Structural determinants of binding of the creatine transporter (creat, SLC6A8) inform the functional annotation of the SLC6 transporters family

被引:0
|
作者
Colas, Claire [1 ]
机构
[1] Univ Vienna, Pharmaceut Chem, Vienna, Austria
关键词
D O I
暂无
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
1213-Pos
引用
收藏
页码:250A / 250A
页数:1
相关论文
共 50 条
  • [21] Cardiac manifestations in a child with a novel mutation in creatine transporter gene SLC6A8
    Anselm, Irina A.
    Coulter, David L.
    Darras, Basil T.
    NEUROLOGY, 2008, 70 (18) : 1642 - 1644
  • [22] PIKfyve in the SGK1 mediated regulation of the creatine transporter SLC6A8
    Strutz-Seebohm, Nathalie
    Shojaiefard, Manzar
    Christie, David L.
    Tavare, Jeremy M.
    Seebohm, Guiscard
    Lang, Florian
    CELLULAR PHYSIOLOGY AND BIOCHEMISTRY, 2007, 20 (06) : 729 - 734
  • [23] The SLC6 orphans form a family of amino acid transporters
    Broer, S.
    JOURNAL OF NEUROCHEMISTRY, 2007, 102 : 10 - 10
  • [24] Deletion of the Creatine Transporter (Slc6a8) in Dopaminergic Neurons Leads to Hyperactivity in Mice
    Zuhair I. Abdulla
    Bahar Pahlevani
    Kerstin H. Lundgren
    Jordan L. Pennington
    Kenea C. Udobi
    Kim B. Seroogy
    Matthew R. Skelton
    Journal of Molecular Neuroscience, 2020, 70 : 102 - 111
  • [25] Classification of the Molecular Defects Associated with Pathogenic Variants of the SLC6A8 Creatine Transporter
    Salazar, Martin D.
    Zelt, Nathan B.
    Saldivar, Robert
    Kuntz, Charles P.
    Chen, Sheng
    Penn, Wesley D.
    Bonneau, Richard
    Leman, Julia Koehler
    Schlebach, Jonathan P.
    BIOCHEMISTRY, 2020, 59 (13) : 1367 - 1377
  • [26] Deletion of the Creatine Transporter (Slc6a8) in Dopaminergic Neurons Leads to Hyperactivity in Mice
    Abdulla, Zuhair I.
    Pahlevani, Bahar
    Lundgren, Kerstin H.
    Pennington, Jordan L.
    Udobi, Kenea C.
    Seroogy, Kim B.
    Skelton, Matthew R.
    JOURNAL OF MOLECULAR NEUROSCIENCE, 2020, 70 (01) : 102 - 111
  • [27] Novel mutation found in creatine transporter gene (SLC6A8) in a patient with intellectual disability
    Rubio Alaejos, A.
    Perez Esteban, G.
    Valina Amado, L.
    Ballesteros Vizoso, M. A.
    Argente Del Castillo, P.
    Bauca, J. M.
    Robles Bauza, J.
    CLINICA CHIMICA ACTA, 2019, 493 : S246 - S246
  • [28] Experimental and Computational Analysis of Newly Identified Pathogenic Mutations in the Creatine Transporter SLC6A8
    Ferrada, Evandro
    Wiedmer, Tabea
    Wang, Wen-An
    Frommelt, Fabian
    Steurer, Barbara
    Klimek, Christoph
    Lindinger, Sabrina
    Osthushenrich, Tanja
    Garofoli, Andrea
    Brocchetti, Silvia
    Bradberry, Samuel
    Huang, Jiahui
    MacNamara, Aidan
    Scarabottolo, Lia
    Ecker, Gerhard F.
    Malarstig, Anders
    Superti-Furga, Giulio
    JOURNAL OF MOLECULAR BIOLOGY, 2024, 436 (02)
  • [29] HOMOCYSTEINE SUPPRESSES PLACENTAL EXPRESSION OF THE CREATINE TRANSPORTER SLC6A8: ROLE OF DNA METHYLATION
    Cash, L.
    Sonne, S.
    Bhatia, J.
    Ganapathy, V
    JOURNAL OF INVESTIGATIVE MEDICINE, 2014, 62 (02) : 575 - 575
  • [30] Mutations in SLC6A8 (creatine transporter) are responsible for about 1% of MR in males.
    Rosenberg, EH
    Almeida, LS
    Clark, AJ
    Stevenson, RE
    Jakobs, C
    Wood, T
    Salomons, GS
    Schwartz, CE
    MOLECULAR GENETICS AND METABOLISM, 2005, 84 (03) : 236 - 236