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Iron in PDB 8hgt: Crystal Structure of the CYP153A Mutant V456A From Marinobacter Aquaeolei

Protein crystallography data

The structure of Crystal Structure of the CYP153A Mutant V456A From Marinobacter Aquaeolei, PDB code: 8hgt was solved by Y.Jiang, X.Tian, Z.Cong, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 31.38 / 2.06
Space group P 1 21 1
Cell size a, b, c (Å), α, β, γ (°) 44.12, 103.312, 52.377, 90, 112.49, 90
R / Rfree (%) 20.2 / 23.8

Iron Binding Sites:

The binding sites of Iron atom in the Crystal Structure of the CYP153A Mutant V456A From Marinobacter Aquaeolei (pdb code 8hgt). 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 the CYP153A Mutant V456A From Marinobacter Aquaeolei, PDB code: 8hgt:

Iron binding site 1 out of 1 in 8hgt

Go back to Iron Binding Sites List in 8hgt
Iron binding site 1 out of 1 in the Crystal Structure of the CYP153A Mutant V456A From Marinobacter Aquaeolei


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 the CYP153A Mutant V456A From Marinobacter Aquaeolei within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe501

b:12.4
occ:1.00
FE A:HEM501 0.0 12.4 1.0
NA A:HEM501 2.0 9.6 1.0
ND A:HEM501 2.0 10.9 1.0
NC A:HEM501 2.0 8.6 1.0
NB A:HEM501 2.0 9.8 1.0
SG A:CYS422 2.5 9.6 1.0
O A:HOH797 2.5 11.3 1.0
C4A A:HEM501 3.0 11.8 1.0
C1B A:HEM501 3.0 8.6 1.0
C4C A:HEM501 3.0 11.3 1.0
C1A A:HEM501 3.0 10.2 1.0
C4D A:HEM501 3.0 12.7 1.0
C1D A:HEM501 3.1 14.2 1.0
C1C A:HEM501 3.1 10.2 1.0
C4B A:HEM501 3.1 8.9 1.0
CB A:CYS422 3.4 15.6 1.0
CHB A:HEM501 3.4 9.8 1.0
CHA A:HEM501 3.4 13.7 1.0
CHD A:HEM501 3.4 13.7 1.0
CHC A:HEM501 3.4 10.1 1.0
O A:GLY311 4.1 16.1 1.0
CA A:CYS422 4.1 15.1 1.0
C3A A:HEM501 4.2 11.7 1.0
C2B A:HEM501 4.3 13.1 1.0
C2A A:HEM501 4.3 10.1 1.0
C3D A:HEM501 4.3 16.4 1.0
C3C A:HEM501 4.3 12.4 1.0
C2D A:HEM501 4.3 13.4 1.0
C2C A:HEM501 4.3 12.3 1.0
C3B A:HEM501 4.3 10.4 1.0
N A:MET423 4.7 17.4 1.0
N A:GLY424 4.7 19.4 1.0
C A:CYS422 4.7 17.9 1.0
C A:GLY311 4.7 15.5 1.0
CA A:GLY311 4.9 13.8 1.0

Reference:

P.Zhao, F.Kong, Y.Jiang, X.Qin, X.Tian, Z.Cong. Enabling Peroxygenase Activity in Cytochrome P450 Monooxygenases By Engineering Hydrogen Peroxide Tunnels. J.Am.Chem.Soc. V. 145 5506 2023.
ISSN: ESSN 1520-5126
PubMed: 36790023
DOI: 10.1021/JACS.3C00195
Page generated: Thu Dec 28 06:01:51 2023

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