Inhibitor binding mode and allosteric regulation of Na + -glucose symporters
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
2041-1723
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
Inhibitor binding mode and allosteric regulation of Na + -glucose symporters ; volume:9 ; number:1 ; day:7 ; month:12 ; year:2018 ; pages:1-10 ; date:12.2018
Nature Communications ; 9, Heft 1 (7.12.2018), 1-10, 12.2018
- Klassifikation
-
Biowissenschaften, Biologie
- Urheber
-
Bisignano, Paola
Ghezzi, Chiara
Jo, Hyunil
Polizzi, Nicholas F.
Althoff, Thorsten
Kalyanaraman, Chakrapani
Friemann, Rosmarie
Jacobson, Matthew P.
Wright, Ernest M.
Grabe, Michael
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
-
10.1038/s41467-018-07700-1
- URN
-
urn:nbn:de:101:1-2019011922511521140494
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:58 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Bisignano, Paola
- Ghezzi, Chiara
- Jo, Hyunil
- Polizzi, Nicholas F.
- Althoff, Thorsten
- Kalyanaraman, Chakrapani
- Friemann, Rosmarie
- Jacobson, Matthew P.
- Wright, Ernest M.
- Grabe, Michael
- SpringerLink (Online service)
Ähnliche Objekte (12)
Binding Modes of Xanthine‐Derived Selective Allosteric Site Inhibitors of MTHFD2
Linking ATP and allosteric sites to achieve superadditive binding with bivalent EGFR kinase inhibitors
Xanomeline displays concomitant orthosteric and allosteric binding modes at the M4 mAChR
2‐Substituted thienotetrahydropyridine derivatives: Allosteric ectonucleotidase inhibitors
Orthosteric and allosteric binding sites of P2X receptors
Covalent-allosteric inhibitors to achieve akt isoform-selectivity
Identification of Allosteric Inhibitors against Active Caspase-6
Covalent‐Allosteric Inhibitors to Achieve Akt Isoform‐Selectivity
Closantel is an allosteric inhibitor of human Taspase1
Synthesis of an HIV-1 Integrase Allosteric Site Inhibitor
Bias-inducing allosteric binding site in mu-opioid receptor signaling
Bias-inducing allosteric binding site in mu-opioid receptor signaling
Binding Modes of Xanthine‐Derived Selective Allosteric Site Inhibitors of MTHFD2
Linking ATP and allosteric sites to achieve superadditive binding with bivalent EGFR kinase inhibitors
Xanomeline displays concomitant orthosteric and allosteric binding modes at the M4 mAChR
2‐Substituted thienotetrahydropyridine derivatives: Allosteric ectonucleotidase inhibitors
Orthosteric and allosteric binding sites of P2X receptors
Covalent-allosteric inhibitors to achieve akt isoform-selectivity
Identification of Allosteric Inhibitors against Active Caspase-6
Covalent‐Allosteric Inhibitors to Achieve Akt Isoform‐Selectivity
Closantel is an allosteric inhibitor of human Taspase1
Synthesis of an HIV-1 Integrase Allosteric Site Inhibitor
Bias-inducing allosteric binding site in mu-opioid receptor signaling
Bias-inducing allosteric binding site in mu-opioid receptor signaling
Binding Modes of Xanthine‐Derived Selective Allosteric Site Inhibitors of MTHFD2
Linking ATP and allosteric sites to achieve superadditive binding with bivalent EGFR kinase inhibitors
Xanomeline displays concomitant orthosteric and allosteric binding modes at the M4 mAChR
2‐Substituted thienotetrahydropyridine derivatives: Allosteric ectonucleotidase inhibitors
Orthosteric and allosteric binding sites of P2X receptors
Covalent-allosteric inhibitors to achieve akt isoform-selectivity
Identification of Allosteric Inhibitors against Active Caspase-6
Covalent‐Allosteric Inhibitors to Achieve Akt Isoform‐Selectivity
Closantel is an allosteric inhibitor of human Taspase1
Synthesis of an HIV-1 Integrase Allosteric Site Inhibitor
Bias-inducing allosteric binding site in mu-opioid receptor signaling