Active state of GluA1/2 in complex with TARP gamma 8, L-glutamate and CTZ. Determined by electron microscopy at 3.5 Å resolution. Released 23 Feb 2022.
Explore 7QHB in 3D Show helices and sheets RCSB PDB PDBe
7QHB contains 102 α-helices and 96 β-strands across 6 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 | 390 | 1 | |
| β-strand | 391-395 | 5 | 1 |
| β-strand | 398 | 1 | 2 |
| β-strand | 402 | 1 | 2 |
| β-strand | 403-404 | 2 | 3 |
| α-helix | 405 | 1 | |
| α-helix | 408-410 | 3 | |
| α-helix | 413-416 | 4 | |
| β-strand | 417-418 | 2 | 3 |
| α-helix | 420-432 | 13 | |
| β-strand | 436-440 | 5 | 1 |
| β-strand | 449 | 1 | 4 |
| β-strand | 456 | 1 | 4 |
| α-helix | 458-464 | 7 | |
| β-strand | 470-471 | 2 | 1 |
| α-helix | 479-484 | 6 | |
| β-strand | 485-487 | 3 | 1 |
| β-strand | 493-494 | 2 | 5 |
| β-strand | 497-501 | 5 | 6 |
| β-strand | 517 | 1 | 7 |
| α-helix | 519-541 | 23 | |
| α-helix | 569-581 | 13 | |
| α-helix | 592-620 | 29 | |
| α-helix | 633-637 | 5 | |
| β-strand | 642 | 1 | 8 |
| β-strand | 646 | 1 | 9 |
| α-helix | 650-657 | 8 | |
| α-helix | 661-670 | 10 | |
| β-strand | 679 | 1 | 9 |
| α-helix | 682-690 | 9 | |
| β-strand | 696 | 1 | 8 |
| β-strand | 698-700 | 3 | 6 |
| α-helix | 703-710 | 8 | |
| β-strand | 716-719 | 4 | 6 |
| β-strand | 726-727 | 2 | 5 |
| β-strand | 731-733 | 3 | 1 |
| α-helix | 739-751 | 13 | |
| α-helix | 754-759 | 6 | |
| α-helix | 760-764 | 5 | |
| α-helix | 782 | 1 | |
| β-strand | 783 | 1 | 10 |
| α-helix | 784 | 1 | |
| α-helix | 785-788 | 4 | |
| α-helix | 790-814 | 25 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 394-399 | 6 | 11 |
| β-strand | 407-408 | 2 | 12 |
| α-helix | 409 | 1 | |
| β-strand | 421-422 | 2 | 12 |
| α-helix | 424-436 | 13 | |
| β-strand | 439-444 | 6 | 11 |
| β-strand | 452-453 | 2 | 13 |
| β-strand | 460-461 | 2 | 13 |
| α-helix | 462-468 | 7 | |
| β-strand | 474-475 | 2 | 11 |
| α-helix | 479 | 1 | |
| β-strand | 480 | 1 | 14 |
| α-helix | 481 | 1 | |
| α-helix | 483-486 | 4 | |
| β-strand | 489-491 | 3 | 11 |
| β-strand | 496-499 | 4 | 14 |
| β-strand | 500-505 | 6 | 15 |
| β-strand | 510 | 1 | 16 |
| α-helix | 512-513 | 2 | |
| α-helix | 516-518 | 3 | |
| β-strand | 521 | 1 | 10 |
| α-helix | 523-546 | 24 | |
| α-helix | 573-584 | 12 | |
| α-helix | 596-623 | 28 | |
| β-strand | 628 | 1 | 16 |
| α-helix | 637-640 | 4 | |
| β-strand | 648 | 1 | 15 |
| α-helix | 654-661 | 8 | |
| α-helix | 665-676 | 12 | |
| α-helix | 686-696 | 11 | |
| β-strand | 702-705 | 4 | 15 |
| α-helix | 706-714 | 9 | |
| β-strand | 720-723 | 4 | 15 |
| β-strand | 729-732 | 4 | 14 |
| β-strand | 735-737 | 3 | 11 |
| α-helix | 743-756 | 14 | |
| α-helix | 758-763 | 6 | |
| α-helix | 764-768 | 5 | |
| α-helix | 786 | 1 | |
| β-strand | 787 | 1 | 17 |
| α-helix | 788 | 1 | |
| α-helix | 789-818 | 30 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 19-39 | 21 | |
| β-strand | 45-49 | 5 | 33 |
| β-strand | 80-84 | 5 | 33 |
| β-strand | 88 | 1 | 34 |
| β-strand | 90-91 | 2 | 33 |
| α-helix | 101 | 1 | |
| β-strand | 102 | 1 | 34 |
| α-helix | 103 | 1 | |
| α-helix | 118-127 | 10 | |
| α-helix | 129-150 | 22 | |
| α-helix | 156-183 | 28 | |
| β-strand | 201 | 1 | 33 |
| α-helix | 203-233 | 31 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Isoform Flip of Glutamate receptor 1 | A, C | protein | 915 | Rattus norvegicus | P19490 (AlphaFold model) |
| Isoform Flip of Glutamate receptor 2 | B, D | protein | 860 | Rattus norvegicus | P19491 (AlphaFold model) |
| Voltage-dependent calcium channel gamma-8 subunit | I, J | protein | 423 | Rattus norvegicus | Q8VHW5 (AlphaFold model) |
>7QHB_1 Isoform Flip of Glutamate receptor 1 (chains A, C) MPYIFAFFCTGFLGAVVGADYKDDDDKNFPNNIQIGGLFPNQQSQEHAAFRFALSQLTEP PKLLPQIDIVNISDSFEMTYRFCSQFSKGVYAIFGFYERRTVNMLTSFCGALHVCFITPS FPVDTSNQFVLQLRPELQEALISIIDHYKWQTFVYIYDADRGLSVLQRVLDTAAEKNWQV TAVNILTTTEEGYRMLFQDLEKKKERLVVVDCESERLNAILGQIVKLEKNGIGYHYILAN LGFMDIDLNKFKESGANVTGFQLVNYTDTIPARIMQQWRTSDSRDHTRVDWKRPKYTSAL TYDGVKVMAEAFQSLRRQRIDISRRGNAGDCLANPAVPWGQGIDIQRALQQVRFEGLTGN VQFNEKGRRTNYTLHVIEMKHDGIRKIGYWNEDDKFVPAATDAQAGGDNSSVQNRTYIVT TILEDPYVMLKKNANQFEGNDRYEGYCVELAAEIAKHVGYSYRLEIVSDGKYGARDPDTK AWNGMVGELVYGRADVAVAPLTITLVREEVIDFSKPFMSLGISIMIKKPQKSKPGVFSFL DPLAYEIWMCIVFAYIGVSVVLFLVSRFSPYEWHSEEFEEGRDQTTSDQSNEFGIFNSLW FSLGAFMQQGCDISPRSLSGRIVGGVWWFFTLIIISSYTANLAAFLTVERMVSPIESAED LAKQTEIAYGTLEAGSTKEFFRRSKIAVFEKMWTYMKSAEPSVFVRTTEEGMIRVRKSKG KYAYLLESTMNEYIEQRKPCDTMKVGGNLDSKGYGIATPKGSALRGPVNLAVLKLSEQGV LDKLKSKWWYDKGECGSKDSGSKDKTSALSLSNVAGVFYILIGGLGLAMLVALIEFCYKS RSESKRMKGFCLIPQQSINEAIRTSTLPRNSGAGASGGGGSGENGRVVSQDFPKSMQSIP CMSHSSGMPLGATGL
>7QHB_2 Isoform Flip of Glutamate receptor 2 (chains B, D) MQKIMHISVLLSPVLWGLIFGVSSNSIQIGGLFPRGADQEYSAFRVGMVQFSTSEFRLTP HIDNLEVANSFAVTNAFCSQFSRGVYAIFGFYDKKSVNTITSFCGTLHVSFITPSFPTDG THPFVIQMRPDLKGALLSLIEYYQWDKFAYLYDSDRGLSTLQAVLDSAAEKKWQVTAINV GNINNDKKDETYRSLFQDLELKKERRVILDCERDKVNDIVDQVITIGKHVKGYHYIIANL GFTDGDLLKIQFGGANVSGFQIVDYDDSLVSKFIERWSTLEEKEYPGAHTATIKYTSALT YDAVQVMTEAFRNLRKQRIEISRRGNAGDCLANPAVPWGQGVEIERALKQVQVEGLSGNI KFDQNGKRINYTINIMELKTNGPRKIGYWSEVDKMVVTLTELPSGNDTSGLENKTVVVTT ILESPYVMMKKNHEMLEGNERYEGYCVDLAAEIAKHCGFKYKLTIVGDGKYGARDADTKI WNGMVGELVYGKADIAIAPLTITLVREEVIDFSKPFMSLGISIMIKKPQKSKPGVFSFLD PLAYEIWMCIVFAYIGVSVVLFLVSRFSPYEWHTEEFEDGRETQSSESTNEFGIFNSLWF SLGAFMRQGCDISPRSLSGRIVGGVWWFFTLIIISSYTANLAAFLTVERMVSPIESAEDL SKQTEIAYGTLDSGSTKEFFRRSKIAVFDKMWTYMRSAEPSVFVRTTAEGVARVRKSKGK YAYLLESTMNEYIEQRKPCDTMKVGGNLDSKGYGIATPKGSSLGTPVNLAVLKLSEQGVL DKLKNKWWYDKGECGAKDSGSKEKTSALSLSNVAGVFYILVGGLGLAMLVALIEFCYKSR AEAKRMKVAKNPQNINPSSS
>7QHB_3 Voltage-dependent calcium channel gamma-8 subunit (chains I, J) GESLKRWNEERGLWCEKGVQVLLTTIGAFAAFGLMTIAISTDYWLYTRALICNTTNLTAG DDGPPHRGGSGSSEKKDPGGLTHSGLWRICCLEGLKRGVCVKINHFPEDTDYDHDSAEYL LRVVRASSIFPILSAILLLLGGVCVAASRVYKSKRNIILGAGILFVAAGLSNIIGVIVYI SANAGEPGPKRDEEKKNHYSYGWSFYFGGLSFILAEVIGVLAVNIYIERSREAHCQSRSD LLKAGGGAGGSGGSGPSAILRLPSYRFRYRRRSRSSSRGSSEASPSRDASPGGPGGPGFA STDISMYTLSRDPSKGSVAAGLASAGGGGGGAGVGAYGGAAGAAGGGGTGSERDRGSSAG FLTLHNAFPKEAASGVTVTVTGPPAAPAPAPPAPAAPAPGTLSKEAAASNTNTLNRKLEV LFQ
| ID | Name | Formula | Copies |
|---|---|---|---|
| PAM | Palmitoleic acid | C16 H30 O2 | 14 |
| GLU | Glutamic acid | C5 H9 N O4 | 4 |
| CYZ | Cyclothiazide | C14 H16 Cl N3 O4 S2 | 4 |
| OLC | (2R)-2,3-dihydroxypropyl (9Z)-octadec-9-enoate | C21 H40 O4 | 2 |
| 79N | (2S)-2,3-dihydroxypropyl (7Z)-hexadec-7-enoate | C19 H36 O4 | 4 |
Mechanisms underlying TARP modulation of the GluA1/2-gamma 8 AMPA receptor. Herguedas, B., Kohegyi, B.K., Dohrke, J.N. et al. Nat Commun (2022) 13:734-734. DOI 10.1038/s41467-022-28404-7 · PubMed
Other PDB entries of the same protein (UniProt P19490 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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