Crystal structure of OspC3-calmodulin-caspase-4 complex. Determined by X-ray diffraction at 2.75 Å resolution. Released 25 Jan 2023.
Explore 7WR4 in 3D Show helices and sheets RCSB PDB PDBe
7WR4 contains 50 α-helices and 28 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 | 52-77 | 26 | |
| α-helix | 80-84 | 5 | |
| α-helix | 90-92 | 3 | |
| α-helix | 100-119 | 20 | |
| α-helix | 125-135 | 11 | |
| β-strand | 139-145 | 7 | 1 |
| β-strand | 150 | 1 | 2 |
| β-strand | 154-156 | 3 | 2 |
| α-helix | 159-166 | 8 | |
| α-helix | 172-175 | 4 | |
| α-helix | 176-180 | 5 | |
| β-strand | 186-193 | 8 | 1 |
| β-strand | 206 | 1 | 3 |
| β-strand | 209 | 1 | 3 |
| β-strand | 214-218 | 5 | 1 |
| β-strand | 226-228 | 3 | 1 |
| α-helix | 237-239 | 3 | |
| α-helix | 240-242 | 3 | |
| α-helix | 246-252 | 7 | |
| α-helix | 256-259 | 4 | |
| β-strand | 276-277 | 2 | 1 |
| α-helix | 281-295 | 15 | |
| α-helix | 299-305 | 7 | |
| α-helix | 312-322 | 11 | |
| β-strand | 326-330 | 5 | 1 |
| β-strand | 333-335 | 3 | 2 |
| β-strand | 339-342 | 4 | 1 |
| α-helix | 348-354 | 7 | |
| α-helix | 357-363 | 7 | |
| α-helix | 367-379 | 13 | |
| α-helix | 383-392 | 10 | |
| α-helix | 397-404 | 8 | |
| α-helix | 410-414 | 5 | |
| α-helix | 417-422 | 6 | |
| α-helix | 425-427 | 3 | |
| α-helix | 428-436 | 9 | |
| α-helix | 444-446 | 3 | |
| β-strand | 449 | 1 | 4 |
| α-helix | 455-462 | 8 | |
| α-helix | 465-473 | 9 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 10-12 | 3 | |
| α-helix | 13-18 | 6 | |
| β-strand | 27-28 | 2 | 5 |
| α-helix | 30-32 | 3 | |
| α-helix | 33-39 | 7 | |
| α-helix | 46-55 | 10 | |
| β-strand | 64-65 | 2 | 5 |
| α-helix | 66-78 | 13 | |
| α-helix | 81-82 | 2 | |
| α-helix | 83-91 | 9 | |
| β-strand | 100 | 1 | 6 |
| α-helix | 103-111 | 9 | |
| α-helix | 119-129 | 11 | |
| β-strand | 138 | 1 | 6 |
| α-helix | 139-146 | 8 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 107-110 | 4 | |
| α-helix | 111-120 | 10 | |
| α-helix | 122-124 | 3 | |
| β-strand | 125 | 1 | 7 |
| β-strand | 137-142 | 6 | 4 |
| α-helix | 155-168 | 14 | |
| β-strand | 172-177 | 6 | 4 |
| α-helix | 181-192 | 12 | |
| α-helix | 195-199 | 5 | |
| β-strand | 203-208 | 6 | 4 |
| β-strand | 211 | 1 | 8 |
| β-strand | 215-217 | 3 | 8 |
| β-strand | 228-230 | 3 | 8 |
| α-helix | 231-237 | 7 | |
| α-helix | 244-246 | 3 | |
| β-strand | 251-256 | 6 | 4 |
| α-helix | 291-296 | 6 | |
| β-strand | 300-305 | 6 | 4 |
| α-helix | 321-333 | 13 | |
| α-helix | 339-349 | 11 | |
| α-helix | 356-358 | 3 | |
| β-strand | 361-363 | 3 | 4 |
| β-strand | 370 | 1 | 7 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| OspC3 | A | protein | 430 | Shigella flexneri | A0A0H2US87 (AlphaFold model) |
| Calmodulin-1 | B | protein | 149 | Homo sapiens | P0DP23 (AlphaFold model) |
| Caspase-4 | C | protein | 280 | Homo sapiens | P49662 (AlphaFold model) |
>7WR4_1 OspC3 (chains A) GPLGSGRPDHCANTVKNFLRKSIAAQSYSKMFSQGTSFKSLNLSLEAPSGARSSFRSLEH LDKVSRHYISEIIQKVHPLSSDERHLLSIIINSNFNFRHQSNSNLSNNILNIKSFDKIQS ENIQTHKNTYSEDIKEISNHDFVFFGVEISNHQEKLPLNKTHHTVDFGANAYIIDHDSPY GYMTLTDHFDNAIPPVFYHEHQSFFLDNFKEVVDEVSRYVHGNQGKTDVPIFNTKDMRLG IGLHLIDFIRKSKDQGFREFCYNKNIDPVSLDRIINFVFQLEYHIPRMLSTDNFKKIKLR DISLEDAIKASNYEEINNKVTDKKMAHQALAYSLGNKKADIALYLLSKFNFTKQDVAEME KMKNNRYCNLYDVEYLLSKDGANYKVLEYFINNGLVDVNKKFQKVNSGDTMLDNAMKSKD SKMIDFLLKN
>7WR4_2 Calmodulin-1 (chains B) MADQLTEEQIAEFKEAFSLFDKDGDGTITTKELGTVMRSLGQNPTEAELQDMINEVDADG NGTIDFPEFLTMMARKMKDTDSEEEIREAFRVFDKDGNGYISAAELRHVMTNLGEKLTDE EVDEMIREADIDGDGQVNYEEFVQMMTAK
>7WR4_3 Caspase-4 (chains C) SGRPSTDALKLCPHEEFLRLCKERAEEIYPIKERNNRTRLALIICNTEFDHLPPRNGADF DITGMKELLEGLDYSVDVEENLTARDMESALRAFATRPEHKSSDSTFLVLMSHGILEGIC GTVHDEKKPDVLLYDTIFQIFNNRNCLSLKDKPKVIIVQAARGANRGELWVRDSPASLEV ASSQSSENLEEDAVYKTHVEKDFIAFCSSTPHNVSWRDSTMGSIFITQLITCFQKYSWCC HLEEVFRKVQQSFETPRAKAQMPTIERLSMTRYFYLFPGN
Structural mechanisms of calmodulin activation of Shigella effector OspC3 to ADP-riboxanate caspase-4/11 and block pyroptosis. Hou, Y., Zeng, H., Li, Z. et al. Nat Struct Mol Biol (2023) 30:261-272. DOI 10.1038/s41594-022-00888-3 · PubMed
Other PDB entries of the same protein (UniProt A0A0H2US87 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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