Fluorine in PDB 7mrd: Crystal Structure of the First Bromodomain (BD1) of Human Brdt Bound to Gxh-II-082

Protein crystallography data

The structure of Crystal Structure of the First Bromodomain (BD1) of Human Brdt Bound to Gxh-II-082, PDB code: 7mrd was solved by A.Chan, E.Schonbrunn, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 56.30 / 1.39
Space group P 21 21 21
Cell size a, b, c (Å), α, β, γ (°) 34.85, 63.17, 112.6, 90, 90, 90
R / Rfree (%) 20.1 / 22.1

Other elements in 7mrd:

The structure of Crystal Structure of the First Bromodomain (BD1) of Human Brdt Bound to Gxh-II-082 also contains other interesting chemical elements:

Chlorine (Cl) 2 atoms

Fluorine Binding Sites:

The binding sites of Fluorine atom in the Crystal Structure of the First Bromodomain (BD1) of Human Brdt Bound to Gxh-II-082 (pdb code 7mrd). This binding sites where shown within 5.0 Angstroms radius around Fluorine atom.
In total 2 binding sites of Fluorine where determined in the Crystal Structure of the First Bromodomain (BD1) of Human Brdt Bound to Gxh-II-082, PDB code: 7mrd:
Jump to Fluorine binding site number: 1; 2;

Fluorine binding site 1 out of 2 in 7mrd

Go back to Fluorine Binding Sites List in 7mrd
Fluorine binding site 1 out of 2 in the Crystal Structure of the First Bromodomain (BD1) of Human Brdt Bound to Gxh-II-082


Mono view


Stereo pair view

A full contact list of Fluorine with other atoms in the F binding site number 1 of Crystal Structure of the First Bromodomain (BD1) of Human Brdt Bound to Gxh-II-082 within 5.0Å range:
probe atom residue distance (Å) B Occ
B:F201

b:26.8
occ:1.00
F77 B:ZMV201 0.0 26.8 1.0
C76 B:ZMV201 1.4 23.1 1.0
C47 B:ZMV201 2.4 24.3 1.0
C75 B:ZMV201 2.4 19.6 1.0
C45 B:ZMV201 2.8 29.5 1.0
N44 B:ZMV201 2.9 27.3 1.0
N62 B:ZMV201 3.2 18.6 1.0
CD2 B:LEU61 3.4 23.0 1.0
O B:HOH372 3.5 26.0 1.0
CB B:LEU61 3.5 19.6 1.0
C50 B:ZMV201 3.6 16.9 1.0
C48 B:ZMV201 3.6 27.2 1.0
O B:LEU61 3.7 19.6 1.0
O64 B:ZMV201 3.7 22.9 1.0
C61 B:ZMV201 3.8 16.6 1.0
O46 B:ZMV201 3.8 26.9 1.0
CG B:LEU61 3.9 19.9 1.0
S63 B:ZMV201 4.0 19.9 1.0
C41 B:ZMV201 4.1 30.9 1.0
CA B:LEU61 4.1 22.2 1.0
C49 B:ZMV201 4.1 18.9 1.0
C70 B:ZMV201 4.2 16.3 1.0
CD1 B:LEU61 4.2 18.5 1.0
C40 B:ZMV201 4.3 30.8 1.0
O65 B:ZMV201 4.3 20.7 1.0
C B:LEU61 4.3 20.2 1.0
O A:HOH211 4.4 35.6 1.0
CD2 B:LEU63 4.6 20.6 1.0
C59 B:ZMV201 4.6 17.0 1.0
N51 B:ZMV201 4.9 16.9 1.0
N53 B:ZMV201 5.0 16.7 1.0

Fluorine binding site 2 out of 2 in 7mrd

Go back to Fluorine Binding Sites List in 7mrd
Fluorine binding site 2 out of 2 in the Crystal Structure of the First Bromodomain (BD1) of Human Brdt Bound to Gxh-II-082


Mono view


Stereo pair view

A full contact list of Fluorine with other atoms in the F binding site number 2 of Crystal Structure of the First Bromodomain (BD1) of Human Brdt Bound to Gxh-II-082 within 5.0Å range:
probe atom residue distance (Å) B Occ
B:F201

b:19.8
occ:1.00
F79 B:ZMV201 0.0 19.8 1.0
C78 B:ZMV201 1.4 15.9 1.0
C80 B:ZMV201 2.4 15.5 1.0
C10 B:ZMV201 2.4 18.1 1.0
N13 B:ZMV201 2.6 20.6 1.0
C11 B:ZMV201 2.8 19.1 1.0
N87 B:ZMV201 3.2 18.8 1.0
O B:HOH344 3.3 18.0 1.0
C86 B:ZMV201 3.5 17.2 1.0
CD2 A:LEU61 3.5 22.6 1.0
C07 B:ZMV201 3.6 15.9 1.0
C09 B:ZMV201 3.6 19.6 1.0
CD1 A:LEU61 3.7 20.8 1.0
CB A:LEU61 3.8 23.1 1.0
C15 B:ZMV201 3.8 22.7 1.0
CG A:LEU61 3.9 20.8 1.0
C14 B:ZMV201 3.9 20.2 1.0
C85 B:ZMV201 3.9 17.0 1.0
O12 B:ZMV201 4.0 22.1 1.0
O90 B:ZMV201 4.1 19.4 1.0
C95 B:ZMV201 4.1 17.2 1.0
C08 B:ZMV201 4.1 20.4 1.0
S88 B:ZMV201 4.1 17.7 1.0
O89 B:ZMV201 4.4 17.6 1.0
CD1 A:LEU63 4.5 19.7 1.0
CL96 B:ZMV201 4.5 20.7 1.0
O A:LEU61 4.5 21.2 1.0
CA A:LEU61 4.7 20.8 1.0
N81 B:ZMV201 4.8 14.3 1.0
C84 B:ZMV201 4.8 16.8 1.0
N06 B:ZMV201 4.9 14.9 1.0
C19 B:ZMV201 4.9 24.0 1.0
CG A:LEU63 4.9 19.6 1.0
CD2 A:LEU63 4.9 21.4 1.0
C97 B:ZMV201 5.0 17.4 1.0

Reference:

X.Guan, N.Cheryala, R.M.Karim, A.Chan, N.Berndt, J.Qi, G.I.Georg, E.Schonbrunn. Bivalent Bet Bromodomain Inhibitors Confer Increased Potency and Selectivity For Brdt Via Protein Conformational Plasticity. J.Med.Chem. V. 65 10441 2022.
ISSN: ISSN 0022-2623
PubMed: 35867655
DOI: 10.1021/ACS.JMEDCHEM.2C00453
Page generated: Fri Aug 2 09:46:08 2024

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