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: Tue Dec 15 05:11:20 2020

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