The crystal structure of the Michaelis-Menten complex of a C1s/C1-INH at 3.94 Angstroms. Determined by X-ray diffraction at 3.94 Å resolution. Released 26 Jun 2024.
Explore 8W18 in 3D Show helices and sheets RCSB PDB PDBe
8W18 contains 32 α-helices and 64 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 | 292-293 | 2 | |
| β-strand | 294 | 1 | 10 |
| α-helix | 295 | 1 | |
| β-strand | 302-304 | 3 | 11 |
| β-strand | 311 | 1 | 10 |
| α-helix | 312 | 1 | |
| β-strand | 316-321 | 6 | 11 |
| β-strand | 325-326 | 2 | 12 |
| β-strand | 327-328 | 2 | 13 |
| β-strand | 333-334 | 2 | 13 |
| β-strand | 336-340 | 5 | 11 |
| β-strand | 341 | 1 | 14 |
| β-strand | 347 | 1 | 14 |
| β-strand | 355-356 | 2 | 12 |
| α-helix | 357 | 1 | |
| β-strand | 358 | 1 | 15 |
| α-helix | 362-364 | 3 | |
| β-strand | 369-370 | 2 | 16 |
| β-strand | 377 | 1 | 15 |
| β-strand | 381-382 | 2 | 17 |
| β-strand | 384-385 | 2 | 16 |
| β-strand | 391 | 1 | 18 |
| β-strand | 401-403 | 3 | 17 |
| β-strand | 409-410 | 2 | 17 |
| β-strand | 411 | 1 | 19 |
| β-strand | 415 | 1 | 19 |
| α-helix | 417-419 | 3 | |
| β-strand | 423 | 1 | 18 |
| α-helix | 431-433 | 3 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 439 | 1 | 6 |
| β-strand | 442-443 | 2 | 4 |
| β-strand | 452-455 | 4 | 7 |
| β-strand | 458-459 | 2 | 5 |
| β-strand | 460-464 | 5 | 7 |
| β-strand | 469-472 | 4 | 7 |
| β-strand | 485-487 | 3 | 7 |
| β-strand | 491 | 1 | 8 |
| α-helix | 494-497 | 4 | |
| β-strand | 501-503 | 3 | 7 |
| β-strand | 505-510 | 6 | 7 |
| β-strand | 531-535 | 5 | 7 |
| α-helix | 547-548 | 2 | |
| β-strand | 549 | 1 | 4 |
| β-strand | 564-569 | 6 | 4 |
| β-strand | 581 | 1 | 8 |
| β-strand | 583-588 | 6 | 4 |
| β-strand | 589-590 | 2 | 9 |
| α-helix | 592-594 | 3 | |
| α-helix | 610-612 | 3 | |
| β-strand | 616-617 | 2 | 4 |
| β-strand | 618-619 | 2 | 9 |
| α-helix | 622-624 | 3 | |
| β-strand | 626 | 1 | 6 |
| β-strand | 635-639 | 5 | 4 |
| β-strand | 647-655 | 9 | 4 |
| β-strand | 664-667 | 4 | 4 |
| α-helix | 669-671 | 3 | |
| α-helix | 672-681 | 10 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 124-131 | 8 | |
| α-helix | 132-137 | 6 | |
| α-helix | 139-158 | 20 | |
| β-strand | 167-169 | 3 | 1 |
| α-helix | 171-182 | 12 | |
| α-helix | 188-196 | 9 | |
| α-helix | 199-200 | 2 | |
| α-helix | 206-212 | 7 | |
| β-strand | 218-226 | 9 | 2 |
| α-helix | 231-233 | 3 | |
| α-helix | 234-243 | 10 | |
| α-helix | 247-248 | 2 | |
| β-strand | 249-250 | 2 | 2 |
| α-helix | 251 | 1 | |
| α-helix | 255-269 | 15 | |
| β-strand | 287-295 | 9 | 2 |
| β-strand | 299-301 | 3 | 3 |
| α-helix | 302-304 | 3 | |
| α-helix | 305-307 | 3 | |
| β-strand | 309-315 | 7 | 1 |
| β-strand | 318-337 | 20 | 1 |
| β-strand | 342-348 | 7 | 1 |
| β-strand | 349 | 1 | 3 |
| β-strand | 353-360 | 8 | 1 |
| α-helix | 367-372 | 6 | |
| α-helix | 376-386 | 11 | |
| α-helix | 390-391 | 2 | |
| β-strand | 392-399 | 8 | 1 |
| β-strand | 401-408 | 8 | 2 |
| α-helix | 409-415 | 7 | |
| β-strand | 440-449 | 10 | 2 |
| β-strand | 453-455 | 3 | 3 |
| β-strand | 465 | 1 | 4 |
| β-strand | 468-469 | 2 | 5 |
| β-strand | 470-472 | 3 | 1 |
| β-strand | 477-483 | 7 | 1 |
| β-strand | 488-489 | 2 | 1 |
| β-strand | 492-495 | 4 | 1 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Plasma protease C1 inhibitor | I | protein | 395 | Homo sapiens | P05155 (AlphaFold model) |
| Complement C1s subcomponent light chain | B | protein | 251 | Homo sapiens | P09871 (AlphaFold model) |
| Complement C1s subcomponent heavy chain | A | protein | 151 | Homo sapiens | P09871 (AlphaFold model) |
>8W18_1 Plasma protease C1 inhibitor (chains I) GSTGSTDSPTQPTTGSFCPGPVTLCSDLESHSTEAVLGDALVDFSLKLYHAFSAMKKVET NMAFSPFSIASLLTQVLLGAGENTKTNLESILSYPKDFTCVHQALKGFTTKGVTSVSQIF HSPDLAIRDTFVNASRTLYSSSPRVLSNNSDANLELINTWVAKNTNNKISRLLDSLPSDT RLVLLNAIYLSAKWKTTFDPKKTRMEPFHFKNSVIKVPMMNSKKYPVAHFIDQTLKAKVG QLQLSHNLSLVILVPQNLKHRLEDMEQALSPSVFKAIMEKLEMSKFQPTLLTLPRIKVTT SQDMLSIMEKLEFFDFSYDLNLCGLTEDPDLQVSAMQHQTVLELTETGVEAAAASAISVA RTLLVFEVQQPFLFVLWDQQHKFPVFMGRVYDPRA
>8W18_2 Complement C1s subcomponent light chain (chains B) IIGGSDADIKNFPWQVFFDNPWAGGALINEYWVLTAAHVVEGNREPTMYVGSTSVQTSRL AKSKMLTPEHVFIHPGWKLLEVPEGRTNFDNDIALVRLKDPVKMGPTVSPICLPGTSSDY NLMDGDLGLISGWGRTEKRDRAVRLKAARLPVAPLRKCKEVKVEKPTADAEAYVFTPNMI CAGGEKGMDSCKGDAGGAFAVQDPNDKTKFYAAGLVSWGPQCGTYGLYTRVKNYVDWIMK TMQENSTPRED
>8W18_3 Complement C1s subcomponent heavy chain (chains A) GSTGSMPCPKEDTPNSVWEPAKAKYVFRDVVQITCLDGFEVVEGRVGATSFYSTCQSNGK WSNSKLKCQPVDCGIPESIENGKVEDPESTLFGSVIRYTCEEPYYYMENGGGGEYHCAGN GSWVNEVLGPELPKCVPVCGVPREPFEEKQR
The Crystal Structure of the Michaelis-Menten Complex of C1 Esterase Inhibitor and C1s Reveals Novel Insights into Complement Regulation. Garrigues, R.J., Garrison, M.P., Garcia, B.L. J Immunol (2024) 213:718-729. DOI 10.4049/jimmunol.2400194 · PubMed
Other PDB entries of the same protein (UniProt P05155 (AlphaFold model), which also has an AlphaFold model), best resolution first:
MolViewer shows 8W18 directly in your browser with nothing to install. Switch between cartoon, ball-and-stick, spacefill and surface views, color by chain, secondary structure or B-factor, measure distances, angles and dihedrals, and share or embed the view.