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Magnesium in PDB 1swv: Crystal Structure of the D12A Mutant of Phosphonoacetaldehyde Hydrolase Complexed with Magnesium

Enzymatic activity of Crystal Structure of the D12A Mutant of Phosphonoacetaldehyde Hydrolase Complexed with Magnesium

All present enzymatic activity of Crystal Structure of the D12A Mutant of Phosphonoacetaldehyde Hydrolase Complexed with Magnesium:
3.11.1.1;

Protein crystallography data

The structure of Crystal Structure of the D12A Mutant of Phosphonoacetaldehyde Hydrolase Complexed with Magnesium, PDB code: 1swv was solved by G.Zhang, M.C.Morais, J.Dai, W.Zhang, D.Dunaway-Mariano, K.N.Allen, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 61.08 / 2.30
Space group P 1 21 1
Cell size a, b, c (Å), α, β, γ (°) 64.503, 62.553, 73.759, 90.00, 108.76, 90.00
R / Rfree (%) 21.6 / 27.8

Magnesium Binding Sites:

The binding sites of Magnesium atom in the Crystal Structure of the D12A Mutant of Phosphonoacetaldehyde Hydrolase Complexed with Magnesium (pdb code 1swv). This binding sites where shown within 5.0 Angstroms radius around Magnesium atom.
In total 2 binding sites of Magnesium where determined in the Crystal Structure of the D12A Mutant of Phosphonoacetaldehyde Hydrolase Complexed with Magnesium, PDB code: 1swv:
Jump to Magnesium binding site number: 1; 2;

Magnesium binding site 1 out of 2 in 1swv

Go back to Magnesium Binding Sites List in 1swv
Magnesium binding site 1 out of 2 in the Crystal Structure of the D12A Mutant of Phosphonoacetaldehyde Hydrolase Complexed with Magnesium


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 1 of Crystal Structure of the D12A Mutant of Phosphonoacetaldehyde Hydrolase Complexed with Magnesium within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Mg501

b:19.6
occ:1.00
OD1 A:ASP186 2.7 14.5 1.0
OD2 A:ASP190 2.7 11.0 1.0
O A:HOH556 2.9 16.3 1.0
O A:ALA14 3.1 12.9 1.0
O A:HOH516 3.3 12.9 1.0
CB A:ALA12 3.4 9.9 1.0
CG A:ASP190 3.6 9.5 1.0
CG A:ASP186 3.6 15.8 1.0
OD1 A:ASP190 3.8 6.4 1.0
CG2 A:THR187 3.9 10.0 1.0
OD2 A:ASP186 4.0 14.0 1.0
NH1 A:ARG160 4.0 15.0 1.0
C A:ALA14 4.3 10.8 1.0
OG1 A:THR16 4.3 11.7 1.0
N A:ASP186 4.4 13.4 1.0
NH2 A:ARG160 4.4 14.6 1.0
CZ A:ARG160 4.4 15.5 1.0
OG1 A:THR187 4.5 13.0 1.0
N A:TRP13 4.5 10.9 1.0
CA A:ALA12 4.6 11.7 1.0
N A:ALA14 4.8 12.1 1.0
O A:HOH531 4.8 13.1 1.0
N A:THR187 4.8 14.8 1.0
CB A:THR187 4.8 13.7 1.0
CB A:ASP186 4.9 14.9 1.0
CA A:GLY50 4.9 13.8 1.0
C A:ALA12 4.9 10.9 1.0
C A:TRP13 5.0 10.7 1.0
CB A:ASP190 5.0 11.3 1.0
CA A:ALA14 5.0 11.6 1.0

Magnesium binding site 2 out of 2 in 1swv

Go back to Magnesium Binding Sites List in 1swv
Magnesium binding site 2 out of 2 in the Crystal Structure of the D12A Mutant of Phosphonoacetaldehyde Hydrolase Complexed with Magnesium


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 2 of Crystal Structure of the D12A Mutant of Phosphonoacetaldehyde Hydrolase Complexed with Magnesium within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Mg502

b:59.2
occ:1.00
O B:HOH560 2.5 29.9 1.0
OD2 B:ASP190 2.7 20.8 1.0
OD1 B:ASP186 2.8 24.7 1.0
O B:HOH602 2.8 23.5 1.0
O B:HOH511 3.1 23.0 1.0
O B:ALA14 3.1 30.3 1.0
CB B:ALA12 3.6 29.0 1.0
CG B:ASP190 3.6 20.4 1.0
CG2 B:THR187 3.7 22.8 1.0
CG B:ASP186 3.8 24.7 1.0
OD1 B:ASP190 3.8 22.2 1.0
NH1 B:ARG160 4.1 24.1 1.0
OD2 B:ASP186 4.1 25.6 1.0
C B:ALA14 4.3 28.4 1.0
OG1 B:THR187 4.4 23.4 1.0
CZ B:ARG160 4.5 21.6 1.0
NH2 B:ARG160 4.5 26.5 1.0
O B:HOH558 4.5 19.2 1.0
OG1 B:THR16 4.6 34.6 1.0
CB B:THR187 4.7 23.1 1.0
N B:TRP13 4.7 29.4 1.0
N B:ASP186 4.7 26.1 1.0
CA B:GLY50 4.8 23.1 1.0
CA B:ALA12 4.8 32.0 1.0
N B:THR187 4.8 24.8 1.0
N B:ALA14 4.9 27.7 1.0
CB B:ASP186 5.0 23.4 1.0

Reference:

G.Zhang, M.C.Morais, J.Dai, W.Zhang, D.Dunaway-Mariano, K.N.Allen. Investigation of Metal Ion Binding in Phosphonoacetaldehyde Hydrolase Identifies Sequence Markers For Metal-Activated Enzymes of the Had Enzyme Superfamily Biochemistry V. 43 4990 2004.
ISSN: ISSN 0006-2960
PubMed: 15109258
DOI: 10.1021/BI036309N
Page generated: Tue Aug 13 14:21:13 2024

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