Atomistry » Sodium » PDB 1s45-1t3p » 1sg8
Atomistry »
  Sodium »
    PDB 1s45-1t3p »
      1sg8 »

Sodium in PDB 1sg8: Crystal Structure of the Procoagulant Fast Form of Thrombin

Enzymatic activity of Crystal Structure of the Procoagulant Fast Form of Thrombin

All present enzymatic activity of Crystal Structure of the Procoagulant Fast Form of Thrombin:
3.4.21.5;

Protein crystallography data

The structure of Crystal Structure of the Procoagulant Fast Form of Thrombin, PDB code: 1sg8 was solved by A.O.Pineda, C.J.Carrell, L.A.Bush, S.Prasad, S.Caccia, Z.W.Chen, F.S.Mathews, E.Di Cera, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 24.64 / 2.30
Space group P 21 21 21
Cell size a, b, c (Å), α, β, γ (°) 59.490, 65.580, 162.440, 90.00, 90.00, 90.00
R / Rfree (%) 21.9 / 28.9

Sodium Binding Sites:

The binding sites of Sodium atom in the Crystal Structure of the Procoagulant Fast Form of Thrombin (pdb code 1sg8). This binding sites where shown within 5.0 Angstroms radius around Sodium atom.
In total 2 binding sites of Sodium where determined in the Crystal Structure of the Procoagulant Fast Form of Thrombin, PDB code: 1sg8:
Jump to Sodium binding site number: 1; 2;

Sodium binding site 1 out of 2 in 1sg8

Go back to Sodium Binding Sites List in 1sg8
Sodium binding site 1 out of 2 in the Crystal Structure of the Procoagulant Fast Form of Thrombin


Mono view


Stereo pair view

A full contact list of Sodium with other atoms in the Na binding site number 1 of Crystal Structure of the Procoagulant Fast Form of Thrombin within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Na1701

b:54.3
occ:1.00
O B:LYS224 2.5 49.8 1.0
O B:ARG221A 2.5 53.2 1.0
O B:HOH549 2.5 45.7 1.0
O B:HOH749 2.7 50.1 1.0
O B:HOH913 2.8 74.8 1.0
O B:HOH766 2.9 50.5 1.0
C B:LYS224 3.5 51.8 1.0
C B:ARG221A 3.6 51.5 1.0
O B:TYR184A 3.9 39.6 1.0
N B:LYS224 4.0 49.3 1.0
O B:HOH542 4.0 47.7 1.0
O B:HOH540 4.1 39.1 1.0
N B:ARG221A 4.2 53.2 1.0
CA B:LYS224 4.2 50.9 1.0
CA B:ASP222 4.3 50.7 1.0
C B:ASP221 4.4 54.2 1.0
N B:ASP222 4.4 50.7 1.0
N B:TYR225 4.4 49.3 1.0
CB B:LYS224 4.6 47.0 1.0
CD1 B:TYR225 4.6 54.7 1.0
N B:GLY223 4.6 52.4 1.0
CA B:ARG221A 4.6 53.4 1.0
CA B:ASP221 4.6 52.7 1.0
CA B:TYR225 4.6 50.1 1.0
CE1 B:TYR225 4.7 53.0 1.0
C B:ASP222 4.7 50.8 1.0
O B:HOH790 4.7 48.6 1.0
OD1 B:ASP221 4.9 45.8 1.0
O B:ASP221 5.0 55.1 1.0

Sodium binding site 2 out of 2 in 1sg8

Go back to Sodium Binding Sites List in 1sg8
Sodium binding site 2 out of 2 in the Crystal Structure of the Procoagulant Fast Form of Thrombin


Mono view


Stereo pair view

A full contact list of Sodium with other atoms in the Na binding site number 2 of Crystal Structure of the Procoagulant Fast Form of Thrombin within 5.0Å range:
probe atom residue distance (Å) B Occ
E:Na1702

b:55.0
occ:1.00
O E:HOH663 2.4 49.1 1.0
O E:HOH651 2.5 38.3 1.0
O E:ARG221A 2.5 51.0 1.0
O E:LYS224 2.5 48.6 1.0
O E:HOH649 2.5 44.4 1.0
O E:HOH664 2.9 58.2 1.0
C E:ARG221A 3.4 51.4 1.0
O E:HOH655 3.6 43.1 1.0
O E:TYR184A 3.7 47.0 1.0
O E:HOH527 3.7 49.4 1.0
C E:LYS224 3.7 50.2 1.0
N E:ARG221A 4.0 56.8 1.0
C E:ASP221 4.1 54.7 1.0
O E:HOH652 4.2 46.0 1.0
N E:ASP222 4.2 48.6 1.0
CA E:ASP222 4.3 48.4 1.0
N E:LYS224 4.3 43.9 1.0
CA E:ARG221A 4.3 51.9 1.0
O E:ASP221 4.4 55.0 1.0
CA E:ASP221 4.5 53.5 1.0
CA E:LYS224 4.6 47.7 1.0
N E:GLY223 4.6 44.5 1.0
N E:TYR225 4.6 51.4 1.0
OD1 E:ASP221 4.7 50.5 1.0
CA E:TYR225 4.7 50.9 1.0
CD1 E:TYR225 4.7 49.6 1.0
C E:ASP222 4.8 44.5 1.0
C E:TYR184A 4.8 46.0 1.0
CE1 E:TYR225 4.9 50.7 1.0
CB E:LYS224 5.0 52.5 1.0

Reference:

A.O.Pineda, C.J.Carrell, L.A.Bush, S.Prasad, S.Caccia, Z.W.Chen, F.S.Mathews, E.Di Cera. Molecular Dissection of Na+ Binding to Thrombin. J.Biol.Chem. V. 279 31842 2004.
ISSN: ISSN 0021-9258
PubMed: 15152000
DOI: 10.1074/JBC.M401756200
Page generated: Tue Dec 15 05:35:56 2020

Last articles

Zn in 8WB0
Zn in 8WAX
Zn in 8WAU
Zn in 8WAZ
Zn in 8WAY
Zn in 8WAV
Zn in 8WAW
Zn in 8WAT
Zn in 8W7M
Zn in 8WD3
© Copyright 2008-2020 by atomistry.com
Home   |    Site Map   |    Copyright   |    Contact us   |    Privacy