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Atomistry » Fluorine » PDB 8d7z-8dxh » 8dxe » |
Fluorine in PDB 8dxe: Hiv-1 Reverse Transcriptase/Rilpivirine with Bound Fragment 2-Amino-6- Fluorobenzonitrile at the Nnrti Adjacent SiteEnzymatic activity of Hiv-1 Reverse Transcriptase/Rilpivirine with Bound Fragment 2-Amino-6- Fluorobenzonitrile at the Nnrti Adjacent Site
All present enzymatic activity of Hiv-1 Reverse Transcriptase/Rilpivirine with Bound Fragment 2-Amino-6- Fluorobenzonitrile at the Nnrti Adjacent Site:
2.7.7.49; 2.7.7.7; 3.1.13.2; 3.1.26.13; Protein crystallography data
The structure of Hiv-1 Reverse Transcriptase/Rilpivirine with Bound Fragment 2-Amino-6- Fluorobenzonitrile at the Nnrti Adjacent Site, PDB code: 8dxe
was solved by
A.Chopra,
F.X.Ruiz,
J.D.Bauman,
E.Arnold,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Other elements in 8dxe:
The structure of Hiv-1 Reverse Transcriptase/Rilpivirine with Bound Fragment 2-Amino-6- Fluorobenzonitrile at the Nnrti Adjacent Site also contains other interesting chemical elements:
Fluorine Binding Sites:
The binding sites of Fluorine atom in the Hiv-1 Reverse Transcriptase/Rilpivirine with Bound Fragment 2-Amino-6- Fluorobenzonitrile at the Nnrti Adjacent Site
(pdb code 8dxe). 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 Hiv-1 Reverse Transcriptase/Rilpivirine with Bound Fragment 2-Amino-6- Fluorobenzonitrile at the Nnrti Adjacent Site, PDB code: 8dxe: Fluorine binding site 1 out of 1 in 8dxeGo back to![]() ![]()
Fluorine binding site 1 out
of 1 in the Hiv-1 Reverse Transcriptase/Rilpivirine with Bound Fragment 2-Amino-6- Fluorobenzonitrile at the Nnrti Adjacent Site
![]() Mono view ![]() Stereo pair view
Reference:
A.Chopra,
J.D.Bauman,
F.X.Ruiz,
E.Arnold.
Halo Library, A Tool For Rapid Identification of Ligand Binding Sites on Proteins Using Crystallographic Fragment Screening. J.Med.Chem. V. 66 6013 2023.
Page generated: Wed Jul 16 03:30:20 2025
ISSN: ISSN 0022-2623 PubMed: 37115705 DOI: 10.1021/ACS.JMEDCHEM.2C01681 |
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