Ion selectivity of OmpF porin soaked in 0.3M KBr. Determined by X-ray diffraction at 2.09 Å resolution. Released 23 Oct 2013.
Explore 4LSI in 3D Show helices and sheets RCSB PDB PDBe
4LSI contains 14 α-helices and 74 β-strands across 3 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 | 9-11 | 3 | 1 |
| β-strand | 14-23 | 10 | 1 |
| β-strand | 31 | 1 | 2 |
| β-strand | 36-37 | 2 | 1 |
| β-strand | 40-50 | 11 | 1 |
| β-strand | 55-66 | 12 | 1 |
| β-strand | 80-90 | 11 | 1 |
| β-strand | 94-102 | 9 | 1 |
| α-helix | 106-109 | 4 | |
| β-strand | 132-141 | 10 | 1 |
| α-helix | 143-146 | 4 | |
| β-strand | 151-158 | 8 | 1 |
| α-helix | 159-160 | 2 | |
| β-strand | 161 | 1 | 3 |
| β-strand | 170 | 1 | 3 |
| β-strand | 173-182 | 10 | 1 |
| β-strand | 185-195 | 11 | 1 |
| α-helix | 196-197 | 2 | |
| α-helix | 198-201 | 4 | |
| β-strand | 205 | 1 | 4 |
| β-strand | 210-222 | 13 | 1 |
| β-strand | 225-235 | 11 | 1 |
| β-strand | 239-242 | 4 | 4 |
| β-strand | 247-250 | 4 | 4 |
| β-strand | 253-263 | 11 | 1 |
| β-strand | 269-283 | 15 | 1 |
| β-strand | 287-302 | 16 | 1 |
| β-strand | 307-316 | 10 | 1 |
| β-strand | 329 | 1 | 2 |
| β-strand | 331-339 | 9 | 1 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 9-23 | 15 | 5 |
| β-strand | 31 | 1 | 6 |
| β-strand | 36-37 | 2 | 5 |
| β-strand | 40-52 | 13 | 5 |
| β-strand | 55-66 | 12 | 5 |
| β-strand | 80-90 | 11 | 5 |
| β-strand | 94-100 | 7 | 5 |
| β-strand | 102 | 1 | 7 |
| α-helix | 106-109 | 4 | |
| β-strand | 132 | 1 | 7 |
| β-strand | 136-141 | 6 | 5 |
| α-helix | 143-146 | 4 | |
| β-strand | 151-158 | 8 | 5 |
| β-strand | 161 | 1 | 8 |
| β-strand | 170 | 1 | 8 |
| β-strand | 173-182 | 10 | 5 |
| β-strand | 185-195 | 11 | 5 |
| α-helix | 196-197 | 2 | |
| α-helix | 198-201 | 4 | |
| β-strand | 205 | 1 | 9 |
| β-strand | 210-222 | 13 | 5 |
| β-strand | 225-235 | 11 | 5 |
| β-strand | 239-242 | 4 | 9 |
| β-strand | 247-250 | 4 | 9 |
| β-strand | 253-263 | 11 | 5 |
| β-strand | 269-283 | 15 | 5 |
| β-strand | 287-302 | 16 | 5 |
| β-strand | 307-316 | 10 | 5 |
| β-strand | 329 | 1 | 6 |
| β-strand | 331-339 | 9 | 5 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 9-11 | 3 | 10 |
| β-strand | 14-23 | 10 | 10 |
| β-strand | 31 | 1 | 11 |
| β-strand | 36-37 | 2 | 10 |
| β-strand | 40-50 | 11 | 10 |
| β-strand | 55-66 | 12 | 10 |
| β-strand | 80-90 | 11 | 10 |
| β-strand | 94-102 | 9 | 10 |
| α-helix | 106-109 | 4 | |
| β-strand | 132-141 | 10 | 10 |
| α-helix | 143-146 | 4 | |
| β-strand | 151-158 | 8 | 10 |
| α-helix | 159-160 | 2 | |
| β-strand | 161 | 1 | 12 |
| β-strand | 170 | 1 | 12 |
| β-strand | 173-182 | 10 | 10 |
| β-strand | 185-195 | 11 | 10 |
| α-helix | 196-197 | 2 | |
| α-helix | 198-201 | 4 | |
| β-strand | 205 | 1 | 10 |
| β-strand | 210-222 | 13 | 10 |
| β-strand | 225-241 | 17 | 10 |
| β-strand | 248-263 | 16 | 10 |
| β-strand | 269-283 | 15 | 10 |
| β-strand | 287-304 | 18 | 10 |
| β-strand | 307-316 | 10 | 10 |
| β-strand | 329 | 1 | 11 |
| β-strand | 331-339 | 9 | 10 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Outer membrane protein F | A, B, C | protein | 341 | Escherichia coli | P02931 (AlphaFold model) |
>4LSI_1 Outer membrane protein F (chains A, B, C) GAEIYNKDGNKVDLYGKAVGLHYFSKGNGENSYGGNGDMTYARLGFKGETQINSDLTGYG QWEYNFQGNNSEGADAQTGNKTRLAFAGLKYADVGSFDYGRNYGVVYDALGYTDMLPEFG GDTAYSDDFFVGRVGGVATYRNSNFFGLVDGLNFAVQYLGKNERDTARRSNGDGVGGSIS YEYEGFGIVGAYGAADRTNLQEAQPLGNGKKAEQWATGLKYDANNIYLAANYGETRNATP ITNKFTNTSGFANKTQDVLLVAQYQFDFGLRPSIAYTKSKAKDVEGIGDVDLVNYFEVGA TYYFNKNMSTYVDYIINQIDSDNKLGVGSDDTVAVGIVYQF
Water and common crystallization additives (PEG, GOL, BR) are not listed.
A structural study of ion permeation in OmpF porin from anomalous X-ray diffraction and molecular dynamics simulations. Dhakshnamoorthy, B., Ziervogel, B.K., Blachowicz, L. et al. J Am Chem Soc (2013) 135:16561-16568. DOI 10.1021/ja407783a · PubMed
Other PDB entries of the same protein (UniProt P02931 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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