6TJQ: Recombinant GBA

Crystal Structure of Recombinant GBA in Complex with 2-Deoxy-2-fluoro-beta-D-glucopyranoside. Determined by X-ray diffraction at 1.41 Å resolution. Released 10 Jun 2020.

Method
X-ray diffraction
Resolution
1.41 Å
Organism
Homo sapiens
Chains
1
Atoms
4,730
Mol. weight
58.46 kDa
Ligands
NAG, NF8
Released
10 Jun 2020

Explore 6TJQ in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

6TJQ contains 25 α-helices and 25 β-strands across 1 chain. Residue ranges use author residue numbering, as in the PDB file, from PDBe. To see them in 3D, choose the Cartoon representation with Secondary structure coloring: helices, sheets and coils get different colors.

Chain BBB: 25 helices, 25 β-strands

ElementResiduesLengthSheet
β-strand6-831
β-strand14-1851
α-helix27-293
β-strand36-4382
β-strand50-5562
α-helix561
β-strand5712
β-strand65-77132
α-helix781
β-strand80-8453
α-helix87-948
α-helix98-10912
β-strand118-12363
α-helix1511
α-helix152-1576
α-helix158-16710
α-helix171-1722
β-strand173-17863
α-helix183-1853
β-strand18614
β-strand19714
α-helix204-22219
β-strand229-23133
α-helix236-2405
α-helix253-2597
α-helix260-2645
α-helix265-2695
β-strand277-28483
α-helix285-2873
α-helix290-2967
α-helix299-3024
β-strand307-31153
α-helix315-3173
α-helix3201
α-helix321-3255
α-helix326-3305
β-strand335-34063
α-helix357-37216
β-strand375-38283
β-strand38511
β-strand402-40541
α-helix406-4083
β-strand410-41341
α-helix415-42410
β-strand432-43872
β-strand444-45072
β-strand456-46272
β-strand468-47472
β-strand478-48472
β-strand488-49472

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
GlucosylceramidaseBBBprotein497Homo sapiensP04062 (AlphaFold model)
Sequence of entity 1 (BBB), FASTA
>6TJQ_1 Glucosylceramidase (chains BBB)
ARPCIPKSFGYSSVVCVCNATYCDSFDPPTFPALGTFSRYESTRSGRRMELSMGPIQANH
TGTGLLLTLQPEQKFQKVKGFGGAMTDAAALNILALSPPAQNLLLKSYFSEEGIGYNIIR
VPMASCDFSIRTYTYADTPDDFQLHNFSLPEEDTKLKIPLIHRALQLAQRPVSLLASPWT
SPTWLKTNGAVNGKGSLKGQPGDIYHQTWARYFVKFLDAYAEHKLQFWAVTAENEPSAGL
LSGYPFQCLGFTPEHQRDFIARDLGPTLANSTHHNVRLLMLDDQRLLLPHWAKVVLTDPE
AAKYVHGIAVHWYLDFLAPAKATLGETHRLFPNTMLFASEACVGSKFWEQSVRLGSWDRG
MQYSHSIITNLLYHVVGWTDWNLALNPEGGPNWVRNFVDSPIIVDITKDTFYKQPMFYHL
GHFSKFIPEGSQRVGLVASQKNDLDAVALMHPDGSAVVVVLNRSSKDVPLTIKDPAVGFL
ETISPGYSIHTYLWRRQ

Ligands and cofactors

IDNameFormulaCopies
NAG2-acetamido-2-deoxy-beta-D-glucopyranoseC8 H15 N O62
NF8(2~{R},3~{S},4~{S},5~{S})-5-fluoranyl-2-(hydroxymethyl)oxane-3,4-diolC6 H11 F O41

Water and common crystallization additives (SO4, EDO) are not listed.

Primary citation

A baculoviral system for the production of human beta-glucocerebrosidase enables atomic resolution analysis. Rowland, R.J., Wu, L., Liu, F. et al. Acta Crystallogr D Struct Biol (2020) 76:565-580. DOI 10.1107/S205979832000501X · PubMed

Other PDB entries of the same protein (UniProt P04062 (AlphaFold model), which also has an AlphaFold model), best resolution first:

Browse structure collections

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