Magnesium in PDB 7mjv: Miab in the Complex with S-Adenosylmethionine and Rna

Enzymatic activity of Miab in the Complex with S-Adenosylmethionine and Rna

All present enzymatic activity of Miab in the Complex with S-Adenosylmethionine and Rna:
2.8.4.3;

Protein crystallography data

The structure of Miab in the Complex with S-Adenosylmethionine and Rna, PDB code: 7mjv was solved by O.A.Esakova, T.L.Grove, N.H.Yennawar, A.J.Arcinas, B.Wang, C.Krebs, S.C.Almo, S.J.Booker, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 45.51 / 2.24
Space group P 21 21 21
Cell size a, b, c (Å), α, β, γ (°) 54.155, 81.442, 109.751, 90, 90, 90
R / Rfree (%) 24.3 / 27.3

Other elements in 7mjv:

The structure of Miab in the Complex with S-Adenosylmethionine and Rna also contains other interesting chemical elements:

Iron (Fe) 7 atoms

Magnesium Binding Sites:

The binding sites of Magnesium atom in the Miab in the Complex with S-Adenosylmethionine and Rna (pdb code 7mjv). This binding sites where shown within 5.0 Angstroms radius around Magnesium atom.
In total 2 binding sites of Magnesium where determined in the Miab in the Complex with S-Adenosylmethionine and Rna, PDB code: 7mjv:
Jump to Magnesium binding site number: 1; 2;

Magnesium binding site 1 out of 2 in 7mjv

Go back to Magnesium Binding Sites List in 7mjv
Magnesium binding site 1 out of 2 in the Miab in the Complex with S-Adenosylmethionine and Rna


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 1 of Miab in the Complex with S-Adenosylmethionine and Rna within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Mg504

b:41.0
occ:1.00
O A:ILE266 2.3 45.5 1.0
O A:VAL272 2.3 34.9 1.0
O A:HOH617 2.3 50.1 1.0
O A:MET269 2.3 43.5 1.0
C A:VAL272 3.4 34.8 1.0
C A:ILE266 3.4 39.8 1.0
C A:MET269 3.5 49.2 1.0
OE2 A:GLU420 3.6 65.4 1.0
N A:VAL272 3.9 36.6 1.0
CA A:PRO270 4.0 39.6 1.0
CA A:VAL272 4.0 35.4 1.0
C A:PRO270 4.1 39.3 1.0
CB A:VAL272 4.1 39.3 1.0
O A:PRO270 4.1 44.2 1.0
CA A:ILE266 4.1 39.4 1.0
N A:PRO270 4.2 43.4 1.0
CG2 A:ILE266 4.2 36.6 1.0
CG A:LYS274 4.2 48.0 1.0
CE A:LYS274 4.4 51.7 1.0
N A:MET269 4.5 55.6 1.0
N A:ALA267 4.5 41.9 1.0
CA A:MET269 4.5 42.1 1.0
N A:CYS273 4.5 35.4 1.0
C A:ALA267 4.6 49.8 1.0
O A:ALA267 4.7 48.9 1.0
N A:ASN271 4.7 42.5 1.0
CA A:ALA267 4.7 41.4 1.0
O A:VAL265 4.8 42.6 1.0
CG1 A:VAL272 4.8 34.6 1.0
C A:CYS273 4.8 40.8 1.0
CB A:ILE266 4.8 38.4 1.0
CA A:CYS273 4.8 42.6 1.0
N A:LYS274 4.8 41.9 1.0
CD A:GLU420 4.9 63.0 1.0
C A:ASN271 4.9 37.2 1.0
CD A:LYS274 5.0 52.1 1.0

Magnesium binding site 2 out of 2 in 7mjv

Go back to Magnesium Binding Sites List in 7mjv
Magnesium binding site 2 out of 2 in the Miab in the Complex with S-Adenosylmethionine and Rna


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 2 of Miab in the Complex with S-Adenosylmethionine and Rna within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Mg505

b:65.7
occ:1.00
O A:HOH603 2.4 46.0 1.0
N A:LYS351 2.9 42.7 1.0
O2' E:A38 3.3 51.4 1.0
O A:LYS351 3.6 43.3 1.0
CB A:LYS351 3.6 46.1 1.0
O3' E:A38 3.7 69.9 1.0
CA A:LYS351 3.8 48.2 1.0
CA A:PHE350 3.8 40.3 1.0
C A:PHE350 3.8 41.2 1.0
CB A:PHE350 3.8 39.7 1.0
CD A:ARG66 4.0 48.1 1.0
CG A:LYS351 4.0 50.7 1.0
C A:LYS351 4.1 47.5 1.0
CE A:LYS351 4.4 55.8 1.0
OP1 E:U39 4.4 64.6 1.0
CD1 A:PHE350 4.5 42.2 1.0
C2' E:A38 4.5 58.8 1.0
NE A:ARG66 4.6 52.8 1.0
C3' E:A38 4.6 65.0 1.0
CG A:PHE350 4.7 38.7 1.0
P E:U39 4.7 60.6 1.0
C4' E:A38 4.8 63.6 1.0
C5' E:U39 4.8 61.5 1.0
CD A:LYS351 4.9 51.5 1.0
OP1 E:A38 4.9 62.8 1.0

Reference:

O.A.Esakova, T.L.Grove, N.H.Yennawar, A.J.Arcinas, B.Wang, C.Krebs, S.C.Almo, S.J.Booker. Structural Basis For Trna Methylthiolation By the Radical Sam Enzyme Miab Nature 2021.
ISSN: ESSN 1476-4687
DOI: 10.1038/S41586-021-03904-6
Page generated: Fri Sep 24 15:26:01 2021

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