Crystal structure of aPKC Iota kinase domain with LLGL2 peptide. Determined by X-ray diffraction at 2.59 Å resolution. Released 20 Nov 2024.
Explore 8R3X in 3D Show helices and sheets RCSB PDB PDBe
8R3X contains 43 α-helices and 32 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 | 251-253 | 3 | |
| β-strand | 254-262 | 9 | 1 |
| β-strand | 266-273 | 8 | 1 |
| β-strand | 279-286 | 8 | 1 |
| α-helix | 287-289 | 3 | |
| α-helix | 293-308 | 16 | |
| β-strand | 315 | 1 | 2 |
| β-strand | 318-323 | 6 | 1 |
| β-strand | 327-332 | 6 | 1 |
| β-strand | 339 | 1 | 2 |
| α-helix | 340-346 | 7 | |
| α-helix | 352-371 | 20 | |
| β-strand | 375 | 1 | 3 |
| α-helix | 381-383 | 3 | |
| β-strand | 384-386 | 3 | 2 |
| β-strand | 392-394 | 3 | 2 |
| β-strand | 401 | 1 | 3 |
| β-strand | 410 | 1 | 4 |
| β-strand | 414-415 | 2 | 5 |
| α-helix | 417-419 | 3 | |
| α-helix | 422-425 | 4 | |
| β-strand | 430 | 1 | 4 |
| α-helix | 433-448 | 16 | |
| α-helix | 462-464 | 3 | |
| α-helix | 467-476 | 10 | |
| α-helix | 480-482 | 3 | |
| α-helix | 487-496 | 10 | |
| α-helix | 512-517 | 6 | |
| α-helix | 520-522 | 3 | |
| α-helix | 527-531 | 5 | |
| α-helix | 536-537 | 2 | |
| α-helix | 549-551 | 3 | |
| α-helix | 554-558 | 5 | |
| α-helix | 563-566 | 4 | |
| α-helix | 568-571 | 4 | |
| α-helix | 576-579 | 4 | |
| β-strand | 584-585 | 2 | 1 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 251-253 | 3 | |
| β-strand | 254-262 | 9 | 6 |
| β-strand | 266-273 | 8 | 6 |
| β-strand | 279-286 | 8 | 6 |
| α-helix | 287-289 | 3 | |
| α-helix | 295-309 | 15 | |
| β-strand | 315 | 1 | 7 |
| β-strand | 318-323 | 6 | 6 |
| β-strand | 327-332 | 6 | 6 |
| β-strand | 339 | 1 | 7 |
| α-helix | 340-346 | 7 | |
| α-helix | 352-371 | 20 | |
| β-strand | 375 | 1 | 8 |
| α-helix | 381-383 | 3 | |
| β-strand | 384-386 | 3 | 7 |
| β-strand | 392-394 | 3 | 7 |
| β-strand | 401 | 1 | 8 |
| β-strand | 410 | 1 | 9 |
| β-strand | 413-415 | 3 | 10 |
| α-helix | 417-419 | 3 | |
| α-helix | 422-425 | 4 | |
| β-strand | 430 | 1 | 9 |
| α-helix | 433-448 | 16 | |
| α-helix | 462-464 | 3 | |
| α-helix | 467-476 | 10 | |
| α-helix | 480-482 | 3 | |
| α-helix | 487-496 | 10 | |
| α-helix | 512-517 | 6 | |
| α-helix | 520-522 | 3 | |
| α-helix | 527-531 | 5 | |
| α-helix | 536-537 | 2 | |
| α-helix | 549-551 | 3 | |
| α-helix | 554-557 | 4 | |
| α-helix | 568-571 | 4 | |
| α-helix | 576-579 | 4 | |
| β-strand | 584-585 | 2 | 6 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 654-655 | 2 | 5 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 654-656 | 3 | 10 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Protein kinase C iota type | A, B | protein | 356 | Homo sapiens | P41743 (AlphaFold model) |
| LLGL scribble cell polarity complex component 2 | C, D | protein | 20 | Homo sapiens | Q6P1M3 (AlphaFold model) |
>8R3X_1 Protein kinase C iota type (chains A, B) ESGKASSSLGLQDFDLLRVIGRGSYAKVLLVRLKKTDRIYAMKVVKKELVNDDEDIDWVQ TEKHVFEQASNHPFLVGLHSCFQTESRLFFVIEYVNGGDLMFHMQRQRKLPEEHARFYSA EISLALNYLHERGIIYRDLKLDNVLLDSEGHIKLTDYGMCKEGLRPGDTTSTFCGTPNYI APEILRGEDYGFSVDWWALGVLMFEMMAGRSPFDIVGSSDNPDQNTEDYLFQVILEKQIR IPRSLSVKAASVLKSFLNKDPKERLGCHPQTGFADIQGHPFFRNVDWDMMEQKQVVPPFK PNISGEFGLDNFDSQFTNEPVQLTPDDDDIVRKIDQSEFEGFEYINPLLMSAEECV
>8R3X_2 LLGL scribble cell polarity complex component 2 (chains C, D) SRVKSLKKSLRQSFRRMRKS
Capture, mutual inhibition and release mechanism for aPKC-Par6 and its multisite polarity substrate Lgl. Earl, C.P., Cobbaut, M., Barros-Carvalho, A. et al. Nat Struct Mol Biol (2025) 32:729-739. DOI 10.1038/s41594-024-01425-0 · PubMed
Other PDB entries of the same protein (UniProt P41743 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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