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Manganese in PDB 1i19: Crystal Structure of Cholesterol Oxidase From B.Sterolicum

Enzymatic activity of Crystal Structure of Cholesterol Oxidase From B.Sterolicum

All present enzymatic activity of Crystal Structure of Cholesterol Oxidase From B.Sterolicum:
1.1.3.6;

Protein crystallography data

The structure of Crystal Structure of Cholesterol Oxidase From B.Sterolicum, PDB code: 1i19 was solved by R.Coulombe, K.Q.Yue, S.Ghisla, A.Vrielink, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 36.91 / 1.70
Space group P 1 21 1
Cell size a, b, c (Å), α, β, γ (°) 77.440, 124.470, 80.840, 90.00, 109.17, 90.00
R / Rfree (%) 18.2 / 20.1

Other elements in 1i19:

The structure of Crystal Structure of Cholesterol Oxidase From B.Sterolicum also contains other interesting chemical elements:

Arsenic (As) 1 atom

Manganese Binding Sites:

The binding sites of Manganese atom in the Crystal Structure of Cholesterol Oxidase From B.Sterolicum (pdb code 1i19). This binding sites where shown within 5.0 Angstroms radius around Manganese atom.
In total 3 binding sites of Manganese where determined in the Crystal Structure of Cholesterol Oxidase From B.Sterolicum, PDB code: 1i19:
Jump to Manganese binding site number: 1; 2; 3;

Manganese binding site 1 out of 3 in 1i19

Go back to Manganese Binding Sites List in 1i19
Manganese binding site 1 out of 3 in the Crystal Structure of Cholesterol Oxidase From B.Sterolicum


Mono view


Stereo pair view

A full contact list of Manganese with other atoms in the Mn binding site number 1 of Crystal Structure of Cholesterol Oxidase From B.Sterolicum within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Mn702

b:20.0
occ:1.00
OD1 B:ASN542 2.2 16.7 1.0
O1 B:CAC703 2.3 22.1 1.0
O B:HOH1863 2.3 18.3 1.0
OE2 B:GLU579 2.3 17.9 1.0
O B:HOH1872 2.4 24.2 1.0
O B:HOH1862 2.5 26.9 1.0
CD B:GLU579 3.2 18.1 1.0
CG B:ASN542 3.3 16.1 1.0
OE1 B:GLU579 3.5 18.2 1.0
AS B:CAC703 3.5 22.6 1.0
C2 B:CAC703 3.8 22.4 1.0
ND2 B:ASN542 4.0 16.5 1.0
O B:HOH1425 4.1 22.8 1.0
O B:HOH1408 4.2 26.3 1.0
O B:HOH1475 4.2 22.1 1.0
O B:HOH1180 4.2 18.8 1.0
O2 B:CAC703 4.4 21.7 1.0
CB B:ASN542 4.4 15.9 1.0
OG1 B:THR547 4.6 16.6 1.0
CG B:GLU579 4.6 18.0 1.0
CA B:ASN542 4.6 15.8 1.0
C B:ASN542 4.9 16.2 1.0
C1 B:CAC703 5.0 22.2 1.0

Manganese binding site 2 out of 3 in 1i19

Go back to Manganese Binding Sites List in 1i19
Manganese binding site 2 out of 3 in the Crystal Structure of Cholesterol Oxidase From B.Sterolicum


Mono view


Stereo pair view

A full contact list of Manganese with other atoms in the Mn binding site number 2 of Crystal Structure of Cholesterol Oxidase From B.Sterolicum within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Mn704

b:42.1
occ:1.00
O B:HOH1925 2.4 34.0 1.0
O B:HOH1875 2.4 27.4 1.0
O B:HOH1480 2.5 27.1 1.0
O B:HOH1924 2.5 34.3 1.0
O B:HOH1898 2.5 35.7 1.0
O B:HOH1322 4.1 25.3 1.0
O B:HOH1912 4.2 36.8 1.0
OD1 B:ASP111 4.3 24.7 1.0
ND1 B:HIS600 4.5 19.4 1.0
O B:HIS600 4.8 17.7 1.0
CB B:HIS600 4.9 18.4 1.0
CA B:HIS600 5.0 17.7 1.0
O B:HOH1967 5.0 42.6 1.0

Manganese binding site 3 out of 3 in 1i19

Go back to Manganese Binding Sites List in 1i19
Manganese binding site 3 out of 3 in the Crystal Structure of Cholesterol Oxidase From B.Sterolicum


Mono view


Stereo pair view

A full contact list of Manganese with other atoms in the Mn binding site number 3 of Crystal Structure of Cholesterol Oxidase From B.Sterolicum within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Mn705

b:41.0
occ:1.00
OD1 B:ASP545 2.2 21.0 1.0
O B:HOH1986 2.4 45.5 1.0
O B:HOH1985 2.5 48.6 1.0
O B:HOH1984 2.6 45.2 1.0
CG B:ASP545 3.2 20.1 1.0
OD2 B:ASP545 3.6 21.0 1.0
OD2 B:ASP544 3.9 24.6 1.0
CB B:ASP544 4.2 21.2 1.0
C B:ASP544 4.4 19.1 1.0
CB B:ASP545 4.4 19.2 1.0
O B:ASP544 4.5 19.1 1.0
N B:ASP545 4.5 18.5 1.0
CA B:ASP545 4.6 18.3 1.0
CG B:ASP544 4.6 22.8 1.0
O B:HOH1391 4.6 22.8 1.0
O B:HOH1781 4.7 36.7 1.0
CA B:ASP544 5.0 19.5 1.0

Reference:

R.Coulombe, K.Q.Yue, S.Ghisla, A.Vrielink. Oxygen Access to the Active Site of Cholesterol Oxidase Through A Narrow Channel Is Gated By An Arg-Glu Pair. J.Biol.Chem. V. 276 30435 2001.
ISSN: ISSN 0021-9258
PubMed: 11397813
DOI: 10.1074/JBC.M104103200
Page generated: Sat Oct 5 10:58:22 2024

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