Iron in PDB 5esl: Saccharomyces Cerevisiae CYP51 (Lanosterol 14-Alpha Demethylase) T322I Mutant Complexed with Itraconazole

Protein crystallography data

The structure of Saccharomyces Cerevisiae CYP51 (Lanosterol 14-Alpha Demethylase) T322I Mutant Complexed with Itraconazole, PDB code: 5esl was solved by A.Sagatova, M.V.Keniya, R.K.Wilson, M.Sabherwal, J.D.A.Tyndall, B.C.Monk, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 50.61 / 2.35
Space group P 1 21 1
Cell size a, b, c (Å), α, β, γ (°) 77.090, 65.390, 80.780, 90.00, 98.42, 90.00
R / Rfree (%) 21 / 26.6

Other elements in 5esl:

The structure of Saccharomyces Cerevisiae CYP51 (Lanosterol 14-Alpha Demethylase) T322I Mutant Complexed with Itraconazole also contains other interesting chemical elements:

Chlorine (Cl) 2 atoms

Iron Binding Sites:

The binding sites of Iron atom in the Saccharomyces Cerevisiae CYP51 (Lanosterol 14-Alpha Demethylase) T322I Mutant Complexed with Itraconazole (pdb code 5esl). This binding sites where shown within 5.0 Angstroms radius around Iron atom.
In total only one binding site of Iron was determined in the Saccharomyces Cerevisiae CYP51 (Lanosterol 14-Alpha Demethylase) T322I Mutant Complexed with Itraconazole, PDB code: 5esl:

Iron binding site 1 out of 1 in 5esl

Go back to Iron Binding Sites List in 5esl
Iron binding site 1 out of 1 in the Saccharomyces Cerevisiae CYP51 (Lanosterol 14-Alpha Demethylase) T322I Mutant Complexed with Itraconazole


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 1 of Saccharomyces Cerevisiae CYP51 (Lanosterol 14-Alpha Demethylase) T322I Mutant Complexed with Itraconazole within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe702

b:32.6
occ:1.00
FE A:HEM702 0.0 32.6 1.0
NC A:HEM702 2.0 32.3 1.0
NA A:HEM702 2.0 31.1 1.0
NB A:HEM702 2.1 29.7 1.0
ND A:HEM702 2.1 29.4 1.0
N39 A:1YN701 2.1 32.2 1.0
SG A:CYS470 2.3 33.7 1.0
C4C A:HEM702 3.0 27.7 1.0
C1C A:HEM702 3.0 33.2 1.0
C40 A:1YN701 3.0 30.2 1.0
C1D A:HEM702 3.0 25.2 1.0
C4A A:HEM702 3.1 30.5 1.0
C4B A:HEM702 3.1 29.6 1.0
C1A A:HEM702 3.1 32.2 1.0
C1B A:HEM702 3.1 30.2 1.0
C4D A:HEM702 3.1 30.7 1.0
C38 A:1YN701 3.2 30.2 1.0
CHD A:HEM702 3.3 29.6 1.0
CB A:CYS470 3.4 28.3 1.0
CHC A:HEM702 3.4 33.6 1.0
CHB A:HEM702 3.4 28.7 1.0
CHA A:HEM702 3.5 32.2 1.0
CA A:CYS470 4.2 33.2 1.0
C3C A:HEM702 4.2 31.7 1.0
C2C A:HEM702 4.2 31.1 1.0
N41 A:1YN701 4.2 34.4 1.0
N37 A:1YN701 4.3 35.5 1.0
C3A A:HEM702 4.3 32.4 1.0
C2A A:HEM702 4.3 31.4 1.0
C2D A:HEM702 4.3 31.0 1.0
C3B A:HEM702 4.3 28.6 1.0
C2B A:HEM702 4.3 31.6 1.0
C3D A:HEM702 4.3 32.1 1.0
N A:GLY472 4.9 30.3 1.0

Reference:

A.Sagatova, M.V.Keniya, R.K.Wilson, M.Sabherwal, J.D.A.Tyndall, B.C.Monk. Structures of Lanosterol 14-Alpha Demethylase Mutants. To Be Published.
Page generated: Sun Dec 13 16:00:54 2020

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