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Keywords: protein-protein interactions
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Biochem J (2024) 481 (23): 1723–1740.
Published: 21 November 2024
... PRMT3 protein arginine methyltransferase protein evolution protein-protein interactions zinc finger ZNF200 Protein arginine methyltransferase 3 (PRMT3) is a type I arginine methyltransferase which generates the asymmetric dimethylation modifications at the arginine residues of the substrate...
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Biochem J (2024) 481 (21): 1535–1556.
Published: 21 October 2024
... disordered region culminating in the transactivation domain (TAD). The TAD participates in many proteinprotein interactions, notably with kinases that promote stability (Aurora-A) or degradation (ERK1, GSK3) via the ubiquitin-proteasome system. We probed the structure, dynamics and interactions of N-myc TAD...
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Biochem J (2024) 481 (14): 945–955.
Published: 10 July 2024
... under a transformative agreement with JISC. PDZ domains peptide interacting motifs proteinprotein interactions The SHANK (SH3 and multiple ankyrin repeat domain) protein acts as a scaffolding protein located at excitatory glutamatergic synapses ( Figure 1 ); it plays a crucial role...
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Biochem J (2024) 481 (14): 903–922.
Published: 10 July 2024
... on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) . apoptosis Bax Bcl-2 BH3-only proteins proteinprotein interactions transmembrane domain When a eukaryotic cell is faced with overwhelming cellular stress that surpasses...
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Biochem J (2023) 480 (12): 875–890.
Published: 22 June 2023
...) that drive adrenal Cushing's syndrome [ 12–18 ]. Most PKAc mutations cluster where the kinase domain interfaces with its regulatory (R) subunits [ 19 ]. This proteinprotein interaction is not only necessary for autoinhibition of kinase activity, but also directs subcellular targeting of PKA holoenzymes...
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Biochem J (2022) 479 (6): 751–766.
Published: 28 March 2022
... structure proteinprotein interactions ubiquitin ubiquitin ligases DNA for the GTPase2 domain of human Miro1 (mG2, residues 402–582) and human CISD1 (residues 32–108) were codon optimized and inserted into His 6 - expression plasmids (ATUM, Newark, CA, U.S.A.). The mG2 protein contained 3...
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Biochem J (2022) 479 (5): 687–700.
Published: 16 March 2022
...Matthew Batchelor; Robert S. Dawber; Andrew J. Wilson; Richard Bayliss How cellular functions are regulated through protein phosphorylation events that promote or inhibit proteinprotein interactions (PPIs) is key to understanding regulatory molecular mechanisms. Whilst phosphorylation can...
Includes: Supplementary data
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Biochem J (2022) 479 (3): 289–304.
Published: 04 February 2022
...). Published by Portland Press Limited on behalf of the Biochemical Society 2022 adenosine diphosphate ribose post-translational modification proteinprotein interactions ubiquitin ligases Ubiquitination is a reversible post-translational protein modification that results in the addition...
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Biochem J (2022) 479 (1): 1–22.
Published: 06 January 2022
...Johanna Kliche; Ylva Ivarsson Cellular function is based on proteinprotein interactions. A large proportion of these interactions involves the binding of short linear motifs (SLiMs) by folded globular domains. These interactions are regulated by post-translational modifications...
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Biochem J (2021) 478 (19): 3643–3654.
Published: 14 October 2021
... membrane proteins protein-protein interactions tetraspanins Tetraspanins (Tspans) are widely expressed membrane proteins of 200–350 amino acids that cross the cell membrane four times [ 1 ]. They are involved in diverse cellular processes, such as cell proliferation, trafficking, signaling...
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Biochem J (2021) 478 (13): 2555–2569.
Published: 09 July 2021
.... GHKL ATPase nucleic acid binding proteins proteinprotein interactions SMC proteins UBL domain In 2008, SMCHD1 was identified as an epigenetic regulator essential for the maintenance of X-chromosome inactivation [ 1 ]. Subsequently, SMCHD1 has been attributed roles in the transcriptional...
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Biochem J (2021) 478 (11): 2163–2178.
Published: 11 June 2021
... bioluminescence resonance energy transfer CYP1A2 cytochrome p450 NADPH-cytochrome P450 reductase proteinprotein interactions The cytochrome P450s (P450s) involved in drug and xenobiotic metabolism are heme-containing, membrane-bound enzymes that reside primarily in the endoplasmic reticulum of cells...
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Biochem J (2021) 478 (7): 1321–1332.
Published: 06 April 2021
... proteinprotein interactions Scribble Vangl2 The establishment of cell polarity, defined as the asymmetric distribution of proteins, carbohydrates and lipids within the cell, is a crucial process for the organization and development of all animal tissues [ 1 ]. In multicellular organisms, four...
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Biochem J (2021) 478 (2): 377–388.
Published: 27 January 2021
... for POR to function. In addition to these functionally required proteinprotein interactions, HO-1 forms homomeric complexes, and several P450s have been shown to form complexes with themselves and with other P450s, raising the question, ‘How are the HO-1 and P450 systems organized in the endoplasmic...
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Biochem J (2020) 477 (9): 1701–1719.
Published: 11 May 2020
...Lidan Aharon; Shay-Lee Aharoni; Evette S. Radisky; Niv Papo To facilitate investigations of proteinprotein interactions (PPIs), we developed a novel platform for quantitative mapping of protein binding specificity landscapes, which combines the multi-target screening of a mutagenesis library...
Includes: Supplementary data
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Biochem J (2020) 477 (7): 1219–1225.
Published: 09 April 2020
...Nikolai N. Sluchanko Many major proteinprotein interaction networks are maintained by ‘hub’ proteins with multiple binding partners, where interactions are often facilitated by intrinsically disordered protein regions that undergo post-translational modifications, such as phosphorylation...
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Biochem J (2019) 476 (23): 3661–3685.
Published: 12 December 2019
... or chemically modified proteins. This includes the incorporation of proteins bearing fluorescent probes and light-activating cross-linkers. Therefore, this strategy may be used for monitoring proteinprotein interactions in HLM with various biophysical techniques, as well as for identifying the P450 interaction...
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Biochem J (2019) 476 (14): 2093–2109.
Published: 31 July 2019
..., with the magnitude of the effect depending on which PTB-AP was co-expressed. Taken together, our results indicate a modulating effect of PTB-APs on PICALM-mediated APP endocytosis and localization. amyloid precursor protein endocytosis PICALM proteinprotein interactions PTB-containing adaptor protein...
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Biochem J (2019) 476 (13): 1875–1887.
Published: 02 July 2019
... Attribution License 4.0 (CC BY) . AAA proteins integrins proteinprotein interactions tetrapyrroles The first committed step in the biosynthesis of chlorophyll is catalysed by magnesium chelatase (MgCH; E.C.6.6.1.1), a large, multisubunit enzyme which catalyses the insertion of a Mg 2+ ion...
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Biochem J (2018) 475 (18): 2969–2983.
Published: 25 September 2018
... This is an open 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) . AMPK glucose transport obesity proteinprotein interactions Rab-GAP signalling AMP-activated protein kinase (AMPK...
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Biochem J (2018) 475 (14): 2293–2304.
Published: 25 July 2018
... GTPases intracellular signaling proteinprotein interactions Heterotrimeric (αβγ) G proteins are molecular switches that mediate signaling initiated by G protein-coupled receptors (GPCRs) and play central roles in numerous cellular signaling cascades [ 1 – 3 ]. G proteins are activated...
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Biochem J (2017) 474 (24): 4035–4051.
Published: 27 November 2017
... intracellular calcium proteinprotein interactions regulation Gap junctions formed by two hemichannels of connexins between two adjacent cells provide a direct pathway for cell communication and the cell-to-cell transfer of small molecules (<1 kDa). This specialized membrane structure integrates...
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Biochem J (2017) 474 (21): 3689–3704.
Published: 25 October 2017
... alternative splicing in human cells, and indeed that tri-snRNP proteins are over-represented in this process [ 28 ]. This study indicates that modulating proteinprotein interactions within the spliceosome can regulate alternative splicing. As part of a larger goal to understand how spliceosomal proteins...
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Biochem J (2017) 474 (15): 2601–2617.
Published: 21 July 2017
...(s); published by Portland Press Limited on behalf of the Biochemical Society 2017 drug design osteoclasts proteinprotein interactions rational protein engineering receptor tyrosine kinases X-ray structure Recombinant protein ligands and receptors have shown great promise...
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Biochem J (2017) 474 (10): 1633–1651.
Published: 04 May 2017
... Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) . epigenetics histone binding PHD finger proteinprotein interactions reader domains Members of the BAZ family of proteins, which includes BAZ1A, also known as Acf1 [ 21 , 22 ], BAZ1B, also known...
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Biochem J (2017) 474 (9): 1509–1528.
Published: 19 April 2017
...–protein interactions proteolysis transcription factors 293HEK and MDCK cells were transiently transfected in triplicate on 24-well plates. In addition to Dok-4 and/or kinase expression constructs, the pFR-Luc vector (Gal-4/luciferase) was transfected in combination with pFA2-Elk-1 CT, pFA2-Elk-4...
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Biochem J (2017) 474 (7): 1273–1287.
Published: 23 March 2017
... The Author(s); published by Portland Press Limited on behalf of the Biochemical Society 2017 crystallography Parkinson's disease proteinprotein interactions All peptides were synthesized via Fmoc solid-phase peptide synthesis making use of an Intavis MultiPep RSi peptide synthesizer...
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Biochem J (2016) 473 (19): 3237–3252.
Published: 27 September 2016
... that there are functional consequences of this interaction, with inhibition of NCC affecting the function of ENaC. This novel finding of an association between ENaC and NCC could alter our understanding of salt transport in the distal tubule. ion channels proteinprotein interactions sodium channel sodium chloride...
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Biochem J (2016) 473 (19): 3269–3290.
Published: 27 September 2016
...–protein interactions serpin α 1 -Antitrypsin (α 1 -AT) is the most abundant circulating protease inhibitor and a member of the serpin superfamily. It is predominantly expressed by hepatocytes in the liver and acts to prevent excessive proteolytic damage by the enzyme neutrophil elastase...
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Biochem J (2015) 469 (1): 159–168.
Published: 19 June 2015
... positions distal from the binding groove through a network of residues undergoing subtle changes of conformation and dynamics. intradomain energetic connectivity PDZ domains pre-steady-state kinetics proteinprotein interactions Microtubule-associated serine threonine kinase 2 (MAST2...
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Biochem J (2012) 446 (3): 489–497.
Published: 28 August 2012
... forms CYP1A2–CYP1A2 complexes that exhibit altered catalytic activity. bioluminescence resonance energy transfer (BRET) cytochrome P450 enzyme kinetics homomeric P450–P450 complexes protein cross-linking proteinprotein interactions Cytochrome P450 plays a major role in the metabolism...
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