Atomistry » Fluorine » PDB 5sol-5srx » 5sr9
Atomistry »
  Fluorine »
    PDB 5sol-5srx »
      5sr9 »

Fluorine in PDB 5sr9: Pandda Analysis Group Deposition -- Crystal Structure of Sars-Cov-2 NSP3 Macrodomain in Complex with Z3562259556 - (R) Isomer

Enzymatic activity of Pandda Analysis Group Deposition -- Crystal Structure of Sars-Cov-2 NSP3 Macrodomain in Complex with Z3562259556 - (R) Isomer

All present enzymatic activity of Pandda Analysis Group Deposition -- Crystal Structure of Sars-Cov-2 NSP3 Macrodomain in Complex with Z3562259556 - (R) Isomer:
3.4.19.121;

Protein crystallography data

The structure of Pandda Analysis Group Deposition -- Crystal Structure of Sars-Cov-2 NSP3 Macrodomain in Complex with Z3562259556 - (R) Isomer, PDB code: 5sr9 was solved by G.J.Correy, J.S.Fraser, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 44.35 / 1.05
Space group P 43
Cell size a, b, c (Å), α, β, γ (°) 88.691, 88.691, 39.442, 90, 90, 90
R / Rfree (%) 13.5 / 15.4

Fluorine Binding Sites:

The binding sites of Fluorine atom in the Pandda Analysis Group Deposition -- Crystal Structure of Sars-Cov-2 NSP3 Macrodomain in Complex with Z3562259556 - (R) Isomer (pdb code 5sr9). This binding sites where shown within 5.0 Angstroms radius around Fluorine atom.
In total only one binding site of Fluorine was determined in the Pandda Analysis Group Deposition -- Crystal Structure of Sars-Cov-2 NSP3 Macrodomain in Complex with Z3562259556 - (R) Isomer, PDB code: 5sr9:

Fluorine binding site 1 out of 1 in 5sr9

Go back to Fluorine Binding Sites List in 5sr9
Fluorine binding site 1 out of 1 in the Pandda Analysis Group Deposition -- Crystal Structure of Sars-Cov-2 NSP3 Macrodomain in Complex with Z3562259556 - (R) Isomer


Mono view


Stereo pair view

A full contact list of Fluorine with other atoms in the F binding site number 1 of Pandda Analysis Group Deposition -- Crystal Structure of Sars-Cov-2 NSP3 Macrodomain in Complex with Z3562259556 - (R) Isomer within 5.0Å range:
probe atom residue distance (Å) B Occ
A:F201

b:15.1
occ:0.20
 F16 A:R0H201 0.0 15.1 0.2
O A:HOH543 1.1 36.7 0.8
C13 A:R0H201 1.4 15.2 0.2
O A:HOH439 1.8 14.4 0.8
C12 A:R0H201 2.4 15.1 0.2
C14 A:R0H201 2.4 15.0 0.2
HB2 A:ALA52 2.6 14.8 0.8
HB2 A:ALA52 2.6 14.7 0.2
H121 A:R0H201 2.7 18.1 0.2
H141 A:R0H201 2.7 18.1 0.2
O A:HOH538 2.9 54.0 1.0
O A:HOH463 3.1 44.6 0.8
CB A:ALA52 3.4 12.2 0.2
CB A:ALA52 3.4 12.3 0.8
HB1 A:ALA52 3.5 14.7 0.2
O A:HOH479 3.5 37.6 1.0
HB1 A:ALA52 3.6 14.8 0.8
O A:HOH536 3.7 33.1 0.8
C15 A:R0H201 3.7 15.2 0.2
C11 A:R0H201 3.7 15.0 0.2
HB3 A:ALA52 3.9 14.7 0.2
HB3 A:ALA52 4.0 14.8 0.8
C10 A:R0H201 4.3 15.4 0.2
O A:GLY48 4.3 11.0 0.8
O A:GLY48 4.3 16.7 0.2
HA A:ALA52 4.3 14.7 0.2
HA A:ALA52 4.4 12.2 0.8
CA A:ALA52 4.4 10.2 0.8
CA A:ALA52 4.5 12.2 0.2
H151 A:R0H201 4.6 18.2 0.2
H A:ALA52 4.6 11.4 0.8
H A:ALA52 4.7 15.0 0.2
N A:ALA52 4.8 9.5 0.8
N A:ALA52 4.9 12.5 0.2
N17 A:R0H201 4.9 14.5 0.2
HA2 A:GLY48 4.9 20.2 0.2
C A:GLY48 5.0 16.3 0.2

Reference:

S.Gahbauer, G.J.Correy, M.Schuller, M.P.Ferla, Y.U.Doruk, M.Rachman, T.Wu, M.Diolaiti, S.Wang, R.J.Neitz, D.Fearon, D.Radchenko, Y.Moroz, J.J.Irwin, A.R.Renslo, J.C.Taylor, J.E.Gestwicki, F.Von Delft, A.Ashworth, I.Ahel, B.K.Shoichet, J.S.Fraser. Structure-Based Inhibitor Optimization For the NSP3 Macrodomain of Sars-Cov-2. Biorxiv 2022.
ISSN: ISSN 2692-8205
PubMed: 35794891
DOI: 10.1101/2022.06.27.497816
Page generated: Tue Jul 15 07:36:04 2025

Last articles

Mg in 7MWN
Mg in 7MWG
Mg in 7MQX
Mg in 7MU0
Mg in 7MTO
Mg in 7MSY
Mg in 7MSU
Mg in 7MSS
Mg in 7MSR
Mg in 7MSP
© Copyright 2008-2020 by atomistry.com
Home   |    Site Map   |    Copyright   |    Contact us   |    Privacy