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Iron in PDB 7v44: Crystal Structure of Class I P450 Monooxygenase (P450TOL) From Rhodococcus Coprophilus Tc-2 in Complex with Meta-Chlorotoluene.

Protein crystallography data

The structure of Crystal Structure of Class I P450 Monooxygenase (P450TOL) From Rhodococcus Coprophilus Tc-2 in Complex with Meta-Chlorotoluene., PDB code: 7v44 was solved by L.L.Zhang, J.W.Huang, W.D.Liu, C.C.Chen, R.T.Guo, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 24.19 / 1.42
Space group P 32 2 1
Cell size a, b, c (Å), α, β, γ (°) 111.063, 111.063, 80.57, 90, 90, 120
R / Rfree (%) 14.9 / 17.2

Other elements in 7v44:

The structure of Crystal Structure of Class I P450 Monooxygenase (P450TOL) From Rhodococcus Coprophilus Tc-2 in Complex with Meta-Chlorotoluene. also contains other interesting chemical elements:

Chlorine (Cl) 1 atom

Iron Binding Sites:

The binding sites of Iron atom in the Crystal Structure of Class I P450 Monooxygenase (P450TOL) From Rhodococcus Coprophilus Tc-2 in Complex with Meta-Chlorotoluene. (pdb code 7v44). 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 Crystal Structure of Class I P450 Monooxygenase (P450TOL) From Rhodococcus Coprophilus Tc-2 in Complex with Meta-Chlorotoluene., PDB code: 7v44:

Iron binding site 1 out of 1 in 7v44

Go back to Iron Binding Sites List in 7v44
Iron binding site 1 out of 1 in the Crystal Structure of Class I P450 Monooxygenase (P450TOL) From Rhodococcus Coprophilus Tc-2 in Complex with Meta-Chlorotoluene.


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 1 of Crystal Structure of Class I P450 Monooxygenase (P450TOL) From Rhodococcus Coprophilus Tc-2 in Complex with Meta-Chlorotoluene. within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe501

b:10.5
occ:1.00
FE A:HEM501 0.0 10.5 1.0
ND A:HEM501 2.0 9.9 1.0
NA A:HEM501 2.0 9.4 1.0
NB A:HEM501 2.1 9.7 1.0
NC A:HEM501 2.1 10.5 1.0
SG A:CYS389 2.4 11.2 1.0
C1D A:HEM501 3.0 10.0 1.0
C1B A:HEM501 3.0 9.0 1.0
C4A A:HEM501 3.0 9.3 1.0
C4C A:HEM501 3.0 10.7 1.0
C4D A:HEM501 3.1 9.9 1.0
C1A A:HEM501 3.1 9.3 1.0
C4B A:HEM501 3.1 10.5 1.0
C1C A:HEM501 3.1 11.5 1.0
CB A:CYS389 3.4 9.7 1.0
CHD A:HEM501 3.4 10.6 1.0
CHB A:HEM501 3.4 10.2 1.0
CHC A:HEM501 3.4 10.9 1.0
CHA A:HEM501 3.4 8.9 1.0
CA A:CYS389 4.0 9.8 1.0
CAH A:C3U502 4.2 23.5 1.0
C2C A:HEM501 4.3 11.6 1.0
C3B A:HEM501 4.3 10.8 1.0
C2A A:HEM501 4.3 9.1 1.0
C3C A:HEM501 4.3 12.2 1.0
C2D A:HEM501 4.3 9.6 1.0
C3A A:HEM501 4.3 9.5 1.0
C2B A:HEM501 4.3 10.5 1.0
C3D A:HEM501 4.3 10.4 1.0
N A:GLY391 4.7 10.8 1.0
C A:CYS389 4.8 10.7 1.0
N A:ILE390 4.8 11.4 1.0
CAF A:C3U502 4.8 21.4 1.0

Reference:

C.C.Chen, M.Dai, L.Zhang, J.Zhao, W.Zeng, M.Shi, J.W.Huang, W.Liu, R.T.Guo, A.Li. Molecular Basis For A Toluene Monooxygenase to Govern Substrate Selectivity Acs Catalysis V. 12 2831 2022.
ISSN: ESSN 2155-5435
DOI: 10.1021/ACSCATAL.1C05845
Page generated: Fri Aug 9 05:23:03 2024

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