Atomistry » Iron » PDB 3whm-3x16 » 3wml
Atomistry »
  Iron »
    PDB 3whm-3x16 »
      3wml »

Iron in PDB 3wml: Structure of Phosphotriesterase Mutant (S308L/Y309A) From Agrobacterium Radiobacter

Enzymatic activity of Structure of Phosphotriesterase Mutant (S308L/Y309A) From Agrobacterium Radiobacter

All present enzymatic activity of Structure of Phosphotriesterase Mutant (S308L/Y309A) From Agrobacterium Radiobacter:
3.1.8.1;

Protein crystallography data

The structure of Structure of Phosphotriesterase Mutant (S308L/Y309A) From Agrobacterium Radiobacter, PDB code: 3wml was solved by C.J.Jackson, P.D.Carr, E.Sugrue, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 29.36 / 1.99
Space group P 31 2 1
Cell size a, b, c (Å), α, β, γ (°) 108.996, 108.996, 61.774, 90.00, 90.00, 120.00
R / Rfree (%) 15.7 / 18.7

Other elements in 3wml:

The structure of Structure of Phosphotriesterase Mutant (S308L/Y309A) From Agrobacterium Radiobacter also contains other interesting chemical elements:

Cobalt (Co) 1 atom

Iron Binding Sites:

The binding sites of Iron atom in the Structure of Phosphotriesterase Mutant (S308L/Y309A) From Agrobacterium Radiobacter (pdb code 3wml). This binding sites where shown within 5.0 Angstroms radius around Iron atom.
In total only one binding site of Iron was determined in the Structure of Phosphotriesterase Mutant (S308L/Y309A) From Agrobacterium Radiobacter, PDB code: 3wml:

Iron binding site 1 out of 1 in 3wml

Go back to Iron Binding Sites List in 3wml
Iron binding site 1 out of 1 in the Structure of Phosphotriesterase Mutant (S308L/Y309A) From Agrobacterium Radiobacter


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 1 of Structure of Phosphotriesterase Mutant (S308L/Y309A) From Agrobacterium Radiobacter within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe401

b:11.8
occ:0.90
 O A:HOH614 1.9 21.1 1.0
NE2 A:HIS57 2.2 11.9 1.0
OD1 A:ASP301 2.2 11.7 1.0
CE1 A:HIS55 2.3 12.3 1.0
OQ1 A:KCX169 2.6 15.7 1.0
CG A:ASP301 3.0 11.8 1.0
CX A:KCX169 3.0 21.3 1.0
CD2 A:HIS57 3.1 12.0 1.0
ND1 A:HIS55 3.2 14.6 1.0
OD2 A:ASP301 3.2 14.0 1.0
CE1 A:HIS57 3.2 12.2 1.0
NE2 A:HIS55 3.3 14.2 1.0
NZ A:KCX169 3.5 22.8 1.0
CO A:CO402 3.7 14.9 0.9
OQ2 A:KCX169 3.8 18.0 1.0
O A:HOH615 4.2 22.0 1.0
NE2 A:HIS230 4.2 17.8 1.0
CG A:HIS57 4.3 12.4 1.0
ND1 A:HIS57 4.3 13.3 1.0
CG2 A:VAL101 4.3 12.1 1.0
CB A:ASP301 4.3 11.2 1.0
CG A:HIS55 4.4 12.5 1.0
CD2 A:HIS55 4.4 11.4 1.0
CE1 A:HIS230 4.6 15.2 1.0
CA A:ASP301 4.8 11.1 1.0
CE A:KCX169 4.9 17.8 1.0

Reference:

T.Naqvi, A.C.Warden, N.French, E.Sugrue, P.D.Carr, C.J.Jackson, C.Scott. A 5000-Fold Increase in the Specificity of A Bacterial Phosphotriesterase For Malathion Through Combinatorial Active Site Mutagenesis Plos One V. 9 94177 2014.
ISSN: ESSN 1932-6203
PubMed: 24721933
DOI: 10.1371/JOURNAL.PONE.0094177
Page generated: Sun Aug 4 22:43:01 2024

Last articles

Zn in 9JYW
Zn in 9IR4
Zn in 9IR3
Zn in 9GMX
Zn in 9GMW
Zn in 9JEJ
Zn in 9ERF
Zn in 9ERE
Zn in 9EGV
Zn in 9EGW
© Copyright 2008-2020 by atomistry.com
Home   |    Site Map   |    Copyright   |    Contact us   |    Privacy