Crystal Structure of Plasmodium falciparum actin I (H74Q) in the Mg-K-ATP state. Determined by X-ray diffraction at 2.0 Å resolution. Released 26 Jun 2019.
Explore 6I4G in 3D Show helices and sheets RCSB PDB PDBe
6I4G contains 60 α-helices and 56 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 | 7-8 | 2 | |
| β-strand | 9-13 | 5 | 1 |
| β-strand | 17-22 | 6 | 1 |
| β-strand | 30-33 | 4 | 1 |
| β-strand | 36-38 | 3 | 2 |
| β-strand | 54-55 | 2 | 2 |
| α-helix | 57-61 | 5 | |
| α-helix | 66 | 1 | |
| β-strand | 67-69 | 3 | 2 |
| β-strand | 72-73 | 2 | 3 |
| β-strand | 76-77 | 2 | 3 |
| α-helix | 80-88 | 9 | |
| α-helix | 89-95 | 7 | |
| β-strand | 97 | 1 | 4 |
| α-helix | 99-101 | 3 | |
| β-strand | 104-108 | 5 | 1 |
| α-helix | 114-126 | 13 | |
| β-strand | 132-137 | 6 | 1 |
| α-helix | 138-145 | 8 | |
| β-strand | 151-156 | 6 | 5 |
| β-strand | 161-167 | 7 | 5 |
| β-strand | 170-171 | 2 | 5 |
| α-helix | 173-175 | 3 | |
| β-strand | 177-179 | 3 | 5 |
| α-helix | 183-197 | 15 | |
| α-helix | 204-217 | 14 | |
| β-strand | 219 | 1 | 6 |
| α-helix | 224-232 | 9 | |
| β-strand | 239-242 | 4 | 7 |
| β-strand | 248-251 | 4 | 7 |
| α-helix | 254-260 | 7 | |
| α-helix | 265-268 | 4 | |
| α-helix | 272-274 | 3 | |
| α-helix | 275-284 | 10 | |
| α-helix | 288-290 | 3 | |
| α-helix | 291-295 | 5 | |
| β-strand | 298-301 | 4 | 5 |
| α-helix | 303-305 | 3 | |
| β-strand | 308 | 1 | 6 |
| α-helix | 310-321 | 12 | |
| α-helix | 327-328 | 2 | |
| β-strand | 330-331 | 2 | 5 |
| α-helix | 336-338 | 3 | |
| α-helix | 339-347 | 9 | |
| α-helix | 351-355 | 5 | |
| β-strand | 358-359 | 2 | 1 |
| α-helix | 360-366 | 7 | |
| α-helix | 368-371 | 4 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 9-13 | 5 | 8 |
| β-strand | 17-22 | 6 | 8 |
| β-strand | 30-33 | 4 | 8 |
| β-strand | 36-38 | 3 | 9 |
| β-strand | 54-55 | 2 | 9 |
| α-helix | 57-61 | 5 | |
| β-strand | 67-69 | 3 | 9 |
| β-strand | 72-73 | 2 | 10 |
| β-strand | 76-77 | 2 | 10 |
| α-helix | 80-88 | 9 | |
| α-helix | 89-95 | 7 | |
| α-helix | 99-101 | 3 | |
| β-strand | 104-108 | 5 | 8 |
| α-helix | 114-126 | 13 | |
| β-strand | 132-137 | 6 | 8 |
| α-helix | 138-145 | 8 | |
| β-strand | 151-156 | 6 | 11 |
| β-strand | 161-167 | 7 | 11 |
| β-strand | 170-171 | 2 | 11 |
| α-helix | 173-175 | 3 | |
| β-strand | 177-179 | 3 | 11 |
| α-helix | 183-197 | 15 | |
| α-helix | 204-217 | 14 | |
| α-helix | 224-232 | 9 | |
| β-strand | 239-242 | 4 | 12 |
| β-strand | 248-251 | 4 | 12 |
| α-helix | 254-260 | 7 | |
| α-helix | 265-268 | 4 | |
| α-helix | 275-284 | 10 | |
| β-strand | 286 | 1 | 4 |
| α-helix | 288-295 | 8 | |
| β-strand | 298-301 | 4 | 11 |
| α-helix | 303-305 | 3 | |
| α-helix | 310-321 | 12 | |
| β-strand | 330-331 | 2 | 11 |
| α-helix | 336-338 | 3 | |
| α-helix | 339-347 | 9 | |
| α-helix | 351-355 | 5 | |
| β-strand | 358-359 | 2 | 8 |
| α-helix | 360-366 | 7 | |
| α-helix | 368-372 | 5 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 8-10 | 3 | |
| β-strand | 16-23 | 8 | 13 |
| β-strand | 26-29 | 4 | 13 |
| α-helix | 30-31 | 2 | |
| α-helix | 32-34 | 3 | |
| β-strand | 37-39 | 3 | 14 |
| β-strand | 43-50 | 8 | 13 |
| β-strand | 58-65 | 8 | 13 |
| α-helix | 71-87 | 17 | |
| β-strand | 93-98 | 6 | 13 |
| α-helix | 104-108 | 5 | |
| β-strand | 115-117 | 3 | 14 |
| α-helix | 121-123 | 3 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 6-10 | 5 | |
| β-strand | 16-22 | 7 | 15 |
| β-strand | 27-29 | 3 | 15 |
| α-helix | 30-31 | 2 | |
| α-helix | 32-34 | 3 | |
| β-strand | 37-39 | 3 | 16 |
| β-strand | 43-51 | 9 | 15 |
| β-strand | 57-65 | 9 | 15 |
| α-helix | 71-87 | 17 | |
| α-helix | 92 | 1 | |
| β-strand | 93-98 | 6 | 15 |
| α-helix | 104-107 | 4 | |
| β-strand | 115-117 | 3 | 16 |
| α-helix | 121-123 | 3 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Actin-1 | A, B | protein | 378 | Plasmodium falciparum | Q8I4X0 (AlphaFold model) |
| Gelsolin | G, H | protein | 127 | Mus musculus | P13020 (AlphaFold model) |
>6I4G_1 Actin-1 (chains A, B) GAMGEEDVQALVVDNGSGNVKAGVAGDDAPRSVFPSIVGRPKNPGIMVGMEEKDAFVGDE AQTKRGILTLKYPIEQGIVTNWDDMEKIWHHTFYNELRAAPEEHPVLLTEAPLNPKGNRE RMTQIMFESFNVPAMYVAIQAVLSLYSSGRTTGIVLDSGDGVSHTVPIYEGYALPHAIMR LDLAGRDLTEYLMKILHERGYGFSTSAEKEIVRDIKEKLCYIALNFDEEMKTSEQSSDIE KSYELPDGNIITVGNERFRCPEALFQPSFLGKEAAGIHTTTFNSIKKCDVDIRKDLYGNI VLSGGTTMYEGIGERLTRDITTLAPSTMKIKVVAPPERKYSVWIGGSILSSLSTFQQMWI TKEEYDESGPSIVHRKCF
>6I4G_2 Gelsolin (chains G, H) GPMVVEHPEFLKAGKEPGLQIWRVEKFDLVPVPPNLYGDFFTGDAYVILKTVQLRNGNLQ YDLHYWLGNECSQDESGAAAIFTVQLDDYLNGRAVQHREVQGFESSTFSGYFKSGLKYKK GGVASGF
| ID | Name | Formula | Copies |
|---|---|---|---|
| SCN | Thiocyanate ion | C N S | 1 |
| CA | Calcium ion | Ca | 4 |
| MG | Magnesium ion | Mg | 2 |
| ATP | Adenosine-5'-triphosphate | C10 H16 N5 O13 P3 | 2 |
Water and common crystallization additives (BME, K) are not listed.
Atomic view into Plasmodium actin polymerization, ATP hydrolysis, and fragmentation. Kumpula, E.P., Lopez, A.J., Tajedin, L. et al. PLoS Biol (2019) 17:e3000315-e3000315. DOI 10.1371/journal.pbio.3000315 · PubMed
Other PDB entries of the same protein (UniProt Q8I4X0 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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