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  1. Article: G

    Millett, Michael / Heuberger, Anika / Castosa, Elisabeth Martin / Comite, Allison / Wagner, Preston / Hall, Dominic / Gallardo, Ignacio / Chambers, Nicole E / Wagner, Lloyd / Moehle, Mark S

    bioRxiv : the preprint server for biology

    2024  

    Abstract: The heterotrimeric G-protein α subunit, Gα ...

    Abstract The heterotrimeric G-protein α subunit, Gα
    Language English
    Publishing date 2024-04-05
    Publishing country United States
    Document type Preprint
    DOI 10.1101/2024.04.03.587766
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: The Concise Guide to PHARMACOLOGY 2023/24: G protein-coupled receptors.

    Alexander, Stephen P H / Christopoulos, Arthur / Davenport, Anthony P / Kelly, Eamonn / Mathie, Alistair A / Peters, John A / Veale, Emma L / Armstrong, Jane F / Faccenda, Elena / Harding, Simon D / Davies, Jamie A / Abbracchio, Maria Pia / Abraham, George / Agoulnik, Alexander / Alexander, Wayne / Al-Hosaini, Khaled / Bäck, Magnus / Baker, Jillian G / Barnes, Nicholas M /
    Bathgate, Ross / Beaulieu, Jean-Martin / Beck-Sickinger, Annette G / Behrens, Maik / Bernstein, Kenneth E / Bettler, Bernhard / Birdsall, Nigel J M / Blaho, Victoria / Boulay, Francois / Bousquet, Corinne / Bräuner-Osborne, Hans / Burnstock, Geoffrey / Caló, Girolamo / Castaño, Justo P / Catt, Kevin J / Ceruti, Stefania / Chazot, Paul / Chiang, Nan / Chini, Bice / Chun, Jerold / Cianciulli, Antonia / Civelli, Olivier / Clapp, Lucie H / Couture, Réjean / Cox, Helen M / Csaba, Zsolt / Dahlgren, Claes / Dent, Gordon / Douglas, Steven D / Dournaud, Pascal / Eguchi, Satoru / Escher, Emanuel / Filardo, Edward J / Fong, Tung / Fumagalli, Marta / Gainetdinov, Raul R / Garelja, Michael L / de Gasparo, Marc / Gerard, Craig / Gershengorn, Marvin / Gobeil, Fernand / Goodfriend, Theodore L / Goudet, Cyril / Grätz, Lukas / Gregory, Karen J / Gundlach, Andrew L / Hamann, Jörg / Hanson, Julien / Hauger, Richard L / Hay, Debbie L / Heinemann, Akos / Herr, Deron / Hollenberg, Morley D / Holliday, Nicholas D / Horiuchi, Mastgugu / Hoyer, Daniel / Hunyady, László / Husain, Ahsan / IJzerman, Adriaan P / Inagami, Tadashi / Jacobson, Kenneth A / Jensen, Robert T / Jockers, Ralf / Jonnalagadda, Deepa / Karnik, Sadashiva / Kaupmann, Klemens / Kemp, Jacqueline / Kennedy, Charles / Kihara, Yasuyuki / Kitazawa, Takio / Kozielewicz, Pawel / Kreienkamp, Hans-Jürgen / Kukkonen, Jyrki P / Langenhan, Tobias / Larhammar, Dan / Leach, Katie / Lecca, Davide / Lee, John D / Leeman, Susan E / Leprince, Jérôme / Li, Xaria X / Lolait, Stephen J / Lupp, Amelie / Macrae, Robyn / Maguire, Janet / Malfacini, Davide / Mazella, Jean / McArdle, Craig A / Melmed, Shlomo / Michel, Martin C / Miller, Laurence J / Mitolo, Vincenzo / Mouillac, Bernard / Müller, Christa E / Murphy, Philip M / Nahon, Jean-Louis / Ngo, Tony / Norel, Xavier / Nyimanu, Duuamene / O'Carroll, Anne-Marie / Offermanns, Stefan / Panaro, Maria Antonietta / Parmentier, Marc / Pertwee, Roger G / Pin, Jean-Philippe / Prossnitz, Eric R / Quinn, Mark / Ramachandran, Rithwik / Ray, Manisha / Reinscheid, Rainer K / Rondard, Philippe / Rovati, G Enrico / Ruzza, Chiara / Sanger, Gareth J / Schöneberg, Torsten / Schulte, Gunnar / Schulz, Stefan / Segaloff, Deborah L / Serhan, Charles N / Singh, Khuraijam Dhanachandra / Smith, Craig M / Stoddart, Leigh A / Sugimoto, Yukihiko / Summers, Roger / Tan, Valerie P / Thal, David / Thomas, Walter Wally / Timmermans, Pieter B M W M / Tirupula, Kalyan / Toll, Lawrence / Tulipano, Giovanni / Unal, Hamiyet / Unger, Thomas / Valant, Celine / Vanderheyden, Patrick / Vaudry, David / Vaudry, Hubert / Vilardaga, Jean-Pierre / Walker, Christopher S / Wang, Ji Ming / Ward, Donald T / Wester, Hans-Jürgen / Willars, Gary B / Williams, Tom Lloyd / Woodruff, Trent M / Yao, Chengcan / Ye, Richard D

    British journal of pharmacology

    2023  Volume 180 Suppl 2, Page(s) S23–S144

    Abstract: ... of this section can be found at http://onlinelibrary.wiley.com/doi/bph.16177. G protein-coupled receptors are one ...

    Abstract The Concise Guide to PHARMACOLOGY 2023/24 is the sixth in this series of biennial publications. The Concise Guide provides concise overviews, mostly in tabular format, of the key properties of approximately 1800 drug targets, and about 6000 interactions with about 3900 ligands. There is an emphasis on selective pharmacology (where available), plus links to the open access knowledgebase source of drug targets and their ligands (https://www.guidetopharmacology.org), which provides more detailed views of target and ligand properties. Although the Concise Guide constitutes almost 500 pages, the material presented is substantially reduced compared to information and links presented on the website. It provides a permanent, citable, point-in-time record that will survive database updates. The full contents of this section can be found at http://onlinelibrary.wiley.com/doi/bph.16177. G protein-coupled receptors are one of the six major pharmacological targets into which the Guide is divided, with the others being: ion channels, nuclear hormone receptors, catalytic receptors, enzymes and transporters. These are presented with nomenclature guidance and summary information on the best available pharmacological tools, alongside key references and suggestions for further reading. The landscape format of the Concise Guide is designed to facilitate comparison of related targets from material contemporary to mid-2023, and supersedes data presented in the 2021/22, 2019/20, 2017/18, 2015/16 and 2013/14 Concise Guides and previous Guides to Receptors and Channels. It is produced in close conjunction with the Nomenclature and Standards Committee of the International Union of Basic and Clinical Pharmacology (NC-IUPHAR), therefore, providing official IUPHAR classification and nomenclature for human drug targets, where appropriate.
    MeSH term(s) Humans ; Databases, Pharmaceutical ; Receptors, G-Protein-Coupled ; Ligands ; Ion Channels/chemistry ; Receptors, Cytoplasmic and Nuclear
    Chemical Substances Receptors, G-Protein-Coupled ; Ligands ; Ion Channels ; Receptors, Cytoplasmic and Nuclear
    Language English
    Publishing date 2023-12-18
    Publishing country England
    Document type Journal Article
    ZDB-ID 80081-8
    ISSN 1476-5381 ; 0007-1188
    ISSN (online) 1476-5381
    ISSN 0007-1188
    DOI 10.1111/bph.16177
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Regulation of the Hippo-YAP Pathway by G-Protein-Coupled Receptor Signaling.

    Yu, Fa-Xing / Zhao, Bin / Panupinthu, Nattapon / Jewell, Jenna L / Lian, Ian / Wang, Lloyd H / Zhao, Jiagang / Yuan, Haixin / Tumaneng, Karen / Li, Hairi / Fu, Xiang-Dong / Mills, Gordon B / Guan, Kun-Liang

    Cell

    2024  Volume 187, Issue 6, Page(s) 1563–1564

    Language English
    Publishing date 2024-03-15
    Publishing country United States
    Document type Published Erratum
    ZDB-ID 187009-9
    ISSN 1097-4172 ; 0092-8674
    ISSN (online) 1097-4172
    ISSN 0092-8674
    DOI 10.1016/j.cell.2024.02.007
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: THE CONCISE GUIDE TO PHARMACOLOGY 2021/22: G protein-coupled receptors.

    Alexander, Stephen Ph / Christopoulos, Arthur / Davenport, Anthony P / Kelly, Eamonn / Mathie, Alistair / Peters, John A / Veale, Emma L / Armstrong, Jane F / Faccenda, Elena / Harding, Simon D / Pawson, Adam J / Southan, Christopher / Davies, Jamie A / Abbracchio, Maria Pia / Alexander, Wayne / Al-Hosaini, Khaled / Bäck, Magnus / Barnes, Nicholas M / Bathgate, Ross /
    Beaulieu, Jean-Martin / Bernstein, Kenneth E / Bettler, Bernhard / Birdsall, Nigel J M / Blaho, Victoria / Boulay, Francois / Bousquet, Corinne / Bräuner-Osborne, Hans / Burnstock, Geoffrey / Caló, Girolamo / Castaño, Justo P / Catt, Kevin J / Ceruti, Stefania / Chazot, Paul / Chiang, Nan / Chini, Bice / Chun, Jerold / Cianciulli, Antonia / Civelli, Olivier / Clapp, Lucie H / Couture, Réjean / Csaba, Zsolt / Dahlgren, Claes / Dent, Gordon / Singh, Khuraijam Dhanachandra / Douglas, Steven D / Dournaud, Pascal / Eguchi, Satoru / Escher, Emanuel / Filardo, Edward J / Fong, Tung / Fumagalli, Marta / Gainetdinov, Raul R / Gasparo, Marc de / Gerard, Craig / Gershengorn, Marvin / Gobeil, Fernand / Goodfriend, Theodore L / Goudet, Cyril / Gregory, Karen J / Gundlach, Andrew L / Hamann, Jörg / Hanson, Julien / Hauger, Richard L / Hay, Debbie L / Heinemann, Akos / Hollenberg, Morley D / Holliday, Nicholas D / Horiuchi, Mastgugu / Hoyer, Daniel / Hunyady, László / Husain, Ahsan / IJzerman, Adriaan P / Inagami, Tadashi / Jacobson, Kenneth A / Jensen, Robert T / Jockers, Ralf / Jonnalagadda, Deepa / Karnik, Sadashiva / Kaupmann, Klemens / Kemp, Jacqueline / Kennedy, Charles / Kihara, Yasuyuki / Kitazawa, Takio / Kozielewicz, Pawel / Kreienkamp, Hans-Jürgen / Kukkonen, Jyrki P / Langenhan, Tobias / Leach, Katie / Lecca, Davide / Lee, John D / Leeman, Susan E / Leprince, Jérôme / Li, Xaria X / Williams, Tom Lloyd / Lolait, Stephen J / Lupp, Amelie / Macrae, Robyn / Maguire, Janet / Mazella, Jean / McArdle, Craig A / Melmed, Shlomo / Michel, Martin C / Miller, Laurence J / Mitolo, Vincenzo / Mouillac, Bernard / Müller, Christa E / Murphy, Philip / Nahon, Jean-Louis / Ngo, Tony / Norel, Xavier / Nyimanu, Duuamene / O'Carroll, Anne-Marie / Offermanns, Stefan / Panaro, Maria Antonietta / Parmentier, Marc / Pertwee, Roger G / Pin, Jean-Philippe / Prossnitz, Eric R / Quinn, Mark / Ramachandran, Rithwik / Ray, Manisha / Reinscheid, Rainer K / Rondard, Philippe / Rovati, G Enrico / Ruzza, Chiara / Sanger, Gareth J / Schöneberg, Torsten / Schulte, Gunnar / Schulz, Stefan / Segaloff, Deborah L / Serhan, Charles N / Stoddart, Leigh A / Sugimoto, Yukihiko / Summers, Roger / Tan, Valerie P / Thal, David / Thomas, Walter Wally / Timmermans, Pieter B M W M / Tirupula, Kalyan / Tulipano, Giovanni / Unal, Hamiyet / Unger, Thomas / Valant, Celine / Vanderheyden, Patrick / Vaudry, David / Vaudry, Hubert / Vilardaga, Jean-Pierre / Walker, Christopher S / Wang, Ji Ming / Ward, Donald T / Wester, Hans-Jürgen / Willars, Gary B / Woodruff, Trent M / Yao, Chengcan / Ye, Richard D

    British journal of pharmacology

    2021  Volume 178 Suppl 1, Page(s) S27–S156

    Abstract: ... The full contents of this section can be found at http://onlinelibrary.wiley.com/doi/bph.15538. G protein ...

    Abstract The Concise Guide to PHARMACOLOGY 2021/22 is the fifth in this series of biennial publications. The Concise Guide provides concise overviews, mostly in tabular format, of the key properties of nearly 1900 human drug targets with an emphasis on selective pharmacology (where available), plus links to the open access knowledgebase source of drug targets and their ligands (www.guidetopharmacology.org), which provides more detailed views of target and ligand properties. Although the Concise Guide constitutes over 500 pages, the material presented is substantially reduced compared to information and links presented on the website. It provides a permanent, citable, point-in-time record that will survive database updates. The full contents of this section can be found at http://onlinelibrary.wiley.com/doi/bph.15538. G protein-coupled receptors are one of the six major pharmacological targets into which the Guide is divided, with the others being: ion channels, nuclear hormone receptors, catalytic receptors, enzymes and transporters. These are presented with nomenclature guidance and summary information on the best available pharmacological tools, alongside key references and suggestions for further reading. The landscape format of the Concise Guide is designed to facilitate comparison of related targets from material contemporary to mid-2021, and supersedes data presented in the 2019/20, 2017/18, 2015/16 and 2013/14 Concise Guides and previous Guides to Receptors and Channels. It is produced in close conjunction with the Nomenclature and Standards Committee of the International Union of Basic and Clinical Pharmacology (NC-IUPHAR), therefore, providing official IUPHAR classification and nomenclature for human drug targets, where appropriate.
    MeSH term(s) Databases, Pharmaceutical ; Humans ; Ion Channels ; Ligands ; Pharmacology ; Receptors, Cytoplasmic and Nuclear ; Receptors, G-Protein-Coupled
    Chemical Substances Ion Channels ; Ligands ; Receptors, Cytoplasmic and Nuclear ; Receptors, G-Protein-Coupled
    Language English
    Publishing date 2021-09-22
    Publishing country England
    Document type Journal Article
    ZDB-ID 80081-8
    ISSN 1476-5381 ; 0007-1188
    ISSN (online) 1476-5381
    ISSN 0007-1188
    DOI 10.1111/bph.15538
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Complete Genome Sequences of Cluster G Mycobacteriophage Darionha, Cluster A Mycobacteriophage Salz, and Cluster J Mycobacteriophage ThreeRngTarjay.

    Sandoval, Andrea M / Abram, Amber M / Alhabib, Zahraa M / Antonyan, Angelina S / Brikho, Salar M / Buhay, Sarah I / Craig, Griffin E / Crile, Karen G / El Yaman, Nour / Garcia-Leon, Lizbeth / Hammoud, Zahraa B / Huffman, Anthony R / Issa, Ali H / Jackman, Alexander B / Krajcz, Victoria K / Lloyd, Yamiya J / Jones, Marcel L / McMahon, Diana L / Murdock, Briana A D /
    Nelson, Jada J / Patel, Tulsi T / Patil, Yashodhara V / Ricketts, Sabriyyah A / Romero-Barajas, Leonardo S / Sareini, Laila H / Sesoko, Channing S / Shammami, Marcelio A / Sheardy, Erin E / Sherwood, John R / Simpson, Arren E / Tiba, Racha H / Conant, Stephanie B / Finkel, Jonathan S / Kagey, Jacob D

    Microbiology resource announcements

    2020  Volume 9, Issue 20

    Abstract: Mycobacteriophages Darionha, Salz, and ThreeRngTarjay are mycobacteriophages isolated using the ... ...

    Abstract Mycobacteriophages Darionha, Salz, and ThreeRngTarjay are mycobacteriophages isolated using the host
    Language English
    Publishing date 2020-05-14
    Publishing country United States
    Document type Journal Article
    ISSN 2576-098X
    ISSN (online) 2576-098X
    DOI 10.1128/MRA.00160-20
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Analyzing kinetic signaling data for G-protein-coupled receptors.

    Hoare, Sam R J / Tewson, Paul H / Quinn, Anne Marie / Hughes, Thomas E / Bridge, Lloyd J

    Scientific reports

    2020  Volume 10, Issue 1, Page(s) 12263

    Abstract: In classical pharmacology, bioassay data are fit to general equations (e.g. the dose response ... equation) to determine empirical drug parameters (e.g. EC ...

    Abstract In classical pharmacology, bioassay data are fit to general equations (e.g. the dose response equation) to determine empirical drug parameters (e.g. EC
    MeSH term(s) Dose-Response Relationship, Drug ; Drug Discovery ; Models, Biological ; Pharmacokinetics ; Receptors, G-Protein-Coupled/metabolism ; Signal Transduction/drug effects
    Chemical Substances Receptors, G-Protein-Coupled
    Language English
    Publishing date 2020-07-23
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 2615211-3
    ISSN 2045-2322 ; 2045-2322
    ISSN (online) 2045-2322
    ISSN 2045-2322
    DOI 10.1038/s41598-020-67844-3
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Conference proceedings ; Online: Piloting the G + Customer and Product Profile Tools for gender-responsive bean breeding in Zimbabwe

    Nchanji, Eileen Bogweh / Lutomia, Cosmas Kweyu / Rubyogo, Jean-Claude / Chirwa, Rowland / Onyango, Patricia / Nyarai, Chisorochengwe / Tsekenedza, Shylet / Gutsa, Freeman / Lloyd, Sondayi

    2023  

    Abstract: ... The tool; G+ product and customer profile recognizes changes in the modern agriculture as production and ...

    Abstract Gender is an integral part of bean breeding initiatives and provides the platform through which plant breeding should be implemented. Gender-sensitive breeding offers a clear focus on addressing gender gap in agriculture by considering different traits preferred by both men and women (Nchanji et al., 2021b). Through the gender lens, critical elements in women and men’s preferences are consulted even though such profiles do not necessarily have different traits for men and women (Nchanji et al., 2021b). Breeding teams are therefore capable of assessing gender-relevant differences in preferences, constraints, needs, and potential impact on women and men’s livelihood strategies. This observation is founded on the critical role women play in production of common beans in Zimbabwe. Therefore, their participation in bean breeding initiatives is considered essential because it is regarded as a women’s crop (PABRA 2015a). The CGIAR gender and breeding initiative has developed an important tool to guide breeders in identifying the gender gaps and preferences of customer to develop and prioritize new product that address persistent gender gaps in crop production. The tool; G+ product and customer profile recognizes changes in the modern agriculture as production and marketing systems transition towards more demand-driven business models for social inclusivity.
    Keywords gender ; gender analysis ; breeding ; product development ; value chains ; género ; análisis de género ; fitomejoramiento
    Language English
    Publishing date 2023-01-04T08:59:02Z
    Publishing country fr
    Document type Conference proceedings ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  8. Article ; Online: Sub-Femto-g Free Fall for Space-Based Gravitational Wave Observatories: LISA Pathfinder Results.

    Armano, M / Audley, H / Auger, G / Baird, J T / Bassan, M / Binetruy, P / Born, M / Bortoluzzi, D / Brandt, N / Caleno, M / Carbone, L / Cavalleri, A / Cesarini, A / Ciani, G / Congedo, G / Cruise, A M / Danzmann, K / de Deus Silva, M / De Rosa, R /
    Diaz-Aguiló, M / Di Fiore, L / Diepholz, I / Dixon, G / Dolesi, R / Dunbar, N / Ferraioli, L / Ferroni, V / Fichter, W / Fitzsimons, E D / Flatscher, R / Freschi, M / García Marín, A F / García Marirrodriga, C / Gerndt, R / Gesa, L / Gibert, F / Giardini, D / Giusteri, R / Guzmán, F / Grado, A / Grimani, C / Grynagier, A / Grzymisch, J / Harrison, I / Heinzel, G / Hewitson, M / Hollington, D / Hoyland, D / Hueller, M / Inchauspé, H / Jennrich, O / Jetzer, P / Johann, U / Johlander, B / Karnesis, N / Kaune, B / Korsakova, N / Killow, C J / Lobo, J A / Lloro, I / Liu, L / López-Zaragoza, J P / Maarschalkerweerd, R / Mance, D / Martín, V / Martin-Polo, L / Martino, J / Martin-Porqueras, F / Madden, S / Mateos, I / McNamara, P W / Mendes, J / Mendes, L / Monsky, A / Nicolodi, D / Nofrarias, M / Paczkowski, S / Perreur-Lloyd, M / Petiteau, A / Pivato, P / Plagnol, E / Prat, P / Ragnit, U / Raïs, B / Ramos-Castro, J / Reiche, J / Robertson, D I / Rozemeijer, H / Rivas, F / Russano, G / Sanjuán, J / Sarra, P / Schleicher, A / Shaul, D / Slutsky, J / Sopuerta, C F / Stanga, R / Steier, F / Sumner, T / Texier, D / Thorpe, J I / Trenkel, C / Tröbs, M / Tu, H B / Vetrugno, D / Vitale, S / Wand, V / Wanner, G / Ward, H / Warren, C / Wass, P J / Wealthy, D / Weber, W J / Wissel, L / Wittchen, A / Zambotti, A / Zanoni, C / Ziegler, T / Zweifel, P

    Physical review letters

    2016  Volume 116, Issue 23, Page(s) 231101

    Abstract: ... of the power spectral density of 5.2±0.1  fm s^{-2}/sqrt[Hz], or (0.54±0.01)×10^{-15}  g/sqrt[Hz], with g ...

    Abstract We report the first results of the LISA Pathfinder in-flight experiment. The results demonstrate that two free-falling reference test masses, such as those needed for a space-based gravitational wave observatory like LISA, can be put in free fall with a relative acceleration noise with a square root of the power spectral density of 5.2±0.1  fm s^{-2}/sqrt[Hz], or (0.54±0.01)×10^{-15}  g/sqrt[Hz], with g the standard gravity, for frequencies between 0.7 and 20 mHz. This value is lower than the LISA Pathfinder requirement by more than a factor 5 and within a factor 1.25 of the requirement for the LISA mission, and is compatible with Brownian noise from viscous damping due to the residual gas surrounding the test masses. Above 60 mHz the acceleration noise is dominated by interferometer displacement readout noise at a level of (34.8±0.3)  fm/sqrt[Hz], about 2 orders of magnitude better than requirements. At f≤0.5  mHz we observe a low-frequency tail that stays below 12  fm s^{-2}/sqrt[Hz] down to 0.1 mHz. This performance would allow for a space-based gravitational wave observatory with a sensitivity close to what was originally foreseen for LISA.
    Language English
    Publishing date 2016-06-10
    Publishing country United States
    Document type Journal Article
    ZDB-ID 208853-8
    ISSN 1079-7114 ; 0031-9007
    ISSN (online) 1079-7114
    ISSN 0031-9007
    DOI 10.1103/PhysRevLett.116.231101
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article: Microscale thermophoresis analysis of the molecular interaction between small nuclear ribonucleoprotein polypeptide G and the RING finger domain of RBBP6 towards anti-cancer drug discovery.

    Mabonga, Lloyd / Masamba, Priscilla / Basson, Albertus Kotze / Kappo, Abidemi Paul

    American journal of translational research

    2021  Volume 13, Issue 11, Page(s) 12775–12785

    Abstract: Regulatory core-splicing proteins are now becoming highly promising therapeutic targets for the development of anti-cancer drugs. SNRPG and RBBP6 are two good examples of regulatory core-splicing proteins involved in tumorigenesis and tumor development ... ...

    Abstract Regulatory core-splicing proteins are now becoming highly promising therapeutic targets for the development of anti-cancer drugs. SNRPG and RBBP6 are two good examples of regulatory core-splicing proteins involved in tumorigenesis and tumor development whose multi-functional role is primarily mediated by protein-protein interactions. Over the years, skepticism abutting from the two onco-proteins has been mounting. Suggestive evidence using yeast 2-hybrid technique observed possible involvement between SNRPG and the RING finger domain of RBBP6. However, the putative interaction remains elusive and yet to be characterized. In this study, we developed the first MST-based assay to confirm the interaction between SNRPG and the RING finger domain of RBBP6. The results demonstrated a strong binding affinity between SNRPG and the RING finger domain of RBBP6 with a K
    Language English
    Publishing date 2021-11-15
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2471058-1
    ISSN 1943-8141
    ISSN 1943-8141
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article: Molecular interaction between small nuclear ribonucleoprotein polypeptide G and heat shock protein 70.14: a microscale thermophoresis exposition towards developing anti-cancer drugs.

    Mabonga, Lloyd / Ikwegbue, Paul Chukwudi / Masamba, Priscilla / Kappo, Abidemi Paul

    American journal of translational research

    2022  Volume 14, Issue 9, Page(s) 6150–6162

    Abstract: ... polypeptide G (SNRPG) and heat shock protein 70.14 (Hsp70.14) have attracted attention as potential smart ...

    Abstract Background: Targeting protein-protein interactions (PPIs) linked to protein quality control (PQC) pathways as potential anti-cancer drug targets have unanimously widened biological insights and the therapeutic potential of PPIs as smart-drug discovery tools in cancer. PPIs between disease-relevant proteins associated with protein homeostasis in PQC pathways have been linked to improved mechanistic understanding associated with conformational abnormalities and impairment, cellular proteotoxicity, induced apoptosis, and pathogenesis in different types of cancers. In this context, PPIs between small nuclear ribonucleoprotein polypeptide G (SNRPG) and heat shock protein 70.14 (Hsp70.14) have attracted attention as potential smart drug discovery tools in cancer diagnostics and therapeutics. Validated evidence of high-quality biological data has shown the presence of the two proteins in different types of cancers including breast cancer. The links between SNRPG and Hsp70.14 in cancer-cell networks remain elusive, overlooked, and uncharacterized.
    Methodology: In this study, we explored the interaction between the two oncogenic proteins using the MST-based assays.
    Results: The results revealed a low K
    Conclusions: The results suggest a possible involvement between the two proteins in hostile tumour microenvironments. Furthermore, these findings offer a different therapeutic perspective that could pave the way for the creation of novel small molecule inhibitors as drugs for the treatment of cancer.
    Language English
    Publishing date 2022-09-15
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2471058-1
    ISSN 1943-8141
    ISSN 1943-8141
    Database MEDical Literature Analysis and Retrieval System OnLINE

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