Crystal structure of Atg7CTD-Atg8-MgATP complex in form II. Determined by X-ray diffraction at 2.15 Å resolution. Released 28 Mar 2018.
Explore 5YEC in 3D Show helices and sheets RCSB PDB PDBe
5YEC contains 47 α-helices and 39 β-strands across 4 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 |
|---|---|---|---|
| α-helix | 297-313 | 17 | |
| α-helix | 319-323 | 5 | |
| β-strand | 326-330 | 5 | 1 |
| α-helix | 334-345 | 12 | |
| β-strand | 350-355 | 6 | 1 |
| β-strand | 358 | 1 | 2 |
| α-helix | 372-374 | 3 | |
| β-strand | 378 | 1 | 2 |
| α-helix | 379-390 | 12 | |
| β-strand | 395-400 | 6 | 1 |
| α-helix | 402-404 | 3 | |
| α-helix | 413-429 | 17 | |
| β-strand | 432-435 | 4 | 1 |
| α-helix | 440-442 | 3 | |
| α-helix | 444-452 | 9 | |
| β-strand | 456-462 | 7 | 1 |
| β-strand | 466-471 | 6 | 1 |
| α-helix | 472-473 | 2 | |
| β-strand | 483 | 1 | 3 |
| α-helix | 488-492 | 5 | |
| α-helix | 513-530 | 18 | |
| α-helix | 532-534 | 3 | |
| β-strand | 539-540 | 2 | 4 |
| β-strand | 543-544 | 2 | 4 |
| β-strand | 548-552 | 5 | 1 |
| β-strand | 557-561 | 5 | 1 |
| β-strand | 564 | 1 | 3 |
| α-helix | 565-566 | 2 | |
| α-helix | 574-583 | 10 | |
| α-helix | 585-593 | 9 | |
| α-helix | 595-602 | 8 | |
| α-helix | 604-615 | 12 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 5-8 | 4 | |
| α-helix | 11-24 | 14 | |
| β-strand | 28-35 | 8 | 5 |
| α-helix | 42-44 | 3 | |
| β-strand | 48-52 | 5 | 5 |
| β-strand | 56 | 1 | 6 |
| α-helix | 57-67 | 11 | |
| β-strand | 77-79 | 3 | 5 |
| β-strand | 90 | 1 | 6 |
| α-helix | 91-98 | 8 | |
| α-helix | 104 | 1 | |
| β-strand | 105-110 | 6 | 5 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 303-313 | 11 | |
| α-helix | 320-323 | 4 | |
| β-strand | 326-330 | 5 | 7 |
| α-helix | 334-345 | 12 | |
| β-strand | 350-355 | 6 | 7 |
| β-strand | 358 | 1 | 8 |
| α-helix | 372-374 | 3 | |
| β-strand | 378 | 1 | 8 |
| α-helix | 379-390 | 12 | |
| β-strand | 395-400 | 6 | 7 |
| α-helix | 402-404 | 3 | |
| α-helix | 413-429 | 17 | |
| β-strand | 432-435 | 4 | 7 |
| α-helix | 440-442 | 3 | |
| α-helix | 444-452 | 9 | |
| β-strand | 456-462 | 7 | 7 |
| β-strand | 466-471 | 6 | 7 |
| α-helix | 472-473 | 2 | |
| β-strand | 483 | 1 | 9 |
| α-helix | 486-492 | 7 | |
| α-helix | 508-511 | 4 | |
| α-helix | 512-529 | 18 | |
| α-helix | 532-534 | 3 | |
| β-strand | 539-540 | 2 | 10 |
| β-strand | 543-544 | 2 | 10 |
| β-strand | 548-552 | 5 | 7 |
| β-strand | 557-561 | 5 | 7 |
| β-strand | 564 | 1 | 9 |
| α-helix | 565-566 | 2 | |
| α-helix | 574-583 | 10 | |
| α-helix | 585-593 | 9 | |
| α-helix | 595-602 | 8 | |
| α-helix | 604-614 | 11 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 5-8 | 4 | |
| α-helix | 11-24 | 14 | |
| β-strand | 28-34 | 7 | 11 |
| β-strand | 48-52 | 5 | 11 |
| β-strand | 56 | 1 | 12 |
| α-helix | 57-68 | 12 | |
| β-strand | 90 | 1 | 12 |
| α-helix | 91-98 | 8 | |
| β-strand | 105-108 | 4 | 11 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Ubiquitin-like modifier-activating enzyme ATG7 | A, C | protein | 340 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | P38862 (AlphaFold model) |
| Autophagy-related protein 8 | B, D | protein | 119 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | P38182 (AlphaFold model) |
>5YEC_1 Ubiquitin-like modifier-activating enzyme ATG7 (chains A, C) GPHMLKIADQSVDLNLKLMKWRILPDLNLDIIKNTKVLLLGAGTLGCYVSRALIAWGVRK ITFVDNGTVSYSNPVRQALYNFEDCGKPKAELAAASLKRIFPLMDATGVKLSIPMIGHKL VNEEAQHKDFDRLRALIKEHDIIFLLVDSRESRWLPSLLSNIENKTVINAALGFDSYLVM RHGNRDEQSSKQLGCYFCHDVVAPTDSLTDRTLDQMCTVTRPGVAMMASSLAVELMTSLL QTKYSGSETTVLGDIPHQIRGFLHNFSILKLETPAYEHCPACSPKVIEAFTDLGWEFVKK ALEHPLYLEEISGLSVIKQEVERLGNDVFEWEDDESDEIA
>5YEC_2 Autophagy-related protein 8 (chains B, D) GPHMKSTFKSEYPFEKRKAESERIADRFPNRIPVICEKAEKSDIPEIDKRKYLVPADLTV GQFVYVIRKRIMLPPEKAIFIFVNDTLPPTAALMSAIYQEHKDKDGFLYVTYSGENTFG
Atg7 Activates an Autophagy-Essential Ubiquitin-like Protein Atg8 through Multi-Step Recognition. Yamaguchi, M., Satoo, K., Suzuki, H. et al. J Mol Biol (2018) 430:249-257. DOI 10.1016/j.jmb.2017.12.002 · PubMed
Other PDB entries of the same protein (UniProt P38862 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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