Crystal structure of MUS81-EME1, apo form. Determined by X-ray diffraction at 2.15 Å resolution. Released 3 Jul 2024.
Explore 9F98 in 3D Show helices and sheets RCSB PDB PDBe
9F98 contains 30 α-helices and 34 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 | 284-293 | 10 | |
| β-strand | 298-301 | 4 | 2 |
| β-strand | 308-314 | 7 | 2 |
| β-strand | 325-336 | 12 | 2 |
| α-helix | 337-345 | 9 | |
| α-helix | 349-357 | 9 | |
| β-strand | 363-369 | 7 | 2 |
| α-helix | 381-393 | 13 | |
| β-strand | 398-402 | 5 | 2 |
| α-helix | 405-422 | 18 | |
| β-strand | 428-430 | 3 | 1 |
| β-strand | 452-453 | 2 | 1 |
| β-strand | 455 | 1 | 2 |
| α-helix | 456-459 | 4 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 252-256 | 5 | 3 |
| α-helix | 258-262 | 5 | |
| α-helix | 266-275 | 10 | |
| β-strand | 279-282 | 4 | 3 |
| β-strand | 290-295 | 6 | 3 |
| β-strand | 307-308 | 2 | 3 |
| α-helix | 309 | 1 | |
| β-strand | 311-317 | 7 | 3 |
| α-helix | 318-327 | 10 | |
| α-helix | 343-353 | 11 | |
| 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 | 325-336 | 12 | 5 |
| α-helix | 337-345 | 9 | |
| 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 | 428-430 | 3 | 4 |
| α-helix | 448 | 1 | |
| α-helix | 450 | 1 | |
| β-strand | 452-453 | 2 | 4 |
| β-strand | 455 | 1 | 5 |
| α-helix | 456-460 | 5 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 253-256 | 4 | 6 |
| α-helix | 258-261 | 4 | |
| α-helix | 266-275 | 10 | |
| β-strand | 279-282 | 4 | 6 |
| β-strand | 290-294 | 5 | 6 |
| β-strand | 308 | 1 | 6 |
| β-strand | 311-317 | 7 | 6 |
| α-helix | 318-327 | 10 | |
| α-helix | 343-353 | 11 | |
| α-helix | 357 | 1 | |
| β-strand | 358-364 | 7 | 6 |
| α-helix | 405-418 | 14 | |
| β-strand | 422-426 | 5 | 6 |
| 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) |
>9F98_1 Crossover junction endonuclease MUS81 (chains A, C) GSSAELASEAGVQQQPLELRPGEYRVLLCVDIGETRGGGHRPELLRELQRLHVTHTVRKL HVGDFVWVAQETNPRDPANPGELVLDHIVERKRLDDLCSSIIDGRFREQKFRLKRCGLER RVYLVEEHGSVHNLSLPESTLLQAVTNTQVIDGFFVKRTADIKESAAYLALLTRGLQRLY QGHTLRSRPWGTPGNPESGAMTSPNPLCSLLTFSDFNAGAIKNKAQSVREVFARQLMQVR GVSGEKAAALVDRYSTPASLLAAYDACATPKEQETLLSTIKCGRLQRNLGPALSRTLSQL YCSYGPLT
>9F98_2 Crossover junction endonuclease EME1 (chains B, D) GEECLKHIIVVLDPVLLQMEGGGQLLGALQTMECRCVIEAQAVPCSVTWRRRAGPSEDRE DWVEEPTVLVLLRAEAFVSMIDNGKQGSLDSTMKGKETLQGFVTDITAKTAGKALSLVIV DQEKCFSAQNPPRRGKQGANKQTKKQQQRQPEASIGSMVSRVDAEEALVDLQLHTEAQAQ IVQSWKELADFTCAFTKAVAEAPFKKLRDETTFSFCLESDWAGGVKVDLAGRGLALVWRR QIQQLNRVSLEMASAVVNAYPSPQLLVQAYQQCFSDKERQNLLADIQVRRGEGVTSTSRR IGPELSRRIYLQMTTLQPHLSLDSAD
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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