Copper in PDB 5jx9: Crystal Structure of Laccase From Thermus Thermophilus HB27 (Cu(II)- Cyclophanes, 5 Min)

All present enzymatic activity of Crystal Structure of Laccase From Thermus Thermophilus HB27 (Cu(II)- Cyclophanes, 5 Min):
1.10.3.2;

The structure of Crystal Structure of Laccase From Thermus Thermophilus HB27 (Cu(II)- Cyclophanes, 5 Min), PDB code: 5jx9 was solved by A.Diaz-Vilchis, R.R.Ruiz-Arellano, E.Rosas-Benitez, E.Rudino-Pinera, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å)	19.63 / 1.60
Space group	C 2 2 21
Cell size a, b, c (Å), α, β, γ (°)	93.440, 109.860, 96.050, 90.00, 90.00, 90.00
R / Rfree (%)	15 / 17.6

The binding sites of Copper atom in the Crystal Structure of Laccase From Thermus Thermophilus HB27 (Cu(II)- Cyclophanes, 5 Min) (pdb code 5jx9). This binding sites where shown within 5.0 Angstroms radius around Copper atom.
In total 3 binding sites of Copper where determined in the Crystal Structure of Laccase From Thermus Thermophilus HB27 (Cu(II)- Cyclophanes, 5 Min), PDB code: 5jx9:
Jump to Copper binding site number: 1; 2; 3;

Copper binding site 1 out of 3 in the Crystal Structure of Laccase From Thermus Thermophilus HB27 (Cu(II)- Cyclophanes, 5 Min)


Mono view


Stereo pair view

A full contact list of Copper with other atoms in the Cu binding site number 1 of Crystal Structure of Laccase From Thermus Thermophilus HB27 (Cu(II)- Cyclophanes, 5 Min) within 5.0Å range: probe atom residue distance (Å) B Occ A:Cu501 b:14.3 occ:0.16 NE2 A:HIS398 1.8 6.3 1.0 NE2 A:HIS444 1.9 7.1 1.0 CE1 A:HIS137 2.3 13.1 0.2 ND1 A:HIS137 2.4 13.0 0.2 CE1 A:HIS398 2.5 4.4 1.0 ND1 A:HIS137 2.6 11.8 0.8 CE1 A:HIS137 2.6 14.2 0.8 CD2 A:HIS444 2.8 6.0 1.0 CE1 A:HIS444 2.9 8.2 1.0 CD2 A:HIS398 3.0 5.3 1.0 NE2 A:HIS137 3.3 18.7 0.2 CD2 A:HIS95 3.5 7.8 1.0 CG A:HIS137 3.6 9.4 0.2 CG A:HIS137 3.6 9.0 0.8 NE2 A:HIS137 3.6 20.1 0.8 O A:HOH625 3.7 13.7 1.0 ND1 A:HIS398 3.7 6.5 1.0 NE2 A:HIS95 3.8 8.9 1.0 CD2 A:HIS396 3.8 6.8 1.0 ND1 A:HIS444 4.0 7.1 1.0 CG A:HIS444 4.0 6.5 1.0 CD2 A:HIS137 4.0 16.3 0.2 CG A:HIS398 4.0 4.6 1.0 CG A:HIS95 4.2 5.4 1.0 CD2 A:HIS137 4.2 17.0 0.8 NE2 A:HIS396 4.3 6.8 1.0 CG2 A:VAL442 4.4 5.8 1.0 CE1 A:HIS95 4.5 7.9 1.0 CB A:HIS137 4.5 9.3 0.8 CB A:HIS137 4.6 9.4 0.2 OE2 A:GLU451 4.7 5.7 0.4 ND1 A:HIS95 4.7 6.6 1.0 CB A:HIS95 4.8 9.4 1.0 OE1 A:GLU451 4.8 10.3 0.4 CD A:GLU451 4.9 5.7 0.4 CE1 A:HIS135 5.0 8.7 1.0

Copper binding site 2 out of 3 in the Crystal Structure of Laccase From Thermus Thermophilus HB27 (Cu(II)- Cyclophanes, 5 Min)


Mono view


Stereo pair view

A full contact list of Copper with other atoms in the Cu binding site number 2 of Crystal Structure of Laccase From Thermus Thermophilus HB27 (Cu(II)- Cyclophanes, 5 Min) within 5.0Å range: probe atom residue distance (Å) B Occ A:Cu502 b:8.8 occ:1.00 ND1 A:HIS97 2.0 6.2 1.0 NE2 A:HIS135 2.0 7.8 1.0 NE2 A:HIS446 2.1 4.0 1.0 CE1 A:HIS97 2.9 6.6 1.0 CE1 A:HIS446 2.9 5.4 1.0 CD2 A:HIS135 3.0 8.2 1.0 CG A:HIS97 3.0 6.0 1.0 CE1 A:HIS135 3.0 8.7 1.0 CD2 A:HIS446 3.1 6.6 1.0 CB A:HIS97 3.4 4.5 1.0 CZ2 A:TRP133 3.5 5.9 1.0 CD2 A:HIS95 3.7 7.8 1.0 CE2 A:TRP133 3.8 4.8 1.0 NE1 A:TRP133 3.9 4.8 1.0 NE2 A:HIS97 4.0 4.4 1.0 ND1 A:HIS446 4.1 7.0 1.0 CD2 A:HIS97 4.1 6.1 1.0 ND1 A:HIS135 4.1 3.7 1.0 CG A:HIS135 4.1 4.0 1.0 CG A:HIS446 4.2 4.2 1.0 CH2 A:TRP133 4.2 5.4 1.0 NE2 A:HIS95 4.3 8.9 1.0 NE2 A:HIS396 4.4 6.8 1.0 CD2 A:HIS396 4.4 6.8 1.0 CA A:HIS97 4.7 7.2 1.0 CD2 A:TRP133 4.8 3.6 1.0 CG A:HIS95 4.8 5.4 1.0 CD1 A:TRP133 4.9 4.1 1.0

Copper binding site 3 out of 3 in the Crystal Structure of Laccase From Thermus Thermophilus HB27 (Cu(II)- Cyclophanes, 5 Min)


Mono view


Stereo pair view

A full contact list of Copper with other atoms in the Cu binding site number 3 of Crystal Structure of Laccase From Thermus Thermophilus HB27 (Cu(II)- Cyclophanes, 5 Min) within 5.0Å range: probe atom residue distance (Å) B Occ A:Cu503 b:9.3 occ:0.90 ND1 A:HIS393 2.0 5.6 1.0 ND1 A:HIS450 2.1 6.6 1.0 SG A:CYS445 2.2 6.5 1.0 CE1 A:HIS393 2.8 10.3 1.0 CG A:HIS450 3.0 4.1 1.0 CE1 A:HIS450 3.1 6.4 1.0 CG A:HIS393 3.1 4.8 1.0 CB A:CYS445 3.3 6.5 1.0 CB A:HIS450 3.4 4.8 1.0 SD A:MET455 3.4 10.5 0.7 CB A:HIS393 3.6 6.0 1.0 SD A:MET455 3.8 4.8 0.3 CA A:HIS393 3.9 6.7 1.0 CD1 A:ILE447 3.9 7.7 1.0 CB A:ILE447 4.0 5.1 1.0 NE2 A:HIS393 4.0 9.0 1.0 NE2 A:HIS450 4.2 7.1 1.0 CD2 A:HIS393 4.2 6.2 1.0 CD2 A:HIS450 4.2 7.1 1.0 O A:ASP392 4.4 6.3 1.0 CG1 A:ILE447 4.4 6.0 1.0 CE A:MET455 4.4 7.3 0.7 CD A:PRO394 4.5 2.8 1.0 CA A:CYS445 4.6 6.6 1.0 O A:ILE447 4.7 6.1 1.0 CE A:MET455 4.7 7.3 0.3 CG2 A:ILE447 4.8 7.2 1.0 N A:ILE447 4.8 5.1 1.0 CA A:HIS450 4.9 5.8 1.0 C A:HIS393 4.9 5.8 1.0 CA A:ILE447 4.9 5.0 1.0 N A:HIS393 5.0 4.8 1.0 N A:PRO394 5.0 4.6 1.0 CG A:MET455 5.0 9.2 0.7

A.Diaz-Vilchis, R.R.Ruiz-Arellano, E.Rosas-Benitez, V.Stojanoff, E.Rudino-Pinera. Preserving Metallic Sites Affected By Radiation Damage: the CUT2 Case in Thermus Thermophilus Multicopper Oxidase To Be Published.