Evidence map›Paper›PMID 25987764›Full record

ArticleBioinformation2015

Interaction pattern for the complex of B-DNA Fullerene compounds with a set of known replication proteins using docking study.

Sumbul Firdaus, Anupam Dhasmana, Vandana Srivastava, Tasneem Bano, Afreen Fatima, Qazi Mohammad Sajid Jamal, Roshan Jahan, Gulshan Wadhwad, Mohtashim Lohani

Open access · hybridAbstract read
In one paragraph

Article in Bioinformation, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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0citing papers in PubMed
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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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3 · Its place in the literature

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0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Sumbul FirdausDepartment of Physics, Integral University, Lucknow, India.
Anupam DhasmanaDepartments of Bioengineering, Integral University, Lucknow, India.
Vandana SrivastavaDepartments of Bioengineering, Integral University, Lucknow, India.
Tasneem BanoDepartments of Bioengineering, Integral University, Lucknow, India.
Afreen FatimaDepartments of Bioengineering, Integral University, Lucknow, India.
Qazi Mohammad Sajid JamalDepartments of Biosciences, Integral University, Lucknow, India.
Roshan JahanDepartments of Biosciences, Integral University, Lucknow, India.
Gulshan WadhwadDepartment of Biotechnology, Ministry of Science and Technology, CGO complex, Lodhi Road, New Delhi-110003, India.
Mohtashim LohaniDepartments of Biosciences, Integral University, Lucknow, India.
Integral University · INMinistry of Science and Technology · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fullerenes have attracted considerable attention due to their unique chemical structure and potential applications which has opened wide venues for possible human exposure to various fullerene types. Therefore, in depth knowledge of how fullerene may interfere with various cellular processes becomes quite imperative. The present study was designed to investigate how the presence of fullerene affect the binding of DNA with different enzymes involved in replication process. Different fullerenes were first docked with DNA and then binding scores of different enzymes was analyzed with fullerene docked DNA. C30, C40 & C50 once docked with DNA, reduced the binding score of primase, whereas no significant change in the binding score was observed with the helicase, ssb protein, dna pol δ, dna pol ε, ligase, DNA clamp, and topoisomerases. On the contrast, the binding score of RPA14 decreases in fluctuating manner while interacting with increasing molecular weight of fullerene bound single-stranded DNA complex. The study revealed the affect of fullerene family interacting with DNA on the binding pattern of enzymes involved in replication process. Study suggests that the presence of most of fullerenes may not affect the activity of these enzymes necessary for replication process whereas C30, C40 & C50 may disrupt the activity of primase, (strating point for DNA polymerase) its docking score decreases from 13820 to 10702.

Indexed as

FullereneFullerene familyreplication enzymesRPA

Identifiers

PMID25987764
PMCPMC4421002
OpenAlexW2016806929

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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.