Manganese in PDB 5t3v: A Novel Domain in Human Exog Converts Apoptotic Endonuclease to Dna- Repair Enzyme

Protein crystallography data

The structure of A Novel Domain in Human Exog Converts Apoptotic Endonuclease to Dna- Repair Enzyme, PDB code: 5t3v was solved by M.R.Szymanski, W.Y.Yin, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 49.71 / 2.60
Space group P 1 21 1
Cell size a, b, c (Å), α, β, γ (°) 73.340, 83.436, 74.771, 90.00, 113.42, 90.00
R / Rfree (%) 17.6 / 22.4

Manganese Binding Sites:

The binding sites of Manganese atom in the A Novel Domain in Human Exog Converts Apoptotic Endonuclease to Dna- Repair Enzyme (pdb code 5t3v). This binding sites where shown within 5.0 Angstroms radius around Manganese atom.
In total 2 binding sites of Manganese where determined in the A Novel Domain in Human Exog Converts Apoptotic Endonuclease to Dna- Repair Enzyme, PDB code: 5t3v:
Jump to Manganese binding site number: 1; 2;

Manganese binding site 1 out of 2 in 5t3v

Go back to Manganese Binding Sites List in 5t3v
Manganese binding site 1 out of 2 in the A Novel Domain in Human Exog Converts Apoptotic Endonuclease to Dna- Repair Enzyme


Mono view


Stereo pair view

A full contact list of Manganese with other atoms in the Mn binding site number 1 of A Novel Domain in Human Exog Converts Apoptotic Endonuclease to Dna- Repair Enzyme within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Mn401

b:69.0
occ:1.00
O A:HOH522 1.9 69.7 1.0
OD1 A:ASN171 2.1 60.3 1.0
O A:HOH505 2.1 40.2 1.0
O A:HOH507 2.2 51.0 1.0
O A:HOH506 2.3 72.2 1.0
O A:HOH510 2.5 49.6 1.0
HD21 A:ASN171 2.9 71.1 1.0
CG A:ASN171 3.0 57.7 1.0
ND2 A:ASN171 3.3 59.3 1.0
H A:HIS140 3.4 57.9 1.0
HB2 A:HIS140 3.7 56.4 1.0
HA2 A:GLY139 3.8 66.0 1.0
HD1 A:TRP175 3.9 64.3 1.0
O A:HOH521 4.0 32.3 1.0
N A:HIS140 4.1 48.2 1.0
OE1 A:GLU179 4.1 60.8 1.0
ND1 A:HIS140 4.2 52.2 1.0
HD22 A:ASN171 4.2 71.1 1.0
O A:ASN171 4.2 45.9 1.0
OE2 A:GLU179 4.3 63.4 1.0
CB A:ASN171 4.4 55.9 1.0
CB A:HIS140 4.5 47.0 1.0
OE1 A:GLN166 4.5 43.2 1.0
HA A:ASN171 4.5 64.1 1.0
CD A:GLU179 4.6 61.0 1.0
CD1 A:TRP175 4.7 53.6 1.0
CA A:GLY139 4.7 55.0 1.0
O A:HIS140 4.7 48.9 1.0
C A:ASN171 4.8 48.8 1.0
HE1 A:TRP175 4.8 62.4 1.0
CG A:HIS140 4.8 51.6 1.0
HB2 A:ASN171 4.8 67.0 1.0
CA A:HIS140 4.8 45.5 1.0
CA A:ASN171 4.8 53.4 1.0
C A:GLY139 4.9 51.7 1.0
HA3 A:GLY139 4.9 66.0 1.0

Manganese binding site 2 out of 2 in 5t3v

Go back to Manganese Binding Sites List in 5t3v
Manganese binding site 2 out of 2 in the A Novel Domain in Human Exog Converts Apoptotic Endonuclease to Dna- Repair Enzyme


Mono view


Stereo pair view

A full contact list of Manganese with other atoms in the Mn binding site number 2 of A Novel Domain in Human Exog Converts Apoptotic Endonuclease to Dna- Repair Enzyme within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Mn401

b:61.2
occ:1.00
OD1 B:ASN171 2.0 78.8 1.0
O B:HOH518 2.3 43.0 1.0
O B:HOH511 2.3 56.7 1.0
O B:HOH508 2.3 65.7 1.0
O B:HOH536 2.4 49.9 1.0
O B:HOH512 2.4 64.9 1.0
CG B:ASN171 3.0 70.7 1.0
HD21 B:ASN171 3.1 89.3 1.0
H B:HIS140 3.4 55.4 1.0
ND2 B:ASN171 3.4 74.5 1.0
HD1 B:TRP175 3.6 58.5 1.0
HA2 B:GLY139 3.8 57.9 1.0
HB2 B:HIS140 3.8 55.8 1.0
OE2 B:GLU179 3.9 57.0 1.0
N B:HIS140 4.1 46.1 1.0
O B:ASN171 4.2 47.8 1.0
ND1 B:HIS140 4.3 53.4 1.0
OE1 B:GLU179 4.3 64.7 1.0
HD22 B:ASN171 4.3 89.3 1.0
OE1 B:GLN166 4.3 43.5 1.0
HA B:ASN171 4.3 65.8 1.0
O B:HOH502 4.3 42.5 1.0
CB B:ASN171 4.4 63.2 1.0
CD1 B:TRP175 4.5 48.7 1.0
CD B:GLU179 4.5 59.0 1.0
CA B:GLY139 4.6 48.2 1.0
CB B:HIS140 4.6 46.5 1.0
O B:HIS140 4.6 37.9 1.0
C B:ASN171 4.7 49.3 1.0
HA3 B:GLY139 4.7 57.9 1.0
CA B:ASN171 4.7 54.8 1.0
HB2 B:ASN171 4.7 75.8 1.0
C B:GLY139 4.8 47.1 1.0
HE1 B:TRP175 4.8 58.5 1.0
HE22 B:GLN166 4.9 53.8 1.0
CA B:HIS140 4.9 43.1 1.0
CG B:HIS140 4.9 49.4 1.0
HB3 B:ASN171 5.0 75.8 1.0

Reference:

M.R.Szymanski, W.Yu, A.M.Gmyrek, M.A.White, I.J.Molineux, J.C.Lee, Y.W.Yin. A Domain in Human Exog Converts Apoptotic Endonuclease to Dna-Repair Exonuclease. Nat Commun V. 8 14959 2017.
ISSN: ESSN 2041-1723
PubMed: 28466855
DOI: 10.1038/NCOMMS14959
Page generated: Tue Dec 15 04:46:40 2020

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