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5FJS

Bacterial beta-glucosidase reveals the structural and functional basis of genetic defects in human glucocerebrosidase 2 (GBA2)

Summary for 5FJS
Entry DOI10.2210/pdb5fjs/pdb
DescriptorGLUCOSYLCERAMIDASE, CALCIUM ION (3 entities in total)
Functional Keywordshydrolase, bile acid beta-glucosidase, glucosylceramidase, gba2, hereditary ataxia
Biological sourceTHERMOANAEROBACTERIUM XYLANOLYTICUM
Total number of polymer chains2
Total formula weight180813.36
Authors
Primary citationCharoenwattanasatien, R.,Pengthaisong, S.,Breen, I.,Mutoha, R.,Sansenya, S.,Hua, Y.,Tankrathok, A.,Wu, L.,Songsiriritthigul, C.,Tanaka, H.,Williams, S.J.,Davies, G.J.,Kurisu, G.,Ketudat Cairns, J.R.
Bacterial Beta-Glucosidase Reveals the Structural and Functional Basis of Genetic Defects in Human Glucocerebrosidase 2 (Gba2)
Acs Chem.Biol., 11:1891-, 2016
Cited by
PubMed Abstract: Human glucosylcerebrosidase 2 (GBA2) of the CAZy family GH116 is responsible for the breakdown of glycosphingolipids on the cytoplasmic face of the endoplasmic reticulum and Golgi apparatus. Genetic defects in GBA2 result in spastic paraplegia and cerebellar ataxia, while cross-talk between GBA2 and GBA1 glucosylceramidases may affect Gaucher disease. Here, we report the first three-dimensional structure for any GH116 enzyme, Thermoanaerobacterium xylanolyticum TxGH116 β-glucosidase, alone and in complex with diverse ligands. These structures allow identification of the glucoside binding and active site residues, which are shown to be conserved with GBA2. Mutagenic analysis of TxGH116 and structural modeling of GBA2 provide a detailed structural and functional rationale for pathogenic missense mutations of GBA2.
PubMed: 27115290
DOI: 10.1021/ACSCHEMBIO.6B00192
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.6 Å)
Structure validation

237735

數據於2025-06-18公開中

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