Iron in PDB 8vfr: The Crystal Structure of 4-Methylbenzoic Acid-Bound Galqe CYP199A4 After Soaking in 10 Mm H2O2 For 5 Minutes

The structure of The Crystal Structure of 4-Methylbenzoic Acid-Bound Galqe CYP199A4 After Soaking in 10 Mm H2O2 For 5 Minutes, PDB code: 8vfr was solved by M.N.Podgorski, S.G.Bell, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å)	42.89 / 2.02
Space group	P 1 21 1
Cell size a, b, c (Å), α, β, γ (°)	44.213, 51.268, 78.417, 90, 92.94, 90
R / Rfree (%)	19.4 / 23.9

The structure of The Crystal Structure of 4-Methylbenzoic Acid-Bound Galqe CYP199A4 After Soaking in 10 Mm H2O2 For 5 Minutes also contains other interesting chemical elements:

Chlorine

(Cl)

1 atom

The binding sites of Iron atom in the The Crystal Structure of 4-Methylbenzoic Acid-Bound Galqe CYP199A4 After Soaking in 10 Mm H2O2 For 5 Minutes (pdb code 8vfr). 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 The Crystal Structure of 4-Methylbenzoic Acid-Bound Galqe CYP199A4 After Soaking in 10 Mm H2O2 For 5 Minutes, PDB code: 8vfr:

Iron binding site 1 out of 1 in the The Crystal Structure of 4-Methylbenzoic Acid-Bound Galqe CYP199A4 After Soaking in 10 Mm H2O2 For 5 Minutes


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 1 of The Crystal Structure of 4-Methylbenzoic Acid-Bound Galqe CYP199A4 After Soaking in 10 Mm H2O2 For 5 Minutes within 5.0Å range: probe atom residue distance (Å) B Occ A:Fe501 b:19.4 occ:1.00 FE A:HEM501 0.0 19.4 1.0 ND A:HEM501 2.0 23.9 1.0 NB A:HEM501 2.0 21.4 1.0 NA A:HEM501 2.0 23.3 1.0 NC A:HEM501 2.1 22.8 1.0 O A:HOH602 2.1 23.1 0.8 SG A:CYS358 2.3 25.7 1.0 C4D A:HEM501 3.1 21.4 1.0 C1C A:HEM501 3.1 21.1 1.0 C4A A:HEM501 3.1 21.4 1.0 C1D A:HEM501 3.1 25.1 1.0 C4B A:HEM501 3.1 21.7 1.0 C1B A:HEM501 3.1 19.3 1.0 C4C A:HEM501 3.1 26.8 1.0 C1A A:HEM501 3.1 23.1 1.0 OAA A:E5X503 3.2 24.5 0.4 CB A:CYS358 3.3 20.6 1.0 CHB A:HEM501 3.4 20.3 1.0 CHC A:HEM501 3.4 20.1 1.0 CHD A:HEM501 3.4 21.1 1.0 CHA A:HEM501 3.4 20.6 1.0 CA A:CYS358 4.1 20.6 1.0 C2C A:HEM501 4.3 22.8 1.0 C3D A:HEM501 4.3 21.9 1.0 C3A A:HEM501 4.3 20.2 1.0 C3C A:HEM501 4.3 21.7 1.0 C2D A:HEM501 4.3 24.9 1.0 C2A A:HEM501 4.3 21.5 1.0 C2B A:HEM501 4.3 18.5 1.0 C3B A:HEM501 4.3 21.6 1.0 OE2 A:GLU252 4.4 30.0 1.0 O A:GLY248 4.4 37.6 1.0 C8 A:4MA502 4.5 22.5 0.5 CAJ A:E5X503 4.6 22.5 0.4 C3 A:4MA502 4.8 23.0 0.5 C A:CYS358 4.9 22.6 1.0 CAG A:E5X503 4.9 23.0 0.4

M.N.Podgorski, J.Akter, L.R.Churchman, J.B.Bruning, J.J.De Voss, S.G.Bell. Engineering Peroxygenase Activity Into Cytochrome P450 Monooxygenases Through Modification of the Oxygen Binding Region Acs Catalysis 7426 2024.
ISSN: ESSN 2155-5435
DOI: 10.1021/ACSCATAL.4C01326