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Iron in PDB 7soj: Structure of V750A Soybean Lipoxygenase at 277K

Protein crystallography data

The structure of Structure of V750A Soybean Lipoxygenase at 277K, PDB code: 7soj was solved by C.L.Gee, A.R.Offenbacher, S.Hu, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 46.35 / 1.85
Space group P 1 21 1
Cell size a, b, c (Å), α, β, γ (°) 91.537, 92.693, 100.27, 90, 93.75, 90
R / Rfree (%) 16.9 / 19.8

Iron Binding Sites:

The binding sites of Iron atom in the Structure of V750A Soybean Lipoxygenase at 277K (pdb code 7soj). This binding sites where shown within 5.0 Angstroms radius around Iron atom.
In total 2 binding sites of Iron where determined in the Structure of V750A Soybean Lipoxygenase at 277K, PDB code: 7soj:
Jump to Iron binding site number: 1; 2;

Iron binding site 1 out of 2 in 7soj

Go back to Iron Binding Sites List in 7soj
Iron binding site 1 out of 2 in the Structure of V750A Soybean Lipoxygenase at 277K


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 1 of Structure of V750A Soybean Lipoxygenase at 277K within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe901

b:32.4
occ:1.00
NE2 A:HIS504 2.1 24.8 1.0
NE2 A:HIS499 2.3 27.9 1.0
O A:HOH1038 2.3 24.2 1.0
NE2 A:HIS690 2.3 16.6 1.0
OXT A:ILE839 2.4 24.6 1.0
CE1 A:HIS504 2.9 25.3 1.0
HE1 A:HIS504 3.0 30.3 1.0
CE1 A:HIS499 3.1 34.9 1.0
CD2 A:HIS690 3.2 17.9 1.0
OD1 A:ASN694 3.2 25.9 1.0
HE1 A:HIS499 3.2 41.9 1.0
CD2 A:HIS504 3.2 21.5 1.0
HD2 A:HIS690 3.3 21.5 1.0
C A:ILE839 3.3 26.8 1.0
CD2 A:HIS499 3.3 27.6 1.0
O A:ILE839 3.4 26.7 1.0
CE1 A:HIS690 3.4 18.2 1.0
HD2 A:HIS504 3.5 25.8 1.0
HD2 A:HIS499 3.6 33.1 1.0
HE1 A:HIS690 3.6 21.9 1.0
HG23 A:ILE837 3.7 21.6 1.0
CG A:ASN694 3.7 20.7 1.0
HB2 A:ASN694 3.8 22.6 1.0
ND1 A:HIS504 4.1 24.3 1.0
CG A:HIS504 4.3 19.3 1.0
ND1 A:HIS499 4.3 28.6 1.0
CB A:ASN694 4.3 18.8 1.0
H A:ILE839 4.3 27.8 1.0
CG A:HIS690 4.4 16.8 1.0
CG A:HIS499 4.4 25.0 1.0
CG2 A:ILE837 4.4 18.0 1.0
ND1 A:HIS690 4.4 16.7 1.0
ND2 A:ASN694 4.5 21.2 1.0
HG22 A:ILE837 4.6 21.6 1.0
HD21 A:ASN694 4.6 25.5 1.0
HG23 A:ILE839 4.6 28.1 1.0
HG21 A:ILE837 4.6 21.6 1.0
CA A:ILE839 4.7 24.4 1.0
HD1 A:HIS504 4.8 29.2 1.0
HB3 A:ASN694 4.8 22.6 1.0
HB3 A:LEU754 4.9 27.2 1.0
N A:ILE839 4.9 23.2 1.0
HD22 A:LEU754 4.9 30.9 1.0
HD13 A:LEU754 5.0 39.5 1.0
OG1 A:THR503 5.0 21.4 1.0

Iron binding site 2 out of 2 in 7soj

Go back to Iron Binding Sites List in 7soj
Iron binding site 2 out of 2 in the Structure of V750A Soybean Lipoxygenase at 277K


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 2 of Structure of V750A Soybean Lipoxygenase at 277K within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Fe901

b:32.1
occ:1.00
NE2 B:HIS504 2.2 24.4 1.0
NE2 B:HIS499 2.2 24.3 1.0
O B:HOH1017 2.3 27.0 1.0
OXT B:ILE839 2.3 20.8 1.0
NE2 B:HIS690 2.4 16.2 1.0
CE1 B:HIS499 3.0 31.9 1.0
CE1 B:HIS504 3.0 24.5 1.0
OD1 B:ASN694 3.1 25.2 1.0
HE1 B:HIS499 3.1 38.3 1.0
HE1 B:HIS504 3.1 29.4 1.0
CD2 B:HIS690 3.2 18.4 1.0
HD2 B:HIS690 3.2 22.1 1.0
CD2 B:HIS504 3.3 23.9 1.0
C B:ILE839 3.3 24.8 1.0
CD2 B:HIS499 3.3 24.9 1.0
O B:ILE839 3.4 24.5 1.0
HD2 B:HIS504 3.5 28.6 1.0
CE1 B:HIS690 3.5 19.4 1.0
HD2 B:HIS499 3.6 29.9 1.0
HG23 B:ILE837 3.7 23.2 1.0
CG B:ASN694 3.7 21.6 1.0
HB2 B:ASN694 3.7 23.5 1.0
HE1 B:HIS690 3.8 23.2 1.0
ND1 B:HIS499 4.2 30.3 1.0
ND1 B:HIS504 4.2 25.8 1.0
CB B:ASN694 4.3 19.6 1.0
CG B:HIS504 4.3 20.8 1.0
CG B:HIS499 4.4 23.3 1.0
H B:ILE839 4.4 26.1 1.0
ND2 B:ASN694 4.4 20.3 1.0
CG B:HIS690 4.4 15.7 1.0
CG2 B:ILE837 4.5 19.3 1.0
HD21 B:ASN694 4.5 24.4 1.0
HG23 B:ILE839 4.5 30.4 1.0
ND1 B:HIS690 4.6 17.2 1.0
HG22 B:ILE837 4.6 23.2 1.0
HG21 B:ILE837 4.6 23.2 1.0
CA B:ILE839 4.7 22.6 1.0
HB3 B:ASN694 4.8 23.5 1.0
HD13 B:LEU754 4.8 36.7 1.0
HD22 B:LEU754 4.9 33.3 1.0
N B:ILE839 4.9 21.8 1.0
HD1 B:HIS499 4.9 36.4 1.0
HD1 B:HIS504 4.9 30.9 1.0

Reference:

J.P.T.Zaragoza, A.R.Offenbacher, S.Hu, C.L.Gee, Z.M.Firestein, N.Minnetian, Z.Deng, A.T.Iavarone, J.P.Klinman. A Dynamically-Activated Protein Quake Controls the Thermal Activation of Enzyme Catalyzed Hydrogen Tunneling To Be Published.
Page generated: Thu Aug 7 05:35:20 2025

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