9DQH: Gq-coupled MRGPRD with a new agonist EP-2825
CryoEM structure of Gq-coupled MRGPRD with a new agonist EP-2825. Determined by electron microscopy at 2.92 Å resolution. Released 11 Dec 2024.
- Method
- Electron microscopy
- Resolution
- 2.92 Å
- Organisms
- Homo sapiens, Mus musculus
- Chains
- 5
- Atoms
- 7,978
- Mol. weight
- 137.68 kDa
- Ligands
- A1BE2
- Released
- 11 Dec 2024
Explore 9DQH in 3D
Show helices and sheets
RCSB PDB
PDBe
Secondary structure: helices and β-sheets
9DQH contains 37 α-helices and 62 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: 14 helices, 0 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 22-51 | 30 | |
| α-helix | 61-86 | 26 | |
| α-helix | 92-128 | 37 | |
| α-helix | 130-135 | 6 | |
| α-helix | 141-162 | 22 | |
| α-helix | 172-185 | 14 | |
| α-helix | 186-190 | 5 | |
| α-helix | 191-206 | 16 | |
| α-helix | 209-211 | 3 | |
| α-helix | 218-229 | 12 | |
| α-helix | 230-234 | 5 | |
| α-helix | 235-243 | 9 | |
| α-helix | 251-273 | 23 | |
| α-helix | 274-278 | 5 | |
Chain B: 10 helices, 7 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 7-31 | 25 | |
| β-strand | 33-35 | 3 | 1 |
| β-strand | 36-39 | 4 | 2 |
| α-helix | 46-48 | 3 | |
| β-strand | 69-76 | 8 | 1 |
| β-strand | 79-86 | 8 | 1 |
| α-helix | 96-101 | 6 | |
| β-strand | 105-111 | 7 | 2 |
| α-helix | 118-129 | 12 | |
| α-helix | 132-134 | 3 | |
| β-strand | 138-144 | 7 | 2 |
| α-helix | 146-155 | 10 | |
| α-helix | 160-163 | 4 | |
| α-helix | 165-167 | 3 | |
| α-helix | 184-203 | 20 | |
| β-strand | 211-215 | 5 | 2 |
| α-helix | 224-242 | 19 | |
Chain C: 5 helices, 28 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 4-25 | 22 | |
| α-helix | 30-33 | 4 | |
| α-helix | 34-36 | 3 | |
| β-strand | 47-51 | 5 | 3 |
| β-strand | 58-63 | 6 | 4 |
| β-strand | 69-74 | 6 | 4 |
| β-strand | 78-83 | 6 | 4 |
| β-strand | 89-94 | 6 | 4 |
| β-strand | 100-105 | 6 | 5 |
| β-strand | 111-116 | 6 | 5 |
| β-strand | 121-125 | 5 | 5 |
| α-helix | 129-131 | 3 | |
| β-strand | 134-139 | 6 | 5 |
| β-strand | 146-151 | 6 | 6 |
| β-strand | 156-161 | 6 | 6 |
| β-strand | 166-170 | 5 | 6 |
| β-strand | 175-180 | 6 | 6 |
| β-strand | 187-192 | 6 | 7 |
| β-strand | 198-203 | 6 | 7 |
| β-strand | 207-212 | 6 | 7 |
| β-strand | 217-223 | 7 | 7 |
| β-strand | 229-234 | 6 | 8 |
| β-strand | 240-245 | 6 | 8 |
| β-strand | 249-254 | 6 | 8 |
| β-strand | 260-264 | 5 | 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 | 304-308 | 5 | 9 |
| β-strand | 315-320 | 6 | 3 |
| β-strand | 327-331 | 5 | 3 |
| β-strand | 336-339 | 4 | 3 |
Chain D: 4 helices, 0 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 12-23 | 12 | |
| α-helix | 30-43 | 14 | |
| α-helix | 45-47 | 3 | |
| α-helix | 53-55 | 3 | |
Chain E: 4 helices, 27 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 3-6 | 4 | 10 |
| β-strand | 11-12 | 2 | 11 |
| β-strand | 18-25 | 8 | 10 |
| α-helix | 29-31 | 3 | |
| β-strand | 33-39 | 7 | 12 |
| β-strand | 45-51 | 7 | 12 |
| α-helix | 53-55 | 3 | |
| β-strand | 58-60 | 3 | 12 |
| β-strand | 68-73 | 6 | 10 |
| β-strand | 78-83 | 6 | 10 |
| β-strand | 92-99 | 8 | 12 |
| β-strand | 110-111 | 2 | 12 |
| β-strand | 113 | 1 | 10 |
| β-strand | 115-117 | 3 | 12 |
| β-strand | 118-119 | 2 | 11 |
| α-helix | 126-127 | 2 | |
| β-strand | 128-129 | 2 | 13 |
| β-strand | 134-136 | 3 | 14 |
| β-strand | 143-147 | 5 | 15 |
| β-strand | 148-149 | 2 | 13 |
| β-strand | 154 | 1 | 16 |
| β-strand | 160 | 1 | 16 |
| β-strand | 162-167 | 6 | 14 |
| β-strand | 174-178 | 5 | 14 |
| β-strand | 182-183 | 2 | 14 |
| β-strand | 192-196 | 5 | 15 |
| β-strand | 199-204 | 6 | 15 |
| β-strand | 214-219 | 6 | 14 |
| α-helix | 225 | 1 | |
| β-strand | 227 | 1 | 14 |
| β-strand | 231-234 | 4 | 14 |
Molecules and chains
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|
| Mas-related G-protein coupled receptor member D | A | protein | 322 | Homo sapiens | Q8TDS7 (AlphaFold model) |
| Gs-mini-Gq chimera | B | protein | 246 | Homo sapiens | A0A590UJY2 (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) |
| scFv16 | E | protein | 257 | Mus musculus | |
Sequence of entity 1 (A), FASTA
>9DQH_1 Mas-related G-protein coupled receptor member D (chains A)
GPNQTLNSSGTVESALNYSRGSTVHTAYLVLSSLAMFTCLCGMAGNSMVIWLLGFRMHRN
PFCIYILNLAAADLLFLFSMASTLSLETQPLVNTTDKVHELMKRLMYFAYTVGLSLLTAI
STQRCLSVLFPIWFKCHRPRHLSAWVCGLLWTLCLLMNGLTSSFCSKFLKFNEDRCFRVD
MVQAALIMGVLTPVMTLSSLTLFVWVRRSSQQWRRQPTRLFVVVLASVLVFLICSLPLSI
YWFVLYWLSLPPEMQVLCFSLSRLSSSVSSSANPVIYFLVGSRRSHRLPTRSLGTVLQQA
LREEPELEGGETPTVGTNEMGA
Sequence of entity 2 (B), FASTA
>9DQH_2 Gs-mini-Gq chimera (chains B)
MGSTVSAEDKAAAERSKMIDKNLREDGEKARRTLRLLLLGADNSGKSTIVKQMRILHGGS
GGSGGTSGIFETKFQVDKVNFHMFDVGGQRDERRKWIQCFNDVTAIIFVVDSSDYNRLQE
ALNDFKSIWNNRWLRTISVILFLNKQDLLAEKVLAGKSKIEDYFPEFARYTTPEDATPEP
GEDPRVTRAKYFIRKEFVDISTASGDGRHICYPHFTCAVDTENARRIFNDCKDIILQMNL
REYNLV
Sequence of entity 3 (C), FASTA
>9DQH_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
>9DQH_4 Guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-2 (chains D)
MASNNTASIAQARKLVEQLKMEANIDRIKVSKAAADLMAYCEAHAKEDPLLTPVPASENP
FREKKFFCAIL
Sequence of entity 5 (E), FASTA
>9DQH_5 scFv16 (chains E)
DVQLVESGGGLVQPGGSRKLSCSASGFAFSSFGMHWVRQAPEKGLEWVAYISSGSGTIYY
ADTVKGRFTISRDDPKNTLFLQMTSLRSEDTAMYYCVRSIYYYGSSPFDFWGQGTTLTVS
SGGGGSGGGGSGGGGSDIVMTQATSSVPVTPGESVSISCRSSKSLLHSNGNTYLYWFLQR
PGQSPQLLIYRMSNLASGVPDRFSGSGSGTAFTLTISRLEAEDVGVYYCMQHLEYPLTFG
AGTKLELKAAALEVLFQ
Ligands and cofactors
| ID | Name | Formula | Copies |
|---|
| A1BE2 | 2-({1-[2-(4-chlorophenyl)-2-methylpropanoyl]piperidin-4-yl}amino)-5,6,7,8-tetra… | C23 H29 Cl N4 O2 | 1 |
Primary citation
High-affinity agonists reveal recognition motifs for the MRGPRD GPCR. Wang, C., Liu, Y., Lanier, M. et al. Cell Rep (2024) 43:114942-114942. DOI 10.1016/j.celrep.2024.114942 · PubMed
Other PDB entries of the same protein (UniProt Q8TDS7 (AlphaFold model), which also has an AlphaFold model), best resolution first:
- 7Y15 2.9 Å, Cryo-EM structure of apo-state MrgD-Gi complex
- 9DQJ 2.9 Å, CryoEM structure of Gq-coupled MRGPRD with a new agonist EP-3945
- 7Y12 3.1 Å, Cryo-EM structure of MrgD-Gi complex with beta-alanine
- 7Y13 3.1 Å, Cryo-EM structure of apo-state MrgD-Gi complex (local)
- 7Y14 3.2 Å, Cryo-EM structure of MrgD-Gi complex with beta-alanine (local)
Browse structure collections
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