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Chlorine in PDB 4xs1: Salmonella Typhimurium Ahpc T43V Mutant

Enzymatic activity of Salmonella Typhimurium Ahpc T43V Mutant

All present enzymatic activity of Salmonella Typhimurium Ahpc T43V Mutant:
1.11.1.15;

Protein crystallography data

The structure of Salmonella Typhimurium Ahpc T43V Mutant, PDB code: 4xs1 was solved by A.Perkins, K.Nelson, D.Parsonage, L.Poole, P.A.Karplus, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 31.60 / 2.10
Space group C 2 2 21
Cell size a, b, c (Å), α, β, γ (°) 126.989, 171.880, 135.920, 90.00, 90.00, 90.00
R / Rfree (%) 18.9 / 21.8

Other elements in 4xs1:

The structure of Salmonella Typhimurium Ahpc T43V Mutant also contains other interesting chemical elements:

Potassium (K) 3 atoms

Chlorine Binding Sites:

The binding sites of Chlorine atom in the Salmonella Typhimurium Ahpc T43V Mutant (pdb code 4xs1). This binding sites where shown within 5.0 Angstroms radius around Chlorine atom.
In total 5 binding sites of Chlorine where determined in the Salmonella Typhimurium Ahpc T43V Mutant, PDB code: 4xs1:
Jump to Chlorine binding site number: 1; 2; 3; 4; 5;

Chlorine binding site 1 out of 5 in 4xs1

Go back to Chlorine Binding Sites List in 4xs1
Chlorine binding site 1 out of 5 in the Salmonella Typhimurium Ahpc T43V Mutant


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 1 of Salmonella Typhimurium Ahpc T43V Mutant within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl202

b:49.2
occ:1.00
O A:HOH403 2.9 38.0 1.0
O A:HOH340 3.0 42.5 1.0
O A:HOH348 3.0 39.3 1.0
N A:LEU2 3.2 29.4 1.0
CB A:SER1 3.5 34.9 1.0
CA A:SER1 3.5 34.9 1.0
CD1 A:ILE133 3.7 25.6 1.0
CG A:LEU2 3.8 36.0 1.0
C A:SER1 3.9 34.0 1.0
CB A:LEU2 3.9 33.8 1.0
CD1 A:LEU2 4.1 32.7 1.0
CA A:LEU2 4.1 31.4 1.0
CE2 A:PHE122 4.2 29.6 1.0
CG2 A:ILE133 4.4 26.9 1.0
CB B:SER1 4.4 37.0 1.0
OG A:SER1 4.6 32.4 1.0
CA B:SER1 4.6 36.7 1.0
O B:HOH343 4.7 42.5 1.0
CZ A:PHE122 4.8 31.8 1.0
CL B:CL202 4.8 49.0 1.0
N B:SER1 4.8 41.7 1.0
O A:PHE107 4.8 32.9 1.0
CG1 A:ILE133 4.9 31.6 1.0
N A:SER1 4.9 35.6 1.0

Chlorine binding site 2 out of 5 in 4xs1

Go back to Chlorine Binding Sites List in 4xs1
Chlorine binding site 2 out of 5 in the Salmonella Typhimurium Ahpc T43V Mutant


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 2 of Salmonella Typhimurium Ahpc T43V Mutant within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Cl202

b:49.0
occ:1.00
O B:HOH341 3.0 33.5 1.0
O A:HOH403 3.0 38.0 1.0
O B:HOH343 3.1 42.5 1.0
N B:LEU2 3.2 34.5 1.0
CB B:SER1 3.5 37.0 1.0
CA B:SER1 3.6 36.7 1.0
CD1 B:ILE133 3.8 31.9 1.0
CG B:LEU2 3.8 35.9 1.0
CB B:LEU2 3.9 31.5 1.0
C B:SER1 3.9 38.2 1.0
CE2 B:PHE122 4.1 28.6 1.0
CD1 B:LEU2 4.1 37.3 1.0
CA B:LEU2 4.2 31.2 1.0
CG2 B:ILE133 4.4 30.3 1.0
CB A:SER1 4.5 34.9 1.0
CZ B:PHE122 4.5 30.2 1.0
OG B:SER1 4.6 35.6 1.0
CA A:SER1 4.6 34.9 1.0
O A:HOH348 4.7 39.3 1.0
N A:SER1 4.7 35.6 1.0
CL A:CL202 4.8 49.2 1.0
O B:PHE107 4.8 35.0 1.0
CG1 B:ILE133 4.9 34.6 1.0
N B:SER1 5.0 41.7 1.0

Chlorine binding site 3 out of 5 in 4xs1

Go back to Chlorine Binding Sites List in 4xs1
Chlorine binding site 3 out of 5 in the Salmonella Typhimurium Ahpc T43V Mutant


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 3 of Salmonella Typhimurium Ahpc T43V Mutant within 5.0Å range:
probe atom residue distance (Å) B Occ
C:Cl201

b:51.8
occ:1.00
O D:HOH321 2.8 39.8 1.0
O D:HOH329 2.9 38.9 1.0
O C:HOH323 3.0 44.6 1.0
N C:LEU2 3.3 39.6 1.0
CB C:SER1 3.6 48.4 1.0
CA C:SER1 3.6 48.7 1.0
CD1 C:ILE133 3.9 34.6 1.0
CG C:LEU2 3.9 42.9 1.0
C C:SER1 3.9 46.5 1.0
CB C:LEU2 4.0 40.4 1.0
CE2 C:PHE122 4.2 33.6 1.0
CD1 C:LEU2 4.2 40.7 1.0
CA C:LEU2 4.2 39.6 1.0
CB D:SER1 4.3 42.8 1.0
CA D:SER1 4.3 42.9 1.0
CG2 C:ILE133 4.4 33.3 1.0
N D:SER1 4.6 42.1 1.0
O D:HOH349 4.6 45.3 1.0
CL D:CL202 4.6 57.5 1.0
OG C:SER1 4.7 44.5 1.0
CZ C:PHE122 4.7 35.7 1.0
O C:PHE107 4.9 39.1 1.0
CG1 C:ILE133 4.9 37.6 1.0
N C:SER1 5.0 50.5 1.0

Chlorine binding site 4 out of 5 in 4xs1

Go back to Chlorine Binding Sites List in 4xs1
Chlorine binding site 4 out of 5 in the Salmonella Typhimurium Ahpc T43V Mutant


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 4 of Salmonella Typhimurium Ahpc T43V Mutant within 5.0Å range:
probe atom residue distance (Å) B Occ
D:Cl202

b:57.5
occ:1.00
O D:HOH331 2.8 42.3 1.0
O D:HOH321 2.9 39.8 1.0
N D:LEU2 3.2 39.3 1.0
O D:HOH349 3.2 45.3 1.0
CB D:SER1 3.6 42.8 1.0
CA D:SER1 3.6 42.9 1.0
CD1 D:ILE133 3.7 35.2 1.0
CB D:LEU2 3.8 37.9 1.0
CG D:LEU2 3.9 38.2 1.0
C D:SER1 3.9 43.7 1.0
CD1 D:LEU2 4.0 38.3 1.0
CE2 D:PHE122 4.1 44.3 1.0
CA D:LEU2 4.1 38.5 1.0
CG2 D:ILE133 4.3 35.1 1.0
CB C:SER1 4.4 48.4 1.0
CA C:SER1 4.5 48.7 1.0
CZ D:PHE122 4.6 43.6 1.0
CL C:CL201 4.6 51.8 1.0
O C:HOH323 4.7 44.6 1.0
OG D:SER1 4.7 41.9 1.0
N C:SER1 4.7 50.5 1.0
CG1 D:ILE133 4.9 38.5 1.0
O D:PHE107 4.9 37.4 1.0

Chlorine binding site 5 out of 5 in 4xs1

Go back to Chlorine Binding Sites List in 4xs1
Chlorine binding site 5 out of 5 in the Salmonella Typhimurium Ahpc T43V Mutant


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 5 of Salmonella Typhimurium Ahpc T43V Mutant within 5.0Å range:
probe atom residue distance (Å) B Occ
E:Cl201

b:75.0
occ:1.00
O E:HOH304 3.0 57.2 1.0
N E:LEU2 3.1 48.3 1.0
CB E:SER1 3.5 55.6 1.0
CA E:SER1 3.6 52.1 1.0
CG E:LEU2 3.8 53.6 1.0
CB E:LEU2 3.8 52.4 1.0
CD1 E:ILE133 3.8 50.9 1.0
C E:SER1 3.8 51.8 1.0
CA E:LEU2 4.0 50.9 1.0
CE2 E:PHE122 4.1 52.8 1.0
CD1 E:LEU2 4.1 55.4 1.0
CG2 E:ILE133 4.4 53.6 1.0
OG E:SER1 4.4 59.3 1.0
CZ E:PHE122 4.6 50.0 1.0
CG1 E:ILE133 4.9 49.6 1.0
O E:PHE107 4.9 51.1 1.0
C E:LEU2 5.0 54.3 1.0

Reference:

K.J.Nelson, A.Perkins, A.E.D.Van Swearingen, S.Hartman, A.E.Brereton, D.Parsonage, F.R.Salsbury Jr., P.A.Karplus, L.B.Poole. Experimentally Dissecting the Origins of Peroxiredoxin Catalysis. Antioxid.Redox Signal. V. 28 521 2018.
ISSN: ESSN 1557-7716
PubMed: 28375740
DOI: 10.1089/ARS.2016.6922
Page generated: Sat Dec 12 11:21:20 2020

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