Cryo-EM structure of human Nav1.7(E406K) in complex with auxiliary beta subunits, huwentoxin-IV and saxitoxin (S6IV alpha helix conformer). Determined by electron microscopy at 3.0 Å resolution. Released 25 May 2022.
Explore 7W9T in 3D Show helices and sheets RCSB PDB PDBe
7W9T contains 96 α-helices and 47 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 |
|---|---|---|---|
| β-strand | 14 | 1 | 1 |
| α-helix | 17-31 | 15 | |
| β-strand | 58 | 1 | 2 |
| α-helix | 61-63 | 3 | |
| α-helix | 66-67 | 2 | |
| β-strand | 75-76 | 2 | 1 |
| α-helix | 80-83 | 4 | |
| β-strand | 87-91 | 5 | 1 |
| β-strand | 96 | 1 | 2 |
| β-strand | 97-101 | 5 | 1 |
| α-helix | 104 | 1 | |
| β-strand | 105 | 1 | 3 |
| β-strand | 109 | 1 | 3 |
| α-helix | 114-123 | 10 | |
| α-helix | 127-143 | 17 | |
| α-helix | 151-171 | 21 | |
| α-helix | 183-185 | 3 | |
| α-helix | 187-205 | 19 | |
| α-helix | 210-215 | 6 | |
| α-helix | 216-218 | 3 | |
| α-helix | 219-222 | 4 | |
| α-helix | 223-226 | 4 | |
| α-helix | 231-243 | 13 | |
| α-helix | 246-267 | 22 | |
| α-helix | 270-272 | 3 | |
| β-strand | 273-277 | 5 | 4 |
| α-helix | 286-292 | 7 | |
| α-helix | 297-302 | 6 | |
| β-strand | 303 | 1 | 4 |
| β-strand | 314 | 1 | 4 |
| β-strand | 328-332 | 5 | 4 |
| α-helix | 338-340 | 3 | |
| α-helix | 347-358 | 12 | |
| α-helix | 363-373 | 11 | |
| α-helix | 376-378 | 3 | |
| α-helix | 379-385 | 7 | |
| α-helix | 386-393 | 8 | |
| α-helix | 394-431 | 38 | |
| α-helix | 729-740 | 12 | |
| α-helix | 743-761 | 19 | |
| α-helix | 770-797 | 28 | |
| α-helix | 800-805 | 6 | |
| α-helix | 807-824 | 18 | |
| α-helix | 828-830 | 3 | |
| α-helix | 831-839 | 9 | |
| α-helix | 840-847 | 8 | |
| α-helix | 850-864 | 15 | |
| α-helix | 867-894 | 28 | |
| α-helix | 896-898 | 3 | |
| α-helix | 913-925 | 13 | |
| α-helix | 929-939 | 11 | |
| α-helix | 941-950 | 10 | |
| α-helix | 951-955 | 5 | |
| α-helix | 956-970 | 15 | |
| α-helix | 973-976 | 4 | |
| α-helix | 987-1013 | 27 | |
| α-helix | 1176-1189 | 14 | |
| α-helix | 1192-1207 | 16 | |
| α-helix | 1208-1211 | 4 | |
| α-helix | 1220-1248 | 29 | |
| α-helix | 1250-1254 | 5 | |
| α-helix | 1258-1278 | 21 | |
| α-helix | 1285-1289 | 5 | |
| α-helix | 1290-1300 | 11 | |
| α-helix | 1305-1343 | 39 | |
| β-strand | 1349-1352 | 4 | 5 |
| β-strand | 1357 | 1 | 5 |
| β-strand | 1366 | 1 | 6 |
| α-helix | 1367-1376 | 10 | |
| β-strand | 1380-1383 | 4 | 5 |
| α-helix | 1384-1385 | 2 | |
| α-helix | 1392-1403 | 12 | |
| α-helix | 1408-1416 | 9 | |
| β-strand | 1423 | 1 | 6 |
| α-helix | 1424-1425 | 2 | |
| α-helix | 1431-1433 | 3 | |
| α-helix | 1434-1441 | 8 | |
| α-helix | 1442-1448 | 7 | |
| α-helix | 1449-1466 | 18 | |
| α-helix | 1476-1487 | 12 | |
| α-helix | 1495-1500 | 6 | |
| α-helix | 1503-1512 | 10 | |
| α-helix | 1515-1533 | 19 | |
| α-helix | 1541-1569 | 29 | |
| α-helix | 1570-1575 | 6 | |
| α-helix | 1577-1601 | 25 | |
| α-helix | 1606-1613 | 8 | |
| α-helix | 1614-1616 | 3 | |
| α-helix | 1617-1620 | 4 | |
| α-helix | 1621-1625 | 5 | |
| α-helix | 1628-1639 | 12 | |
| α-helix | 1641-1666 | 26 | |
| α-helix | 1684-1695 | 12 | |
| α-helix | 1700-1707 | 8 | |
| α-helix | 1719-1721 | 3 | |
| α-helix | 1733-1767 | 35 | |
| α-helix | 1776-1789 | 14 | |
| β-strand | 1796-1798 | 3 | 7 |
| α-helix | 1799-1805 | 7 | |
| α-helix | 1809-1810 | 2 | |
| α-helix | 1820-1825 | 6 | |
| β-strand | 1829-1831 | 3 | 7 |
| β-strand | 1835-1837 | 3 | 7 |
| α-helix | 1838-1850 | 13 | |
| α-helix | 1854-1868 | 15 | |
| α-helix | 1874-1876 | 3 | |
| β-strand | 1879-1882 | 4 | 7 |
| α-helix | 1883-1890 | 8 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 25-27 | 3 | |
| β-strand | 29-31 | 3 | 8 |
| β-strand | 36-38 | 3 | 9 |
| β-strand | 50-51 | 2 | 10 |
| β-strand | 55-61 | 7 | 11 |
| β-strand | 68-74 | 7 | 11 |
| β-strand | 77-80 | 4 | 11 |
| α-helix | 84-86 | 3 | |
| β-strand | 90-92 | 3 | 9 |
| β-strand | 106-108 | 3 | 9 |
| α-helix | 113-115 | 3 | |
| β-strand | 117-123 | 7 | 11 |
| β-strand | 126-128 | 3 | 10 |
| β-strand | 133-135 | 3 | 10 |
| β-strand | 138-144 | 7 | 11 |
| β-strand | 145-147 | 3 | 8 |
| α-helix | 151-153 | 3 | |
| α-helix | 154-191 | 38 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 31-33 | 3 | 12 |
| β-strand | 37-41 | 5 | 13 |
| β-strand | 46-48 | 3 | 14 |
| β-strand | 51-53 | 3 | 12 |
| β-strand | 64-70 | 7 | 13 |
| β-strand | 78-84 | 7 | 13 |
| β-strand | 86-89 | 4 | 13 |
| α-helix | 93-95 | 3 | |
| β-strand | 99-101 | 3 | 14 |
| β-strand | 104 | 1 | 12 |
| α-helix | 105-107 | 3 | |
| β-strand | 109 | 1 | 12 |
| β-strand | 112-114 | 3 | 14 |
| α-helix | 119-121 | 3 | |
| β-strand | 123-130 | 8 | 13 |
| α-helix | 137 | 1 | |
| β-strand | 138-147 | 10 | 13 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Sodium channel protein type 9 subunit alpha | A | protein | 2031 | Homo sapiens | Q15858 (AlphaFold model) |
| Sodium channel subunit beta-1 | B | protein | 218 | Homo sapiens | Q07699 (AlphaFold model) |
| Sodium channel subunit beta-2 | C | protein | 215 | Homo sapiens | O60939 (AlphaFold model) |
>7W9T_1 Sodium channel protein type 9 subunit alpha (chains A) MASWSHPQFEKGGGARGGSGGGSWSHPQFEKGFDYKDDDDKGTMAMLPPPGPQSFVHFTK QSLALIEQRIAERKSKEPKEEKKDDDEEAPKPSSDLEAGKQLPFIYGDIPPGMVSEPLED LDPYYADKKTFIVLNKGKTIFRFNATPALYMLSPFSPLRRISIKILVHSLFSMLIMCTIL TNCIFMTMNNPPDWTKNVEYTFTGIYTFESLVKILARGFCVGEFTFLRDPWNWLDFVVIV FAYLTEFVNLGNVSALRTFRVLRALKTISVIPGLKTIVGALIQSVKKLSDVMILTVFCLS VFALIGLQLFMGNLKHKCFRNSLENNETLESIMNTLESEEDFRKYFYYLEGSKDALLCGF STDSGQCPEGYTCVKIGRNPDYGYTSFDTFSWAFLALFRLMTQDYWENLYQQTLRAAGKT YMIFFVVVIFLGSFYLINLILAVVAMAYKEQNQANIEEAKQKELEFQQMLDRLKKEQEEA EAIAAAAAEYTSIRRSRIMGLSESSSETSKLSSKSAKERRNRRKKKNQKKLSSGEEKGDA EKLSKSESEDSIRRKSFHLGVEGHRRAHEKRLSTPNQSPLSIRGSLFSARRSSRTSLFSF KGRGRDIGSETEFADDEHSIFGDNESRRGSLFVPHRPQERRSSNISQASRSPPMLPVNGK MHSAVDCNGVVSLVDGRSALMLPNGQLLPEVIIDKATSDDSGTTNQIHKKRRCSSYLLSE DMLNDPNLRQRAMSRASILTNTVEELEESRQKCPPWWYRFAHKFLIWNCSPYWIKFKKCI YFIVMDPFVDLAITICIVLNTLFMAMEHHPMTEEFKNVLAIGNLVFTGIFAAEMVLKLIA MDPYEYFQVGWNIFDSLIVTLSLVELFLADVEGLSVLRSFRLLRVFKLAKSWPTLNMLIK IIGNSVGALGNLTLVLAIIVFIFAVVGMQLFGKSYKECVCKINDDCTLPRWHMNDFFHSF LIVFRVLCGEWIETMWDCMEVAGQAMCLIVYMMVMVIGNLVVLNLFLALLLSSFSSDNLT AIEEDPDANNLQIAVTRIKKGINYVKQTLREFILKAFSKKPKISREIRQAEDLNTKKENY ISNHTLAEMSKGHNFLKEKDKISGFGSSVDKHLMEDSDGQSFIHNPSLTVTVPIAPGESD LENMNAEELSSDSDSEYSKVRLNRSSSSECSTVDNPLPGEGEEAEAEPMNSDEPEACFTD GCVWRFSCCQVNIESGKGKIWWNIRKTCYKIVEHSWFESFIVLMILLSSGALAFEDIYIE RKKTIKIILEYADKIFTYIFILEMLLKWIAYGYKTYFTNAWCWLDFLIVDVSLVTLVANT LGYSDLGPIKSLRTLRALRPLRALSRFEGMRVVVNALIGAIPSIMNVLLVCLIFWLIFSI MGVNLFAGKFYECINTTDGSRFPASQVPNRSECFALMNVSQNVRWKNLKVNFDNVGLGYL SLLQVATFKGWTIIMYAAVDSVNVDKQPKYEYSLYMYIYFVVFIIFGSFFTLNLFIGVII DNFNQQKKKLGGQDIFMTEEQKKYYNAMKKLGSKKPQKPIPRPGNKIQGCIFDLVTNQAF DISIMVLICLNMVTMMVEKEGQSQHMTEVLYWINVVFIILFTGECVLKLISLRHYYFTVG WNIFDFVVVIISIVGMFLADLIETYFVSPTLFRVIRLARIGRILRLVKGAKGIRTLLFAL MMSLPALFNIGLLLFLVMFIYAIFGMSNFAYVKKEDGINDMFNFETFGNSMICLFQITTS AGWDGLLAPILNSKPPDCDPKKVHPGSSVEGDCGNPSVGIFYFVSYIIISFLVVVNMYIA VILENFSVATEESTEPLSEDDFEMFYEVWEKFDPDATQFIEFSKLSDFAAALDPPLLIAK PNKVQLIAMDLPMVSGDRIHCLDILFAFTKRVLGESGEMDSLRSQMEERFMSANPSKVSY EPITTTLKRKQEDVSATVIQRAYRRYRLRQNVKNISSIYIKDGDRDDDLLNKKDMAFDNV NENSSPEKTDATSSTTSPPSYDSVTKPDKEKYEQDRTEKEDKGKDSKESKK
>7W9T_2 Sodium channel subunit beta-1 (chains B) MGRLLALVVGAALVSSACGGCVEVDSETEAVYGMTFKILCISCKRRSETNAETFTEWTFR QKGTEEFVKILRYENEVLQLEEDERFEGRVVWNGSRGTKDLQDLSIFITNVTYNHSGDYE CHVYRLLFFENYEHNTSVVKKIHIEVVDKANRDMASIVSEIMMYVLIVVLTIWLVAEMIY CYKKIAAATETAAQENASEYLAITSESKENCTGVQVAE
>7W9T_3 Sodium channel subunit beta-2 (chains C) MHRDAWLPRPAFSLTGLSLFFSLVPPGRSMEVTVPATLNVLNGSDARLPCTFNSCYTVNH KQFSLNWTYQECNNCSEEMFLQFRMKIINLKLERFQDRVEFSGNPSKYDVSVMLRNVQPE DEGIYNCYIMNPPDRHRGHGKIHLQVLMEEPPERDSTVAVIVGASVGGFLAVVILVLMVV KCVRRKKEQKLSTDDLKTEEEGKTDGEGNPDDGAK
| ID | Name | Formula | Copies |
|---|---|---|---|
| 9Z9 | (3beta,14beta,17beta,25R)-3-[4-methoxy-3-(methoxymethyl)butoxy]spirost-5-en | C34 H56 O5 | 1 |
| Y01 | Cholesterol hemisuccinate | C31 H50 O4 | 5 |
| P5S | O-[(R)-{[(2R)-2,3-bis(octadecanoyloxy)propyl]oxy}(hydroxy)phosphoryl]-L-serine | C42 H82 N O10 P | 2 |
| NAG | 2-acetamido-2-deoxy-beta-D-glucopyranose | C8 H15 N O6 | 5 |
| 9SL | [(3aS,4R,10aS)-2,6-diamino-10,10-dihydroxy-3a,4,9,10-tetrahydro-3H,8H-pyrrolo[1… | C10 H17 N7 O4 | 1 |
| PCW | 1,2-dioleoyl-sn-glycero-3-phosphocholine | C44 H85 N O8 P | 5 |
| LPE | 1-O-octadecyl-sn-glycero-3-phosphocholine | C26 H57 N O6 P | 14 |
High-resolution structures of human Na v 1.7 reveal gating modulation through alpha-pi helical transition of S6 IV. Huang, G., Liu, D., Wang, W. et al. Cell Rep (2022) 39:110735-110735. DOI 10.1016/j.celrep.2022.110735 · PubMed
Other PDB entries of the same protein (UniProt Q15858 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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