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CORDIS Web 30th anniversary CORDIS Web 30th anniversary

EUbOPEN: Enabling and Unlocking biology in the OPEN

CORDIS oferuje możliwość skorzystania z odnośników do publicznie dostępnych publikacji i rezultatów projektów realizowanych w ramach programów ramowych HORYZONT.

Odnośniki do rezultatów i publikacji związanych z poszczególnymi projektami 7PR, a także odnośniki do niektórych konkretnych kategorii wyników, takich jak zbiory danych i oprogramowanie, są dynamicznie pobierane z systemu OpenAIRE .

Rezultaty

300 proteins purified in year 1

1,500 proteins purified at a rate of approximately 300 per year (reported at M12, M36, M60). Expression constructs and proteins will be produced by UOXF, GUF, KI, UNIVDUN, LUMC, with contributions from EFPIA and Associated Partners where applicable.

Applied to ≥2 new chemical series in year 3

First version of platform for automated compound synthesis applied to 2 new scaffoldsyear M36 M60

Additional ten PCAs established and/or optimised (20 in total)

Ten PCAs established and/or optimised (20 in total, 10 by month 24 and additional 10 by month 48).

Family wide screening platform for kinases using NanoBRET or ABPP technology

Family wide screening platform for kinases and one new family using NanoBRET or ABPP technology M24 M60

40 CRISPR knockout cell lines in year 1

40 CRISPR knockout cell lines per year (total 160) (M12, M36, M48).

First set of community engagement events or symposium held

Community engagement events and symposia held

Deposit intermediate set of data in sustainable resources
Evaluation of Raman assays and establishment of protocols in cell culture and patient-derived tissues

Evaluation of Raman assays and establishment of protocols in cell culture and patient-derived tissues.

Data for initial CG set released

Data for each Chemogenomic set release in EUbOPEN gateway Zenodo

50 targets enabled with in vitro assays and 30 targets with cellular assays

D5.1 250 targets enabled with assays for chemical probe discovery and optimisation at a rate of approximately 50 per year and 150 targets enabled with an in-cell target engagement assay at a rate of about 30 per year (M12, M36, M60).

EUbOPEN database gateway development

EUbOPEN database gateway specification and further development

Acquisition of > 500 compounds for CGL covering >250 targets

Acquisition of CG compounds (500 compounds/year) from commercial sources, academic partners and EFPIA.

EUbOPEN database gateway specification

EUbOPEN database gateway specification and further development.

Guiding principles for global network with similar organisations

Guiding principles for global network with similar organisations.

Five aggregated, anonymized and quality assured screening data sets released to the public

Five aggregated anonymized and quality assured screening data sets released to the public on annual basis through project website and other dissemination channels

20 recombinant antibodies or binders in year 2 and 3

50 recombinant antibodies or other binders at a rate of about 10 per year reported at M12 M36 M60 Binders will be generated by KI and ReSOLUTE with donations from Pharma partners

100 protein structures in year 1

100 protein structures in year 1.

Standardized chip design and processing established

Standardized chip design and processing established.

20 CP in year 1

20 EUbOPEN-generated CPs in year 1, including EFPIA contributions and jointly generated CPs as well as contributions from other scientists outside EUbOPEN.

First version of platform for automated compound synthesis

First version of platform for automated compound synthesis M24

Additional five aggregated, anonymized and quality assured screening data sets released to the public

Five aggregated anonymized and quality assured screening data sets released to the public on annual basis through project website and other dissemination channels

First EUbOPEN website review and development

EUbOPEN website development with regular reviews and updates

Update on web-based internal database system development

Webbased internal database system implementation and development

Intermediate release of curated CG compound profiling data

Release of curated CGL profiling data

First review of data ontology

Data ontology defined by working group and regularly reviewed

Acquisition of > 2,000 compounds for CGL covering >750 new targets

Acquisition of CG compounds (500 compounds/year) from commercial sources, academic partners and EFPIA.

Web-based internal database system initial implementation

Web-based internal database system implementation and development.

LiP-MS or BioID datasets of ≥10 probe-cell interactions

LiPMS datasets of 5 probecell interactionsyear M36 M60

Agreed quality control criteria approved by JMC

Agreed quality control criteria approved by JMC.

Ten PCAs established and/or optimised (20 in total)

Ten PCAs established andor optimised 20 in total 10 by month 24 and additional 10 by month 48

>1500 novel CG compounds sourced

At least 1500 CG compounds sourced or synthesised .

600 proteins purified in year 2 and 3

1500 proteins purified at a rate of approximately 300 per year reported at M12 M36 M60 Expression constructs and proteins will be produced by UOXF GUF KI UNIVDUN LUMC with contributions from EFPIA and Associated Partners where applicable

Data ontology defined by working group

Data ontology defined by working group.

A total of fifteen aggregated, anonymized and quality assured screening data sets released to the public

Five aggregated, anonymized and quality assured screening data sets released to the public on annual basis through project website and other dissemination channels.

40 CP in year 2 and 3

40 EUbOPENgenerated CPs in year 2 and 3 to a total of 60 CPs The CPs will include EFPIA contributions and jointly generated CPs as well as contributions from other scientists outside EUbOPEN

10 recombinant antibodies or binders in year 1

50 recombinant antibodies or other binders at a rate of about 10 per year (reported at M12, M36, M60). Binders will be generated by KI and ReSOLUTE with donations from Pharma partners.

Data deposition of genome/proteome wide analysis for >60 CG compounds

Genomeproteome wide analysis of subset of CG compounds 150 in total and deposition of data in sustainable resources M24 M60

100 targets enabled with in vitro assays and 60 targets with cellular assays in year 2 and 3

D51 250 targets enabled with assays for chemical probe discovery and optimisation at a rate of approximately 50 per year and 150 targets enabled with an incell target engagement assay at a rate of about 30 per year M12 M36 M60

Steady state sample access (1-2 per week) from IBD and CRC

Steady state sample access (1-2 per week) from IBD and CRC.

Establish data publication standard and database
200 protein structures in years 2 and 3

200 protein structures in year 2 and 3

Assembly of expanded reaction toolkit and fragment set for plate-based chemistry

Assembly of expanded reaction toolkit and fragment set for platebased chemistry

New protein family sentinel selectivity panel

New protein family sentinel selectivity panel for three families

Initial protocols made openly available through portal and public databases

Protocols made openly available through portal and public databases

Partnerships with >25 international partners

Partnerships with 25 international organisations with efforts in screening assay development patientderived cell assays chemical screening chemical probe generation and compound profiling established

80 CRISPR knockout cell lines in years 2 and 3

40 CRISPR knockout cell lines per year total 160 M12 M36 M48

Online compound ordering system for the public

Online compound ordering system for the public operational.

EUbOPEN website implementation

EUbOPEN website development with regular reviews and updates (M3, M36, M60).

Define criteria for compounds of CGL

The criteria underlying the list of targets to be covered by the CGL will be defined by the JMC and TPN (M3), and surveyed in regular meetings to govern the activities of Pillar 1.

Define target list of 1,000 targets

Defined target list of 1,000 proteins covered by the CGL.

Revised target list

The target list will be revised during the project.

Distribution of additionally approved CG sets and CP

Additionally approved CGs and CPs will be assembled and released with appropriate instructions to the public.

Extended FRAGALYSIS cloud infrastructure for in silico compound design

Extended FRAGALYSIS cloud infrastructure for in silico compound design Comprehensive compound prioritisation based on commercially available compounds

Extended FRAGALYSIS cloud infrastructure for de novo compound design

FRAGALYSIS de novo compound design interface compatible with platforms for automated compound synthesis.

Distribution of approved CG sets and CP

Newly approved CGs and CPs will be assembled and released with appropriate instructions to the public.

Publikacje

Comparative structural analyses of the NHL domains from the human E3 ligase TRIM-NHL family

Autorzy: Chaikuad A, Zhubi R, Tredup C, Knapp S.
Opublikowane w: IUCr, 2022, ISSN 2052-2525
Wydawca: IUCr Journals
DOI: 10.1107/s2052252522008582

Technologies for Direct Detection of Covalent Protein–Drug Adducts

Autorzy: Elma Mons, Robbert Q. Kim, Monique P. C. Mulder
Opublikowane w: Pharmaceuticals, 2023, ISSN 1424-8247
Wydawca: Multidisciplinary Digital Publishing Institute (MDPI)
DOI: 10.3390/ph16040547

DIP-MS: ultra-deep interaction proteomics for the deconvolution of protein complexes

Autorzy: Frommelt F, Fossati A, Uliana F, Wendt F, Xue P, Heusel M, Wollscheid B, Aebersold R, Ciuffa R, Gstaiger M.
Opublikowane w: Nat Methods, 2024, ISSN 1548-7091
Wydawca: Nature Publishing Group
DOI: 10.1038/s41592-024-02211-y

Systematic Design of Adenosine Analogs as Inhibitors of a Clostridioides difficile-Specific DNA Adenine Methyltransferase Required for Normal Sporulation and Persistence.

Autorzy: Zhou J, Horton JR, Menna M, Fiorentino F, Ren R, Yu D, Hajian T, Vedadi M, Mazzoccanti G, Ciogli A, Weinhold E, Hüben M, Blumenthal RM, Zhang X, Mai A, Rotili D, Cheng X
Opublikowane w: J Med Chem, 2022, ISSN 0022-2623
Wydawca: American Chemical Society
DOI: 10.1021/acs.jmedchem.2c01789

Building ubiquitination machineries: E3 ligase multi-subunit assembly and substrate targeting by PROTACs and molecular glues

Autorzy: Sarath Ramachandran, Alessio Ciulli
Opublikowane w: Current Opinion in Structural Biology, Numer 67, 2021, Strona(/y) 110-119, ISSN 0959-440X
Wydawca: Elsevier BV
DOI: 10.1016/j.sbi.2020.10.009

Development of a Selective Dual Discoidin Domain Receptor (DDR)/p38 Kinase Chemical Probe.

Autorzy: Rohm, S., Berger, B. T., Schroder, M., Chatterjee, D., Mathea, S., Joerger, A. C., Pinkas, D. M., Bufton, J. C., Tjaden, A., Kovooru, L., Kudolo, M., Pohl, C., Bullock, A. N., Muller, S., Laufer, S. and Knapp, S
Opublikowane w: J Med Chem., 2021, ISSN 0022-2623
Wydawca: American Chemical Society
DOI: 10.1021/acs.jmedchem.1c00868

Development and Characterization of Type I, Type II, and Type III LIM-Kinase Chemical Probes

Autorzy: Hanke T, Mathea S, Woortman J, Salah E, Berger BT, Tumber A, Kashima R, Hata A, Kuster B, Müller S, Knapp S. J Med Chem 2022. 
Opublikowane w: Journal of Medicinal Chemistry, 2022, ISSN 0022-2623
Wydawca: American Chemical Society
DOI: 10.1021/acs.jmedchem.2c01106

Mechanism and evolutionary origins of alanine-tail C-degron recognition by E3 ligases Pirh2 and CRL2-KLHDC10.

Autorzy: Patil PR, Burroughs AM, Misra M, Cerullo F, Costas-Insua C, Hung HC, Dikic I, Aravind L, Joazeiro CAP
Opublikowane w: Cell Rep, 2023, ISSN 2211-1247
Wydawca: Cell Press
DOI: 10.1016/j.celrep.2023.113100

Breaking free from the crystal lattice: Structural biology in solution to study protein degraders

Autorzy: Kevin Haubrich; Valentina A. Spiteri; William Farnaby; Frank Sobott; Alessio Ciulli
Opublikowane w: Crossref, Numer 2, 2023, ISSN 0346-251X
Wydawca: Pergamon Press Ltd.
DOI: 10.1016/j.sbi.2023.102534

Ubiquitin ligases: guardians of mammalian development

Autorzy: Cruz Walma, D. A., Chen, Z., Bullock, A. N. and Yamada, K. M
Opublikowane w: Nat Rev Mol Cell Biol, 2022, ISSN 1471-0072
Wydawca: Nature Publishing Group
DOI: 10.1038/s41580-021-00448-5

Hepatic miR-144 Drives Fumarase Activity Preventing NRF2 Activation During Obesity

Autorzy: Azzimato, V., Chen, P., Barreby, E., Morgantini, C., Levi, L., Vankova, A., ... & Aouadi, M.
Opublikowane w: Gastroenterology, 2021, ISSN 0016-5085
Wydawca: W. B. Saunders Co., Ltd.
DOI: 10.1053/j.gastro.2021.08.030

Structure and activity of human TMPRSS2 protease implicated in SARS-CoV-2 activation.

Autorzy: Fraser BJ, Beldar S, Seitova A, Hutchinson A, Mannar D, Li Y, Kwon D, Tan R, Wilson RP, Leopold K, Subramaniam S, Halabelian L, Arrowsmith CH, Bénard F
Opublikowane w: Nat Chem Biol, 2022, ISSN 1552-4450
Wydawca: Nature Publishing Group
DOI: 10.1038/s41589-022-01059-7

The ethnogeographic variability of genetic factors underlying G6PD deficiency

Autorzy: Koromina, M., Pandi, M. T., van der Spek, P. J., Patrinos, G. P., & Lauschke, V. M.
Opublikowane w: Pharmacological Research, 2021, ISSN 1043-6618
Wydawca: Academic Press
DOI: 10.1016/j.phrs.2021.105904

Small-molecule activation of OGG1 increases oxidative DNA damage repair by gaining a new function. 

Autorzy: Michel M, Benítez-Buelga C, Calvo PA, Hanna BMF, Mortusewicz O, Masuyer G, Davies J, Wallner O, Sanjiv K, Albers JJ, Castañeda-Zegarra S, Jemth AS, Visnes T, Sastre-Perona A, Danda AN, Homan EJ, Marimuthu K, Zhenjun Z, Chi CN, Sarno A, Wiita E, von Nicolai C, Komor AJ, Rajagopal V, Müller S, Hank EC, Varga M, Scaletti ER, Pandey M, Karsten S, Haslene-Hox H, Loevenich S, Marttila P, Rasti A, Mam
Opublikowane w: Science, 2023, ISSN 0036-8075
Wydawca: American Association for the Advancement of Science
DOI: 10.1126/science.abf8980

Population-scale predictions of DPD and TPMT phenotypes using a quantitative pharmacogene-specific ensemble classifier

Autorzy: Yitian Zhou, Carolina Dagli Hernandez, Volker M. Lauschke
Opublikowane w: British Journal of Cancer, Numer 123/12, 2020, Strona(/y) 1782-1789, ISSN 0007-0920
Wydawca: Nature Publishing Group
DOI: 10.1038/s41416-020-01084-0

Harnessing CD3 diversity to optimize CAR T cells.

Autorzy: Velasco Cárdenas RM, Brandl SM, Meléndez AV, Schlaak AE, Buschky A, Peters T, Beier F, Serrels B, Taromi S, Raute K, Hauri S, Gstaiger M, Lassmann S, Huppa JB, Boerries M, Andrieux G, Bengsch B, Schamel WW, Minguet S.
Opublikowane w: Nat Immunol., 2024, ISSN 1529-2908
Wydawca: Nature Publishing Group
DOI: 10.1038/s41590-023-01658-z

Histone lysine methacrylation is a dynamic post-translational modification regulated by HAT1 and SIRT2

Autorzy: Delaney K, Tan M, Zhu Z, Gao J, Dai L, Kim S, Ding J, He M, Halabelian L, Yang L, Nagarajan P, Parthun MR, Lee S, Khochbin S, Zheng YG, Zhao Y
Opublikowane w: Cell Discov, 2022, ISSN 2056-5968
Wydawca: Nature Publishing Group
DOI: 10.1038/s41421-021-00344-4

PRMT inhibition induces a viral mimicry response in triple-negative breast cancer.

Autorzy: Wu Q, Nie DY, Ba-Alawi W, Ji Y, Zhang Z, Cruickshank J, Haight J, Ciamponi FE, Chen J, Duan S, Shen Y, Liu J, Marhon SA, Mehdipour P, Szewczyk MM, Dogan-Artun N, Chen W, Zhang LX, Deblois G, Prinos P, Massirer KB, Barsyte-Lovejoy D, Jin J, De Carvalho DD, Haibe-Kains B, Wang X, Cescon DW, Lupien M, Arrowsmith CH
Opublikowane w: Nature Chemical Biology, 2022, ISSN 1552-4450
Wydawca: Nature Publishing Group
DOI: 10.1038/s41589-022-01024-4

Proteomic workflows for deep phenotypic profiling of 3D organotypic liver models

Autorzy: Stefania Koutsilieri, Evgeniya Mickols, Ákos Végvári, Volker M Lauschke
Opublikowane w: Biotechnol J, 2023, ISSN 1860-6768
Wydawca: Wiley - VCH Verlag GmbH & CO. KGaA
DOI: 10.1002/biot.202300684

High-content live-cell multiplex screen for chemogenomic compound annotation based on nuclear morphology

Autorzy: Tjaden A, Giessmann RT, Knapp S, Schröder M, Müller S.
Opublikowane w: STAR Protoc., 2022, ISSN 2666-1667
Wydawca: Cell Press
DOI: 10.1016/j.xpro.2022.101791

No shortcuts to SARS-CoV-2 antivirals.

Autorzy: Edwards A, Hartung IV
Opublikowane w: Science, 2021, ISSN 0036-8075
Wydawca: American Association for the Advancement of Science
DOI: 10.1126/science.abj9488

Crystal Structure-Guided Design of Bisubstrate Inhibitors and Photoluminescent Probes for Protein Kinases of the PIM Family

Autorzy: Olivier E. Nonga, Darja Lavogina, Erki Enkvist, Katrin Kestav, Apirat Chaikuad, Sarah E. Dixon-Clarke, Alex N. Bullock, Sergei Kopanchuk, Taavi Ivan, Ramesh Ekambaram, Kaido Viht, Stefan Knapp, Asko Uri
Opublikowane w: Molecules, Numer 26/14, 2021, Strona(/y) 4353, ISSN 1420-3049
Wydawca: Multidisciplinary Digital Publishing Institute (MDPI)
DOI: 10.3390/molecules26144353

Mutation in Abl kinase with altered drug-binding kinetics indicates a novel mechanism of imatinib resistance

Autorzy: Lyczek A, Berger BT, Rangwala AM, Paung Y, Tom J, Philipose H, Guo J, Albanese SK, Robers MB, Knapp S, Chodera JD, Seeliger MA.
Opublikowane w: Proc Natl Acad Sci U S A, 2021, ISSN 0027-8424
Wydawca: National Academy of Sciences
DOI: 10.1073/pnas.2111451118

RNF8 ubiquitylation of XRN2 facilitates R-loop resolution and restrains genomic instability in BRCA1 mutant cells

Autorzy: Rehna Krishnan, Mariah Lapierre, Brandon Gautreau, Kevin C J Nixon, Samah El Ghamrasni, Parasvi S Patel, Jun Hao, V Talya Yerlici, Kiran Kumar Naidu Guturi, Jonathan St-Germain, Francesca Mateo, Amine Saad, Arash Algouneh, Rebecca Earnshaw, Duan Shili, Alma Seitova, Joshua Miller, Negin Khosraviani, Adam Penn, Brandon Ho, Otto Sanchez, M Prakash Hande, Jean-Yves Masson, Grant W Brown, Moulay Alaou
Opublikowane w: Nucleic Acids Res, 2023, ISSN 0305-1048
Wydawca: Oxford University Press
DOI: 10.1093/nar/gkad733

The Kinase Chemogenomic Set (KCGS): An Open Science Resource for Kinase Vulnerability Identification

Autorzy: Carrow I. Wells, Hassan Al-Ali, David M. Andrews, Christopher R. M. Asquith, Alison D. Axtman, Ivan Dikic, Daniel Ebner, Peter Ettmayer, Christian Fischer, Mathias Frederiksen, Robert E. Futrell, Nathanael S. Gray, Stephanie B. Hatch, Stefan Knapp, Ulrich Lücking, Michael Michaelides, Caitlin E. Mills, Susanne Müller, Dafydd Owen, Alfredo Picado, Kumar S. Saikatendu, Martin Schröder, Alexandra
Opublikowane w: International Journal of Molecular Sciences, Numer 22/2, 2021, Strona(/y) 566, ISSN 1422-0067
Wydawca: Multidisciplinary Digital Publishing Institute (MDPI)
DOI: 10.3390/ijms22020566

Post-transcriptional and Post-translational Modifications of Primary Cilia: How to Fine Tune Your Neuronal Antenna.

Autorzy: Rocha C, Prinos P
Opublikowane w: Front Cell Neurosci, 2022, ISSN 1662-5102
Wydawca: Frontiers Research Foundation
DOI: 10.3389/fncel.2022.809917

DFG-1 Residue Controls Inhibitor Binding Mode and Affinity, Providing a Basis for Rational Design of Kinase Inhibitor Selectivity

Autorzy: Martin Schröder, Alex N. Bullock, Oleg Fedorov, Franz Bracher, Apirat Chaikuad, Stefan Knapp
Opublikowane w: Journal of Medicinal Chemistry, Numer 63/18, 2020, Strona(/y) 10224-10234, ISSN 0022-2623
Wydawca: American Chemical Society
DOI: 10.1021/acs.jmedchem.0c00898

Genotoxicity and Epigenotoxicity of Carbazole-Derived Molecules on MCF-7 Breast Cancer Cells

Autorzy: Claudio Luparello, Ilenia Cruciata, Andreas C. Joerger, Cory A. Ocasio, Rhiannon Jones, Raysa Khan Tareque, Mark C. Bagley, John Spencer, Martin Walker, Carol Austin, Tiziana Ferrara, Pietro D′Oca, Rossella Bellina, Rossella Branni, Fabio Caradonna
Opublikowane w: International Journal of Molecular Sciences, Numer 22/7, 2021, Strona(/y) 3410, ISSN 1422-0067
Wydawca: Multidisciplinary Digital Publishing Institute (MDPI)
DOI: 10.3390/ijms22073410

Autoantibodies against Four-and-a-Half-LIM Domain 1 (FHL1) in Inflammatory Myopathies: Results from an Australian Single-Center Cohort.

Autorzy: Galindo-Feria AS, Horuluoglu B, Day J, Fernandes-Cerqueira C, Wigren E, Gräslund S, Proudman S, Lundberg IE, Limaye V
Opublikowane w: Rheumatology, 2022, ISSN 1462-0324
Wydawca: Oxford University Press
DOI: 10.1093/rheumatology/keac003

Structural insights into a regulatory mechanism of FIR RRM1-FUSE interaction

Autorzy: Ni X, Joerger AC, Chaikuad A, Knapp S.
Opublikowane w: Open Biol., 2023, ISSN 2046-2441
Wydawca: Royal Society Publishing
DOI: 10.1098/rsob.230031

SS148 and WZ16 inhibit the activities of nsp10-nsp16 complexes from all seven human pathogenic coronaviruses.

Autorzy: Li F, Ghiabi P, Hajian T, Klima M, Li ASM, Yazdi AK, Chau I, Loppnau P, Kutera M, Seitova A, Bolotokova A, Hutchinson A, Perveen S, Boura E, Vedadi M
Opublikowane w: Biochim Biophys Acta, 2023, ISSN 0304-4165
Wydawca: Elsevier BV
DOI: 10.1016/j.bbagen.2023.130319

Adjudin improves beta cell maturation, hepatic glucose uptake and glucose homeostasis

Autorzy: Lipeng Ren, Jérémie Charbord, Lianhe Chu, Aurino M Kemas, Maria Bertuzzi, Jiarui Mi, Chen Xing, Volker M Lauschke, Olov Andersson
Opublikowane w: Diabetologia, 2023, ISSN 0012-186X
Wydawca: Springer Verlag
DOI: 10.1007/s00125-023-06020-4

Prediction and Validation of a Protein's Free Energy Surface Using Hydrogen Exchange and (Importantly) Its Denaturant Dependence.

Autorzy: Peng X, Baxa M, Faruk N, Sachleben JR, Pintscher S, Gagnon IA, Houliston S, Arrowsmith CH, Freed KF, Rocklin GJ, Sosnick TR
Opublikowane w: J Chem Theory Comput, 2021, ISSN 1549-9618
Wydawca: American Chemical Society
DOI: 10.1021/acs.jctc.1c00960

Discovery and Characterization of BAY-805, a Potent and Selective Inhibitor of Ubiquitin-Specific Protease USP21

Autorzy: Fabian Göricke; Victoria Vu; Leanna Smith; Ulrike Scheib; Raphael Böhm; Namik Akkilic; Gerd Wohlfahrt; Jörg Weiske; Ulf Bömer; Krzysztof Brzezinka; Niels Lindner; Philip Lienau; Stefan Gradl; Hartmut Beck; Peter J. Brown; Vijayaratnam Santhakumar; Masoud Vedadi; Dalia Barsyte-Lovejoy; Cheryl H. Arrowsmith; Norbert Schmees; Kirstin Petersen
Opublikowane w: Crossref, Numer 3, 2023, ISSN 0022-2623
Wydawca: American Chemical Society
DOI: 10.1021/acs.jmedchem.2c01933

Editorial: The next generation of tools and technologies for studying human neurons in a dish

Autorzy: Thomas M. Durcan and Alison D. Axtman
Opublikowane w: Front Cell Neurosci, 2023, ISSN 1662-5102
Wydawca: Frontiers Research Foundation
DOI: 10.3389/fncel.2023.1196543

7-(2-Anilinopyrimidin-4-yl)-1-benzazepin-2-ones Designed by a “Cut and Glue” Strategy Are Dual Aurora A/VEGF-R Kinase Inhibitors

Autorzy: Mehmet Karatas, Apirat Chaikuad, Bianca Berger, Michael H. G. Kubbutat, Frank Totzke, Stefan Knapp, Conrad Kunick
Opublikowane w: Molecules, Numer 26/6, 2021, Strona(/y) 1611, ISSN 1420-3049
Wydawca: Multidisciplinary Digital Publishing Institute (MDPI)
DOI: 10.3390/molecules26061611

Pharmacogenomics in the era of next generation sequencing – from byte to bedside

Autorzy: Laura E. Russell, Yitian Zhou, Ahmed A. Almousa, Jasleen K. Sodhi, Chukwunonso K. Nwabufo, Volker M. Lauschke
Opublikowane w: Drug Metabolism Reviews, 2021, Strona(/y) 1-26, ISSN 0360-2532
Wydawca: Marcel Dekker Inc.
DOI: 10.1080/03602532.2021.1909613

Structure and Function of Protein Arginine Methyltransferase PRMT7.

Autorzy: Halabelian L, Barsyte-Lovejoy D
Opublikowane w: Life (Basel), 2021, ISSN 2075-1729
Wydawca: MDPI
DOI: 10.3390/life11080768

Scaffold hopping from amodiaquine to novel Nurr1 agonist chemotypes via microscale analogue libraries.

Autorzy: Willems, S.; Müller, M.; Ohrndorf, J.; Heering, J.; Proschak, E.; Merk, D.
Opublikowane w: ChemMedChem, 2022, ISSN 1860-7179
Wydawca: Wiley - V C H Verlag GmbbH & Co.
DOI: 10.1002/cmdc.202200026

Conformation and dynamics of the kinase domain drive subcellular location and activation of LRRK2

Autorzy: Sven H. Schmidt, Jui-Hung Weng, Phillip C. Aoto, Daniela Boassa, Sebastian Mathea, Steve Silletti, Junru Hu, Maximilian Wallbott, Elizabeth A. Komives, Stefan Knapp, Friedrich W. Herberg, Susan S. Taylor
Opublikowane w: Proceedings of the National Academy of Sciences, Numer 118/23, 2021, Strona(/y) e2100844118, ISSN 0027-8424
Wydawca: National Academy of Sciences
DOI: 10.1073/pnas.2100844118

Integrated analysis of Shank1 PDZ interactions with C-terminal and internal binding motifs

Autorzy: Muhammad Ali, Mishal Mariam McAuley, Susanne Lüchow, Stefan Knapp, Andreas C. Joerger, Ylva Ivarsson
Opublikowane w: Current Research in Structural Biology, Numer 3, 2021, Strona(/y) 41-50, ISSN 2665-928X
Wydawca: Elsevier
DOI: 10.1016/j.crstbi.2021.01.001

Disease-associated KBTBD4 mutations in medulloblastoma elicit neomorphic ubiquitylation activity to promote CoREST degradation

Autorzy: Chen, Z., Ioris, R. M., Richardson, S., Van Ess, A. N., Vendrell, I., Kessler, B.M., Buffa, F.M., Busino, L., Clifford, S. C., Bullock, A. N. D'Angiolella, V.
Opublikowane w: Cell Death Differ., 2022, ISSN 1350-9047
Wydawca: Nature Publishing Group
DOI: 10.1038/s41418-022-00983-4

Huntingtin structure is orchestrated by HAP40 and shows a polyglutamine expansion-specific interaction with exon 1.

Autorzy: Harding RJ, Deme JC, Hevler JF, Tamara S, Lemak A, Cantle JP, Szewczyk MM, Begeja N, Goss S, Zuo X, Loppnau P, Seitova A, Hutchinson A, Fan L, Truant R, Schapira M, Carroll JB, Heck AJR, Lea SM, Arrowsmith CH
Opublikowane w: Commun Biol, 2021, ISSN 2399-3642
Wydawca: Springer Nature
DOI: 10.1038/s42003-021-02895-4

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The genetic landscape of major drug metabolizing cytochrome P450 genes—an updated analysis of population-scale sequencing data

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Practice guidance documents for the diagnosis and management of non-alcoholic fatty liver disease—recent updates and open questions

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Trivalent PROTACs enhance protein degradation via combined avidity and cooperativity

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Population pharmacogenomics: an update on ethnogeographic differences and opportunities for precision public health

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Nucelotide Binding, Evolutionary Insights and Interaction Partners of the Pseudokinase Unc-51-like Kinase 4

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ALK2 Receptor Kinase Association with FKBP12.6 Is Structurally Conserved with the ALK2-FKBP12 Complex

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Calcium measurements in enzymatically dissociated or mechanically microdissected mouse primary skeletal muscle fibers

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Targeting TRIM Proteins: A Quest towards Drugging an Emerging Protein Class

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Phosphorylation of the DNA repair scaffold SLX4drives folding of the SAP domain and activation of theMUS81-EME1 endonucleas

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JAK inhibition reduces SARS-CoV-2 liver infectivity and modulates inflammatory responses to reduce morbidity and mortality

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CACHE (Critical Assessment of Computational Hit-finding Experiments): A public–private partnership benchmarking initiative to enable the development of computational methods for hit-finding

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Crimean-Congo haemorrhagic fever virus uses LDLR to bind and enter host cells.

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Structural basis of the TAM domain of BAZ2A in binding toDNA or RNA independent of methylation status

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Cellular Validation of a Chemically Improved Inhibitor Identifies Monoubiquitination on OTUB2

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JAK Inhibitors — More Than Just Glucocorticoids

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Probing the mechanism of Cbl-b inhibition by a small molecule inhibitor

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Rewiring of catecholamine-induced calcium signalling is an early event in non-alcoholic fatty liver disease

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