Chlorine in PDB 7ab1: Crystal Structure of Mertk Kinase Domain in Complex with Gilteritinib

All present enzymatic activity of Crystal Structure of Mertk Kinase Domain in Complex with Gilteritinib:
2.7.10.1;

The structure of Crystal Structure of Mertk Kinase Domain in Complex with Gilteritinib, PDB code: 7ab1 was solved by A.Pflug, M.Schimpl, W.Mccoull, J.W.M.Nissink, R.C.Overman, P.B.Rawlins, C.Truman, E.Underwood, J.Warwicker, J.Winter-Holt, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å)	46.65 / 1.93
Space group	C 2 2 21
Cell size a, b, c (Å), α, β, γ (°)	93.302, 94.120, 70.734, 90.00, 90.00, 90.00
R / Rfree (%)	23.4 / 29.8

The binding sites of Chlorine atom in the Crystal Structure of Mertk Kinase Domain in Complex with Gilteritinib (pdb code 7ab1). This binding sites where shown within 5.0 Angstroms radius around Chlorine atom.
In total 4 binding sites of Chlorine where determined in the Crystal Structure of Mertk Kinase Domain in Complex with Gilteritinib, PDB code: 7ab1:
Jump to Chlorine binding site number: 1; 2; 3; 4;

Chlorine binding site 1 out of 4 in the Crystal Structure of Mertk Kinase Domain in Complex with Gilteritinib


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 1 of Crystal Structure of Mertk Kinase Domain in Complex with Gilteritinib within 5.0Å range: probe atom residue distance (Å) B Occ A:Cl902 b:44.8 occ:1.00 N A:LYS820 3.3 43.4 1.0 CA A:TYR801 3.8 41.2 1.0 CA A:LEU819 3.8 45.9 1.0 CB A:LYS820 3.8 46.4 1.0 CD2 A:LEU819 3.8 47.4 1.0 CD A:PRO802 3.9 38.7 1.0 CD A:LYS820 3.9 65.3 1.0 CG A:LYS820 3.9 54.1 1.0 C A:LEU819 4.1 48.3 1.0 N A:TYR801 4.1 44.2 1.0 CA A:LYS820 4.2 45.2 1.0 CZ2 A:TRP791 4.2 39.7 1.0 CD1 A:TYR801 4.4 44.7 1.0 CB A:LEU819 4.4 47.2 1.0 CG A:PRO802 4.6 42.1 1.0 N A:PRO802 4.6 41.5 1.0 CB A:TYR801 4.6 41.1 1.0 C A:TYR801 4.7 44.4 1.0 CE A:LYS820 4.7 69.1 1.0 CG A:LEU819 4.7 45.5 1.0 O A:ARG818 4.8 44.4 1.0 CG A:TYR801 4.8 39.8 1.0 CE2 A:TRP791 4.8 40.2 1.0 O A:LYS820 4.9 46.4 1.0 NE1 A:TRP791 4.9 43.8 1.0 N A:LEU819 4.9 45.9 1.0 CH2 A:TRP791 4.9 40.3 1.0

Chlorine binding site 2 out of 4 in the Crystal Structure of Mertk Kinase Domain in Complex with Gilteritinib


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 2 of Crystal Structure of Mertk Kinase Domain in Complex with Gilteritinib within 5.0Å range: probe atom residue distance (Å) B Occ A:Cl903 b:60.3 occ:0.50 NH2 A:ARG687 2.9 56.9 1.0 O A:HOH1041 3.2 37.0 1.0 CZ A:ARG687 3.8 58.9 1.0 CG A:MET798 3.8 53.6 1.0 CA A:MET798 3.8 40.0 1.0 NH1 A:ARG687 3.8 55.6 1.0 O A:GLY797 3.9 38.0 1.0 N A:MET798 4.0 41.2 1.0 C A:GLY797 4.1 37.5 1.0 CB A:MET798 4.4 45.1 1.0 CD2 A:LEU684 4.4 41.3 1.0 C A:MET798 5.0 36.0 1.0

Chlorine binding site 3 out of 4 in the Crystal Structure of Mertk Kinase Domain in Complex with Gilteritinib


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 3 of Crystal Structure of Mertk Kinase Domain in Complex with Gilteritinib within 5.0Å range: probe atom residue distance (Å) B Occ A:Cl904 b:77.0 occ:1.00 NH2 A:ARG732 3.2 90.5 1.0 O A:HOH1052 3.2 60.4 1.0 N A:ARG651 3.6 48.8 1.0 CE A:MET674 3.8 63.4 1.0 CG A:PRO672 3.8 42.5 1.0 CZ A:ARG732 3.8 80.3 1.0 CB A:ARG651 3.9 56.2 1.0 NE A:ARG732 4.0 77.5 1.0 O A:VAL649 4.2 45.5 1.0 CA A:ILE650 4.2 48.0 1.0 CA A:ARG651 4.4 49.8 1.0 C A:ILE650 4.4 48.2 1.0 CG1 A:ILE650 4.6 49.6 1.0 CB A:PRO672 4.6 44.4 1.0 NH1 A:ARG732 4.7 78.0 1.0 SG A:CYS738 4.8 60.4 1.0 C A:VAL649 5.0 45.1 1.0

Chlorine binding site 4 out of 4 in the Crystal Structure of Mertk Kinase Domain in Complex with Gilteritinib


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 4 of Crystal Structure of Mertk Kinase Domain in Complex with Gilteritinib within 5.0Å range: probe atom residue distance (Å) B Occ A:Cl905 b:65.3 occ:1.00 NH2 A:ARG584 3.3 53.8 1.0 N A:LEU589 3.3 46.7 1.0 CA A:ILE588 3.7 53.3 1.0 NH1 A:ARG584 3.8 62.9 1.0 C A:ILE588 4.0 52.9 1.0 CZ A:ARG584 4.0 55.7 1.0 O A:LEU587 4.1 49.8 1.0 CB A:LEU589 4.2 52.9 1.0 CG2 A:ILE588 4.2 63.7 1.0 CA A:LEU589 4.3 52.8 1.0 CD1 A:ILE588 4.3 63.9 1.0 CG A:LEU589 4.4 56.9 1.0 O A:LEU589 4.5 51.7 1.0 CB A:ILE588 4.5 58.9 1.0 CD1 A:LEU589 4.7 57.4 1.0 N A:ILE588 4.7 55.1 1.0 C A:LEU587 4.8 52.6 1.0 C A:LEU589 4.9 57.5 1.0

A.Pflug, M.Schimpl, J.W.M.Nissink, R.C.Overman, P.B.Rawlins, C.Truman, E.Underwood, J.Warwicker, J.Winter-Holt, W.Mccoull. A-Loop Interactions in Mer Tyrosine Kinase Give Rise to Inhibitors with Two-Step Mechanism and Long Residence Time of Binding. Biochem.J. V. 477 4443 2020.
ISSN: ESSN 1470-8728
PubMed: 33119085
DOI: 10.1042/BCJ20200735