6YTR: Recombinant human beta-glucocerebrosidase

Structure of recombinant human beta-glucocerebrosidase in complex with cyclophellitol aziridine inhibitor. Determined by X-ray diffraction at 1.7 Å resolution. Released 12 May 2021.

Method
X-ray diffraction
Resolution
1.7 Å
Organism
Homo sapiens
Chains
2
Atoms
9,172
Mol. weight
117.01 kDa
Ligands
PO8, NAG
Released
12 May 2021

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

Secondary structure: helices and β-sheets

6YTR contains 49 α-helices and 51 β-strands across 2 chains. 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 AAA: 24 helices, 27 β-strands

ElementResiduesLengthSheet
β-strand211
β-strand6-722
β-strand15-1842
β-strand2511
α-helix26-294
β-strand36-4383
β-strand50-5563
α-helix561
β-strand5713
β-strand65-77133
α-helix781
β-strand80-8454
α-helix87-948
α-helix98-10912
β-strand118-12364
α-helix1511
α-helix152-1576
α-helix158-16710
α-helix171-1722
β-strand173-17864
α-helix183-1853
β-strand18615
β-strand19715
α-helix204-22219
β-strand229-23134
α-helix236-2405
α-helix253-2597
α-helix260-2645
α-helix265-2695
β-strand277-28484
α-helix285-2873
α-helix290-2967
α-helix299-3024
β-strand307-31154
α-helix315-3173
α-helix321-3255
α-helix326-3305
β-strand335-34064
α-helix357-37216
β-strand375-38284
β-strand38512
β-strand402-40542
α-helix406-4083
β-strand410-41342
α-helix415-42410
β-strand432-43873
β-strand444-45073
β-strand456-46273
β-strand468-47473
β-strand478-48473
β-strand488-49473
Chain BBB: 25 helices, 24 β-strands
ElementResiduesLengthSheet
α-helix2-43
β-strand6-726
β-strand15-1846
α-helix27-304
β-strand36-4387
β-strand50-5787
β-strand65-77137
α-helix781
β-strand80-8458
α-helix87-948
α-helix98-10912
β-strand118-12368
α-helix1511
α-helix152-1576
α-helix158-16710
α-helix171-1722
β-strand173-17868
α-helix183-1853
β-strand18619
β-strand19719
α-helix204-22219
β-strand229-23138
α-helix236-2405
α-helix253-2597
α-helix260-2645
α-helix265-2695
β-strand277-28488
α-helix285-2873
α-helix290-2967
α-helix299-3024
β-strand307-31158
α-helix315-3173
α-helix3201
α-helix321-3255
α-helix326-3305
β-strand335-34068
α-helix357-37216
β-strand375-38288
β-strand38516
β-strand402-40546
α-helix406-4083
β-strand410-41346
α-helix415-42410
β-strand432-43877
β-strand444-45077
β-strand456-46277
β-strand468-47477
β-strand478-48477
β-strand488-49477

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Lysosomal acid glucosylceramidaseAAA, BBBprotein497Homo sapiensP04062 (AlphaFold model)
Sequence of entity 1 (AAA, BBB), FASTA
>6YTR_1 Lysosomal acid glucosylceramidase (chains AAA, BBB)
ARPCIPKSFGYSSVVCVCNATYCDSFDPPTFPALGTFSRYESTRSGRRMELSMGPIQANH
TGTGLLLTLQPEQKFQKVKGFGGAMTDAAALNILALSPPAQNLLLKSYFSEEGIGYNIIR
VPMASCDFSIRTYTYADTPDDFQLHNFSLPEEDTKLKIPLIHRALQLAQRPVSLLASPWT
SPTWLKTNGAVNGKGSLKGQPGDIYHQTWARYFVKFLDAYAEHKLQFWAVTAENEPSAGL
LSGYPFQCLGFTPEHQRDFIARDLGPTLANSTHHNVRLLMLDDQRLLLPHWAKVVLTDPE
AAKYVHGIAVHWYLDFLAPAKATLGETHRLFPNTMLFASEACVGSKFWEQSVRLGSWDRG
MQYSHSIITNLLYHVVGWTDWNLALNPEGGPNWVRNFVDSPIIVDITKDTFYKQPMFYHL
GHFSKFIPEGSQRVGLVASQKNDLDAVALMHPDGSAVVVVLNRSSKDVPLTIKDPAVGFL
ETISPGYSIHTYLWRRQ

Ligands and cofactors

IDNameFormulaCopies
PO8(1~{R},2~{S},3~{S},4~{S},5~{R},6~{R})-5-azanyl-6-(hydroxymethyl)cyclohexane-1,2…C7 H16 N O52
NAG2-acetamido-2-deoxy-beta-D-glucopyranoseC8 H15 N O61

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

Primary citation

Design, Synthesis and Structural Analysis of Glucocerebrosidase Imaging Agents. Rowland, R.J., Chen, Y., Breen, I. et al. Chemistry (2021) 27:16377-16388. DOI 10.1002/chem.202102359 · PubMed

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

Browse structure collections

About this viewer

MolViewer shows 6YTR directly in your browser with nothing to install. Switch between cartoon, ball-and-stick, spacefill and surface views, color by chain, secondary structure or B-factor, measure distances, angles and dihedrals, and share or embed the view.