Atomistry » Sodium » PDB 3p2y-3pkh » 3paq
Atomistry »
  Sodium »
    PDB 3p2y-3pkh »
      3paq »

Sodium in PDB 3paq: Surfactant Protein A Neck and Carbohydrate Recognition Domain (Ncrd) Complexed with Alpha-Methylmannose

Protein crystallography data

The structure of Surfactant Protein A Neck and Carbohydrate Recognition Domain (Ncrd) Complexed with Alpha-Methylmannose, PDB code: 3paq was solved by F.Shang, M.J.Rynkiewicz, F.X.Mccormack, H.Wu, T.M.Cafarella, J.Head, B.A.Seaton, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 30.73 / 2.10
Space group P 63
Cell size a, b, c (Å), α, β, γ (°) 97.452, 97.452, 44.848, 90.00, 90.00, 120.00
R / Rfree (%) 22.3 / 24.4

Other elements in 3paq:

The structure of Surfactant Protein A Neck and Carbohydrate Recognition Domain (Ncrd) Complexed with Alpha-Methylmannose also contains other interesting chemical elements:

Calcium (Ca) 1 atom

Sodium Binding Sites:

The binding sites of Sodium atom in the Surfactant Protein A Neck and Carbohydrate Recognition Domain (Ncrd) Complexed with Alpha-Methylmannose (pdb code 3paq). This binding sites where shown within 5.0 Angstroms radius around Sodium atom.
In total only one binding site of Sodium was determined in the Surfactant Protein A Neck and Carbohydrate Recognition Domain (Ncrd) Complexed with Alpha-Methylmannose, PDB code: 3paq:

Sodium binding site 1 out of 1 in 3paq

Go back to Sodium Binding Sites List in 3paq
Sodium binding site 1 out of 1 in the Surfactant Protein A Neck and Carbohydrate Recognition Domain (Ncrd) Complexed with Alpha-Methylmannose


Mono view


Stereo pair view

A full contact list of Sodium with other atoms in the Na binding site number 1 of Surfactant Protein A Neck and Carbohydrate Recognition Domain (Ncrd) Complexed with Alpha-Methylmannose within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Na301

b:55.7
occ:1.00
OE1 A:GLU171 2.6 56.6 1.0
O A:GLU202 2.7 49.7 1.0
N A:GLY200 3.0 59.5 1.0
N A:GLU202 3.1 55.1 1.0
CD A:GLU171 3.2 56.8 1.0
OE2 A:GLU171 3.2 58.4 1.0
C A:GLU202 3.2 51.4 1.0
OD2 A:ASP215 3.3 42.0 1.0
O A:HOH560 3.3 49.0 1.0
CA A:GLY200 3.4 58.9 1.0
CA A:GLU202 3.5 52.7 1.0
N A:LYS201 3.6 57.9 1.0
C A:GLY200 3.6 58.3 1.0
C A:GLY198 3.7 57.4 1.0
CB A:GLU202 3.8 52.2 1.0
N A:GLN199 3.9 58.8 1.0
CA A:GLY198 4.0 56.2 1.0
O A:GLY198 4.0 57.5 1.0
C A:GLN199 4.0 61.1 1.0
N A:LYS203 4.2 49.8 1.0
C A:LYS201 4.2 56.9 1.0
N A:GLY198 4.3 54.2 1.0
CG A:ASP215 4.4 41.9 1.0
CA A:GLN199 4.4 61.2 1.0
O A:GLY200 4.5 58.7 1.0
CA A:LYS201 4.5 57.5 1.0
CG A:GLU171 4.6 56.2 1.0
CZ A:PHE178 4.6 42.4 1.0
CG A:GLU202 4.7 52.5 1.0
CB A:ASP215 4.7 39.0 1.0
CA A:LYS203 4.8 49.8 1.0
CB A:GLU171 4.8 56.0 1.0

Reference:

F.Shang, M.J.Rynkiewicz, F.X.Mccormack, H.Wu, T.M.Cafarella, J.F.Head, B.A.Seaton. Crystallographic Complexes of Surfactant Protein A and Carbohydrates Reveal Ligand-Induced Conformational Change. J.Biol.Chem. V. 286 757 2011.
ISSN: ISSN 0021-9258
PubMed: 21047777
DOI: 10.1074/JBC.M110.175265
Page generated: Mon Oct 7 12:12:18 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