9KXU: Human B0AT1-ACE2 complex with compound 2

Structure of human B0AT1-ACE2 complex with compound 2. Determined by electron microscopy at 2.87 Å resolution. Released 10 Dec 2025.

Method
Electron microscopy
Resolution
2.87 Å
Organism
Homo sapiens
Chains
2
Atoms
5,056
Mol. weight
166.95 kDa
Ligands
NAG, A1L6V
Released
10 Dec 2025

Explore 9KXU in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

9KXU contains 40 α-helices and 4 β-strands across 2 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.

Chain A: 39 helices, 4 β-strands

ElementResiduesLengthSheet
α-helix18-3114
α-helix38-5013
α-helix57-637
α-helix71-777
α-helix78-825
α-helix83-9614
α-helix100-1078
α-helix109-1135
α-helix114-14128
β-strand15511
β-strand16211
α-helix164-1685
α-helix171-1744
α-helix175-1806
α-helix195-21117
α-helix216-22611
α-helix229-2335
α-helix236-2427
α-helix247-2559
α-helix259-2624
α-helix265-27814
α-helix285-2906
α-helix299-34749
α-helix358-36710
α-helix386-3894
α-helix3971
α-helix398-4025
α-helix403-4075
α-helix413-44533
α-helix455-46915
α-helix472-4743
α-helix478-4847
α-helix488-4903
α-helix492-50716
α-helix511-52212
α-helix528-5325
α-helix533-5375
α-helix538-55215
β-strand559-56242
β-strand574-57742
α-helix578-5792
α-helix582-59413
α-helix596-60510
Chain B: 1 helix, 0 β-strands
ElementResiduesLengthSheet
α-helix741-76626

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Sodium-dependent neutral amino acid transporter B(0)AT1Aprotein654Homo sapiensQ695T7 (AlphaFold model)
Angiotensin-converting enzyme 2Bprotein806Homo sapiensQ9BYF1 (AlphaFold model)
Sequence of entity 1 (A), FASTA
>9KXU_1 Sodium-dependent neutral amino acid transporter B(0)AT1 (chains A)
MADYKDDDDKSGPDEVDASGRVRLVLPNPGLDARIPSLAELETIEQEEASSRPKWDNKAQ
YMLTCLGFCVGLGNVWRFPYLCQSHGGGAFMIPFLILLVLEGIPLLYLEFAIGQRLRRGS
LGVWSSIHPALKGLGLASMLTSFMVGLYYNTIISWIMWYLFNSFQEPLPWSDCPLNENQT
GYVDECARSSPVDYFWYRETLNISTSISDSGSIQWWMLLCLACAWSVLYMCTIRGIETTG
KAVYITSTLPYVVLTIFLIRGLTLKGATNGIVFLFTPNVTELAQPDTWLDAGAQVFFSFS
LAFGGLISFSSYNSVHNNCEKDSVIVSIINGFTSVYVAIVVYSVIGFRATQRYDDCFSTN
ILTLINGFDLPEGNVTQENFVDMQQRCNASDPAAYAQLVFQTCDINAFLSEAVEGTGLAF
IVFTEAITKMPLSPLWSVLFFIMLFCLGLSSMFGNMEGVVVPLQDLRVIPPKWPKEVLTG
LICLGTFLIGFIFTLNSGQYWLSLLDSYAGSIPLLIIAFCEMFSVVYVYGVDRFNKDIEF
MIGHKPNIFWQVTWRVVSPLLMLIIFLFFFVVEVSQELTYSIWDPGYEEFPKSQKISYPN
WVYVVVVIVAGVPSLTIPGYAIYKLIRNHCQKPGDHQGLVSTLSTASMNGDLKY
Sequence of entity 2 (B), FASTA
>9KXU_2 Angiotensin-converting enzyme 2 (chains B)
MRSSSSWLLLSLVAVTAAQSTIEEQAKTFLDKFNHEAEDLFYQSSLASWNYNTNITEENV
QNMNNAGDKWSAFLKEQSTLAQMYPLQEIQNLTVKLQLQALQQNGSSVLSEDKSKRLNTI
LNTMSTIYSTGKVCNPDNPQECLLLEPGLNEIMANSLDYNERLWAWESWRSEVGKQLRPL
YEEYVVLKNEMARANHYEDYGDYWRGDYEVNGVDGYDYSRGQLIEDVEHTFEEIKPLYEH
LHAYVRAKLMNAYPSYISPIGCLPAHLLGDMWGRFWTNLYSLTVPFGQKPNIDVTDAMVD
QAWDAQRIFKEAEKFFVSVGLPNMTQGFWENSMLTDPGNVQKAVCHPTAWDLGKGDFRIL
MCTKVTMDDFLTAHHEMGHIQYDMAYAAQPFLLRNGANEGFHEAVGEIMSLSAATPKHLK
SIGLLSPDFQEDNETEINFLLKQALTIVGTLPFTYMLEKWRWMVFKGEIPKDQWMKKWWE
MKREIVGVVEPVPHDETYCDPASLFHVSNDYSFIRYYTRTLYQFQFQEALCQAAKHEGPL
HKCDISNSTEAGQKLFNMLRLGKSEPWTLALENVVGAKNMNVRPLLNYFEPLFTWLKDQN
KNSFVGWSTDWSPYADQSIKVRISLKSALGDKAYEWNDNEMYLFRSSVAYAMRQYFLKVK
NQMILFGEEDVRVANLKPRISFNFFVTAPKNVSDIIPRTEVEKAIRMSRSRINDAFRLND
NSLEFLGIQPTLGPPNQPPVSIWLIVFGVVMGVIVVGIVILIFTGIRDRKKKNKARSGEN
PYASIDISKGENNPGFQNTDDVQTSF

Ligands and cofactors

IDNameFormulaCopies
NAG2-acetamido-2-deoxy-beta-D-glucopyranoseC8 H15 N O61
A1L6V(~{E})-~{N}-[2-(dimethylamino)-2-oxidanylidene-ethyl]-3-[4-(trifluoromethyl)phe…C14 H15 F3 N2 O21

Primary citation

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:

Browse structure collections

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