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Keywords: mutagenesis
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Articles
Biochem J (2023) 480 (9): 573–585.
Published: 04 May 2023
...) alkyl-formamidopyrimidine alkylation damage fluorination mutagenesis N7-alkylguanine translesion DNA synthesis Guanine N7 is the most nucleophilic atom within DNA, thereby reacting with a wide range of endogenous and exogenous alkylating agents (e.g. S -adenosylmethionine, temozolomide...
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Biochem J (2021) 478 (9): 1769–1781.
Published: 10 May 2021
... by Portland Press Limited on behalf of the Biochemical Society 2021 8-oxoadenine DNA polymerase geometric selection mutagenesis translesion synthesis Our kinetic studies showed that Dpo4's efficiency of the oxoA:dG extension was only ∼5-fold less efficient than that of the oxoA:dT extension...
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Biochem J (2020) 477 (24): 4797–4810.
Published: 24 December 2020
... predominantly pairs with cytosine to promote A to G mutations. Despite the known promutagenicity of the major deaminated purines, structures of DNA polymerase bypassing these lesions have not been reported. To gain insights into the deaminated-induced mutagenesis, we solved crystal structures of human DNA...
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Biochem J (2020) 477 (23): 4543–4558.
Published: 03 December 2020
... for kinetic and crystallographic studies. 5′-CAT(NHMG)CTCACACT-3′: C 125 H 161 O 71 N 42 F 1 P 11 Mass calculated [M]: 3745.74; observed [M+1]: 3746.52. © 2020 The Author(s). Published by Portland Press Limited on behalf of the Biochemical Society 2020 mutagenesis nitrogen mustards polymerase eta...
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Biochem J (2020) 477 (15): 2859–2871.
Published: 12 August 2020
... to the lesion's conformational flexibility that enables Hoogsteen base pairing with dATP in the confines of DNA polymerases. The mutagenesis mechanism of oxoA, which preferentially causes A to C transversions, remains poorly characterized. While structures for oxoA bypass by human DNA polymerases are available...
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Biochem J (2020) 477 (5): 937–951.
Published: 06 March 2020
...′-GGTGATGGGC-3′, and the downstream primer sequence was 5′-phosphate/GTGGG-3′. cisplatin DNA intrastrand cross-link DNA polymerase mutagenesis translesion synthesis Cisplatin ( cis -diamminedichloroplatinum(II)) is one of the most commonly employed anti-cancer drugs. Over the past four...
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Biochem J (2019) 476 (7): 1109–1119.
Published: 10 April 2019
... through site-directed mutagenesis. Amino acid substitutions at the sites involved in binding of the Fe(II) cofactor, 2OG cosubstrate and (2 S )- N ε -trimethyllysine substrate provide a basic insight into the binding requirements that determine an efficient TMLH-catalyzed conversion of (2 S )- N ε...
Includes: Supplementary data
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Biochem J (2018) 475 (2): 415–428.
Published: 23 January 2018
... access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) . anomalous dispersion bacterial chitinase secretion crystal structure mutagenesis peptidoglycan hydrolase zinc enzyme...
Includes: Supplementary data
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Biochem J (2017) 474 (11): 1837–1852.
Published: 16 May 2017
... Poznański ( [email protected] ) 15 11 2016 7 4 2017 13 4 2017 13 4 2017 © 2017 The Author(s); published by Portland Press Limited on behalf of the Biochemical Society 2017 acrolein AlkB dioxygenase DNA repair mutagenesis substrate binding Acrolein (ACR), a highly...
Includes: Supplementary data
Articles
Biochem J (2016) 473 (14): 2073–2085.
Published: 12 July 2016
... eight conserved cysteine residues as potential co-ordinating ligands for Fe–S clusters but their functional importance and the type of bound clusters is unclear. In the present study, we use a combination of mutagenesis, cell biological and biochemical as well as UV–visible, EPR and Mössbauer...
Includes: Supplementary data
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Biochem J (2014) 459 (2): 289–299.
Published: 28 March 2014
... catalytically important residues. Site-directed mutagenesis experiments confirmed the role of the identified residues, and demonstrated the importance of selected acidic residues and a conserved G 108 NYFWTHYFF 117 motif. The mutated isomerases were assayed both in vivo by quantification of cycloeucalenol...
Includes: Supplementary data
Articles
Biochem J (2013) 452 (1): 121–129.
Published: 25 April 2013
... of whole-cell patch voltage-clamp, immunoprecipitation, Western blotting and mutagenesis. We found that the hSKCa1 current was inhibited by the broad-spectrum PTK inhibitor genistein, the selective EGFR (epidermal growth factor receptor) kinase inhibitors T25 (tyrphostin 25) and AG556 (tyrphostin AG 556...
Articles
Biochem J (2012) 444 (2): 199–204.
Published: 11 May 2012
... be addressed (email [email protected] ). 18 1 2012 5 3 2012 7 3 2012 7 3 2012 © The Authors Journal compilation © 2012 Biochemical Society 2012 cytochrome c oxidase energy coupling mutagenesis proton channel subunit I yeast C c O (cytochrome c oxidase, also...
Includes: Supplementary data
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Biochem J (2012) 443 (3): 841–850.
Published: 16 April 2012
... Biochemical Society 2012 chimaeric receptor evolution mutagenesis orphan G-protein-coupled receptor (GPCR) structure–function relationship GPR34 is an orphan GPCR (G-protein-coupled receptor) and was first discovered by mining GenBank® for novel GPCR sequences and homology cloning. It has...
Includes: Supplementary data
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Biochem J (2011) 438 (1): 155–164.
Published: 27 July 2011
... (IL27R) Janus kinase/signal transducer and activator of transcription (JAK/STAT) mutagenesis transformation Random mutagenesis of IL27R was performed essentially as described previously [ 39 ]. A full-length human IL27R cDNA in the pEYK3.1 retroviral vector was transformed into XL-1 Red bacteria...
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Biochem J (2011) 437 (2): 243–253.
Published: 28 June 2011
...) in an apo state and in complex with the non-hydrolysable substrate α,β-imido dUTP or dUMP product. Alanine-replacement mutagenesis of the active-site residues revealed seven residues important for activity including the conserved triad Asp 87 /Arg 137 /Asp 85 . The Y88A mutant protein was equally active...
Includes: Multimedia, Supplementary data
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Biochem J (2009) 421 (2): 231–241.
Published: 26 June 2009
...] is the regulatory enzyme for the biosynthesis of shikonin, a naphthoquinone pigment, and was utilized in the present study as a representative of membrane-type AS-PTs to clarify the function of this enzyme family at the molecular level. Site-directed mutagenesis of LePGT1 with a yeast expression system indicated...
Includes: Supplementary data
Articles
Biochem J (2009) 420 (2): 201–209.
Published: 13 May 2009
..., serine and arginine residues. Site-directed mutagenesis and kinetic analysis strongly suggest that Lys 57 is important for the fumarate-induced activation and quaternary structural organization of the enzyme. Lys 57 mutant enzymes demonstrate a reduction of K m and an elevation of k cat following...
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Biochem J (2008) 415 (3): 449–454.
Published: 15 October 2008
..., suggesting a two-metal-ion mechanism as is known for class II and class III adenylate cyclases. Twelve residues which are essential for catalysis were identified by mutagenesis of a total of 20 polar residues conserved in all class I adenylate cyclases. Five essential residues (Ser 103 , Ser 113 , Asp 114...
Includes: Supplementary data
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Biochem J (2008) 415 (2): 217–223.
Published: 25 September 2008
... structures of both human and A. fumigatus GNA1, as well as their kinetic characterization. The structures show significant differences in the sugar-binding site with, in particular, several non-conservative substitutions near the phosphate-binding pocket. Mutagenesis targeting these differences revealed...
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Biochem J (2008) 413 (1): 135–142.
Published: 12 June 2008
.... Mutagenesis of Arg 347 to other amino acids also decreased the inhibitory potency, with aspartate producing near total loss of CFTR inh -172 activity. The results of the present study provide evidence that CFTR inh -172 interacts directly with CFTR, and that Arg 347 is important for the interaction. 1...
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Biochem J (2008) 412 (1): 113–121.
Published: 25 April 2008
... of CTPS from inactive dimers to active tetramers. In the present study, site-directed mutagenesis was used to replace the fully conserved glycine residues 142 and 143 within the UTP-binding site and 146 within the CTP-binding site of Escherchia coli CTPS. CD spectral analyses of wild-type CTPS...
Includes: Supplementary data
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Biochem J (2008) 412 (1): 103–112.
Published: 25 April 2008
... 3 RΔi3 constructs containing a single mutation were generated by PCR-based site-directed mutagenesis and fragment replacement strategies. All PCR-derived sequences were confirmed by restriction enzyme analysis and DNA sequencing. To generate libraries of mutated M 3 Rs, an error-prone PCR...
Includes: Supplementary data
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Biochem J (2007) 405 (2): 277–286.
Published: 27 June 2007
... -R (human P2Y 11 receptor), however, is coupled with stimulation of both the adenylate cyclase and the phospholipase C pathways [ 5 ]. This is a unique feature among the P2Y-R family. ligand binding molecular dynamics mutagenesis nucleotide receptor P2Y receptor virtual screening (ii...
Includes: Supplementary data
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Biochem J (2006) 397 (2): 297–304.
Published: 28 June 2006
.... In the present study, we investigated whether TWEAK binding to this CRD was dependent on selected evolutionarily conserved amino acid residues by using a site-specific mutagenesis approach and several different ligand-binding assays. Our results indicate that three residues within the predicted Fn14 CRD A1...
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Biochem J (2006) 397 (1): 47–52.
Published: 14 June 2006
... xanthus protoporphyrin (IX) ferrochelatase ligates a [2Fe-2S] cluster via cysteine residues present in an internal segment. Site-directed mutagenesis of this ferrochelatase demonstrates that changing one cysteine ligand into serine results in loss of the cluster, but unlike eukaryotic protoporphyrin (IX...
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Biochem J (2006) 393 (1): 161–169.
Published: 12 December 2005
...Paula Sjödin; Sara K. S. Holmberg; Helena Åkerberg; Magnus M. Berglund; Nina Mohell; Dan Larhammar Interactions of the human NPY (neuropeptide Y) receptor Y1 with the two endogenous agonists NPY and peptide YY and two non-peptide antagonists were investigated using site-directed mutagenesis at 17...
Includes: Supplementary data
Articles
Biochem J (2005) 392 (3): 601–606.
Published: 06 December 2005
...-trisphosphate receptor (IP 3 R) ER-associated degradation (ERAD) mutagenesis αT3-1 cells ubiquitination The effects of the intracellular messenger IP 3 (inositol 1,4,5-trisphosphate) are mediated by IP 3 Rs (IP 3 receptor), which form tetrameric channels in membranes of the ER (endoplasmic...
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Biochem J (2005) 391 (2): 285–289.
Published: 10 October 2005
... 3.1.4.50), an 813–816 amino acid protein found in nearly every cell type [ 4 , 5 ]. In vivo , either endogenous or overexpressed GPI-PLD cleaves and releases GPI-anchored proteins [ 6 , 7 ]. β-propeller domain catalytic activity glycosylphosphatidylinositol histidine mutagenesis phospholipase D...
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Biochem J (2005) 391 (1): 105–114.
Published: 26 September 2005
... 2 6 2005 The Biochemical Society, London 2005 glycosome Leishmania mutagenesis peroxin (PEX) peroxisomal targeting signal 1 (PTS1) protein–protein interaction The human protozoan pathogens Leishmania , Trypanosoma brucei and T. cruzi are nucleated cells...
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Biochem J (2005) 390 (2): 395–405.
Published: 23 August 2005
... coupled site-directed mutagenesis of the recombinant cABC I with a structural model of the enzyme–substrate complex in order to investigate in detail the roles of active site amino acids in the catalytic action of the enzyme. The putative catalytic residues His-501, Tyr-508, Arg-560 and Glu-653 were...
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Biochem J (2005) 389 (1): 173–180.
Published: 21 June 2005
... Society, London 2005 epimerase mutagenesis specificity structure substrate UDP- N -acetylglucosamine In summary, previous work has identified a limited number of residues that are potentially responsible for substrate specificity, but very few mutagenesis and biochemical studies...
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Biochem J (2005) 387 (3): 849–858.
Published: 26 April 2005
... receptor cytoplasmic domain filamin A GPIb/V/IX mutagenesis platelet Flow-based adhesion assays were performed as described previously using glass microslides (VitroCom, NJ, U.S.A.) coated with 10 μg/ml BvWf (bovine vWf) [ 19 ]. For cell-rolling velocity analysis, 25 cells were analysed from five...
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Biochem J (2005) 387 (1): 101–108.
Published: 22 March 2005
... domains supported α9β1-dependent cell adhesion. Recognition by both α4β1 and α4β7 of ADAM7 and ADAM28 was activation-dependent, requiring either the presence of Mn 2+ or an activating monoclonal antibody for cell attachment. Charge-to-alanine mutagenesis experiments revealed that the same residues within...
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Biochem J (2005) 386 (3): 423–431.
Published: 08 March 2005
... Evaluation Server ( www.doe-mbi.ucla/Services/Verify_3D.htlm ). The best model was depicted with Molscript [ 20 , 21 ] and Raster3D [ 22 ] ( Figure 1 C). fluorescence GABA B(1b) receptor G-protein-coupled receptor ligand-binding domain minimal functional domain mutagenesis The complex...
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Biochem J (2005) 386 (3): 453–460.
Published: 08 March 2005
.... These conformational changes will then stabilize the Hsp70 and peptide substrate complexes [ 1 , 12 ] and allow the subsequent protein folding to occur. crystal structure heat-shock protein 40 (Hsp40) Hsp70 mutagenesis substrate binding The mechanism by which molecular chaperone Hsp40s interact...
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Biochem J (2004) 384 (1): 87–92.
Published: 09 November 2004
...-hypertensives and anti-inflammatories. hOAT4-mediated transport of the organic anion oestrone sulphate in COS-7 cells was inhibited by the histidine-modifying reagent DEPC (diethyl pyrocarbonate). Therefore the role of histidine residues in the function of hOAT4 was examined by site-directed mutagenesis. All...
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