Human Nav1.2-beta2-KIIIA ternary complex. Determined by electron microscopy at 3.0 Å resolution. Released 27 Feb 2019.
Explore 6J8E in 3D Show helices and sheets RCSB PDB PDBe
6J8E contains 68 α-helices and 22 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 | 118-121 | 4 | |
| α-helix | 124-127 | 4 | |
| α-helix | 129-145 | 17 | |
| α-helix | 156-174 | 19 | |
| α-helix | 190-202 | 13 | |
| α-helix | 204-206 | 3 | |
| α-helix | 218-224 | 7 | |
| α-helix | 227-230 | 4 | |
| α-helix | 234-245 | 12 | |
| α-helix | 246-249 | 4 | |
| α-helix | 251-269 | 19 | |
| α-helix | 273-275 | 3 | |
| β-strand | 276-280 | 5 | 4 |
| α-helix | 281-282 | 2 | |
| β-strand | 342 | 1 | 5 |
| β-strand | 344 | 1 | 5 |
| β-strand | 351-355 | 5 | 4 |
| α-helix | 370-381 | 12 | |
| α-helix | 386-396 | 11 | |
| α-helix | 399-401 | 3 | |
| α-helix | 402-408 | 7 | |
| α-helix | 409-414 | 6 | |
| α-helix | 415-440 | 26 | |
| α-helix | 742-753 | 12 | |
| α-helix | 763-777 | 15 | |
| α-helix | 788-807 | 20 | |
| α-helix | 823-840 | 18 | |
| α-helix | 847-862 | 16 | |
| α-helix | 865-878 | 14 | |
| α-helix | 882-902 | 21 | |
| α-helix | 904-909 | 6 | |
| α-helix | 928-938 | 11 | |
| α-helix | 944-954 | 11 | |
| α-helix | 956-985 | 30 | |
| α-helix | 1195-1205 | 11 | |
| α-helix | 1208-1223 | 16 | |
| α-helix | 1224-1227 | 4 | |
| α-helix | 1232-1235 | 4 | |
| α-helix | 1239-1264 | 26 | |
| α-helix | 1266-1269 | 4 | |
| α-helix | 1273-1294 | 22 | |
| α-helix | 1302-1305 | 4 | |
| α-helix | 1306-1316 | 11 | |
| α-helix | 1321-1330 | 10 | |
| α-helix | 1331-1333 | 3 | |
| α-helix | 1334-1358 | 25 | |
| β-strand | 1365-1368 | 4 | 6 |
| β-strand | 1373-1374 | 2 | 6 |
| α-helix | 1375-1376 | 2 | |
| β-strand | 1382 | 1 | 7 |
| α-helix | 1383-1390 | 8 | |
| β-strand | 1397-1399 | 3 | 6 |
| α-helix | 1409-1420 | 12 | |
| α-helix | 1424-1432 | 9 | |
| β-strand | 1439 | 1 | 7 |
| α-helix | 1447-1449 | 3 | |
| α-helix | 1450-1457 | 8 | |
| α-helix | 1458-1463 | 6 | |
| α-helix | 1464-1482 | 19 | |
| α-helix | 1492-1496 | 5 | |
| α-helix | 1501-1505 | 5 | |
| α-helix | 1520-1528 | 9 | |
| α-helix | 1531-1549 | 19 | |
| α-helix | 1557-1584 | 28 | |
| α-helix | 1593-1615 | 23 | |
| α-helix | 1622-1628 | 7 | |
| α-helix | 1629-1633 | 5 | |
| α-helix | 1636-1641 | 6 | |
| α-helix | 1646-1654 | 9 | |
| α-helix | 1657-1681 | 25 | |
| α-helix | 1700-1710 | 11 | |
| α-helix | 1716-1720 | 5 | |
| α-helix | 1749-1784 | 36 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 32-33 | 2 | 1 |
| β-strand | 37-41 | 5 | 2 |
| β-strand | 46-48 | 3 | 3 |
| β-strand | 51-52 | 2 | 1 |
| β-strand | 64-70 | 7 | 2 |
| β-strand | 77-84 | 8 | 2 |
| β-strand | 86-89 | 4 | 2 |
| β-strand | 99-101 | 3 | 3 |
| β-strand | 104 | 1 | 1 |
| α-helix | 105-107 | 3 | |
| β-strand | 109 | 1 | 1 |
| β-strand | 112-114 | 3 | 3 |
| α-helix | 119-121 | 3 | |
| β-strand | 123-130 | 8 | 2 |
| α-helix | 136-137 | 2 | |
| β-strand | 138-147 | 10 | 2 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 7-12 | 6 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Sodium channel subunit beta-2 | C | protein | 122 | Homo sapiens | O60939 (AlphaFold model) |
| Sodium channel protein type 2 subunit alpha | A | protein | 2048 | Homo sapiens | Q99250 (AlphaFold model) |
| Mu-conotoxin KIIIA | D | protein | 16 | Conus kinoshitai | P0C195 (AlphaFold model) |
>6J8E_1 Sodium channel subunit beta-2 (chains C) GRSMEVTVPATLNVLNGSDARLPCTFNSCYTVNHKQFSLNWTYQECNNCSEEMFLQFRMK IINLKLERFQDRVEFSGNPSKYDVSVMLRNVQPEDEGIYNCYIMNPPDRHRGHGKIHLQV LM
>6J8E_2 Sodium channel protein type 2 subunit alpha (chains A) MASWSHPQFEKGGGARGGSGGGSWSHPQFEKGFDYKDDDDKGTMAQSVLVPPGPDSFRFF TRESLAAIEQRIAEEKAKRPKQERKDEDDENGPKPNSDLEAGKSLPFIYGDIPPEMVSVP LEDLDPYYINKKTFIVLNKGKAISRFSATPALYILTPFNPIRKLAIKILVHSLFNMLIMC TILTNCVFMTMSNPPDWTKNVEYTFTGIYTFESLIKILARGFCLEDFTFLRDPWNWLDFT VITFAYVTEFVDLGNVSALRTFRVLRALKTISVIPGLKTIVGALIQSVKKLSDVMILTVF CLSVFALIGLQLFMGNLRNKCLQWPPDNSSFEINITSFFNNSLDGNGTTFNRTVSIFNWD EYIEDKSHFYFLEGQNDALLCGNSSDAGQCPEGYICVKAGRNPNYGYTSFDTFSWAFLSL FRLMTQDFWENLYQLTLRAAGKTYMIFFVLVIFLGSFYLINLILAVVAMAYEEQNQATLE EAEQKEAEFQQMLEQLKKQQEEAQAAAAAASAESRDFSGAGGIGVFSESSSVASKLSSKS EKELKNRRKKKKQKEQSGEEEKNDRVRKSESEDSIRRKGFRFSLEGSRLTYEKRFSSPHQ SLLSIRGSLFSPRRNSRASLFSFRGRAKDIGSENDFADDEHSTFEDNDSRRDSLFVPHRH GERRHSNVSQASRASRVLPILPMNGKMHSAVDCNGVVSLVGGPSTLTSAGQLLPEGTTTE TEIRKRRSSSYHVSMDLLEDPTSRQRAMSIASILTNTMEELEESRQKCPPCWYKFANMCL IWDCCKPWLKVKHLVNLVVMDPFVDLAITICIVLNTLFMAMEHYPMTEQFSSVLSVGNLV FTGIFTAEMFLKIIAMDPYYYFQEGWNIFDGFIVSLSLMELGLANVEGLSVLRSFRLLRV FKLAKSWPTLNMLIKIIGNSVGALGNLTLVLAIIVFIFAVVGMQLFGKSYKECVCKISND CELPRWHMHDFFHSFLIVFRVLCGEWIETMWDCMEVAGQTMCLTVFMMVMVIGNLVVLNL FLALLLSSFSSDNLAATDDDNEMNNLQIAVGRMQKGIDFVKRKIREFIQKAFVRKQKALD EIKPLEDLNNKKDSCISNHTTIEIGKDLNYLKDGNGTTSGIGSSVEKYVVDESDYMSFIN NPSLTVTVPIAVGESDFENLNTEEFSSESDMEESKEKLNATSSSEGSTVDIGAPAEGEQP EVEPEESLEPEACFTEDCVRKFKCCQISIEEGKGKLWWNLRKTCYKIVEHNWFETFIVFM ILLSSGALAFEDIYIEQRKTIKTMLEYADKVFTYIFILEMLLKWVAYGFQVYFTNAWCWL DFLIVDVSLVSLTANALGYSELGAIKSLRTLRALRPLRALSRFEGMRVVVNALLGAIPSI MNVLLVCLIFWLIFSIMGVNLFAGKFYHCINYTTGEMFDVSVVNNYSECKALIESNQTAR WKNVKVNFDNVGLGYLSLLQVATFKGWMDIMYAAVDSRNVELQPKYEDNLYMYLYFVIFI IFGSFFTLNLFIGVIIDNFNQQKKKFGGQDIFMTEEQKKYYNAMKKLGSKKPQKPIPRPA NKFQGMVFDFVTKQVFDISIMILICLNMVTMMVETDDQSQEMTNILYWINLVFIVLFTGE CVLKLISLRYYYFTIGWNIFDFVVVILSIVGMFLAELIEKYFVSPTLFRVIRLARIGRIL RLIKGAKGIRTLLFALMMSLPALFNIGLLLFLVMFIYAIFGMSNFAYVKREVGIDDMFNF ETFGNSMICLFQITTSAGWDGLLAPILNSGPPDCDPDKDHPGSSVKGDCGNPSVGIFFFV SYIIISFLVVVNMYIAVILENFSVATEESAEPLSEDDFEMFYEVWEKFDPDATQFIEFAK LSDFADALDPPLLIAKPNKVQLIAMDLPMVSGDRIHCLDILFAFTKRVLGESGEMDALRI QMEERFMASNPSKVSYEPITTTLKRKQEEVSAIIIQRAYRRYLLKQKVKKVSSIYKKDKG KECDGTPIKEDTLIDKLNENSTPEKTDMTPSTTSPPSYDSVTKPEKEKFEKDKSEKEDKG KDIRESKK
>6J8E_3 Mu-conotoxin KIIIA (chains D) CCNCSSKWCRDHSRCC
| ID | Name | Formula | Copies |
|---|---|---|---|
| 9Z9 | (3beta,14beta,17beta,25R)-3-[4-methoxy-3-(methoxymethyl)butoxy]spirost-5-en | C34 H56 O5 | 1 |
| NAG | 2-acetamido-2-deoxy-beta-D-glucopyranose | C8 H15 N O6 | 1 |
Water and common crystallization additives (NA) are not listed.
Molecular basis for pore blockade of human Na+channel Nav1.2 by the mu-conotoxin KIIIA. Pan, X., Li, Z., Huang, X. et al. Science (2019) 363:1309-1313. DOI 10.1126/science.aaw2999 · PubMed
Other PDB entries of the same protein (UniProt O60939 (AlphaFold model), which also has an AlphaFold model), best resolution first:
6J8E is part of these collections:
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