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  1. Article ; Online: Ubiquitin-regulating effector proteins from Legionella.

    Jeong, Minwoo / Jeon, Hayoung / Shin, Donghyuk

    BMB reports

    2022  Volume 55, Issue 7, Page(s) 316–322

    Abstract: Ubiquitin is relatively modest in size but involves almost entire cellular signaling pathways. The primary role of ubiquitin is maintaining cellular protein homeostasis. Ubiquitination regulates the fate of target proteins using the proteasome- or ... ...

    Abstract Ubiquitin is relatively modest in size but involves almost entire cellular signaling pathways. The primary role of ubiquitin is maintaining cellular protein homeostasis. Ubiquitination regulates the fate of target proteins using the proteasome- or autophagymediated degradation of ubiquitinated substrates, which can be either intracellular or foreign proteins from invading pathogens. Legionella, a gram-negative intracellular pathogen, hinders the host-ubiquitin system by translocating hundreds of effector proteins into the host cell's cytoplasm. In this review, we describe the current understanding of ubiquitin machinery from Legionella. We summarize structural and biochemical differences between the host-ubiquitin system and ubiquitin-related effectors of Legionella. Some of these effectors act much like canonical host-ubiquitin machinery, whereas others have distinctive structures and accomplish non-canonical ubiquitination via novel biochemical mechanisms. [BMB Reports 2022; 55(7): 316-322].
    MeSH term(s) Bacterial Proteins/metabolism ; Legionella/metabolism ; Legionella pneumophila/metabolism ; Ubiquitin/metabolism ; Ubiquitination
    Chemical Substances Bacterial Proteins ; Ubiquitin
    Language English
    Publishing date 2022-06-24
    Publishing country Korea (South)
    Document type News ; Review
    ZDB-ID 2410389-5
    ISSN 1976-670X ; 1976-6696
    ISSN (online) 1976-670X
    ISSN 1976-6696
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Structural insights into ubiquitin chain cleavage by

    Kang, Sangwoo / Kim, Gyuhee / Choi, Minhyeong / Jeong, Minwoo / van der Heden van Noort, Gerbrand J / Roh, Soung-Hun / Shin, Donghyuk

    Life science alliance

    2023  Volume 6, Issue 7

    Abstract: Although ubiquitin is found only in eukaryotes, several pathogenic bacteria and viruses possess proteins that hinder the host ubiquitin system. ...

    Abstract Although ubiquitin is found only in eukaryotes, several pathogenic bacteria and viruses possess proteins that hinder the host ubiquitin system.
    MeSH term(s) Female ; Humans ; Ubiquitin/metabolism ; Polyubiquitin/chemistry ; Polyubiquitin/metabolism ; Legionella/metabolism ; Deubiquitinating Enzymes/genetics ; Deubiquitinating Enzymes/metabolism ; Ovarian Neoplasms/genetics
    Chemical Substances Ubiquitin ; Polyubiquitin (120904-94-1) ; Deubiquitinating Enzymes (EC 3.4.19.12)
    Language English
    Publishing date 2023-04-26
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ISSN 2575-1077
    ISSN (online) 2575-1077
    DOI 10.26508/lsa.202201876
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Effect of N doping on the microstructure and dry etch properties of amorphous carbon deposited with a DC sputtering system.

    Kim, Sungtae / Jeong, Min-Woo / Kim, Kuntae / Kim, Ung-Gi / Kim, Miyoung / Lee, So-Yeon / Joo, Young-Chang

    RSC advances

    2023  Volume 13, Issue 3, Page(s) 2131–2139

    Abstract: The importance of developing a hardmask with excellent performance, and physical and chemical properties to utilize in long-term etching is spotlighted due to the acceleration of development in high-density semiconductors. To develop such a hardmask, ... ...

    Abstract The importance of developing a hardmask with excellent performance, and physical and chemical properties to utilize in long-term etching is spotlighted due to the acceleration of development in high-density semiconductors. To develop such a hardmask, amorphous carbon hardmasks doped with various concentrations of N were fabricated with a DC magnetron sputtering system using varying inert gas (Ar to N
    Language English
    Publishing date 2023-01-12
    Publishing country England
    Document type Journal Article
    ISSN 2046-2069
    ISSN (online) 2046-2069
    DOI 10.1039/d2ra06808g
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Book ; Online: Connecting Low-Loss Subspace for Personalized Federated Learning

    Hahn, Seok-Ju / Jeong, Minwoo / Lee, Junghye

    2021  

    Abstract: Due to the curse of statistical heterogeneity across clients, adopting a personalized federated learning method has become an essential choice for the successful deployment of federated learning-based services. Among diverse branches of personalization ... ...

    Abstract Due to the curse of statistical heterogeneity across clients, adopting a personalized federated learning method has become an essential choice for the successful deployment of federated learning-based services. Among diverse branches of personalization techniques, a model mixture-based personalization method is preferred as each client has their own personalized model as a result of federated learning. It usually requires a local model and a federated model, but this approach is either limited to partial parameter exchange or requires additional local updates, each of which is helpless to novel clients and burdensome to the client's computational capacity. As the existence of a connected subspace containing diverse low-loss solutions between two or more independent deep networks has been discovered, we combined this interesting property with the model mixture-based personalized federated learning method for improved performance of personalization. We proposed SuPerFed, a personalized federated learning method that induces an explicit connection between the optima of the local and the federated model in weight space for boosting each other. Through extensive experiments on several benchmark datasets, we demonstrated that our method achieves consistent gains in both personalization performance and robustness to problematic scenarios possible in realistic services.

    Comment: Appears at ACM SIGKDD 2022. Code available at http://github.com/vaseline555/SuPerFed
    Keywords Computer Science - Machine Learning ; Computer Science - Artificial Intelligence
    Subject code 006
    Publishing date 2021-09-15
    Publishing country us
    Document type Book ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  5. Article: CWAS-Plus: Estimating category-wide association of rare noncoding variation from whole-genome sequencing data with cell-type-specific functional data.

    Kim, Yujin / Jeong, Minwoo / Koh, In Gyeong / Kim, Chanhee / Lee, Hyeji / Kim, Jae Hyun / Yurko, Ronald / Kim, Il Bin / Park, Jeongbin / Werling, Donna M / Sanders, Stephan J / An, Joon-Yong

    medRxiv : the preprint server for health sciences

    2024  

    Abstract: Variants in cis-regulatory elements link the noncoding genome to human brain pathology; however, detailed analytic tools for understanding the association between cell-level brain pathology and noncoding variants are lacking. CWAS-Plus, adapted from a ... ...

    Abstract Variants in cis-regulatory elements link the noncoding genome to human brain pathology; however, detailed analytic tools for understanding the association between cell-level brain pathology and noncoding variants are lacking. CWAS-Plus, adapted from a Python package for category-wide association testing (CWAS) employs both whole-genome sequencing and user-provided functional data to enhance noncoding variant analysis, with a faster and more efficient execution of the CWAS workflow. Here, we used single-nuclei assay for transposase-accessible chromatin with sequencing to facilitate CWAS-guided noncoding variant analysis at cell-type specific enhancers and promoters. Examining autism spectrum disorder whole-genome sequencing data (n = 7,280), CWAS-Plus identified noncoding
    Language English
    Publishing date 2024-04-15
    Publishing country United States
    Document type Preprint
    DOI 10.1101/2024.04.15.24305828
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: Bonding structure and etching characteristics of amorphous carbon for a hardmask deposited by DC sputtering

    Lee, So-Yeon / Jang, Kyung-Tae / Jeong, Min-Woo / Joo, Young-Chang / Kim, Kuntae / Kim, Miyoung / Kim, Sungtae / Lee, Gun-Do / Park, Hwanyeol

    Carbon. 2019 Dec., v. 154

    2019  

    Abstract: An amorphous carbon hardmask was fabricated by DC sputtering to evaluate the etching characteristics for semiconductor microstructure patterning. The bonding structure of the carbon films deposited by sputtering was modified by the DC sputtering ... ...

    Abstract An amorphous carbon hardmask was fabricated by DC sputtering to evaluate the etching characteristics for semiconductor microstructure patterning. The bonding structure of the carbon films deposited by sputtering was modified by the DC sputtering conditions and the deposition pressure. In the case of a low-pressure deposition process, an sp3-bonding-rich amorphous carbon film was fabricated and had excellent etching resistance. On the other hand, during the high-pressure deposition process, an sp2-bonding-rich amorphous carbon film was fabricated and had poor etching resistance. To understand the degradation process of the carbon hardmask induced by the penetration of fluorine ions into the film during dry etching, the phenomenon of fluorine penetration into the film and the interaction between fluorine and the carbon bonds were studied by density functional theory (DFT). Through the DFT calculations, it is unveiled that the energy barrier for the migration of a fluorine atom through the sp3 bonding path is much larger than that of a fluorine atom through the sp2 bonding path in amorphous carbon.
    Keywords carbon ; density functional theory ; energy ; fluorine ; ions ; microstructure ; semiconductors
    Language English
    Dates of publication 2019-12
    Size p. 277-284.
    Publishing place Elsevier Ltd
    Document type Article
    ISSN 0008-6223
    DOI 10.1016/j.carbon.2019.08.013
    Database NAL-Catalogue (AGRICOLA)

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  7. Book ; Online: Natural language dialog systems and intelligent assistants

    Jeong, Minwoo / Kim, Hong Kook / Kim, Ji-Hwan / Lee, Gary Geunbae

    2015  

    Author's details Gary Geunbae Lee, Hong Kook Kim, Minwoo Jeong, Ji-Hwan Kim, editors
    Keywords Human-computer interaction ; Human-robot interaction ; Natural language processing (Computer science)
    Language English
    Size Online-Ressource (x, 275 pages)
    Publisher Springer
    Publishing place Cham
    Document type Book ; Online
    Note Includes bibliographical references and index
    ISBN 3319192914 ; 9783319192901 ; 9783319192918 ; 3319192906
    Database Library catalogue of the German National Library of Science and Technology (TIB), Hannover

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  8. Article ; Online: New pathway for the formation of metallic cubic phase Ge-Sb-Te compounds induced by an electric current.

    Park, Yong-Jin / Cho, Ju-Young / Jeong, Min-Woo / Na, Sekwon / Joo, Young-Chang

    Scientific reports

    2016  Volume 6, Page(s) 21466

    Abstract: The novel discovery of a current-induced transition from insulator to metal in the crystalline phase of Ge2Sb2Te5 and GeSb4Te7 have been studied by means of a model using line-patterned samples. The resistivity of cubic phase Ge-Sb-Te compound was ... ...

    Abstract The novel discovery of a current-induced transition from insulator to metal in the crystalline phase of Ge2Sb2Te5 and GeSb4Te7 have been studied by means of a model using line-patterned samples. The resistivity of cubic phase Ge-Sb-Te compound was reduced by an electrical current (~1 MA/cm(2)), and the final resistivity was determined based on the stress current density, regardless of the initial resistivity and temperature, which indicates that the conductivity of Ge-Sb-Te compound can be modulated by an electrical current. The minimum resistivity of Ge-Sb-Te materials can be achieved at high kinetic rates by applying an electrical current, and the material properties change from insulating to metallic behavior without a phase transition. The current-induced metal transition is more effective in GeSb4Te7 than Ge2Sb2Te5, which depends on the intrinsic vacancy of materials. Electromigration, which is the migration of atoms induced by a momentum transfer from charge carriers, can easily promote the rearrangement of vacancies in the cubic phase of Ge-Sb-Te compound. This behavior differs significantly from thermal annealing, which accompanies a phase transition to the hexagonal phase. This result suggests a new pathway for modulating the electrical conductivity and material properties of chalcogenide materials by applying an electrical current.
    Language English
    Publishing date 2016-02-23
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2615211-3
    ISSN 2045-2322 ; 2045-2322
    ISSN (online) 2045-2322
    ISSN 2045-2322
    DOI 10.1038/srep21466
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: HnRNP A1 phosphorylated by VRK1 stimulates telomerase and its binding to telomeric DNA sequence.

    Choi, Yoon Ha / Lim, Jong-Kwan / Jeong, Min-Woo / Kim, Kyong-Tai

    Nucleic acids research

    2012  Volume 40, Issue 17, Page(s) 8499–8518

    Abstract: The telomere integrity is maintained via replication machinery, telomere associated proteins and telomerase. Many telomere associated proteins are regulated in a cell cycle-dependent manner. Heterogeneous nuclear ribonucleoprotein A1 (hnRNP A1), a single- ...

    Abstract The telomere integrity is maintained via replication machinery, telomere associated proteins and telomerase. Many telomere associated proteins are regulated in a cell cycle-dependent manner. Heterogeneous nuclear ribonucleoprotein A1 (hnRNP A1), a single-stranded oligonucleotide binding protein, is thought to play a pivotal role in telomere maintenance. Here, we identified hnRNP A1 as a novel substrate for vaccinia-related kinase 1 (VRK1), a cell cycle regulating kinase. Phosphorylation by VRK1 potentiates the binding of hnRNP A1 to telomeric ssDNA and telomerase RNA in vitro and enhances its function for telomerase reaction. VRK1 deficiency induces a shortening of telomeres with an abnormal telomere arrangement and activation of DNA-damage signaling in mouse male germ cells. Together, our data suggest that VRK1 is required for telomere maintenance via phosphorylation of hnRNP A1, which regulates proteins associated with the telomere and telomerase RNA.
    MeSH term(s) Animals ; Base Sequence ; Binding Sites ; Cell Cycle/genetics ; DNA, Single-Stranded/chemistry ; DNA, Single-Stranded/metabolism ; HeLa Cells ; Heterogeneous Nuclear Ribonucleoprotein A1 ; Heterogeneous-Nuclear Ribonucleoprotein Group A-B/chemistry ; Heterogeneous-Nuclear Ribonucleoprotein Group A-B/metabolism ; Humans ; Intracellular Signaling Peptides and Proteins/metabolism ; Male ; Mice ; Phosphorylation ; Protein-Serine-Threonine Kinases/deficiency ; Protein-Serine-Threonine Kinases/metabolism ; RNA/metabolism ; Spermatogonia/metabolism ; Telomerase/metabolism ; Telomere/chemistry ; Telomere/metabolism ; Telomere Homeostasis
    Chemical Substances DNA, Single-Stranded ; Heterogeneous Nuclear Ribonucleoprotein A1 ; Heterogeneous-Nuclear Ribonucleoprotein Group A-B ; Hnrnpa1 protein, mouse ; Intracellular Signaling Peptides and Proteins ; hnRNPA1 protein, human ; telomerase RNA ; RNA (63231-63-0) ; Protein-Serine-Threonine Kinases (EC 2.7.11.1) ; VRK1 protein, human (EC 2.7.11.1) ; Vrk1 protein, mouse (EC 2.7.11.1) ; Telomerase (EC 2.7.7.49)
    Language English
    Publishing date 2012-06-26
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 186809-3
    ISSN 1362-4962 ; 1362-4954 ; 0301-5610 ; 0305-1048
    ISSN (online) 1362-4962 ; 1362-4954
    ISSN 0301-5610 ; 0305-1048
    DOI 10.1093/nar/gks634
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Mitogen-activated protein kinase phosphatase 2 regulates histone H3 phosphorylation via interaction with vaccinia-related kinase 1.

    Jeong, Min-Woo / Kang, Tae-Hong / Kim, Wanil / Choi, Yoon Ha / Kim, Kyong-Tai

    Molecular biology of the cell

    2012  Volume 24, Issue 3, Page(s) 373–384

    Abstract: Mitogen-activated protein kinase phosphatase 2 (MKP2) is a member of the dual-specificity MKPs that regulate MAP kinase signaling. However, MKP2 functions are still largely unknown. In this study, we showed that MKP2 could regulate histone H3 ... ...

    Abstract Mitogen-activated protein kinase phosphatase 2 (MKP2) is a member of the dual-specificity MKPs that regulate MAP kinase signaling. However, MKP2 functions are still largely unknown. In this study, we showed that MKP2 could regulate histone H3 phosphorylation under oxidative stress conditions. We found that MKP2 inhibited histone H3 phosphorylation by suppressing vaccinia-related kinase 1 (VRK1) activity. Moreover, this regulation was dependent on the selective interaction with VRK1, regardless of its phosphatase activity. The interaction between MKP2 and VRK1 mainly occurred in the chromatin, where histones are abundant. We also observed that the protein level of MKP2 and its interaction with histone H3 increased from G1 to M phase during the cell cycle, which is similar to the VRK1 profile. Furthermore, MKP2 specifically regulated the VRK1-mediated histone H3 phosphorylation at M phase. Taken together, these data suggest a novel function of MKP2 as a negative regulator of VRK1-mediated histone H3 phosphorylation.
    MeSH term(s) Cell Division ; Chromatin/enzymology ; Dual-Specificity Phosphatases/metabolism ; HeLa Cells ; Histones/metabolism ; Humans ; Hydrogen Peroxide/metabolism ; Intracellular Signaling Peptides and Proteins/metabolism ; Mitogen-Activated Protein Kinase Phosphatases/metabolism ; Oxidative Stress ; Phosphorylation ; Protein Processing, Post-Translational ; Protein Transport ; Protein-Serine-Threonine Kinases/metabolism
    Chemical Substances Chromatin ; Histones ; Intracellular Signaling Peptides and Proteins ; Hydrogen Peroxide (BBX060AN9V) ; Protein-Serine-Threonine Kinases (EC 2.7.11.1) ; VRK1 protein, human (EC 2.7.11.1) ; Mitogen-Activated Protein Kinase Phosphatases (EC 3.1.3.16) ; DUSP4 protein, human (EC 3.1.3.48) ; Dual-Specificity Phosphatases (EC 3.1.3.48)
    Language English
    Publishing date 2012-12-05
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1098979-1
    ISSN 1939-4586 ; 1059-1524
    ISSN (online) 1939-4586
    ISSN 1059-1524
    DOI 10.1091/mbc.E12-06-0456
    Database MEDical Literature Analysis and Retrieval System OnLINE

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