Atomistry » Magnesium » PDB 7f6n-7fs9 » 7fs2
Atomistry »
  Magnesium »
    PDB 7f6n-7fs9 »
      7fs2 »

Magnesium in PDB 7fs2: Structure of Liver Pyruvate Kinase in Complex with Allosteric Modulator 13

Enzymatic activity of Structure of Liver Pyruvate Kinase in Complex with Allosteric Modulator 13

All present enzymatic activity of Structure of Liver Pyruvate Kinase in Complex with Allosteric Modulator 13:
2.7.1.40;

Protein crystallography data

The structure of Structure of Liver Pyruvate Kinase in Complex with Allosteric Modulator 13, PDB code: 7fs2 was solved by A.Lulla, O.Nilsson, P.Brear, A.Nain-Perez, M.Grotli, M.Hyvonen, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 187.60 / 2.37
Space group C 1 2 1
Cell size a, b, c (Å), α, β, γ (°) 207.669, 113.013, 187.767, 90, 92.41, 90
R / Rfree (%) 20.3 / 24

Other elements in 7fs2:

The structure of Structure of Liver Pyruvate Kinase in Complex with Allosteric Modulator 13 also contains other interesting chemical elements:

Potassium (K) 8 atoms

Magnesium Binding Sites:

The binding sites of Magnesium atom in the Structure of Liver Pyruvate Kinase in Complex with Allosteric Modulator 13 (pdb code 7fs2). This binding sites where shown within 5.0 Angstroms radius around Magnesium atom.
In total 8 binding sites of Magnesium where determined in the Structure of Liver Pyruvate Kinase in Complex with Allosteric Modulator 13, PDB code: 7fs2:
Jump to Magnesium binding site number: 1; 2; 3; 4; 5; 6; 7; 8;

Magnesium binding site 1 out of 8 in 7fs2

Go back to Magnesium Binding Sites List in 7fs2
Magnesium binding site 1 out of 8 in the Structure of Liver Pyruvate Kinase in Complex with Allosteric Modulator 13


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 1 of Structure of Liver Pyruvate Kinase in Complex with Allosteric Modulator 13 within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Mg603

b:41.0
occ:1.00
 OD2 A:ASP308 1.9 74.1 1.0
O2 A:OXL602 2.0 80.5 1.0
O1 A:OXL602 2.1 79.9 1.0
OE2 A:GLU284 2.2 78.2 1.0
C1 A:OXL602 2.7 80.1 1.0
C2 A:OXL602 2.8 80.3 1.0
CG A:ASP308 3.1 71.5 1.0
CD A:GLU284 3.2 76.1 1.0
OE1 A:GLU284 3.5 77.2 1.0
CB A:ASP308 3.8 64.7 1.0
O4 A:OXL602 4.0 80.1 1.0
O3 A:OXL602 4.0 80.1 1.0
OD1 A:ASP308 4.1 72.7 1.0
NZ A:LYS282 4.2 66.5 1.0
N A:ASP308 4.5 61.2 1.0
CG A:GLU284 4.6 69.3 1.0
CE A:LYS282 4.6 65.1 1.0
CE1 A:PHE256 4.7 74.0 1.0
CA A:ASP308 4.8 62.1 1.0
CB A:ALA305 4.8 55.4 1.0
CB A:GLU284 4.9 64.7 1.0

Magnesium binding site 2 out of 8 in 7fs2

Go back to Magnesium Binding Sites List in 7fs2
Magnesium binding site 2 out of 8 in the Structure of Liver Pyruvate Kinase in Complex with Allosteric Modulator 13


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 2 of Structure of Liver Pyruvate Kinase in Complex with Allosteric Modulator 13 within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Mg603

b:40.8
occ:1.00
 O4 B:OXL602 1.9 63.3 1.0
OD2 B:ASP308 1.9 61.4 1.0
OE2 B:GLU284 2.0 59.8 1.0
O3 B:OXL602 2.3 62.3 1.0
C2 B:OXL602 2.8 63.3 1.0
C1 B:OXL602 2.9 62.4 1.0
CD B:GLU284 3.0 59.4 1.0
CG B:ASP308 3.1 58.7 1.0
OE1 B:GLU284 3.3 62.7 1.0
CB B:ASP308 3.8 51.2 1.0
O2 B:OXL602 4.0 63.7 1.0
O1 B:OXL602 4.1 61.9 1.0
OD1 B:ASP308 4.1 60.1 1.0
NZ B:LYS282 4.2 50.8 1.0
CG B:GLU284 4.4 52.1 1.0
CE B:LYS282 4.5 48.2 1.0
N B:ASP308 4.6 46.5 1.0
CE1 B:PHE256 4.6 52.3 1.0
O B:HOH779 4.6 44.1 1.0
CB B:GLU284 4.7 46.8 1.0
CB B:ALA305 4.7 44.7 1.0
CA B:ASP308 4.8 48.0 1.0
CD1 B:PHE256 4.9 51.7 1.0

Magnesium binding site 3 out of 8 in 7fs2

Go back to Magnesium Binding Sites List in 7fs2
Magnesium binding site 3 out of 8 in the Structure of Liver Pyruvate Kinase in Complex with Allosteric Modulator 13


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 3 of Structure of Liver Pyruvate Kinase in Complex with Allosteric Modulator 13 within 5.0Å range:
probe atom residue distance (Å) B Occ
C:Mg603

b:31.1
occ:1.00
 OE2 C:GLU284 1.9 43.5 1.0
OD2 C:ASP308 2.0 59.9 1.0
O3 C:OXL602 2.1 74.4 1.0
O4 C:OXL602 2.2 75.8 1.0
CD C:GLU284 2.8 47.6 1.0
C1 C:OXL602 2.8 74.5 1.0
C2 C:OXL602 2.9 75.2 1.0
OE1 C:GLU284 3.0 50.5 1.0
CG C:ASP308 3.2 57.9 1.0
CB C:ASP308 3.9 52.4 1.0
NZ C:LYS282 4.0 50.0 1.0
O1 C:OXL602 4.1 74.0 1.0
O2 C:OXL602 4.1 74.9 1.0
CG C:GLU284 4.2 47.4 1.0
OD1 C:ASP308 4.2 58.9 1.0
CE1 C:PHE256 4.4 53.0 1.0
CE C:LYS282 4.4 48.4 1.0
CB C:GLU284 4.6 47.4 1.0
CD1 C:PHE256 4.6 52.1 1.0
CB C:ALA305 4.8 47.5 1.0
N C:ASP308 4.8 49.5 1.0
CA C:ASP308 4.9 50.3 1.0

Magnesium binding site 4 out of 8 in 7fs2

Go back to Magnesium Binding Sites List in 7fs2
Magnesium binding site 4 out of 8 in the Structure of Liver Pyruvate Kinase in Complex with Allosteric Modulator 13


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 4 of Structure of Liver Pyruvate Kinase in Complex with Allosteric Modulator 13 within 5.0Å range:
probe atom residue distance (Å) B Occ
D:Mg603

b:26.5
occ:1.00
 OD2 D:ASP308 1.9 56.3 1.0
O1 D:OXL602 1.9 64.3 1.0
O2 D:OXL602 1.9 62.3 1.0
OE2 D:GLU284 2.2 51.7 1.0
C1 D:OXL602 2.7 63.5 1.0
C2 D:OXL602 2.7 62.7 1.0
CG D:ASP308 3.1 52.4 1.0
CD D:GLU284 3.1 51.2 1.0
OE1 D:GLU284 3.4 53.4 1.0
CB D:ASP308 3.8 43.8 1.0
O4 D:OXL602 3.9 62.3 1.0
O3 D:OXL602 4.0 63.1 1.0
OD1 D:ASP308 4.1 53.8 1.0
NZ D:LYS282 4.2 43.1 1.0
CG D:GLU284 4.5 46.0 1.0
CE1 D:PHE256 4.5 47.0 1.0
CE D:LYS282 4.6 39.9 1.0
N D:ASP308 4.6 38.4 1.0
CB D:GLU284 4.8 41.3 1.0
CA D:ASP308 4.9 40.4 1.0
CB D:ALA305 4.9 31.0 1.0
CD1 D:PHE256 4.9 46.3 1.0

Magnesium binding site 5 out of 8 in 7fs2

Go back to Magnesium Binding Sites List in 7fs2
Magnesium binding site 5 out of 8 in the Structure of Liver Pyruvate Kinase in Complex with Allosteric Modulator 13


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 5 of Structure of Liver Pyruvate Kinase in Complex with Allosteric Modulator 13 within 5.0Å range:
probe atom residue distance (Å) B Occ
E:Mg603

b:33.2
occ:1.00
 OE2 E:GLU284 1.9 62.9 1.0
OD2 E:ASP308 1.9 68.5 1.0
O3 E:OXL602 2.0 72.6 1.0
O4 E:OXL602 2.3 71.1 1.0
O E:HOH727 2.5 39.9 1.0
CD E:GLU284 2.8 62.3 1.0
C1 E:OXL602 2.9 72.5 1.0
C2 E:OXL602 3.0 71.6 1.0
OE1 E:GLU284 3.1 62.3 1.0
CG E:ASP308 3.1 66.4 1.0
CB E:ASP308 3.8 58.8 1.0
NZ E:LYS282 4.0 57.8 1.0
O1 E:OXL602 4.1 72.9 1.0
OD1 E:ASP308 4.1 68.6 1.0
O2 E:OXL602 4.2 71.3 1.0
CG E:GLU284 4.2 60.6 1.0
CE1 E:PHE256 4.3 62.3 1.0
CE E:LYS282 4.4 56.4 1.0
CB E:GLU284 4.6 58.1 1.0
CD1 E:PHE256 4.6 61.6 1.0
N E:ASP308 4.7 54.7 1.0
CB E:ALA305 4.8 53.1 1.0
CA E:ASP308 4.9 55.6 1.0

Magnesium binding site 6 out of 8 in 7fs2

Go back to Magnesium Binding Sites List in 7fs2
Magnesium binding site 6 out of 8 in the Structure of Liver Pyruvate Kinase in Complex with Allosteric Modulator 13


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 6 of Structure of Liver Pyruvate Kinase in Complex with Allosteric Modulator 13 within 5.0Å range:
probe atom residue distance (Å) B Occ
F:Mg603

b:27.8
occ:1.00
 OE2 F:GLU284 1.9 49.8 1.0
OD2 F:ASP308 1.9 53.9 1.0
O1 F:OXL602 1.9 67.8 1.0
O F:HOH725 2.3 27.8 1.0
O2 F:OXL602 2.7 70.0 1.0
CD F:GLU284 2.9 49.9 1.0
C1 F:OXL602 3.0 68.2 1.0
CG F:ASP308 3.1 53.0 1.0
OE1 F:GLU284 3.2 53.5 1.0
C2 F:OXL602 3.3 69.5 1.0
CB F:ASP308 3.8 44.5 1.0
NZ F:LYS282 4.0 37.8 1.0
O3 F:OXL602 4.1 67.7 1.0
OD1 F:ASP308 4.2 56.2 1.0
CG F:GLU284 4.2 43.9 1.0
CE F:LYS282 4.4 35.4 1.0
CE1 F:PHE256 4.5 48.6 1.0
O4 F:OXL602 4.5 69.8 1.0
CB F:GLU284 4.6 41.1 1.0
N F:ASP308 4.6 39.4 1.0
CB F:ALA305 4.6 38.4 1.0
CD1 F:PHE256 4.8 47.8 1.0
CA F:ASP308 4.8 40.9 1.0

Magnesium binding site 7 out of 8 in 7fs2

Go back to Magnesium Binding Sites List in 7fs2
Magnesium binding site 7 out of 8 in the Structure of Liver Pyruvate Kinase in Complex with Allosteric Modulator 13


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 7 of Structure of Liver Pyruvate Kinase in Complex with Allosteric Modulator 13 within 5.0Å range:
probe atom residue distance (Å) B Occ
G:Mg603

b:15.8
occ:1.00
 OE2 G:GLU284 1.9 42.5 1.0
O2 G:OXL602 2.0 52.5 1.0
O1 G:OXL602 2.0 50.5 1.0
OD2 G:ASP308 2.0 53.4 1.0
O G:HOH716 2.2 32.1 1.0
O G:HOH745 2.5 43.9 1.0
C2 G:OXL602 2.6 51.9 1.0
C1 G:OXL602 2.7 50.9 1.0
CD G:GLU284 2.9 45.3 1.0
CG G:ASP308 3.1 50.5 1.0
OE1 G:GLU284 3.3 48.5 1.0
CB G:ASP308 3.7 44.2 1.0
O3 G:OXL602 3.9 50.3 1.0
O4 G:OXL602 4.0 51.9 1.0
NZ G:LYS282 4.1 41.6 1.0
OD1 G:ASP308 4.2 51.3 1.0
CG G:GLU284 4.3 41.6 1.0
N G:ASP308 4.4 41.9 1.0
CE G:LYS282 4.5 39.0 1.0
CB G:ALA305 4.6 40.9 1.0
CE1 G:PHE256 4.6 46.3 1.0
CB G:GLU284 4.6 40.5 1.0
CA G:ASP308 4.7 41.7 1.0
CD1 G:PHE256 4.9 45.7 1.0

Magnesium binding site 8 out of 8 in 7fs2

Go back to Magnesium Binding Sites List in 7fs2
Magnesium binding site 8 out of 8 in the Structure of Liver Pyruvate Kinase in Complex with Allosteric Modulator 13


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 8 of Structure of Liver Pyruvate Kinase in Complex with Allosteric Modulator 13 within 5.0Å range:
probe atom residue distance (Å) B Occ
H:Mg603

b:18.9
occ:1.00
 OE2 H:GLU284 1.9 48.9 1.0
OD2 H:ASP308 1.9 47.8 1.0
O3 H:OXL602 1.9 58.5 1.0
O4 H:OXL602 2.0 56.9 1.0
O H:HOH708 2.1 25.6 1.0
O H:HOH703 2.1 32.7 1.0
C2 H:OXL602 2.6 57.3 1.0
C1 H:OXL602 2.6 58.2 1.0
CD H:GLU284 3.0 47.9 1.0
CG H:ASP308 3.0 45.5 1.0
OE1 H:GLU284 3.4 51.3 1.0
CB H:ASP308 3.6 39.2 1.0
O1 H:OXL602 3.8 58.6 1.0
O2 H:OXL602 3.9 56.9 1.0
OD1 H:ASP308 4.1 46.5 1.0
NZ H:LYS282 4.2 33.0 1.0
CG H:GLU284 4.3 42.3 1.0
N H:ASP308 4.3 35.0 1.0
CB H:ALA305 4.5 30.8 1.0
CA H:ASP308 4.5 37.4 1.0
CE H:LYS282 4.5 31.0 1.0
CB H:GLU284 4.6 37.8 1.0
CE1 H:PHE256 4.6 39.3 1.0
CD1 H:PHE256 4.9 38.8 1.0

Reference:

A.Nain-Perez, O.Nilsson, A.Lulla, L.Haversen, P.Brear, S.Liljenberg, M.Hyvonen, J.Boren, M.Grotli. Tuning Liver Pyruvate Kinase Activity Up or Down with A New Class of Allosteric Modulators. Eur.J.Med.Chem. V. 250 15177 2023.
ISSN: ISSN 0223-5234
PubMed: 36753880
DOI: 10.1016/J.EJMECH.2023.115177
Page generated: Wed Oct 2 21:40:26 2024

Last articles

Zn in 9MJ5
Zn in 9HNW
Zn in 9G0L
Zn in 9FNE
Zn in 9DZN
Zn in 9E0I
Zn in 9D32
Zn in 9DAK
Zn in 8ZXC
Zn in 8ZUF
© Copyright 2008-2020 by atomistry.com
Home   |    Site Map   |    Copyright   |    Contact us   |    Privacy