WT CRISPR-Cas12a with the target strand in the RuvC active site. Determined by electron microscopy at 3.8 Å resolution. Released 3 Jul 2024.
Explore 8SFP in 3D Show helices and sheets RCSB PDB PDBe
8SFP contains 64 α-helices and 51 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 | 8 | 1 | 1 |
| β-strand | 11 | 1 | 2 |
| β-strand | 13-23 | 11 | 3 |
| α-helix | 27-34 | 8 | |
| α-helix | 36-65 | 30 | |
| α-helix | 66-68 | 3 | |
| α-helix | 74-85 | 12 | |
| α-helix | 89-111 | 23 | |
| α-helix | 119-129 | 11 | |
| α-helix | 135-137 | 3 | |
| α-helix | 141-145 | 5 | |
| α-helix | 153-160 | 8 | |
| α-helix | 166-169 | 4 | |
| α-helix | 170-179 | 10 | |
| α-helix | 189-191 | 3 | |
| α-helix | 192-197 | 6 | |
| α-helix | 198-214 | 17 | |
| α-helix | 219-229 | 11 | |
| α-helix | 244-247 | 4 | |
| α-helix | 252-263 | 12 | |
| α-helix | 277-285 | 9 | |
| α-helix | 290-297 | 8 | |
| α-helix | 304-308 | 5 | |
| α-helix | 320-323 | 4 | |
| α-helix | 326-342 | 17 | |
| α-helix | 345-356 | 12 | |
| β-strand | 365-366 | 2 | 4 |
| α-helix | 371-378 | 8 | |
| α-helix | 384-395 | 12 | |
| α-helix | 404-413 | 10 | |
| β-strand | 418-419 | 2 | 4 |
| α-helix | 420-426 | 7 | |
| α-helix | 429-451 | 23 | |
| α-helix | 453-455 | 3 | |
| α-helix | 461-481 | 21 | |
| β-strand | 484 | 1 | 4 |
| α-helix | 494-507 | 14 | |
| α-helix | 509-521 | 13 | |
| α-helix | 524-526 | 3 | |
| β-strand | 531-532 | 2 | 3 |
| β-strand | 554-559 | 6 | 3 |
| β-strand | 562-567 | 6 | 3 |
| α-helix | 569-570 | 2 | |
| β-strand | 571 | 1 | 5 |
| β-strand | 574 | 1 | 5 |
| β-strand | 582 | 1 | 3 |
| β-strand | 589-597 | 9 | 3 |
| α-helix | 601-609 | 9 | |
| α-helix | 613-621 | 9 | |
| β-strand | 626-628 | 3 | 6 |
| β-strand | 632 | 1 | 7 |
| α-helix | 635 | 1 | |
| β-strand | 636-638 | 3 | 6 |
| α-helix | 639 | 1 | |
| α-helix | 640-646 | 7 | |
| α-helix | 657-663 | 7 | |
| α-helix | 666-686 | 21 | |
| β-strand | 687 | 1 | 7 |
| α-helix | 698-700 | 3 | |
| α-helix | 701-703 | 3 | |
| α-helix | 707-714 | 8 | |
| α-helix | 715-717 | 3 | |
| β-strand | 719-727 | 9 | 3 |
| α-helix | 728-736 | 9 | |
| β-strand | 741-746 | 6 | 3 |
| α-helix | 757-759 | 3 | |
| α-helix | 760-769 | 10 | |
| α-helix | 771-775 | 5 | |
| β-strand | 780-781 | 2 | 3 |
| β-strand | 786-790 | 5 | 3 |
| α-helix | 862-864 | 3 | |
| β-strand | 868-877 | 10 | 3 |
| β-strand | 882 | 1 | 2 |
| α-helix | 888-898 | 11 | |
| β-strand | 904-909 | 6 | 8 |
| β-strand | 915-920 | 6 | 8 |
| β-strand | 926-931 | 6 | 8 |
| β-strand | 934-935 | 2 | 9 |
| β-strand | 938-939 | 2 | 9 |
| α-helix | 940-956 | 17 | |
| α-helix | 965-986 | 22 | |
| β-strand | 989-994 | 6 | 8 |
| α-helix | 997-1006 | 10 | |
| α-helix | 1014-1024 | 11 | |
| β-strand | 1026 | 1 | 1 |
| β-strand | 1036 | 1 | 10 |
| β-strand | 1041 | 1 | 10 |
| β-strand | 1043 | 1 | 1 |
| α-helix | 1047-1049 | 3 | |
| β-strand | 1058-1059 | 2 | 8 |
| β-strand | 1062-1066 | 5 | 8 |
| β-strand | 1083 | 1 | 11 |
| α-helix | 1091-1099 | 9 | |
| β-strand | 1104-1106 | 3 | 12 |
| β-strand | 1113-1117 | 5 | 12 |
| β-strand | 1126 | 1 | 11 |
| β-strand | 1136-1140 | 5 | 12 |
| β-strand | 1145-1147 | 3 | 13 |
| β-strand | 1153-1155 | 3 | 13 |
| β-strand | 1159-1166 | 8 | 14 |
| β-strand | 1169-1176 | 8 | 14 |
| α-helix | 1178-1189 | 12 | |
| α-helix | 1199-1204 | 6 | |
| α-helix | 1209-1222 | 14 | |
| β-strand | 1226-1229 | 4 | 15 |
| β-strand | 1234-1237 | 4 | 15 |
| β-strand | 1238 | 1 | 16 |
| β-strand | 1241 | 1 | 12 |
| β-strand | 1243 | 1 | 17 |
| β-strand | 1247 | 1 | 17 |
| β-strand | 1250 | 1 | 16 |
| α-helix | 1251-1253 | 3 | |
| α-helix | 1262-1283 | 22 | |
| 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 (5'-d(p*cp*tp*tp*cp*cp*gp*ap*tp*cp*tp*tp*tp*tp*ap*gp*tp*gp*ap*tp*a)-3') | D | DNA | 56 | synthetic construct |
>8SFP_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
>8SFP_2 RNA (39-MER) (chains B) UUUUUAAUUUCUACUCUUGUAGAUGUGAUAAGUGGAAUGCCAUGUGGA
>8SFP_3 DNA (40-MER) (chains C) AGCACAGTAGCTACTCCACATGGCATTCCACTTATCACTAAAAGATCGGAAGAGCG
>8SFP_4 DNA (5'-D(P*CP*TP*TP*CP*CP*GP*AP*TP*CP*TP*TP*TP*TP*AP*GP*TP*GP*AP*TP*A)-3') (chains D) CGCTCTTCCGATCTTTTAGTGATAAGTGGAATGCCATGTGGAGTAGCTACTGTGCT
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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