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Manganese in PDB 5bkd: Crystal Structure of Aad-1 in Complex with (R)-Cyhalofop, Mn(II), and 2-Oxoglutarate

Enzymatic activity of Crystal Structure of Aad-1 in Complex with (R)-Cyhalofop, Mn(II), and 2-Oxoglutarate

All present enzymatic activity of Crystal Structure of Aad-1 in Complex with (R)-Cyhalofop, Mn(II), and 2-Oxoglutarate:
1.14.11.44;

Protein crystallography data

The structure of Crystal Structure of Aad-1 in Complex with (R)-Cyhalofop, Mn(II), and 2-Oxoglutarate, PDB code: 5bkd was solved by J.R.Chekan, S.K.Nair, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 56.74 / 1.90
Space group P 21 21 2
Cell size a, b, c (Å), α, β, γ (°) 85.531, 97.421, 69.804, 90.00, 90.00, 90.00
R / Rfree (%) 17.5 / 21.8

Other elements in 5bkd:

The structure of Crystal Structure of Aad-1 in Complex with (R)-Cyhalofop, Mn(II), and 2-Oxoglutarate also contains other interesting chemical elements:

Fluorine (F) 2 atoms

Manganese Binding Sites:

The binding sites of Manganese atom in the Crystal Structure of Aad-1 in Complex with (R)-Cyhalofop, Mn(II), and 2-Oxoglutarate (pdb code 5bkd). This binding sites where shown within 5.0 Angstroms radius around Manganese atom.
In total 2 binding sites of Manganese where determined in the Crystal Structure of Aad-1 in Complex with (R)-Cyhalofop, Mn(II), and 2-Oxoglutarate, PDB code: 5bkd:
Jump to Manganese binding site number: 1; 2;

Manganese binding site 1 out of 2 in 5bkd

Go back to Manganese Binding Sites List in 5bkd
Manganese binding site 1 out of 2 in the Crystal Structure of Aad-1 in Complex with (R)-Cyhalofop, Mn(II), and 2-Oxoglutarate


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 Aad-1 in Complex with (R)-Cyhalofop, Mn(II), and 2-Oxoglutarate within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Mn501

b:14.5
occ:1.00
O1 A:AKG502 2.1 17.2 1.0
OD1 A:ASP113 2.1 11.3 1.0
NE2 A:HIS270 2.2 14.2 1.0
NE2 A:HIS111 2.2 16.7 1.0
O5 A:AKG502 2.4 12.7 1.0
C1 A:AKG502 2.9 15.2 1.0
C2 A:AKG502 3.0 17.0 1.0
CE1 A:HIS111 3.1 14.2 1.0
CE1 A:HIS270 3.1 14.7 1.0
CD2 A:HIS270 3.2 12.8 1.0
CD2 A:HIS111 3.2 13.1 1.0
CG A:ASP113 3.2 14.7 1.0
OD2 A:ASP113 3.6 15.1 1.0
O2 A:AKG502 4.1 20.0 1.0
ND1 A:HIS111 4.2 13.1 1.0
ND1 A:HIS270 4.2 11.4 1.0
C18 A:RCF503 4.2 22.3 1.0
CG A:HIS111 4.3 15.2 1.0
CG A:HIS270 4.3 15.7 1.0
NH1 A:ARG285 4.4 13.6 1.0
CZ2 A:TRP263 4.4 14.6 1.0
C15 A:RCF503 4.4 19.5 1.0
CB A:ASP113 4.5 12.7 1.0
C3 A:AKG502 4.5 11.6 1.0
C19 A:RCF503 4.7 22.4 1.0
CA A:ASP113 4.7 13.4 1.0
CH2 A:TRP263 4.7 13.0 1.0
N A:ASP113 4.8 14.6 1.0
C22 A:RCF503 4.9 25.0 1.0
O21 A:RCF503 4.9 22.1 1.0
C16 A:RCF503 4.9 20.6 1.0

Manganese binding site 2 out of 2 in 5bkd

Go back to Manganese Binding Sites List in 5bkd
Manganese binding site 2 out of 2 in the Crystal Structure of Aad-1 in Complex with (R)-Cyhalofop, Mn(II), and 2-Oxoglutarate


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 Aad-1 in Complex with (R)-Cyhalofop, Mn(II), and 2-Oxoglutarate within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Mn501

b:18.5
occ:1.00
NE2 B:HIS270 2.1 16.1 1.0
O2 B:AKG502 2.1 18.9 1.0
NE2 B:HIS111 2.2 15.7 1.0
OD1 B:ASP113 2.2 17.1 1.0
O5 B:AKG502 2.4 16.7 1.0
C1 B:AKG502 3.0 23.5 1.0
CE1 B:HIS270 3.0 13.8 1.0
CE1 B:HIS111 3.0 19.5 1.0
C2 B:AKG502 3.1 20.1 1.0
CD2 B:HIS270 3.1 14.9 1.0
CD2 B:HIS111 3.2 20.1 1.0
CG B:ASP113 3.2 20.6 1.0
OD2 B:ASP113 3.6 19.9 1.0
C18 B:RCF503 4.0 36.6 1.0
ND1 B:HIS270 4.2 17.2 1.0
O1 B:AKG502 4.2 21.9 1.0
ND1 B:HIS111 4.2 15.6 1.0
CG B:HIS270 4.2 11.4 1.0
CG B:HIS111 4.3 18.1 1.0
NH1 B:ARG285 4.4 13.8 1.0
C15 B:RCF503 4.4 35.0 1.0
C22 B:RCF503 4.4 27.8 1.0
CZ2 B:TRP263 4.5 14.9 1.0
C3 B:AKG502 4.6 21.0 1.0
CB B:ASP113 4.6 15.3 1.0
C19 B:RCF503 4.6 35.4 1.0
CH2 B:TRP263 4.8 17.3 1.0
CA B:ASP113 4.8 21.7 1.0
C16 B:RCF503 4.9 33.4 1.0
N B:ASP113 4.9 15.3 1.0
C14 B:RCF503 4.9 35.6 1.0

Reference:

J.R.Chekan, C.Ongpipattanakul, T.R.Wright, B.Zhang, J.M.Bollinger Jr., L.J.Rajakovich, C.Krebs, R.M.Cicchillo, S.K.Nair. Molecular Basis For Enantioselective Herbicide Degradation Imparted By Aryloxyalkanoate Dioxygenases in Transgenic Plants. Proc.Natl.Acad.Sci.Usa V. 116 13299 2019.
ISSN: ESSN 1091-6490
PubMed: 31209034
DOI: 10.1073/PNAS.1900711116
Page generated: Sat Oct 5 23:37:53 2024

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