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Chlorine in PDB 5vcw: Crystal Structure of Human MYT1 Kinase Domain in Complex with Pelitinib

Enzymatic activity of Crystal Structure of Human MYT1 Kinase Domain in Complex with Pelitinib

All present enzymatic activity of Crystal Structure of Human MYT1 Kinase Domain in Complex with Pelitinib:
2.7.11.1;

Protein crystallography data

The structure of Crystal Structure of Human MYT1 Kinase Domain in Complex with Pelitinib, PDB code: 5vcw was solved by J.-Y.Zhu, E.Schonbrunn, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 36.43 / 2.25
Space group P 1 21 1
Cell size a, b, c (Å), α, β, γ (°) 50.510, 112.900, 72.710, 90.00, 109.27, 90.00
R / Rfree (%) 19.6 / 24.6

Other elements in 5vcw:

The structure of Crystal Structure of Human MYT1 Kinase Domain in Complex with Pelitinib also contains other interesting chemical elements:

Fluorine (F) 2 atoms

Chlorine Binding Sites:

The binding sites of Chlorine atom in the Crystal Structure of Human MYT1 Kinase Domain in Complex with Pelitinib (pdb code 5vcw). This binding sites where shown within 5.0 Angstroms radius around Chlorine atom.
In total 2 binding sites of Chlorine where determined in the Crystal Structure of Human MYT1 Kinase Domain in Complex with Pelitinib, PDB code: 5vcw:
Jump to Chlorine binding site number: 1; 2;

Chlorine binding site 1 out of 2 in 5vcw

Go back to Chlorine Binding Sites List in 5vcw
Chlorine binding site 1 out of 2 in the Crystal Structure of Human MYT1 Kinase Domain in Complex with Pelitinib


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 Human MYT1 Kinase Domain in Complex with Pelitinib within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl401

b:58.1
occ:1.00
CL1 A:93J401 0.0 58.1 1.0
C21 A:93J401 1.7 51.7 1.0
C22 A:93J401 2.7 49.5 1.0
C20 A:93J401 2.7 51.9 1.0
F01 A:93J401 2.9 58.0 1.0
O A:LEU185 3.2 52.3 1.0
N A:LYS139 3.5 46.1 1.0
CG2 A:THR187 3.5 53.8 1.0
CB A:LYS139 3.6 43.6 1.0
OG1 A:THR187 3.7 47.8 1.0
O A:ALA137 4.0 55.0 1.0
C23 A:93J401 4.0 49.3 1.0
C A:LEU185 4.0 48.5 1.0
C19 A:93J401 4.1 55.2 1.0
CA A:LYS139 4.1 59.0 1.0
N A:THR187 4.2 53.4 1.0
CB A:THR187 4.2 49.4 1.0
C A:ALA137 4.2 60.1 1.0
C A:VAL138 4.2 56.4 1.0
CB A:LEU185 4.2 54.8 1.0
CA A:VAL138 4.3 51.7 1.0
N04 A:93J401 4.3 43.1 1.0
CB A:ALA137 4.4 56.0 1.0
N A:VAL138 4.4 57.8 1.0
C24 A:93J401 4.5 48.5 1.0
C18 A:93J401 4.7 55.7 1.0
CG1 A:VAL124 4.8 45.4 1.0
N A:GLN186 4.8 47.1 1.0
CA A:LEU185 4.8 51.7 1.0
CA A:THR187 4.8 55.6 1.0
CA A:GLN186 4.9 58.2 1.0
C A:GLN186 4.9 59.2 1.0
CA A:ALA137 5.0 56.5 1.0
CG A:LYS139 5.0 52.5 1.0

Chlorine binding site 2 out of 2 in 5vcw

Go back to Chlorine Binding Sites List in 5vcw
Chlorine binding site 2 out of 2 in the Crystal Structure of Human MYT1 Kinase Domain in Complex with Pelitinib


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 Human MYT1 Kinase Domain in Complex with Pelitinib within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Cl401

b:62.0
occ:1.00
CL1 B:93J401 0.0 62.0 1.0
C21 B:93J401 1.7 54.6 1.0
C20 B:93J401 2.7 46.0 1.0
C22 B:93J401 2.7 53.6 1.0
F01 B:93J401 2.9 53.2 1.0
O B:LEU185 3.2 56.8 1.0
O B:ALA137 3.5 57.1 1.0
N B:LYS139 3.5 48.9 1.0
CG2 B:THR187 3.6 51.4 1.0
OG1 B:THR187 3.6 52.0 1.0
CB B:LYS139 3.7 44.8 1.0
C B:ALA137 4.0 60.0 1.0
C23 B:93J401 4.0 49.8 1.0
C19 B:93J401 4.0 49.0 1.0
C B:LEU185 4.1 54.2 1.0
C B:VAL138 4.1 54.9 1.0
N B:THR187 4.2 54.0 1.0
CA B:LYS139 4.2 57.1 1.0
CB B:THR187 4.2 53.6 1.0
N04 B:93J401 4.3 45.7 1.0
CA B:VAL138 4.3 57.5 1.0
N B:VAL138 4.4 58.2 1.0
CB B:LEU185 4.4 50.9 1.0
CB B:ALA137 4.4 53.4 1.0
C24 B:93J401 4.5 48.2 1.0
C18 B:93J401 4.6 57.7 1.0
CA B:THR187 4.8 55.4 1.0
CA B:ALA137 4.9 55.7 1.0
CG1 B:VAL124 4.9 54.0 1.0
N B:GLN186 4.9 53.9 1.0
CA B:LEU185 4.9 52.2 1.0
C B:GLN186 4.9 58.8 1.0
CA B:GLN186 4.9 51.5 1.0

Reference:

J.Y.Zhu, R.A.Cuellar, N.Berndt, H.E.Lee, S.H.Olesen, M.P.Martin, J.T.Jensen, G.I.Georg, E.Schonbrunn. Structural Basis of Wee Kinases Functionality and Inactivation By Diverse Small Molecule Inhibitors. J. Med. Chem. V. 60 7863 2017.
ISSN: ISSN 1520-4804
PubMed: 28792760
DOI: 10.1021/ACS.JMEDCHEM.7B00996
Page generated: Fri Jul 26 18:46:51 2024

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