Crystal structure of the HCoV-HKU1 RBD in complex with Fab. Determined by X-ray diffraction at 1.8 Å resolution. Released 30 Jul 2025.
Explore 9JCY in 3D Show helices and sheets RCSB PDB PDBe
9JCY contains 33 α-helices and 72 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 | 324-325 | 2 | |
| β-strand | 326 | 1 | 1 |
| α-helix | 329-333 | 5 | |
| β-strand | 337-339 | 3 | 2 |
| α-helix | 341-343 | 3 | |
| β-strand | 345-349 | 5 | 3 |
| β-strand | 352-354 | 3 | 1 |
| α-helix | 356-362 | 7 | |
| β-strand | 364-371 | 8 | 3 |
| α-helix | 375-377 | 3 | |
| β-strand | 382-383 | 2 | 1 |
| β-strand | 385-392 | 8 | 3 |
| α-helix | 395-401 | 7 | |
| α-helix | 408-412 | 5 | |
| β-strand | 422-430 | 9 | 3 |
| β-strand | 435-437 | 3 | 2 |
| α-helix | 443-447 | 5 | |
| α-helix | 450-453 | 4 | |
| β-strand | 459-463 | 5 | 4 |
| β-strand | 467-468 | 2 | 5 |
| β-strand | 477 | 1 | 6 |
| α-helix | 478 | 1 | |
| α-helix | 479-482 | 4 | |
| β-strand | 487 | 1 | 7 |
| α-helix | 489-491 | 3 | |
| β-strand | 492 | 1 | 6 |
| β-strand | 494 | 1 | 8 |
| α-helix | 495-496 | 2 | |
| α-helix | 501-503 | 3 | |
| β-strand | 504-509 | 6 | 7 |
| β-strand | 512-518 | 7 | 7 |
| β-strand | 536-537 | 2 | 5 |
| α-helix | 544-546 | 3 | |
| β-strand | 551 | 1 | 9 |
| α-helix | 553-555 | 3 | |
| β-strand | 556 | 1 | 10 |
| β-strand | 558 | 1 | 6 |
| β-strand | 566 | 1 | 8 |
| β-strand | 569 | 1 | 10 |
| α-helix | 571-573 | 3 | |
| β-strand | 574 | 1 | 9 |
| β-strand | 577-581 | 5 | 4 |
| β-strand | 583-584 | 2 | 3 |
| β-strand | 587-597 | 11 | 3 |
| β-strand | 604-606 | 3 | 1 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 4-7 | 4 | 16 |
| β-strand | 10-14 | 5 | 17 |
| β-strand | 19-25 | 7 | 16 |
| β-strand | 33-38 | 6 | 17 |
| β-strand | 45-49 | 5 | 17 |
| β-strand | 53-54 | 2 | 17 |
| α-helix | 55 | 1 | |
| β-strand | 62-67 | 6 | 16 |
| β-strand | 70-75 | 6 | 16 |
| α-helix | 80-82 | 3 | |
| β-strand | 84-90 | 7 | 17 |
| β-strand | 97-98 | 2 | 17 |
| β-strand | 102-107 | 6 | 17 |
| β-strand | 111 | 1 | 18 |
| α-helix | 112-113 | 2 | |
| β-strand | 114-118 | 5 | 19 |
| α-helix | 119-121 | 3 | |
| α-helix | 122-126 | 5 | |
| β-strand | 129-139 | 11 | 19 |
| β-strand | 140 | 1 | 18 |
| β-strand | 145-150 | 6 | 20 |
| β-strand | 153-154 | 2 | 20 |
| β-strand | 159-163 | 5 | 19 |
| α-helix | 164-167 | 4 | |
| β-strand | 173-182 | 10 | 19 |
| α-helix | 183-186 | 4 | |
| β-strand | 191-197 | 7 | 20 |
| β-strand | 205-210 | 6 | 20 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 3-7 | 5 | 7 |
| β-strand | 11-12 | 2 | 11 |
| β-strand | 18-25 | 8 | 7 |
| β-strand | 34-40 | 7 | 12 |
| β-strand | 47-52 | 6 | 12 |
| β-strand | 58-60 | 3 | 12 |
| α-helix | 62-64 | 3 | |
| β-strand | 68-73 | 6 | 7 |
| β-strand | 78-83 | 6 | 7 |
| α-helix | 88-90 | 3 | |
| β-strand | 92-101 | 10 | 12 |
| β-strand | 109-112 | 4 | 12 |
| β-strand | 118-120 | 3 | 12 |
| β-strand | 121-122 | 2 | 11 |
| α-helix | 126-127 | 2 | |
| β-strand | 128 | 1 | 13 |
| α-helix | 129-130 | 2 | |
| β-strand | 131-135 | 5 | 14 |
| α-helix | 136-138 | 3 | |
| β-strand | 146-156 | 11 | 14 |
| β-strand | 157 | 1 | 13 |
| β-strand | 162-165 | 4 | 15 |
| α-helix | 166-168 | 3 | |
| β-strand | 170 | 1 | 15 |
| β-strand | 174-176 | 3 | 14 |
| α-helix | 177-179 | 3 | |
| β-strand | 180-181 | 2 | 14 |
| β-strand | 187-196 | 10 | 14 |
| α-helix | 197-199 | 3 | |
| β-strand | 206-211 | 6 | 15 |
| α-helix | 212-214 | 3 | |
| β-strand | 216-221 | 6 | 15 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Spike protein S1 | A | protein | 308 | Human coronavirus HKU1 (isolate N1) | Q5MQD0 (AlphaFold model) |
| Heavy chain of Fab | C | protein | 235 | Homo sapiens | |
| Light chain of Fab | B | protein | 214 | Homo sapiens |
>9JCY_1 Spike protein S1 (chains A) DLPDCDIDKWLNNFNVPSPLNWERKIFSNCNFNLSTLLRLVHTDSFSCNNFDESKIYGSC FKSIVLDKFAIPNSRRSDLQLGSSGFLQSSNYKIDTTSSSCQLYYSLPAINVTINNYNPS SWNRRYGFNNFNLSSHSVVYSRYCFSVNNTFCPCAKPSFASSCKSHKPPSASCPIGTNYR SCESTTVLDHTDWCRCSCLPDPITAYDPRSCSQKKSLVGVGEHCAGFGVDEEKCGVLDGS YNVSCLCSTDAFLGWSYDTCVSNNRCNIFSNFILNGINSGTTCSNDLSGLEVLFQGPGGS HHHHHHHH
>9JCY_2 Heavy chain of Fab (chains C) QVQLQESGPGLVKPSGTLSLTCAVSGGSISSSNWWSWVRQPPGKGLEWIGSMHYSGSSHY KPSLKSRIAMSVDTSKNQFSLNLNSVTAADTAVYYCAREGGSSGYDYVYYFDDWGQGTTV TVSSASTKGPSVFPLAPSSKSTSGGTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAV LQSSGLYSLSSVVTVPSSSLGTQTYICNVNHKPSNTKVDKKVEPKSCGSHHHHHH
>9JCY_3 Light chain of Fab (chains B) DIQMTQSPSSLSASVGDRVTITCRASQSISSYLNWYQQKPGKAPKLLIYAASSLQSGVPS RFSGSGSGTDFTLTISSLQPEDFATYYCQQSYSTPRTFGQGTKVEIKRTVAAPSVFIFPP SDEQLKSGTASVVCLLNNFYPREAKVQWKVDNALQSGNSQESVTEQDSKDSTYSLSSTLT LSKADYEKHKVYACEVTHQGLSSPVTKSFNRGEC
| ID | Name | Formula | Copies |
|---|---|---|---|
| NAG | 2-acetamido-2-deoxy-beta-D-glucopyranose | C8 H15 N O6 | 2 |
Water and common crystallization additives (GOL) are not listed.
The crystal structure of coronavirus RBD-TMPRSS2 complex provides basis for the discovery of therapeutic antibodies. Zhao, Z., Yang, Q., Liu, X. et al. Nat Commun (2025) 16:6636-6636. DOI 10.1038/s41467-025-62023-2 · PubMed
Other PDB entries of the same protein (UniProt Q5MQD0 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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