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Iron in PDB 4o6s: 1.32A Resolution Structure of the Hemophore Hasa From Pseudomonas Aeruginosa (H83A Mutant, Zinc Bound)

Protein crystallography data

The structure of 1.32A Resolution Structure of the Hemophore Hasa From Pseudomonas Aeruginosa (H83A Mutant, Zinc Bound), PDB code: 4o6s was solved by S.Lovell, R.Kumar, K.P.Battaile, H.Matsumura, H.Yao, J.C.Rodriguez, P.Moenne-Loccoz, M.Rivera, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 34.63 / 1.32
Space group P 1 21 1
Cell size a, b, c (Å), α, β, γ (°) 34.898, 66.232, 40.999, 90.00, 97.13, 90.00
R / Rfree (%) 14.3 / 16.8

Other elements in 4o6s:

The structure of 1.32A Resolution Structure of the Hemophore Hasa From Pseudomonas Aeruginosa (H83A Mutant, Zinc Bound) also contains other interesting chemical elements:

Zinc (Zn) 9 atoms

Iron Binding Sites:

The binding sites of Iron atom in the 1.32A Resolution Structure of the Hemophore Hasa From Pseudomonas Aeruginosa (H83A Mutant, Zinc Bound) (pdb code 4o6s). 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 1.32A Resolution Structure of the Hemophore Hasa From Pseudomonas Aeruginosa (H83A Mutant, Zinc Bound), PDB code: 4o6s:

Iron binding site 1 out of 1 in 4o6s

Go back to Iron Binding Sites List in 4o6s
Iron binding site 1 out of 1 in the 1.32A Resolution Structure of the Hemophore Hasa From Pseudomonas Aeruginosa (H83A Mutant, Zinc Bound)


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 1 of 1.32A Resolution Structure of the Hemophore Hasa From Pseudomonas Aeruginosa (H83A Mutant, Zinc Bound) within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe205

b:7.0
occ:1.00
FE A:HEM205 0.0 7.0 1.0
ND A:HEM205 2.0 6.6 1.0
NA A:HEM205 2.0 6.3 1.0
NE2 A:HIS32 2.0 6.3 1.0
NC A:HEM205 2.0 6.5 1.0
NB A:HEM205 2.1 6.7 1.0
OH A:TYR75 2.1 6.4 1.0
CE1 A:HIS32 3.0 7.0 1.0
C4C A:HEM205 3.0 5.7 1.0
CZ A:TYR75 3.0 6.1 1.0
C4A A:HEM205 3.0 7.8 1.0
C1D A:HEM205 3.0 6.5 1.0
CD2 A:HIS32 3.0 7.2 1.0
C4D A:HEM205 3.0 7.4 1.0
C1A A:HEM205 3.1 7.9 1.0
C1B A:HEM205 3.1 7.1 1.0
C1C A:HEM205 3.1 6.5 1.0
C4B A:HEM205 3.1 6.6 1.0
CHD A:HEM205 3.4 6.5 1.0
CHB A:HEM205 3.4 8.1 1.0
CHA A:HEM205 3.4 7.7 1.0
CHC A:HEM205 3.4 6.8 1.0
CE2 A:TYR75 3.8 7.2 1.0
CE1 A:TYR75 3.8 7.2 1.0
ND1 A:HIS32 4.1 8.2 1.0
CG A:HIS32 4.2 7.2 1.0
O2 A:EDO201 4.2 15.7 1.0
C2A A:HEM205 4.3 9.9 1.0
C3D A:HEM205 4.3 7.4 1.0
C3C A:HEM205 4.3 6.8 1.0
C3A A:HEM205 4.3 9.4 1.0
C2C A:HEM205 4.3 7.2 1.0
C2D A:HEM205 4.3 7.0 1.0
C3B A:HEM205 4.3 8.0 1.0
C2B A:HEM205 4.3 8.0 1.0
C2 A:EDO201 4.5 20.7 1.0
CB A:ALA83 4.8 8.4 1.0
CD2 A:TYR75 5.0 5.7 1.0

Reference:

R.Kumar, H.Matsumura, S.Lovell, H.Yao, J.C.Rodriguez, K.P.Battaile, P.Moenne-Loccoz, M.Rivera. Replacing the Axial Ligand Tyrosine 75 or Its Hydrogen Bond Partner Histidine 83 Minimally Affects Hemin Acquisition By the Hemophore Hasap From Pseudomonas Aeruginosa. Biochemistry V. 53 2112 2014.
ISSN: ISSN 0006-2960
PubMed: 24625274
DOI: 10.1021/BI500030P
Page generated: Sun Dec 13 15:43:31 2020

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