Atomistry » Sodium » PDB 3q11-3qpz » 3qel
Atomistry »
  Sodium »
    PDB 3q11-3qpz »
      3qel »

Sodium in PDB 3qel: Crystal Structure of Amino Terminal Domains of the Nmda Receptor Subunit GLUN1 and GLUN2B in Complex with Ifenprodil

Protein crystallography data

The structure of Crystal Structure of Amino Terminal Domains of the Nmda Receptor Subunit GLUN1 and GLUN2B in Complex with Ifenprodil, PDB code: 3qel was solved by E.Karakas, N.Simorowski, H.Furukawa, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 29.98 / 2.60
Space group C 1 2 1
Cell size a, b, c (Å), α, β, γ (°) 267.993, 60.869, 144.923, 90.00, 116.49, 90.00
R / Rfree (%) 18.8 / 23.8

Sodium Binding Sites:

The binding sites of Sodium atom in the Crystal Structure of Amino Terminal Domains of the Nmda Receptor Subunit GLUN1 and GLUN2B in Complex with Ifenprodil (pdb code 3qel). 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 Amino Terminal Domains of the Nmda Receptor Subunit GLUN1 and GLUN2B in Complex with Ifenprodil, PDB code: 3qel:
Jump to Sodium binding site number: 1; 2;

Sodium binding site 1 out of 2 in 3qel

Go back to Sodium Binding Sites List in 3qel
Sodium binding site 1 out of 2 in the Crystal Structure of Amino Terminal Domains of the Nmda Receptor Subunit GLUN1 and GLUN2B in Complex with Ifenprodil


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 Amino Terminal Domains of the Nmda Receptor Subunit GLUN1 and GLUN2B in Complex with Ifenprodil within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Na501

b:49.0
occ:1.00
O A:PHE137 2.1 38.9 1.0
O A:ASP364 2.4 38.9 1.0
O A:HOH440 2.4 38.5 1.0
O A:HOH441 2.6 42.4 1.0
O A:HOH458 3.1 43.2 1.0
C A:PHE137 3.2 34.8 1.0
C A:ASP364 3.5 36.5 1.0
O A:HOH451 3.5 47.8 1.0
O A:TYR128 3.9 40.3 1.0
CB A:PHE137 4.0 30.4 1.0
CA A:PHE137 4.0 33.6 1.0
CA A:GLY365 4.0 33.9 1.0
N A:PHE137 4.0 39.4 1.0
N A:GLY365 4.2 34.7 1.0
N A:LEU138 4.2 35.1 1.0
O A:HIS134 4.4 35.5 1.0
CA A:LEU138 4.4 36.4 1.0
C A:GLY365 4.5 34.7 1.0
CD2 A:PHE137 4.5 35.0 1.0
CA A:ASP364 4.5 35.2 1.0
CA A:SER129 4.8 38.6 1.0
CG A:PHE137 4.8 34.5 1.0
O A:GLY365 4.8 32.8 1.0
CB A:ASP364 5.0 43.2 1.0
C A:TYR128 5.0 36.8 1.0

Sodium binding site 2 out of 2 in 3qel

Go back to Sodium Binding Sites List in 3qel
Sodium binding site 2 out of 2 in the Crystal Structure of Amino Terminal Domains of the Nmda Receptor Subunit GLUN1 and GLUN2B in Complex with Ifenprodil


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 Amino Terminal Domains of the Nmda Receptor Subunit GLUN1 and GLUN2B in Complex with Ifenprodil within 5.0Å range:
probe atom residue distance (Å) B Occ
C:Na501

b:63.9
occ:1.00
O C:PHE137 2.1 56.9 1.0
O C:HOH423 2.3 51.8 1.0
O C:ASP364 2.4 68.1 1.0
O C:HOH424 2.4 55.8 1.0
O C:HOH425 2.9 57.9 1.0
C C:PHE137 3.3 53.0 1.0
C C:ASP364 3.5 66.7 1.0
CA C:GLY365 3.7 55.9 1.0
O C:TYR128 3.8 57.3 1.0
N C:GLY365 4.0 55.1 1.0
CA C:PHE137 4.0 50.4 1.0
CB C:PHE137 4.0 50.3 1.0
N C:PHE137 4.2 53.4 1.0
O C:HIS134 4.3 48.7 1.0
N C:LEU138 4.3 49.8 1.0
C C:GLY365 4.4 54.8 1.0
CD2 C:PHE137 4.5 56.0 1.0
CA C:LEU138 4.5 49.8 1.0
CA C:ASP364 4.6 68.9 1.0
O C:LEU135 4.7 83.0 1.0
CA C:SER129 4.7 51.5 1.0
OD1 C:ASP366 4.8 58.9 1.0
CG C:PHE137 4.8 55.1 1.0
O C:GLY365 4.8 49.9 1.0
O C:SER129 4.9 54.2 1.0
C C:TYR128 4.9 59.2 1.0
N C:ASP366 5.0 56.0 1.0

Reference:

E.Karakas, N.Simorowski, H.Furukawa. Subunit Arrangement and Phenylethanolamine Binding in GLUN1/GLUN2B Nmda Receptors. Nature V. 475 249 2011.
ISSN: ISSN 0028-0836
PubMed: 21677647
DOI: 10.1038/NATURE10180
Page generated: Mon Oct 7 12:28:59 2024

Last articles

Zn in 9JYW
Zn in 9IR4
Zn in 9IR3
Zn in 9GMX
Zn in 9GMW
Zn in 9JEJ
Zn in 9ERF
Zn in 9ERE
Zn in 9EGV
Zn in 9EGW
© Copyright 2008-2020 by atomistry.com
Home   |    Site Map   |    Copyright   |    Contact us   |    Privacy