نتایج جستجو برای: binding protein c mutation

تعداد نتایج: 2414558  

Journal: :Molecules 2021

Identification of molecular determinants receptor-ligand binding could significantly increase the quality structure-based virtual screening protocols. In turn, drug design process, especially fragment-based approaches, benefit from knowledge. Retrospective campaigns by employing AutoDock Vina followed protein-ligand interaction fingerprinting (PLIF) identification using recently published PyPLI...

Journal: :Journal of molecular graphics & modelling 2012
Akos Gellért Katalin Nemes Katalin Kádár Katalin Salánki Ervin Balázs

The main function of the 2b protein of Cucumber mosaic virus (CMV) is binding permanently the double stranded siRNA molecules in the suppression process of post-transcriptional gene silencing (PTGS). The crystal structure of the homologue Tomato aspermy virus (TAV) 2b protein is known, but without the C-terminal domain. The biologically active form is a tetramer: four 2b protein molecules and t...

Journal: :The Journal of biological chemistry 2003
Aimee L Eggler Shelley L Lusetti Michael M Cox

The nucleation step of Escherichia coli RecA filament formation on single-stranded DNA (ssDNA) is strongly inhibited by prebound E. coli ssDNA-binding protein (SSB). The capacity of RecA protein to displace SSB is dramatically enhanced in RecA proteins with C-terminal deletions. The displacement of SSB by RecA protein is progressively improved when 6, 13, and 17 C-terminal amino acids are remov...

Journal: :FEBS Letters 2021

Recently, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants (B.1.1.7 and B.1351) have emerged harbouring mutations that make them highly contagious. The N501Y mutation within the receptor-binding domain (RBD) of spike protein these SARS-CoV-2 may enhance binding to human angiotensin-converting enzyme (hACE2). However, no molecular explanation for such an enhanced affinity ha...

2011
Margaret E. Graham Gerald R. Prescott James R. Johnson Mathew Jones Alice Walmesley Lee P. Haynes Alan Morgan Robert D. Burgoyne Jeff W. Barclay

Munc18-1 is an essential synaptic protein functioning during multiple stages of the exocytotic process including vesicle recruitment, docking and fusion. These functions require a number of distinct syntaxin-dependent interactions; however, Munc18-1 also regulates vesicle fusion via syntaxin-independent interactions with other exocytotic proteins. Although the structural regions of the Munc18-1...

Delavar Shahbaz Zadeh Hamid Mirmohammad Sadeghi Jamshid Faghri, Kamran Pooshang Bagheri, Rahmatolah Yazdani Sharareh Moghim

Objective(s) Staphylococcus aureus is a leading cause of many nosocomial and community acquired infections. According to many reports, antibiotic therapy can not guarantee the eradication of S. aureus infections. Thus designing an adhesin based vaccine could restrain the S. aureus infections. This study designed for construction of a new fusion protein vaccine against S. aureus infections base...

امانی, جعفر, سروری زنجانی, رحیم, موسوی, سید لطیف, نظریان, شهرام,

Background and Objective: Botulinum neurotoxin type A, structurally consists of a 50KD light chain and a 100 KD heavy chain linked by a disulfide bond. The protein can further be divided into three functional domains of which catalytic domain corresponds to the light chain. In this research we aimed to produce recombinant catalytic domain in order to obtain a protective protein. Materials and M...

Objective(s): Non-syndromic sensorineural hearing loss (NSHL) is a common disorder affecting approximately 1 in 500 newborns. This type of hearing loss is extremely heterogeneous and includes over 100 loci. Mutations in the GJB2 gene have been implicated in about half of autosomal recessive NSHL (ARNSHL) cases, making this the most common cause of ARNSHL. For the latter form of deafness, most f...

Journal: :The Biochemical journal 2008
René Assenberg Michelle Webb Edward Connolly Katherine Stott Matthew Watson Josie Hobbs Jean O Thomas

The structure-specific DNA-binding protein HMGB1 (high-mobility group protein B1) which comprises two tandem HMG boxes (A and B) and an acidic C-terminal tail, is acetylated in vivo at Lys(2) and Lys(11) in the A box. Mutation to alanine of both residues in the isolated A domain, which has a strong preference for pre-bent DNA, abolishes binding to four-way junctions and 88 bp DNA minicircles. T...

Journal: :Social Science Research Network 2021

Analysis of large scale human genomic data has yielded unexplained mutations known to cause severe disease in healthy individuals. Here we report the unexpected recovery a rare dominant lethal mutation TPM1, sarcomeric actin-binding protein, 8 individuals with atrial septal defect (ASD) 5-generation pedigree. Mice TPM1 exhibited early embryonic lethality disrupted myofibril assembly and no hear...

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