Evidence map›Paper›PMID 10749667›Full record

ArticleThe Biochemical journal2000

Expression and characterization of a recombinant cysteine proteinase of Leishmania mexicana.

S J Sanderson, K G Pollock, J D Hilley, M Meldal, P S Hilaire, M A Juliano, L Juliano, J C Mottram, G H Coombs

Open access · greenAbstract read
In one paragraph

Article in The Biochemical journal, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
6.8field-weighted citation impact, top 3% 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

16 citing papers in PubMed, 72 citations in OpenAlex.

  1. Article
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  7. Synthesis of C3/C1-Substituted Tetrahydroisoquinolines.Molecules (Basel, Switzerland) · 2015
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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

9 authors at 3 institutions in 3 countries.

S J SandersonDivision of Infection and Immunity, Joseph Black Building, Institute of Biomedical and Life Sciences, University of Glasgow, University Avenue, Glasgow G12 8QQ, UK. s.sanderson@bio.gla.ac.uk
K G Pollock
J D Hilley
M Meldal
P S Hilaire
M A Juliano
L Juliano
J C Mottram
G H Coombs
Associação Paulista de Medicina · BRCarlsberg Laboratory · DKUniversity of Glasgow · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A major cysteine proteinase (CPB) of Leishmania mexicana, that is predominantly expressed in the form of the parasite that causes disease in mammals, has been overexpressed in Escherichia coli and purified from inclusion bodies to apparent homogeneity. The CPB enzyme, CPB2.8, was expressed as an inactive pro-form lacking the characteristic C-terminal extension (CPB2.8DeltaCTE). Pro-region processing was initiated during protein refolding and proceeded through several intermediate stages. Maximum enzyme activity accompanied removal of the entire pro-region. This was facilitated by acidification. Purified mature enzyme gave a single band on SDS/PAGE and gelatin SDS/PAGE gels, co-migrated with native enzyme in L. mexicana lysates, and had the same N-terminal sequence as the native enzyme. The procedure yielded >3.5 mg of active enzyme per litre of E. coli culture.

Indexed as

Amino Acid SequenceAnimalsBlotting, WesternCysteine EndopeptidasesEnzyme ActivationEscherichia coliHumansInclusion BodiesKineticsLeishmania mexicanaMolecular Sequence DataProtein RenaturationRecombinant ProteinsSequence AlignmentCysteine EndopeptidasesRecombinant Proteins

Identifiers

PMID10749667
PMCPMC1220970
OpenAlexW2123441430

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.