Atomistry » Calcium » PDB 4qn5-4r90 » 4qra
Atomistry »
  Calcium »
    PDB 4qn5-4r90 »
      4qra »

Calcium in PDB 4qra: Structure and Specificity of L-D-Transpeptidase From Mycobacterium Tuberculosis and Antibiotic Resistance: Calcium Binding Promotes Dimer Formation

Protein crystallography data

The structure of Structure and Specificity of L-D-Transpeptidase From Mycobacterium Tuberculosis and Antibiotic Resistance: Calcium Binding Promotes Dimer Formation, PDB code: 4qra was solved by K.Gokulan, K.I.Varughese, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 34.86 / 2.29
Space group C 1 2 1
Cell size a, b, c (Å), α, β, γ (°) 113.758, 88.132, 90.512, 90.00, 90.02, 90.00
R / Rfree (%) 18.2 / 22.6

Calcium Binding Sites:

The binding sites of Calcium atom in the Structure and Specificity of L-D-Transpeptidase From Mycobacterium Tuberculosis and Antibiotic Resistance: Calcium Binding Promotes Dimer Formation (pdb code 4qra). This binding sites where shown within 5.0 Angstroms radius around Calcium atom.
In total only one binding site of Calcium was determined in the Structure and Specificity of L-D-Transpeptidase From Mycobacterium Tuberculosis and Antibiotic Resistance: Calcium Binding Promotes Dimer Formation, PDB code: 4qra:

Calcium binding site 1 out of 1 in 4qra

Go back to Calcium Binding Sites List in 4qra
Calcium binding site 1 out of 1 in the Structure and Specificity of L-D-Transpeptidase From Mycobacterium Tuberculosis and Antibiotic Resistance: Calcium Binding Promotes Dimer Formation


Mono view


Stereo pair view

A full contact list of Calcium with other atoms in the Ca binding site number 1 of Structure and Specificity of L-D-Transpeptidase From Mycobacterium Tuberculosis and Antibiotic Resistance: Calcium Binding Promotes Dimer Formation within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Ca501

b:32.0
occ:1.00
O B:LEU151 2.3 28.7 1.0
O B:HOH525 2.4 26.6 1.0
O A:LEU151 2.4 30.2 1.0
O A:HOH624 2.4 22.8 1.0
O B:HOH527 2.4 22.3 1.0
O A:HOH625 2.5 28.4 1.0
O B:HOH526 2.6 29.0 1.0
C B:LEU151 3.5 27.4 1.0
C A:LEU151 3.5 27.4 1.0
N A:LEU151 4.2 28.2 1.0
OE2 A:GLU176 4.3 33.4 1.0
CA A:LEU151 4.3 26.7 1.0
OE2 B:GLU176 4.3 32.8 1.0
N B:LEU151 4.3 28.2 1.0
CA B:LEU151 4.3 27.6 1.0
OE1 B:GLU240 4.4 44.8 1.0
N B:THR152 4.4 26.7 1.0
N A:THR152 4.5 26.9 1.0
CB A:LEU151 4.5 27.4 1.0
OE1 A:GLU240 4.5 46.1 1.0
CB B:LEU151 4.5 26.8 1.0
CA B:THR152 4.5 27.5 1.0
CA A:THR152 4.5 27.6 1.0
OD1 B:ASP175 4.6 26.2 1.0
OD1 A:ASP175 4.6 26.0 1.0
OD2 B:ASP175 4.7 29.4 1.0
OD2 A:ASP175 4.7 28.3 1.0
CG B:GLU176 4.9 30.4 1.0
CG A:GLU176 4.9 31.4 1.0
CG B:ASP175 5.0 26.5 1.0
CG A:ASP175 5.0 26.2 1.0

Reference:

K.Gokulan, S.Khare, C.E.Cerniglia, S.L.Foley, K.I.Varughese. Structure and Specificity of L-D-Transpeptidase From Mycobacterium Tuberculosis and Antibiotic Resistance: Calcium Binding Promotes Dimer Formation To Be Published.
Page generated: Sun Jul 14 12:30:27 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