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Iron in PDB 4g3r: Crystal Structure of Nitrosyl Cytochrome P450CAM

Enzymatic activity of Crystal Structure of Nitrosyl Cytochrome P450CAM

All present enzymatic activity of Crystal Structure of Nitrosyl Cytochrome P450CAM:
1.14.15.1;

Protein crystallography data

The structure of Crystal Structure of Nitrosyl Cytochrome P450CAM, PDB code: 4g3r was solved by Y.Madrona, S.M.Tripathi, H.Li, T.L.Poulos, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 33.10 / 2.20
Space group P 1 21 1
Cell size a, b, c (Å), α, β, γ (°) 67.553, 62.269, 95.490, 90.00, 90.06, 90.00
R / Rfree (%) 19 / 25

Other elements in 4g3r:

The structure of Crystal Structure of Nitrosyl Cytochrome P450CAM also contains other interesting chemical elements:

Potassium (K) 2 atoms

Iron Binding Sites:

The binding sites of Iron atom in the Crystal Structure of Nitrosyl Cytochrome P450CAM (pdb code 4g3r). 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 Nitrosyl Cytochrome P450CAM, PDB code: 4g3r:
Jump to Iron binding site number: 1; 2;

Iron binding site 1 out of 2 in 4g3r

Go back to Iron Binding Sites List in 4g3r
Iron binding site 1 out of 2 in the Crystal Structure of Nitrosyl Cytochrome P450CAM


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 Nitrosyl Cytochrome P450CAM within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe501

b:29.4
occ:1.00
FE A:HEM501 0.0 29.4 1.0
NA A:HEM501 2.2 23.8 1.0
ND A:HEM501 2.2 24.6 1.0
NB A:HEM501 2.2 23.9 1.0
NC A:HEM501 2.2 24.6 1.0
SG A:CYS357 2.3 22.5 1.0
C1A A:HEM501 3.1 21.9 1.0
C4D A:HEM501 3.1 24.5 1.0
C4B A:HEM501 3.1 24.4 1.0
C1C A:HEM501 3.2 24.8 1.0
C1B A:HEM501 3.2 28.2 1.0
C4A A:HEM501 3.2 23.0 1.0
C1D A:HEM501 3.2 27.8 1.0
C4C A:HEM501 3.2 26.6 1.0
CB A:CYS357 3.4 27.7 1.0
CHA A:HEM501 3.4 20.7 1.0
CHC A:HEM501 3.5 24.4 1.0
CHB A:HEM501 3.5 24.7 1.0
CHD A:HEM501 3.6 27.4 1.0
C5 A:CAM502 4.0 33.4 1.0
CA A:CYS357 4.0 27.5 1.0
C3B A:HEM501 4.3 25.6 1.0
C2A A:HEM501 4.4 19.6 1.0
C2B A:HEM501 4.4 26.1 1.0
C3A A:HEM501 4.4 20.9 1.0
C2C A:HEM501 4.4 23.6 1.0
C3D A:HEM501 4.4 22.9 1.0
C2D A:HEM501 4.4 25.6 1.0
C3C A:HEM501 4.4 28.8 1.0
N A:GLY359 4.5 31.8 1.0
C4 A:CAM502 4.6 32.2 1.0
N A:LEU358 4.7 30.0 1.0
C A:CYS357 4.7 27.7 1.0
CA A:GLY359 4.9 31.9 1.0
C9 A:CAM502 5.0 24.1 1.0

Iron binding site 2 out of 2 in 4g3r

Go back to Iron Binding Sites List in 4g3r
Iron binding site 2 out of 2 in the Crystal Structure of Nitrosyl Cytochrome P450CAM


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 Nitrosyl Cytochrome P450CAM within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Fe501

b:34.5
occ:1.00
FE B:HEM501 0.0 34.5 1.0
N B:NO504 1.8 58.9 0.9
NA B:HEM501 2.2 33.3 1.0
NB B:HEM501 2.2 27.4 1.0
ND B:HEM501 2.3 33.0 1.0
NC B:HEM501 2.3 27.7 1.0
SG B:CYS357 2.3 34.1 1.0
O B:NO504 2.9 60.3 0.9
C1A B:HEM501 3.1 31.8 1.0
C4D B:HEM501 3.2 30.2 1.0
C4A B:HEM501 3.2 35.9 1.0
C4B B:HEM501 3.2 29.3 1.0
C1C B:HEM501 3.2 29.1 1.0
C1B B:HEM501 3.2 31.8 1.0
C1D B:HEM501 3.2 32.5 1.0
C4C B:HEM501 3.2 29.6 1.0
CB B:CYS357 3.3 35.5 1.0
CHA B:HEM501 3.5 30.9 1.0
CHC B:HEM501 3.5 28.5 1.0
CHB B:HEM501 3.5 32.2 1.0
CHD B:HEM501 3.5 28.2 1.0
CA B:CYS357 4.0 36.1 1.0
C2A B:HEM501 4.4 34.8 1.0
C3A B:HEM501 4.4 33.0 1.0
C3B B:HEM501 4.4 31.4 1.0
C2B B:HEM501 4.4 31.5 1.0
C3D B:HEM501 4.4 32.0 1.0
C2C B:HEM501 4.4 33.8 1.0
C2D B:HEM501 4.4 33.6 1.0
C3C B:HEM501 4.5 31.2 1.0
C5 B:CAM502 4.5 34.8 1.0
N B:GLY359 4.6 37.7 1.0
N B:LEU358 4.6 35.9 1.0
C B:CYS357 4.7 36.1 1.0
C9 B:CAM502 4.8 31.6 1.0
CA B:GLY359 5.0 36.8 1.0

Reference:

Y.Madrona, S.Tripathi, H.Li, T.L.Poulos. Crystal Structures of Substrate-Free and Nitrosyl Cytochrome P450CIN: Implications For O(2) Activation. Biochemistry V. 51 6623 2012.
ISSN: ISSN 0006-2960
PubMed: 22775403
DOI: 10.1021/BI300666U
Page generated: Tue Aug 5 10:33:12 2025

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