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: Sat Apr 8 07:44:23 2023

Last articles

Zn in 8WB0
Zn in 8WAX
Zn in 8WAU
Zn in 8WAZ
Zn in 8WAY
Zn in 8WAV
Zn in 8WAW
Zn in 8WAT
Zn in 8W7M
Zn in 8WD3
© Copyright 2008-2020 by atomistry.com
Home   |    Site Map   |    Copyright   |    Contact us   |    Privacy