MAGI1_2 complexed with a phosphomimetic RSK1 peptide. Determined by X-ray diffraction at 2.3 Å resolution. Released 1 Apr 2020.
Explore 6TWY in 3D Show helices and sheets RCSB PDB PDBe
6TWY contains 48 α-helices and 17 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 | 463-465 | 3 | |
| β-strand | 469-476 | 8 | 1 |
| β-strand | 478 | 1 | 2 |
| β-strand | 481 | 1 | 2 |
| β-strand | 484-488 | 5 | 1 |
| β-strand | 496-501 | 6 | 1 |
| α-helix | 506-510 | 5 | |
| β-strand | 518-522 | 5 | 1 |
| β-strand | 526 | 1 | 1 |
| α-helix | 532-541 | 10 | |
| β-strand | 547-554 | 8 | 1 |
| α-helix | 574-585 | 12 | |
| α-helix | 592-599 | 8 | |
| α-helix | 604-618 | 15 | |
| α-helix | 622-629 | 8 | |
| α-helix | 632-642 | 11 | |
| α-helix | 645-656 | 12 | |
| α-helix | 664-673 | 10 | |
| α-helix | 676-690 | 15 | |
| α-helix | 694-701 | 8 | |
| α-helix | 704-714 | 11 | |
| α-helix | 718-721 | 4 | |
| α-helix | 727-739 | 13 | |
| α-helix | 749-758 | 10 | |
| α-helix | 761-774 | 14 | |
| α-helix | 779-786 | 8 | |
| α-helix | 789-803 | 15 | |
| α-helix | 805-817 | 13 | |
| α-helix | 824-834 | 11 | |
| α-helix | 839-850 | 12 | |
| α-helix | 854-861 | 8 | |
| α-helix | 864-874 | 11 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 463-465 | 3 | |
| β-strand | 469-476 | 8 | 3 |
| β-strand | 478 | 1 | 4 |
| β-strand | 481 | 1 | 4 |
| β-strand | 484-488 | 5 | 3 |
| β-strand | 496-501 | 6 | 3 |
| α-helix | 506-510 | 5 | |
| β-strand | 518-522 | 5 | 3 |
| β-strand | 525-526 | 2 | 3 |
| α-helix | 532-541 | 10 | |
| α-helix | 543 | 1 | |
| β-strand | 547-554 | 8 | 3 |
| α-helix | 574-586 | 13 | |
| α-helix | 592-599 | 8 | |
| α-helix | 604-618 | 15 | |
| α-helix | 622-629 | 8 | |
| α-helix | 632-642 | 11 | |
| α-helix | 645-656 | 12 | |
| α-helix | 664-673 | 10 | |
| α-helix | 676-690 | 15 | |
| α-helix | 694-701 | 8 | |
| α-helix | 704-714 | 11 | |
| α-helix | 718-722 | 5 | |
| α-helix | 727-740 | 14 | |
| α-helix | 749-758 | 10 | |
| α-helix | 761-771 | 11 | |
| α-helix | 779-786 | 8 | |
| α-helix | 789-817 | 29 | |
| α-helix | 824-833 | 10 | |
| α-helix | 839-850 | 12 | |
| α-helix | 854-861 | 8 | |
| α-helix | 864-874 | 11 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 732-734 | 3 | 3 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Membrane-associated guanylate kinase, WW and PDZ domain-containing protein 1,Annexin A2 | A, B | protein | 427 | Homo sapiens | P07355 (AlphaFold model), Q96QZ7 (AlphaFold model) |
| Phosphomimetic RSK1 peptide | C | protein | 11 | Homo sapiens | Q15418 (AlphaFold model) |
>6TWY_1 Membrane-associated guanylate kinase, WW and PDZ domain-containing protein 1,Annexin A2 (chains A, B) GSMGKPFFTRNPSELKGKFIHTKLRKSSRGFGFTVVGGDEPDEFLQIKSLVLDGPAALDG KMETGDVIVSVNDTCVLGHTHAQVVKIFQSIPIGASVDLELCRGYPLGSSAYGSVKAYTN FDAERDALNIETAIKTKGVDEVTIVNILTNRSNEQRQDIAFAYQRRTKKELASALKSALS GHLETVILGLLKTPAQYDASELKASMKGLGTDEDSLIEIICSRTNQELQEINRVYKEMYK TDLEKDIISDTSGDFRKLMVALAKGRRAEDGSVIDYELIDQDARDLYDAGVKRKGTDVPK WISIMTERSVPHLQKVFDRYKSYSPYDMLESIRKEVKGDLENAFLNLVQCIQNKPLYFAD RLYDSMKGKGTRDKVLIRIMVSRSEVDMLKIRSEFKRKYGKSLYYYIQQDTKGDYQKALL YLCGGDD
>6TWY_2 Phosphomimetic RSK1 peptide (chains C) RRVRKLPETTL
Water and common crystallization additives (GOL) are not listed.
Dual Specificity PDZ- and 14-3-3-Binding Motifs: A Structural and Interactomics Study. Gogl, G., Jane, P., Caillet-Saguy, C. et al. Structure (2020) 28:747-759.e3. DOI 10.1016/j.str.2020.03.010 · PubMed
Other PDB entries of the same protein (UniProt P07355 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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