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Magnesium in PDB 4zrt: PTP1BC215S Bound to Nephrin Peptide Substrate

Enzymatic activity of PTP1BC215S Bound to Nephrin Peptide Substrate

All present enzymatic activity of PTP1BC215S Bound to Nephrin Peptide Substrate:
3.1.3.48;

Protein crystallography data

The structure of PTP1BC215S Bound to Nephrin Peptide Substrate, PDB code: 4zrt was solved by N.G.Selner, C.E.Bell, D.Pei, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 19.95 / 1.74
Space group P 1 21 1
Cell size a, b, c (Å), α, β, γ (°) 43.848, 88.725, 50.043, 90.00, 97.25, 90.00
R / Rfree (%) 16.8 / 20.7

Other elements in 4zrt:

The structure of PTP1BC215S Bound to Nephrin Peptide Substrate also contains other interesting chemical elements:

Chlorine (Cl) 2 atoms

Magnesium Binding Sites:

The binding sites of Magnesium atom in the PTP1BC215S Bound to Nephrin Peptide Substrate (pdb code 4zrt). This binding sites where shown within 5.0 Angstroms radius around Magnesium atom.
In total only one binding site of Magnesium was determined in the PTP1BC215S Bound to Nephrin Peptide Substrate, PDB code: 4zrt:

Magnesium binding site 1 out of 1 in 4zrt

Go back to Magnesium Binding Sites List in 4zrt
Magnesium binding site 1 out of 1 in the PTP1BC215S Bound to Nephrin Peptide Substrate


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 1 of PTP1BC215S Bound to Nephrin Peptide Substrate within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Mg301

b:23.8
occ:1.00
O A:HOH478 2.0 22.9 1.0
O A:HOH607 2.0 39.7 1.0
O A:HOH418 2.1 28.9 1.0
OE1 A:GLU130 4.1 16.7 1.0
O A:HOH600 4.2 29.7 1.0
OE2 A:GLU130 4.2 23.5 1.0
O A:HOH477 4.4 34.7 1.0
OE1 A:GLU129 4.4 17.6 1.0
O A:HOH567 4.5 23.7 1.0
CD A:GLU130 4.6 20.4 1.0
O A:HOH640 4.7 37.7 1.0
CG A:LYS128 4.9 22.0 1.0

Reference:

N.G.Selner, R.Luechapanichkul, X.Chen, B.G.Neel, Z.Y.Zhang, S.Knapp, C.E.Bell, D.Pei. Diverse Levels of Sequence Selectivity and Catalytic Efficiency of Protein-Tyrosine Phosphatases. Biochemistry V. 53 397 2014.
ISSN: ISSN 0006-2960
PubMed: 24359314
DOI: 10.1021/BI401223R
Page generated: Sun Sep 29 00:09:14 2024

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