Iron in PDB 6bpt: Crystal Structure of Ferrous Form of the Uncrosslinked F2-TYR157 Human Cysteine Dioxygenase

Enzymatic activity of Crystal Structure of Ferrous Form of the Uncrosslinked F2-TYR157 Human Cysteine Dioxygenase

All present enzymatic activity of Crystal Structure of Ferrous Form of the Uncrosslinked F2-TYR157 Human Cysteine Dioxygenase:
1.13.11.20;

Protein crystallography data

The structure of Crystal Structure of Ferrous Form of the Uncrosslinked F2-TYR157 Human Cysteine Dioxygenase, PDB code: 6bpt was solved by A.Liu, J.Li, I.Shin, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 38.04 / 2.40
Space group P 65
Cell size a, b, c (Å), α, β, γ (°) 131.783, 131.783, 34.316, 90.00, 90.00, 120.00
R / Rfree (%) 15.6 / 20.2

Other elements in 6bpt:

The structure of Crystal Structure of Ferrous Form of the Uncrosslinked F2-TYR157 Human Cysteine Dioxygenase also contains other interesting chemical elements:

Fluorine (F) 2 atoms

Iron Binding Sites:

The binding sites of Iron atom in the Crystal Structure of Ferrous Form of the Uncrosslinked F2-TYR157 Human Cysteine Dioxygenase (pdb code 6bpt). 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 Crystal Structure of Ferrous Form of the Uncrosslinked F2-TYR157 Human Cysteine Dioxygenase, PDB code: 6bpt:

Iron binding site 1 out of 1 in 6bpt

Go back to Iron Binding Sites List in 6bpt
Iron binding site 1 out of 1 in the Crystal Structure of Ferrous Form of the Uncrosslinked F2-TYR157 Human Cysteine Dioxygenase


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 1 of Crystal Structure of Ferrous Form of the Uncrosslinked F2-TYR157 Human Cysteine Dioxygenase within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe301

b:14.8
occ:1.00
 NE2 A:HIS86 2.2 16.4 1.0
NE2 A:HIS88 2.2 19.0 1.0
NE2 A:HIS140 2.3 17.2 1.0
O A:HOH420 2.4 28.5 1.0
O A:HOH484 2.5 22.6 1.0
O A:HOH491 2.5 15.6 1.0
CE1 A:HIS86 3.1 21.4 1.0
CD2 A:HIS88 3.2 15.0 1.0
CE1 A:HIS88 3.2 21.3 1.0
CD2 A:HIS86 3.2 19.9 1.0
CE1 A:HIS140 3.2 14.9 1.0
CD2 A:HIS140 3.2 20.0 1.0
OH A:F2Y157 3.9 29.8 1.0
ND1 A:HIS86 4.3 20.7 1.0
O A:HOH512 4.3 34.4 1.0
ND1 A:HIS88 4.3 25.2 1.0
CG A:HIS88 4.3 17.9 1.0
CG A:HIS86 4.3 17.2 1.0
ND1 A:HIS140 4.3 14.7 1.0
O A:HOH426 4.3 31.8 1.0
SG A:CYS93 4.4 18.9 0.3
CG A:HIS140 4.4 17.1 1.0
O A:HOH445 4.5 42.2 1.0
O A:HOH506 4.8 29.9 1.0
CZ A:F2Y157 4.9 23.8 1.0

Reference:

J.Li, W.P.Griffith, I.Davis, I.Shin, J.Wang, F.Li, Y.Wang, D.J.Wherritt, A.Liu. Cleavage of A Carbon-Fluorine Bond By An Engineered Cysteine Dioxygenase. Nat. Chem. Biol. V. 14 853 2018.
ISSN: ESSN 1552-4469
PubMed: 29942080
DOI: 10.1038/S41589-018-0085-5
Page generated: Tue Aug 6 14:37:44 2024

Last articles

Zn in 9JPJ
Zn in 9JP7
Zn in 9JPK
Zn in 9JPL
Zn in 9GN6
Zn in 9GN7
Zn in 9GKU
Zn in 9GKW
Zn in 9GKX
Zn in 9GL0
© Copyright 2008-2020 by atomistry.com
Home   |    Site Map   |    Copyright   |    Contact us   |    Privacy