Atomistry » Iron » PDB 5fp4-5g6e » 5fyf
Atomistry »
  Iron »
    PDB 5fp4-5g6e »
      5fyf »

Iron in PDB 5fyf: Structure of CYP153A From Marinobacter Aquaeolei

Protein crystallography data

The structure of Structure of CYP153A From Marinobacter Aquaeolei, PDB code: 5fyf was solved by H.R.Danesh Azari, C.Spandolf, S.M.Hoffman, M.Weissenborn, B.Hauer, G.Grogan, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 107.59 / 2.04
Space group P 21 21 21
Cell size a, b, c (Å), α, β, γ (°) 59.590, 71.110, 215.180, 90.00, 90.00, 90.00
R / Rfree (%) 19.8 / 23.7

Iron Binding Sites:

The binding sites of Iron atom in the Structure of CYP153A From Marinobacter Aquaeolei (pdb code 5fyf). This binding sites where shown within 5.0 Angstroms radius around Iron atom.
In total 2 binding sites of Iron where determined in the Structure of CYP153A From Marinobacter Aquaeolei, PDB code: 5fyf:
Jump to Iron binding site number: 1; 2;

Iron binding site 1 out of 2 in 5fyf

Go back to Iron Binding Sites List in 5fyf
Iron binding site 1 out of 2 in the Structure of CYP153A From Marinobacter Aquaeolei


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 1 of Structure of CYP153A From Marinobacter Aquaeolei within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe1475

b:27.3
occ:1.00
FE A:HEM1475 0.0 27.3 1.0
ND A:HEM1475 1.9 24.2 1.0
NB A:HEM1475 2.0 22.3 1.0
NA A:HEM1475 2.0 22.2 1.0
NC A:HEM1475 2.1 27.3 1.0
SG A:CYS422 2.3 30.1 1.0
C4D A:HEM1475 3.0 25.9 1.0
C1D A:HEM1475 3.0 27.3 1.0
C1B A:HEM1475 3.0 27.8 1.0
C4A A:HEM1475 3.0 21.2 1.0
C4B A:HEM1475 3.0 30.1 1.0
C1A A:HEM1475 3.0 24.0 1.0
C4C A:HEM1475 3.0 27.0 1.0
C1C A:HEM1475 3.1 29.9 1.0
CB A:CYS422 3.4 29.5 1.0
CHB A:HEM1475 3.4 24.9 1.0
CHA A:HEM1475 3.4 27.0 1.0
CHD A:HEM1475 3.4 26.4 1.0
CHC A:HEM1475 3.5 27.2 1.0
O A:GLY311 4.0 32.0 1.0
CA A:CYS422 4.1 27.0 1.0
C2B A:HEM1475 4.2 26.4 1.0
C3A A:HEM1475 4.2 22.9 1.0
C3D A:HEM1475 4.2 23.8 1.0
C2D A:HEM1475 4.2 26.2 1.0
C3B A:HEM1475 4.2 25.4 1.0
C2A A:HEM1475 4.2 24.1 1.0
C3C A:HEM1475 4.3 31.3 1.0
C2C A:HEM1475 4.3 28.6 1.0
N A:GLY424 4.6 30.6 1.0
C A:GLY311 4.7 30.7 1.0
C A:CYS422 4.7 28.5 1.0
N A:MET423 4.8 29.3 1.0
CA A:GLY311 4.9 31.8 1.0

Iron binding site 2 out of 2 in 5fyf

Go back to Iron Binding Sites List in 5fyf
Iron binding site 2 out of 2 in the Structure of CYP153A From Marinobacter Aquaeolei


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 2 of Structure of CYP153A From Marinobacter Aquaeolei within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Fe1475

b:38.4
occ:1.00
FE B:HEM1475 0.0 38.4 1.0
ND B:HEM1475 1.9 44.0 1.0
NA B:HEM1475 2.0 37.7 1.0
NC B:HEM1475 2.1 37.4 1.0
NB B:HEM1475 2.1 35.7 1.0
SG B:CYS422 2.3 39.5 1.0
C1D B:HEM1475 2.9 38.3 1.0
C4D B:HEM1475 2.9 40.6 1.0
C4A B:HEM1475 3.0 39.3 1.0
C1A B:HEM1475 3.0 44.9 1.0
C4C B:HEM1475 3.0 39.5 1.0
C1B B:HEM1475 3.1 38.6 1.0
C4B B:HEM1475 3.1 38.1 1.0
C1C B:HEM1475 3.1 39.0 1.0
CHD B:HEM1475 3.3 38.7 1.0
CHB B:HEM1475 3.4 37.2 1.0
CHA B:HEM1475 3.4 42.6 1.0
CB B:CYS422 3.4 42.3 1.0
CHC B:HEM1475 3.5 40.5 1.0
O B:GLY311 4.0 36.7 1.0
CA B:CYS422 4.2 42.2 1.0
C3A B:HEM1475 4.2 44.1 1.0
C2D B:HEM1475 4.2 43.0 1.0
C3D B:HEM1475 4.2 43.3 1.0
C2A B:HEM1475 4.2 42.9 1.0
C3C B:HEM1475 4.3 39.6 1.0
C2B B:HEM1475 4.3 32.6 1.0
C2C B:HEM1475 4.3 34.9 1.0
C3B B:HEM1475 4.4 34.9 1.0
N B:GLY424 4.6 39.2 1.0
C B:GLY311 4.7 42.7 1.0
C B:CYS422 4.8 33.8 1.0
N B:MET423 4.8 38.0 1.0
CA B:GLY311 4.9 41.0 1.0

Reference:

S.M.Hoffman, H.-R.Danesh Azari, C.Spandolf, M.Weissenborn, G.Grogan, B.Hauer. Structure-Guided Redesign of CYP153AM.Aqfor the Improved Terminal Hydroxylation of Fatty Acids Chemcatchem 2016.
ISSN: ESSN 1867-3899
DOI: 10.1002/CCTC.201600680
Page generated: Tue Aug 6 01:23:48 2024

Last articles

Zn in 9JYW
Zn in 9IR4
Zn in 9IR3
Zn in 9GMX
Zn in 9GMW
Zn in 9JEJ
Zn in 9ERF
Zn in 9ERE
Zn in 9EGV
Zn in 9EGW
© Copyright 2008-2020 by atomistry.com
Home   |    Site Map   |    Copyright   |    Contact us   |    Privacy