8XOR: Tethered agonist-bound human PAR1-Gq complex
Cryo-EM structure of the tethered agonist-bound human PAR1-Gq complex. Determined by electron microscopy at 3.0 Å resolution. Released 18 Sept 2024.
- Method
- Electron microscopy
- Resolution
- 3.0 Å
- Organisms
- Rattus, Bos taurus, Homo sapiens
- Chains
- 5
- Atoms
- 8,979
- Mol. weight
- 184.14 kDa
- Ligands
- CLR
- Released
- 18 Sept 2024
Explore 8XOR in 3D
Show helices and sheets
RCSB PDB
PDBe
Secondary structure: helices and β-sheets
8XOR contains 46 α-helices and 64 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: 11 helices, 6 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 7-23 | 17 | |
| α-helix | 24-28 | 5 | |
| β-strand | 34-40 | 7 | 8 |
| α-helix | 46-53 | 8 | |
| β-strand | 184-191 | 8 | 8 |
| β-strand | 194-201 | 8 | 8 |
| α-helix | 211-217 | 7 | |
| β-strand | 220-226 | 7 | 8 |
| α-helix | 230-244 | 15 | |
| α-helix | 249-251 | 3 | |
| β-strand | 253-259 | 7 | 8 |
| α-helix | 261-269 | 9 | |
| α-helix | 275-277 | 3 | |
| α-helix | 280-284 | 5 | |
| α-helix | 301-317 | 17 | |
| β-strand | 326-330 | 5 | 8 |
| α-helix | 338-357 | 20 | |
Chain B: 5 helices, 28 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 4-25 | 22 | |
| α-helix | 30-33 | 4 | |
| α-helix | 34-36 | 3 | |
| α-helix | 38-40 | 3 | |
| β-strand | 47-52 | 6 | 1 |
| β-strand | 58-63 | 6 | 2 |
| β-strand | 69-74 | 6 | 2 |
| β-strand | 78-83 | 6 | 2 |
| β-strand | 89-94 | 6 | 2 |
| β-strand | 100-105 | 6 | 3 |
| β-strand | 111-116 | 6 | 3 |
| β-strand | 121-125 | 5 | 3 |
| β-strand | 134-139 | 6 | 3 |
| β-strand | 146-151 | 6 | 4 |
| β-strand | 156-161 | 6 | 4 |
| β-strand | 166-170 | 5 | 4 |
| β-strand | 175-180 | 6 | 4 |
| β-strand | 187-192 | 6 | 5 |
| β-strand | 198-203 | 6 | 5 |
| β-strand | 207-212 | 6 | 5 |
| β-strand | 218-222 | 5 | 5 |
| β-strand | 229-234 | 6 | 6 |
| β-strand | 240-245 | 6 | 6 |
| β-strand | 250-254 | 5 | 6 |
| β-strand | 259-264 | 6 | 6 |
| α-helix | 272 | 1 | |
| β-strand | 273-278 | 6 | 7 |
| β-strand | 284-289 | 6 | 7 |
| β-strand | 294-298 | 5 | 7 |
| β-strand | 303-308 | 6 | 7 |
| β-strand | 315-320 | 6 | 1 |
| β-strand | 327-331 | 5 | 1 |
| β-strand | 335-339 | 5 | 1 |
Chain C: 3 helices, 0 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 12-23 | 12 | |
| α-helix | 30-43 | 14 | |
| α-helix | 53-55 | 3 | |
Chain E: 6 helices, 25 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 3-6 | 4 | 9 |
| β-strand | 11-12 | 2 | 10 |
| β-strand | 17-25 | 9 | 9 |
| α-helix | 29-31 | 3 | |
| β-strand | 33-39 | 7 | 11 |
| β-strand | 45-51 | 7 | 11 |
| α-helix | 53-55 | 3 | |
| β-strand | 58-60 | 3 | 11 |
| β-strand | 68-73 | 6 | 9 |
| α-helix | 74-76 | 3 | |
| β-strand | 78-84 | 7 | 9 |
| α-helix | 88-90 | 3 | |
| β-strand | 92-99 | 8 | 11 |
| β-strand | 110-117 | 8 | 11 |
| β-strand | 118-119 | 2 | 10 |
| α-helix | 136-138 | 3 | |
| β-strand | 140-142 | 3 | 12 |
| β-strand | 147-148 | 2 | 13 |
| β-strand | 155-161 | 7 | 12 |
| β-strand | 166 | 1 | 14 |
| β-strand | 172 | 1 | 14 |
| β-strand | 174-179 | 6 | 15 |
| β-strand | 185-190 | 6 | 15 |
| β-strand | 194-195 | 2 | 15 |
| α-helix | 196 | 1 | |
| β-strand | 203-207 | 5 | 12 |
| β-strand | 211-216 | 6 | 12 |
| β-strand | 226-231 | 6 | 15 |
| β-strand | 239 | 1 | 15 |
| β-strand | 243-244 | 2 | 15 |
| β-strand | 245-246 | 2 | 13 |
Chain R: 21 helices, 5 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 43-46 | 4 | 16 |
| β-strand | 87-88 | 2 | 16 |
| α-helix | 90-97 | 8 | |
| α-helix | 99 | 1 | |
| α-helix | 100-104 | 5 | |
| α-helix | 105-125 | 21 | |
| α-helix | 126-130 | 5 | |
| α-helix | 136-163 | 28 | |
| α-helix | 171-205 | 35 | |
| α-helix | 207-213 | 7 | |
| α-helix | 216-239 | 24 | |
| β-strand | 243-245 | 3 | 17 |
| α-helix | 246 | 1 | |
| β-strand | 252-254 | 3 | 17 |
| β-strand | 257-259 | 3 | 16 |
| α-helix | 260-262 | 3 | |
| α-helix | 263-267 | 5 | |
| α-helix | 268-275 | 8 | |
| α-helix | 276-280 | 5 | |
| α-helix | 281-298 | 18 | |
| α-helix | 300-305 | 6 | |
| α-helix | 309-338 | 30 | |
| α-helix | 343-360 | 18 | |
| α-helix | 363-368 | 6 | |
| α-helix | 369-373 | 5 | |
| α-helix | 376-379 | 4 | |
Molecules and chains
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|
| Guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1 | B | protein | 379 | Rattus | P54311 (AlphaFold model) |
| Guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-2 | C | protein | 67 | Bos taurus | P63212 (AlphaFold model) |
| G subunit q (Gi1-Gq chimeric) | A | protein | 361 | Homo sapiens | P63096 (AlphaFold model) |
| scFv16 | E | protein | 303 | Mus musculus | |
| Proteinase-activated receptor 1 LgBiT | R | protein | 532 | Homo sapiens | P25116 (AlphaFold model) |
Sequence of entity 1 (B), FASTA
>8XOR_1 Guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1 (chains B)
MVSGWRLFKKISGSSGGGGSGGGGSSGGSLLQSELDQLRQEAEQLKNQIRDARKACADAT
LSQITNNIDPVGRIQMRTRRTLRGHLAKIYAMHWGTDSRLLVSASQDGKLIIWDSYTTNK
VHAIPLRSSWVMTCAYAPSGNYVACGGLDNICSIYNLKTREGNVRVSRELAGHTGYLSCC
RFLDDNQIVTSSGDTTCALWDIETGQQTTTFTGHTGDVMSLSLAPDTRLFVSGACDASAK
LWDVREGMCRQTFTGHESDINAICFFPNGNAFATGSDDATCRLFDLRADQELMTYSHDNI
ICGITSVSFSKSGRLLLAGYDDFNCNVWDALKADRAGVLAGHDNRVSCLGVTDDGMAVAT
GSWDSFLKIWNHHHHHHHH
Sequence of entity 2 (C), FASTA
>8XOR_2 Guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-2 (chains C)
ASNNTASIAQARKLVEQLKMEANIDRIKVSKAAADLMAYCEAHAKEDPLLTPVPASENPF
REKKFFC
Sequence of entity 3 (A), FASTA
>8XOR_3 G subunit q (Gi1-Gq chimeric) (chains A)
MGCTLSAEDKAAVERSKMIEKQLQKDKQVYRRTLRLLLLGADNSGKSTIVKQMRIYHVNG
YSEEECKQYKAVVYSNTIQSIIAIIRAMGRLKIDFGDSARADDARQLFVLAGAAEEGFMT
AELAGVIKRLWKDSGVQACFNRSREYQLNDSAAYYLNDLDRIAQPNYIPTQQDVLRTRVK
TSGIFETKFQVDKVNFHMFDVGAQRDERRKWIQCFNDVTAIIFVVDSSDYNRLQEALNDF
KSIWNNRWLRTISVILFLNKQDLLAEKVLAGKSKIEDYFPEFARYTTPEDATPEPGEDPR
VTRAKYFIRKEFVDISTASGDGRHICYPHFTCAVDTENARRIFNDCKDIILQMNLREYNL
V
Sequence of entity 4 (E), FASTA
>8XOR_4 scFv16 (chains E)
LLVNQSHQGFNKEHTSKMVSAIVLYVLLAAAAHSAFAVQLVESGGGLVQPGGSRKLSCSA
SGFAFSSFGMHWVRQAPEKGLEWVAYISSGSGTIYYADTVKGRFTISRDDPKNTLFLQMT
SLRSEDTAMYYCVRSIYYYGSSPFDFWGQGTTLTVSAGGGGSGGGGSGGGGSADIVMTQA
TSSVPVTPGESVSISCRSSKSLLHSNGNTYLYWFLQRPGQSPQLLIYRMSNLASGVPDRF
SGSGSGTAFTLTISRLEAEDVGVYYCMQHLEYPLTFGAGTKLELVDENLYFQGASHHHHH
HHH
Sequence of entity 5 (R), FASTA
>8XOR_5 Proteinase-activated receptor 1 LgBiT (chains R)
SFLLRNPNDKYEPFWEDEEKNESGLTEYRLVSINKSSPLQKQLPAFISEDASGYLTSSWL
TLFVPSVYTGVFVVSLPLNIMAIVVFILKMKVKKPAVVYMLHLATADVLFVSVLPFKISY
YFSGSDWQFGSELCRFVTAAFYCNMYASILLMTVISIDRFLAVVYPMQSLSWRTLGRASF
TCLAIWALAIAGVVPLLLKEQTIQVPGLNITTCHDVLNETLLEGYYAYYFSAFSAVFFFV
PLIISTVCYVSIIRCLSSSAVANRSKKSRALFLSAAVFCIFIICFGPTNVLLIAHYSFLS
HTSTTEAAYFAYLLCVCVSSISCCIDPLIYYYASSECQRYVYSILCCKESSDPSSYGSSG
GGGSGGGGSSGVFTLEDFVGDWEQTAAYNLDQVLEQGGVSSLLQNLAVSVTPIQRIVRSG
ENALKIDIHVIIPYEGLSADQMAQIEEVFKVVYPVDDHHFKVILPYGTLVIDGVTPNMLN
YFGRPYEGIAVFDGKKITVTGTLWNGNKIIDERLITPDGSMLFRVTINSGGS
Ligands and cofactors
| ID | Name | Formula | Copies |
|---|
| CLR | Cholesterol | C27 H46 O | 6 |
Primary citation
Structural basis of tethered agonism and G protein coupling of protease-activated receptors. Guo, J., Zhou, Y.L., Yang, Y. et al. Cell Res (2024) 34:725-734. DOI 10.1038/s41422-024-00997-2 · PubMed
Other PDB entries of the same protein (UniProt P54311 (AlphaFold model), which also has an AlphaFold model), best resolution first:
- 7MBX 1.95 Å, Human Cholecystokinin 1 receptor (CCK1R) Gs complex
- 9EJZ 2.06 Å, Human M5 muscarinic acetylcholine receptor complex with mini-Gq, agonist acetylcholine…
- 9IJE 2.34 Å, Epinephrine-activated human beta3 adrenergic receptor
- 8YK0 2.4 Å, Cryo-EM structure of human GPR156-Gi3 complex
- 8Z9O 2.4 Å, Cryo-EM structure of human GPR4-Gs complex
- 22ES 2.43 Å, Gi bound kappa-opioid receptor in complex with difelikefalin
- 7MBY 2.44 Å, Human Cholecystokinin 1 receptor (CCK1R) Gq chimera (mGsqi) complex
- 9WG6 2.44 Å, D1R-Gs in complexed with Dopamine/LY3154207/BMSA1/UNC9815
- 8JIS 2.46 Å, Cryo-EM structure of the GLP-1R/GCGR dual agonist peptide15-bound human GLP-1R-Gs complex
- 9M0R 2.47 Å, Structure of neuropeptide FF receptor 1 complex with NPVF
- 8YKV 2.48 Å, Cryo-EM structure of succinate receptor SUCR1 bound to compound 31
- 9M1O 2.49 Å, Cryo-EM structures of NPFFR2 complex with neuropeptide FF
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