Structure of Xenopus KCNQ1-CaM in complex with ML277. Determined by electron microscopy at 3.9 Å resolution. Released 6 Jul 2022.
Explore 7TCI in 3D Show helices and sheets RCSB PDB PDBe
7TCI contains 108 α-helices and 24 β-strands across 8 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 | 96-105 | 10 | |
| α-helix | 110-134 | 25 | |
| α-helix | 140-167 | 28 | |
| α-helix | 176-184 | 9 | |
| α-helix | 187-205 | 19 | |
| α-helix | 219-227 | 9 | |
| α-helix | 228-231 | 4 | |
| α-helix | 233-235 | 3 | |
| α-helix | 238-247 | 10 | |
| α-helix | 249-273 | 25 | |
| β-strand | 278 | 1 | 1 |
| β-strand | 284 | 1 | 1 |
| α-helix | 289-300 | 12 | |
| α-helix | 313-349 | 37 | |
| α-helix | 352-353 | 2 | |
| α-helix | 354-356 | 3 | |
| α-helix | 358-375 | 18 | |
| α-helix | 498-522 | 25 | |
| α-helix | 524-525 | 2 | |
| α-helix | 527-555 | 29 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 11-21 | 11 | |
| β-strand | 28 | 1 | 2 |
| α-helix | 30-40 | 11 | |
| α-helix | 46-56 | 11 | |
| β-strand | 64 | 1 | 2 |
| α-helix | 66-74 | 9 | |
| α-helix | 80-93 | 14 | |
| α-helix | 95-97 | 3 | |
| β-strand | 100-102 | 3 | 3 |
| α-helix | 103-112 | 10 | |
| α-helix | 119-129 | 11 | |
| β-strand | 136-138 | 3 | 3 |
| α-helix | 139-145 | 7 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Potassium voltage-gated channel subfamily KQT member 1 | A, C, E, G | protein | 548 | Xenopus laevis | P70057 (AlphaFold model) |
| Calmodulin-1 | B, D, F, H | protein | 149 | Homo sapiens | P0DP23 (AlphaFold model) |
>7TCI_1 Potassium voltage-gated channel subfamily KQT member 1 (chains A, C, E, G) MATDPPRPTINLDPRVSIYSGRRPLLSRTNIQGRVYNFLERPTGWKCFVYHFTVFLIVLI CLIFSVLSTIQQYNNLATETLFWMEIVLVVFFGAEYVVRLWSAGCRSKYVGVWGRLRFAR KPISVIDLIVVVASVIVLCVGSNGQVFATSAIRGIRFLQILRMLHVDRQGGTWRLLGSVV FIHRQELITTLYIGFLGLIFSSYFVYLAEKDAIDSSGEYQFGSYADALWWGVVTVTTIGY GDKVPQTWIGKTIASCFSVFAISFFALPAGILGSGFALKVQQKQRQKHFNRQIPAAASLI QTAWRCYAAENPDSATWKIYIRKQSRNHHLMSPSPKPKKSAMVKKKKIRTERDEGSTDKM LNIPHITYDHVADDRKNDGYSVESYENTVRKPFGFLDPSTGPFIRTSSFTDDLDMEGDTL LTPITHISELKEHHRAAIKVIRRMQYFVAKKKFQQARKPYDVRDVIEQYSQGHLNLMVRI KELQRRLDQSLGKPSLFLSVSDKVKDKGINTIGSRLNRVEDKVTQMDHKLNLITDMLHHL LTNQQSNS
>7TCI_2 Calmodulin-1 (chains B, D, F, H) MADQLTEEQIAEFKEAFSLFDKDGDGTITTKELGTVMRSLGQNPTEAELQDMINEVDADG NGTIDFPEFLTMMARKMKDTDSEEEIREAFRVFDKDGNGYISAAELRHVMTNLGEKLTDE EVDEMIREADIDGDGQVNYEEFVQMMTAK
| ID | Name | Formula | Copies |
|---|---|---|---|
| I0S | (2R)-N-[4-(4-methoxyphenyl)-1,3-thiazol-2-yl]-1-(4-methylbenzene-1-sulfonyl)pip… | C23 H25 N3 O4 S2 | 4 |
| CA | Calcium ion | Ca | 12 |
Structural and electrophysiological basis for the modulation of KCNQ1 channel currents by ML277. Willegems, K., Eldstrom, J., Kyriakis, E. et al. Nat Commun (2022) 13:3760-3760. DOI 10.1038/s41467-022-31526-7 · PubMed
Other PDB entries of the same protein (UniProt P70057 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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