Crystal structure of Anthrax Lethal Factor active site mutant protein complexed with an optimised peptide substrate in the presence of zinc. Determined by X-ray diffraction at 2.8 Å resolution. Released 27 Jan 2004.
Explore 1PWW in 3D Show helices and sheets RCSB PDB PDBe
1PWW contains 92 α-helices and 54 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 | 31-43 | 13 | |
| β-strand | 44-47 | 4 | 1 |
| α-helix | 55-63 | 9 | |
| α-helix | 68-76 | 9 | |
| β-strand | 80-84 | 5 | 1 |
| α-helix | 88-90 | 3 | |
| α-helix | 100-102 | 3 | |
| β-strand | 105 | 1 | 2 |
| β-strand | 111 | 1 | 2 |
| β-strand | 119-122 | 4 | 1 |
| β-strand | 128-131 | 4 | 1 |
| α-helix | 141-153 | 13 | |
| α-helix | 154-159 | 6 | |
| α-helix | 160-163 | 4 | |
| α-helix | 168-178 | 11 | |
| α-helix | 184-189 | 6 | |
| α-helix | 192-195 | 4 | |
| α-helix | 203-207 | 5 | |
| α-helix | 210-225 | 16 | |
| α-helix | 230-236 | 7 | |
| α-helix | 238-246 | 9 | |
| α-helix | 247-251 | 5 | |
| α-helix | 253-261 | 9 | |
| α-helix | 264-277 | 14 | |
| α-helix | 279-284 | 6 | |
| α-helix | 287-295 | 9 | |
| β-strand | 300 | 1 | 3 |
| α-helix | 301-303 | 3 | |
| α-helix | 304-309 | 6 | |
| α-helix | 313-321 | 9 | |
| α-helix | 324-326 | 3 | |
| α-helix | 332-344 | 13 | |
| α-helix | 370-382 | 13 | |
| β-strand | 386 | 1 | 3 |
| α-helix | 388-395 | 8 | |
| α-helix | 406-422 | 17 | |
| β-strand | 426 | 1 | 4 |
| β-strand | 429 | 1 | 5 |
| β-strand | 432 | 1 | 5 |
| β-strand | 436-441 | 6 | 6 |
| α-helix | 443-445 | 3 | |
| α-helix | 448-451 | 4 | |
| β-strand | 455 | 1 | 7 |
| β-strand | 463 | 1 | 7 |
| α-helix | 465-472 | 8 | |
| β-strand | 477-480 | 4 | 6 |
| β-strand | 485-487 | 3 | 6 |
| β-strand | 499-504 | 6 | 6 |
| β-strand | 510 | 1 | 4 |
| β-strand | 511-513 | 3 | 6 |
| β-strand | 518-521 | 4 | 6 |
| α-helix | 522 | 1 | |
| β-strand | 525-536 | 12 | 6 |
| β-strand | 541-550 | 10 | 6 |
| α-helix | 552-574 | 23 | |
| β-strand | 583-586 | 4 | 8 |
| α-helix | 592-607 | 16 | |
| α-helix | 612-624 | 13 | |
| β-strand | 629-632 | 4 | 8 |
| α-helix | 636-638 | 3 | |
| α-helix | 640-643 | 4 | |
| α-helix | 649-651 | 3 | |
| β-strand | 657-660 | 4 | 8 |
| α-helix | 661-663 | 3 | |
| β-strand | 665-669 | 5 | 8 |
| β-strand | 674 | 1 | 9 |
| α-helix | 680-700 | 21 | |
| α-helix | 708-710 | 3 | |
| α-helix | 712-720 | 9 | |
| α-helix | 729-731 | 3 | |
| α-helix | 733-744 | 12 | |
| α-helix | 749-756 | 8 | |
| α-helix | 760-775 | 16 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 29-43 | 15 | |
| β-strand | 44-45 | 2 | 10 |
| α-helix | 54-64 | 11 | |
| α-helix | 68-76 | 9 | |
| β-strand | 80-83 | 4 | 10 |
| α-helix | 88-90 | 3 | |
| α-helix | 94-96 | 3 | |
| α-helix | 99-102 | 4 | |
| β-strand | 103-105 | 3 | 11 |
| β-strand | 111-113 | 3 | 11 |
| β-strand | 119-122 | 4 | 10 |
| β-strand | 128-131 | 4 | 10 |
| α-helix | 136-139 | 4 | |
| α-helix | 141-153 | 13 | |
| α-helix | 154-159 | 6 | |
| α-helix | 161-163 | 3 | |
| α-helix | 168-178 | 11 | |
| α-helix | 184-189 | 6 | |
| α-helix | 192-195 | 4 | |
| α-helix | 203-208 | 6 | |
| α-helix | 210-225 | 16 | |
| α-helix | 227-236 | 10 | |
| α-helix | 238-246 | 9 | |
| α-helix | 247-251 | 5 | |
| α-helix | 252-260 | 9 | |
| α-helix | 264-277 | 14 | |
| α-helix | 279-282 | 4 | |
| α-helix | 287-297 | 11 | |
| α-helix | 299 | 1 | |
| β-strand | 300 | 1 | 12 |
| α-helix | 301-302 | 2 | |
| α-helix | 304-309 | 6 | |
| α-helix | 313-321 | 9 | |
| α-helix | 324-326 | 3 | |
| α-helix | 332-345 | 14 | |
| α-helix | 370-382 | 13 | |
| β-strand | 386 | 1 | 12 |
| α-helix | 388-395 | 8 | |
| α-helix | 406-420 | 15 | |
| β-strand | 426 | 1 | 13 |
| β-strand | 436-441 | 6 | 14 |
| α-helix | 444-453 | 10 | |
| β-strand | 455 | 1 | 15 |
| β-strand | 463 | 1 | 15 |
| α-helix | 465-472 | 8 | |
| β-strand | 477-480 | 4 | 14 |
| β-strand | 485-487 | 3 | 14 |
| β-strand | 499-504 | 6 | 14 |
| β-strand | 510 | 1 | 13 |
| β-strand | 511-514 | 4 | 14 |
| β-strand | 518-521 | 4 | 14 |
| α-helix | 522 | 1 | |
| β-strand | 525-537 | 13 | 14 |
| β-strand | 540-550 | 11 | 14 |
| α-helix | 552-574 | 23 | |
| β-strand | 583-586 | 4 | 16 |
| α-helix | 592-609 | 18 | |
| α-helix | 612-624 | 13 | |
| β-strand | 629-632 | 4 | 16 |
| α-helix | 636-638 | 3 | |
| α-helix | 640-643 | 4 | |
| β-strand | 657-660 | 4 | 16 |
| β-strand | 665-669 | 5 | 16 |
| α-helix | 680-700 | 21 | |
| α-helix | 708-710 | 3 | |
| α-helix | 712-721 | 10 | |
| α-helix | 729-731 | 3 | |
| α-helix | 733-744 | 12 | |
| α-helix | 749-758 | 10 | |
| α-helix | 760-774 | 15 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 9 | 1 | 8 |
| β-strand | 13 | 1 | 9 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 9 | 1 | 16 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Lethal factor | A, B | protein | 776 | Bacillus anthracis | P15917 (AlphaFold model) |
| LF20 | C, D | protein | 20 |
>1PWW_1 Lethal factor (chains A, B) AGGHGDVGMHVKEKEKNKDENKRKDEERNKTQEEHLKEIMKHIVKIEVKGEEAVKKEAAE KLLEKVPSDVLEMYKAIGGKIYIVDGDITKHISLEALSEDKKKIKDIYGKDALLHEHYVY AKEGYEPVLVIQSSEDYVENTEKALNVYYEIGKILSRDILSKINQPYQKFLDVLNTIKNA SDSDGQDLLFTNQLKEHPTDFSVEFLEQNSNEVQEVFAKAFAYYIEPQHRDVLQLYAPEA FNYMDKFNEQEINLSLEELKDQRMLSRYEKWEKIKQHYQHWSDSLSEEGRGLLKKLQIPI EPKKDDIIHSLSQEEKELLKRIQIDSSDFLSTEEKEFLKKLQIDIRDSLSEEEKELLNRI QVDSSNPLSEKEKEFLKKLKLDIQPYDINQRLQDTGGLIDSPSINLDVRKQYKRDIQNID ALLHQSIGSTLYNKIYLYENMNINNLTATLGADLVDSTDNTKINRGIFNEFKKNFKYSIS SNYMIVDINERPALDNERLKWRIQLSPDTRAGYLENGKLILQRNIGLEIKDVQIIKQSEK EYIRIDAKVVPKSKIDTKIQEAQLNINQEWNKALGLPKYTKLITFNVHNRYASNIVESAY LILNEWKNNIQSDLIKKVTNYLVDGNGRFVFTDITLPNIAEQYTHQDEIYEQVHSKGLYV PESRSILLHGPSKGVELRNDSEGFIHCFGHAVDDYAGYLLDKNQSDLVTNSKKFIDIFKE EGSNLTSYGRTNEAEFFAEAFRLMHSTDHAERLKVQKNAPKTFQFINDQIKFIINS
>1PWW_2 LF20 (chains C, D) MLARRKKVYPYPMEPTIAEG
| ID | Name | Formula | Copies |
|---|---|---|---|
| ZN | Zinc ion | Zn | 2 |
The structural basis for substrate and inhibitor selectivity of the anthrax lethal factor. Turk, B.E., Wong, T.Y., Schwarzenbacher, R. et al. Nat Struct Mol Biol (2004) 11:60-66. DOI 10.1038/nsmb708 · PubMed
Other PDB entries of the same protein (UniProt P15917 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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