Current Protein Identity:Q8I6T3 New Search
Main Difference Dimensions in This Set
Different construct Different assembly state Different ligand/ion 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
5FMG Structure and function based design of Plasmodium-selective proteasome inhibitors Deposited 2015-11-04 Assembly 1 Protein heterocomplex Heteromer;Protein × 28 PDB declaration: 28-meric(28) Consistent with protein count
Chain I 42–270(229 aa)
Chain W 42–270(229 aa)
Not recorded 7F1 (2S)-N-[(E,2S)-1-(1H-indol-3-yl)-4-methylsulfonyl-but-3-en-2-yl]-2-[[(2S)-3-(1H-indol-3-yl)-2-(2-morpholin-4-ylethanoylamino)propanoyl]amino]-4-methyl-pentanamide × 2 ELECTRON MICROSCOPY
cryo-EM buffer 50MM TRIS HCL, 5MM MGCL2, 1MM DITHIOTREITOL;pH 7.5;50MM TRIS HCL, 5MM MGCL2, 1MM DITHIOTREITOL
cryo-EM vitrification conditions Cryogen ETHANE;VITRIFICATION 1 -- CRYOGEN- ETHANE, HUMIDITY- 95, INSTRUMENT- FEI VITROBOT MARK III, METHOD- BLOT 2.5 SECONDS BEFORE PLUNGING,
Resolution 3.60 Å
6MUV The structure of the Plasmodium falciparum 20S proteasome in complex with two PA28 activators Deposited 2018-10-23 Assembly 1 Protein heterocomplex Heteromer;Protein × 42 PDB declaration: 42-meric(42) Consistent with protein count
Chain I 42–270(229 aa)
Chain W 42–270(229 aa)
Not recorded No recorded non-water small molecule ELECTRON MICROSCOPY
cryo-EM buffer pH 7.4
cryo-EM vitrification conditions Cryogen ETHANE;wait time 0sec blot time 2sec blot force -1
Resolution 3.80 Å
6MUW The structure of the Plasmodium falciparum 20S proteasome. Deposited 2018-10-23 Assembly 1 Protein heterocomplex Heteromer;Protein × 28 PDB declaration: 28-meric(28) Consistent with protein count
Chain I 42–270(229 aa)
Chain W 42–270(229 aa)
Not recorded No recorded non-water small molecule ELECTRON MICROSCOPY
cryo-EM buffer pH 7.4
cryo-EM vitrification conditions Cryogen ETHANE;wait time 0sec blot time 2sec blot force -1
Resolution 3.60 Å
6MUX The structure of the Plasmodium falciparum 20S proteasome in complex with one PA28 activator Deposited 2018-10-23 Assembly 1 Protein heterocomplex Heteromer;Protein × 35 PDB declaration: 35-meric(35) Consistent with protein count
Chain I 42–270(229 aa)
Chain W 42–270(229 aa)
Not recorded No recorded non-water small molecule ELECTRON MICROSCOPY
cryo-EM buffer pH 7.4
cryo-EM vitrification conditions Cryogen ETHANE;wait time 0sec blot time 2sec blot force -1
Resolution 3.90 Å
7LXT Structure of Plasmodium falciparum 20S proteasome with bound bortezomib Deposited 2021-03-05 Assembly 1 Protein heterocomplex Heteromer;Protein × 28 PDB declaration: 28-meric(28) Consistent with protein count
Chain I 42–270(229 aa)
Chain W 42–270(229 aa)
Not recorded BO2 N-[(1R)-1-(DIHYDROXYBORYL)-3-METHYLBUTYL]-N-(PYRAZIN-2-YLCARBONYL)-L-PHENYLALANINAMIDE × 6 ELECTRON MICROSCOPY
cryo-EM buffer pH 7.4
cryo-EM vitrification conditions Cryogen ETHANE
Resolution 3.40 Å
7LXU Structure of Plasmodium falciparum 20S proteasome with bound MPI-5 Deposited 2021-03-05 Assembly 1 Protein heterocomplex Heteromer;Protein × 28 PDB declaration: 28-meric(28) Consistent with protein count
Chain I 42–270(229 aa)
Chain W 42–270(229 aa)
Not recorded YHD N-[(1R)-2-([1,1'-biphenyl]-4-yl)-1-boronoethyl]-1-methyl-L-prolinamide × 2 ELECTRON MICROSCOPY
cryo-EM buffer pH 7.4
cryo-EM vitrification conditions Cryogen ETHANE
Resolution 3.10 Å
8G6F Structure of the Plasmodium falciparum 20S proteasome beta-6 A117D mutant complexed with inhibitor WLW-vs Deposited 2023-02-15 Assembly 1 Protein heterocomplex Heteromer;Protein × 28 PDB declaration: 28-meric(28) Consistent with protein count
Chain I 42–270(229 aa)
Chain W 42–270(229 aa)
Not recorded 7F1 (2S)-N-[(E,2S)-1-(1H-indol-3-yl)-4-methylsulfonyl-but-3-en-2-yl]-2-[[(2S)-3-(1H-indol-3-yl)-2-(2-morpholin-4-ylethanoylamino)propanoyl]amino]-4-methyl-pentanamide × 4 ELECTRON MICROSCOPY
cryo-EM buffer pH 7.5
cryo-EM vitrification conditions Cryogen ETHANE
Resolution 2.58 Å
8W2F Plasmodium falciparum 20S proteasome bound to an inhibitor Deposited 2024-02-20 Assembly 1 Protein heterocomplex Heteromer;Protein × 28 PDB declaration: 28-meric(28) Consistent with protein count
Chain I 42–270(229 aa)
Chain W 42–270(229 aa)
Not recorded A1AE6 (3S)-1-[(2-fluoroethoxy)acetyl]-N-{[(4P)-4-(6-methylpyridin-3-yl)-1,3-thiazol-2-yl]methyl}piperidine-3-carboxamide × 2 ELECTRON MICROSCOPY
cryo-EM buffer pH 7.6
cryo-EM vitrification conditions Cryogen ETHANE
Resolution 3.10 Å
9O3E Plasmodium falciparum 20S proteasome bound to inhibitor 159 Deposited 2025-04-07 Assembly 1 Protein heterocomplex Heteromer;Protein × 28 PDB declaration: 28-meric(28) Consistent with protein count
Chain I 42–270(229 aa)
Chain W 42–270(229 aa)
Not recorded A1B74 (3S)-N~3~-{(1S)-1-[4-(4-cyanophenyl)-1,3-thiazol-2-yl]ethyl}-N~1~-ethoxypiperidine-1,3-dicarboxamide × 2 ELECTRON MICROSCOPY
cryo-EM buffer pH 7.6
cryo-EM vitrification conditions Cryogen ETHANE
Resolution 2.79 Å
9O3F Plasmodium falciparum 20S proteasome bound to inhibitor 296 Deposited 2025-04-07 Assembly 1 Protein heterocomplex Heteromer;Protein × 28 PDB declaration: 28-meric(28) Consistent with protein count
Chain I 42–270(229 aa)
Chain W 42–270(229 aa)
Not recorded A1B73 (3S)-1-({[(3S)-piperidin-3-yl]oxy}acetyl)-N-({4-[4-(trifluoromethyl)phenyl]-1,3-thiazol-2-yl}methyl)piperidine-3-carboxamide × 2 ELECTRON MICROSCOPY
cryo-EM buffer pH 7.6
cryo-EM vitrification conditions Cryogen ETHANE
Resolution 2.28 Å
9Y0K Structure of Plasmodium falciparum 20S proteasome with bound J80 Deposited 2025-08-28 Assembly 1 Protein heterocomplex Heteromer;Protein × 28 PDB declaration: 28-meric(28) Consistent with protein count
Chain I 42–270(229 aa)
Chain W 42–270(229 aa)
Not recorded A1CRO N,N-diethyl-N~2~-hexanoyl-D-asparaginyl-N-{(1S)-2-(2,4-difluorophenyl)-1-[(2S,3S,5S,6S)-5-formyl-2-hydroxy-3-(hydroxymethyl)-3,6-dimethylmorpholin-2-yl]ethyl}-4-fluoro-L-phenylalaninamide × 2 ELECTRON MICROSCOPY
cryo-EM buffer pH 7.5
cryo-EM vitrification conditions Cryogen ETHANE
Resolution 3.00 Å
9Y1O The structure of the Plasmodium falciparum 20S proteasome Deposited 2025-08-29 Assembly 1 Protein heterocomplex Heteromer;Protein × 28 PDB declaration: 28-meric(28) Consistent with protein count
Chain I 42–270(229 aa)
Chain W 42–270(229 aa)
Not recorded No recorded non-water small molecule ELECTRON MICROSCOPY
cryo-EM buffer pH 7.5
cryo-EM vitrification conditions Cryogen ETHANE
Resolution 3.10 Å
9YUY Structure of the Plasmodium falciparum 20S proteasome in complex with a beta5-selective covalent syringolin analogue inhibitor. Deposited 2025-10-23 Assembly 1 Protein heterocomplex Heteromer;Protein × 28 PDB declaration: 28-meric(28) Consistent with protein count
Chain I 1–270(270 aa)
Chain W 1–270(270 aa)
Not recorded A1CY6 methyl N-{[(2R)-1-({(5R,8R)-5-[(3-fluorophenyl)methyl]-2,7-dioxo-1,6-diazacyclododecan-8-yl}amino)-1-oxo-3-phenylpropan-2-yl]carbamoyl}-L-valinate × 2 ELECTRON MICROSCOPY
cryo-EM buffer pH 7.5
cryo-EM vitrification conditions Cryogen ETHANE
Resolution 2.70 Å