. In studying the structure of Trypanosoma brucei 20 S proteasomes, we isolated by two-dimensional (2D) gel electrophoresis a 27 kDa subunit protein with an estimated pI of 4.7 and subjected it to mass spectrometric analysis. A tryptic peptide sequence from the protein was found identical with that of the rat alpha5 subunit. With the use of antiserum against T. brucei 20 S proteasomes to screen a T. b. rhodesiense lambda expression cDNA library, we obtained a cDNA clone encoding a full-length protein of 246 amino acid residues with a calculated molecular mass of 27174 Da and a pI of 4.71. It bears 50. 0% and 46.3% sequence identity with rat and yeast proteasome subunit alpha5 respectively, and matches all the peptide sequences derived from MS of the 2D gel-purified protein. The protein is thus designated the alpha5 subunit of T. brucei 20 S proteasome (TbPSA5). The recombinant protein, expressed in plasmid-transformed Escherichia coli, was found in a 27 kDa monomer form as well as polymerized forms with estimated molecular masses ranging from 190 to 800 kDa. Under the electron microscope, the most highly polymerized forms bear the appearance of cylinders of four-stacked heptamer rings with an estimated outer diameter of 14.5 nm and a length of 18 nm, which were immunoprecipitable by anti-(T. brucei 20 S proteasome) antiserum. In view of the documented self-assembly of the archaeon proteasome alpha subunit into double heptamer rings and the spontaneous assembly of the two alpha subunits from the 20 S proteasome of Rhodococcus erythropolis, the self-assembly of the T. brucei alpha subunit might reflect a common feature of proteasome biogenesis shared by prokaryotes and primitive eukaryotes such as the trypanosomes but apparently lost among the higher forms of eukaryote such as the yeast and the mammals.

Indexed as

Amino Acid SequenceAnimalsCysteine EndopeptidasesGene DosageGene LibraryMolecular Sequence DataMultienzyme ComplexesPrecipitin TestsProteasome Endopeptidase ComplexProtein BindingProtozoan ProteinsRecombinant ProteinsSequence Analysis, DNASequence Homology, Amino AcidSpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationTrypanosoma brucei bruceiCysteine EndopeptidasesMultienzyme ComplexesProteasome Endopeptidase ComplexProtozoan ProteinsRecombinant Proteins

Identifiers

PMID10567215
PMCPMC1220650
OpenAlexW2084682671

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.