Literature DB >> 33847952

Comparing SSB-PriA Functional and Physical Interactions in Gram-Positive and -Negative Bacteria.

Yen-Hua Huang1, Cheng-Yang Huang2,3.   

Abstract

Single-stranded DNA (ssDNA)-binding protein (SSB) is essential for DNA metabolic processes. SSB also binds to many DNA-binding proteins that constitute the SSB interactome. The mechanism through which PriA helicase, an initiator protein in the DNA replication restart process, is stimulated by SSB in Escherichia coli (EcSSB) has been established. However, some Gram-positive bacterial SSBs such as Bacillus subtilis SsbA (a counterpart of EcSSB), Staphylococcus aureus SsbA, SsbB, and SsbC do not activate PriA helicase. Here, we describe some of the methods used in our laboratory to compare SSB-PriA functional and physical interactions in Gram-positive and -negative bacteria.

Entities:  

Keywords:  ATPase; ConSurf; PriA; Protein-protein interaction; SPR; SSB; SsbA; Stimulation; ssDNA-binding protein

Year:  2021        PMID: 33847952     DOI: 10.1007/978-1-0716-1290-3_4

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  2 in total

1.  Real-time biospecific interaction analysis using surface plasmon resonance and a sensor chip technology.

Authors:  U Jönsson; L Fägerstam; B Ivarsson; B Johnsson; R Karlsson; K Lundh; S Löfås; B Persson; H Roos; I Rönnberg
Journal:  Biotechniques       Date:  1991-11       Impact factor: 1.993

2.  Structural insight into the DNA-binding mode of the primosomal proteins PriA, PriB, and DnaT.

Authors:  Yen-Hua Huang; Cheng-Yang Huang
Journal:  Biomed Res Int       Date:  2014-07-21       Impact factor: 3.411

  2 in total
  1 in total

1.  A Complexed Crystal Structure of a Single-Stranded DNA-Binding Protein with Quercetin and the Structural Basis of Flavonol Inhibition Specificity.

Authors:  En-Shyh Lin; Ren-Hong Luo; Cheng-Yang Huang
Journal:  Int J Mol Sci       Date:  2022-01-06       Impact factor: 5.923

  1 in total

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