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Zinc in PDB 8b26: Dihydroprecondylocarpine Acetate Synthase 2 From Tabernanthe Iboga

Protein crystallography data

The structure of Dihydroprecondylocarpine Acetate Synthase 2 From Tabernanthe Iboga, PDB code: 8b26 was solved by C.Langley, J.Basquin, L.Caputi, S.E.O'connor, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 41.64 / 2.42
Space group P 21 21 21
Cell size a, b, c (Å), α, β, γ (°) 74.422, 78.124, 131.207, 90, 90, 90
R / Rfree (%) 21.4 / 25.8

Zinc Binding Sites:

The binding sites of Zinc atom in the Dihydroprecondylocarpine Acetate Synthase 2 From Tabernanthe Iboga (pdb code 8b26). This binding sites where shown within 5.0 Angstroms radius around Zinc atom.
In total 2 binding sites of Zinc where determined in the Dihydroprecondylocarpine Acetate Synthase 2 From Tabernanthe Iboga, PDB code: 8b26:
Jump to Zinc binding site number: 1; 2;

Zinc binding site 1 out of 2 in 8b26

Go back to Zinc Binding Sites List in 8b26
Zinc binding site 1 out of 2 in the Dihydroprecondylocarpine Acetate Synthase 2 From Tabernanthe Iboga


Mono view


Stereo pair view

A full contact list of Zinc with other atoms in the Zn binding site number 1 of Dihydroprecondylocarpine Acetate Synthase 2 From Tabernanthe Iboga within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Zn401

b:66.9
occ:0.85
SG A:CYS108 2.3 73.4 1.0
SG A:CYS111 2.3 66.8 1.0
SG A:CYS119 2.3 73.3 1.0
SG A:CYS105 2.3 69.5 1.0
CB A:CYS119 3.2 64.3 1.0
CB A:CYS108 3.4 71.7 1.0
CB A:CYS105 3.5 65.3 1.0
CB A:CYS111 3.6 72.3 1.0
N A:GLY106 3.7 69.7 1.0
N A:CYS108 3.7 73.3 1.0
N A:CYS105 3.9 70.9 1.0
CA A:CYS105 4.1 70.8 1.0
CA A:CYS108 4.1 67.3 1.0
CA A:CYS119 4.1 70.4 1.0
N A:LYS107 4.3 79.9 1.0
C A:CYS105 4.3 67.5 1.0
N A:CYS111 4.3 74.4 1.0
CD A:PRO120 4.4 71.7 1.0
CB A:THR104 4.5 65.1 1.0
CA A:CYS111 4.5 75.5 1.0
CA A:GLY106 4.6 64.7 1.0
C A:CYS108 4.8 69.8 1.0
C A:THR104 4.8 68.4 1.0
N A:PRO120 4.9 63.1 1.0
C A:LYS107 4.9 80.7 1.0
C A:CYS119 4.9 69.8 1.0
C A:GLY106 4.9 77.1 1.0
O A:CYS108 4.9 74.7 1.0

Zinc binding site 2 out of 2 in 8b26

Go back to Zinc Binding Sites List in 8b26
Zinc binding site 2 out of 2 in the Dihydroprecondylocarpine Acetate Synthase 2 From Tabernanthe Iboga


Mono view


Stereo pair view

A full contact list of Zinc with other atoms in the Zn binding site number 2 of Dihydroprecondylocarpine Acetate Synthase 2 From Tabernanthe Iboga within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Zn401

b:64.8
occ:0.73
SG B:CYS111 2.3 70.6 1.0
SG B:CYS108 2.3 77.1 1.0
SG B:CYS119 2.3 74.0 1.0
SG B:CYS105 2.3 71.3 1.0
O B:HOH511 2.4 69.6 1.0
CB B:CYS119 3.2 64.2 1.0
CB B:CYS108 3.4 72.6 1.0
CB B:CYS105 3.5 71.6 1.0
CB B:CYS111 3.5 77.8 1.0
N B:GLY106 3.9 71.6 1.0
N B:CYS105 3.9 74.8 1.0
N B:CYS108 3.9 79.4 1.0
CA B:CYS119 4.0 68.0 1.0
CA B:CYS105 4.1 70.8 1.0
CA B:CYS108 4.2 77.4 1.0
CD B:PRO120 4.2 73.8 1.0
N B:CYS111 4.2 77.5 1.0
CA B:CYS111 4.4 80.1 1.0
C B:CYS105 4.4 70.9 1.0
N B:LYS107 4.6 82.8 1.0
CB B:THR104 4.6 68.6 1.0
N B:PRO120 4.7 77.5 1.0
C B:CYS119 4.7 71.4 1.0
C B:CYS108 4.8 74.7 1.0
CA B:GLY106 4.8 75.6 1.0
C B:THR104 4.9 71.3 1.0
O B:CYS108 5.0 71.1 1.0

Reference:

C.Langley, E.Tatsis, B.Hong, Y.Nakamura, C.Paetz, C.E.M.Stevenson, J.Basquin, D.M.Lawson, L.Caputi, S.E.O'connor. Expansion of the Catalytic Repertoire of Alcohol Dehydrogenases in Plant Metabolism. Angew.Chem.Int.Ed.Engl. V. 61 10934 2022.
ISSN: ESSN 1521-3773
PubMed: 36198083
DOI: 10.1002/ANIE.202210934
Page generated: Wed Oct 30 18:07:14 2024

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