Zinc in PDB 7k32: Crystal Structure of Endonuclease Q Complex with 27-Mer Duplex Substrate with An Abasic Lesion at the Active Site

Protein crystallography data

The structure of Crystal Structure of Endonuclease Q Complex with 27-Mer Duplex Substrate with An Abasic Lesion at the Active Site, PDB code: 7k32 was solved by K.Shi, N.M.Moeller, S.Banerjee, L.Yin, K.Orellana, H.Aihara, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 88.59 / 3.11
Space group H 3
Cell size a, b, c (Å), α, β, γ (°) 154.02, 154.02, 118.51, 90, 90, 120
R / Rfree (%) 19.9 / 24.7

Other elements in 7k32:

The structure of Crystal Structure of Endonuclease Q Complex with 27-Mer Duplex Substrate with An Abasic Lesion at the Active Site also contains other interesting chemical elements:

Bromine (Br) 1 atom
Magnesium (Mg) 1 atom

Zinc Binding Sites:

The binding sites of Zinc atom in the Crystal Structure of Endonuclease Q Complex with 27-Mer Duplex Substrate with An Abasic Lesion at the Active Site (pdb code 7k32). This binding sites where shown within 5.0 Angstroms radius around Zinc atom.
In total 2 binding sites of Zinc where determined in the Crystal Structure of Endonuclease Q Complex with 27-Mer Duplex Substrate with An Abasic Lesion at the Active Site, PDB code: 7k32:
Jump to Zinc binding site number: 1; 2;

Zinc binding site 1 out of 2 in 7k32

Go back to Zinc Binding Sites List in 7k32
Zinc binding site 1 out of 2 in the Crystal Structure of Endonuclease Q Complex with 27-Mer Duplex Substrate with An Abasic Lesion at the Active Site


Mono view


Stereo pair view

A full contact list of Zinc with other atoms in the Zn binding site number 1 of Crystal Structure of Endonuclease Q Complex with 27-Mer Duplex Substrate with An Abasic Lesion at the Active Site within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Zn501

b:151.6
occ:1.00
SG A:CYS252 2.3 151.0 1.0
SG A:CYS249 2.3 215.9 1.0
SG A:CYS271 2.3 141.9 1.0
SG A:CYS268 2.3 156.3 1.0
CB A:CYS271 2.7 162.8 1.0
CB A:CYS249 3.0 176.4 1.0
CB A:CYS268 3.3 158.2 1.0
N A:CYS252 3.4 175.7 1.0
CB A:CYS252 3.5 144.8 1.0
CA A:CYS252 3.9 163.2 1.0
CA A:CYS271 4.2 177.8 1.0
CB A:ARG251 4.4 159.3 1.0
N A:TYR253 4.4 157.1 1.0
CA A:CYS249 4.4 144.3 1.0
C A:ARG251 4.5 171.8 1.0
N A:ARG251 4.5 123.5 1.0
C A:CYS252 4.5 171.4 1.0
CA A:ARG251 4.7 155.4 1.0
OH A:TYR256 4.7 169.5 1.0
N A:GLY273 4.8 153.1 1.0
CA A:CYS268 4.8 153.9 1.0
C A:CYS271 4.8 164.9 1.0
N A:CYS271 4.9 190.8 1.0
OG1 A:THR254 4.9 166.8 1.0
C A:CYS249 5.0 139.3 1.0
CA A:GLY273 5.0 152.6 1.0
N A:THR254 5.0 136.8 1.0

Zinc binding site 2 out of 2 in 7k32

Go back to Zinc Binding Sites List in 7k32
Zinc binding site 2 out of 2 in the Crystal Structure of Endonuclease Q Complex with 27-Mer Duplex Substrate with An Abasic Lesion at the Active Site


Mono view


Stereo pair view

A full contact list of Zinc with other atoms in the Zn binding site number 2 of Crystal Structure of Endonuclease Q Complex with 27-Mer Duplex Substrate with An Abasic Lesion at the Active Site within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Zn502

b:174.8
occ:1.00
OE2 A:GLU76 2.0 205.6 1.0
NE2 A:HIS139 2.1 153.7 1.0
OE1 A:GLU76 2.1 191.6 1.0
ND1 A:HIS84 2.1 141.4 1.0
OD1 A:ASN193 2.2 281.2 1.0
CD A:GLU76 2.4 168.9 1.0
OP2 C:3DR14 2.7 168.3 1.0
CE1 A:HIS84 2.9 138.0 1.0
CE1 A:HIS139 3.0 127.9 1.0
CD2 A:HIS139 3.1 139.2 1.0
CG A:ASN193 3.3 237.9 1.0
CG A:HIS84 3.3 118.1 1.0
OP1 C:3DR14 3.3 190.6 1.0
P C:3DR14 3.5 176.1 1.0
CB A:HIS84 3.9 102.5 1.0
ND2 A:ASN193 3.9 244.7 1.0
CG A:GLU76 3.9 119.5 1.0
NE2 A:HIS84 4.1 137.3 1.0
ND1 A:HIS139 4.1 125.2 1.0
CE1 A:HIS8 4.1 116.8 1.0
NE2 A:HIS8 4.1 110.4 1.0
CG A:HIS139 4.2 119.8 1.0
CD2 A:HIS84 4.3 125.9 1.0
NH1 A:ARG114 4.5 116.0 1.0
NE2 A:HIS10 4.5 109.0 1.0
CB A:ASN193 4.6 191.5 1.0
O5' C:3DR14 4.6 159.0 1.0
O3' C:DC13 4.7 187.9 1.0
C5' C:3DR14 4.7 130.9 1.0
CZ A:ARG114 4.8 111.8 1.0
CB A:GLU76 4.9 86.1 1.0

Reference:

K.Shi, N.H.Moeller, S.Banerjee, J.L.Mccann, M.A.Carpenter, L.Yin, R.Moorthy, K.Orellana, D.A.Harki, R.S.Harris, H.Aihara. Structural Basis For Recognition of Distinct Deaminated Dna Lesions By Endonuclease Q. Proc.Natl.Acad.Sci.Usa V. 118 2021.
ISSN: ESSN 1091-6490
PubMed: 33658373
DOI: 10.1073/PNAS.2021120118
Page generated: Sat Apr 3 18:35:39 2021

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