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Fluorine in PDB 5eto: E. Coli 6-Hydroxymethyl-7,8-Dihydropterin Pyrophosphokinase Complexed with Ampcpp and Inhibitor at 1.07 Angstrom Resolution

Enzymatic activity of E. Coli 6-Hydroxymethyl-7,8-Dihydropterin Pyrophosphokinase Complexed with Ampcpp and Inhibitor at 1.07 Angstrom Resolution

All present enzymatic activity of E. Coli 6-Hydroxymethyl-7,8-Dihydropterin Pyrophosphokinase Complexed with Ampcpp and Inhibitor at 1.07 Angstrom Resolution:
2.7.6.3;

Protein crystallography data

The structure of E. Coli 6-Hydroxymethyl-7,8-Dihydropterin Pyrophosphokinase Complexed with Ampcpp and Inhibitor at 1.07 Angstrom Resolution, PDB code: 5eto was solved by M.L.Dennis, T.S.Peat, J.D.Swarbrick, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 34.69 / 1.07
Space group P 1 21 1
Cell size a, b, c (Å), α, β, γ (°) 35.770, 57.750, 38.420, 90.00, 115.46, 90.00
R / Rfree (%) 12.9 / 15

Other elements in 5eto:

The structure of E. Coli 6-Hydroxymethyl-7,8-Dihydropterin Pyrophosphokinase Complexed with Ampcpp and Inhibitor at 1.07 Angstrom Resolution also contains other interesting chemical elements:

Calcium (Ca) 4 atoms
Chlorine (Cl) 2 atoms

Fluorine Binding Sites:

The binding sites of Fluorine atom in the E. Coli 6-Hydroxymethyl-7,8-Dihydropterin Pyrophosphokinase Complexed with Ampcpp and Inhibitor at 1.07 Angstrom Resolution (pdb code 5eto). 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 E. Coli 6-Hydroxymethyl-7,8-Dihydropterin Pyrophosphokinase Complexed with Ampcpp and Inhibitor at 1.07 Angstrom Resolution, PDB code: 5eto:

Fluorine binding site 1 out of 1 in 5eto

Go back to Fluorine Binding Sites List in 5eto
Fluorine binding site 1 out of 1 in the E. Coli 6-Hydroxymethyl-7,8-Dihydropterin Pyrophosphokinase Complexed with Ampcpp and Inhibitor at 1.07 Angstrom Resolution


Mono view


Stereo pair view

A full contact list of Fluorine with other atoms in the F binding site number 1 of E. Coli 6-Hydroxymethyl-7,8-Dihydropterin Pyrophosphokinase Complexed with Ampcpp and Inhibitor at 1.07 Angstrom Resolution within 5.0Å range:
probe atom residue distance (Å) B Occ
A:F201

b:17.2
occ:1.00
 F21 A:5RY201 0.0 17.2 1.0
C8 A:5RY201 1.3 12.6 1.0
C4 A:5RY201 2.3 15.2 1.0
C6 A:5RY201 2.3 14.8 1.0
C13 A:5RY201 2.9 16.7 1.0
CZ A:ARG121 3.2 5.8 1.0
CZ A:PHE123 3.2 7.3 1.0
NE A:ARG121 3.2 6.7 1.0
CE2 A:PHE123 3.3 8.3 1.0
NH1 A:ARG121 3.4 6.5 1.0
C5 A:5RY201 3.5 13.9 1.0
C3 A:5RY201 3.6 14.4 1.0
NH2 A:ARG121 3.6 7.0 1.0
N16 A:5RY201 3.7 11.0 1.0
CD A:ARG121 3.7 6.7 1.0
C12 A:5RY201 3.7 11.3 1.0
C9 A:5RY201 4.0 7.9 1.0
C2 A:5RY201 4.0 16.3 1.0
N18 A:5RY201 4.1 10.4 1.0
S22 A:5RY201 4.2 15.1 1.0
C7 A:5RY201 4.2 7.9 1.0
CG A:ARG121 4.2 6.5 1.0
CB A:LEU45 4.3 10.5 1.0
CE1 A:PHE123 4.4 6.9 1.0
N15 A:5RY201 4.6 6.2 1.0
C1 A:5RY201 4.7 19.0 1.0
O A:LEU45 4.7 9.2 1.0
CD2 A:PHE123 4.7 7.4 1.0
C A:LEU45 5.0 8.0 1.0

Reference:

M.L.Dennis, N.P.Pitcher, M.D.Lee, A.J.Debono, Z.C.Wang, J.R.Harjani, R.Rahmani, B.Cleary, T.S.Peat, J.B.Baell, J.D.Swarbrick. Structural Basis For the Selective Binding of Inhibitors to 6-Hydroxymethyl-7,8-Dihydropterin Pyrophosphokinase From Staphylococcus Aureus and Escherichia Coli. J.Med.Chem. V. 59 5248 2016.
ISSN: ISSN 0022-2623
PubMed: 27094768
DOI: 10.1021/ACS.JMEDCHEM.6B00002
Page generated: Thu Aug 1 09:14:20 2024

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