메뉴 건너뛰기




Volumn 1848, Issue 11, 2015, Pages 2799-2804

Binding interaction of SGLT with sugar and thiosugar by the molecular dynamics simulation

Author keywords

Bennett's acceptance ratio method; Binding free energy; Co transporter; Luseogliflozin; Molecular dynamics

Indexed keywords

SODIUM GLUCOSE COTRANSPORTER 1; SUGAR; THIOSUGAR; BACTERIAL PROTEIN; GALACTOSE; GLUCOSE; PROTEIN BINDING; SLC5A2 PROTEIN, HUMAN; SODIUM; SODIUM GLUCOSE COTRANSPORTER; SODIUM GLUCOSE COTRANSPORTER 2;

EID: 84941332884     PISSN: 00052736     EISSN: 18792642     Source Type: Journal    
DOI: 10.1016/j.bbamem.2015.08.001     Document Type: Article
Times cited : (6)

References (31)
  • 1
    • 84919662775 scopus 로고    scopus 로고
    • Sodium glucose co-transporter-2 (SGLT2) inhibitors: A review of their basic and clinical pharmacology
    • S. Kalra Sodium glucose co-transporter-2 (SGLT2) inhibitors: a review of their basic and clinical pharmacology Diabetes Ther. 5 2014 355 366
    • (2014) Diabetes Ther. , vol.5 , pp. 355-366
    • Kalra, S.1
  • 2
    • 84908066747 scopus 로고    scopus 로고
    • Update on developments with SGLT2 inhibitors in the management of type 2 diabetes
    • M.A. Nauck Update on developments with SGLT2 inhibitors in the management of type 2 diabetes Drug Des. Devel. Ther. 8 2014 1335 1380
    • (2014) Drug Des. Devel. Ther. , vol.8 , pp. 1335-1380
    • Nauck, M.A.1
  • 3
    • 84877922239 scopus 로고    scopus 로고
    • Ipragliflozin and other sodium-glucose cotransporter-2 (SGLT2) inhibitors in the treatment of type 2 diabetes: Preclinical and clinical data
    • E. Kurosaki, and H. Ogasawara Ipragliflozin and other sodium-glucose cotransporter-2 (SGLT2) inhibitors in the treatment of type 2 diabetes: preclinical and clinical data Pharmacol. Ther. 139 2013 51 59
    • (2013) Pharmacol. Ther. , vol.139 , pp. 51-59
    • Kurosaki, E.1    Ogasawara, H.2
  • 5
    • 84902240389 scopus 로고    scopus 로고
    • Luseogliflozin: First global approval
    • A. Markham, and S. Elkinson Luseogliflozin: First global approval Drugs 74 2014 945 950
    • (2014) Drugs , vol.74 , pp. 945-950
    • Markham, A.1    Elkinson, S.2
  • 6
    • 84910685028 scopus 로고    scopus 로고
    • Luseogliflozin for the treatment of type 2 diabetes
    • Y. Seino Luseogliflozin for the treatment of type 2 diabetes Expert. Opin. Pharmacother. 15 2014 2741 2749
    • (2014) Expert. Opin. Pharmacother. , vol.15 , pp. 2741-2749
    • Seino, Y.1
  • 7
    • 84903557735 scopus 로고    scopus 로고
    • Efficacy and safety of luseogliflozin as monotherapy in Japanese patients with type 2 diabetes mellitus: A randomized, double-blind, placebo-controlled, phase 3 study
    • Y. Seino, T. Sasaki, A. Fukatsu, M. Ubukata, S. Sakai, and Y. Samukawa Efficacy and safety of luseogliflozin as monotherapy in Japanese patients with type 2 diabetes mellitus: a randomized, double-blind, placebo-controlled, phase 3 study Curr. Med. Res. Opin. 30 2014 1245 1255
    • (2014) Curr. Med. Res. Opin. , vol.30 , pp. 1245-1255
    • Seino, Y.1    Sasaki, T.2    Fukatsu, A.3    Ubukata, M.4    Sakai, S.5    Samukawa, Y.6
  • 8
    • 84899904943 scopus 로고    scopus 로고
    • Renal sodium glucose cotransporter 2 inhibitors as a novel therapeutic approach to treatment of type 2 diabetes: Clinical data and mechanism of action
    • Y. Fujita, and N. Inagaki Renal sodium glucose cotransporter 2 inhibitors as a novel therapeutic approach to treatment of type 2 diabetes: clinical data and mechanism of action J. Diabetes Investig. 5 2014 265 275
    • (2014) J. Diabetes Investig. , vol.5 , pp. 265-275
    • Fujita, Y.1    Inagaki, N.2
  • 9
    • 84930083149 scopus 로고    scopus 로고
    • In vitro characterization of luseogliflozin, a potent and competitive sodium glucose co-transporter 2 inhibitor: Inhibition kinetics and binding studies
    • S. Uchida, A. Mitani, E. Gunji, T. Takahashi, and K. Yamamoto In vitro characterization of luseogliflozin, a potent and competitive sodium glucose co-transporter 2 inhibitor: inhibition kinetics and binding studies J. Pharmacol. Sci. 128 2015 54 57
    • (2015) J. Pharmacol. Sci. , vol.128 , pp. 54-57
    • Uchida, S.1    Mitani, A.2    Gunji, E.3    Takahashi, T.4    Yamamoto, K.5
  • 12
  • 13
    • 84855427590 scopus 로고    scopus 로고
    • A gate-free pathway for substrate release from the inward-facing state of the Na(+)-galactose transporter
    • J. Li, and E. Tajkhorshid A gate-free pathway for substrate release from the inward-facing state of the Na(+)-galactose transporter Biochim. Biophys. Acta 1818 2011 263 271
    • (2011) Biochim. Biophys. Acta , vol.1818 , pp. 263-271
    • Li, J.1    Tajkhorshid, E.2
  • 17
    • 84855757480 scopus 로고    scopus 로고
    • Chemical Computing Group, Inc. (CCG) Montreal, Quebec, Canada
    • Molecular Operating Environment (MOE) 2008 Chemical Computing Group, Inc. (CCG) Montreal, Quebec, Canada
    • (2008) Molecular Operating Environment (MOE)
  • 18
    • 33748518255 scopus 로고    scopus 로고
    • Comparison of multiple Amber force fields and development of improved protein backbone parameters
    • V. Hornak, R. Abel, A. Okur, B. Strockbine, A. Roitberg, and C. Simmerling Comparison of multiple Amber force fields and development of improved protein backbone parameters Proteins 65 2006 712 725
    • (2006) Proteins , vol.65 , pp. 712-725
    • Hornak, V.1    Abel, R.2    Okur, A.3    Strockbine, B.4    Roitberg, A.5    Simmerling, C.6
  • 21
    • 3042524904 scopus 로고
    • A well-behaved electrostatic potential based method using charge restraints for deriving atomic charges: The RESP model
    • C.I. Bayly, P. Cieplak, W. Cornell, and P.A. Kollman A well-behaved electrostatic potential based method using charge restraints for deriving atomic charges: the RESP model J. Phys. Chem. 97 1993 10269 10280
    • (1993) J. Phys. Chem. , vol.97 , pp. 10269-10280
    • Bayly, C.I.1    Cieplak, P.2    Cornell, W.3    Kollman, P.A.4
  • 22
    • 46249092554 scopus 로고    scopus 로고
    • GROMACS 4: Algorithms for highly efficient, load-balanced, and scalable molecular simulation
    • B. Hess, C. Kutzner, D. Van Der Spoel, and E. Lindahl GROMACS 4: algorithms for highly efficient, load-balanced, and scalable molecular simulation J. Chem. Theory Comput. 4 2008 435 447
    • (2008) J. Chem. Theory Comput. , vol.4 , pp. 435-447
    • Hess, B.1    Kutzner, C.2    Van Der Spoel, D.3    Lindahl, E.4
  • 24
    • 33846823909 scopus 로고
    • Particle mesh Ewald: An N·log(N) method for Ewald sums in large systems
    • T. Darden, D. York, and L. Pedersen Particle mesh Ewald: an N·log(N) method for Ewald sums in large systems J. Chem. Phys. 98 1993 10089 10092
    • (1993) J. Chem. Phys. , vol.98 , pp. 10089-10092
    • Darden, T.1    York, D.2    Pedersen, L.3
  • 25
    • 0025319621 scopus 로고
    • Calculation of the relative binding free energy of 2′GMP and 2′AMP to ribonuclease T1 using molecular dynamics/free energy perturbation approaches
    • S. Hirono, and P.A. Kollman Calculation of the relative binding free energy of 2′GMP and 2′AMP to ribonuclease T1 using molecular dynamics/free energy perturbation approaches J. Mol. Biol. 212 1990 197 209
    • (1990) J. Mol. Biol. , vol.212 , pp. 197-209
    • Hirono, S.1    Kollman, P.A.2
  • 26
    • 5244304444 scopus 로고
    • Efficient estimation of free energy differences from Monte Carlo data
    • C.H. Bennett Efficient estimation of free energy differences from Monte Carlo data J. Comput. Phys. 22 1976 245 268
    • (1976) J. Comput. Phys. , vol.22 , pp. 245-268
    • Bennett, C.H.1
  • 28
    • 0033117937 scopus 로고    scopus 로고
    • Investigating protein dynamics in collective coordinate space
    • A. Kitao, and N. Go Investigating protein dynamics in collective coordinate space Curr. Opin. Struct. Biol. 9 1999 164 169
    • (1999) Curr. Opin. Struct. Biol. , vol.9 , pp. 164-169
    • Kitao, A.1    Go, N.2
  • 30
    • 0035312645 scopus 로고    scopus 로고
    • Steered molecular dynamics and mechanical functions of proteins
    • B. Isralewitz, M. Gao, and K. Schulten Steered molecular dynamics and mechanical functions of proteins Curr. Opin. Struct. Biol. 11 2001 224 230
    • (2001) Curr. Opin. Struct. Biol. , vol.11 , pp. 224-230
    • Isralewitz, B.1    Gao, M.2    Schulten, K.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.