Receptor-binding domain (RBD) of the spike protein of the bat coronavirus RaTG13 virus in complex with the extracellular domain of human angiotensin-converting enzyme 2 (ACE2) - Crystal form 1. Determined by X-ray diffraction at 4.5 Å resolution. Released 3 Aug 2022.
Explore 7P8I in 3D Show helices and sheets RCSB PDB PDBe
7P8I contains 90 α-helices and 49 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 | 21-51 | 31 | |
| α-helix | 56-80 | 25 | |
| α-helix | 85-87 | 3 | |
| α-helix | 91-101 | 11 | |
| α-helix | 104-107 | 4 | |
| α-helix | 110-129 | 20 | |
| β-strand | 131-133 | 3 | 1 |
| β-strand | 141-143 | 3 | 1 |
| α-helix | 144-148 | 5 | |
| α-helix | 149-154 | 6 | |
| α-helix | 158-168 | 11 | |
| α-helix | 169-173 | 5 | |
| α-helix | 174-193 | 20 | |
| α-helix | 199-204 | 6 | |
| α-helix | 205-207 | 3 | |
| β-strand | 209 | 1 | 2 |
| β-strand | 217 | 1 | 2 |
| α-helix | 221-251 | 31 | |
| α-helix | 261 | 1 | |
| β-strand | 262-263 | 2 | 3 |
| α-helix | 264-266 | 3 | |
| α-helix | 276-278 | 3 | |
| α-helix | 279-282 | 4 | |
| α-helix | 289-290 | 2 | |
| α-helix | 294-299 | 6 | |
| α-helix | 304-316 | 13 | |
| α-helix | 320-324 | 5 | |
| α-helix | 325-330 | 6 | |
| β-strand | 332 | 1 | 4 |
| β-strand | 347-352 | 6 | 4 |
| β-strand | 355-359 | 5 | 4 |
| α-helix | 366-383 | 18 | |
| α-helix | 390-392 | 3 | |
| α-helix | 400-413 | 14 | |
| α-helix | 415-421 | 7 | |
| α-helix | 432-446 | 15 | |
| α-helix | 449-465 | 17 | |
| α-helix | 470-472 | 3 | |
| α-helix | 473-485 | 13 | |
| β-strand | 487-488 | 2 | 3 |
| α-helix | 499-502 | 4 | |
| α-helix | 504-507 | 4 | |
| α-helix | 513-532 | 20 | |
| α-helix | 539-541 | 3 | |
| α-helix | 548-558 | 11 | |
| α-helix | 566-574 | 9 | |
| α-helix | 582-598 | 17 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 354-358 | 5 | 5 |
| β-strand | 361-362 | 2 | 6 |
| α-helix | 368-370 | 3 | |
| α-helix | 373-374 | 2 | |
| β-strand | 376-379 | 4 | 5 |
| β-strand | 395-402 | 8 | 5 |
| α-helix | 405-409 | 5 | |
| α-helix | 417-422 | 6 | |
| β-strand | 431-437 | 7 | 5 |
| β-strand | 448 | 1 | 7 |
| β-strand | 452-454 | 3 | 8 |
| α-helix | 460-462 | 3 | |
| β-strand | 473-474 | 2 | 9 |
| β-strand | 488-489 | 2 | 9 |
| β-strand | 492-494 | 3 | 8 |
| β-strand | 497 | 1 | 7 |
| α-helix | 503-505 | 3 | |
| β-strand | 508-514 | 7 | 5 |
| β-strand | 524-525 | 2 | 6 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 21-51 | 31 | |
| α-helix | 56-80 | 25 | |
| α-helix | 85-87 | 3 | |
| α-helix | 91-101 | 11 | |
| α-helix | 104-107 | 4 | |
| α-helix | 110-129 | 20 | |
| β-strand | 132-133 | 2 | 10 |
| β-strand | 141-142 | 2 | 10 |
| α-helix | 144-147 | 4 | |
| α-helix | 148-152 | 5 | |
| α-helix | 158-168 | 11 | |
| α-helix | 169-173 | 5 | |
| α-helix | 174-193 | 20 | |
| α-helix | 199-204 | 6 | |
| α-helix | 205-207 | 3 | |
| β-strand | 209 | 1 | 11 |
| β-strand | 217 | 1 | 11 |
| α-helix | 221-251 | 31 | |
| β-strand | 260 | 1 | 12 |
| α-helix | 261 | 1 | |
| β-strand | 262-263 | 2 | 13 |
| α-helix | 264-266 | 3 | |
| α-helix | 276-278 | 3 | |
| α-helix | 279-282 | 4 | |
| α-helix | 289-290 | 2 | |
| α-helix | 294-299 | 6 | |
| α-helix | 304-316 | 13 | |
| α-helix | 320-324 | 5 | |
| α-helix | 325-330 | 6 | |
| β-strand | 332 | 1 | 14 |
| β-strand | 347-352 | 6 | 14 |
| β-strand | 355-359 | 5 | 14 |
| α-helix | 366-384 | 19 | |
| α-helix | 390-392 | 3 | |
| α-helix | 400-413 | 14 | |
| α-helix | 415-421 | 7 | |
| α-helix | 432-446 | 15 | |
| α-helix | 449-465 | 17 | |
| α-helix | 470-472 | 3 | |
| α-helix | 473-480 | 8 | |
| α-helix | 481-485 | 5 | |
| β-strand | 487-488 | 2 | 13 |
| α-helix | 499-502 | 4 | |
| α-helix | 504-507 | 4 | |
| α-helix | 514-532 | 19 | |
| α-helix | 539-541 | 3 | |
| α-helix | 548-558 | 11 | |
| α-helix | 566-574 | 9 | |
| α-helix | 582-587 | 6 | |
| α-helix | 589-598 | 10 | |
| β-strand | 607 | 1 | 12 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 336 | 1 | 15 |
| α-helix | 339-342 | 4 | |
| β-strand | 349 | 1 | 16 |
| β-strand | 354-357 | 4 | 16 |
| β-strand | 361 | 1 | 15 |
| β-strand | 362 | 1 | 17 |
| α-helix | 366-371 | 6 | |
| β-strand | 376-379 | 4 | 16 |
| β-strand | 392 | 1 | 18 |
| β-strand | 394-402 | 9 | 16 |
| α-helix | 404-409 | 6 | |
| α-helix | 418-421 | 4 | |
| β-strand | 431-437 | 7 | 16 |
| β-strand | 452-454 | 3 | 19 |
| α-helix | 460-462 | 3 | |
| β-strand | 473-474 | 2 | 20 |
| β-strand | 488-489 | 2 | 20 |
| β-strand | 492-494 | 3 | 19 |
| α-helix | 503-505 | 3 | |
| β-strand | 508-516 | 9 | 16 |
| β-strand | 524 | 1 | 18 |
| β-strand | 525 | 1 | 17 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Processed angiotensin-converting enzyme 2 | A, C | protein | 602 | Homo sapiens | Q9BYF1 (AlphaFold model) |
| Spike glycoprotein | B, D | protein | 233 | Bat coronavirus RaTG13 | A0ABF7PLN6 |
>7P8I_1 Processed angiotensin-converting enzyme 2 (chains A, C) GSSTIEEQAKTFLDKFNHEAEDLFYQSSLASWNYNTNITEENVQNMNNAGDKWSAFLKEQ STLAQMYPLQEIQNLTVKLQLQALQQNGSSVLSEDKSKRLNTILNTMSTIYSTGKVCNPD NPQECLLLEPGLNEIMANSLDYNERLWAWESWRSEVGKQLRPLYEEYVVLKNEMARANHY EDYGDYWRGDYEVNGVDGYDYSRGQLIEDVEHTFEEIKPLYEHLHAYVRAKLMNAYPSYI SPIGCLPAHLLGDMWGRFWTNLYSLTVPFGQKPNIDVTDAMVDQAWDAQRIFKEAEKFFV SVGLPNMTQGFWENSMLTDPGNVQKAVCHPTAWDLGKGDFRILMCTKVTMDDFLTAHHEM GHIQYDMAYAAQPFLLRNGANEGFHEAVGEIMSLSAATPKHLKSIGLLSPDFQEDNETEI NFLLKQALTIVGTLPFTYMLEKWRWMVFKGEIPKDQWMKKWWEMKREIVGVVEPVPHDET YCDPASLFHVSNDYSFIRYYTRTLYQFQFQEALCQAAKHEGPLHKCDISNSTEAGQKLFN MLRLGKSEPWTLALENVVGAKNMNVRPLLNYFEPLFTWLKDQNKNSFVGWSTDWSPYADA AA
>7P8I_2 Spike glycoprotein (chains B, D) GSRVQPTDSIVRFPNITNLCPFGEVFNATTFASVYAWNRKRISNCVADYSVLYNSTSFST FKCYGVSPTKLNDLCFTNVYADSFVITGDEVRQIAPGQTGKIADYNYKLPDDFTGCVIAW NSKHIDAKEGGNFNYLYRLFRKANLKPFERDISTEIYQAGSKPCNGQTGLNCYYPLYRYG FYPTDGVGHQPYRVVVLSFELLNAPATVCGPKKSTNLVKNKCVNFAAHHHHHH
| ID | Name | Formula | Copies |
|---|---|---|---|
| NAG | 2-acetamido-2-deoxy-beta-D-glucopyranose | C8 H15 N O6 | 3 |
Evidence of SARS-CoV-2 Direct Evolution in R. affinis Bats Driven by Affinity and Dynamics Optimization of the Spike Protein. Castelli, M., Scietti, L., Faravelli, S. et al. To be published.
Other PDB entries of the same protein (UniProt Q9BYF1 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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