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Magnesium in PDB 1z88: Crystal Structure of LYS154ARG Mutant of Mature Apha of S. Typhimurium

Enzymatic activity of Crystal Structure of LYS154ARG Mutant of Mature Apha of S. Typhimurium

All present enzymatic activity of Crystal Structure of LYS154ARG Mutant of Mature Apha of S. Typhimurium:
3.1.3.2;

Protein crystallography data

The structure of Crystal Structure of LYS154ARG Mutant of Mature Apha of S. Typhimurium, PDB code: 1z88 was solved by R.D.Makde, G.D.Gupta, V.Kumar, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 20.00 / 2.10
Space group P 21 21 21
Cell size a, b, c (Å), α, β, γ (°) 70.650, 84.210, 149.410, 90.00, 90.00, 90.00
R / Rfree (%) 16.7 / 20.7

Magnesium Binding Sites:

The binding sites of Magnesium atom in the Crystal Structure of LYS154ARG Mutant of Mature Apha of S. Typhimurium (pdb code 1z88). This binding sites where shown within 5.0 Angstroms radius around Magnesium atom.
In total 4 binding sites of Magnesium where determined in the Crystal Structure of LYS154ARG Mutant of Mature Apha of S. Typhimurium, PDB code: 1z88:
Jump to Magnesium binding site number: 1; 2; 3; 4;

Magnesium binding site 1 out of 4 in 1z88

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Magnesium binding site 1 out of 4 in the Crystal Structure of LYS154ARG Mutant of Mature Apha of S. Typhimurium


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 LYS154ARG Mutant of Mature Apha of S. Typhimurium within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Mg601

b:12.2
occ:1.00
O A:HOH603 1.9 13.2 1.0
O A:HOH698 2.1 10.1 1.0
OD2 A:ASP46 2.1 20.0 1.0
O A:ASP48 2.1 12.0 1.0
OD1 A:ASP169 2.1 15.7 1.0
O A:HOH604 2.2 17.5 1.0
CG A:ASP46 3.0 20.6 1.0
CG A:ASP169 3.1 15.1 1.0
C A:ASP48 3.3 14.7 1.0
OD1 A:ASP46 3.4 17.4 1.0
OD2 A:ASP169 3.4 18.2 1.0
OG A:SER170 3.8 16.9 1.0
OD2 A:ASP173 4.0 17.6 1.0
CA A:ASP48 4.1 14.2 1.0
OG1 A:THR50 4.1 14.8 1.0
O A:HOH702 4.1 37.3 1.0
O A:HOH602 4.2 21.4 1.0
N A:ASP48 4.2 15.2 1.0
CB A:ASP48 4.2 17.8 1.0
CB A:ASP46 4.4 19.7 1.0
N A:ASP49 4.4 15.3 1.0
O A:HOH655 4.4 25.4 1.0
CB A:ASP49 4.4 15.4 1.0
CB A:ASP169 4.5 13.7 1.0
N A:ASP169 4.6 15.5 1.0
O A:HOH609 4.7 22.8 1.0
N A:SER170 4.7 14.3 1.0
N A:THR50 4.7 14.9 1.0
CA A:ASP49 4.7 16.5 1.0
O A:HOH608 4.7 19.7 1.0
CB A:SER170 4.8 14.8 1.0
C A:ASP49 4.8 17.2 1.0
C A:ILE47 4.9 16.8 1.0
CB A:THR50 5.0 14.3 1.0

Magnesium binding site 2 out of 4 in 1z88

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Magnesium binding site 2 out of 4 in the Crystal Structure of LYS154ARG Mutant of Mature Apha of S. Typhimurium


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 LYS154ARG Mutant of Mature Apha of S. Typhimurium within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Mg602

b:18.5
occ:1.00
O B:ASP48 2.1 13.8 1.0
OD2 B:ASP46 2.1 20.8 1.0
O B:HOH609 2.1 16.7 1.0
O B:HOH690 2.2 15.0 1.0
O B:HOH689 2.2 21.2 1.0
OD1 B:ASP169 2.2 18.0 1.0
CG B:ASP46 3.0 20.7 1.0
CG B:ASP169 3.2 17.3 1.0
C B:ASP48 3.2 15.9 1.0
OD1 B:ASP46 3.4 23.5 1.0
OD2 B:ASP169 3.5 14.8 1.0
O B:HOH675 3.6 49.9 1.0
CA B:ASP48 3.9 16.4 1.0
OG1 B:THR50 4.0 17.1 1.0
OG B:SER170 4.0 19.6 1.0
CB B:ASP48 4.0 17.4 1.0
OD2 B:ASP173 4.1 23.5 1.0
N B:ASP48 4.1 13.6 1.0
O B:HOH612 4.2 18.2 1.0
O B:HOH608 4.3 33.5 1.0
N B:ASP49 4.3 16.0 1.0
CB B:ASP46 4.4 20.3 1.0
CB B:ASP49 4.4 16.3 1.0
CB B:ASP169 4.5 16.8 1.0
O B:HOH606 4.7 20.8 1.0
N B:ASP169 4.7 16.4 1.0
CA B:ASP49 4.7 17.9 1.0
N B:THR50 4.7 16.4 1.0
C B:ILE47 4.8 12.9 1.0
C B:ASP49 4.8 18.8 1.0
O B:HOH607 4.8 30.1 1.0
N B:SER170 4.9 18.3 1.0
CB B:THR50 4.9 15.9 1.0
CB B:SER170 4.9 18.5 1.0

Magnesium binding site 3 out of 4 in 1z88

Go back to Magnesium Binding Sites List in 1z88
Magnesium binding site 3 out of 4 in the Crystal Structure of LYS154ARG Mutant of Mature Apha of S. Typhimurium


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 3 of Crystal Structure of LYS154ARG Mutant of Mature Apha of S. Typhimurium within 5.0Å range:
probe atom residue distance (Å) B Occ
C:Mg604

b:16.1
occ:1.00
OD2 C:ASP46 1.9 18.9 1.0
O C:HOH683 2.1 11.2 1.0
O C:ASP48 2.1 12.4 1.0
O C:HOH611 2.1 13.6 1.0
OD1 C:ASP169 2.1 17.0 1.0
O C:HOH610 2.2 19.8 1.0
CG C:ASP46 3.0 22.5 1.0
CG C:ASP169 3.1 16.3 1.0
C C:ASP48 3.2 15.7 1.0
OD1 C:ASP46 3.4 21.5 1.0
OD2 C:ASP169 3.5 15.7 1.0
OG C:SER170 3.9 18.7 1.0
OG1 C:THR50 3.9 13.3 1.0
CA C:ASP48 4.0 16.3 1.0
O C:HOH695 4.0 50.6 1.0
O C:HOH609 4.1 19.5 1.0
OD2 C:ASP173 4.1 17.7 1.0
N C:ASP48 4.1 16.6 1.0
CB C:ASP48 4.2 18.2 1.0
CB C:ASP46 4.2 19.6 1.0
N C:ASP49 4.3 14.8 1.0
CB C:ASP49 4.4 14.4 1.0
CB C:ASP169 4.5 15.1 1.0
O C:HOH612 4.5 28.2 1.0
N C:THR50 4.6 15.2 1.0
N C:ASP169 4.6 17.1 1.0
O C:HOH616 4.7 23.1 1.0
CA C:ASP49 4.7 15.0 1.0
C C:ASP49 4.7 14.8 1.0
O C:HOH613 4.8 33.0 1.0
CB C:THR50 4.8 16.4 1.0
C C:ILE47 4.8 18.9 1.0
N C:SER170 4.9 16.5 1.0
CB C:SER170 4.9 17.7 1.0

Magnesium binding site 4 out of 4 in 1z88

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Magnesium binding site 4 out of 4 in the Crystal Structure of LYS154ARG Mutant of Mature Apha of S. Typhimurium


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 4 of Crystal Structure of LYS154ARG Mutant of Mature Apha of S. Typhimurium within 5.0Å range:
probe atom residue distance (Å) B Occ
D:Mg603

b:16.7
occ:1.00
O D:ASP48 2.1 14.8 1.0
O D:HOH613 2.1 9.9 1.0
O D:HOH714 2.1 11.5 1.0
OD1 D:ASP169 2.2 16.5 1.0
O D:HOH713 2.2 17.3 1.0
OD2 D:ASP46 2.2 15.1 1.0
CG D:ASP169 3.1 15.3 1.0
CG D:ASP46 3.1 14.3 1.0
C D:ASP48 3.2 15.0 1.0
OD2 D:ASP169 3.4 18.0 1.0
OD1 D:ASP46 3.5 15.8 1.0
O D:HOH715 3.7 34.3 1.0
OG D:SER170 3.9 17.5 1.0
CA D:ASP48 4.0 15.1 1.0
OG1 D:THR50 4.0 14.5 1.0
CB D:ASP48 4.1 16.6 1.0
OD2 D:ASP173 4.2 18.9 1.0
O D:HOH612 4.2 20.9 1.0
N D:ASP48 4.2 13.6 1.0
N D:ASP49 4.3 13.2 1.0
CB D:ASP49 4.4 12.7 1.0
O D:HOH693 4.4 39.4 1.0
CB D:ASP46 4.5 15.3 1.0
CB D:ASP169 4.5 15.7 1.0
O D:HOH614 4.6 17.2 1.0
O D:HOH672 4.6 36.1 1.0
N D:ASP169 4.7 13.4 1.0
CA D:ASP49 4.7 14.3 1.0
N D:THR50 4.7 12.9 1.0
C D:ASP49 4.8 15.0 1.0
N D:SER170 4.8 13.5 1.0
C D:ILE47 4.9 12.8 1.0
CB D:SER170 4.9 15.3 1.0
CB D:THR50 5.0 14.6 1.0

Reference:

R.D.Makde, G.D.Gupta, S.K.Mahajan, V.Kumar. Structural and Mutational Analyses Reveal the Functional Role of Active-Site Lys-154 and Asp-173 of Salmonella Typhimurium Apha Protein. Arch.Biochem.Biophys. V. 464 70 2007.
ISSN: ISSN 0003-9861
PubMed: 17570338
DOI: 10.1016/J.ABB.2007.03.043
Page generated: Mon Dec 14 07:11:33 2020

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