Evidence map›Paper›PMID 21903402›Full record

ArticleBioorganic & medicinal chemistry2011

Identification of novel small molecule inhibitors of 4-diphosphocytidyl-2-C-methyl-D-erythritol (CDP-ME) kinase of Gram-negative bacteria.

M Tang, S I Odejinmi, Y M Allette, H Vankayalapati, K Lai

Open access · greenAbstract read
In one paragraph

Article in Bioorganic & medicinal chemistry, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

10 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
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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

5 authors at 3 institutions in 1 country.

M TangDivision of Medical Genetics, Department of Pediatrics, University of Utah School of Medicine, 50 N. Mario Capecchi Drive, SOM Room 2C412, Salt Lake City, UT 84132, USA.
S I Odejinmi
Y M Allette
H Vankayalapati
K Lai
University of Utah · USHuntsman Cancer Institute · USIndiana University School of Medicine

Funding

Innovative Therapies and Clinical Studies for Classic GalactosemiaR01HD054744 · NICHD · UNIVERSITY OF UTAH · PI LAI, KENT · 2007 to 2011
$1.6M
Toward Improved Therapy for Classic GalactosemiaR03MH085689 · NIMH · UNIVERSITY OF UTAH · PI LAI, KENT · 2008 to 2008
$24k
NICHD NIH HHS 5R01 HD054744-04NICHD NIH HHS 5R01 HD054744-04S1NICHD NIH HHS R01 HD054744NIMH NIH HHS 7R03 MH085689-02NIMH NIH HHS R03 MH085689
6 · The paper itself

Abstract

The biosyntheses of isoprenoids is essential for the survival in all living organisms, and requires one of the two biochemical pathways: (a) Mevalonate (MVA) Pathway or (b) Methylerythritol Phosphate (MEP) Pathway. The latter pathway, which is used by all Gram-negative bacteria, some Gram-positive bacteria and a few apicomplexan protozoa, provides an attractive target for the development of new antimicrobials because of its absence in humans. In this report, we describe two different approaches that we used to identify novel small molecule inhibitors of Escherichia coli and Yersinia pestis 4-diphosphocytidyl-2-C-methyl D-erythritol (CDP-ME) kinases, key enzymes of the MEP pathway encoded by the E. coli ispE and Y. pestisipk genes, respectively. In the first approach, we explored existing inhibitors of the GHMP kinases while in the second approach; we performed computational high-throughput screening of compound libraries by targeting the CDP-ME binding site of the two bacterial enzymes. From the first approach, we identified two compounds with 6-(benzylthio)-2-(2-hydroxyphenyl)-4-oxo-3,4-dihydro-2H-1,3-thiazine-5-carbonitrile and (Z)-3-methyl-4-((5-phenylfuran-2-yl)methylene)isoxazol-5(4H)-one scaffolds which inhibited E. coli CDP-ME kinase in vitro. We then performed substructure search and docking experiments based on these two scaffolds and identified twenty three analogs for structure-activity relationship (SAR) studies. Three new compounds from the isoxazol-5(4H)-one series have shown inhibitory activities against E. coli and Y. pestis CDP-ME kinases with the IC(50) values ranging from 7 to 13 μM. The second approach by computational high-throughput screening (HTS) of two million drug-like compounds yielded two compounds with benzenesulfonamide and acetamide moieties which, at a concentration of 20 μM, inhibited 80% and 65%, respectively, of control CDP-ME kinase activity.

Indexed as

Amino Acid SequenceBacterial ProteinsBinding SitesComputer SimulationEnzyme InhibitorsEscherichia coliEscherichia coli ProteinsMolecular Sequence DataPhosphotransferases (Alcohol Group Acceptor)Sequence Homology, Amino AcidSmall Molecule LibrariesStructure-Activity RelationshipYersinia pestisBacterial ProteinsEnzyme InhibitorsEscherichia coli ProteinsIspE protein, E coliPhosphotransferases (Alcohol Group Acceptor)Small Molecule Libraries

Identifiers

PMID21903402
PMCPMC3188437
OpenAlexW2052139414

What OpenQuestion holds

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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.