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Magnesium in PDB 6fbo: Human Methionine Adenosyltransferase II Mutant (S114A) in I222 Crystal Form

Enzymatic activity of Human Methionine Adenosyltransferase II Mutant (S114A) in I222 Crystal Form

All present enzymatic activity of Human Methionine Adenosyltransferase II Mutant (S114A) in I222 Crystal Form:
2.5.1.6;

Protein crystallography data

The structure of Human Methionine Adenosyltransferase II Mutant (S114A) in I222 Crystal Form, PDB code: 6fbo was solved by J.Panmanee, S.V.Antonyuk, S.S.Hasnain, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 58.28 / 1.80
Space group I 2 2 2
Cell size a, b, c (Å), α, β, γ (°) 66.621, 94.682, 116.550, 90.00, 90.00, 90.00
R / Rfree (%) 15.1 / 17.4

Other elements in 6fbo:

The structure of Human Methionine Adenosyltransferase II Mutant (S114A) in I222 Crystal Form also contains other interesting chemical elements:

Potassium (K) 2 atoms

Magnesium Binding Sites:

The binding sites of Magnesium atom in the Human Methionine Adenosyltransferase II Mutant (S114A) in I222 Crystal Form (pdb code 6fbo). This binding sites where shown within 5.0 Angstroms radius around Magnesium atom.
In total 2 binding sites of Magnesium where determined in the Human Methionine Adenosyltransferase II Mutant (S114A) in I222 Crystal Form, PDB code: 6fbo:
Jump to Magnesium binding site number: 1; 2;

Magnesium binding site 1 out of 2 in 6fbo

Go back to Magnesium Binding Sites List in 6fbo
Magnesium binding site 1 out of 2 in the Human Methionine Adenosyltransferase II Mutant (S114A) in I222 Crystal Form


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 1 of Human Methionine Adenosyltransferase II Mutant (S114A) in I222 Crystal Form within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Mg402

b:13.7
occ:1.00
O1A A:PPK401 2.0 14.9 1.0
O2G A:PPK401 2.0 17.3 1.0
O1B A:PPK401 2.1 16.6 1.0
OD2 A:ASP31 2.1 12.8 1.0
O A:HOH513 2.2 13.6 1.0
O A:HOH504 2.2 15.2 1.0
CG A:ASP31 3.0 13.6 1.0
PB A:PPK401 3.1 19.9 1.0
OD1 A:ASP31 3.2 13.4 1.0
PG A:PPK401 3.3 18.0 1.0
PA A:PPK401 3.3 15.2 1.0
NZ A:LYS265 3.5 15.8 1.0
O3A A:PPK401 3.5 17.5 1.0
N3B A:PPK401 3.6 16.7 1.0
K A:K404 3.7 10.4 0.5
NH2 A:ARG264 4.1 18.0 1.0
OD2 A:ASP258 4.1 21.6 0.8
O3G A:PPK401 4.1 17.6 1.0
CE1 A:HIS29 4.1 13.0 1.0
O4A A:PPK401 4.2 14.2 1.0
O A:ALA259 4.3 18.1 1.0
O2A A:PPK401 4.3 16.0 1.0
CB A:ASP31 4.3 12.5 1.0
O1G A:PPK401 4.4 18.3 1.0
O2B A:PPK401 4.4 22.2 1.0
NE A:ARG264 4.5 16.9 1.0
CB A:ARG264 4.6 14.4 1.0
CZ A:ARG264 4.6 16.9 1.0
CE A:LYS265 4.6 14.9 1.0
NE2 A:HIS29 4.7 13.1 1.0
O A:ARG264 4.8 13.3 1.0
CG A:ASP258 5.0 21.9 0.8
OD1 A:ASP258 5.0 20.9 0.8

Magnesium binding site 2 out of 2 in 6fbo

Go back to Magnesium Binding Sites List in 6fbo
Magnesium binding site 2 out of 2 in the Human Methionine Adenosyltransferase II Mutant (S114A) in I222 Crystal Form


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 2 of Human Methionine Adenosyltransferase II Mutant (S114A) in I222 Crystal Form within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Mg403

b:19.0
occ:1.00
O4A A:PPK401 2.1 14.2 1.0
O3G A:PPK401 2.1 17.6 1.0
O A:HOH548 2.2 13.9 0.8
O A:HOH561 2.3 18.2 1.0
PA A:PPK401 3.4 15.2 1.0
PG A:PPK401 3.4 18.0 1.0
N3B A:PPK401 3.5 16.7 1.0
O3A A:PPK401 3.8 17.5 1.0
NZ A:LYS265 3.8 15.8 1.0
OE2 A:GLU23 4.0 17.0 1.0
O1A A:PPK401 4.1 14.9 1.0
NZ A:LYS181 4.1 17.2 1.0
O A:HOH577 4.2 14.0 1.0
O2G A:PPK401 4.4 17.3 1.0
PB A:PPK401 4.4 19.9 1.0
CE A:LYS265 4.4 14.9 1.0
O1G A:PPK401 4.4 18.3 1.0
O2A A:PPK401 4.4 16.0 1.0
OE1 A:GLU23 4.5 19.2 1.0
CD A:GLU23 4.7 18.8 1.0

Reference:

J.Panmanee, J.Bradley-Clarke, J.M.Mato, P.M.O'neill, S.V.Antonyuk, S.S.Hasnain. Control and Regulation of S-Adenosylmethionine Biosynthesis By the Regulatory Beta Subunit and Quinolone-Based Compounds. Febs J. V. 286 2135 2019.
ISSN: ISSN 1742-464X
PubMed: 30776190
DOI: 10.1111/FEBS.14790
Page generated: Tue Oct 1 00:19:01 2024

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