Crystal Structure of Calcineurin in Complex with the Calcineurin-Inhibiting Domain of the African Swine Fever Virus Protein A238L. Determined by X-ray diffraction at 1.7 Å resolution. Released 6 Mar 2013.
Explore 4F0Z in 3D Show helices and sheets RCSB PDB PDBe
4F0Z contains 38 α-helices and 27 β-strands across 3 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 | 22-25 | 4 | |
| α-helix | 27-28 | 2 | |
| β-strand | 29 | 1 | 1 |
| α-helix | 30 | 1 | |
| α-helix | 31-34 | 4 | |
| β-strand | 35 | 1 | 2 |
| β-strand | 41 | 1 | 2 |
| α-helix | 43-51 | 9 | |
| β-strand | 56 | 1 | 1 |
| α-helix | 58-73 | 16 | |
| β-strand | 78-81 | 4 | 3 |
| α-helix | 82 | 1 | |
| β-strand | 85-88 | 4 | 4 |
| β-strand | 90 | 1 | 5 |
| α-helix | 95-105 | 11 | |
| β-strand | 113-115 | 3 | 4 |
| α-helix | 126-139 | 14 | |
| β-strand | 144-146 | 3 | 4 |
| α-helix | 154-159 | 6 | |
| α-helix | 162-169 | 8 | |
| α-helix | 172-183 | 12 | |
| β-strand | 188-191 | 4 | 3 |
| β-strand | 195-198 | 4 | 3 |
| α-helix | 210-213 | 4 | |
| α-helix | 221-222 | 2 | |
| α-helix | 226-232 | 7 | |
| β-strand | 234-235 | 2 | 6 |
| β-strand | 248-250 | 3 | 6 |
| β-strand | 258-260 | 3 | 6 |
| α-helix | 262-271 | 10 | |
| β-strand | 276-279 | 4 | 3 |
| β-strand | 288-290 | 3 | 3 |
| α-helix | 292 | 1 | |
| β-strand | 293 | 1 | 7 |
| α-helix | 294 | 1 | |
| β-strand | 300 | 1 | 7 |
| β-strand | 302-305 | 4 | 3 |
| β-strand | 306 | 1 | 5 |
| α-helix | 311-313 | 3 | |
| α-helix | 317-318 | 2 | |
| β-strand | 319-325 | 7 | 4 |
| β-strand | 328-334 | 7 | 4 |
| α-helix | 344-346 | 3 | |
| α-helix | 349-369 | 21 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 8-10 | 3 | |
| α-helix | 16-29 | 14 | |
| β-strand | 36-37 | 2 | 8 |
| α-helix | 39-43 | 5 | |
| α-helix | 46-48 | 3 | |
| α-helix | 54-61 | 8 | |
| β-strand | 69-70 | 2 | 8 |
| α-helix | 71-79 | 9 | |
| α-helix | 87-98 | 12 | |
| β-strand | 105-106 | 2 | 9 |
| α-helix | 108-119 | 12 | |
| α-helix | 120-122 | 3 | |
| α-helix | 125-139 | 15 | |
| β-strand | 147-148 | 2 | 9 |
| α-helix | 149-156 | 8 | |
| α-helix | 157-159 | 3 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 206 | 1 | |
| β-strand | 207-211 | 5 | 4 |
| α-helix | 214-216 | 3 | |
| α-helix | 219-223 | 5 | |
| α-helix | 231-233 | 3 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Serine/threonine-protein phosphatase 2B catalytic subunit alpha isoform | A | protein | 372 | Homo sapiens | Q08209 (AlphaFold model) |
| Calcineurin subunit B type 1 | B | protein | 170 | Homo sapiens | P63098 (AlphaFold model) |
| Ankyrin repeat domain-containing protein A238L | C | protein | 43 | African swine fever virus Malawi LIL 20/1 | O36972 |
>4F0Z_1 Serine/threonine-protein phosphatase 2B catalytic subunit alpha isoform (chains A) GHMSEPKAIDPKLSTTDRVVKAVPFPPSHRLTAKEVFDNDGKPRVDILKAHLMKEGRLEE SVALRIITEGASILRQEKNLLDIDAPVTVCGDIHGQFFDLMKLFEVGGSPANTRYLFLGD YVDRGYFSIECVLYLWALKILYPKTLFLLRGNHECRHLTEYFTFKQECKIKYSERVYDAC MDAFDCLPLAALMNQQFLCVHGGLSPEINTLDDIRKLDRFKEPPAYGPMCDILWSDPLED FGNEKTQEHFTHNTVRGCSYFYSYPAVCEFLQHNNLLSILRAHEAQDAGYRMYRKSQTTG FPSLITIFSAPNYLDVYNNKAAVLKYENNVMNIRQFNCSPHPYWLPNFMDVFTWSLPFVG EKVTEMLVNVLN
>4F0Z_2 Calcineurin subunit B type 1 (chains B) MGNEASYPLEMCSHFDADEIKRLGKRFKKLDLDNSGSLSVEEFMSLPELQQNPLVQRVID IFDTDGNGEVDFKEFIEGVSQFSVKGDKEQKLRFAFRIYDMDKDGYISNGELFQVLKMMV GNNLKDTQLQQIVDKTIINADKDGDGRISFEEFCAVVGGLDIHKKMVVDV
>4F0Z_3 Ankyrin repeat domain-containing protein A238L (chains C) GHMRRFKKKPKIIITGCEDNVYEKLPEQNSNFLCVKKLNKYGK
| ID | Name | Formula | Copies |
|---|---|---|---|
| CA | Calcium ion | Ca | 4 |
Water and common crystallization additives (GOL) are not listed.
The molecular mechanism of substrate engagement and immunosuppressant inhibition of calcineurin. Grigoriu, S., Bond, R., Cossio, P. et al. PLoS Biol (2013) 11:e1001492-e1001492. DOI 10.1371/journal.pbio.1001492 · PubMed
Other PDB entries of the same protein (UniProt Q08209 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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