The DOI matches its Crossref record; 73 of the 73 references it cites were found in a registry or an index.
The structure and function of G-protein-coupled receptors
Open accessAbstract
G-protein-coupled receptors (GPCRs) mediate most of our physiological responses to hormones, neurotransmitters and environmental stimulants, and so have great potential as therapeutic targets for a broad spectrum of diseases. They are also fascinating molecules from the perspective of membrane-protein structure and biology. Great progress has been made over the past three decades in understanding diverse GPCRs, from pharmacology to functional characterization in vivo. Recent high-resolution structural studies have provided insights into the molecular mechanisms of GPCR activation and constitutive activity.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“GPR20 belongs to the family of the G-protein-coupled receptors, which participate in intracellular second messenger systems triggered by different hormones and neurotransmitters, and amyloid β.53, 54, 55”
From APOE*E2 allele delays age of onset in PSEN1 E280A Alzheimer’s disease (2016) · cites this paper as [54]
In the citing paper
“Both theoretical and experimental results do not offer any clear conclusions with respect to the vibrational theory of neurotransmission for adenosine, serotonin and histamine receptors and their related ligands.”
From Quantum effects in the brain: A review (2020) · cites this paper as [115]
In the citing paper
“Understanding the mechanism or mechanisms of ligand-GPCR interaction is particularly important due to the fact that GPCRs are a major drug target associated with one third of all pharmaceuticals 103,115 .”
From Quantum effects in the brain: A review (2020) · cites this paper as [115]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Crystal Structure of Rhodopsin: A G Protein-Coupled Receptor
Palczewski, K., Kumasaka, T., Hori, T., Behnke, C. A., Motoshima, H., Fox, B. A., Trong, I. L., Teller, D. C., Okada, T., Stenkamp, R. E., et al. (2000) · Science · doi:10.1126/science.289.5480.739 · Cited by 5,637
High-Resolution Crystal Structure of an Engineered Human β 2 -Adrenergic G Protein–Coupled Receptor
Cherezov, V., Rosenbaum, D. M., Hanson, M. A., Rasmussen, S. G. F., Thian, F. S., Kobilka, T. S., Choi, H., Kühn, P., Weis, W. I., Kobilka, B. K., et al. (2007) · Science · doi:10.1126/science.1150577 · Cited by 3,280
Self-citationBallesteros, J. A., & Weinstein, H. (1995) · Methods in neurosciences · doi:10.1016/s1043-9471(05)80049-7 · Cited by 3,001 · cited 1×
“48 (human β 2 AR, with Ballesteros/Weinstein numberin”
Fredriksson, R., Lagerström, M. C., Lundin, L.-G., & Schiöth, H. B. (2003) · Molecular Pharmacology · doi:10.1124/mol.63.6.1256 · Cited by 2,941 · cited 1×
“GPCRs in vertebrates are commonly divided into five families on the basis of their sequence and structural similarity”
Crystal structure of the human β2 adrenergic G-protein-coupled receptor
Rasmussen, S. G. F., Choi, H., Rosenbaum, D. M., Kobilka, T. S., Thian, F. S., Edwards, P. C., Burghammer, M. C., Ratnala, V. R. P., Sanishvili, R., Fischetti, R. F., et al. (2007) · Nature · doi:10.1038/nature06325 · Cited by 1,935
Self-citationThe 2.6 Angstrom Crystal Structure of a Human A 2A Adenosine Receptor Bound to an Antagonist
Jaakola, V., Griffith, M. T., Hanson, M. A., Cherezov, V., Chien, E. Y. T., Lane, J. R., IJzerman, A. P., & Stevens, R. C. (2008) · Science · doi:10.1126/science.1164772 · Cited by 1,786
Léan, A. D., Stadel, J. M., & Lefkowitz, R. J. (1980) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(20)79672-9 · Cited by 1,606
Structure of a β1-adrenergic G-protein-coupled receptor
Warne, T., Serrano‐Vega, M. J., Baker, J. G., Moukhametzianov, R., Edwards, P. C., Henderson, R. A., Leslie, A. G. W., Tate, C. G., & Schertler, G. F. X. (2008) · Nature · doi:10.1038/nature07101 · Cited by 1,377
GPCR Engineering Yields High-Resolution Structural Insights into β 2 -Adrenergic Receptor Function
Rosenbaum, D. M., Cherezov, V., Hanson, M. A., Rasmussen, S. G. F., Thian, F. S., Kobilka, T. S., Choi, H., Yao, X.-J., Weis, W. I., Stevens, R. C., et al. (2007) · Science · doi:10.1126/science.1150609 · Cited by 1,335
Self-citationCloning of the gene and cDNA for mammalian β-adrenergic receptor and homology with rhodopsin
Dixon, R. A. F., Kobilka, B. K., Strader, D. J., Benovic, J., Dohlman, H. G., Frielle, T., Bolanowski, M. A., Bennett, C. D., Rands, E., Diehl, R. E., et al. (1986) · Nature · doi:10.1038/321075a0 · Cited by 1,275 · cited 1×
“The clustering of these residues in the cytoplasmic half of the transmembrane bundle reflects the basic conservation of mechanism across GPCRs, a remarkable structural affirmation of a hypothesis made more than 20 years ag”
Self-citation
Flagged first, then by citations
Cited by
Sorted by citations
Items 301–400 of 1,002
Membrane Lipids in the Function of Serotonin and Adrenergic Receptors
Jafurulla, M., & Chattopadhyay, A. (2012) · Current Medicinal Chemistry · doi:10.2174/09298673130106 · Cited by 77
Fanelli, F., & Benedetti, P. G. D. (2011) · Chemical Reviews · doi:10.1021/cr100437t · Cited by 77
Sengupta, D., Prasanna, X., Mohole, M., & Chattopadhyay, A. (2018) · The Journal of Physical Chemistry B · doi:10.1021/acs.jpcb.8b01657 · Cited by 80
The Emerging Role of Adhesion GPCRs in Cancer
Gad, A. A., & Balenga, N. A. B. (2020) · ACS Pharmacology & Translational Science · doi:10.1021/acsptsci.9b00093 · Cited by 74
Su, M., Zhu, L., Zhang, Y., Paknejad, N., Dey, R., Huang, J., Lee, M.-Y., Williams, D., Jordan, K. D., Eng, E. T., et al. (2020) · Molecular Cell · doi:10.1016/j.molcel.2020.08.001 · Cited by 75
Crystal structure of jumping spider rhodopsin-1 as a light sensitive GPCR
Varma, N., Mutt, E., Mühle, J., Panneels, V., Terakita, A., Deupí, X., Nogły, P., Schertler, G. F. X., & Lesca, E. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1902192116 · Cited by 74
Proteins at Interfaces Probed by Chiral Vibrational Sum Frequency Generation Spectroscopy
Yan, E. C. Y., Wang, Z., & Fu, L. (2015) · The Journal of Physical Chemistry B · doi:10.1021/jp508926e · Cited by 76
Orlandi, C., Omori, Y., Wang, Y., Cao, Y., Ueno, A. M., Roux, M. J., Condomitti, G., de Wit, J., Kanagawa, M., Furukawa, T., et al. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.08.068 · Cited by 78
“A wide variety of extracellular domains allows this large receptor family to sense a range of changes in the extracellular environment, including detection of all known neurotransmitters (Rosenbaum et al., 2009).”
A biased ligand for OXE-R uncouples Gα and Gβγ signaling within a heterotrimer
Blättermann, S., Peters, L., Ottersbach, P. A., Böck, A., Kónya, V., Weaver, C. D., González, Á., Schröder, R. J., Tyagi, R., Luschnig, P., et al. (2012) · Nature Chemical Biology · doi:10.1038/nchembio.962 · Cited by 78
Paradis, J. S., Acosta, M., Saddawi‐Konefka, R., Kishore, A., Lubrano, S., Gomes, F., Arang, N., Tiago, M., Coma, S., Wu, X., et al. (2021) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-20-3363 · Cited by 81
Genetics of ankylosing spondylitis
Brown, M. A. (2010) · Current Opinion in Rheumatology · doi:10.1097/bor.0b013e3283364483 · Cited by 78
“Generally these receptors are not well characterized, but are known to mediate a wide range of cellular signalling (Rosenbaum et al., 2009).”
BackgroundBaltoumas, F. A., Theodoropoulou, M. C., & Hamodrakas, S. J. (2013) · Journal of Structural Biology · doi:10.1016/j.jsb.2013.03.004 · Cited by 83
Endocrinology and the brain: corticotropin-releasing hormone signaling
Inda, C., Armando, N. G., Claro, P. A. D. S., & Silberstein, S. (2017) · Endocrine Connections · doi:10.1530/ec-17-0111 · Cited by 81
Lin, Y., & Smrcka, A. V. (2011) · Molecular Pharmacology · doi:10.1124/mol.111.073072 · Cited by 77
Diverse Roles of Protein Palmitoylation in Cancer Progression, Immunity, Stemness, and Beyond
Li, M., Zhang, L., & Chen, C.-W. D. (2023) · Cells · doi:10.3390/cells12182209 · Cited by 76
Singh, N., Chakraborty, R., Bhullar, R. P., & Chelikani, P. (2014) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2014.02.140 · Cited by 75
Fuxe, K., Marcellino, D., Borroto-Escuela, D. O., Frankowska, M., Ferraro, L., Guidolin, D., Ciruela, F., & Agnati, L. F. (2010) · Journal of Receptors and Signal Transduction · doi:10.3109/10799893.2010.506191 · Cited by 74
Lightening Up Membrane Receptors with Fluorescent Molecular Probes and Supramolecular Materials
He, X., & Tian, H. (2017) · Chem · doi:10.1016/j.chempr.2017.11.006 · Cited by 75
Kiss, B., Laszlovszky, I., Krámos, B., Visegrády, A., Bobok, A. Á., Lévay, G. I., Lendvai, B., & Román, V. (2021) · Biomolecules · doi:10.3390/biom11010104 · Cited by 74
“Native ligands of aminergic GPCRs bind directly to the transmembrane domain, which is composed of seven transmembrane (TM) helices embedded in the cell membrane connected by three extracellular (EL) and three intracellular (IL) loops [61].”
BackgroundMembrane cholesterol stabilizes the human serotonin1A receptor
Saxena, R., & Chattopadhyay, A. (2012) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2012.07.032 · Cited by 74
Ligand-specific Conformation of Extracellular Loop-2 in the Angiotensin II Type 1 Receptor
Ünal, H., Jagannathan, R., Bhat, M. B., & Karnik, S. S. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.094870 · Cited by 74
Selective phosphorylation modulates the PIP2 sensitivity of the CaM–SK channel complex
Zhang, M., Meng, X.-Y., Cui, M., Pascal, J. M., Logothetis, D. E., & Zhang, J.-F. (2014) · Nature Chemical Biology · doi:10.1038/nchembio.1592 · Cited by 75
Structure‐Based and Fragment‐Based GPCR Drug Discovery
Andrews, S. P., Brown, G. A., & Christopher, J. A. (2013) · ChemMedChem · doi:10.1002/cmdc.201300382 · Cited by 72
El‐Battrawy, I., Zhao, Z., Lan, H., Schünemann, J.-D., Sattler, K., Buljubasic, F., Patocskai, B., Li, X., Yücel, G., Lang, S., et al. (2018) · International Journal of Cardiology · doi:10.1016/j.ijcard.2017.11.007 · Cited by 73
Stereospecific requirement of cholesterol in the function of the serotonin1A receptor
Jafurulla, M., Rao, B. D., Sugunan, S., Ruysschaert, J., Covey, D. F., & Chattopadhyay, A. (2013) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2013.08.015 · Cited by 73
Chang, D.-K., Peterson, E., Sun, J., Goudie, C., Drapkin, R., Liu, J. F., Matulonis, U. A., Zhu, Q. K., & Marasco, W. A. (2015) · OncoImmunology · doi:10.1080/2162402x.2015.1090075 · Cited by 76
Targeting of peptide‐binding receptors on cancer cells with peptide‐drug conjugates
Worm, D. J., Els‐Heindl, S., & Beck‐Sickinger, A. G. (2020) · Peptide Science · doi:10.1002/pep2.24171 · Cited by 76
Ligand functional selectivity and quantitative pharmacology at G protein-coupled receptors
Stallaert, W., Christopoulos, A., & Bouvier, M. (2011) · Expert Opinion on Drug Discovery · doi:10.1517/17460441.2011.586691 · Cited by 72
Structural equilibrium underlying ligand-dependent activation of β2-adrenoreceptor
Imai, S., Yokomizo, T., Kofuku, Y., Shiraishi, Y., Ueda, T., & Shimada, I. (2020) · Nature Chemical Biology · doi:10.1038/s41589-019-0457-5 · Cited by 75
Ricarte, A., Dalton, J. A. R., & Giraldo, J. (2021) · Journal of Chemical Information and Modeling · doi:10.1021/acs.jcim.0c00890 · Cited by 72
Molecular determinants of ligand efficacy and potency in GPCR signaling
Heydenreich, F. M., Martí-Solano, M., Sandhu, M., Kobilka, B. K., Bouvier, M., & Babu, M. M. (2023) · Science · doi:10.1126/science.adh1859 · Cited by 77
Self-citationS1PR5 is pivotal for the homeostasis of patrolling monocytes
Debien, E., Mayol, K., Biajoux, V., Daussy, C., de Agüero, M. G., Taillardet, M., Dagany, N., Brinza, L., Henry, T., Dubois, B., et al. (2013) · European Journal of Immunology · doi:10.1002/eji.201343312 · Cited by 77
Li, T., Liu, L., Zhang, L., & Liu, N. (2014) · Scientific Reports · doi:10.1038/srep06474 · Cited by 72
Enemy attraction: bacterial agonists for leukocyte chemotaxis receptors
Bloes, D. A., Kretschmer, D., & Peschel, A. (2014) · Nature Reviews Microbiology · doi:10.1038/nrmicro3390 · Cited by 73
Pless, S. A., & Ahern, C. A. (2013) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev-pharmtox-011112-140343 · Cited by 74
Challenges for and current status of research into positive modulators of AMPA receptors
Ward, S. E., Bax, B. D., & Harries, M. H. (2010) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2010.00726.x · Cited by 72
Calcitonin Gene-Related Peptide Receptor Antagonists: New Therapeutic Agents for Migraine
Bell, I. M. (2014) · Journal of Medicinal Chemistry · doi:10.1021/jm500364u · Cited by 72
Lambert, N. A. (2010) · Science Signaling · doi:10.1126/scisignal.3115pe12 · Cited by 71
Dynamics and modulation of metabotropic glutamate receptors
Rondard, P., & Pin, J. (2014) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2014.12.001 · Cited by 71
Structure-Based Drug Design for G Protein-Coupled Receptors
Congreve, M., Dias, J. M., & Marshall, F. H. (2014) · Progress in medicinal chemistry · doi:10.1016/b978-0-444-63380-4.00001-9 · Cited by 74
Direct Interaction between an Allosteric Agonist Pepducin and the Chemokine Receptor CXCR4
Janz, J. M., Ren, Y., Looby, R. J., Kazmi, M. A., Sachdev, P., Grunbeck, A., Haggis, L., Chinnapen, D. J. ‐., Lin, A. Y. J., Seibert, C., et al. (2011) · Journal of the American Chemical Society · doi:10.1021/ja206661w · Cited by 71
The BAI subfamily of adhesion GPCRs: synaptic regulation and beyond
Stephenson, J. R., Purcell, R. H., & Hall, R. A. (2014) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2014.02.002 · Cited by 75
“GPCRs recognize a diverse array of extracellular stimuli and transduce intracellular signaling cascades via heterotrimeric G proteins and other signaling intermediates to control cellular physiology [2].”
BackgroundNew developments in C5a receptor signaling
Ward, P. A., & Sarma, J. V. (2012) · Cell Health and Cytoskeleton · doi:10.2147/chc.s27233 · Cited by 71
Structure Determination of Membrane Proteins by Nuclear Magnetic Resonance Spectroscopy
Opella, S. J. (2013) · Annual Review of Analytical Chemistry · doi:10.1146/annurev-anchem-062012-092631 · Cited by 71
Fuller, B. B. (2019) · Cosmetics · doi:10.3390/cosmetics6010006 · Cited by 73
New Routes in GPCR/β-Arrestin-Driven Signaling in Cancer Progression and Metastasis
Bagnato, A., & Rosanò, L. (2019) · Frontiers in Pharmacology · doi:10.3389/fphar.2019.00114 · Cited by 70
Maurice, P., Daulat, A. M., Tureček, R., Ivankova-Susankova, K., Zamponi, F., Kamal, M. T., Clément, N., Guillaume, J., Bettler, B., Galès, C., et al. (2010) · The EMBO Journal · doi:10.1038/emboj.2010.236 · Cited by 70
Stalder, A. K., Lott, D., Strasser, D. S., Cruz, H. G., Krause, A., Groenen, P. M. A., & Dingemanse, J. (2016) · British Journal of Clinical Pharmacology · doi:10.1111/bcp.13149 · Cited by 70
Structure–Function Relationships of Olfactory and Taste Receptors
Behrens, M., Briand, L. V., de March, C. A., Matsunami, H., Yamashita, A., Meyerhof, W., & Weyand, S. N. (2018) · Chemical Senses · doi:10.1093/chemse/bjx083 · Cited by 70
“The structures have been instrumental in developing a unified theory of how the conformation change in the receptor that occurs upon agonist binding results in G protein coupling on the intracellular face of the receptor (Katritch et al. 2013; Rosenbaum et al. 2009; Venkatakrishnan et al. 2016; Venkatakrishnan et al.…”
BackgroundLigands and Beyond: Mechanosensitive Adhesion GPCRs
Lin, H., Ng, K., Chen, T., & Tseng, W.-Y. (2022) · Pharmaceuticals · doi:10.3390/ph15020219 · Cited by 71
Coskuner‐Weber, O., Mirzanli, O., & Uversky, V. N. (2022) · Biophysical Reviews · doi:10.1007/s12551-022-00968-0 · Cited by 70
Genetic loss or pharmacological blockade of testes-expressed taste genes causes male sterility
Mosinger, B. J., Redding, K., Parker, M. R., Yevshayeva, V., Yee, K. K., Dyomina, K., Li, Y., & Margolskee, R. F. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1302827110 · Cited by 69
Optogenetic toolkit for precise control of calcium signaling
Ma, G., Wen, S., He, L., Huang, Y., Wang, Y., & Zhou, Y. (2017) · Cell Calcium · doi:10.1016/j.ceca.2017.01.004 · Cited by 69
Ferro, A., Marinato, G. M., Mulargiu, C., Marino, M., Pasello, G., Guarneri, V., & Bonanno, L. (2024) · Critical Reviews in Oncology/Hematology · doi:10.1016/j.critrevonc.2024.104295 · Cited by 72
Mumford, A. D., Dawood, B. B., Daly, M. E., Murden, S. L., Williams, M. D., Protty, M. B., Spalton, J. C., Wheatley, M., Mundell, S. J., & Watson, S. P. (2009) · Blood · doi:10.1182/blood-2009-08-236976 · Cited by 68
Molecular Dynamics Simulations Reveal Insights into Key Structural Elements of Adenosine Receptors
Rodriguez, D. J., Piñeiro, Á., & Gutiérrez‐de‐Terán, H. (2011) · Biochemistry · doi:10.1021/bi200100t · Cited by 68
Singh, S., & Bowman, G. R. (2017) · Journal of Chemical Theory and Computation · doi:10.1021/acs.jctc.6b01181 · Cited by 66
Kynde, S., Skar‐Gislinge, N., Pedersen, M. C., Midtgaard, S. R., Simonsen, J. B., Schweins, R., Mortensen, K., & Arleth, L. (2014) · Acta Crystallographica Section D Biological Crystallography · doi:10.1107/s1399004713028344 · Cited by 67
“These central features imply that despite the remarkable breakthroughs in the last few years (Morth et al., 2007; Rosenbaum et al., 2009), it is still regarded as extraordinarily challenging to crystallize membrane proteins to obtain high-resolution structural information.”
BackgroundRomo, T. D., Grossfield, A. M., & Pitman, M. C. (2010) · Biophysical Journal · doi:10.1016/j.bpj.2009.09.046 · Cited by 67
Ligand binding to a G protein–coupled receptor captured in a mass spectrometer
Yen, H., Hopper, J. T. S., Liko, I., Allison, T. M., Zhu, Y., Wang, D., Stegmann, M., Mohammed, S., Wu, B., & Robinson, C. V. (2017) · Science Advances · doi:10.1126/sciadv.1701016 · Cited by 71
Bocquet, N., Kohler, J., Hug, M. N., Kusznir, E. A., Rufer, A. C., Dawson, R. J. P., Hennig, M., Ruf, A., Huber, W., & Huber, S. (2015) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2015.02.014 · Cited by 74
“While the crystal structures of themain classes of GPCRs have been elucidated in presence of agonists, antagonists or inverse agonistswithin the last decade, greatly increasing our understanding of the molecular mechanisms underlying ligand binding and receptor activation [3–5], studies about the kinetics of these com…”
Backgroundvan Breda, S. G., Claessen, S. M. H., van Herwijnen, M. H. M., Theunissen, D. H. J., Jennen, D. G. J., de Kok, T. M. C. M., & Kleinjans, J. C. S. (2017) · Toxicology · doi:10.1016/j.tox.2017.11.013 · Cited by 66
The Role of G Protein-coupled Receptor Kinases in Cancer
Yu, S., Sun, L., Jiao, Y., & Lee, L. T. O. (2018) · International Journal of Biological Sciences · doi:10.7150/ijbs.22896 · Cited by 66
Zhang, L.-L., Wang, J., Liu, Y., Lu, X., Kuang, Y., Wan, Y.-H., Chen, Y., Yan, H., Fei, J., & Wang, Z.-G. (2011) · Neuroscience · doi:10.1016/j.neuroscience.2011.08.069 · Cited by 67
Kuang, H., Ku, S. H., & Kokkoli, E. (2016) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2016.08.005 · Cited by 66
Lian, H., Xu, P., He, S., Jun, W., Pan, J., Wang, W., Xu, F., Wang, S., Pan, J., Huang, J., et al. (2018) · Molecular Plant · doi:10.1016/j.molp.2018.08.004 · Cited by 65
Androgen Therapy in Neurodegenerative Diseases
Bianchi, V. E., Rizzi, L., Bresciani, E., Omeljaniuk, R. J., & Torsello, A. (2020) · Journal of the Endocrine Society · doi:10.1210/jendso/bvaa120 · Cited by 69
“Among mARs, GPRC6A is a membrane protein involved in physiological responses to hormones and environmental stimuli regulating the effect of androgens in various tissues [12].”
BackgroundCao, A.-M., Quast, R. B., Fatemi, F., Rondard, P., Pin, J., & Margeat, E. (2021) · Nature Communications · doi:10.1038/s41467-021-25620-5 · Cited by 68
Molecular targeting of Gα and Gβγ subunits: a potential approach for cancer therapeutics
Smrcka, A. V. (2013) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2013.02.006 · Cited by 64
C4a: An Anaphylatoxin in Name Only
Barnum, S. R. (2015) · Journal of Innate Immunity · doi:10.1159/000371423 · Cited by 65
MARCH2 promotes endocytosis and lysosomal sorting of carvedilol-bound β2-adrenergic receptors
Han, S.-O., Xiao, K., Kim, J., Wu, J., Wisler, J. W., Nakamura, N., Freedman, N. J., & Shenoy, S. K. (2012) · The Journal of Cell Biology · doi:10.1083/jcb.201208192 · Cited by 65
Jung, G., Fajardo, G., Ribeiro, A. J. S., Kooiker, K. B., Coronado, M. J., Zhao, M., Hu, D., Reddy, S., Kodo, K., Sriram, K., et al. (2015) · The FASEB Journal · doi:10.1096/fj.15-280982 · Cited by 66
The G protein-coupled estrogen receptor as a modulator of neoplastic transformation
Jacenik, D., Cygankiewicz, A. I., & Krajewska, W. M. (2016) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2016.04.011 · Cited by 65
Cholesterol interaction motifs in G protein‐coupled receptors: Slippery hot spots?
Sarkar, P., & Chattopadhyay, A. (2020) · WIREs Systems Biology and Medicine · doi:10.1002/wsbm.1481 · Cited by 65
When simple agonism is not enough: Emerging modalities of GPCR ligands
Smith, N. J., Bennett, K. A., & Milligan, G. (2010) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2010.07.009 · Cited by 64
Li, Y., Heng, J., Sun, D., Zhang, B., Zhang, X., Zheng, Y., Shi, W., Wang, T., Li, J., Sun, X., et al. (2021) · Journal of the American Chemical Society · doi:10.1021/jacs.1c07369 · Cited by 62
Self-citationHelical membrane protein conformations and their environment
Cross, T. A., Murray, D. T., & Watts, A. G. (2013) · European Biophysics Journal · doi:10.1007/s00249-013-0925-x · Cited by 64
Interactions of the GnRH receptor with heterotrimeric G proteins
Naor, Z., & Huhtaniemi, I. T. (2012) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2012.11.001 · Cited by 64
Buckley, S. J., Fitzgibbon, Q. P., Smith, G. G., & Ventura, T. (2016) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2016.02.001 · Cited by 64
CCR5-Mediated Signaling is Involved in Invasion of Glioblastoma Cells in Its Microenvironment
Novak, M., Krajnc, M. K., Hrastar, B., Breznik, B., Majc, B., Mlinar, M., Rotter, A., Porčnik, A., Mlakar, J., Stare, K., et al. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21124199 · Cited by 63
“Most promising is CCR5 blocking by synthetic drug maraviroc, an allosteric inverse CCR5 agonist [56], which has been proven to significantly inhibit proliferation, colony formation, and migration of several carcinomas, including breast [42] and prostate cancer [55].”
BackgroundWang, Y., Yu, Z., Xiao, W., Lu, S., & Zhang, J. (2020) · Drug Discovery Today · doi:10.1016/j.drudis.2020.12.001 · Cited by 66
The function, structure, and origins of the ER membrane protein complex
Hegde, R. S. (2022) · Annual Review of Biochemistry · doi:10.1146/annurev-biochem-032620-104553 · Cited by 61
Leukotriene BLT2 Receptor Monomers Activate the Gi2 GTP-binding Protein More Efficiently than Dimers
Arcemisbéhère, L., Sen, T., Boudier, L., Balestre, M., Gaibelet, G., Detouillon, E., Orcel, H., Mendre, C., Rahmeh, R., Granier, S., et al. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.083477 · Cited by 63
‘PUFA–GPR40–CREB signaling’ hypothesis for the adult primate neurogenesis
Yamashima, T. (2012) · Progress in Lipid Research · doi:10.1016/j.plipres.2012.02.001 · Cited by 68
Paila, Y. D., Kombrabail, M. H., Krishnamoorthy, G., & Chattopadhyay, A. (2011) · The Journal of Physical Chemistry B · doi:10.1021/jp201458h · Cited by 63
Triggering ubiquitination of IFNAR1 protects tissues from inflammatory injury
Bhattacharya, S., Katlinski, K. V., Reichert, M., Takano, S., Brice, A. K., Zhao, B., Yu, Q., Zheng, H., Carbone, C. J., Katlinskaya, Y. V., et al. (2014) · EMBO Molecular Medicine · doi:10.1002/emmm.201303236 · Cited by 63
Identification of an antithrombotic allosteric modulator that acts through helix 8 of PAR1
Dowal, L. M., Sim, D., Dilks, J. R., Blair, P. S., Beaudry, S., Denker, B. M., Κούκος, Γ., Kuliopulos, A., & Flaumenhaft, R. C. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1014863108 · Cited by 62
New insights into GPCR coupling and dimerisation from cryo-EM structures
Gusach, A., García‐Nafría, J., & Tate, C. G. (2023) · Current Opinion in Structural Biology · doi:10.1016/j.sbi.2023.102574 · Cited by 62
“One mechanism in the cell to terminate GPCR-G protein signalling at the plasma membrane is through receptor phosphorylation by GRKs, recruitment of arrestin via the phosphorylated C-terminus/ICL3 and then clathrin-mediated endocytosis mediated by arrestin-clathrin/AP2 interactions [27].”
de la Fuente, T., Martín‐Fontecha, M., Sallander, J., Benhamú, B., Campillo, M., Medina, R. A., Pellissier, L. P., Claeysen, S., Dumuis, A., Pardo, L., et al. (2010) · Journal of Medicinal Chemistry · doi:10.1021/jm901672k · Cited by 63
Karpenko, J., Kreder, R., Valencia, C., Villa, P., Mendre, C., Mouillac, B., Mély, Y., Hibert, M., Bonnet, D., & Klymchenko, A. S. (2014) · ChemBioChem · doi:10.1002/cbic.201300738 · Cited by 62
Improvement of drug-like properties of peptides: the somatostatin paradigm
Ovadia, O., Greenberg, S., Laufer, B., Gilon, C., Hoffman, A., & Kessler, H. (2010) · Expert Opinion on Drug Discovery · doi:10.1517/17460441.2010.493935 · Cited by 65
Paila, Y. D., Tiwari, S., Sengupta, D., & Chattopadhyay, A. (2010) · Molecular BioSystems · doi:10.1039/c0mb00148a · Cited by 62
Mahmoudi, M., Aslani, S., Nicknam, M. H., Karami, J., & Jamshidi, A. (2016) · Modern Rheumatology · doi:10.1080/14397595.2016.1206174 · Cited by 62
The ganglioside GM1 interacts with the serotonin 1A receptor via the sphingolipid binding domain
Prasanna, X., Jafurulla, M., Sengupta, D., & Chattopadhyay, A. (2016) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2016.08.009 · Cited by 64
Nanobodies: New avenues for imaging, stabilizing and modulating GPCRs
Groof, T. W. M. D., Bobkov, V., Heukers, R., & Smit, M. J. (2019) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2019.01.021 · Cited by 64
Sansuk, K., Deupí, X., Torrecillas, I. R., Jongejan, A., Nijmeijer, S., Bakker, R. A., Pardo, L., & Leurs, R. (2010) · Molecular Pharmacology · doi:10.1124/mol.110.066068 · Cited by 62
In vitro profiling of orphan G protein coupled receptor (GPCR) constitutive activity
Watkins, L. R., & Orlandi, C. (2021) · British Journal of Pharmacology · doi:10.1111/bph.15468 · Cited by 59
GPCRs in Intracellular Compartments: New Targets for Drug Discovery
Fasciani, I., Carli, M., Petragnano, F., Colaianni, F., Aloisi, G., Maggio, R., Scarselli, M., & Rossi, M. (2022) · Biomolecules · doi:10.3390/biom12101343 · Cited by 69
“Many proteins are sorted by short signal peptides attached to the N-terminus (or occasionally at the C-terminus or along the internal sequence) of the protein [68].”
BackgroundPharmacological Chaperones for Misfolded Gonadotropin-Releasing Hormone Receptors
Conn, P. M., & Ulloa‐Aguirre, A. (2011) · Advances in pharmacology · doi:10.1016/b978-0-12-385952-5.00008-7 · Cited by 64
Conserved activation pathways in G-protein-coupled receptors
Deupí, X., Standfuss, J., & Schertler, G. F. X. (2012) · Biochemical Society Transactions · doi:10.1042/bst20120001 · Cited by 62
Metadata
- Authors
- Rosenbaum, D. M., Rasmussen, S. G. F., & Kobilka, B. K.
- Affiliations
- Stanford Medicine (US)
- Venue
- Nature
- Published
- 2009-05
- Volume
- 459
- Issue
- 7245
- Pages
- 356-363
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC3967846
- OpenAlex
- W1988097700
- Cited by
- 2,534
- References
- 73
- Citations by year
- 2026: 108 · 2025: 171 · 2024: 175 · 2023: 140 · 2022: 196 · 2021: 177 · 2020: 150 · 2019: 172 · 2018: 122 · 2017: 136 · 2016: 132 · 2015: 120 · 2014: 133 · 2013: 135 · 2012: 146
- FWCI
- 11.79
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- Lundbeckfonden (R19-2008-2113)
- National Institute of General Medical Sciences (F32GM082028, R01GM083118)
- National Institute of Neurological Disorders and Stroke (R01NS28471, R01NS028471)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Receptor Mechanisms and Signaling
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Kinase Regulation and GTPase Signaling
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- G protein-coupled receptors, GPCR structure, GPCR activation, constitutive activity, membrane protein structure, therapeutic target, hormone signaling, neurotransmitter signaling
- MeSH terms
- Animals, Cytoplasm, Humans, Protein Conformation, Signal Transduction, Conserved Sequence, Receptors, G-Protein-Coupled, Opsins
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review