8T3O: TUG-891 bound FFA4-Gq complex
Cryo-EM structure of the TUG-891 bound FFA4-Gq complex. Determined by electron microscopy at 3.06 Å resolution. Released 17 Jan 2024.
- Method
- Electron microscopy
- Resolution
- 3.06 Å
- Organisms
- Homo sapiens, Mus musculus
- Chains
- 5
- Atoms
- 9,109
- Mol. weight
- 134.19 kDa
- Ligands
- PLM, 2Y5, YN9
- Released
- 17 Jan 2024
Explore 8T3O in 3D
Show helices and sheets
RCSB PDB
PDBe
Secondary structure: helices and β-sheets
8T3O contains 36 α-helices and 67 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, 11 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 7-31 | 25 | |
| β-strand | 34-35 | 2 | 9 |
| β-strand | 38-39 | 2 | 10 |
| β-strand | 72-76 | 5 | 9 |
| β-strand | 79-83 | 5 | 9 |
| β-strand | 85 | 1 | 10 |
| α-helix | 99-101 | 3 | |
| β-strand | 105-106 | 2 | 11 |
| β-strand | 107-108 | 2 | 10 |
| β-strand | 109-111 | 3 | 12 |
| α-helix | 118-129 | 12 | |
| α-helix | 132-134 | 3 | |
| α-helix | 137 | 1 | |
| β-strand | 138-139 | 2 | 11 |
| β-strand | 142-144 | 3 | 12 |
| α-helix | 146-155 | 10 | |
| α-helix | 160-163 | 4 | |
| α-helix | 165-169 | 5 | |
| α-helix | 172-173 | 2 | |
| α-helix | 184-202 | 19 | |
| β-strand | 215 | 1 | 12 |
| α-helix | 223-242 | 20 | |
Chain B: 4 helices, 28 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 4-25 | 22 | |
| α-helix | 30-33 | 4 | |
| α-helix | 38-39 | 2 | |
| β-strand | 45-51 | 7 | 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 |
| α-helix | 95 | 1 | |
| 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 | 176-181 | 6 | 5 |
| β-strand | 187-192 | 6 | 6 |
| β-strand | 198-203 | 6 | 6 |
| β-strand | 207-212 | 6 | 6 |
| β-strand | 220-223 | 4 | 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 | 8 |
| β-strand | 284-289 | 6 | 8 |
| β-strand | 294-298 | 5 | 8 |
| β-strand | 303-307 | 5 | 8 |
| β-strand | 315-320 | 6 | 2 |
| β-strand | 327-331 | 5 | 2 |
| β-strand | 336-341 | 6 | 2 |
Chain G: 3 helices, 0 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 8-23 | 16 | |
| α-helix | 30-43 | 14 | |
| α-helix | 53-55 | 3 | |
Chain N: 5 helices, 26 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 3-7 | 5 | 13 |
| β-strand | 11-12 | 2 | 14 |
| β-strand | 18-25 | 8 | 13 |
| α-helix | 29-31 | 3 | |
| β-strand | 33-39 | 7 | 15 |
| β-strand | 45-51 | 7 | 15 |
| β-strand | 58-60 | 3 | 15 |
| β-strand | 68-73 | 6 | 13 |
| β-strand | 78-83 | 6 | 13 |
| α-helix | 88-90 | 3 | |
| β-strand | 92-94 | 3 | 16 |
| β-strand | 95-99 | 5 | 15 |
| β-strand | 110-111 | 2 | 15 |
| β-strand | 115-117 | 3 | 16 |
| β-strand | 118-119 | 2 | 14 |
| α-helix | 138-140 | 3 | |
| β-strand | 141-143 | 3 | 17 |
| β-strand | 147-149 | 3 | 18 |
| β-strand | 156-162 | 7 | 17 |
| β-strand | 167 | 1 | 19 |
| β-strand | 173 | 1 | 19 |
| β-strand | 175-180 | 6 | 18 |
| β-strand | 187-191 | 5 | 18 |
| β-strand | 195-196 | 2 | 18 |
| α-helix | 197 | 1 | |
| β-strand | 204-208 | 5 | 17 |
| β-strand | 212-217 | 6 | 17 |
| β-strand | 226-232 | 7 | 18 |
| α-helix | 238 | 1 | |
| β-strand | 240 | 1 | 18 |
| β-strand | 244-247 | 4 | 18 |
Chain R: 13 helices, 2 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 36-70 | 35 | |
| α-helix | 73-75 | 3 | |
| α-helix | 78-88 | 11 | |
| α-helix | 92-101 | 10 | |
| α-helix | 108-138 | 31 | |
| α-helix | 139-143 | 5 | |
| α-helix | 152-175 | 24 | |
| β-strand | 177-181 | 5 | 1 |
| β-strand | 192-196 | 5 | 1 |
| α-helix | 201-213 | 13 | |
| α-helix | 217-243 | 27 | |
| α-helix | 249-255 | 7 | |
| α-helix | 258-276 | 19 | |
| α-helix | 279-290 | 12 | |
| α-helix | 300-320 | 21 | |
Molecules and chains
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|
| Free fatty acid receptor 4 | R | protein | 297 | Homo sapiens | Q5NUL3 (AlphaFold model) |
| Guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1 | B | protein | 342 | Homo sapiens | P62873 (AlphaFold model) |
| Guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-2 | G | protein | 57 | Homo sapiens | P59768 (AlphaFold model) |
| Guanine nucleotide-binding protein G(q) | A | protein | 230 | Homo sapiens | |
| scFv16 | N | protein | 266 | Mus musculus | |
Sequence of entity 1 (R), FASTA
>8T3O_1 Free fatty acid receptor 4 (chains R)
RTRFPFFSDVKGDHRLVLAAVETTVLVLIFAVSLLGNVCALVLVARRRRRGATACLVLNL
FCADLLFISAIPLVLAVRWTEAWLLGPVACHLLFYVMTLSGSVTILTLAAVSLERMVCIV
HLQRGPGRRARAVLLALIWGYSAVAALPLCVFFRVVPQRISICTLIWPTIPGEISWDVSF
VTLNFLVPGLVIVISYSKILQITKASRKRLTVSLAYSESHQIRVSQQDFRLFRTLFLLMV
SFFIMWSPIIITILLILIQNFKQDLVIWPSLFFWVVAFTFANSALNPILYNMTLCRN
Sequence of entity 2 (B), FASTA
>8T3O_2 Guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1 (chains B)
SELDQLRQEAEQLKNQIRDARKACADATLSQITNNIDPVGRIQMRTRRTLRGHLAKIYAM
HWGTDSRLLVSASQDGKLIIWDSYTTNKVHAIPLRSSWVMTCAYAPSGNYVACGGLDNIC
SIYNLKTREGNVRVSRELAGHTGYLSCCRFLDDNQIVTSSGDTTCALWDIETGQQTTTFT
GHTGDVMSLSLAPDTRLFVSGACDASAKLWDVREGMCRQTFTGHESDINAICFFPNGNAF
ATGSDDATCRLFDLRADQELMTYSHDNIICGITSVSFSKSGRLLLAGYDDFNCNVWDALK
ADRAGVLAGHDNRVSCLGVTDDGMAVATGSWDSFLKIWNGSS
Sequence of entity 3 (G), FASTA
>8T3O_3 Guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-2 (chains G)
TASIAQARKLVEQLKMEANIDRIKVSKAAADLMAYCEAHAKEDPLLTPVPASENPFR
Sequence of entity 4 (A), FASTA
>8T3O_4 Guanine nucleotide-binding protein G(q) (chains A)
VSAEDKAAAERSKMIDKNLREDGEKARRTLRLLLLGADNSGKSTIVKQMTSGIFETKFQV
DKVNFHMFDVGGQRDERRKWIQCFNDVTAIIFVVDSSDYNRLQEALNDFKSIWNNRWLRT
ISVILFLNKQDLLAEKVLAGKSKIEDYFPEFARYTTPEDATPEPGEDPRVTRAKYFIRKE
FVDISTASGDGRHICYPHFTCAVDTENARRIFNDCKDIILQMNLREYNLV
Sequence of entity 5 (N), FASTA
>8T3O_5 scFv16 (chains N)
VQLVESGGGLVQPGGSRKLSCSASGFAFSSFGMHWVRQAPEKGLEWVAYISSGSGTIYYA
DTVKGRFTISRDDPKNTLFLQMTSLRSEDTAMYYCVRSIYYYGSSPFDFWGQGTTLTVSA
GGGGSGGGGSGGGGSADIVMTQATSSVPVTPGESVSISCRSSKSLLHSNGNTYLYWFLQR
PGQSPQLLIYRMSNLASGVPDRFSGSGSGTAFTLTISRLEAEDVGVYYCMQHLEYPLTFG
AGTKLELLEENLYFQGASHHHHHHHH
Ligands and cofactors
| ID | Name | Formula | Copies |
|---|
| PLM | Palmitic acid | C16 H32 O2 | 1 |
| 2Y5 | (2R)-1-{[(R)-hydroxy{[(1R,2R,3R,4R,5S,6R)-2,3,5,6-tetrahydroxy-4-(phosphonooxy)… | C47 H84 O16 P2 | 1 |
| YN9 | 3-{4-[(4-fluoro-4'-methyl[1,1'-biphenyl]-2-yl)methoxy]phenyl}propanoic acid | C23 H21 F O3 | 1 |
Primary citation
Structural basis for the ligand recognition and signaling of free fatty acid receptors. Zhang, X., Guseinov, A.A., Jenkins, L. et al. Sci Adv (2024) 10:eadj2384-eadj2384. DOI 10.1126/sciadv.adj2384 · PubMed
Other PDB entries of the same protein (UniProt Q5NUL3 (AlphaFold model), which also has an AlphaFold model), best resolution first:
- 8G59 2.64 Å, Cryo-EM structure of the TUG891 bound GPR120-Giq complex
- 24XB 2.65 Å, Cryo-EM Structure of the Apo FFAR4-Gq Complex
- 24QH 2.74 Å, Cryo-EM Structure of the FFAR4-Gi complex with unknown density
- 8ID6 2.8 Å, Cryo-EM structure of the oleic acid bound GPR120-Gi complex
- 8IYS 2.95 Å, TUG891-bound FFAR4 in complex with Gq
- 9XFI 2.99 Å, Cryo-EM structure of the Bavachalcone bound FFAR4-Giq complex
- 8ID8 3.0 Å, Cryo-EM structure of the TUG891 bound GPR120-Gi complex
- 8ID9 3.0 Å, Cryo-EM structure of the eicosapentaenoic acid bound GPR120-Gi complex
- 8H4I 3.06 Å, DHA-bound FFAR4 in complex with Gs
- 8H4L 3.07 Å, DHA-bound FFAR4 in complex with Gq
- 8H4K 3.1 Å, GW9508-bound FFAR4 in complex with Gq
- 8ID3 3.1 Å, Cryo-EM structure of the 9-hydroxystearic acid bound GPR120-Gi complex
Browse structure collections
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