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Chlorine in PDB 2aik: Formylglycine Generating Enzyme C336S Mutant Covalently Bound to Substrate Peptide Lctpsra

Protein crystallography data

The structure of Formylglycine Generating Enzyme C336S Mutant Covalently Bound to Substrate Peptide Lctpsra, PDB code: 2aik was solved by D.Roeser, M.G.Rudolph, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 29.71 / 1.73
Space group P 21 21 2
Cell size a, b, c (Å), α, β, γ (°) 61.719, 109.517, 43.520, 90.00, 90.00, 90.00
R / Rfree (%) 14.1 / 17.4

Other elements in 2aik:

The structure of Formylglycine Generating Enzyme C336S Mutant Covalently Bound to Substrate Peptide Lctpsra also contains other interesting chemical elements:

Calcium (Ca) 2 atoms

Chlorine Binding Sites:

The binding sites of Chlorine atom in the Formylglycine Generating Enzyme C336S Mutant Covalently Bound to Substrate Peptide Lctpsra (pdb code 2aik). 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 Formylglycine Generating Enzyme C336S Mutant Covalently Bound to Substrate Peptide Lctpsra, PDB code: 2aik:

Chlorine binding site 1 out of 1 in 2aik

Go back to Chlorine Binding Sites List in 2aik
Chlorine binding site 1 out of 1 in the Formylglycine Generating Enzyme C336S Mutant Covalently Bound to Substrate Peptide Lctpsra


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 1 of Formylglycine Generating Enzyme C336S Mutant Covalently Bound to Substrate Peptide Lctpsra within 5.0Å range:
probe atom residue distance (Å) B Occ
X:Cl1003

b:28.2
occ:1.00
OG X:SER333 3.0 21.1 1.0
O P:HOH77 3.2 39.9 1.0
NE1 X:TRP299 3.2 21.4 1.0
OG X:SER336 3.2 19.9 1.0
ND2 X:ASN360 3.6 21.7 1.0
SG X:CYS341 3.7 34.5 1.0
CB P:CYS69 3.7 41.1 1.0
CB X:MET335 3.8 19.3 1.0
N X:SER336 3.9 20.0 1.0
CB X:SER333 3.9 19.6 1.0
O P:CYS69 4.0 38.3 1.0
CD1 X:TRP299 4.0 21.6 1.0
CA X:SER336 4.1 19.9 1.0
CE2 X:TRP299 4.1 20.8 1.0
C X:MET335 4.2 19.5 1.0
CB X:SER336 4.2 20.8 1.0
N X:SER333 4.3 19.3 1.0
CB X:CYS341 4.4 30.6 1.0
CA P:CYS69 4.4 41.5 1.0
SG P:CYS69 4.4 42.3 1.0
CZ2 X:TRP299 4.5 22.3 1.0
CA X:MET335 4.5 19.7 1.0
C P:CYS69 4.6 40.0 1.0
CA X:SER333 4.6 19.4 1.0
O X:HOH1173 4.7 35.2 1.0
O X:MET335 4.7 21.2 1.0
N X:MET335 4.7 18.4 1.0
CG X:ASN360 4.8 20.8 1.0
SD X:MET335 4.9 22.6 1.0
CG X:MET335 4.9 20.8 1.0
O X:SER333 5.0 18.9 1.0
C X:SER333 5.0 18.9 1.0

Reference:

D.Roeser, A.Preusser-Kunze, B.Schmidt, K.Gasow, J.G.Wittmann, T.Dierks, K.Von Figura, M.G.Rudolph. A General Binding Mechanism For All Human Sulfatases By the Formylglycine-Generating Enzyme Proc.Natl.Acad.Sci.Usa V. 103 81 2006.
ISSN: ISSN 0027-8424
PubMed: 16368756
DOI: 10.1073/PNAS.0507592102
Page generated: Sat Dec 12 08:58:47 2020

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