Structure of the SecA/SecYE/proOmpA(4Y)-sfGFP complex with ADP. Determined by electron microscopy at 3.33 Å resolution. Released 11 Jan 2023.
Explore 7XHB in 3D Show helices and sheets RCSB PDB PDBe
7XHB contains 59 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 |
|---|---|---|---|
| α-helix | 15-32 | 18 | |
| α-helix | 38-53 | 16 | |
| α-helix | 62-77 | 16 | |
| α-helix | 83-93 | 11 | |
| β-strand | 97-99 | 3 | 1 |
| α-helix | 107-118 | 12 | |
| β-strand | 123-128 | 6 | 2 |
| α-helix | 131-145 | 15 | |
| β-strand | 152 | 1 | 2 |
| α-helix | 161-168 | 8 | |
| β-strand | 172-176 | 5 | 2 |
| α-helix | 177-187 | 11 | |
| β-strand | 201-206 | 6 | 2 |
| α-helix | 209-210 | 2 | |
| α-helix | 211-215 | 5 | |
| β-strand | 221-225 | 5 | 3 |
| α-helix | 232-241 | 10 | |
| β-strand | 246 | 1 | 4 |
| β-strand | 250-251 | 2 | 4 |
| β-strand | 260-261 | 2 | 4 |
| α-helix | 263-272 | 10 | |
| α-helix | 284-294 | 11 | |
| α-helix | 295-299 | 5 | |
| α-helix | 302-305 | 4 | |
| β-strand | 306-308 | 3 | 5 |
| β-strand | 313-316 | 4 | 5 |
| β-strand | 323-324 | 2 | 5 |
| β-strand | 327-329 | 3 | 3 |
| α-helix | 334-340 | 7 | |
| β-strand | 350-355 | 6 | 3 |
| α-helix | 357-362 | 6 | |
| β-strand | 366-367 | 2 | 2 |
| β-strand | 371 | 1 | 1 |
| α-helix | 376-384 | 9 | |
| β-strand | 389-391 | 3 | 1 |
| α-helix | 392-394 | 3 | |
| β-strand | 401-402 | 2 | 6 |
| α-helix | 403-405 | 3 | |
| β-strand | 406-407 | 2 | 7 |
| α-helix | 411-428 | 18 | |
| β-strand | 432-435 | 4 | 6 |
| α-helix | 439-451 | 13 | |
| β-strand | 457-459 | 3 | 6 |
| α-helix | 464-466 | 3 | |
| α-helix | 467-473 | 7 | |
| β-strand | 480-483 | 4 | 6 |
| β-strand | 505-509 | 5 | 6 |
| α-helix | 516-523 | 8 | |
| β-strand | 533-537 | 5 | 6 |
| β-strand | 539 | 1 | 7 |
| α-helix | 544-548 | 5 | |
| α-helix | 552-558 | 7 | |
| β-strand | 569-570 | 2 | 7 |
| α-helix | 572-619 | 48 | |
| α-helix | 624-642 | 19 | |
| α-helix | 654-664 | 11 | |
| α-helix | 674-676 | 3 | |
| α-helix | 681-700 | 20 | |
| α-helix | 706-737 | 32 | |
| α-helix | 738-744 | 7 | |
| α-helix | 748-776 | 29 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 4-20 | 17 | |
| β-strand | 48-53 | 6 | 3 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 3-14 | 12 | |
| α-helix | 15-17 | 3 | |
| β-strand | 19 | 1 | 8 |
| α-helix | 20-22 | 3 | |
| α-helix | 23-58 | 36 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 3-9 | 7 | |
| α-helix | 12-33 | 22 | |
| α-helix | 41-47 | 7 | |
| α-helix | 75-86 | 12 | |
| α-helix | 93-100 | 8 | |
| α-helix | 104-135 | 32 | |
| α-helix | 149-172 | 24 | |
| α-helix | 178-188 | 11 | |
| α-helix | 191-202 | 12 | |
| α-helix | 215-235 | 21 | |
| β-strand | 238-241 | 4 | 8 |
| β-strand | 244 | 1 | 9 |
| β-strand | 262-265 | 4 | 8 |
| α-helix | 272-282 | 11 | |
| α-helix | 284-287 | 4 | |
| α-helix | 295-303 | 9 | |
| α-helix | 309-330 | 22 | |
| α-helix | 333-342 | 10 | |
| β-strand | 346 | 1 | 9 |
| β-strand | 347 | 1 | 10 |
| β-strand | 350 | 1 | 10 |
| α-helix | 355-380 | 26 | |
| α-helix | 383-386 | 4 | |
| α-helix | 400-416 | 17 | |
| α-helix | 420-423 | 4 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Protein translocase subunit SecA | A | protein | 778 | Bacillus subtilis subsp. subtilis str. 168 | P28366 (AlphaFold model) |
| Protein translocase subunit SecY | Y | protein | 430 | Geobacillus thermodenitrificans NG80-2 | A4IJK8 (AlphaFold model) |
| Protein translocase subunit SecE | E | protein | 60 | Geobacillus thermodenitrificans NG80-2 | A4IJH4 (AlphaFold model) |
| Translocating peptide | B | protein | 345 | Escherichia coli |
>7XHB_1 Protein translocase subunit SecA (chains A) MLGILNKMFDPTKRTLNRYEKIANDIDAIRGDYENLSDDALKHKTIEFKERLEKGATTDD LLVEAFAVVREASRRVTGMFPFKVQLMGGVALHDGNIAEMKTGEGKTLTSTLPVYLNALT GKGVHVVTVNEYLASRDAEQMGKIFEFLGLTVGLNLNSMSKDEKREAYAADITYSTNNEL GFDYLRDNMVLYKEQMVQRPLHFAVIDEVDSILIDEARTPLIISGQAAKSTKLYVQANAF VRTLKAEKDYTYDIKTKAVQLTEEGMTKAEKAFGIDNLFDVKHVALNHHINQALKAHVAM QKDVDYVVEDGQVVIVDSFTGRLMKGRRYSEGLHQAIEAKEGLEIQNESMTLATITFQNY FRMYEKLAGMTGTAKTEEEEFRNIYNMQVVTIPTNRPVVRDDRPDLIYRTMEGKFKAVAE DVAQRYMTGQPVLVGTVAVETSELISKLLKNKGIPHQVLNAKNHEREAQIIEEAGQKGAV TIATNMAGRGTDIKLGEGVKELGGLAVVGTERHESRRIDNQLRGRSGRQGDPGITQFYLS MEDELMRRFGAERTMAMLDRFGMDDSTPIQSKMVSRAVESSQKRVEGNNFDSRKQLLQYD DVLRQQREVIYKQRFEVIDSENLREIVENMIKSSLERAIAAYTPREELPEEWKLDGLVDL INTTYLDEGALEKSDIFGKEPDEMLELIMDRIITKYNEKEEQFGKEQMREFEKVIVLRAV DSKWMDHIDAMDQLRQGIHLRAYAQTNPLREYQMEGFAMFEHMIESIEDEVAKFVMKA
>7XHB_2 Protein translocase subunit SecY (chains Y) MFRTISNFMRVSDIRNKIIFTLLMLIVFRIGTFIPVPSVNTDVLKLQDQLNAFGVLNIFC GGALQNFSIFAMGVMPYITASIIVQLLQMDVVPKFAEWSKQGEMGRRKLAQFTRYFTIVL GFIQALGMSYGFNNLAGGMLIQNPGIGTYLLIAVVLTAGTAFLMWLGEQITAKGVGNGIS IIIFAGIVSGIPTILNQIYAQQFENVGEDLFLRIVRLLLVALAVVAVIVGVIYIQQAFRK IPIQYAKRLEGRNPVGGHSTHLPLKVNPAGVIPVIFAVSFLIAPPTIASFFGTNDVTLWI RRTFDYTHPVGMTIYVVLIIAFTYFYAFVQVNPEQMADNLKKQGGYIPGIRPGKNTQEYV TRILYRLTLVGSLFLAFIAVLPVFFVNFANLPPSAQIGGTSLLIVVGVALETMKQLESQL VKRHYRGFIK
>7XHB_3 Protein translocase subunit SecE (chains E) MQRVTNFFKEVVRELKKVSWPNRKELVNYTAVVLATVAFFTVFFAVIDLGISQLIRLVFE
>7XHB_4 Translocating peptide (chains B) MAKKTAIAIAVALAGFATVASYAQYEDGCSGELERQHTFAGGARSIASGYYYYSGDKLPE GVLQSGGSGSKGEELFTGVVPILVELDGDVNGHKFSVRGEGEGDATNGKLTLKFICTTGK LPVPWPTLVTTLTYGVQCFSRYPDHMKRHDFFKSAMPEGYVQERTISFKDDGTYKTRAEV KFEGDTLVNRIELKGIDFKEDGNILGHKLEYNFNSHNVYITADKQKNGIKANFKIRHNVE DGSVQLADHYQQNTPIGDGPVLLPDNHYLSTQSVLSKDPNEKRDHMVLLEFVTAAGITHG SAGLEVLFQGPANGGSAWSHPQFEKGGGSGGGSGGGSWSHPQFEK
Structural basis of SecA-mediated protein translocation. Dong, L., Yang, S., Chen, J. et al. Proc Natl Acad Sci U S A (2023) 120:e2208070120-e2208070120. DOI 10.1073/pnas.2208070120 · PubMed
Other PDB entries of the same protein (UniProt P28366 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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