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Iron in PDB 6ajs: H109S Mutant Form of Uracil Dna Glycosylase X.

Protein crystallography data

The structure of H109S Mutant Form of Uracil Dna Glycosylase X., PDB code: 6ajs was solved by W.C.Ahn, S.Aroli, U.Varshney, E.J.Woo, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 28.02 / 1.63
Space group P 1 21 1
Cell size a, b, c (Å), α, β, γ (°) 36.229, 51.393, 54.444, 90.00, 105.21, 90.00
R / Rfree (%) 16 / 19.7

Iron Binding Sites:

The binding sites of Iron atom in the H109S Mutant Form of Uracil Dna Glycosylase X. (pdb code 6ajs). This binding sites where shown within 5.0 Angstroms radius around Iron atom.
In total 4 binding sites of Iron where determined in the H109S Mutant Form of Uracil Dna Glycosylase X., PDB code: 6ajs:
Jump to Iron binding site number: 1; 2; 3; 4;

Iron binding site 1 out of 4 in 6ajs

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Iron binding site 1 out of 4 in the H109S Mutant Form of Uracil Dna Glycosylase X.


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 1 of H109S Mutant Form of Uracil Dna Glycosylase X. within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe301

b:16.0
occ:1.00
FE1 A:SF4301 0.0 16.0 1.0
S3 A:SF4301 2.3 15.6 1.0
S2 A:SF4301 2.3 15.8 1.0
SG A:CYS120 2.3 15.7 1.0
S4 A:SF4301 2.3 16.6 1.0
FE3 A:SF4301 2.7 16.4 1.0
FE4 A:SF4301 2.7 17.2 1.0
FE2 A:SF4301 2.7 17.0 1.0
CB A:CYS120 3.2 16.2 1.0
CA A:CYS120 3.9 16.7 1.0
S1 A:SF4301 3.9 17.2 1.0
N A:LYS94 4.0 14.7 1.0
CD1 A:TRP123 4.2 16.3 1.0
CB A:LYS94 4.4 17.3 1.0
NE1 A:TRP123 4.5 16.7 1.0
ND1 A:HIS95 4.6 16.4 1.0
CG A:LYS94 4.6 27.7 1.0
SG A:CYS24 4.7 16.9 1.0
CA A:LYS94 4.7 15.1 1.0
N A:CYS120 4.7 16.0 1.0
SG A:CYS27 4.8 17.6 1.0
CA A:VAL93 4.9 15.4 1.0
CB A:VAL93 4.9 19.2 1.0
N A:HIS95 4.9 14.2 1.0
C A:VAL93 5.0 15.5 1.0

Iron binding site 2 out of 4 in 6ajs

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Iron binding site 2 out of 4 in the H109S Mutant Form of Uracil Dna Glycosylase X.


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 2 of H109S Mutant Form of Uracil Dna Glycosylase X. within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe301

b:17.0
occ:1.00
FE2 A:SF4301 0.0 17.0 1.0
S4 A:SF4301 2.3 16.6 1.0
S1 A:SF4301 2.3 17.2 1.0
S3 A:SF4301 2.3 15.6 1.0
SG A:CYS27 2.4 17.6 1.0
FE4 A:SF4301 2.6 17.2 1.0
FE1 A:SF4301 2.7 16.0 1.0
FE3 A:SF4301 2.7 16.4 1.0
N A:CYS27 3.4 15.3 1.0
CB A:CYS27 3.4 18.0 1.0
CA A:CYS27 3.8 16.3 1.0
S2 A:SF4301 3.9 15.8 1.0
C A:GLY26 4.2 19.0 1.0
C A:CYS27 4.2 16.1 1.0
O A:CYS27 4.4 20.0 1.0
CB A:LEU29 4.5 16.9 1.0
ND1 A:HIS95 4.5 16.4 1.0
N A:GLY26 4.6 17.8 1.0
CA A:GLY26 4.6 16.3 1.0
N A:LEU29 4.6 18.1 1.0
SG A:CYS120 4.7 15.7 1.0
CB A:CYS120 4.8 16.2 1.0
CG A:LEU29 4.9 16.9 1.0
SG A:CYS24 5.0 16.9 1.0
O A:GLY26 5.0 21.9 1.0
N A:GLY28 5.0 20.2 1.0

Iron binding site 3 out of 4 in 6ajs

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Iron binding site 3 out of 4 in the H109S Mutant Form of Uracil Dna Glycosylase X.


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 3 of H109S Mutant Form of Uracil Dna Glycosylase X. within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe301

b:16.4
occ:1.00
FE3 A:SF4301 0.0 16.4 1.0
S4 A:SF4301 2.3 16.6 1.0
S2 A:SF4301 2.3 15.8 1.0
S1 A:SF4301 2.3 17.2 1.0
SG A:CYS24 2.4 16.9 1.0
FE4 A:SF4301 2.7 17.2 1.0
FE1 A:SF4301 2.7 16.0 1.0
FE2 A:SF4301 2.7 17.0 1.0
CB A:CYS24 3.3 16.8 1.0
N A:GLY26 3.6 17.8 1.0
S3 A:SF4301 3.9 15.6 1.0
CA A:GLY26 4.0 16.3 1.0
NE1 A:TRP123 4.1 16.7 1.0
C A:CYS24 4.2 17.0 1.0
N A:CYS27 4.3 15.3 1.0
O A:CYS24 4.3 18.6 1.0
CA A:CYS24 4.3 16.0 1.0
ND1 A:HIS95 4.4 16.4 1.0
N A:ARG25 4.4 17.1 1.0
CB A:ALA4 4.4 18.7 1.0
C A:GLY26 4.5 19.0 1.0
C A:ARG25 4.5 18.4 1.0
CD1 A:TRP123 4.6 16.3 1.0
CE1 A:HIS95 4.6 18.8 1.0
SG A:CYS120 4.7 15.7 1.0
CA A:ARG25 4.8 17.6 1.0

Iron binding site 4 out of 4 in 6ajs

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Iron binding site 4 out of 4 in the H109S Mutant Form of Uracil Dna Glycosylase X.


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 4 of H109S Mutant Form of Uracil Dna Glycosylase X. within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe301

b:17.2
occ:1.00
FE4 A:SF4301 0.0 17.2 1.0
ND1 A:HIS95 2.1 16.4 1.0
S3 A:SF4301 2.3 15.6 1.0
S2 A:SF4301 2.3 15.8 1.0
S1 A:SF4301 2.3 17.2 1.0
FE2 A:SF4301 2.6 17.0 1.0
FE3 A:SF4301 2.7 16.4 1.0
FE1 A:SF4301 2.7 16.0 1.0
CE1 A:HIS95 3.0 18.8 1.0
CG A:HIS95 3.2 17.1 1.0
CB A:HIS95 3.6 16.8 1.0
S4 A:SF4301 3.8 16.6 1.0
N A:HIS95 4.0 14.2 1.0
NE2 A:HIS95 4.1 18.0 1.0
CD2 A:HIS95 4.3 15.0 1.0
CA A:HIS95 4.4 14.7 1.0
C A:LYS94 4.5 17.6 1.0
N A:TYR30 4.5 18.1 1.0
SG A:CYS27 4.7 17.6 1.0
CB A:TYR30 4.7 17.7 1.0
CB A:LYS94 4.7 17.3 1.0
CB A:LEU29 4.7 16.9 1.0
N A:LYS94 4.8 14.7 1.0
SG A:CYS24 4.8 16.9 1.0
SG A:CYS120 4.8 15.7 1.0
CB A:CYS24 4.9 16.8 1.0
CA A:TYR30 4.9 17.7 1.0
CA A:LYS94 4.9 15.1 1.0
O A:CYS24 4.9 18.6 1.0

Reference:

W.C.Ahn, S.Aroli, J.H.Kim, J.H.Moon, G.S.Lee, M.H.Lee, P.B.Sang, B.H.Oh, U.Varshney, E.J.Woo. Covalent Binding of Uracil Dna Glycosylase Udgx to Abasic Dna Upon Uracil Excision. Nat.Chem.Biol. V. 15 607 2019.
ISSN: ESSN 1552-4469
PubMed: 31101917
DOI: 10.1038/S41589-019-0289-3
Page generated: Tue Aug 6 13:45:08 2024

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