Structure of E. coli Exonuclease I in complex with a 5cy-dT13 oligonucleotide. Determined by X-ray diffraction at 1.95 Å resolution. Released 8 May 2013.
Explore 4JRP in 3D Show helices and sheets RCSB PDB PDBe
4JRP contains 69 α-helices and 29 β-strands across 2 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 | 10-18 | 9 | 1 |
| β-strand | 28-37 | 10 | 1 |
| β-strand | 42 | 1 | 1 |
| β-strand | 47-50 | 4 | 1 |
| β-strand | 51 | 1 | 2 |
| α-helix | 52-54 | 3 | |
| α-helix | 61-67 | 7 | |
| α-helix | 71-77 | 7 | |
| β-strand | 79 | 1 | 2 |
| α-helix | 81-92 | 12 | |
| β-strand | 97-100 | 4 | 1 |
| α-helix | 108-118 | 11 | |
| α-helix | 125-127 | 3 | |
| α-helix | 129-131 | 3 | |
| β-strand | 133-134 | 2 | 1 |
| α-helix | 137-147 | 11 | |
| α-helix | 153-155 | 3 | |
| β-strand | 156 | 1 | 3 |
| β-strand | 162 | 1 | 3 |
| α-helix | 166-171 | 6 | |
| α-helix | 183-200 | 18 | |
| α-helix | 202-210 | 9 | |
| α-helix | 214-218 | 5 | |
| β-strand | 229-232 | 4 | 4 |
| α-helix | 234-236 | 3 | |
| α-helix | 238-240 | 3 | |
| β-strand | 243-251 | 9 | 4 |
| β-strand | 258-263 | 6 | 4 |
| α-helix | 269-273 | 5 | |
| α-helix | 276-283 | 8 | |
| α-helix | 294-296 | 3 | |
| β-strand | 298-302 | 5 | 4 |
| β-strand | 308-311 | 4 | 4 |
| α-helix | 312-314 | 3 | |
| α-helix | 317-323 | 7 | |
| α-helix | 327-338 | 12 | |
| α-helix | 342-350 | 9 | |
| α-helix | 363-365 | 3 | |
| α-helix | 367-369 | 3 | |
| α-helix | 374-385 | 12 | |
| α-helix | 388-393 | 6 | |
| α-helix | 402-414 | 13 | |
| α-helix | 416-418 | 3 | |
| α-helix | 421-434 | 14 | |
| α-helix | 437-453 | 17 | |
| α-helix | 458-474 | 17 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 10-18 | 9 | 5 |
| β-strand | 28-37 | 10 | 5 |
| β-strand | 42-50 | 9 | 5 |
| β-strand | 51 | 1 | 6 |
| α-helix | 52-54 | 3 | |
| α-helix | 61-67 | 7 | |
| α-helix | 71-77 | 7 | |
| β-strand | 79 | 1 | 6 |
| α-helix | 81-92 | 12 | |
| β-strand | 97-100 | 4 | 5 |
| α-helix | 104-106 | 3 | |
| α-helix | 108-118 | 11 | |
| α-helix | 125-127 | 3 | |
| α-helix | 129-131 | 3 | |
| β-strand | 133-134 | 2 | 5 |
| α-helix | 137-147 | 11 | |
| β-strand | 156 | 1 | 7 |
| α-helix | 161 | 1 | |
| β-strand | 162 | 1 | 7 |
| α-helix | 163 | 1 | |
| α-helix | 166-172 | 7 | |
| α-helix | 183-200 | 18 | |
| α-helix | 202-210 | 9 | |
| α-helix | 214-218 | 5 | |
| β-strand | 229-232 | 4 | 8 |
| α-helix | 234-236 | 3 | |
| α-helix | 238-240 | 3 | |
| β-strand | 243-251 | 9 | 8 |
| β-strand | 258-263 | 6 | 8 |
| α-helix | 269-273 | 5 | |
| α-helix | 276-283 | 8 | |
| α-helix | 294-296 | 3 | |
| β-strand | 298-302 | 5 | 8 |
| α-helix | 303-305 | 3 | |
| β-strand | 308-311 | 4 | 8 |
| α-helix | 312-314 | 3 | |
| α-helix | 317-323 | 7 | |
| α-helix | 327-339 | 13 | |
| α-helix | 341-351 | 11 | |
| α-helix | 354-355 | 2 | |
| α-helix | 357-360 | 4 | |
| α-helix | 363-365 | 3 | |
| α-helix | 367-369 | 3 | |
| α-helix | 371-373 | 3 | |
| α-helix | 374-385 | 12 | |
| α-helix | 388-390 | 3 | |
| α-helix | 391-394 | 4 | |
| α-helix | 402-414 | 13 | |
| α-helix | 416-418 | 3 | |
| α-helix | 421-434 | 14 | |
| α-helix | 437-453 | 17 | |
| α-helix | 458-473 | 16 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| 5cy-dT13 | C, D | DNA | 14 | ||
| Exodeoxyribonuclease I | A, B | protein | 478 | Escherichia coli | P04995 (AlphaFold model) |
>4JRP_1 5cy-dT13 (chains C, D) XTTTTTTTTTTTTT
>4JRP_2 Exodeoxyribonuclease I (chains A, B) GSHMMNDGKQQSTFLFHDYETFGTHPALDRPAQFAAIRTDSEFNVIGEPEVFYCKPADDY LPQPGAVLITGITPQEARAKGENEAAFAARIHSLFTVPKTCILGYNNVRFDDEVTRNIFY RNFYDPYAWSWQHDNSRWDLLDVMRACYALRPEGINWPENDDGLPSFRLEHLTKANGIEH SNAHDAMADVYATIAMAKLVKTRQPRLFDYLFTHRNKHKLMALIDVPQMKPLVHVSGMFG AWRGNTSWVAPLAWHPENRNAVIMVDLAGDISPLLELDSDTLRERLYTAKTDLGDNAAVP VKLVHINKCPVLAQANTLRPEDADRLGINRQHCLDNLKILRENPQVREKVVAIFAEAEPF TPSDNVDAQLYNGFFSDADRAAMKIVLETEPRNLPALDITFVDKRIEKLLFNYRARNFPG TLDYAEQQRWLEHRRQVFTPEFLQGYADELQMLVQQYADDKEKVALLKALWQYAEEIV
Water and common crystallization additives (GOL, SO4) are not listed.
Crystal structures of Escherichia coli exonuclease I in complex with single-stranded DNA provide insights into the mechanism of processive digestion. Korada, S.K., Johns, T.D., Smith, C.E. et al. Nucleic Acids Res (2013) 41:5887-5897. DOI 10.1093/nar/gkt278 · PubMed
Other PDB entries of the same protein (UniProt P04995 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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