Calcium in PDB 5eaj: Crystal Structure of Dhfr in 0% Isopropanol

Enzymatic activity of Crystal Structure of Dhfr in 0% Isopropanol

All present enzymatic activity of Crystal Structure of Dhfr in 0% Isopropanol:
1.5.1.3;

Protein crystallography data

The structure of Crystal Structure of Dhfr in 0% Isopropanol, PDB code: 5eaj was solved by M.J.Cuneo, P.K.Agarwal, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 38.92 / 1.70
Space group P 61
Cell size a, b, c (Å), α, β, γ (°) 91.947, 91.947, 73.097, 90.00, 90.00, 120.00
R / Rfree (%) 19.8 / 22.5

Other elements in 5eaj:

The structure of Crystal Structure of Dhfr in 0% Isopropanol also contains other interesting chemical elements:

Chlorine (Cl) 4 atoms

Calcium Binding Sites:

The binding sites of Calcium atom in the Crystal Structure of Dhfr in 0% Isopropanol (pdb code 5eaj). 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 Crystal Structure of Dhfr in 0% Isopropanol, PDB code: 5eaj:

Calcium binding site 1 out of 1 in 5eaj

Go back to Calcium Binding Sites List in 5eaj
Calcium binding site 1 out of 1 in the Crystal Structure of Dhfr in 0% Isopropanol


Mono view


Stereo pair view

A full contact list of Calcium with other atoms in the Ca binding site number 1 of Crystal Structure of Dhfr in 0% Isopropanol within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Ca202

b:20.1
occ:1.00
O B:SER135 2.3 21.8 1.0
O B:HOH312 2.5 16.4 1.0
O B:HOH319 3.1 35.0 1.0
C B:SER135 3.5 20.0 1.0
CA B:VAL136 4.3 15.4 1.0
N B:VAL136 4.4 17.9 1.0
CB B:SER135 4.4 20.3 1.0
CA B:SER135 4.4 17.0 1.0
OG B:SER135 4.6 22.7 1.0
N B:SER135 4.7 16.7 1.0
OE2 B:GLU134 4.7 24.5 1.0
CG B:GLU134 4.8 20.9 1.0
CL B:CL204 4.8 32.0 1.0
C B:VAL136 5.0 23.9 1.0

Reference:

M.R.Duff Jr., J.M.Borreguero, M.J.Cuneo, A.Ramanathan, J.He, G.Kamath, S.C.Chennubhotla, F.Meilleur, E.E.Howell, K.W.Herwig, D.A.A.Myles, P.K.Agarwal. Modulating Enzyme Activity By Altering Protein Dynamics with Solvent. Biochemistry V. 57 4263 2018.
ISSN: ISSN 1520-4995
PubMed: 29901984
DOI: 10.1021/ACS.BIOCHEM.8B00424
Page generated: Sat Dec 12 05:23:10 2020

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