Current Protein Identity:P28222 New Search
Main Difference Dimensions in This Set
Different construct Different mutation/modification Different assembly state Different ligand/ion Different experimental method Different experimental conditions Different structure-quality metrics

Difference tags compare only the current result set; every original PDB and assembly record remains separate.

Related-Structure Differences

Each row represents one biological assembly in one PDB entry; multiple monomers of the same protein are listed separately.

PDB Entry Assembly / Oligomeric State Construct Mutations and Modifications Ligands, Ions and Non-polymers Experimental Method Experimental Conditions Structure Quality
4IAQ Crystal structure of the chimeric protein of 5-HT1B-BRIL in complex with dihydroergotamine (PSI Community Target) Deposited 2012-12-07 Assembly 1 Insufficient information Homooligomer;Protein × 2 PDB declaration: dimeric(2) Consistent with protein count
Chain A 33–239(207 aa)
Chain A 304–390(87 aa)
Mutation:L138W, M29W, H124I, R128L Mutation:L138W, M29W, H124I, R128L 2GM Dihydroergotamine × 2 X-RAY DIFFRACTION
X-ray crystallization conditions Lipid Cubic Phase (LCP);pH 8.7;293 K;100 mM Tris pH 8.7, 32-36% (v/v) PEG400, 90 mM sodium citrate tribasic dihydrate, 120 mM ammonium sulfate , Lipid Cubic Phase (LCP), temperature 293K
Resolution 2.80 Å R-free 0.257
4IAR Crystal structure of the chimeric protein of 5-HT1B-BRIL in complex with ergotamine (PSI Community Target) Deposited 2012-12-07 Assembly 1 Insufficient information Monomer;Protein × 1 PDB declaration: monomeric(1) Consistent with protein count
Chain A 33–239(207 aa)
Chain A 306–390(85 aa)
Mutation:L138W, M29W, H124I, R128L Mutation:L138W, M29W, H124I, R128L ERM Ergotamine × 1 OLB (2S)-2,3-dihydroxypropyl (9Z)-octadec-9-enoate × 1 X-RAY DIFFRACTION
X-ray crystallization conditions Lipid Cubic Phase (LCP);pH 7.5;293 K;100 mM Tris pH 7.5, 30% (v/v) PEG400, 400 mM lithium chloride , Lipid Cubic Phase (LCP), temperature 293K
Resolution 2.70 Å R-free 0.261
5V54 Crystal structure of 5-HT1B receptor in complex with methiothepin Deposited 2017-03-13 Assembly 1 Protein homooligomer Homooligomer;Protein × 2 PDB declaration: dimeric(2) Consistent with protein count
Chain A 37–239(203 aa) Fragment:UNP residues 37-239,UNP residues 304-390
Chain A 304–390(87 aa) Fragment:UNP residues 37-239,UNP residues 304-390
Chain B 37–239(203 aa) Fragment:UNP residues 37-239,UNP residues 304-390
Chain B 304–390(87 aa) Fragment:UNP residues 37-239,UNP residues 304-390
Mutation:L138W Mutation:L138W Mutation:L138W Mutation:L138W 89F 1-methyl-4-[(5~{S})-3-methylsulfanyl-5,6-dihydrobenzo[b][1]benzothiepin-5-yl]piperazine × 2 X-RAY DIFFRACTION
X-ray crystallization conditions LIPIDIC CUBIC PHASE;293 K;100mM Bis-Tris (pH7.0), 155mM Ammonium phosphate monobasic, 26% PEG300, 0.01M GSH (L-Glutathione reduced), GSSG (L-Glutathione oxidized)
Resolution 3.90 Å R-free 0.288
6G79 Coupling specificity of heterotrimeric Go to the serotonin 5-HT1B receptor Deposited 2018-04-05 Assembly 1 Insufficient information Heteromer;Protein × 4 PDB declaration: tetrameric(4) Consistent with protein count
Chain S 34–390(357 aa)
Not recorded EP5 2-[5-[2-[4-(4-cyanophenyl)piperazin-1-yl]-2-oxidanylidene-ethoxy]-1~{H}-indol-3-yl]ethylazanium × 1 ELECTRON MICROSCOPY
cryo-EM buffer pH 7.5
cryo-EM vitrification conditions Cryogen ETHANE
Resolution 3.78 Å
7C61 Crystal structure of 5-HT1B-BRIL and SRP2070_Fab complex Deposited 2020-05-21 Assembly 1 Insufficient information Heteromer;Protein × 3 PDB declaration: trimeric(3) Consistent with protein count
Chain A 33–239(207 aa)
Chain A 306–390(85 aa)
Mutation:L138W,M1007W,H1102I,R1106L Mutation:L138W,M1007W,H1102I,R1106L ERM Ergotamine × 1 X-RAY DIFFRACTION
X-ray crystallization conditions LIPIDIC CUBIC PHASE;293 K;30% PEG400, 0.4M SODIUM THIOCYANATE, 0.1M SODIUM ACETATE PH 5.5
Resolution 3.00 Å R-free 0.290