4LSI: Ion selectivity of OmpF porin soaked in 0.3M KBr

Ion selectivity of OmpF porin soaked in 0.3M KBr. Determined by X-ray diffraction at 2.09 Å resolution. Released 23 Oct 2013.

Method
X-ray diffraction
Resolution
2.09 Å
Organism
Escherichia coli
Chains
3
Atoms
8,472
Mol. weight
114.98 kDa
Ligands
C8E, MG
Released
23 Oct 2013

Explore 4LSI in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

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.

Chain A: 5 helices, 25 β-strands

ElementResiduesLengthSheet
β-strand9-1131
β-strand14-23101
β-strand3112
β-strand36-3721
β-strand40-50111
β-strand55-66121
β-strand80-90111
β-strand94-10291
α-helix106-1094
β-strand132-141101
α-helix143-1464
β-strand151-15881
α-helix159-1602
β-strand16113
β-strand17013
β-strand173-182101
β-strand185-195111
α-helix196-1972
α-helix198-2014
β-strand20514
β-strand210-222131
β-strand225-235111
β-strand239-24244
β-strand247-25044
β-strand253-263111
β-strand269-283151
β-strand287-302161
β-strand307-316101
β-strand32912
β-strand331-33991
Chain B: 4 helices, 26 β-strands
ElementResiduesLengthSheet
β-strand9-23155
β-strand3116
β-strand36-3725
β-strand40-52135
β-strand55-66125
β-strand80-90115
β-strand94-10075
β-strand10217
α-helix106-1094
β-strand13217
β-strand136-14165
α-helix143-1464
β-strand151-15885
β-strand16118
β-strand17018
β-strand173-182105
β-strand185-195115
α-helix196-1972
α-helix198-2014
β-strand20519
β-strand210-222135
β-strand225-235115
β-strand239-24249
β-strand247-25049
β-strand253-263115
β-strand269-283155
β-strand287-302165
β-strand307-316105
β-strand32916
β-strand331-33995
Chain C: 5 helices, 23 β-strands
ElementResiduesLengthSheet
β-strand9-11310
β-strand14-231010
β-strand31111
β-strand36-37210
β-strand40-501110
β-strand55-661210
β-strand80-901110
β-strand94-102910
α-helix106-1094
β-strand132-1411010
α-helix143-1464
β-strand151-158810
α-helix159-1602
β-strand161112
β-strand170112
β-strand173-1821010
β-strand185-1951110
α-helix196-1972
α-helix198-2014
β-strand205110
β-strand210-2221310
β-strand225-2411710
β-strand248-2631610
β-strand269-2831510
β-strand287-3041810
β-strand307-3161010
β-strand329111
β-strand331-339910

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Outer membrane protein FA, B, Cprotein341Escherichia coliP02931 (AlphaFold model)
Sequence of entity 1 (A, B, C), FASTA
>4LSI_1 Outer membrane protein F (chains A, B, C)
GAEIYNKDGNKVDLYGKAVGLHYFSKGNGENSYGGNGDMTYARLGFKGETQINSDLTGYG
QWEYNFQGNNSEGADAQTGNKTRLAFAGLKYADVGSFDYGRNYGVVYDALGYTDMLPEFG
GDTAYSDDFFVGRVGGVATYRNSNFFGLVDGLNFAVQYLGKNERDTARRSNGDGVGGSIS
YEYEGFGIVGAYGAADRTNLQEAQPLGNGKKAEQWATGLKYDANNIYLAANYGETRNATP
ITNKFTNTSGFANKTQDVLLVAQYQFDFGLRPSIAYTKSKAKDVEGIGDVDLVNYFEVGA
TYYFNKNMSTYVDYIINQIDSDNKLGVGSDDTVAVGIVYQF

Ligands and cofactors

IDNameFormulaCopies
C8E(hydroxyethyloxy)tri(ethyloxy)octaneC16 H34 O54
MGMagnesium ionMg8

Water and common crystallization additives (PEG, GOL, BR) are not listed.

Primary citation

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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