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Zinc in PDB 2e47: Crystal Structure Analysis of the Clock Protein EA4 (Glycosylation Form)

Protein crystallography data

The structure of Crystal Structure Analysis of the Clock Protein EA4 (Glycosylation Form), PDB code: 2e47 was solved by S.-Y.Park, T.Hiraki, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 20.00 / 2.11
Space group P 1 21 1
Cell size a, b, c (Å), α, β, γ (°) 47.098, 73.894, 47.446, 90.00, 104.07, 90.00
R / Rfree (%) 17 / 25.1

Other elements in 2e47:

The structure of Crystal Structure Analysis of the Clock Protein EA4 (Glycosylation Form) also contains other interesting chemical elements:

Copper (Cu) 2 atoms

Zinc Binding Sites:

The binding sites of Zinc atom in the Crystal Structure Analysis of the Clock Protein EA4 (Glycosylation Form) (pdb code 2e47). This binding sites where shown within 5.0 Angstroms radius around Zinc atom.
In total 2 binding sites of Zinc where determined in the Crystal Structure Analysis of the Clock Protein EA4 (Glycosylation Form), PDB code: 2e47:
Jump to Zinc binding site number: 1; 2;

Zinc binding site 1 out of 2 in 2e47

Go back to Zinc Binding Sites List in 2e47
Zinc binding site 1 out of 2 in the Crystal Structure Analysis of the Clock Protein EA4 (Glycosylation Form)


Mono view


Stereo pair view

A full contact list of Zinc with other atoms in the Zn binding site number 1 of Crystal Structure Analysis of the Clock Protein EA4 (Glycosylation Form) within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Zn172

b:24.3
occ:1.00
ND1 A:HIS67 2.0 16.8 1.0
ND1 A:HIS75 2.1 22.7 1.0
OD1 A:ASP87 2.1 20.1 1.0
ND1 A:HIS84 2.1 23.8 1.0
CE1 A:HIS84 2.9 25.5 1.0
CE1 A:HIS75 2.9 23.6 1.0
CG A:ASP87 3.0 23.6 1.0
CG A:HIS67 3.0 22.6 1.0
CE1 A:HIS67 3.1 24.6 1.0
CG A:HIS75 3.2 21.7 1.0
OD2 A:ASP87 3.2 22.5 1.0
CG A:HIS84 3.2 26.5 1.0
CB A:HIS67 3.3 23.2 1.0
CB A:HIS75 3.6 24.4 1.0
CB A:HIS84 3.7 22.4 1.0
O A:LYS140 3.8 31.0 1.0
CA A:HIS75 3.9 25.6 1.0
NE2 A:HIS84 4.1 28.0 1.0
NE2 A:HIS75 4.1 24.6 1.0
CD2 A:HIS67 4.2 20.9 1.0
NE2 A:HIS67 4.2 25.6 1.0
CD2 A:HIS84 4.2 26.0 1.0
CD2 A:HIS75 4.2 21.9 1.0
CB A:ASP87 4.4 20.3 1.0
O A:HOH1014 4.5 26.4 1.0
C A:LYS140 4.7 32.0 1.0
CA A:ASP87 4.8 21.9 1.0
N A:HIS84 4.8 22.7 1.0
CA A:HIS67 4.9 23.0 1.0
N A:HIS75 4.9 25.6 1.0
N A:GLY76 4.9 25.5 1.0
CA A:HIS84 4.9 22.6 1.0
C A:HIS75 4.9 25.7 1.0
CA A:THR141 5.0 29.5 1.0
N A:ASP87 5.0 21.4 1.0

Zinc binding site 2 out of 2 in 2e47

Go back to Zinc Binding Sites List in 2e47
Zinc binding site 2 out of 2 in the Crystal Structure Analysis of the Clock Protein EA4 (Glycosylation Form)


Mono view


Stereo pair view

A full contact list of Zinc with other atoms in the Zn binding site number 2 of Crystal Structure Analysis of the Clock Protein EA4 (Glycosylation Form) within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Zn172

b:25.8
occ:1.00
OD1 B:ASP87 2.1 23.2 1.0
ND1 B:HIS84 2.1 21.2 1.0
ND1 B:HIS75 2.1 20.8 1.0
ND1 B:HIS67 2.1 26.5 1.0
CE1 B:HIS75 2.8 24.3 1.0
CE1 B:HIS84 2.9 18.0 1.0
CG B:HIS67 3.0 25.6 1.0
CG B:ASP87 3.0 27.9 1.0
CG B:HIS84 3.2 21.9 1.0
CE1 B:HIS67 3.2 25.5 1.0
CB B:HIS67 3.2 22.9 1.0
CG B:HIS75 3.3 29.2 1.0
OD2 B:ASP87 3.4 28.0 1.0
CB B:HIS84 3.7 23.2 1.0
O B:LYS140 3.7 39.0 1.0
CB B:HIS75 3.8 30.0 1.0
NE2 B:HIS75 4.0 25.5 1.0
NE2 B:HIS84 4.1 21.4 1.0
CA B:HIS75 4.1 31.2 1.0
CD2 B:HIS67 4.2 25.9 1.0
CD2 B:HIS84 4.2 19.3 1.0
NE2 B:HIS67 4.2 30.4 1.0
CD2 B:HIS75 4.3 27.1 1.0
CB B:ASP87 4.4 25.3 1.0
C B:LYS140 4.8 39.6 1.0
CA B:HIS67 4.8 24.2 1.0
CA B:ASP87 4.8 26.1 1.0
N B:HIS84 4.8 24.6 1.0
CA B:HIS84 4.9 23.3 1.0
N B:GLY76 5.0 29.7 1.0

Reference:

T.Hiraki, N.Shibayama, J.R.M.Tame, S.Akashi, S.-Y.Park. The Clock Protein EA4 Ticks Away with Movement of A Mobile Copper Ion To Be Published.
Page generated: Wed Oct 16 22:58:44 2024

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