Atomistry » Iron » PDB 8k6y-8p02 » 8kht
Atomistry »
  Iron »
    PDB 8k6y-8p02 »
      8kht »

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: Thu Aug 7 18:56:09 2025

Last articles

Mg in 5XTM
Mg in 5XUT
Mg in 5XUS
Mg in 5XUJ
Mg in 5XUI
Mg in 5XU1
Mg in 5XT8
Mg in 5XT2
Mg in 5XR7
Mg in 5XR6
© Copyright 2008-2020 by atomistry.com
Home   |    Site Map   |    Copyright   |    Contact us   |    Privacy