Fluorine in PDB 7t09: Cryptococcus Neoformans Protein Farnesyltransferase in Complex with Fpp and Inhibitor 2D

Enzymatic activity of Cryptococcus Neoformans Protein Farnesyltransferase in Complex with Fpp and Inhibitor 2D

All present enzymatic activity of Cryptococcus Neoformans Protein Farnesyltransferase in Complex with Fpp and Inhibitor 2D:
2.5.1.58;

Protein crystallography data

The structure of Cryptococcus Neoformans Protein Farnesyltransferase in Complex with Fpp and Inhibitor 2D, PDB code: 7t09 was solved by Y.Wang, Y.Shi, L.S.Beese, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 46.82 / 1.98
Space group P 43 21 2
Cell size a, b, c (Å), α, β, γ (°) 141.915, 141.915, 130.226, 90, 90, 90
R / Rfree (%) 17.2 / 19.4

Other elements in 7t09:

The structure of Cryptococcus Neoformans Protein Farnesyltransferase in Complex with Fpp and Inhibitor 2D also contains other interesting chemical elements:

Zinc (Zn) 1 atom

Fluorine Binding Sites:

The binding sites of Fluorine atom in the Cryptococcus Neoformans Protein Farnesyltransferase in Complex with Fpp and Inhibitor 2D (pdb code 7t09). This binding sites where shown within 5.0 Angstroms radius around Fluorine atom.
In total 3 binding sites of Fluorine where determined in the Cryptococcus Neoformans Protein Farnesyltransferase in Complex with Fpp and Inhibitor 2D, PDB code: 7t09:
Jump to Fluorine binding site number: 1; 2; 3;

Fluorine binding site 1 out of 3 in 7t09

Go back to Fluorine Binding Sites List in 7t09
Fluorine binding site 1 out of 3 in the Cryptococcus Neoformans Protein Farnesyltransferase in Complex with Fpp and Inhibitor 2D


Mono view


Stereo pair view

A full contact list of Fluorine with other atoms in the F binding site number 1 of Cryptococcus Neoformans Protein Farnesyltransferase in Complex with Fpp and Inhibitor 2D within 5.0Å range:
probe atom residue distance (Å) B Occ
B:F605

b:30.5
occ:1.00
 F35 B:XMV605 0.0 30.5 1.0
C34 B:XMV605 1.4 29.4 1.0
F36 B:XMV605 2.2 30.7 1.0
F37 B:XMV605 2.2 26.6 1.0
O33 B:XMV605 2.3 27.2 1.0
C29 B:XMV605 2.8 28.2 1.0
C28 B:XMV605 3.0 28.5 1.0
O B:HOH883 3.0 28.5 1.0
CE1 B:TYR409 3.3 27.7 1.0
CZ2 B:TRP94 3.3 24.9 1.0
CD1 B:TYR409 3.3 27.7 1.0
NE1 B:TRP94 3.7 25.3 1.0
CE2 B:TRP94 3.9 24.8 1.0
C30 B:XMV605 3.9 26.6 1.0
C27 B:XMV605 4.1 26.3 1.0
CE3 B:TRP90 4.1 25.8 1.0
CZ3 B:TRP90 4.2 25.4 1.0
CZ2 B:TRP329 4.2 27.1 1.0
CH2 B:TRP94 4.5 26.1 1.0
CD2 B:TRP90 4.5 24.8 1.0
CZ B:TYR409 4.6 27.0 1.0
CG B:TYR409 4.7 25.5 1.0
CH2 B:TRP90 4.7 24.3 1.0
CH2 B:TRP329 4.7 26.2 1.0
ND2 B:ASN413 4.7 25.1 1.0
C06 B:XMV605 4.8 28.2 1.0
C31 B:XMV605 4.8 29.5 1.0
N07 B:XMV605 4.9 27.2 1.0
C32 B:XMV605 4.9 29.1 1.0
CE2 B:TRP90 5.0 27.1 1.0

Fluorine binding site 2 out of 3 in 7t09

Go back to Fluorine Binding Sites List in 7t09
Fluorine binding site 2 out of 3 in the Cryptococcus Neoformans Protein Farnesyltransferase in Complex with Fpp and Inhibitor 2D


Mono view


Stereo pair view

A full contact list of Fluorine with other atoms in the F binding site number 2 of Cryptococcus Neoformans Protein Farnesyltransferase in Complex with Fpp and Inhibitor 2D within 5.0Å range:
probe atom residue distance (Å) B Occ
B:F605

b:30.7
occ:1.00
 F36 B:XMV605 0.0 30.7 1.0
C34 B:XMV605 1.4 29.4 1.0
F37 B:XMV605 2.2 26.6 1.0
F35 B:XMV605 2.2 30.5 1.0
O33 B:XMV605 2.3 27.2 1.0
C28 B:XMV605 2.9 28.5 1.0
C29 B:XMV605 3.0 28.2 1.0
C14 B:FPP606 3.6 24.9 1.0
C9 B:FPP606 3.6 27.7 1.0
C25 B:XMV605 3.6 27.0 1.0
N26 B:XMV605 3.6 28.9 1.0
C21 B:XMV605 3.7 27.9 1.0
C11 B:FPP606 3.7 26.3 1.0
CZ2 B:TRP329 3.8 27.1 1.0
C13 B:FPP606 3.9 23.4 1.0
C12 B:FPP606 4.0 24.8 1.0
CE1 B:TYR409 4.0 27.7 1.0
C22 B:XMV605 4.1 29.0 1.0
CH2 B:TRP329 4.2 26.2 1.0
C27 B:XMV605 4.3 26.3 1.0
C8 B:FPP606 4.3 27.0 1.0
C30 B:XMV605 4.4 26.6 1.0
O B:HOH883 4.5 28.5 1.0
CD1 B:TYR409 4.7 27.7 1.0
CE2 B:TRP329 4.8 24.8 1.0
C20 B:XMV605 4.8 24.4 1.0
C10 B:FPP606 4.8 25.3 1.0
N07 B:XMV605 4.9 27.2 1.0
CZ B:TYR409 4.9 27.0 1.0
OH B:TYR409 5.0 26.0 1.0
C15 B:FPP606 5.0 27.6 1.0

Fluorine binding site 3 out of 3 in 7t09

Go back to Fluorine Binding Sites List in 7t09
Fluorine binding site 3 out of 3 in the Cryptococcus Neoformans Protein Farnesyltransferase in Complex with Fpp and Inhibitor 2D


Mono view


Stereo pair view

A full contact list of Fluorine with other atoms in the F binding site number 3 of Cryptococcus Neoformans Protein Farnesyltransferase in Complex with Fpp and Inhibitor 2D within 5.0Å range:
probe atom residue distance (Å) B Occ
B:F605

b:26.6
occ:1.00
 F37 B:XMV605 0.0 26.6 1.0
C34 B:XMV605 1.4 29.4 1.0
F36 B:XMV605 2.2 30.7 1.0
F35 B:XMV605 2.2 30.5 1.0
O33 B:XMV605 2.3 27.2 1.0
CH2 B:TRP90 3.1 24.3 1.0
CZ3 B:TRP90 3.2 25.4 1.0
C14 B:FPP606 3.3 24.9 1.0
O B:HOH883 3.3 28.5 1.0
C13 B:FPP606 3.5 23.4 1.0
C29 B:XMV605 3.6 28.2 1.0
CZ2 B:TRP90 3.7 25.9 1.0
CH2 B:TRP329 3.7 26.2 1.0
CE3 B:TRP90 3.8 25.8 1.0
C15 B:FPP606 3.8 27.6 1.0
CZ2 B:TRP329 3.9 27.1 1.0
C12 B:FPP606 4.0 24.8 1.0
CE2 B:TRP90 4.2 27.1 1.0
C28 B:XMV605 4.2 28.5 1.0
CD2 B:TRP90 4.3 24.8 1.0
C11 B:FPP606 4.6 26.3 1.0
C30 B:XMV605 4.6 26.6 1.0
C9 B:FPP606 4.8 27.7 1.0
CZ3 B:TRP329 4.9 25.3 1.0
NE1 B:TRP94 5.0 25.3 1.0

Reference:

Y.Wang, F.Xu, C.B.Nichols, Y.Shi, H.W.Hellinga, J.A.Alspaugh, M.D.Distefano, L.S.Beese. Structure-Guided Discovery of Potent Antifungals That Prevent Ras Signaling By Inhibiting Protein Farnesyltransferase. J.Med.Chem. V. 65 13753 2022.
ISSN: ISSN 0022-2623
PubMed: 36218371
DOI: 10.1021/ACS.JMEDCHEM.2C00902
Page generated: Fri Aug 2 13:11:04 2024

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