Atomistry » Chlorine » PDB 6aq4-6axt » 6av7
Atomistry »
  Chlorine »
    PDB 6aq4-6axt »
      6av7 »

Chlorine in PDB 6av7: Structure of Human Endothelial Nitric Oxide Synthase Heme Domain in Complex with HW69

Enzymatic activity of Structure of Human Endothelial Nitric Oxide Synthase Heme Domain in Complex with HW69

All present enzymatic activity of Structure of Human Endothelial Nitric Oxide Synthase Heme Domain in Complex with HW69:
1.14.13.39;

Protein crystallography data

The structure of Structure of Human Endothelial Nitric Oxide Synthase Heme Domain in Complex with HW69, PDB code: 6av7 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) 39.03 / 1.92
Space group P 1 21 1
Cell size a, b, c (Å), α, β, γ (°) 59.445, 152.355, 108.655, 90.00, 90.79, 90.00
R / Rfree (%) 20.4 / 25.4

Other elements in 6av7:

The structure of Structure of Human Endothelial Nitric Oxide Synthase Heme Domain in Complex with HW69 also contains other interesting chemical elements:

Fluorine (F) 4 atoms
Zinc (Zn) 2 atoms
Iron (Fe) 4 atoms
Gadolinium (Gd) 4 atoms

Chlorine Binding Sites:

The binding sites of Chlorine atom in the Structure of Human Endothelial Nitric Oxide Synthase Heme Domain in Complex with HW69 (pdb code 6av7). This binding sites where shown within 5.0 Angstroms radius around Chlorine atom.
In total 4 binding sites of Chlorine where determined in the Structure of Human Endothelial Nitric Oxide Synthase Heme Domain in Complex with HW69, PDB code: 6av7:
Jump to Chlorine binding site number: 1; 2; 3; 4;

Chlorine binding site 1 out of 4 in 6av7

Go back to Chlorine Binding Sites List in 6av7
Chlorine binding site 1 out of 4 in the Structure of Human Endothelial Nitric Oxide Synthase Heme Domain in Complex with HW69


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 1 of Structure of Human Endothelial Nitric Oxide Synthase Heme Domain in Complex with HW69 within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl508

b:63.5
occ:1.00
OH A:TYR357 2.8 55.5 1.0
ND2 A:ASN366 3.1 50.1 1.0
CE1 A:TYR357 3.4 50.6 1.0
NE2 A:GLN247 3.5 69.0 1.0
CZ A:TYR357 3.6 53.1 1.0
OD1 A:ASN366 3.7 50.7 1.0
OH A:TYR331 3.8 71.8 1.0
CG A:ASN366 3.8 58.6 1.0
NH2 A:ARG250 4.2 74.8 1.0
OE1 A:GLN247 4.3 61.1 1.0
CD A:GLN247 4.3 65.3 1.0
NE1 A:TRP330 4.4 60.6 1.0
CZ2 A:TRP330 4.4 55.6 1.0
C08 A:W69503 4.7 94.6 1.0
CD1 A:TYR357 4.7 52.2 1.0
CE2 A:TRP330 4.8 53.8 1.0
CZ A:TYR331 4.8 70.7 1.0
OE1 A:GLU361 4.8 53.8 1.0
CE2 A:TYR357 4.9 54.6 1.0
NH2 A:ARG372 5.0 61.6 1.0

Chlorine binding site 2 out of 4 in 6av7

Go back to Chlorine Binding Sites List in 6av7
Chlorine binding site 2 out of 4 in the Structure of Human Endothelial Nitric Oxide Synthase Heme Domain in Complex with HW69


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 2 of Structure of Human Endothelial Nitric Oxide Synthase Heme Domain in Complex with HW69 within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Cl506

b:44.2
occ:1.00
OH B:TYR357 2.9 35.7 1.0
O B:HOH663 3.0 42.9 1.0
O B:HOH619 3.1 43.5 1.0
ND2 B:ASN366 3.2 29.2 1.0
NE2 B:GLN247 3.2 33.5 1.0
CE1 B:TYR357 3.5 30.9 1.0
CZ B:TYR357 3.7 39.1 1.0
NH2 B:ARG250 3.7 50.1 1.0
OD1 B:ASN366 3.9 40.1 1.0
OH B:TYR331 3.9 40.5 1.0
CG B:ASN366 4.0 38.1 1.0
CD B:GLN247 4.1 35.0 1.0
OE1 B:GLN247 4.2 38.1 1.0
O B:HOH708 4.5 42.2 1.0
C08 B:W69503 4.6 40.4 1.0
CZ2 B:TRP330 4.6 36.4 1.0
NE1 B:TRP330 4.7 35.4 1.0
CZ B:ARG250 4.8 59.8 1.0
OE1 B:GLU361 4.8 44.8 1.0
CD1 B:TYR357 4.8 33.3 1.0
CZ B:TYR331 5.0 33.0 1.0

Chlorine binding site 3 out of 4 in 6av7

Go back to Chlorine Binding Sites List in 6av7
Chlorine binding site 3 out of 4 in the Structure of Human Endothelial Nitric Oxide Synthase Heme Domain in Complex with HW69


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 3 of Structure of Human Endothelial Nitric Oxide Synthase Heme Domain in Complex with HW69 within 5.0Å range:
probe atom residue distance (Å) B Occ
C:Cl509

b:56.5
occ:1.00
OH C:TYR357 3.0 46.9 1.0
ND2 C:ASN366 3.2 46.8 1.0
NE2 C:GLN247 3.4 57.3 1.0
CE1 C:TYR357 3.5 49.0 1.0
CZ C:TYR357 3.7 45.7 1.0
OD1 C:ASN366 3.9 46.1 1.0
CG C:ASN366 4.0 48.5 1.0
NH2 C:ARG250 4.0 57.2 1.0
OH C:TYR331 4.1 58.0 1.0
C08 C:W69503 4.3 76.3 1.0
CD C:GLN247 4.3 62.6 1.0
OE1 C:GLN247 4.4 59.8 1.0
CD1 C:TYR357 4.7 48.3 1.0
CZ2 C:TRP330 4.9 55.2 1.0
NE1 C:TRP330 4.9 45.1 1.0

Chlorine binding site 4 out of 4 in 6av7

Go back to Chlorine Binding Sites List in 6av7
Chlorine binding site 4 out of 4 in the Structure of Human Endothelial Nitric Oxide Synthase Heme Domain in Complex with HW69


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 4 of Structure of Human Endothelial Nitric Oxide Synthase Heme Domain in Complex with HW69 within 5.0Å range:
probe atom residue distance (Å) B Occ
D:Cl507

b:45.8
occ:1.00
OH D:TYR357 2.9 38.5 1.0
O D:HOH614 3.1 56.3 1.0
ND2 D:ASN366 3.2 36.5 1.0
NE2 D:GLN247 3.3 41.1 1.0
O D:HOH617 3.3 54.0 1.0
NH2 D:ARG250 3.6 55.5 1.0
CE1 D:TYR357 3.6 30.7 1.0
CZ D:TYR357 3.7 32.5 1.0
OD1 D:ASN366 3.9 47.1 1.0
CG D:ASN366 4.0 42.6 1.0
OH D:TYR331 4.0 41.1 1.0
CD D:GLN247 4.2 50.9 1.0
OE1 D:GLN247 4.2 49.0 1.0
C08 D:W69503 4.5 42.3 1.0
CZ D:ARG250 4.6 59.5 1.0
OE1 D:GLU361 4.7 41.7 1.0
NE1 D:TRP330 4.8 43.4 1.0
O D:HOH721 4.8 48.6 1.0
CZ2 D:TRP330 4.8 39.0 1.0
CD1 D:TYR357 4.9 35.0 1.0

Reference:

H.T.Do, H.Y.Wang, H.Li, G.Chreifi, T.L.Poulos, R.B.Silverman. Improvement of Cell Permeability of Human Neuronal Nitric Oxide Synthase Inhibitors Using Potent and Selective 2-Aminopyridine-Based Scaffolds with A Fluorobenzene Linker. J. Med. Chem. V. 60 9360 2017.
ISSN: ISSN 1520-4804
PubMed: 29091437
DOI: 10.1021/ACS.JMEDCHEM.7B01356
Page generated: Fri Jul 26 22:18:48 2024

Last articles

Zn in 9JPJ
Zn in 9JP7
Zn in 9JPK
Zn in 9JPL
Zn in 9GN6
Zn in 9GN7
Zn in 9GKU
Zn in 9GKW
Zn in 9GKX
Zn in 9GL0
© Copyright 2008-2020 by atomistry.com
Home   |    Site Map   |    Copyright   |    Contact us   |    Privacy