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Iron in PDB 3n60: Structure of Neuronal Nitric Oxide Synthase Heme Domain in Complex with 6,6'-(2,2'-(5-Amino-1,3-Phenylene)Bis(Ethane-2,1-Diyl))Bis(4- Methylpyridin-2-Amine)

Enzymatic activity of Structure of Neuronal Nitric Oxide Synthase Heme Domain in Complex with 6,6'-(2,2'-(5-Amino-1,3-Phenylene)Bis(Ethane-2,1-Diyl))Bis(4- Methylpyridin-2-Amine)

All present enzymatic activity of Structure of Neuronal Nitric Oxide Synthase Heme Domain in Complex with 6,6'-(2,2'-(5-Amino-1,3-Phenylene)Bis(Ethane-2,1-Diyl))Bis(4- Methylpyridin-2-Amine):
1.14.13.39;

Protein crystallography data

The structure of Structure of Neuronal Nitric Oxide Synthase Heme Domain in Complex with 6,6'-(2,2'-(5-Amino-1,3-Phenylene)Bis(Ethane-2,1-Diyl))Bis(4- Methylpyridin-2-Amine), PDB code: 3n60 was solved by H.Li, S.L.Delker, T.L.Poulos, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 37.63 / 1.98
Space group P 21 21 21
Cell size a, b, c (Å), α, β, γ (°) 51.860, 111.170, 164.020, 90.00, 90.00, 90.00
R / Rfree (%) 19.1 / 23.2

Other elements in 3n60:

The structure of Structure of Neuronal Nitric Oxide Synthase Heme Domain in Complex with 6,6'-(2,2'-(5-Amino-1,3-Phenylene)Bis(Ethane-2,1-Diyl))Bis(4- Methylpyridin-2-Amine) also contains other interesting chemical elements:

Chlorine (Cl) 4 atoms
Zinc (Zn) 3 atoms

Iron Binding Sites:

The binding sites of Iron atom in the Structure of Neuronal Nitric Oxide Synthase Heme Domain in Complex with 6,6'-(2,2'-(5-Amino-1,3-Phenylene)Bis(Ethane-2,1-Diyl))Bis(4- Methylpyridin-2-Amine) (pdb code 3n60). 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 Neuronal Nitric Oxide Synthase Heme Domain in Complex with 6,6'-(2,2'-(5-Amino-1,3-Phenylene)Bis(Ethane-2,1-Diyl))Bis(4- Methylpyridin-2-Amine), PDB code: 3n60:
Jump to Iron binding site number: 1; 2;

Iron binding site 1 out of 2 in 3n60

Go back to Iron Binding Sites List in 3n60
Iron binding site 1 out of 2 in the Structure of Neuronal Nitric Oxide Synthase Heme Domain in Complex with 6,6'-(2,2'-(5-Amino-1,3-Phenylene)Bis(Ethane-2,1-Diyl))Bis(4- Methylpyridin-2-Amine)


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 1 of Structure of Neuronal Nitric Oxide Synthase Heme Domain in Complex with 6,6'-(2,2'-(5-Amino-1,3-Phenylene)Bis(Ethane-2,1-Diyl))Bis(4- Methylpyridin-2-Amine) within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe750

b:33.3
occ:1.00
 FE A:HEM750 0.0 33.3 1.0
ND A:HEM750 2.1 32.8 1.0
NC A:HEM750 2.1 30.8 1.0
NA A:HEM750 2.1 34.5 1.0
NB A:HEM750 2.1 32.4 1.0
SG A:CYS415 2.4 35.8 1.0
C4D A:HEM750 3.1 34.7 1.0
C4C A:HEM750 3.1 32.3 1.0
C4A A:HEM750 3.1 34.3 1.0
C1B A:HEM750 3.1 35.1 1.0
C1C A:HEM750 3.1 32.4 1.0
C1D A:HEM750 3.1 33.8 1.0
C1A A:HEM750 3.1 29.9 1.0
C4B A:HEM750 3.1 35.4 1.0
CB A:CYS415 3.4 34.1 1.0
CHB A:HEM750 3.4 33.0 1.0
CHA A:HEM750 3.5 32.5 1.0
CHD A:HEM750 3.5 33.9 1.0
CHC A:HEM750 3.5 31.2 1.0
C37 A:XFN800 3.7 36.7 1.0
C36 A:XFN800 3.9 39.6 1.0
C38 A:XFN800 4.0 37.5 1.0
C42 A:XFN800 4.0 39.7 1.0
CA A:CYS415 4.2 33.8 1.0
C3C A:HEM750 4.3 33.9 1.0
C3D A:HEM750 4.3 33.6 1.0
C2B A:HEM750 4.3 36.5 1.0
C2C A:HEM750 4.3 33.2 1.0
C3A A:HEM750 4.3 32.9 1.0
C2D A:HEM750 4.3 30.9 1.0
C3B A:HEM750 4.3 36.4 1.0
C2A A:HEM750 4.4 34.3 1.0
C35 A:XFN800 4.4 39.6 1.0
C39 A:XFN800 4.4 39.3 1.0
NE1 A:TRP409 4.5 34.7 1.0
N40 A:XFN800 4.6 38.4 1.0
C A:CYS415 5.0 34.0 1.0

Iron binding site 2 out of 2 in 3n60

Go back to Iron Binding Sites List in 3n60
Iron binding site 2 out of 2 in the Structure of Neuronal Nitric Oxide Synthase Heme Domain in Complex with 6,6'-(2,2'-(5-Amino-1,3-Phenylene)Bis(Ethane-2,1-Diyl))Bis(4- Methylpyridin-2-Amine)


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 2 of Structure of Neuronal Nitric Oxide Synthase Heme Domain in Complex with 6,6'-(2,2'-(5-Amino-1,3-Phenylene)Bis(Ethane-2,1-Diyl))Bis(4- Methylpyridin-2-Amine) within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Fe750

b:32.8
occ:1.00
 FE B:HEM750 0.0 32.8 1.0
ND B:HEM750 2.0 33.6 1.0
NC B:HEM750 2.1 30.3 1.0
NB B:HEM750 2.1 35.0 1.0
NA B:HEM750 2.1 35.8 1.0
SG B:CYS415 2.5 33.1 1.0
C4D B:HEM750 3.0 35.7 1.0
C1D B:HEM750 3.0 32.9 1.0
C4B B:HEM750 3.1 35.5 1.0
C1A B:HEM750 3.1 32.5 1.0
C1C B:HEM750 3.1 32.1 1.0
C4C B:HEM750 3.1 28.9 1.0
C1B B:HEM750 3.1 37.1 1.0
C4A B:HEM750 3.1 35.1 1.0
CB B:CYS415 3.3 31.3 1.0
CHA B:HEM750 3.4 35.1 1.0
CHD B:HEM750 3.4 32.1 1.0
CHC B:HEM750 3.4 35.2 1.0
CHB B:HEM750 3.5 34.8 1.0
C37 B:XFN800 3.8 38.6 1.0
C36 B:XFN800 3.8 38.0 1.0
C38 B:XFN800 4.0 38.4 1.0
CA B:CYS415 4.2 32.1 1.0
C42 B:XFN800 4.2 41.9 1.0
C35 B:XFN800 4.2 38.4 1.0
C2D B:HEM750 4.3 33.2 1.0
C3D B:HEM750 4.3 34.8 1.0
C3C B:HEM750 4.3 29.6 1.0
C2C B:HEM750 4.3 31.1 1.0
C2A B:HEM750 4.3 36.3 1.0
C3B B:HEM750 4.3 35.7 1.0
C2B B:HEM750 4.3 35.8 1.0
C39 B:XFN800 4.3 35.9 1.0
C3A B:HEM750 4.3 34.6 1.0
NE1 B:TRP409 4.4 35.5 1.0
N40 B:XFN800 4.4 36.1 1.0
N B:GLY417 4.9 34.8 1.0
C B:CYS415 5.0 32.4 1.0

Reference:

S.L.Delker, F.Xue, H.Li, J.Jamal, R.B.Silverman, T.L.Poulos. Role of Zinc in Isoform-Selective Inhibitor Binding to Neuronal Nitric Oxide Synthase . Biochemistry V. 49 10803 2010.
ISSN: ISSN 0006-2960
PubMed: 21138269
DOI: 10.1021/BI1013479
Page generated: Tue Aug 5 04:38:50 2025

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