Calcium in PDB 6s39: Fragment Az-018 Binding at the P53PT387/14-3-3 Sigma Interface

Protein crystallography data

The structure of Fragment Az-018 Binding at the P53PT387/14-3-3 Sigma Interface, PDB code: 6s39 was solved by S.Genet, M.Wolter, X.Guillory, B.Somsen, S.Leysen, P.Castaldi, C.Ottmann, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 26.59 / 1.88
Space group C 2 2 21
Cell size a, b, c (Å), α, β, γ (°) 82.110, 111.990, 62.520, 90.00, 90.00, 90.00
R / Rfree (%) 35.4 / 38.8

Calcium Binding Sites:

The binding sites of Calcium atom in the Fragment Az-018 Binding at the P53PT387/14-3-3 Sigma Interface (pdb code 6s39). This binding sites where shown within 5.0 Angstroms radius around Calcium atom.
In total only one binding site of Calcium was determined in the Fragment Az-018 Binding at the P53PT387/14-3-3 Sigma Interface, PDB code: 6s39:

Calcium binding site 1 out of 1 in 6s39

Go back to Calcium Binding Sites List in 6s39
Calcium binding site 1 out of 1 in the Fragment Az-018 Binding at the P53PT387/14-3-3 Sigma Interface


Mono view


Stereo pair view

A full contact list of Calcium with other atoms in the Ca binding site number 1 of Fragment Az-018 Binding at the P53PT387/14-3-3 Sigma Interface within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Ca302

b:15.9
occ:1.00
O A:HOH464 2.7 9.4 1.0
CA A:TYR84 3.8 6.5 1.0
O A:GLU83 3.8 6.1 1.0
CD A:LYS87 3.9 9.9 1.0
C A:GLU83 3.9 6.6 1.0
CB A:LYS87 3.9 8.1 1.0
N A:TYR84 4.0 6.4 1.0
CD1 A:TYR84 4.1 6.4 1.0
CB A:TYR84 4.2 6.4 1.0
CB A:GLU83 4.4 6.9 1.0
CG A:LYS87 4.4 8.9 1.0
CG A:TYR84 4.6 6.4 1.0
O A:HOH440 4.7 9.7 1.0
CA A:GLU83 4.8 7.0 1.0
C A:TYR84 5.0 6.4 1.0

Reference:

X.Guillory, M.Wolter, S.Leysen, J.F.Neves, A.Kuusk, S.Genet, B.Somsen, J.Morrow, E.Rivers, L.Van Beek, J.Patel, R.Goodnow, H.Schoenherr, N.Fuller, Q.Cao, R.G.Doveston, L.Brunsveld, M.R.Arkin, M.P.Castaldi, H.Boyd, I.Landrieu, H.Chen, C.Ottmann. Fragment-Based Differential Targeting of Ppi Stabilizer Interfaces. J.Med.Chem. 2020.
ISSN: ISSN 0022-2623
PubMed: 32501690
DOI: 10.1021/ACS.JMEDCHEM.9B01942
Page generated: Sat Dec 12 07:31:53 2020

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