Atomistry » Copper » PDB 1mg2-1oe1 » 1n19
Atomistry »
  Copper »
    PDB 1mg2-1oe1 »
      1n19 »

Copper in PDB 1n19: Structure of the Hsod A4V Mutant

Enzymatic activity of Structure of the Hsod A4V Mutant

All present enzymatic activity of Structure of the Hsod A4V Mutant:
1.15.1.1;

Protein crystallography data

The structure of Structure of the Hsod A4V Mutant, PDB code: 1n19 was solved by R.M.F.Cardoso, M.M.Thayer, M.Didonato, T.P.Lo, C.K.Bruns, E.D.Getzoff, J.A.Tainer, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 27.90 / 1.86
Space group C 1 2 1
Cell size a, b, c (Å), α, β, γ (°) 114.700, 47.900, 56.200, 90.00, 96.80, 90.00
R / Rfree (%) 20.7 / 26

Other elements in 1n19:

The structure of Structure of the Hsod A4V Mutant also contains other interesting chemical elements:

Zinc (Zn) 2 atoms

Copper Binding Sites:

The binding sites of Copper atom in the Structure of the Hsod A4V Mutant (pdb code 1n19). This binding sites where shown within 5.0 Angstroms radius around Copper atom.
In total 2 binding sites of Copper where determined in the Structure of the Hsod A4V Mutant, PDB code: 1n19:
Jump to Copper binding site number: 1; 2;

Copper binding site 1 out of 2 in 1n19

Go back to Copper Binding Sites List in 1n19
Copper binding site 1 out of 2 in the Structure of the Hsod A4V Mutant


Mono view


Stereo pair view

A full contact list of Copper with other atoms in the Cu binding site number 1 of Structure of the Hsod A4V Mutant within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cu154

b:38.2
occ:1.00
NE2 A:HIS120 2.0 28.4 1.0
NE2 A:HIS48 2.1 32.2 1.0
ND1 A:HIS46 2.1 36.8 1.0
CD2 A:HIS120 2.9 30.6 1.0
CD2 A:HIS48 3.0 31.1 1.0
CE1 A:HIS46 3.0 36.0 1.0
CE1 A:HIS120 3.1 31.8 1.0
CE1 A:HIS48 3.1 32.6 1.0
CG A:HIS46 3.1 34.9 1.0
NE2 A:HIS63 3.3 42.4 1.0
CB A:HIS46 3.5 33.7 1.0
CD2 A:HIS63 3.6 42.4 1.0
CB A:VAL118 4.0 32.1 1.0
CG A:HIS120 4.1 30.9 1.0
ND1 A:HIS120 4.1 33.0 1.0
NE2 A:HIS46 4.2 36.6 1.0
N A:HIS46 4.2 33.6 1.0
CG1 A:VAL118 4.2 30.9 1.0
CG A:HIS48 4.2 30.9 1.0
ND1 A:HIS48 4.2 30.9 1.0
CD2 A:HIS46 4.2 34.1 1.0
CE1 A:HIS63 4.3 43.7 1.0
CA A:HIS46 4.3 32.7 1.0
O A:HOH158 4.4 40.2 1.0
O A:HIS46 4.6 30.0 1.0
O A:VAL118 4.6 34.8 1.0
C A:HIS46 4.6 32.5 1.0
CG A:HIS63 4.7 40.9 1.0
CG2 A:VAL118 4.8 32.8 1.0
C A:VAL118 5.0 31.9 1.0
ND1 A:HIS63 5.0 42.0 1.0

Copper binding site 2 out of 2 in 1n19

Go back to Copper Binding Sites List in 1n19
Copper binding site 2 out of 2 in the Structure of the Hsod A4V Mutant


Mono view


Stereo pair view

A full contact list of Copper with other atoms in the Cu binding site number 2 of Structure of the Hsod A4V Mutant within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Cu154

b:41.5
occ:1.00
ND1 B:HIS46 2.0 33.9 1.0
NE2 B:HIS48 2.1 29.1 1.0
NE2 B:HIS120 2.1 35.0 1.0
CE1 B:HIS46 2.7 36.3 1.0
CD2 B:HIS120 2.9 34.6 1.0
CD2 B:HIS48 3.0 30.0 1.0
CE1 B:HIS48 3.1 31.7 1.0
CE1 B:HIS120 3.2 38.2 1.0
CG B:HIS46 3.2 32.6 1.0
NE2 B:HIS63 3.4 31.9 1.0
CD2 B:HIS63 3.6 32.0 1.0
CB B:HIS46 3.7 29.6 1.0
O B:HOH340 3.8 40.1 1.0
NE2 B:HIS46 3.9 35.0 1.0
CB B:VAL118 4.0 31.2 1.0
CG B:HIS120 4.1 36.3 1.0
CD2 B:HIS46 4.2 33.7 1.0
CG B:HIS48 4.2 30.1 1.0
CG1 B:VAL118 4.2 31.2 1.0
ND1 B:HIS48 4.2 30.3 1.0
N B:HIS46 4.2 30.3 1.0
ND1 B:HIS120 4.2 37.1 1.0
CE1 B:HIS63 4.4 31.0 1.0
CA B:HIS46 4.4 29.1 1.0
O B:HIS46 4.5 26.9 1.0
O B:VAL118 4.5 33.3 1.0
C B:HIS46 4.7 29.1 1.0
CG B:HIS63 4.7 29.6 1.0
CG2 B:VAL118 4.8 30.1 1.0
C B:VAL118 4.9 33.2 1.0

Reference:

R.M.F.Cardoso, M.M.Thayer, M.Didonato, T.P.Lo, C.K.Bruns, E.D.Getzoff, J.A.Tainer. Insights Into Lou Gehrig'S Disease From the Structure and Instability of the A4V Mutant of Human Cu,Zn Superoxide Dismutase. J.Mol.Biol. V. 324 247 2002.
ISSN: ISSN 0022-2836
PubMed: 12441104
DOI: 10.1016/S0022-2836(02)01090-2
Page generated: Tue Jul 30 22:22:28 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