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Chlorine in PDB 3zxd: Wild-Type Lysenin

Protein crystallography data

The structure of Wild-Type Lysenin, PDB code: 3zxd was solved by L.De Colibus, A.F.P.Sonnen, K.J.Morris, C.A.Siebert, P.Abrusci, J.Plitzko, V.Hodnik, M.Leippe, E.Volpi, G.Anderluh, R.J.C.Gilbert, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 29.09 / 3.30
Space group P 1
Cell size a, b, c (Å), α, β, γ (°) 58.910, 85.560, 108.810, 98.88, 96.84, 90.04
R / Rfree (%) 21.3 / 23.6

Other elements in 3zxd:

The structure of Wild-Type Lysenin also contains other interesting chemical elements:

Magnesium (Mg) 6 atoms
Sodium (Na) 6 atoms

Chlorine Binding Sites:

The binding sites of Chlorine atom in the Wild-Type Lysenin (pdb code 3zxd). This binding sites where shown within 5.0 Angstroms radius around Chlorine atom.
In total only one binding site of Chlorine was determined in the Wild-Type Lysenin, PDB code: 3zxd:

Chlorine binding site 1 out of 1 in 3zxd

Go back to Chlorine Binding Sites List in 3zxd
Chlorine binding site 1 out of 1 in the Wild-Type Lysenin


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 1 of Wild-Type Lysenin within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl469

b:61.1
occ:1.00
O A:SER186 3.6 82.7 1.0
CB A:TRP187 3.7 72.6 1.0
CG A:TRP187 3.9 73.9 1.0
CE2 A:TYR221 4.0 62.0 1.0
CZ A:TYR221 4.1 67.4 1.0
CA A:TRP187 4.2 76.1 1.0
C A:SER186 4.3 83.4 1.0
CD2 A:TYR221 4.4 60.8 1.0
OH A:TYR221 4.4 70.8 1.0
CE1 A:TYR221 4.4 58.6 1.0
CD2 A:TRP187 4.4 71.6 1.0
CD1 A:TRP187 4.5 79.2 1.0
N A:TRP187 4.6 78.8 1.0
CD1 A:TYR221 4.7 56.7 1.0
CG A:TYR221 4.7 56.8 1.0
CE3 A:TRP187 4.8 70.0 1.0
CG A:TYR218 4.9 79.7 1.0
CD2 A:TYR218 5.0 84.2 1.0

Reference:

L.De Colibus, A.F.P.Sonnen, K.J.Morris, C.A.Siebert, P.Abrusci, J.Plitzko, V.Hodnik, M.Leippe, E.Volpi, G.Anderluh, R.J.C.Gilbert. Structures of Lysenin Reveal A Shared Evolutionary Origin For Pore-Forming Proteins and Its Mode of Sphingomyelin Recognition. Structure V. 20 1498 2012.
ISSN: ISSN 0969-2126
PubMed: 22819216
DOI: 10.1016/J.STR.2012.06.011
Page generated: Fri Jul 11 12:35:10 2025

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