XChem group deposition -- Crystal Structure of human ACVR1 in complex with FM010926a. Determined by X-ray diffraction at 1.3 Å resolution. Released 23 Jun 2021.
Explore 5S7T in 3D Show helices and sheets RCSB PDB PDBe
5S7T contains 35 α-helices and 35 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 | 209-217 | 9 | 1 |
| β-strand | 220-227 | 8 | 1 |
| β-strand | 230-237 | 8 | 1 |
| α-helix | 239-241 | 3 | |
| α-helix | 242-254 | 13 | |
| β-strand | 262 | 1 | 2 |
| α-helix | 263-264 | 2 | |
| β-strand | 265-272 | 8 | 1 |
| β-strand | 277-283 | 7 | 1 |
| β-strand | 290 | 1 | 2 |
| α-helix | 291-296 | 6 | |
| β-strand | 300 | 1 | 3 |
| α-helix | 302-320 | 19 | |
| β-strand | 323 | 1 | 4 |
| β-strand | 329 | 1 | 4 |
| β-strand | 332-333 | 2 | 5 |
| α-helix | 339-341 | 3 | |
| β-strand | 342-344 | 3 | 2 |
| β-strand | 350-352 | 3 | 2 |
| β-strand | 359-360 | 2 | 5 |
| α-helix | 379-381 | 3 | |
| α-helix | 384-387 | 4 | |
| α-helix | 396-415 | 20 | |
| β-strand | 418 | 1 | 3 |
| β-strand | 420 | 1 | 6 |
| β-strand | 423 | 1 | 6 |
| α-helix | 425-427 | 3 | |
| α-helix | 441-445 | 5 | |
| α-helix | 446-450 | 5 | |
| α-helix | 459-463 | 5 | |
| α-helix | 465-475 | 11 | |
| α-helix | 482-484 | 3 | |
| α-helix | 486-487 | 2 | |
| α-helix | 488-496 | 9 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 209-217 | 9 | 7 |
| β-strand | 220-227 | 8 | 7 |
| β-strand | 230-236 | 7 | 7 |
| α-helix | 239-241 | 3 | |
| α-helix | 242-252 | 11 | |
| α-helix | 255-257 | 3 | |
| β-strand | 262 | 1 | 8 |
| α-helix | 263-264 | 2 | |
| β-strand | 265-273 | 9 | 7 |
| β-strand | 276-284 | 9 | 7 |
| β-strand | 290 | 1 | 8 |
| α-helix | 291-295 | 5 | |
| β-strand | 300 | 1 | 9 |
| α-helix | 302-320 | 19 | |
| β-strand | 323 | 1 | 10 |
| β-strand | 329 | 1 | 10 |
| β-strand | 331-333 | 3 | 11 |
| α-helix | 339-341 | 3 | |
| β-strand | 342-344 | 3 | 8 |
| β-strand | 350-352 | 3 | 8 |
| β-strand | 359-362 | 4 | 11 |
| β-strand | 367-369 | 3 | 11 |
| α-helix | 379-381 | 3 | |
| α-helix | 384-387 | 4 | |
| α-helix | 396-415 | 20 | |
| β-strand | 418 | 1 | 9 |
| β-strand | 420 | 1 | 12 |
| β-strand | 423 | 1 | 12 |
| α-helix | 425-427 | 3 | |
| α-helix | 441-445 | 5 | |
| α-helix | 446-450 | 5 | |
| α-helix | 459-463 | 5 | |
| α-helix | 465-477 | 13 | |
| α-helix | 482-484 | 3 | |
| α-helix | 486-487 | 2 | |
| α-helix | 488-497 | 10 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Activin receptor type-1 | A, B | protein | 301 | Homo sapiens | Q04771 (AlphaFold model) |
>5S7T_1 Activin receptor type-1 (chains A, B) SMQRTVARDITLLECVGKGRYGEVWRGSWQGENVAVKIFSSRDEKSWFRETELYNTVMLR HENILGFIASDMTSRHSSTQLWLITHYHEMGSLYDYLQLTTLDTVSCLRIVLSIASGLAH LHIEIFGTQGKPAIAHRDLKSKNILVKKNGQCCIADLGLAVMHSQSTNQLDVGNNPRVGT KRYMAPEVLDETIQVDCFDSYKRVDIWAFGLVLWEVARRMVSNGIVEDYKPPFYDVVPND PSFEDMRKVVCVDQQRPNIPNRWFSDPTLTSLAKLMKECWYQNPSARLTALRIKKTLTKI D
| ID | Name | Formula | Copies |
|---|---|---|---|
| XGJ | (3S)-1,2,4-triazolidin-3-amine | C2 H8 N4 | 6 |
| LU8 | 4-methyl-3-[4-(1-methylpiperidin-4-yl)phenyl]-5-(3,4,5-trimethoxyphenyl)pyridine | C27 H32 N2 O3 | 4 |
Water and common crystallization additives (SO4, DMS, EDO) are not listed.
XChem group deposition. Williams, E.P., Adamson, R.J., Smil, D. et al. To be published.
Other PDB entries of the same protein (UniProt Q04771 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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