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.
Explore 6YTR in 3D Show helices and sheets RCSB PDB PDBe
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.
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 2 | 1 | 1 |
| β-strand | 6-7 | 2 | 2 |
| β-strand | 15-18 | 4 | 2 |
| β-strand | 25 | 1 | 1 |
| α-helix | 26-29 | 4 | |
| β-strand | 36-43 | 8 | 3 |
| β-strand | 50-55 | 6 | 3 |
| α-helix | 56 | 1 | |
| β-strand | 57 | 1 | 3 |
| β-strand | 65-77 | 13 | 3 |
| α-helix | 78 | 1 | |
| β-strand | 80-84 | 5 | 4 |
| α-helix | 87-94 | 8 | |
| α-helix | 98-109 | 12 | |
| β-strand | 118-123 | 6 | 4 |
| α-helix | 151 | 1 | |
| α-helix | 152-157 | 6 | |
| α-helix | 158-167 | 10 | |
| α-helix | 171-172 | 2 | |
| β-strand | 173-178 | 6 | 4 |
| α-helix | 183-185 | 3 | |
| β-strand | 186 | 1 | 5 |
| β-strand | 197 | 1 | 5 |
| α-helix | 204-222 | 19 | |
| β-strand | 229-231 | 3 | 4 |
| α-helix | 236-240 | 5 | |
| α-helix | 253-259 | 7 | |
| α-helix | 260-264 | 5 | |
| α-helix | 265-269 | 5 | |
| β-strand | 277-284 | 8 | 4 |
| α-helix | 285-287 | 3 | |
| α-helix | 290-296 | 7 | |
| α-helix | 299-302 | 4 | |
| β-strand | 307-311 | 5 | 4 |
| α-helix | 315-317 | 3 | |
| α-helix | 321-325 | 5 | |
| α-helix | 326-330 | 5 | |
| β-strand | 335-340 | 6 | 4 |
| α-helix | 357-372 | 16 | |
| β-strand | 375-382 | 8 | 4 |
| β-strand | 385 | 1 | 2 |
| β-strand | 402-405 | 4 | 2 |
| α-helix | 406-408 | 3 | |
| β-strand | 410-413 | 4 | 2 |
| α-helix | 415-424 | 10 | |
| β-strand | 432-438 | 7 | 3 |
| β-strand | 444-450 | 7 | 3 |
| β-strand | 456-462 | 7 | 3 |
| β-strand | 468-474 | 7 | 3 |
| β-strand | 478-484 | 7 | 3 |
| β-strand | 488-494 | 7 | 3 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 2-4 | 3 | |
| β-strand | 6-7 | 2 | 6 |
| β-strand | 15-18 | 4 | 6 |
| α-helix | 27-30 | 4 | |
| β-strand | 36-43 | 8 | 7 |
| β-strand | 50-57 | 8 | 7 |
| β-strand | 65-77 | 13 | 7 |
| α-helix | 78 | 1 | |
| β-strand | 80-84 | 5 | 8 |
| α-helix | 87-94 | 8 | |
| α-helix | 98-109 | 12 | |
| β-strand | 118-123 | 6 | 8 |
| α-helix | 151 | 1 | |
| α-helix | 152-157 | 6 | |
| α-helix | 158-167 | 10 | |
| α-helix | 171-172 | 2 | |
| β-strand | 173-178 | 6 | 8 |
| α-helix | 183-185 | 3 | |
| β-strand | 186 | 1 | 9 |
| β-strand | 197 | 1 | 9 |
| α-helix | 204-222 | 19 | |
| β-strand | 229-231 | 3 | 8 |
| α-helix | 236-240 | 5 | |
| α-helix | 253-259 | 7 | |
| α-helix | 260-264 | 5 | |
| α-helix | 265-269 | 5 | |
| β-strand | 277-284 | 8 | 8 |
| α-helix | 285-287 | 3 | |
| α-helix | 290-296 | 7 | |
| α-helix | 299-302 | 4 | |
| β-strand | 307-311 | 5 | 8 |
| α-helix | 315-317 | 3 | |
| α-helix | 320 | 1 | |
| α-helix | 321-325 | 5 | |
| α-helix | 326-330 | 5 | |
| β-strand | 335-340 | 6 | 8 |
| α-helix | 357-372 | 16 | |
| β-strand | 375-382 | 8 | 8 |
| β-strand | 385 | 1 | 6 |
| β-strand | 402-405 | 4 | 6 |
| α-helix | 406-408 | 3 | |
| β-strand | 410-413 | 4 | 6 |
| α-helix | 415-424 | 10 | |
| β-strand | 432-438 | 7 | 7 |
| β-strand | 444-450 | 7 | 7 |
| β-strand | 456-462 | 7 | 7 |
| β-strand | 468-474 | 7 | 7 |
| β-strand | 478-484 | 7 | 7 |
| β-strand | 488-494 | 7 | 7 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Lysosomal acid glucosylceramidase | AAA, BBB | protein | 497 | Homo sapiens | P04062 (AlphaFold model) |
>6YTR_1 Lysosomal acid glucosylceramidase (chains AAA, BBB) ARPCIPKSFGYSSVVCVCNATYCDSFDPPTFPALGTFSRYESTRSGRRMELSMGPIQANH TGTGLLLTLQPEQKFQKVKGFGGAMTDAAALNILALSPPAQNLLLKSYFSEEGIGYNIIR VPMASCDFSIRTYTYADTPDDFQLHNFSLPEEDTKLKIPLIHRALQLAQRPVSLLASPWT SPTWLKTNGAVNGKGSLKGQPGDIYHQTWARYFVKFLDAYAEHKLQFWAVTAENEPSAGL LSGYPFQCLGFTPEHQRDFIARDLGPTLANSTHHNVRLLMLDDQRLLLPHWAKVVLTDPE AAKYVHGIAVHWYLDFLAPAKATLGETHRLFPNTMLFASEACVGSKFWEQSVRLGSWDRG MQYSHSIITNLLYHVVGWTDWNLALNPEGGPNWVRNFVDSPIIVDITKDTFYKQPMFYHL GHFSKFIPEGSQRVGLVASQKNDLDAVALMHPDGSAVVVVLNRSSKDVPLTIKDPAVGFL ETISPGYSIHTYLWRRQ
| ID | Name | Formula | Copies |
|---|---|---|---|
| PO8 | (1~{R},2~{S},3~{S},4~{S},5~{R},6~{R})-5-azanyl-6-(hydroxymethyl)cyclohexane-1,2… | C7 H16 N O5 | 2 |
| NAG | 2-acetamido-2-deoxy-beta-D-glucopyranose | C8 H15 N O6 | 1 |
Water and common crystallization additives (SO4, EDO, NA) are not listed.
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:
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