Structure of BACE Bound to SCH736062. Determined by X-ray diffraction at 1.53 Å resolution. Released 16 Feb 2010.
Explore 3L5E in 3D Show helices and sheets RCSB PDB PDBe
3L5E contains 26 α-helices and 56 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 | 67-70 | 4 | 1 |
| β-strand | 74-81 | 8 | 1 |
| β-strand | 86-93 | 8 | 1 |
| β-strand | 99-102 | 4 | 1 |
| α-helix | 115-117 | 3 | |
| β-strand | 122-132 | 11 | 1 |
| β-strand | 135-147 | 13 | 1 |
| β-strand | 155-167 | 13 | 1 |
| β-strand | 178-181 | 4 | 1 |
| α-helix | 185-187 | 3 | |
| α-helix | 197-204 | 8 | |
| β-strand | 211-215 | 5 | 1 |
| α-helix | 224-229 | 6 | |
| β-strand | 233-237 | 5 | 1 |
| α-helix | 242-244 | 3 | |
| β-strand | 245-253 | 9 | 1 |
| β-strand | 257 | 1 | 2 |
| β-strand | 260 | 1 | 2 |
| β-strand | 261 | 1 | 3 |
| β-strand | 264-269 | 6 | 4 |
| β-strand | 272-273 | 2 | 4 |
| α-helix | 278-282 | 5 | |
| β-strand | 286-288 | 3 | 3 |
| β-strand | 295-298 | 4 | 3 |
| α-helix | 299-312 | 14 | |
| α-helix | 320-323 | 4 | |
| β-strand | 329-331 | 3 | 5 |
| α-helix | 338-340 | 3 | |
| α-helix | 342-343 | 2 | |
| β-strand | 344-349 | 6 | 4 |
| β-strand | 355-361 | 7 | 4 |
| α-helix | 363-366 | 4 | |
| β-strand | 367-370 | 4 | 5 |
| β-strand | 379-383 | 5 | 5 |
| β-strand | 385-388 | 4 | 3 |
| β-strand | 392-394 | 3 | 3 |
| α-helix | 396-399 | 4 | |
| β-strand | 402-407 | 6 | 1 |
| β-strand | 412-418 | 7 | 1 |
| β-strand | 430-436 | 7 | 4 |
| α-helix | 440-443 | 4 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 67-70 | 4 | 6 |
| β-strand | 74-81 | 8 | 6 |
| β-strand | 86-93 | 8 | 6 |
| β-strand | 99-102 | 4 | 6 |
| α-helix | 115-117 | 3 | |
| β-strand | 122-130 | 9 | 6 |
| β-strand | 137-147 | 11 | 6 |
| β-strand | 155-166 | 12 | 6 |
| β-strand | 178-181 | 4 | 6 |
| α-helix | 185-187 | 3 | |
| α-helix | 197-204 | 8 | |
| β-strand | 211-215 | 5 | 6 |
| α-helix | 224-229 | 6 | |
| β-strand | 233-237 | 5 | 6 |
| α-helix | 242-244 | 3 | |
| β-strand | 245-253 | 9 | 6 |
| β-strand | 257 | 1 | 7 |
| β-strand | 260 | 1 | 7 |
| β-strand | 261 | 1 | 8 |
| β-strand | 264-269 | 6 | 9 |
| β-strand | 272-273 | 2 | 9 |
| α-helix | 278-281 | 4 | |
| β-strand | 286-288 | 3 | 8 |
| β-strand | 295-298 | 4 | 8 |
| α-helix | 299-312 | 14 | |
| α-helix | 320-323 | 4 | |
| β-strand | 329-331 | 3 | 10 |
| α-helix | 338-340 | 3 | |
| α-helix | 342-343 | 2 | |
| β-strand | 344-349 | 6 | 9 |
| β-strand | 355-361 | 7 | 9 |
| α-helix | 363-366 | 4 | |
| β-strand | 367-370 | 4 | 10 |
| β-strand | 379-383 | 5 | 10 |
| β-strand | 385-388 | 4 | 8 |
| β-strand | 392-394 | 3 | 8 |
| α-helix | 396-399 | 4 | |
| β-strand | 402-407 | 6 | 6 |
| β-strand | 412-418 | 7 | 6 |
| β-strand | 430-436 | 7 | 9 |
| α-helix | 440-443 | 4 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Beta-secretase 1 | A, B | protein | 414 | Homo sapiens | P56817 (AlphaFold model) |
>3L5E_1 Beta-secretase 1 (chains A, B) LRLPRETDEEPEEPGRRGSFVEMVDNLRGKSGQGYYVEMTVGSPPQTLNILVDTGSSNFA VGAAPHPFLHRYYQRQLSSTYRDLRKGVYVPYTQGKWEGELGTDLVSIPHGPNVTVRANI AAITESDKFFINGSNWEGILGLAYAEIARPDDSLEPFFDSLVKQTHVPNLFSLQLCGAGF PLNQSEVLASVGGSMIIGGIDHSLYTGSLWYTPIRREWYYEVIIVRVEINGQDLKMDCKE YNYDKSIVDSGTTNLRLPKKVFEAAVKSIKAASSTEKFPDGFWLGEQLVCWQAGTTPWNI FPVISLYLMGEVTNQSFRITILPQQYLRPVEDVATSQDDCYKFAISQSSTGTVMGAVIME GFYVVFDRARKRIGFAVSACHVHDEFRTAAVEGPFVTLDMEDCGYNIPQTDEST
| ID | Name | Formula | Copies |
|---|---|---|---|
| BDW | (4S)-1-(4-{[(2Z,4R)-4-(2-cyclohexylethyl)-4-(cyclohexylmethyl)-2-imino-5-oxoimi… | C32 H49 N5 O2 | 2 |
| TAR | D(-)-tartaric acid | C4 H6 O6 | 3 |
Discovery of Cyclic Acylguanidines as Highly Potent and Selective beta-Site Amyloid Cleaving Enzyme (BACE) Inhibitors: Part I-Inhibitor Design and Validation. Zhu, Z., Sun, Z.Y., Ye, Y. et al. J Med Chem (2010) 53:951-965. DOI 10.1021/jm901408p · PubMed
Other PDB entries of the same protein (UniProt P56817 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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