Crystal structure of MUS81-EME1 bound by compound 21. Determined by X-ray diffraction at 2.47 Å resolution. Released 19 Jun 2024.
Explore 9F9M in 3D Show helices and sheets RCSB PDB PDBe
9F9M contains 32 α-helices and 36 β-strands across 4 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.
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 261-262 | 2 | 1 |
| β-strand | 267-274 | 8 | 2 |
| α-helix | 275-278 | 4 | |
| α-helix | 288-293 | 6 | |
| β-strand | 298-301 | 4 | 2 |
| β-strand | 308-314 | 7 | 2 |
| β-strand | 325-336 | 12 | 2 |
| α-helix | 337-346 | 10 | |
| α-helix | 349-357 | 9 | |
| β-strand | 363-369 | 7 | 2 |
| α-helix | 381-393 | 13 | |
| α-helix | 397 | 1 | |
| β-strand | 398-402 | 5 | 2 |
| α-helix | 405-423 | 19 | |
| β-strand | 428-431 | 4 | 1 |
| β-strand | 452-454 | 3 | 1 |
| β-strand | 455 | 1 | 2 |
| α-helix | 456-460 | 5 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 253-256 | 4 | 3 |
| α-helix | 258-261 | 4 | |
| α-helix | 266-275 | 10 | |
| β-strand | 279-282 | 4 | 3 |
| β-strand | 290-294 | 5 | 3 |
| β-strand | 308 | 1 | 3 |
| β-strand | 311-317 | 7 | 3 |
| α-helix | 318-326 | 9 | |
| α-helix | 343-354 | 12 | |
| β-strand | 358-364 | 7 | 3 |
| α-helix | 405-418 | 14 | |
| β-strand | 422-426 | 5 | 3 |
| α-helix | 429-445 | 17 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 261-262 | 2 | 4 |
| β-strand | 267-274 | 8 | 5 |
| α-helix | 275-278 | 4 | |
| α-helix | 286-293 | 8 | |
| β-strand | 298-301 | 4 | 5 |
| β-strand | 308-314 | 7 | 5 |
| β-strand | 326 | 1 | 6 |
| β-strand | 327-336 | 10 | 5 |
| α-helix | 337-346 | 10 | |
| α-helix | 349-357 | 9 | |
| β-strand | 363-369 | 7 | 5 |
| α-helix | 381-393 | 13 | |
| α-helix | 397 | 1 | |
| β-strand | 398-402 | 5 | 5 |
| α-helix | 405-423 | 19 | |
| β-strand | 428-429 | 2 | 4 |
| β-strand | 430-431 | 2 | 7 |
| α-helix | 448 | 1 | |
| α-helix | 450 | 1 | |
| β-strand | 453-454 | 2 | 7 |
| β-strand | 455 | 1 | 6 |
| α-helix | 456-460 | 5 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 253-256 | 4 | 8 |
| α-helix | 258-262 | 5 | |
| α-helix | 266-275 | 10 | |
| β-strand | 279-282 | 4 | 8 |
| β-strand | 290-294 | 5 | 8 |
| α-helix | 307 | 1 | |
| β-strand | 308 | 1 | 8 |
| α-helix | 309 | 1 | |
| β-strand | 311-317 | 7 | 8 |
| α-helix | 318-326 | 9 | |
| α-helix | 343-354 | 12 | |
| β-strand | 358-364 | 7 | 8 |
| α-helix | 405-418 | 14 | |
| β-strand | 422-426 | 5 | 8 |
| α-helix | 429-445 | 17 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Crossover junction endonuclease MUS81 | A, C | protein | 308 | Homo sapiens | Q96NY9 (AlphaFold model) |
| Crossover junction endonuclease EME1 | B, D | protein | 326 | Homo sapiens | Q96AY2 (AlphaFold model) |
>9F9M_1 Crossover junction endonuclease MUS81 (chains A, C) GSSAELASEAGVQQQPLELRPGEYRVLLCVDIGETRGGGHRPELLRELQRLHVTHTVRKL HVGDFVWVAQETNPRDPANPGELVLDHIVERKRLDDLCSSIIDGRFREQKFRLKRCGLER RVYLVEEHGSVHNLSLPESTLLQAVTNTQVIDGFFVKRTADIKESAAYLALLTRGLQRLY QGHTLRSRPWGTPGNPESGAMTSPNPLCSLLTFSDFNAGAIKNKAQSVREVFARQLMQVR GVSGEKAAALVDRYSTPASLLAAYDACATPKEQETLLSTIKCGRLQRNLGPALSRTLSQL YCSYGPLT
>9F9M_2 Crossover junction endonuclease EME1 (chains B, D) GEECLKHIIVVLDPVLLQMEGGGQLLGALQTMECRCVIEAQAVPCSVTWRRRAGPSEDRE DWVEEPTVLVLLRAEAFVSMIDNGKQGSLDSTMKGKETLQGFVTDITAKTAGKALSLVIV DQEKCFSAQNPPRRGKQGANKQTKKQQQRQPEASIGSMVSRVDAEEALVDLQLHTEAQAQ IVQSWKELADFTCAFTKAVAEAPFKKLRDETTFSFCLESDWAGGVKVDLAGRGLALVWRR QIQQLNRVSLEMASAVVNAYPSPQLLVQAYQQCFSDKERQNLLADIQVRRGEGVTSTSRR IGPELSRRIYLQMTTLQPHLSLDSAD
| ID | Name | Formula | Copies |
|---|---|---|---|
| MG | Magnesium ion | Mg | 4 |
| A1IA4 | 5-oxidanyl-4-oxidanylidene-1-(4-piperazin-1-ylphenyl)pyridine-3-carboxylic acid | C16 H17 N3 O4 | 2 |
Fragment-Based Discovery of Novel MUS81 Inhibitors. Collie, G.W., Borjesson, U., Chen, Y. et al. ACS Med Chem Lett (2024) 15:1151-1158. DOI 10.1021/acsmedchemlett.3c00453 · PubMed
Other PDB entries of the same protein (UniProt Q96NY9 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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