Structure of human B0AT1-ACE2 complex with compound1. Determined by electron microscopy at 2.8 Å resolution. Released 10 Dec 2025.
Explore 9KY1 in 3D Show helices and sheets RCSB PDB PDBe
9KY1 contains 167 α-helices and 38 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 | 11-14 | 4 | |
| α-helix | 16-17 | 2 | |
| α-helix | 21-24 | 4 | |
| α-helix | 39-49 | 11 | |
| α-helix | 53-56 | 4 | |
| α-helix | 58-64 | 7 | |
| α-helix | 68-77 | 10 | |
| α-helix | 78-82 | 5 | |
| α-helix | 83-96 | 14 | |
| α-helix | 100-107 | 8 | |
| α-helix | 109-111 | 3 | |
| α-helix | 112-141 | 30 | |
| α-helix | 164-167 | 4 | |
| α-helix | 171-174 | 4 | |
| α-helix | 175-180 | 6 | |
| α-helix | 195-212 | 18 | |
| α-helix | 216-241 | 26 | |
| α-helix | 247-254 | 8 | |
| α-helix | 259-263 | 5 | |
| α-helix | 265-278 | 14 | |
| α-helix | 285-290 | 6 | |
| α-helix | 299-348 | 50 | |
| α-helix | 350-351 | 2 | |
| α-helix | 360-370 | 11 | |
| α-helix | 372-377 | 6 | |
| α-helix | 385-389 | 5 | |
| α-helix | 396-397 | 2 | |
| α-helix | 398-403 | 6 | |
| α-helix | 404-408 | 5 | |
| α-helix | 413-445 | 33 | |
| α-helix | 455-469 | 15 | |
| α-helix | 472-474 | 3 | |
| α-helix | 478-487 | 10 | |
| α-helix | 492-503 | 12 | |
| α-helix | 504-508 | 5 | |
| α-helix | 511-521 | 11 | |
| α-helix | 525-527 | 3 | |
| α-helix | 528-532 | 5 | |
| α-helix | 533-537 | 5 | |
| α-helix | 538-552 | 15 | |
| β-strand | 559-561 | 3 | 1 |
| β-strand | 575-577 | 3 | 1 |
| α-helix | 582-590 | 9 | |
| α-helix | 592-608 | 17 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 22-52 | 31 | |
| α-helix | 59-76 | 18 | |
| α-helix | 77-79 | 3 | |
| α-helix | 91-99 | 9 | |
| α-helix | 104-107 | 4 | |
| α-helix | 110-128 | 19 | |
| β-strand | 131-133 | 3 | 2 |
| β-strand | 141-143 | 3 | 2 |
| α-helix | 144-148 | 5 | |
| α-helix | 149-154 | 6 | |
| α-helix | 158-168 | 11 | |
| α-helix | 169-173 | 5 | |
| α-helix | 174-192 | 19 | |
| α-helix | 199-204 | 6 | |
| β-strand | 209 | 1 | 3 |
| β-strand | 217 | 1 | 3 |
| α-helix | 219-231 | 13 | |
| α-helix | 234-251 | 18 | |
| β-strand | 260 | 1 | 4 |
| α-helix | 261 | 1 | |
| β-strand | 262-263 | 2 | 5 |
| α-helix | 264-266 | 3 | |
| α-helix | 276-281 | 6 | |
| α-helix | 294-300 | 7 | |
| α-helix | 306-317 | 12 | |
| α-helix | 320-324 | 5 | |
| α-helix | 325-329 | 5 | |
| β-strand | 332 | 1 | 6 |
| β-strand | 347-352 | 6 | 6 |
| β-strand | 355-359 | 5 | 6 |
| α-helix | 366-384 | 19 | |
| α-helix | 400-413 | 14 | |
| α-helix | 415-420 | 6 | |
| α-helix | 432-446 | 15 | |
| α-helix | 450-465 | 16 | |
| α-helix | 473-480 | 8 | |
| α-helix | 481-485 | 5 | |
| β-strand | 487-488 | 2 | 5 |
| α-helix | 499-502 | 4 | |
| α-helix | 504-507 | 4 | |
| α-helix | 514-532 | 19 | |
| α-helix | 539-541 | 3 | |
| α-helix | 548-560 | 13 | |
| α-helix | 566-574 | 9 | |
| α-helix | 582-587 | 6 | |
| α-helix | 589-598 | 10 | |
| β-strand | 607 | 1 | 4 |
| β-strand | 618-622 | 5 | 7 |
| α-helix | 624-628 | 5 | |
| α-helix | 632-634 | 3 | |
| α-helix | 637-657 | 21 | |
| β-strand | 670-676 | 7 | 7 |
| β-strand | 680-685 | 6 | 7 |
| β-strand | 686-687 | 2 | 8 |
| β-strand | 690-694 | 5 | 8 |
| α-helix | 697-713 | 17 | |
| β-strand | 722-725 | 4 | 7 |
| α-helix | 741-765 | 25 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 11-14 | 4 | |
| α-helix | 18-28 | 11 | |
| α-helix | 39-49 | 11 | |
| α-helix | 53-56 | 4 | |
| α-helix | 58-64 | 7 | |
| α-helix | 67-70 | 4 | |
| α-helix | 71-77 | 7 | |
| α-helix | 78-82 | 5 | |
| α-helix | 83-96 | 14 | |
| α-helix | 100-107 | 8 | |
| α-helix | 109-111 | 3 | |
| α-helix | 112-141 | 30 | |
| α-helix | 149-151 | 3 | |
| α-helix | 164-168 | 5 | |
| α-helix | 171-174 | 4 | |
| α-helix | 175-179 | 5 | |
| α-helix | 195-212 | 18 | |
| α-helix | 216-241 | 26 | |
| α-helix | 247-254 | 8 | |
| α-helix | 259-263 | 5 | |
| α-helix | 265-278 | 14 | |
| α-helix | 285-291 | 7 | |
| α-helix | 299-348 | 50 | |
| α-helix | 350-351 | 2 | |
| α-helix | 360-370 | 11 | |
| α-helix | 372-377 | 6 | |
| α-helix | 385-390 | 6 | |
| α-helix | 396-397 | 2 | |
| α-helix | 398-403 | 6 | |
| α-helix | 404-408 | 5 | |
| α-helix | 413-445 | 33 | |
| α-helix | 455-470 | 16 | |
| α-helix | 471-474 | 4 | |
| α-helix | 478-487 | 10 | |
| α-helix | 492-503 | 12 | |
| α-helix | 504-510 | 7 | |
| α-helix | 511-521 | 11 | |
| α-helix | 525-527 | 3 | |
| α-helix | 528-532 | 5 | |
| α-helix | 533-537 | 5 | |
| α-helix | 538-552 | 15 | |
| β-strand | 559-561 | 3 | 9 |
| β-strand | 575-577 | 3 | 9 |
| α-helix | 578-579 | 2 | |
| α-helix | 582-590 | 9 | |
| α-helix | 592-608 | 17 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 22-51 | 30 | |
| α-helix | 56-82 | 27 | |
| α-helix | 91-101 | 11 | |
| α-helix | 104-107 | 4 | |
| α-helix | 110-129 | 20 | |
| β-strand | 131-133 | 3 | 10 |
| β-strand | 141-143 | 3 | 10 |
| 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 | |
| β-strand | 209 | 1 | 11 |
| β-strand | 217 | 1 | 11 |
| α-helix | 219-231 | 13 | |
| α-helix | 234-251 | 18 | |
| 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 | 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 | 366-383 | 18 | |
| α-helix | 400-412 | 13 | |
| α-helix | 415-420 | 6 | |
| α-helix | 432-446 | 15 | |
| α-helix | 450-464 | 15 | |
| 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 | 548-560 | 13 | |
| α-helix | 566-574 | 9 | |
| α-helix | 582-587 | 6 | |
| α-helix | 589-598 | 10 | |
| β-strand | 607 | 1 | 12 |
| β-strand | 618-622 | 5 | 15 |
| α-helix | 624-627 | 4 | |
| α-helix | 632-634 | 3 | |
| α-helix | 637-657 | 21 | |
| β-strand | 670-673 | 4 | 15 |
| β-strand | 680-685 | 6 | 15 |
| β-strand | 686-687 | 2 | 16 |
| β-strand | 690-694 | 5 | 16 |
| α-helix | 697-714 | 18 | |
| β-strand | 722-723 | 2 | 15 |
| α-helix | 741-766 | 26 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Sodium-dependent neutral amino acid transporter B(0)AT1 | A, C | protein | 654 | Homo sapiens | Q695T7 (AlphaFold model) |
| Angiotensin-converting enzyme 2 | B, D | protein | 806 | Homo sapiens | Q9BYF1 (AlphaFold model) |
>9KY1_1 Sodium-dependent neutral amino acid transporter B(0)AT1 (chains A, C) MADYKDDDDKSGPDEVDASGRVRLVLPNPGLDARIPSLAELETIEQEEASSRPKWDNKAQ YMLTCLGFCVGLGNVWRFPYLCQSHGGGAFMIPFLILLVLEGIPLLYLEFAIGQRLRRGS LGVWSSIHPALKGLGLASMLTSFMVGLYYNTIISWIMWYLFNSFQEPLPWSDCPLNENQT GYVDECARSSPVDYFWYRETLNISTSISDSGSIQWWMLLCLACAWSVLYMCTIRGIETTG KAVYITSTLPYVVLTIFLIRGLTLKGATNGIVFLFTPNVTELAQPDTWLDAGAQVFFSFS LAFGGLISFSSYNSVHNNCEKDSVIVSIINGFTSVYVAIVVYSVIGFRATQRYDDCFSTN ILTLINGFDLPEGNVTQENFVDMQQRCNASDPAAYAQLVFQTCDINAFLSEAVEGTGLAF IVFTEAITKMPLSPLWSVLFFIMLFCLGLSSMFGNMEGVVVPLQDLRVIPPKWPKEVLTG LICLGTFLIGFIFTLNSGQYWLSLLDSYAGSIPLLIIAFCEMFSVVYVYGVDRFNKDIEF MIGHKPNIFWQVTWRVVSPLLMLIIFLFFFVVEVSQELTYSIWDPGYEEFPKSQKISYPN WVYVVVVIVAGVPSLTIPGYAIYKLIRNHCQKPGDHQGLVSTLSTASMNGDLKY
>9KY1_2 Angiotensin-converting enzyme 2 (chains B, D) MRSSSSWLLLSLVAVTAAQSTIEEQAKTFLDKFNHEAEDLFYQSSLASWNYNTNITEENV QNMNNAGDKWSAFLKEQSTLAQMYPLQEIQNLTVKLQLQALQQNGSSVLSEDKSKRLNTI LNTMSTIYSTGKVCNPDNPQECLLLEPGLNEIMANSLDYNERLWAWESWRSEVGKQLRPL YEEYVVLKNEMARANHYEDYGDYWRGDYEVNGVDGYDYSRGQLIEDVEHTFEEIKPLYEH LHAYVRAKLMNAYPSYISPIGCLPAHLLGDMWGRFWTNLYSLTVPFGQKPNIDVTDAMVD QAWDAQRIFKEAEKFFVSVGLPNMTQGFWENSMLTDPGNVQKAVCHPTAWDLGKGDFRIL MCTKVTMDDFLTAHHEMGHIQYDMAYAAQPFLLRNGANEGFHEAVGEIMSLSAATPKHLK SIGLLSPDFQEDNETEINFLLKQALTIVGTLPFTYMLEKWRWMVFKGEIPKDQWMKKWWE MKREIVGVVEPVPHDETYCDPASLFHVSNDYSFIRYYTRTLYQFQFQEALCQAAKHEGPL HKCDISNSTEAGQKLFNMLRLGKSEPWTLALENVVGAKNMNVRPLLNYFEPLFTWLKDQN KNSFVGWSTDWSPYADQSIKVRISLKSALGDKAYEWNDNEMYLFRSSVAYAMRQYFLKVK NQMILFGEEDVRVANLKPRISFNFFVTAPKNVSDIIPRTEVEKAIRMSRSRINDAFRLND NSLEFLGIQPTLGPPNQPPVSIWLIVFGVVMGVIVVGIVILIFTGIRDRKKKNKARSGEN PYASIDISKGENNPGFQNTDDVQTSF
| ID | Name | Formula | Copies |
|---|---|---|---|
| NAG | 2-acetamido-2-deoxy-beta-D-glucopyranose | C8 H15 N O6 | 2 |
Structure-guided development of a potent human B 0 AT1 inhibitor effective in a mouse model of phenylketonuria. Imazu, T., Akashi, T., Hiraizumi, M. et al. Commun Biol (2026). DOI 10.1038/s42003-026-10535-y · PubMed
Other PDB entries of the same protein (UniProt Q695T7 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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