7T8X: ACh-bound M2R-Go signaling complex in S1 state
Cryo-EM structure of ACh-bound M2R-Go signaling complex in S1 state. Determined by electron microscopy at 3.21 Å resolution. Released 25 Jan 2023.
- Method
- Electron microscopy
- Resolution
- 3.21 Å
- Organisms
- Homo sapiens, Mus musculus
- Chains
- 5
- Atoms
- 8,555
- Mol. weight
- 152.91 kDa
- Ligands
- ACH
- Released
- 25 Jan 2023
Explore 7T8X in 3D
Show helices and sheets
RCSB PDB
PDBe
Secondary structure: helices and β-sheets
7T8X contains 36 α-helices and 61 β-strands across 5 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: 17 helices, 0 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 22-50 | 29 | |
| α-helix | 60-71 | 12 | |
| α-helix | 72-77 | 6 | |
| α-helix | 78-86 | 9 | |
| α-helix | 92-126 | 35 | |
| α-helix | 130-134 | 5 | |
| α-helix | 137-166 | 30 | |
| α-helix | 179-181 | 3 | |
| α-helix | 184-191 | 8 | |
| α-helix | 192-196 | 5 | |
| α-helix | 197-211 | 15 | |
| α-helix | 378-380 | 3 | |
| α-helix | 381-412 | 32 | |
| α-helix | 414-416 | 3 | |
| α-helix | 419-431 | 13 | |
| α-helix | 436-439 | 4 | |
| α-helix | 445-451 | 7 | |
Chain B: 9 helices, 7 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 11-29 | 19 | |
| β-strand | 33-35 | 3 | 1 |
| β-strand | 38-39 | 2 | 1 |
| α-helix | 46-52 | 7 | |
| β-strand | 186-192 | 7 | 1 |
| β-strand | 195-201 | 7 | 1 |
| α-helix | 209-211 | 3 | |
| α-helix | 214-216 | 3 | |
| β-strand | 222-227 | 6 | 1 |
| α-helix | 243-255 | 13 | |
| β-strand | 265-270 | 6 | 1 |
| α-helix | 272-281 | 10 | |
| α-helix | 284-286 | 3 | |
| α-helix | 297-309 | 13 | |
| β-strand | 319-323 | 5 | 1 |
| α-helix | 332-351 | 20 | |
Chain C: 4 helices, 30 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 4-25 | 22 | |
| α-helix | 30-33 | 4 | |
| α-helix | 38-39 | 2 | |
| β-strand | 47-50 | 4 | 2 |
| β-strand | 58-63 | 6 | 3 |
| β-strand | 69-74 | 6 | 3 |
| β-strand | 78-83 | 6 | 3 |
| β-strand | 88-94 | 7 | 3 |
| β-strand | 100-105 | 6 | 4 |
| β-strand | 111-116 | 6 | 4 |
| β-strand | 121-125 | 5 | 4 |
| β-strand | 134-139 | 6 | 4 |
| β-strand | 146-151 | 6 | 5 |
| β-strand | 156-161 | 6 | 5 |
| β-strand | 165-170 | 6 | 5 |
| β-strand | 175-181 | 7 | 5 |
| β-strand | 187 | 1 | 6 |
| β-strand | 191-192 | 2 | 7 |
| β-strand | 198-202 | 5 | 7 |
| β-strand | 203 | 1 | 6 |
| β-strand | 208-212 | 5 | 7 |
| β-strand | 220-222 | 3 | 7 |
| β-strand | 229-234 | 6 | 8 |
| β-strand | 240-245 | 6 | 8 |
| β-strand | 250-254 | 5 | 8 |
| β-strand | 259-264 | 6 | 8 |
| α-helix | 272 | 1 | |
| β-strand | 273-278 | 6 | 9 |
| β-strand | 284-289 | 6 | 9 |
| β-strand | 294-298 | 5 | 9 |
| β-strand | 303-308 | 6 | 9 |
| β-strand | 315-320 | 6 | 2 |
| β-strand | 327-331 | 5 | 2 |
| β-strand | 336-339 | 4 | 2 |
Chain D: 3 helices, 0 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 8-22 | 15 | |
| α-helix | 30-42 | 13 | |
| α-helix | 53-55 | 3 | |
Chain E: 3 helices, 24 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 3-7 | 5 | 10 |
| β-strand | 11-12 | 2 | 11 |
| β-strand | 17-25 | 9 | 10 |
| α-helix | 29-31 | 3 | |
| β-strand | 34-39 | 6 | 12 |
| β-strand | 45-51 | 7 | 12 |
| β-strand | 58-60 | 3 | 12 |
| β-strand | 68-73 | 6 | 10 |
| α-helix | 74-76 | 3 | |
| β-strand | 78-84 | 7 | 10 |
| β-strand | 93-98 | 6 | 12 |
| β-strand | 110-111 | 2 | 12 |
| β-strand | 115 | 1 | 12 |
| β-strand | 118-119 | 2 | 11 |
| β-strand | 141 | 1 | 13 |
| β-strand | 146-149 | 4 | 14 |
| β-strand | 155-160 | 6 | 13 |
| β-strand | 166 | 1 | 15 |
| β-strand | 172 | 1 | 15 |
| β-strand | 174-179 | 6 | 14 |
| β-strand | 186-190 | 5 | 14 |
| β-strand | 194-195 | 2 | 14 |
| β-strand | 204-208 | 5 | 13 |
| β-strand | 211-216 | 6 | 13 |
| β-strand | 226-231 | 6 | 14 |
| α-helix | 237 | 1 | |
| β-strand | 243-247 | 5 | 14 |
Molecules and chains
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|
| Muscarinic acetylcholine receptor M2,muscarinic acetylcholine receptor M2 chimera | A | protein | 353 | Homo sapiens | P08172 (AlphaFold model) |
| Guanine nucleotide-binding protein G(o) subunit alpha | B | protein | 354 | Homo sapiens | P09471 (AlphaFold model) |
| Guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1 | C | protein | 345 | Homo sapiens | P62873 (AlphaFold model) |
| Guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-2 | D | protein | 71 | Homo sapiens | P59768 (AlphaFold model) |
| Antibody fragment | E | protein | 256 | Mus musculus | |
Sequence of entity 1 (A), FASTA
>7T8X_1 Muscarinic acetylcholine receptor M2,muscarinic acetylcholine receptor M2 chimera (chains A)
DYKDDDDASTDSSDNSLALTSPYKTFEVVFIVLVAGSLSLVTIIGNILVMVSIKVNRHLQ
TVNNYFLFSLACADLIIGVFSMNLYTLYTVIGYWPLGPVVCDLWLALDYVVSNASVMNLL
IISFDRYFCVTKPLTYPVKRTTKMAGMMIAAAWVLSFILWAPAILFWQFIVGVRTVEDGE
CYIQFFSNAAVTFGTAIAAFYLPVIIMTVLYWHISRASKSRIKKDKKEPVANQDPVSIVA
RKIVKMTKQPAKKKPPPSREKKVTRTILAILLAFIITWAPYNVMVLINTFCAPCIPNTVW
TIGYWLCYINSTINPACYALCNATFKKTFKHLLMCHYKNIGATRPAGLEVLFQ
Sequence of entity 2 (B), FASTA
>7T8X_2 Guanine nucleotide-binding protein G(o) subunit alpha (chains B)
MGCTLSAEDKAAVERSKMIEKNLKEDGISAAKDVKLLLLGAGESGKSTIVKQMKIIHEDG
FSGEDVKQYKPVVYSNTIQSLAAIVRAMDTLGIEYGDKERKADAKMVCDVVSRMEDTEPF
SAELLSAMMRLWGDSGIQECFNRSREYQLNDSAKYYLDSLDRIGAADYQPTEQDILRTRV
KTTGIVETHFTFKNLHFRLFDVGGQRSERKKWIHCFEDVTAIIFCVALSGYDQVLHEDET
TNRMHESLMLFDSICNNKFFIDTSIILFLNKKDLFGEKIKKSPLTICFPEYTGPNTYEDA
AAYIQAQFESKNRSPNKEIYCHMTCATDTNNIQVVFDAVTDIIIANNLRGCGLY
Sequence of entity 3 (C), FASTA
>7T8X_3 Guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1 (chains C)
GPGSSGSELDQLRQEAEQLKNQIRDARKACADATLSQITNNIDPVGRIQMRTRRTLRGHL
AKIYAMHWGTDSRLLVSASQDGKLIIWDSYTTNKVHAIPLRSSWVMTCAYAPSGNYVACG
GLDNICSIYNLKTREGNVRVSRELAGHTGYLSCCRFLDDNQIVTSSGDTTCALWDIETGQ
QTTTFTGHTGDVMSLSLAPDTRLFVSGACDASAKLWDVREGMCRQTFTGHESDINAICFF
PNGNAFATGSDDATCRLFDLRADQELMTYSHDNIICGITSVSFSKSGRLLLAGYDDFNCN
VWDALKADRAGVLAGHDNRVSCLGVTDDGMAVATGSWDSFLKIWN
Sequence of entity 4 (D), FASTA
>7T8X_4 Guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-2 (chains D)
MASNNTASIAQARKLVEQLKMEANIDRIKVSKAAADLMAYCEAHAKEDPLLTPVPASENP
FREKKFFCAIL
Sequence of entity 5 (E), FASTA
>7T8X_5 Antibody fragment (chains E)
DVQLVESGGGLVQPGGSRKLSCSASGFAFSSFGMHWVRQAPEKGLEWVAYISSGSGTIYY
ADTVKGRFTISRDDPKNTLFLQMTSLRSEDTAMYYCVRSIYYYGSSPFDFWGQGTTLTVS
SGGGGSGGGGSGGGGSDIVMTQATSSVPVTPGESVSISCRSSKSLLHSNGNTYLYWFLQR
PGQSPQLLIYRMSNLASGVPDRFSGSGSGTAFTLTISRLEAEDVGVYYCMQHLEYPLTFG
AGTKLELKGSLEVLFQ
Ligands and cofactors
| ID | Name | Formula | Copies |
|---|
| ACH | Acetylcholine | C7 H16 N O2 | 1 |
Primary citation
Structural and dynamic insights into supra-physiological activation and allosteric modulation of a muscarinic acetylcholine receptor. Xu, J., Wang, Q., Hubner, H. et al. Nat Commun (2023) 14:376-376. DOI 10.1038/s41467-022-35726-z · PubMed
Other PDB entries of the same protein (UniProt P08172 (AlphaFold model), which also has an AlphaFold model), best resolution first:
- 5ZKC 2.3 Å, Crystal structure of rationally thermostabilized M2 muscarinic acetylcholine receptor…
- 5YC8 2.5 Å, Crystal structure of rationally thermostabilized M2 muscarinic acetylcholine receptor…
- 5ZK3 2.6 Å, Crystal structure of rationally thermostabilized M2 muscarinic acetylcholine receptor…
- 8J8R 2.9 Å, Structure of beta-arrestin2 in complex with M2Rpp
- 5ZKB 2.95 Å, Crystal structure of rationally thermostabilized M2 muscarinic acetylcholine receptor…
- 3UON 3.0 Å, Structure of the human M2 muscarinic acetylcholine receptor bound to an antagonist
- 5ZK8 3.0 Å, Crystal structure of M2 muscarinic acetylcholine receptor bound with NMS
- 8JAF 3.1 Å, Structure of Muscarinic receptor (M2R) in complex with beta-arrestin1 (Local Refine,…
- 7T94 3.16 Å, Cryo-EM structure of S1 state ACh-bound M2R-Go signaling complex with a PAM
- 8J97 3.2 Å, Structure of Muscarinic receptor (M2R) in complex with beta-arrestin1 (Local refine,…
- 7T96 3.22 Å, Cryo-EM structure of S2 state ACh-bound M2R-Go signaling complex with a PAM
- 7T90 3.32 Å, Cryo-EM structure of ACh-bound M2R-Go signaling complex in S2 state
Browse structure collections
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