Atomistry » Manganese » PDB 6zbn-7bm0 » 6zk6
Atomistry »
  Manganese »
    PDB 6zbn-7bm0 »
      6zk6 »

Manganese in PDB 6zk6: Protein Phosphatase 1 (PP1) T320E Mutant

Enzymatic activity of Protein Phosphatase 1 (PP1) T320E Mutant

All present enzymatic activity of Protein Phosphatase 1 (PP1) T320E Mutant:
3.1.3.16;

Protein crystallography data

The structure of Protein Phosphatase 1 (PP1) T320E Mutant, PDB code: 6zk6 was solved by F.Salvi, O.Barabas, M.Koehn, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 36.22 / 1.90
Space group P 2 21 21
Cell size a, b, c (Å), α, β, γ (°) 38.546, 68.749, 127.846, 90.00, 90.00, 90.00
R / Rfree (%) 15.9 / 19.4

Other elements in 6zk6:

The structure of Protein Phosphatase 1 (PP1) T320E Mutant also contains other interesting chemical elements:

Iron (Fe) 2 atoms

Manganese Binding Sites:

The binding sites of Manganese atom in the Protein Phosphatase 1 (PP1) T320E Mutant (pdb code 6zk6). This binding sites where shown within 5.0 Angstroms radius around Manganese atom.
In total 2 binding sites of Manganese where determined in the Protein Phosphatase 1 (PP1) T320E Mutant, PDB code: 6zk6:
Jump to Manganese binding site number: 1; 2;

Manganese binding site 1 out of 2 in 6zk6

Go back to Manganese Binding Sites List in 6zk6
Manganese binding site 1 out of 2 in the Protein Phosphatase 1 (PP1) T320E Mutant


Mono view


Stereo pair view

A full contact list of Manganese with other atoms in the Mn binding site number 1 of Protein Phosphatase 1 (PP1) T320E Mutant within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Mn401

b:26.8
occ:0.50
FE A:FE403 0.5 23.2 0.5
O A:HOH542 1.8 31.6 1.0
O3 A:PO4405 2.1 30.6 1.0
ND1 A:HIS248 2.2 27.9 1.0
OD2 A:ASP92 2.3 31.2 1.0
NE2 A:HIS173 2.3 28.8 1.0
OD1 A:ASN124 2.5 28.3 1.0
MN A:MN402 2.7 32.3 0.5
CE1 A:HIS248 3.0 29.0 1.0
CE1 A:HIS173 3.2 25.1 1.0
P A:PO4405 3.2 33.8 1.0
CG A:ASP92 3.3 28.0 1.0
FE A:FE404 3.3 31.1 0.5
CG A:HIS248 3.3 28.6 1.0
O1 A:PO4405 3.4 32.6 1.0
CD2 A:HIS173 3.4 24.4 1.0
CG A:ASN124 3.5 26.9 1.0
CA A:HIS248 3.6 26.8 1.0
OD1 A:ASP92 3.7 25.5 1.0
ND2 A:ASN124 3.8 25.8 1.0
CB A:HIS248 3.8 25.9 1.0
O4 A:PO4405 3.8 34.6 1.0
OD2 A:ASP64 3.8 36.3 1.0
O A:HIS248 3.9 31.4 1.0
NE2 A:HIS248 4.2 30.0 1.0
C A:HIS248 4.2 31.6 1.0
ND1 A:HIS173 4.3 24.8 1.0
CD2 A:HIS248 4.4 27.3 1.0
CB A:ASP92 4.4 26.7 1.0
CG A:HIS173 4.5 23.3 1.0
CD2 A:HIS125 4.5 26.3 1.0
O2 A:PO4405 4.5 34.9 1.0
N A:HIS248 4.7 25.1 1.0
CG A:ASP64 4.7 32.7 1.0
O A:HOH550 4.8 30.3 1.0
N A:ASN124 4.8 23.2 1.0
CB A:ASN124 4.8 25.0 1.0
O A:HOH507 4.8 41.1 1.0
OD1 A:ASP64 4.8 32.6 1.0
NE2 A:HIS66 4.9 33.3 1.0
O A:LEU205 4.9 28.1 1.0

Manganese binding site 2 out of 2 in 6zk6

Go back to Manganese Binding Sites List in 6zk6
Manganese binding site 2 out of 2 in the Protein Phosphatase 1 (PP1) T320E Mutant


Mono view


Stereo pair view

A full contact list of Manganese with other atoms in the Mn binding site number 2 of Protein Phosphatase 1 (PP1) T320E Mutant within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Mn402

b:32.3
occ:0.50
FE A:FE404 0.7 31.1 0.5
O A:HOH542 1.9 31.6 1.0
OD2 A:ASP92 2.0 31.2 1.0
OD2 A:ASP64 2.0 36.3 1.0
O1 A:PO4405 2.2 32.6 1.0
NE2 A:HIS66 2.4 33.3 1.0
O A:HOH550 2.6 30.3 1.0
MN A:MN401 2.7 26.8 0.5
CG A:ASP92 3.0 28.0 1.0
FE A:FE403 3.1 23.2 0.5
CG A:ASP64 3.2 32.7 1.0
CE1 A:HIS66 3.2 30.7 1.0
P A:PO4405 3.3 33.8 1.0
O3 A:PO4405 3.3 30.6 1.0
CD2 A:HIS66 3.4 30.1 1.0
CB A:ASP92 3.5 26.7 1.0
O4 A:PO4405 3.9 34.6 1.0
OD1 A:ASP64 4.0 32.6 1.0
NE2 A:HIS173 4.1 28.8 1.0
OD1 A:ASP92 4.1 25.5 1.0
O A:HOH507 4.1 41.1 1.0
CE1 A:HIS173 4.1 25.1 1.0
CB A:ASP64 4.2 32.4 1.0
CD2 A:HIS125 4.3 26.3 1.0
NH2 A:ARG96 4.3 33.6 1.0
ND1 A:HIS66 4.4 30.7 1.0
O A:HIS248 4.5 31.4 1.0
CA A:HIS248 4.5 26.8 1.0
O2 A:PO4405 4.5 34.9 1.0
CG A:HIS66 4.5 30.4 1.0
ND1 A:HIS248 4.6 27.9 1.0
OD1 A:ASN124 4.6 28.3 1.0
OH A:TYR272 4.7 41.9 1.0
NE2 A:HIS125 4.7 27.7 1.0
C A:HIS248 4.8 31.6 1.0
CE1 A:PHE267 4.9 32.7 1.0
CA A:ASP92 5.0 27.7 1.0

Reference:

M.Kohn, F.Salvi, B.Hoermann, J.Del Pino Garcia, M.Fontanillo, R.Derua, M.Beullens, M.Bollen, O.Barabas. Towards Dissecting the Mechanism of Protein Phosphatase-1 Inhibition By Its C-Terminal Phosphorylation. Chembiochem 2020.
ISSN: ESSN 1439-7633
PubMed: 33085143
DOI: 10.1002/CBIC.202000669
Page generated: Sun Oct 6 08:01:08 2024

Last articles

Zn in 9JYW
Zn in 9IR4
Zn in 9IR3
Zn in 9GMX
Zn in 9GMW
Zn in 9JEJ
Zn in 9ERF
Zn in 9ERE
Zn in 9EGV
Zn in 9EGW
© Copyright 2008-2020 by atomistry.com
Home   |    Site Map   |    Copyright   |    Contact us   |    Privacy