Iron in PDB 8kht: The Structure of RV0097 with Substrate

Protein crystallography data

The structure of The Structure of RV0097 with Substrate, PDB code: 8kht was solved by J.Chen, J.Zhou, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 28.37 / 2.05
Space group P 1 21 1
Cell size a, b, c (Å), α, β, γ (°) 56.74, 89.07, 63.51, 90, 90.03, 90
R / Rfree (%) 20.7 / 26.6

Iron Binding Sites:

The binding sites of Iron atom in the The Structure of RV0097 with Substrate (pdb code 8kht). This binding sites where shown within 5.0 Angstroms radius around Iron atom.
In total 2 binding sites of Iron where determined in the The Structure of RV0097 with Substrate, PDB code: 8kht:
Jump to Iron binding site number: 1; 2;

Iron binding site 1 out of 2 in 8kht

Go back to Iron Binding Sites List in 8kht
Iron binding site 1 out of 2 in the The Structure of RV0097 with Substrate


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 1 of The Structure of RV0097 with Substrate within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe401

b:55.6
occ:1.00
NE2 A:HIS113 2.3 32.5 1.0
NE2 A:HIS276 2.4 29.6 1.0
OD1 A:ASP115 2.4 32.0 1.0
O A:HOH596 2.4 35.5 1.0
O A:HOH598 2.4 33.3 1.0
O A:HOH554 2.5 33.3 1.0
CE1 A:HIS113 3.1 30.7 1.0
CD2 A:HIS276 3.3 26.7 1.0
CE1 A:HIS276 3.4 33.4 1.0
CD2 A:HIS113 3.4 30.3 1.0
CG A:ASP115 3.4 36.4 1.0
OD2 A:ASP115 3.7 31.4 1.0
O A:HOH534 3.8 33.5 1.0
O A:HOH518 3.8 36.1 1.0
NH1 A:ARG291 4.0 31.1 1.0
O A:HOH602 4.0 40.9 1.0
ND1 A:HIS113 4.3 37.3 1.0
CG A:HIS276 4.4 31.1 1.0
CG A:HIS113 4.4 34.3 1.0
ND1 A:HIS276 4.4 31.5 1.0
CB A:ASP115 4.7 31.8 1.0

Iron binding site 2 out of 2 in 8kht

Go back to Iron Binding Sites List in 8kht
Iron binding site 2 out of 2 in the The Structure of RV0097 with Substrate


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 2 of The Structure of RV0097 with Substrate within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Fe401

b:56.1
occ:1.00
NE2 B:HIS113 2.3 33.3 1.0
NE2 B:HIS276 2.4 33.3 1.0
OD1 B:ASP115 2.4 28.0 1.0
O B:HOH595 2.4 32.5 1.0
O B:HOH546 2.4 33.3 1.0
O B:HOH587 2.4 35.7 1.0
CE1 B:HIS113 3.2 33.5 1.0
CD2 B:HIS276 3.2 26.9 1.0
CG B:ASP115 3.4 38.1 1.0
CD2 B:HIS113 3.4 28.7 1.0
CE1 B:HIS276 3.4 31.2 1.0
OD2 B:ASP115 3.6 32.0 1.0
O B:HOH603 3.8 41.3 1.0
O B:HOH545 3.8 38.1 1.0
NH1 B:ARG291 3.9 32.7 1.0
O B:HOH527 3.9 35.2 1.0
ND1 B:HIS113 4.3 38.2 1.0
CG B:HIS276 4.4 32.0 1.0
CG B:HIS113 4.4 36.0 1.0
ND1 B:HIS276 4.5 30.1 1.0
CB B:ASP115 4.7 29.3 1.0

Reference:

T.Y.Chen, J.Chen, M.W.Ruszczycky, D.Hilovsky, T.Hostetler, X.Liu, J.Zhou, W.Chang. Variation in Biosynthesis and Metal-Binding Properties of Isonitrile-Containing Peptides Produced By Mycobacteria Versus Streptomyces. Acs Catalysis V. 14 4975 2024.
ISSN: ESSN 2155-5435
DOI: 10.1021/ACSCATAL.4C00645
Page generated: Sat Aug 10 07:38:43 2024

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