Evidence map›Paper›PMID 21778233›Full record

ArticleThe Journal of biological chemistry2011

Mining endonuclease cleavage determinants in genomic sequence data.

Mindy D Szeto, Sandrine J S Boissel, David Baker, Summer B Thyme

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological 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, 15 citations in OpenAlex.

  1. Review
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  10. Targeted gene therapies: tools, applications, optimization.Critical reviews in biochemistry and molecular biology
    Review
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

4 authors at 1 institution in 1 country.

Mindy D SzetoDepartment of Biochemistry, Howard Hughes Medical Institute, University of Washington, Seattle, Washington 98195, USA.
Sandrine J S Boissel
David Baker
Summer B Thyme
Howard Hughes Medical Institute · US

Funding

Directed Protein Evolution for Design of LAGLIDADGs with Novel Recognition SpeciRL1CA133832 · NCI · SEATTLE CHILDREN'S HOSPITAL · PI SCHARENBERG, ANDREW M. · 2007 to 2011
$2.2M
Computational Design of an LAGLIDADGs with Novel Recognition Specificities (CompoRL1GM084433 · NIGMS · UNIVERSITY OF WASHINGTON · PI BAKER, DAVID · 2007 to 2011
$1.9M
Howard Hughes Medical InstituteNCI NIH HHS RL1 CA133832NCI NIH HHS RL1CA133832NIGMS NIH HHS GM084433NIGMS NIH HHS RL1 GM084433
6 · The paper itself

Abstract

Homing endonucleases have great potential as tools for targeted gene therapy and gene correction, but identifying variants of these enzymes capable of cleaving specific DNA targets of interest is necessary before the widespread use of such technologies is possible. We identified homologues of the LAGLIDADG homing endonuclease I-AniI and their putative target insertion sites by BLAST searches followed by examination of the sequences of the flanking genomic regions. Amino acid substitutions in these homologues that were located close to the target site DNA, and thus potentially conferring differences in target specificity, were grafted onto the I-AniI scaffold. Many of these grafts exhibited novel and unexpected specificities. These findings show that the information present in genomic data can be exploited for endonuclease specificity redesign.

Indexed as

EndodeoxyribonucleasesRestriction MappingDNAGenomeDNAEndodeoxyribonucleases

Identifiers

PMID21778233
PMCPMC3173205
OpenAlexW2060664433

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.