8DWC: Gq-coupled MRGPRX1 with peptide agonist BAM8-22
CryoEM structure of Gq-coupled MRGPRX1 with peptide agonist BAM8-22. Determined by electron microscopy at 2.87 Å resolution. Released 2 Nov 2022.
- Method
- Electron microscopy
- Resolution
- 2.87 Å
- Organisms
- Bos taurus, Homo sapiens, Mus musculus
- Chains
- 6
- Atoms
- 8,298
- Mol. weight
- 139.36 kDa
- Released
- 2 Nov 2022
Explore 8DWC in 3D
Show helices and sheets
RCSB PDB
PDBe
Secondary structure: helices and β-sheets
8DWC contains 36 α-helices and 58 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.
Chain A: 1 helix, 0 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 17-19 | 3 | |
Chain B: 11 helices, 6 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 7-31 | 25 | |
| β-strand | 33-39 | 7 | 14 |
| α-helix | 46-48 | 3 | |
| β-strand | 69-76 | 8 | 14 |
| β-strand | 79-86 | 8 | 14 |
| α-helix | 96-100 | 5 | |
| β-strand | 105-111 | 7 | 14 |
| α-helix | 115-117 | 3 | |
| α-helix | 118-129 | 12 | |
| α-helix | 132-134 | 3 | |
| β-strand | 138-144 | 7 | 14 |
| α-helix | 146-155 | 10 | |
| α-helix | 160-163 | 4 | |
| α-helix | 165-167 | 3 | |
| α-helix | 184-203 | 20 | |
| β-strand | 211-213 | 3 | 14 |
| α-helix | 223-242 | 20 | |
Chain C: 3 helices, 29 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 4-23 | 20 | |
| α-helix | 30-33 | 4 | |
| α-helix | 34-36 | 3 | |
| β-strand | 43 | 1 | 1 |
| β-strand | 47-51 | 5 | 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 | 146-153 | 8 | 5 |
| β-strand | 156-161 | 6 | 5 |
| β-strand | 165-170 | 6 | 5 |
| β-strand | 175-181 | 7 | 5 |
| β-strand | 187-192 | 6 | 6 |
| β-strand | 198-203 | 6 | 6 |
| β-strand | 208-212 | 5 | 6 |
| β-strand | 217-222 | 6 | 6 |
| β-strand | 229-234 | 6 | 7 |
| β-strand | 240-245 | 6 | 7 |
| β-strand | 250-254 | 5 | 7 |
| β-strand | 259-264 | 6 | 7 |
| β-strand | 273-278 | 6 | 1 |
| β-strand | 284-289 | 6 | 1 |
| β-strand | 294-298 | 5 | 1 |
| β-strand | 304-308 | 5 | 1 |
| 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 | 13-23 | 11 | |
| α-helix | 30-43 | 14 | |
| α-helix | 53-55 | 3 | |
Chain E: 4 helices, 23 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 3-7 | 5 | 8 |
| β-strand | 10-12 | 3 | 9 |
| β-strand | 19-25 | 7 | 8 |
| α-helix | 29-31 | 3 | |
| β-strand | 33-39 | 7 | 9 |
| β-strand | 45-51 | 7 | 9 |
| α-helix | 53-55 | 3 | |
| β-strand | 58-60 | 3 | 9 |
| β-strand | 68-73 | 6 | 8 |
| β-strand | 78-83 | 6 | 8 |
| β-strand | 92-99 | 8 | 9 |
| β-strand | 111-119 | 9 | 9 |
| β-strand | 128-129 | 2 | 10 |
| β-strand | 134-136 | 3 | 11 |
| β-strand | 143-147 | 5 | 12 |
| β-strand | 148-149 | 2 | 10 |
| β-strand | 154 | 1 | 13 |
| β-strand | 160 | 1 | 13 |
| β-strand | 162-167 | 6 | 11 |
| β-strand | 174-178 | 5 | 11 |
| β-strand | 182-183 | 2 | 11 |
| α-helix | 184 | 1 | |
| β-strand | 191-196 | 6 | 12 |
| β-strand | 199-204 | 6 | 12 |
| β-strand | 214-219 | 6 | 11 |
| α-helix | 225 | 1 | |
| β-strand | 231-234 | 4 | 11 |
Chain R: 14 helices, 0 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 24-54 | 31 | |
| α-helix | 60-85 | 26 | |
| α-helix | 94-125 | 32 | |
| α-helix | 127-128 | 2 | |
| α-helix | 129-133 | 5 | |
| α-helix | 138-160 | 23 | |
| α-helix | 171-203 | 33 | |
| α-helix | 212-226 | 15 | |
| α-helix | 231-238 | 8 | |
| α-helix | 246-249 | 4 | |
| α-helix | 250-254 | 5 | |
| α-helix | 255-268 | 14 | |
| α-helix | 269-274 | 6 | |
| α-helix | 275-277 | 3 | |
Molecules and chains
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|
| Proenkephalin-A | A | protein | 15 | Bos taurus | P01210 (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) |
| Mas-related G-protein coupled receptor member X1 | R | protein | 323 | Homo sapiens | Q96LB2 (AlphaFold model) |
| scFv16 | E | protein | 257 | Mus musculus | |
| Gs-mini-Gq chimera | B | protein | 246 | Homo sapiens | |
Sequence of entity 1 (A), FASTA
>8DWC_1 Proenkephalin-A (chains A)
VGRPEWWMDYQKRYG
Sequence of entity 2 (C), FASTA
>8DWC_2 Guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1 (chains C)
GPGSSGSELDQLRQEAEQLKNQIRDARKACADATLSQITNNIDPVGRIQMRTRRTLRGHL
AKIYAMHWGTDSRLLVSASQDGKLIIWDSYTTNKVHAIPLRSSWVMTCAYAPSGNYVACG
GLDNICSIYNLKTREGNVRVSRELAGHTGYLSCCRFLDDNQIVTSSGDTTCALWDIETGQ
QTTTFTGHTGDVMSLSLAPDTRLFVSGACDASAKLWDVREGMCRQTFTGHESDINAICFF
PNGNAFATGSDDATCRLFDLRADQELMTYSHDNIICGITSVSFSKSGRLLLAGYDDFNCN
VWDALKADRAGVLAGHDNRVSCLGVTDDGMAVATGSWDSFLKIWN
Sequence of entity 3 (D), FASTA
>8DWC_3 Guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-2 (chains D)
MASNNTASIAQARKLVEQLKMEANIDRIKVSKAAADLMAYCEAHAKEDPLLTPVPASENP
FREKKFFCAIL
Sequence of entity 4 (R), FASTA
>8DWC_4 Mas-related G-protein coupled receptor member X1 (chains R)
GPDPTISTLDTELTPINGTEETLCYKQTLSLTVLTCIVSLVGLTGNAVVLWLLGCRMRRN
AFSIYILNLAAADFLFLSGRLIYSLLSFISIPHTISKILYPVMMFSYFAGLSFLSAVSTE
RCLSVLWPIWYRCHRPTHLSAVVCVLLWALSLLRSILEWMLCGFLFSGADSAWCQTSDFI
TVAWLIFLCVVLCGSSLVLLIRILCGSRKIPLTRLYVTILLTVLVFLLCGLPFGIQFFLF
LWIHVDREVLFCHVHLVSIFLSALNSSANPIIYFFVGSFRQRQNRQNLKLVLQRALQDAS
EVDEGGGQLPEEILELSGSRLEQ
Sequence of entity 5 (E), FASTA
>8DWC_5 scFv16 (chains E)
DVQLVESGGGLVQPGGSRKLSCSASGFAFSSFGMHWVRQAPEKGLEWVAYISSGSGTIYY
ADTVKGRFTISRDDPKNTLFLQMTSLRSEDTAMYYCVRSIYYYGSSPFDFWGQGTTLTVS
SGGGGSGGGGSGGGGSDIVMTQATSSVPVTPGESVSISCRSSKSLLHSNGNTYLYWFLQR
PGQSPQLLIYRMSNLASGVPDRFSGSGSGTAFTLTISRLEAEDVGVYYCMQHLEYPLTFG
AGTKLELKAAALEVLFQ
Sequence of entity 6 (B), FASTA
>8DWC_6 Gs-mini-Gq chimera (chains B)
MGSTVSAEDKAAAERSKMIDKNLREDGEKARRTLRLLLLGADNSGKSTIVKQMRILHGGS
GGSGGTSGIFETKFQVDKVNFHMFDVGGQRDERRKWIQCFNDVTAIIFVVDSSDYNRLQE
ALNDFKSIWNNRWLRTISVILFLNKQDLLAEKVLAGKSKIEDYFPEFARYTTPEDATPEP
GEDPRVTRAKYFIRKEFVDISTASGDGRHICYPHFTCAVDTENARRIFNDCKDIILQMNL
REYNLV
Primary citation
Ligand recognition and allosteric modulation of the human MRGPRX1 receptor. Liu, Y., Cao, C., Huang, X.P. et al. Nat Chem Biol (2023) 19:416-422. DOI 10.1038/s41589-022-01173-6 · PubMed
Other PDB entries of the same protein (UniProt P01210 (AlphaFold model), which also has an AlphaFold model), best resolution first:
- 5E33 1.84 Å, Structure of human DPP3 in complex with met-enkephalin
- 5E3A 2.05 Å, Structure of human DPP3 in complex with opioid peptide leu-enkephalin
- 8JGF 2.7 Å, CryoEM structure of Gq-coupled MRGPRX1 with peptide agonist BAM8-22
- 8DWG 2.71 Å, CryoEM structure of Gq-coupled MRGPRX1 with peptide ligand BAM8-22 and positive…
- 8JGG 3.0 Å, CryoEM structure of Gi-coupled MRGPRX1 with peptide agonist BAM8-22
- 1PLW NMR structure of Methionine-Enkephalin in fast tumbling DMPC/DHPC bicelles
- 1PLX NMR structure of Methionine-Enkephalin in fast tumbling Bicelles/DMPG
- 2LWC Met-enkephalin in DPMC SUV
Browse structure collections
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