Manganese in PDB 8a1c: Trai Trans-Esterase Domain From PKM101 (Dna Bound)

The structure of Trai Trans-Esterase Domain From PKM101 (Dna Bound), PDB code: 8a1c was solved by A.Breidenstein, R.P.-A.Berntsson, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å)	40.82 / 2.10
Space group	P 21 21 21
Cell size a, b, c (Å), α, β, γ (°)	43.444, 81.643, 90.785, 90, 90, 90
R / Rfree (%)	22.5 / 26.7

The binding sites of Manganese atom in the Trai Trans-Esterase Domain From PKM101 (Dna Bound) (pdb code 8a1c). This binding sites where shown within 5.0 Angstroms radius around Manganese atom.
In total only one binding site of Manganese was determined in the Trai Trans-Esterase Domain From PKM101 (Dna Bound), PDB code: 8a1c:

Manganese binding site 1 out of 1 in the Trai Trans-Esterase Domain From PKM101 (Dna Bound)


Mono view


Stereo pair view

A full contact list of Manganese with other atoms in the Mn binding site number 1 of Trai Trans-Esterase Domain From PKM101 (Dna Bound) within 5.0Å range: probe atom residue distance (Å) B Occ A:Mn401 b:39.9 occ:1.00 NE2 A:HIS162 2.1 51.1 1.0 O A:HOH529 2.1 55.3 1.0 ND1 A:HIS149 2.2 50.2 1.0 NE2 A:HIS160 2.3 47.4 1.0 HO3' C:DT11 2.9 126.9 1.0 CD2 A:HIS162 3.0 48.2 1.0 HB2 A:HIS149 3.1 53.0 1.0 HD2 A:HIS162 3.1 58.3 1.0 CE1 A:HIS162 3.2 58.0 1.0 CE1 A:HIS149 3.2 53.6 1.0 CE1 A:HIS160 3.2 49.2 1.0 CG A:HIS149 3.3 48.6 1.0 CD2 A:HIS160 3.3 49.3 1.0 HE1 A:HIS149 3.3 64.7 1.0 HE1 A:HIS160 3.3 59.4 1.0 HE1 A:HIS162 3.4 70.0 1.0 O A:HOH515 3.4 56.7 1.0 HD2 A:HIS160 3.4 59.5 1.0 CB A:HIS149 3.6 43.8 1.0 O3' C:DT11 3.7 105.5 1.0 HB3 A:HIS149 3.7 53.0 1.0 H3' C:DT11 4.1 136.0 1.0 CG A:HIS162 4.2 47.3 1.0 ND1 A:HIS162 4.2 51.4 1.0 NE2 A:HIS149 4.3 48.3 1.0 ND1 A:HIS160 4.3 47.2 1.0 CD2 A:HIS149 4.4 48.7 1.0 CG A:HIS160 4.4 48.4 1.0 C3' C:DT11 4.5 113.0 1.0 OD2 A:ASP21 4.6 59.7 1.0 HB3 A:ASP21 4.8 67.7 1.0 O A:THR151 4.9 46.4 1.0 HB2 A:ASP21 5.0 67.7 1.0 CA A:HIS149 5.0 46.1 1.0

A.Breidenstein, J.Ter Beek, R.P.-A.Berntsson. Structural and Functional Characterization of Trai From PKM101 Reveals Basis For Dna Processing To Be Published.