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Keywords: protein engineering
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Biochem J (2023) 480 (16): 1317–1330.
Published: 25 August 2023
... and deubiquitinase activity with the OTUD1 substrate RIPK1 were inhibited. Herein we describe the development of molecular tools for exploring the activity of OTUD1 in a cellular context, towards protein-based therapeutics. deubiquitinases inhibitor phage display protein engineering ubiquitin variants UIM...
Includes: Supplementary data
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Biochem J (2023) 480 (14): 1097–1107.
Published: 17 July 2023
... in an all-inclusive Read & Publish agreement with Portland Press and the Biochemical Society under a transformative agreement with MALMAD. auto-cleavage auto-degradation enzyme engineering matrix metalloproteases MMP-9 protein engineering Matrix metalloproteinases (MMPs...
Includes: Supplementary data
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Biochem J (2023) 480 (2): 127–140.
Published: 23 January 2023
... 2023 The Author(s). Published by Portland Press Limited on behalf of the Biochemical Society 2023 protein engineering signaling pathways synthetic biology All these data concerning the molecular means by which information is allosterically transmitted from the sensory end...
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Biochem J (2021) 478 (15): 3047–3062.
Published: 13 August 2021
... enzyme activation metalloenzymes molecular mechanisms protein engineering Metals are present as structural features in over one-third of proteins, underscoring their importance for protein structure and function [ 1 , 2 ]. The incorporation of divalent metal ions into protein structures...
Includes: Supplementary data
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Biochem J (2020) 477 (9): 1701–1719.
Published: 11 May 2020
... Papo ( [email protected] ) 3 3 2020 11 4 2020 14 4 2020 15 4 2020 © 2020 The Author(s). Published by Portland Press Limited on behalf of the Biochemical Society 2020 metalloproteases next-generation sequencing protease inhibitor protein engineering protein–protein...
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Biochem J (2020) 477 (8): 1483–1497.
Published: 29 April 2020
... to previous studies from a structural perspective. These clashes would potentially lead to reduced substrate binding affinity of McTadA, consistent with our in vitro deamination activity and binding assays. To rescue the deamination activity of McTadA, we carried out two rounds of protein engineering through...
Includes: Supplementary data
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Biochem J (2019) 476 (23): 3631–3647.
Published: 10 December 2019
... protein engineering protein folding Instances of so-called imperfect (poor or suboptimal) ‘design’ have been extensively studied in records of evolutionary history, and have served as evidence that living organisms, rather than being designed, are the products of complex evolutionary forces...
Includes: Supplementary data
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Biochem J (2018) 475 (23): 3887–3901.
Published: 12 December 2018
... of the Biochemical Society 2018 homoserine malate dehydrogenase protein engineering site-directed mutagenesis synthetic biology A central challenge in the creation of a resource-efficient and sustainable bioeconomy lies in the reduction in our dependence on fossil resources and a shift in focus...
Includes: Supplementary data
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Biochem J (2018) 475 (7): 1335–1352.
Published: 16 April 2018
.... directed evolution protease inhibitor protein engineering protein–protein interactions (PPIs) serine proteases Extracellular proteases that are aberrantly expressed in the tumor microenvironment are key contributors to cancer growth, progression and metastasis [ 1 – 3 ] and hence constitute...
Includes: Supplementary data
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Biochem J (2016) 473 (20): 3611–3620.
Published: 11 October 2016
... approach to expand the capability of ancestral reconstruction to search sequence space for extreme protein properties of biotechnological interest. protein engineering protein stability resurrected proteins thioredoxin The engineering of proteins with enhanced stability has drawn...
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Biochem J (2016) 473 (11): 1563–1578.
Published: 27 May 2016
...) and alternative drug candidates compared with current biopharmaceutical treatments. Aβ peptide lipocalin neurodegeneration protein engineering Alzheimer's disease (AD) is the most prevalent form of dementia, with 10% of the human population older than 65 years and 40% older than 85 years affected...
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Biochem J (2011) 435 (2): 345–354.
Published: 29 March 2011
... ). 1 9 2010 14 1 2011 4 2 2011 4 2 2011 © The Authors Journal compilation © 2011 Biochemical Society 2011 haloalkane dehalogenase phylogenetic analysis principal component analysis protein engineering substrate specificity Enzymes are biological catalysts...
Includes: Supplementary data
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Biochem J (2011) 435 (1): 55–63.
Published: 15 March 2011
...://creativecommons.org/licenses/by-nc/2.5/ ) which permits unrestricted non-commercial use, distribution and reproduction in any medium, provided the original work is properly cited. avidin biotin protein engineering protein–ligand interaction streptavidin traptavidin The capture of the small molecule...
Includes: Supplementary data
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Biochem J (2011) 435 (1): 1–16.
Published: 15 March 2011
... © 2011 Biochemical Society 2011 procoagulant protease therapy protein degradation protein engineering trypsin fold Sequencing of the human genome revealed that more than 2% of our genes encode proteases, suggesting that these enzymes possess functions more complex than the simple...
Includes: Supplementary data
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Biochem J (2008) 414 (2): 205–214.
Published: 12 August 2008
[email protected] ). 27 3 2008 2 5 2008 19 5 2008 19 5 2008 © The Authors Journal compilation © 2008 Biochemical Society 2008 chaperonin CO 2 fixation directed evolution protein engineering RbcX ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco) Rubisco...
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Biochem J (2007) 404 (3): 517–524.
Published: 29 May 2007
... protein engineering ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco) Rubisco (ribulose-1,5-bisphosphate carboxylase/oxygenase) catalyses the nucleophilic carboxylation of ribulose-P 2 ( D -ribulose-1,5-bisphosphate). This conversion of inorganic CO 2 into carbohydrate is frequently...
Includes: Supplementary data
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Biochem J (2006) 397 (2): 305–312.
Published: 28 June 2006
... pyralis protein engineering Beetle luciferases catalyse the efficient transfer of chemical energy into light via a two-step process, utilizing ATP-Mg 2+ , firefly luciferin ( D -LH 2 ) and molecular oxygen, yielding oxyluciferin (LO): A wide range of novel in vitro and in vivo...
Includes: Supplementary data
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Biochem J (2006) 394 (1): 85–93.
Published: 27 January 2006
... 2005 21 11 2005 21 11 2005 The Biochemical Society, London 2006 cyclic protein cyclotide haemolytic activity kalata NMR protein engineering The cyclotides [ 1 ] are a fascinating family of plant proteins that are distinguished by a head-to-tail peptide backbone...
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Biochem J (2005) 392 (3): 485–491.
Published: 06 December 2005
... chain. In contrast with wild-type avidin, which contains four identical avidin monomers, scAvd enables each one of the four avidin domains to be independently modified by protein engineering. Therefore the scAvd scaffold can be used to construct spatially and stoichiometrically defined pseudotetrameric...
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Biochem J (2004) 382 (3): 885–893.
Published: 07 September 2004
... 3GA glutathione S-transferase herbicide detoxification ligandin protein engineering triazine dye GSTs (glutathione S-transferases; EC 2.5.1.18) are dimeric detoxification enzymes that catalyse a wide variety of conjugations of GSH to hydrophobic electrophilic compounds [ 1 , 2 ]. Each GST...
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Biochem J (2001) 359 (3): 715–720.
Published: 25 October 2001
... 9 2001 The Biochemical Society, London ©2001 2001 non-coded amino acids protein engineering semisynthesis structure–function Biochem. J. (2001) 359, 715 720 (Printed in Great Britain) 715 Conserved tryptophan in cytochrome c : importance of the unique side-chain features...
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Biochem J (2001) 358 (1): 101–110.
Published: 08 August 2001
...2001 2001 essential dynamics herbicide detoxification molecular dynamics protein engineering Abbreviations used: CDNB, 1-chloro-2,4-dinitrobenzene; G-site, GSH binding site; GST, glutathione S-transferase; H-site, electrophile binding site; Ni-NTA, Ni 2+ -nitrilotriacetate. Biochem...
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Biochem J (2001) 354 (2): 455–463.
Published: 22 February 2001
... properties of His- 311 are important for enzyme function. An important structural role has also been attributed to cis-Pro-288. This residue may provide the key residues Gln-287 and His-311 with the proper orientation for productive binding of formate. Key words: kinetic mechanism, protein engineering, site...
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Biochem J (2000) 352 (2): 257–266.
Published: 24 November 2000
... and R184 located close to the adenosine ribose 2«-phosphate group, and R144 likely to interact with the nicotinamide ribose 5«-phosphate group. Key words: coenzyme affinity, enzyme kinetics, flavodoxin NADP+ oxidoreductase, protein engineering. with other members of the ferredoxin reductase family...
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Biochem J (1999) 341 (1): 139–145.
Published: 24 June 1999
... activity, protein engineering, Vipera ammodytes ammodytes. have been used, from comparison of their primary and tertiary structures, chemical modification and the use of specific site- directed antibodies to acceptor-binding studies. Despite nu- merous attempts, toxic PLA # s still remain a complex multi...
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Biochem J (1999) 339 (2): 309–317.
Published: 08 April 1999
... to denaturants such as guanidine HCl and urea was revealed; the wild-type protein always proved to be the most resistant. The results obtained show the importance of hydrogen bonds and ion pairs in determining protein stability and confirm that simulation methods are able to direct protein engineering in site...