WT CRISPR-Cas12a with a 20bp R-loop and nontarget strand in the RuvC active site. Determined by electron microscopy at 3.3 Å resolution. Released 3 Jul 2024.
Explore 8SFO in 3D Show helices and sheets RCSB PDB PDBe
8SFO contains 70 α-helices and 49 β-strands across 1 chain. 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 |
|---|---|---|---|
| α-helix | 4-6 | 3 | |
| β-strand | 11 | 1 | 1 |
| β-strand | 13-23 | 11 | 2 |
| α-helix | 24 | 1 | |
| α-helix | 27-33 | 7 | |
| α-helix | 36-66 | 31 | |
| α-helix | 74-85 | 12 | |
| α-helix | 89-111 | 23 | |
| α-helix | 119-130 | 12 | |
| α-helix | 136-139 | 4 | |
| α-helix | 143-146 | 4 | |
| α-helix | 153-160 | 8 | |
| α-helix | 166-169 | 4 | |
| α-helix | 170-177 | 8 | |
| α-helix | 189-191 | 3 | |
| α-helix | 192-197 | 6 | |
| α-helix | 198-214 | 17 | |
| α-helix | 217-229 | 13 | |
| α-helix | 237-240 | 4 | |
| α-helix | 243-247 | 5 | |
| α-helix | 252-263 | 12 | |
| α-helix | 272-275 | 4 | |
| α-helix | 277-286 | 10 | |
| α-helix | 290-297 | 8 | |
| α-helix | 302-308 | 7 | |
| α-helix | 311-313 | 3 | |
| α-helix | 326-343 | 18 | |
| α-helix | 345-354 | 10 | |
| α-helix | 355-358 | 4 | |
| α-helix | 361-363 | 3 | |
| β-strand | 365-366 | 2 | 3 |
| α-helix | 371-378 | 8 | |
| α-helix | 383-395 | 13 | |
| α-helix | 404-415 | 12 | |
| β-strand | 418-419 | 2 | 3 |
| α-helix | 420-427 | 8 | |
| α-helix | 429-451 | 23 | |
| α-helix | 453-455 | 3 | |
| α-helix | 461-481 | 21 | |
| β-strand | 484 | 1 | 3 |
| α-helix | 494-507 | 14 | |
| α-helix | 510-521 | 12 | |
| α-helix | 524-526 | 3 | |
| β-strand | 531-533 | 3 | 2 |
| β-strand | 545 | 1 | 2 |
| α-helix | 549-552 | 4 | |
| β-strand | 554-559 | 6 | 2 |
| β-strand | 562-567 | 6 | 2 |
| α-helix | 569-570 | 2 | |
| β-strand | 571 | 1 | 4 |
| β-strand | 574 | 1 | 4 |
| β-strand | 589-596 | 8 | 2 |
| α-helix | 601-609 | 9 | |
| α-helix | 613-618 | 6 | |
| β-strand | 626-628 | 3 | 5 |
| β-strand | 632 | 1 | 6 |
| β-strand | 636-638 | 3 | 5 |
| α-helix | 640-646 | 7 | |
| α-helix | 657-663 | 7 | |
| α-helix | 666-686 | 21 | |
| β-strand | 687 | 1 | 6 |
| α-helix | 695-697 | 3 | |
| α-helix | 699-700 | 2 | |
| α-helix | 701-703 | 3 | |
| α-helix | 707-714 | 8 | |
| α-helix | 715-718 | 4 | |
| β-strand | 720-727 | 8 | 2 |
| α-helix | 728-737 | 10 | |
| β-strand | 741-746 | 6 | 2 |
| α-helix | 748-750 | 3 | |
| α-helix | 757-759 | 3 | |
| α-helix | 760-768 | 9 | |
| α-helix | 771-775 | 5 | |
| β-strand | 779-781 | 3 | 2 |
| β-strand | 786-790 | 5 | 2 |
| α-helix | 862-865 | 4 | |
| β-strand | 868-877 | 10 | 2 |
| β-strand | 882 | 1 | 1 |
| α-helix | 888-898 | 11 | |
| β-strand | 904 | 1 | 7 |
| β-strand | 907-909 | 3 | 7 |
| β-strand | 915-920 | 6 | 7 |
| β-strand | 926-931 | 6 | 7 |
| β-strand | 934 | 1 | 8 |
| β-strand | 939 | 1 | 8 |
| α-helix | 940-954 | 15 | |
| α-helix | 965-986 | 22 | |
| β-strand | 989 | 1 | 7 |
| β-strand | 990-994 | 5 | 9 |
| α-helix | 997-1006 | 10 | |
| α-helix | 1016-1024 | 9 | |
| β-strand | 1026 | 1 | 10 |
| β-strand | 1043 | 1 | 10 |
| α-helix | 1047-1049 | 3 | |
| β-strand | 1058-1059 | 2 | 9 |
| β-strand | 1062-1066 | 5 | 9 |
| β-strand | 1083 | 1 | 11 |
| α-helix | 1085-1087 | 3 | |
| α-helix | 1091-1099 | 9 | |
| β-strand | 1104-1106 | 3 | 12 |
| β-strand | 1113-1118 | 6 | 12 |
| β-strand | 1126 | 1 | 11 |
| β-strand | 1135-1140 | 6 | 12 |
| β-strand | 1145-1147 | 3 | 13 |
| β-strand | 1153-1155 | 3 | 13 |
| β-strand | 1159-1162 | 4 | 14 |
| β-strand | 1173-1176 | 4 | 14 |
| α-helix | 1178-1189 | 12 | |
| α-helix | 1200-1204 | 5 | |
| α-helix | 1209-1222 | 14 | |
| β-strand | 1226 | 1 | 15 |
| β-strand | 1229 | 1 | 16 |
| β-strand | 1234 | 1 | 16 |
| β-strand | 1237 | 1 | 15 |
| β-strand | 1238-1242 | 5 | 17 |
| β-strand | 1248-1250 | 3 | 17 |
| α-helix | 1251-1253 | 3 | |
| α-helix | 1262-1281 | 20 | |
| α-helix | 1295-1306 | 12 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| CRISPR-associated endonuclease Cas12a | A | protein | 1311 | Acidaminococcus sp. BV3L6 | U2UMQ6 (AlphaFold model) |
| RNA (39-mer) | B | RNA | 48 | synthetic construct | |
| DNA (40-mer) | C | DNA | 56 | synthetic construct | |
| DNA (35-mer) | D | DNA | 56 | synthetic construct |
>8SFO_1 CRISPR-associated endonuclease Cas12a (chains A) GAASMTQFEGFTNLYQVSKTLRFELIPQGKTLKHIQEQGFIEEDKARNDHYKELKPIIDR IYKTYADQCLQLVQLDWENLSAAIDSYRKEKTEETRNALIEEQATYRNAIHDYFIGRTDN LTDAINKRHAEIYKGLFKAELFNGKVLKQLGTVTTTEHENALLRSFDKFTTYFSGFYENR KNVFSAEDISTAIPHRIVQDNFPKFKENCHIFTRLITAVPSLREHFENVKKAIGIFVSTS IEEVFSFPFYNQLLTQTQIDLYNQLLGGISREAGTEKIKGLNEVLNLAIQKNDETAHIIA SLPHRFIPLFKQILSDRNTLSFILEEFKSDEEVIQSFCKYKTLLRNENVLETAEALFNEL NSIDLTHIFISHKKLETISSALCDHWDTLRNALYERRISELTGKITKSAKEKVQRSLKHE DINLQEIISAAGKELSEAFKQKTSEILSHAHAALDQPLPTTLKKQEEKEILKSQLDSLLG LYHLLDWFAVDESNEVDPEFSARLTGIKLEMEPSLSFYNKARNYATKKPYSVEKFKLNFQ MPTLASGWDVNKEKNNGAILFVKNGLYYLGIMPKQKGRYKALSFEPTEKTSEGFDKMYYD YFPDAAKMIPKCSTQLKAVTAHFQTHTTPILLSNNFIEPLEITKEIYDLNNPEKEPKKFQ TAYAKKTGDQKGYREALCKWIDFTRDFLSKYTKTTSIDLSSLRPSSQYKDLGEYYAELNP LLYHISFQRIAEKEIMDAVETGKLYLFQIYNKDFAKGHHGKPNLHTLYWTGLFSPENLAK TSIKLNGQAELFYRPKSRMKRMAHRLGEKMLNKKLKDQKTPIPDTLYQELYDYVNHRLSH DLSDEARALLPNVITKEVSHEIIKDRRFTSDKFFFHVPITLNYQAANSPSKFNQRVNAYL KEHPETPIIGIDRGERNLIYITVIDSTGKILEQRSLNTIQQFDYQKKLDNREKERVAARQ AWSVVGTIKDLKQGYLSQVIHEIVDLMIHYQAVVVLENLNFGFKSKRTGIAEKAVYQQFE KMLIDKLNCLVLKDYPAEKVGGVLNPYQLTDQFTSFAKMGTQSGFLFYVPAPYTSKIDPL TGFVDPFVWKTIKNHESRKHFLEGFDFLHYDVKTGDFILHFKMNRNLSFQRGLPGFMPAW DIVFEKNETQFDAKGTPFIAGKRIVPVIENHRFTGRYRDLYPANELIALLEEKGIVFRDG SNILPKLLENDDSHAIDTMVALIRSVLQMRNSNAATGEDYINSPVRDLNGVCFDSRFQNP EWPMDADANGAYHIALKGQLLLNHLKESKDLKLQNGISNQDWLAYIQELRN
>8SFO_2 RNA (39-MER) (chains B) UUUUUAAUUUCUACUCUUGUAGAUGUGAUAAGUGGAAUGCCAUGUGGA
>8SFO_3 DNA (40-MER) (chains C) AGCACAGTAGCTACTCCACATGGCATTCCACTTATCACTAAAAGATCGGAAGAGCG
>8SFO_4 DNA (35-MER) (chains D) CGCTCTTCCGATCTTTTAGTGATAAGTGGAATGCCATGTGGAGTAGCTACTGTGCT
| ID | Name | Formula | Copies |
|---|---|---|---|
| MG | Magnesium ion | Mg | 2 |
Cas12a domain flexibility guides R-loop formation and forces RuvC resetting. Strohkendl, I., Saha, A., Moy, C. et al. Mol Cell (2024) 84:2717-2731.e6. DOI 10.1016/j.molcel.2024.06.007 · PubMed
Other PDB entries of the same protein (UniProt U2UMQ6 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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