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Iron in PDB 4dtw: Cytochrome P450 BM3H-8C8 Mri Sensor Bound to Serotonin

Enzymatic activity of Cytochrome P450 BM3H-8C8 Mri Sensor Bound to Serotonin

All present enzymatic activity of Cytochrome P450 BM3H-8C8 Mri Sensor Bound to Serotonin:
1.14.14.1;

Protein crystallography data

The structure of Cytochrome P450 BM3H-8C8 Mri Sensor Bound to Serotonin, PDB code: 4dtw was solved by E.M.Brustad, V.S.Lelyveld, C.D.Snow, N.Crook, F.M.Martinez, T.J.Scholl, A.Jasanoff, F.H.Arnold, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 38.87 / 1.80
Space group P 1 21 1
Cell size a, b, c (Å), α, β, γ (°) 58.606, 146.249, 64.064, 90.00, 97.51, 90.00
R / Rfree (%) 19.2 / 25.4

Other elements in 4dtw:

The structure of Cytochrome P450 BM3H-8C8 Mri Sensor Bound to Serotonin also contains other interesting chemical elements:

Magnesium (Mg) 1 atom

Iron Binding Sites:

The binding sites of Iron atom in the Cytochrome P450 BM3H-8C8 Mri Sensor Bound to Serotonin (pdb code 4dtw). This binding sites where shown within 5.0 Angstroms radius around Iron atom.
In total 2 binding sites of Iron where determined in the Cytochrome P450 BM3H-8C8 Mri Sensor Bound to Serotonin, PDB code: 4dtw:
Jump to Iron binding site number: 1; 2;

Iron binding site 1 out of 2 in 4dtw

Go back to Iron Binding Sites List in 4dtw
Iron binding site 1 out of 2 in the Cytochrome P450 BM3H-8C8 Mri Sensor Bound to Serotonin


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 1 of Cytochrome P450 BM3H-8C8 Mri Sensor Bound to Serotonin within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Fe501

b:9.4
occ:1.00
FE B:HEM501 0.0 9.4 1.0
NZ B:SRO502 1.9 7.5 1.0
NB B:HEM501 2.0 6.5 1.0
NA B:HEM501 2.0 12.6 1.0
NC B:HEM501 2.1 13.1 1.0
ND B:HEM501 2.1 5.6 1.0
SG B:CYS400 2.2 8.6 1.0
C1B B:HEM501 3.0 13.7 1.0
C4B B:HEM501 3.0 9.2 1.0
C4A B:HEM501 3.0 9.6 1.0
C4C B:HEM501 3.1 9.3 1.0
C1A B:HEM501 3.1 8.9 1.0
C1D B:HEM501 3.1 9.8 1.0
C4D B:HEM501 3.1 11.3 1.0
C1C B:HEM501 3.1 7.5 1.0
CA B:SRO502 3.2 14.4 1.0
CB B:CYS400 3.2 10.9 1.0
CHB B:HEM501 3.4 12.2 1.0
CHC B:HEM501 3.5 10.0 1.0
CHD B:HEM501 3.5 8.6 1.0
CHA B:HEM501 3.5 7.2 1.0
CA B:CYS400 4.0 9.7 1.0
C2B B:HEM501 4.2 8.4 1.0
C3B B:HEM501 4.2 6.2 1.0
C3C B:HEM501 4.3 11.1 1.0
C2A B:HEM501 4.3 7.7 1.0
C3A B:HEM501 4.3 8.9 1.0
C2D B:HEM501 4.3 9.5 1.0
C2C B:HEM501 4.3 9.9 1.0
C3D B:HEM501 4.3 9.3 1.0
CB B:SRO502 4.6 20.2 1.0
C B:CYS400 4.8 10.5 1.0
O B:ALA264 4.8 23.8 1.0
N B:GLY402 4.8 10.1 1.0
N B:ILE401 5.0 9.1 1.0

Iron binding site 2 out of 2 in 4dtw

Go back to Iron Binding Sites List in 4dtw
Iron binding site 2 out of 2 in the Cytochrome P450 BM3H-8C8 Mri Sensor Bound to Serotonin


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 2 of Cytochrome P450 BM3H-8C8 Mri Sensor Bound to Serotonin within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe500

b:9.7
occ:1.00
FE A:HEM500 0.0 9.7 1.0
NB A:HEM500 1.9 6.0 1.0
NZ A:SRO501 1.9 8.4 1.0
ND A:HEM500 2.0 8.2 1.0
NA A:HEM500 2.0 11.9 1.0
NC A:HEM500 2.1 13.4 1.0
SG A:CYS400 2.2 11.1 1.0
C4B A:HEM500 3.0 8.6 1.0
C1B A:HEM500 3.0 9.0 1.0
C4D A:HEM500 3.0 10.5 1.0
C1D A:HEM500 3.0 10.6 1.0
C1A A:HEM500 3.1 7.0 1.0
C1C A:HEM500 3.1 6.7 1.0
C4C A:HEM500 3.1 13.1 1.0
C4A A:HEM500 3.1 11.8 1.0
CB A:CYS400 3.2 8.5 1.0
CA A:SRO501 3.3 17.2 1.0
CHC A:HEM500 3.4 5.3 1.0
CHA A:HEM500 3.4 6.9 1.0
CHD A:HEM500 3.5 11.0 1.0
CHB A:HEM500 3.5 9.7 1.0
CA A:CYS400 4.0 10.4 1.0
C2B A:HEM500 4.2 7.0 1.0
C3B A:HEM500 4.2 9.5 1.0
C2D A:HEM500 4.3 10.4 1.0
C3C A:HEM500 4.3 10.1 1.0
C2C A:HEM500 4.3 10.8 1.0
C3D A:HEM500 4.3 6.2 1.0
C2A A:HEM500 4.3 7.5 1.0
C3A A:HEM500 4.3 9.6 1.0
CB A:SRO501 4.6 23.5 1.0
O A:ALA264 4.7 15.1 1.0
C A:CYS400 4.8 11.1 1.0
N A:GLY402 4.8 10.3 1.0
N A:ILE401 5.0 11.6 1.0

Reference:

E.M.Brustad, V.S.Lelyveld, C.D.Snow, N.Crook, S.T.Jung, F.M.Martinez, T.J.Scholl, A.Jasanoff, F.H.Arnold. Structure-Guided Directed Evolution of Highly Selective P450-Based Magnetic Resonance Imaging Sensors For Dopamine and Serotonin. J.Mol.Biol. V. 422 245 2012.
ISSN: ISSN 0022-2836
PubMed: 22659321
DOI: 10.1016/J.JMB.2012.05.029
Page generated: Tue Aug 5 09:54:42 2025

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