Iron in PDB 9iss: Crystal Structure of Cytochrome P450BM3 III-10C1 Mutant Heme Domain with N-Decanoyl-L-Homoserine Lactone

All present enzymatic activity of Crystal Structure of Cytochrome P450BM3 III-10C1 Mutant Heme Domain with N-Decanoyl-L-Homoserine Lactone:
1.14.14.1; 1.6.2.4;

The structure of Crystal Structure of Cytochrome P450BM3 III-10C1 Mutant Heme Domain with N-Decanoyl-L-Homoserine Lactone, PDB code: 9iss was solved by Y.Yokoyama, O.Shoji, H.Sugimoto, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å)	47.44 / 1.46
Space group	P 1 21 1
Cell size a, b, c (Å), α, β, γ (°)	58.575, 145.442, 63.106, 90, 97.37, 90
R / Rfree (%)	16.6 / 18.2

The binding sites of Iron atom in the Crystal Structure of Cytochrome P450BM3 III-10C1 Mutant Heme Domain with N-Decanoyl-L-Homoserine Lactone (pdb code 9iss). This binding sites where shown within 5.0 Angstroms radius around Iron atom.
In total 2 binding sites of Iron where determined in the Crystal Structure of Cytochrome P450BM3 III-10C1 Mutant Heme Domain with N-Decanoyl-L-Homoserine Lactone, PDB code: 9iss:
Jump to Iron binding site number: 1; 2;

Iron binding site 1 out of 2 in the Crystal Structure of Cytochrome P450BM3 III-10C1 Mutant Heme Domain with N-Decanoyl-L-Homoserine Lactone


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 Cytochrome P450BM3 III-10C1 Mutant Heme Domain with N-Decanoyl-L-Homoserine Lactone within 5.0Å range: probe atom residue distance (Å) B Occ A:Fe501 b:11.0 occ:1.00 FE A:HEM501 0.0 11.0 1.0 ND A:HEM501 2.0 9.5 1.0 NA A:HEM501 2.0 9.7 1.0 NC A:HEM501 2.1 9.4 1.0 NB A:HEM501 2.1 9.2 1.0 SG A:CYS400 2.3 12.6 1.0 S A:DMS503 2.4 18.5 0.7 C1D A:HEM501 3.0 9.8 1.0 C4D A:HEM501 3.0 10.2 1.0 C4B A:HEM501 3.0 9.7 1.0 C1B A:HEM501 3.0 9.8 1.0 C4C A:HEM501 3.0 10.8 1.0 C1A A:HEM501 3.1 9.4 1.0 C1C A:HEM501 3.1 10.0 1.0 C4A A:HEM501 3.1 9.8 1.0 O A:DMS503 3.4 20.0 0.7 CB A:CYS400 3.4 12.8 1.0 CHC A:HEM501 3.4 10.6 1.0 CHD A:HEM501 3.4 11.1 1.0 CHB A:HEM501 3.4 10.7 1.0 CHA A:HEM501 3.5 10.8 1.0 C2 A:DMS503 3.6 17.9 0.7 C1 A:DMS503 3.6 21.2 0.7 CA A:CYS400 4.0 11.2 1.0 C3B A:HEM501 4.2 11.6 1.0 C2C A:HEM501 4.3 11.3 1.0 C3A A:HEM501 4.3 10.1 1.0 C3C A:HEM501 4.3 11.2 1.0 C3D A:HEM501 4.3 10.8 1.0 C2D A:HEM501 4.3 10.4 1.0 C2B A:HEM501 4.3 10.9 1.0 C2A A:HEM501 4.3 10.4 1.0 N A:GLY402 4.8 11.1 1.0 C A:CYS400 4.8 11.1 1.0 N A:ILE401 4.9 11.4 1.0

Iron binding site 2 out of 2 in the Crystal Structure of Cytochrome P450BM3 III-10C1 Mutant Heme Domain with N-Decanoyl-L-Homoserine Lactone


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 2 of Crystal Structure of Cytochrome P450BM3 III-10C1 Mutant Heme Domain with N-Decanoyl-L-Homoserine Lactone within 5.0Å range: probe atom residue distance (Å) B Occ B:Fe501 b:11.1 occ:1.00 FE B:HEM501 0.0 11.1 1.0 ND B:HEM501 2.0 9.3 1.0 NA B:HEM501 2.0 9.2 1.0 NC B:HEM501 2.0 10.1 1.0 NB B:HEM501 2.1 9.3 1.0 SG B:CYS400 2.3 12.8 1.0 S B:DMS503 2.4 18.7 0.7 C4C B:HEM501 3.0 10.8 1.0 C1B B:HEM501 3.0 9.6 1.0 C1D B:HEM501 3.0 10.4 1.0 C4D B:HEM501 3.0 9.2 1.0 C1C B:HEM501 3.1 9.9 1.0 C4B B:HEM501 3.1 9.9 1.0 C4A B:HEM501 3.1 9.5 1.0 C1A B:HEM501 3.1 9.0 1.0 CB B:CYS400 3.3 11.3 1.0 O B:DMS503 3.3 22.2 0.7 CHD B:HEM501 3.4 11.1 1.0 CHC B:HEM501 3.4 10.4 1.0 CHA B:HEM501 3.4 9.8 1.0 CHB B:HEM501 3.5 10.1 1.0 C2 B:DMS503 3.6 20.7 0.7 C1 B:DMS503 3.7 17.9 0.7 CA B:CYS400 4.0 11.0 1.0 C2C B:HEM501 4.2 11.0 1.0 C3C B:HEM501 4.3 11.8 1.0 C2D B:HEM501 4.3 10.1 1.0 C3A B:HEM501 4.3 9.7 1.0 C2B B:HEM501 4.3 10.1 1.0 C3B B:HEM501 4.3 10.2 1.0 C2A B:HEM501 4.3 10.3 1.0 C3D B:HEM501 4.3 10.5 1.0 C B:CYS400 4.8 10.8 1.0 N B:GLY402 4.8 12.6 1.0 N B:ILE401 4.9 10.9 1.0

Y.Yokoyama, S.Ariyasu, M.Karasawa, C.Kasai, Y.Aiba, H.Sugimoto, O.Shoji. Bacterial Acyl Homoserine Lactones Triggered Non-Native Substrate Hydroxylation Catalyzed By Directed-Evolution-Derived Cytochrome P450BM3 Mutants Chemcatchem 2024.
ISSN: ESSN 1867-3899
DOI: 10.1002/CCTC.202401641