Vaccinia C16 protein bound to Ku70/Ku80. Determined by electron microscopy at 3.47 Å resolution. Released 9 Nov 2022.
Explore 8AG5 in 3D Show helices and sheets RCSB PDB PDBe
8AG5 contains 65 α-helices and 102 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 | 36-43 | 8 | 1 |
| α-helix | 46-49 | 4 | |
| α-helix | 59-77 | 19 | |
| β-strand | 82-88 | 7 | 1 |
| β-strand | 102-109 | 8 | 1 |
| α-helix | 113-120 | 8 | |
| α-helix | 124-134 | 11 | |
| α-helix | 143-155 | 13 | |
| β-strand | 162-169 | 8 | 1 |
| α-helix | 180-196 | 17 | |
| β-strand | 199-202 | 4 | 1 |
| β-strand | 205 | 1 | 2 |
| α-helix | 213-216 | 4 | |
| α-helix | 232-235 | 4 | |
| β-strand | 236 | 1 | 2 |
| α-helix | 239-250 | 12 | |
| α-helix | 251-253 | 3 | |
| β-strand | 257 | 1 | 3 |
| β-strand | 260-262 | 3 | 3 |
| β-strand | 268-274 | 7 | 3 |
| β-strand | 277 | 1 | 4 |
| α-helix | 279-285 | 7 | |
| β-strand | 286 | 1 | 5 |
| β-strand | 288 | 1 | 6 |
| β-strand | 295 | 1 | 6 |
| β-strand | 299-303 | 5 | 7 |
| α-helix | 313-315 | 3 | |
| β-strand | 316-322 | 7 | 8 |
| β-strand | 325-329 | 5 | 8 |
| α-helix | 331-336 | 6 | |
| β-strand | 344-352 | 9 | 3 |
| α-helix | 353-355 | 3 | |
| β-strand | 366-370 | 5 | 3 |
| β-strand | 375-376 | 2 | 9 |
| α-helix | 378-392 | 15 | |
| β-strand | 394-401 | 8 | 3 |
| β-strand | 409-416 | 8 | 3 |
| β-strand | 419-420 | 2 | 10 |
| β-strand | 426-428 | 3 | 10 |
| β-strand | 431-436 | 6 | 3 |
| α-helix | 440-442 | 3 | |
| β-strand | 443 | 1 | 11 |
| α-helix | 444-448 | 5 | |
| α-helix | 456-468 | 13 | |
| β-strand | 470 | 1 | 11 |
| α-helix | 481-494 | 14 | |
| α-helix | 499-502 | 4 | |
| α-helix | 511-518 | 8 | |
| α-helix | 521-529 | 9 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 3 | 1 | 12 |
| β-strand | 8-15 | 8 | 13 |
| β-strand | 24 | 1 | 14 |
| β-strand | 27 | 1 | 14 |
| α-helix | 30-47 | 18 | |
| β-strand | 53-59 | 7 | 13 |
| β-strand | 65 | 1 | 13 |
| β-strand | 77-84 | 8 | 13 |
| α-helix | 88-96 | 9 | |
| α-helix | 107-121 | 15 | |
| β-strand | 129-135 | 7 | 13 |
| α-helix | 147-156 | 10 | |
| β-strand | 159-165 | 7 | 13 |
| α-helix | 199-215 | 17 | |
| α-helix | 218-223 | 6 | |
| β-strand | 224-226 | 3 | 13 |
| α-helix | 227-230 | 4 | |
| α-helix | 235-237 | 3 | |
| α-helix | 243 | 1 | |
| β-strand | 244 | 1 | 12 |
| α-helix | 245-246 | 2 | |
| β-strand | 247-252 | 6 | 11 |
| β-strand | 258-267 | 10 | 11 |
| α-helix | 276 | 1 | |
| β-strand | 277-280 | 4 | 8 |
| α-helix | 286-288 | 3 | |
| β-strand | 290-294 | 5 | 7 |
| β-strand | 313-315 | 3 | 5 |
| β-strand | 320-322 | 3 | 5 |
| α-helix | 323-325 | 3 | |
| β-strand | 339-347 | 9 | 11 |
| α-helix | 348-350 | 3 | |
| α-helix | 353-355 | 3 | |
| β-strand | 357-366 | 10 | 11 |
| α-helix | 367 | 1 | |
| α-helix | 371-387 | 17 | |
| β-strand | 389-396 | 8 | 11 |
| α-helix | 402-403 | 2 | |
| β-strand | 404-412 | 9 | 11 |
| β-strand | 417-424 | 8 | 11 |
| α-helix | 427-429 | 3 | |
| β-strand | 430 | 1 | 4 |
| α-helix | 448-460 | 13 | |
| β-strand | 462 | 1 | 3 |
| β-strand | 464-466 | 3 | 15 |
| β-strand | 473-475 | 3 | 15 |
| α-helix | 479-481 | 3 | |
| α-helix | 483-484 | 2 | |
| α-helix | 485-499 | 15 | |
| α-helix | 504-509 | 6 | |
| α-helix | 510-515 | 6 | |
| α-helix | 520-525 | 6 | |
| α-helix | 527-536 | 10 | |
| β-strand | 540-541 | 2 | 9 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 2-4 | 3 | 16 |
| β-strand | 10-15 | 6 | 16 |
| α-helix | 23-29 | 7 | |
| β-strand | 38-41 | 4 | 16 |
| α-helix | 48-59 | 12 | |
| β-strand | 66-69 | 4 | 16 |
| β-strand | 73-78 | 6 | 16 |
| β-strand | 85-86 | 2 | 17 |
| β-strand | 98-108 | 11 | 16 |
| β-strand | 113 | 1 | 18 |
| β-strand | 116-119 | 4 | 17 |
| β-strand | 124-127 | 4 | 17 |
| β-strand | 130-134 | 5 | 16 |
| β-strand | 138-141 | 4 | 17 |
| α-helix | 142-143 | 2 | |
| β-strand | 144 | 1 | 18 |
| β-strand | 149-159 | 11 | 16 |
| β-strand | 165-167 | 3 | 19 |
| β-strand | 175-177 | 3 | 19 |
| β-strand | 178 | 1 | 20 |
| β-strand | 186-193 | 8 | 20 |
| β-strand | 203-208 | 6 | 20 |
| β-strand | 214-218 | 5 | 20 |
| α-helix | 224-228 | 5 | |
| β-strand | 231-232 | 2 | 20 |
| α-helix | 235-238 | 4 | |
| α-helix | 239-243 | 5 | |
| α-helix | 247-250 | 4 | |
| β-strand | 255-256 | 2 | 20 |
| α-helix | 268-273 | 6 | |
| α-helix | 283-297 | 15 | |
| β-strand | 304-310 | 7 | 20 |
| β-strand | 316-327 | 12 | 20 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 2-4 | 3 | 16 |
| β-strand | 10-15 | 6 | 16 |
| α-helix | 23-30 | 8 | |
| β-strand | 38-42 | 5 | 16 |
| α-helix | 48-60 | 13 | |
| β-strand | 64-69 | 6 | 16 |
| β-strand | 72-78 | 7 | 16 |
| β-strand | 84 | 1 | 17 |
| β-strand | 98-108 | 11 | 16 |
| β-strand | 116-118 | 3 | 17 |
| β-strand | 124-127 | 4 | 17 |
| β-strand | 130-134 | 5 | 16 |
| β-strand | 139-141 | 3 | 17 |
| β-strand | 149-160 | 12 | 16 |
| β-strand | 164-168 | 5 | 21 |
| β-strand | 174-178 | 5 | 21 |
| β-strand | 186-193 | 8 | 21 |
| α-helix | 194-195 | 2 | |
| β-strand | 199 | 1 | 22 |
| β-strand | 203-209 | 7 | 21 |
| β-strand | 214-218 | 5 | 21 |
| α-helix | 224-227 | 4 | |
| β-strand | 231-232 | 2 | 21 |
| α-helix | 235-242 | 8 | |
| β-strand | 244 | 1 | 22 |
| β-strand | 255-256 | 2 | 21 |
| α-helix | 282-298 | 17 | |
| β-strand | 304-310 | 7 | 21 |
| β-strand | 313 | 1 | 12 |
| α-helix | 315 | 1 | |
| β-strand | 316-327 | 12 | 21 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Ku70-Xrcc6 | A | protein | 651 | Homo sapiens | P12956 (AlphaFold model) |
| X-ray repair cross-complementing protein 5 | B | protein | 755 | Homo sapiens | P13010 (AlphaFold model) |
| Protein C10 | C, D | protein | 369 | Vaccinia virus Western Reserve | P03296 (AlphaFold model) |
>8AG5_1 Ku70-Xrcc6 (chains A) MSAWSHPQFEKGSAGSAAGSGAGWSHPQFEKLEVLFQGPGGSMSGWESYYKTEGDEEAEE EQEENLEASGDYKYSGRDSLIFLVDASKAMFESQSEDELTPFDMSIQCIQSVYISKIISS DRDLLAVVFYGTEKDKNSVNFKNIYVLQELDNPGAKRILELDQFKGQQGQKRFQDMMGHG SDYSLSEVLWVCANLFSDVQFKMSHKRIMLFTNEDNPHGNDSAKASRARTKAGDLRDTGI FLDLMHLKKPGGFDISLFYRDIISIAEDEDLRVHFEESSKLEDLLRKVRAKETRKRALSR LKLKLNKDIVISVGIYNLVQKALKPPPIKLYRETNEPVKTKTRTFNTSTGGLLLPSDTKR SQIYGSRQIILEKEETEELKRFDDPGLMLMGFKPLVLLKKHHYLRPSLFVYPEESLVIGS STLFSALLIKCLEKEVAALCRYTPRRNIPPYFVALVPQEEELDDQKIQVTPPGFQLVFLP FADDKRKMPFTEKIMATPEQVGKMKAIVEKLRFTYRSDSFENPVLQQHFRNLEALALDLM EPEQAVDLTLPKVEAMNKRLGSLVDEFKELVYPPDYNPEGKVTKRKHDNEGSGSKRPKVE YSEEELKTHISKGTLGKFTVPMLKEACRAYGLKSGLKKQELLEALTKHFQD
>8AG5_2 X-ray repair cross-complementing protein 5 (chains B) MAHHHHHHHHHHGALEVLFQGPHMVRSGNKAAVVLCMDVGFTMSNSIPGIESPFEQAKKV ITMFVQRQVFAENKDEIALVLFGTDGTDNPLSGGDQYQNITVHRHLMLPDFDLLEDIESK IQPGSQQADFLDALIVSMDVIQHETIGKKFEKRHIEIFTDLSSRFSKSQLDIIIHSLKKC DISLQFFLPFSLGKEDGSGDRGDGPFRLGGHGPSFPLKGITEQQKEGLEIVKMVMISLEG EDGLDEIYSFSESLRKLCVFKKIERHSIHWPCRLTIGSNLSIRIAAYKSILQERVKKTWT VVDAKTLKKEDIQKETVYCLNDDDETEVLKEDIIQGFRYGSDIVPFSKVDEEQMKYKSEG KCFSVLGFCKSSQVQRRFFMGNQVLKVFAARDDEAAAVALSSLIHALDDLDMVAIVRYAY DKRANPQVGVAFPHIKHNYECLVYVQLPFMEDLRQYMFSSLKNSKKYAPTEAQLNAVDAL IDSMSLAKKDEKTDTLEDLFPTTKIPNPRFQRLFQCLLHRALHPREPLPPIQQHIWNMLN PPAEVTTKSQIPLSKIKTLFPLIEAKKKDQVTAQEIFQDNHEDGPTAKKLKTEQGGAHFS VSSLAEGSVTSVGSVNPAENFRVLVKQKKASFEEASNQLINHIEQFLDTNETPYFMKSID CIRAFREEAIKFSEEQRFNNFLKALQEKVEIKQLNHFWEIVVQDGITLITKEEASGSSVT AEEAKKFLAPKDKPSGDTAAVFEEGGDVDDLLDMI
>8AG5_3 Protein C10 (chains C, D) MDIYDDKGLQTIKLFNNEFDCIRNDIRELFKHVTDSDSIQLPMEDNSDIIENIRKILYRR LKNVECVDIDSTITFMKYDPNDDNKRTCSNWVPLTNNYMEYCLVIYLETPICGGKIKLYH PTGNIKSDKDIMFAKTLDFKSKKVLTGRKTIAVLDISVSYNRSMTTIHYNDDVDIDIHTD KNGKELCYCYITIDDHYLVDVETIGVIVNRSGKCLLVNNHLGIGIVKDKRISDSFGDVCM DTIFDFSEARELFSLTNDDNRNIAWDTDKLDDDTDIWTPVTEDDYKFLSRLVLYAKSQSD TVFDYYVLTGDTEPPTVFIFKVTRFYFNMPKGGENLYFQGWSHPQFEKGGGSGGGSGGSS AWSHPQFEK
Structural basis for the inactivation of cytosolic DNA sensing by the vaccinia virus. Rivera-Calzada, A., Arribas-Bosacoma, R., Ruiz-Ramos, A. et al. Nat Commun (2022) 13:7062-7062. DOI 10.1038/s41467-022-34843-z · PubMed
Other PDB entries of the same protein (UniProt P12956 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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