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Iron in PDB 8e7w: Rstspo A139T with Heme

Protein crystallography data

The structure of Rstspo A139T with Heme, PDB code: 8e7w was solved by J.Liu, C.Hiser, F.Li, R.Garavito, S.Ferguson-Miller, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 28.95 / 2.10
Space group C 1 2 1
Cell size a, b, c (Å), α, β, γ (°) 58.399, 99.568, 95.812, 90, 100.16, 90
R / Rfree (%) 19.5 / 25.3

Iron Binding Sites:

The binding sites of Iron atom in the Rstspo A139T with Heme (pdb code 8e7w). 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 Rstspo A139T with Heme, PDB code: 8e7w:

Iron binding site 1 out of 1 in 8e7w

Go back to Iron Binding Sites List in 8e7w
Iron binding site 1 out of 1 in the Rstspo A139T with Heme


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 1 of Rstspo A139T with Heme within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Fe201

b:32.4
occ:0.77
FE B:HEM201 0.0 32.4 0.8
NB B:HEM201 2.0 33.4 0.6
NC B:HEM201 2.1 30.7 0.7
NA B:HEM201 2.1 43.1 1.0
ND B:HEM201 2.1 39.0 1.0
O B:HOH336 2.7 43.0 1.0
C1B B:HEM201 3.0 37.9 1.0
C4A B:HEM201 3.0 40.4 1.0
C4B B:HEM201 3.1 33.2 0.6
C1D B:HEM201 3.1 36.3 1.0
C4C B:HEM201 3.1 35.5 1.0
C1C B:HEM201 3.1 32.8 0.6
C1A B:HEM201 3.1 39.4 1.0
C4D B:HEM201 3.1 44.0 1.0
CHB B:HEM201 3.4 38.2 1.0
CHD B:HEM201 3.4 33.4 1.0
CHC B:HEM201 3.4 33.5 1.0
CHA B:HEM201 3.5 42.2 1.0
NE1 B:TRP50 4.0 30.6 1.0
C2B B:HEM201 4.3 40.5 1.0
C3A B:HEM201 4.3 39.3 1.0
C3B B:HEM201 4.3 39.3 1.0
C2A B:HEM201 4.3 40.5 1.0
C2D B:HEM201 4.3 40.6 1.0
C3D B:HEM201 4.3 43.9 1.0
CD1 B:TRP50 4.3 36.4 1.0
C3C B:HEM201 4.3 33.1 1.0
C2C B:HEM201 4.3 31.9 0.7
CD1 B:PHE46 4.3 33.9 1.0
CE2 B:PHE92 4.4 30.6 1.0
O B:HOH331 4.5 41.5 1.0
O B:HOH306 4.6 42.0 1.0
CB B:PHE46 4.6 37.2 1.0
CG B:PHE46 4.7 36.0 1.0
CZ3 B:TRP87 4.7 30.7 1.0
OG1 B:THR88 4.9 31.3 1.0

Reference:

J.Liu, C.Hiser, F.Li, R.Hall, R.M.Garavito, S.Ferguson-Miller. New Tspo Crystal Structures of Mutant and Heme-Bound Forms with Altered Flexibility, Ligand Binding, and Porphyrin Degradation Activity. Biochemistry 2023.
ISSN: ISSN 0006-2960
PubMed: 36947867
DOI: 10.1021/ACS.BIOCHEM.2C00612
Page generated: Sat Aug 10 00:54:06 2024

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