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Iron in PDB 1yqp: T268N Mutant Cytochrome Domain of Flavocytochrome P450 BM3

Enzymatic activity of T268N Mutant Cytochrome Domain of Flavocytochrome P450 BM3

All present enzymatic activity of T268N Mutant Cytochrome Domain of Flavocytochrome P450 BM3:
1.14.14.1; 1.6.2.4;

Protein crystallography data

The structure of T268N Mutant Cytochrome Domain of Flavocytochrome P450 BM3, PDB code: 1yqp was solved by J.P.Clark, C.S.Miles, C.G.Mowat, M.D.Walkinshaw, G.A.Reid, S.N.Daff, S.K.Chapman, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 24.00 / 1.80
Space group P 1 21 1
Cell size a, b, c (Å), α, β, γ (°) 58.876, 153.241, 61.607, 90.00, 94.48, 90.00
R / Rfree (%) 17.4 / 21

Iron Binding Sites:

The binding sites of Iron atom in the T268N Mutant Cytochrome Domain of Flavocytochrome P450 BM3 (pdb code 1yqp). This binding sites where shown within 5.0 Angstroms radius around Iron atom.
In total 2 binding sites of Iron where determined in the T268N Mutant Cytochrome Domain of Flavocytochrome P450 BM3, PDB code: 1yqp:
Jump to Iron binding site number: 1; 2;

Iron binding site 1 out of 2 in 1yqp

Go back to Iron Binding Sites List in 1yqp
Iron binding site 1 out of 2 in the T268N Mutant Cytochrome Domain of Flavocytochrome P450 BM3


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 1 of T268N Mutant Cytochrome Domain of Flavocytochrome P450 BM3 within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe460

b:17.3
occ:1.00
FE A:HEM460 0.0 17.3 1.0
NB A:HEM460 2.0 16.6 1.0
NC A:HEM460 2.1 16.9 1.0
NA A:HEM460 2.1 15.3 1.0
ND A:HEM460 2.1 15.1 1.0
SG A:CYS400 2.3 15.4 1.0
O A:HOH623 2.6 25.4 1.0
C1B A:HEM460 3.0 15.0 1.0
C4B A:HEM460 3.0 15.3 1.0
C1C A:HEM460 3.1 13.9 1.0
C4A A:HEM460 3.1 15.4 1.0
C4C A:HEM460 3.1 15.4 1.0
C4D A:HEM460 3.1 16.3 1.0
C1A A:HEM460 3.1 15.7 1.0
C1D A:HEM460 3.1 15.2 1.0
CB A:CYS400 3.3 14.8 1.0
CHB A:HEM460 3.4 15.4 1.0
CHC A:HEM460 3.4 15.1 1.0
CHA A:HEM460 3.5 14.5 1.0
CHD A:HEM460 3.5 14.7 1.0
CA A:CYS400 4.0 14.4 1.0
O A:ALA264 4.2 27.1 1.0
C3B A:HEM460 4.2 16.4 1.0
C2B A:HEM460 4.3 15.6 1.0
C2C A:HEM460 4.3 16.0 1.0
C3C A:HEM460 4.3 15.2 1.0
C3A A:HEM460 4.3 15.4 1.0
C3D A:HEM460 4.3 13.5 1.0
C2A A:HEM460 4.3 14.4 1.0
C2D A:HEM460 4.4 12.7 1.0
O A:HOH715 4.5 28.3 1.0
ND2 A:ASN268 4.6 22.0 1.0
C A:CYS400 4.7 15.0 1.0
N A:GLY402 4.8 15.1 1.0
CB A:ALA264 4.8 24.2 1.0
C A:ALA264 4.9 24.8 1.0
N A:ILE401 4.9 14.6 1.0

Iron binding site 2 out of 2 in 1yqp

Go back to Iron Binding Sites List in 1yqp
Iron binding site 2 out of 2 in the T268N Mutant Cytochrome Domain of Flavocytochrome P450 BM3


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 2 of T268N Mutant Cytochrome Domain of Flavocytochrome P450 BM3 within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Fe460

b:18.1
occ:1.00
FE B:HEM460 0.0 18.1 1.0
NC B:HEM460 2.0 15.2 1.0
NB B:HEM460 2.1 14.9 1.0
NA B:HEM460 2.1 15.8 1.0
ND B:HEM460 2.1 15.5 1.0
SG B:CYS400 2.3 16.3 1.0
O B:HOH731 2.7 30.4 1.0
C4C B:HEM460 3.0 16.3 1.0
C4B B:HEM460 3.1 15.7 1.0
C1C B:HEM460 3.1 15.4 1.0
C1D B:HEM460 3.1 16.8 1.0
C1B B:HEM460 3.1 15.5 1.0
C4A B:HEM460 3.1 14.9 1.0
C4D B:HEM460 3.1 15.6 1.0
C1A B:HEM460 3.1 15.1 1.0
CB B:CYS400 3.3 15.7 1.0
CHD B:HEM460 3.4 15.0 1.0
CHC B:HEM460 3.4 14.4 1.0
CHB B:HEM460 3.4 14.8 1.0
CHA B:HEM460 3.5 14.9 1.0
CA B:CYS400 3.9 15.2 1.0
O B:ALA264 4.2 25.4 1.0
C3C B:HEM460 4.3 17.1 1.0
C3B B:HEM460 4.3 13.8 1.0
C2C B:HEM460 4.3 14.8 1.0
C2B B:HEM460 4.3 13.4 1.0
C3A B:HEM460 4.3 14.5 1.0
C2D B:HEM460 4.3 14.9 1.0
C2A B:HEM460 4.3 14.7 1.0
C3D B:HEM460 4.4 13.9 1.0
ND2 B:ASN268 4.5 19.1 1.0
O B:HOH465 4.5 29.3 1.0
C B:CYS400 4.7 15.6 1.0
N B:GLY402 4.8 16.3 1.0
C B:ALA264 4.9 23.8 1.0
N B:ILE401 4.9 15.0 1.0

Reference:

J.P.Clark, C.S.Miles, C.G.Mowat, M.D.Walkinshaw, G.A.Reid, S.N.Daff, S.K.Chapman. The Role of THR268 and PHE393 in Cytochrome P450 BM3. J.Inorg.Biochem. V. 100 1075 2006.
ISSN: ISSN 0162-0134
PubMed: 16403573
DOI: 10.1016/J.JINORGBIO.2005.11.020
Page generated: Sat Aug 3 18:04:58 2024

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