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Arsenic in PDB 5vv6: Structure of Bovine Endothelial Nitric Oxide Synthase Heme Domain in Complex with 7-(((4-(Dimethylamino)Phenethyl)Amino)Methyl)Quinolin-2- Amine

Enzymatic activity of Structure of Bovine Endothelial Nitric Oxide Synthase Heme Domain in Complex with 7-(((4-(Dimethylamino)Phenethyl)Amino)Methyl)Quinolin-2- Amine

All present enzymatic activity of Structure of Bovine Endothelial Nitric Oxide Synthase Heme Domain in Complex with 7-(((4-(Dimethylamino)Phenethyl)Amino)Methyl)Quinolin-2- Amine:
1.14.13.39;

Protein crystallography data

The structure of Structure of Bovine Endothelial Nitric Oxide Synthase Heme Domain in Complex with 7-(((4-(Dimethylamino)Phenethyl)Amino)Methyl)Quinolin-2- Amine, PDB code: 5vv6 was solved by H.Li, T.L.Poulos, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 39.17 / 2.00
Space group P 21 21 21
Cell size a, b, c (Å), α, β, γ (°) 57.800, 106.196, 156.672, 90.00, 90.00, 90.00
R / Rfree (%) 17 / 22

Other elements in 5vv6:

The structure of Structure of Bovine Endothelial Nitric Oxide Synthase Heme Domain in Complex with 7-(((4-(Dimethylamino)Phenethyl)Amino)Methyl)Quinolin-2- Amine also contains other interesting chemical elements:

Iron (Fe) 2 atoms
Zinc (Zn) 1 atom

Arsenic Binding Sites:

The binding sites of Arsenic atom in the Structure of Bovine Endothelial Nitric Oxide Synthase Heme Domain in Complex with 7-(((4-(Dimethylamino)Phenethyl)Amino)Methyl)Quinolin-2- Amine (pdb code 5vv6). This binding sites where shown within 5.0 Angstroms radius around Arsenic atom.
In total 2 binding sites of Arsenic where determined in the Structure of Bovine Endothelial Nitric Oxide Synthase Heme Domain in Complex with 7-(((4-(Dimethylamino)Phenethyl)Amino)Methyl)Quinolin-2- Amine, PDB code: 5vv6:
Jump to Arsenic binding site number: 1; 2;

Arsenic binding site 1 out of 2 in 5vv6

Go back to Arsenic Binding Sites List in 5vv6
Arsenic binding site 1 out of 2 in the Structure of Bovine Endothelial Nitric Oxide Synthase Heme Domain in Complex with 7-(((4-(Dimethylamino)Phenethyl)Amino)Methyl)Quinolin-2- Amine


Mono view


Stereo pair view

A full contact list of Arsenic with other atoms in the As binding site number 1 of Structure of Bovine Endothelial Nitric Oxide Synthase Heme Domain in Complex with 7-(((4-(Dimethylamino)Phenethyl)Amino)Methyl)Quinolin-2- Amine within 5.0Å range:
probe atom residue distance (Å) B Occ
A:As384

b:57.6
occ:1.00
 AS A:CAS384 0.0 57.6 1.0
CE2 A:CAS384 2.0 35.8 1.0
CE1 A:CAS384 2.0 52.3 1.0
SG A:CAS384 2.4 31.8 1.0
CB A:CAS384 3.2 29.1 1.0
CA A:CAS384 3.8 31.0 1.0
N A:CAS384 4.5 35.3 1.0
CD1 A:LEU328 4.7 31.7 1.0
CE3 A:TRP324 4.7 31.1 1.0
CD2 A:TRP324 4.8 30.3 1.0
CB A:TRP324 4.9 31.1 1.0
CG A:TRP324 5.0 29.9 1.0
C A:CAS384 5.0 33.0 1.0

Arsenic binding site 2 out of 2 in 5vv6

Go back to Arsenic Binding Sites List in 5vv6
Arsenic binding site 2 out of 2 in the Structure of Bovine Endothelial Nitric Oxide Synthase Heme Domain in Complex with 7-(((4-(Dimethylamino)Phenethyl)Amino)Methyl)Quinolin-2- Amine


Mono view


Stereo pair view

A full contact list of Arsenic with other atoms in the As binding site number 2 of Structure of Bovine Endothelial Nitric Oxide Synthase Heme Domain in Complex with 7-(((4-(Dimethylamino)Phenethyl)Amino)Methyl)Quinolin-2- Amine within 5.0Å range:
probe atom residue distance (Å) B Occ
B:As384

b:58.5
occ:1.00
 AS B:CAS384 0.0 58.5 1.0
CE2 B:CAS384 2.0 52.7 1.0
CE1 B:CAS384 2.0 60.7 1.0
SG B:CAS384 2.4 57.4 1.0
CB B:CAS384 3.0 41.8 1.0
CA B:CAS384 3.8 46.8 1.0
CE3 B:TRP324 4.1 47.6 1.0
CB B:TRP324 4.2 47.5 1.0
CD2 B:TRP324 4.3 52.8 1.0
CG B:TRP324 4.4 53.1 1.0
N B:CAS384 4.7 44.5 1.0
CD2 B:LEU328 4.8 36.5 1.0
C B:CAS384 4.9 44.4 1.0
CZ3 B:TRP324 4.9 48.7 1.0
O B:CAS384 5.0 46.2 1.0

Reference:

A.V.Pensa, M.A.Cinelli, H.Li, G.Chreifi, P.Mukherjee, L.J.Roman, P.Martasek, T.L.Poulos, R.B.Silverman. Hydrophilic, Potent, and Selective 7-Substituted 2-Aminoquinolines As Improved Human Neuronal Nitric Oxide Synthase Inhibitors. J. Med. Chem. V. 60 7146 2017.
ISSN: ISSN 1520-4804
PubMed: 28776992
DOI: 10.1021/ACS.JMEDCHEM.7B00835
Page generated: Sat Dec 12 01:47:50 2020

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