Literature DB >> 8451638

Molecular matchmakers.

A Sancar1, J E Hearst.   

Abstract

Molecular matchmakers are a class of proteins that use the energy released from the hydrolysis of adenosine triphosphate to cause a conformational change in one or both components of a DNA binding protein pair to promote formation of a metastable DNA-protein complex. After matchmaking the matchmaker dissociates from the complex, permitting the matched protein to engage in other protein-protein interactions to bring about the effector function. Matchmaking is most commonly used under circumstances that require targeted, high-avidity DNA binding without relying solely on sequence specificity. Molecular matchmaking is an extensively used mechanism in repair, replication, and transcription and most likely in recombination and transposition reactions, too.

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Year:  1993        PMID: 8451638     DOI: 10.1126/science.8451638

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  52 in total

1.  An ATP/ADP-dependent molecular switch regulates the stability of p53-DNA complexes.

Authors:  A L Okorokov; J Milner
Journal:  Mol Cell Biol       Date:  1999-11       Impact factor: 4.272

2.  Mechanism of the gBP21-mediated RNA/RNA annealing reaction: matchmaking and charge reduction.

Authors:  Ulrich F Müller; H Ulrich Göringer
Journal:  Nucleic Acids Res       Date:  2002-01-15       Impact factor: 16.971

Review 3.  Handoff from recombinase to replisome: insights from transposition.

Authors:  H Nakai; V Doseeva; J M Jones
Journal:  Proc Natl Acad Sci U S A       Date:  2001-07-17       Impact factor: 11.205

4.  Heteroduplexes in mixed-template amplifications: formation, consequence and elimination by 'reconditioning PCR'.

Authors:  Janelle R Thompson; Luisa A Marcelino; Martin F Polz
Journal:  Nucleic Acids Res       Date:  2002-05-01       Impact factor: 16.971

5.  Purification and characterization of human DNA damage checkpoint Rad complexes.

Authors:  L A Lindsey-Boltz; V P Bermudez; J Hurwitz; A Sancar
Journal:  Proc Natl Acad Sci U S A       Date:  2001-09-25       Impact factor: 11.205

6.  Functional studies on the candidate ATPase domains of Saccharomyces cerevisiae MutLalpha.

Authors:  P T Tran; R M Liskay
Journal:  Mol Cell Biol       Date:  2000-09       Impact factor: 4.272

7.  Human MutSalpha recognizes damaged DNA base pairs containing O6-methylguanine, O4-methylthymine, or the cisplatin-d(GpG) adduct.

Authors:  D R Duckett; J T Drummond; A I Murchie; J T Reardon; A Sancar; D M Lilley; P Modrich
Journal:  Proc Natl Acad Sci U S A       Date:  1996-06-25       Impact factor: 11.205

8.  An Atypical AAA+ ATPase Assembly Controls Efficient Transposition through DNA Remodeling and Transposase Recruitment.

Authors:  Ernesto Arias-Palomo; James M Berger
Journal:  Cell       Date:  2015-08-13       Impact factor: 41.582

9.  Imp3p and Imp4p mediate formation of essential U3-precursor rRNA (pre-rRNA) duplexes, possibly to recruit the small subunit processome to the pre-rRNA.

Authors:  Tímea Gérczei; Carl C Correll
Journal:  Proc Natl Acad Sci U S A       Date:  2004-10-15       Impact factor: 11.205

10.  The Streptomyces peucetius drrC gene encodes a UvrA-like protein involved in daunorubicin resistance and production.

Authors:  N Lomovskaya; S K Hong; S U Kim; L Fonstein; K Furuya; R C Hutchinson
Journal:  J Bacteriol       Date:  1996-06       Impact factor: 3.490

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