Copper in PDB 3nsc: C500S Mutant of Cueo Bound to Cu(II)

The structure of C500S Mutant of Cueo Bound to Cu(II), PDB code: 3nsc was solved by S.A.Roberts, W.R.Montfort, S.K.Singh, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å)	20.30 / 1.50
Space group	P 1 21 1
Cell size a, b, c (Å), α, β, γ (°)	50.329, 91.574, 54.248, 90.00, 102.48, 90.00
R / Rfree (%)	18.1 / 21.3

The binding sites of Copper atom in the C500S Mutant of Cueo Bound to Cu(II) (pdb code 3nsc). This binding sites where shown within 5.0 Angstroms radius around Copper atom.
In total 3 binding sites of Copper where determined in the C500S Mutant of Cueo Bound to Cu(II), PDB code: 3nsc:
Jump to Copper binding site number: 1; 2; 3;

Copper binding site 1 out of 3 in the C500S Mutant of Cueo Bound to Cu(II)


Mono view


Stereo pair view

A full contact list of Copper with other atoms in the Cu binding site number 1 of C500S Mutant of Cueo Bound to Cu(II) within 5.0Å range: probe atom residue distance (Å) B Occ A:Cu602 b:19.7 occ:1.00 ND1 A:HIS103 1.9 13.0 1.0 NE2 A:HIS141 2.0 17.1 1.0 NE2 A:HIS501 2.1 16.2 1.0 CE1 A:HIS103 2.9 17.2 1.0 CD2 A:HIS141 3.0 16.2 1.0 O A:HOH534 3.0 32.2 1.0 CG A:HIS103 3.0 15.3 1.0 CE1 A:HIS141 3.0 18.0 1.0 CE1 A:HIS501 3.1 17.0 1.0 CD2 A:HIS501 3.1 16.4 1.0 CB A:HIS103 3.4 16.1 1.0 CZ2 A:TRP139 3.7 16.0 1.0 CE2 A:TRP139 4.0 14.0 1.0 NE2 A:HIS103 4.0 17.2 1.0 CD2 A:HIS103 4.1 15.0 1.0 ND1 A:HIS141 4.1 17.2 1.0 CG A:HIS141 4.1 15.3 1.0 NE1 A:TRP139 4.1 15.0 1.0 O A:HOH933 4.2 31.2 1.0 ND1 A:HIS501 4.2 17.4 1.0 CG A:HIS501 4.2 16.8 1.0 CD2 A:HIS101 4.3 16.1 1.0 CU A:CU603 4.3 19.9 1.0 CH2 A:TRP139 4.4 15.4 1.0 CD2 A:HIS446 4.5 16.6 1.0 NE2 A:HIS446 4.5 15.3 1.0 NE2 A:HIS101 4.7 16.9 1.0 CA A:HIS103 4.7 15.8 1.0 CU A:CU604 4.8 22.0 1.0 CD2 A:TRP139 5.0 12.9 1.0

Copper binding site 2 out of 3 in the C500S Mutant of Cueo Bound to Cu(II)


Mono view


Stereo pair view

A full contact list of Copper with other atoms in the Cu binding site number 2 of C500S Mutant of Cueo Bound to Cu(II) within 5.0Å range: probe atom residue distance (Å) B Occ A:Cu603 b:19.9 occ:1.00 NE2 A:HIS101 2.0 16.9 1.0 NE2 A:HIS446 2.0 15.3 1.0 O A:ACT1 2.4 14.3 0.5 CE1 A:HIS101 2.9 19.6 1.0 CE1 A:HIS446 2.9 16.0 1.0 CD2 A:HIS446 2.9 16.6 1.0 CD2 A:HIS101 3.0 16.1 1.0 CD2 A:HIS448 3.2 17.6 1.0 NE2 A:HIS448 3.3 15.9 1.0 C A:ACT1 3.4 15.1 0.5 OXT A:ACT1 3.5 15.2 0.5 CG A:HIS103 3.6 15.3 1.0 CA A:HIS103 3.6 15.8 1.0 O A:HOH534 3.7 32.2 1.0 ND1 A:HIS103 3.8 13.0 1.0 CB A:HIS103 3.8 16.1 1.0 CG A:HIS448 3.8 17.2 1.0 CU A:CU604 3.9 22.0 1.0 ND1 A:HIS101 4.0 18.5 1.0 CE1 A:HIS448 4.0 18.6 1.0 ND1 A:HIS446 4.0 17.9 1.0 CG A:HIS446 4.1 14.5 1.0 CG A:HIS101 4.1 17.1 1.0 CD2 A:HIS103 4.1 15.0 1.0 ND1 A:HIS448 4.3 18.6 1.0 CE1 A:HIS103 4.3 17.2 1.0 CU A:CU602 4.3 19.7 1.0 N A:GLY104 4.3 15.9 1.0 NE2 A:HIS103 4.5 17.2 1.0 C A:HIS103 4.5 16.3 1.0 N A:HIS103 4.5 15.8 1.0 CA A:HIS448 4.6 18.7 1.0 O A:HOH971 4.6 24.6 0.5 O A:HOH970 4.6 23.4 0.5 CB A:HIS448 4.7 18.1 1.0 CH3 A:ACT1 4.7 16.6 0.5 O A:TRP102 4.8 18.7 1.0 C A:TRP102 5.0 17.2 1.0

Copper binding site 3 out of 3 in the C500S Mutant of Cueo Bound to Cu(II)


Mono view


Stereo pair view

A full contact list of Copper with other atoms in the Cu binding site number 3 of C500S Mutant of Cueo Bound to Cu(II) within 5.0Å range: probe atom residue distance (Å) B Occ A:Cu604 b:22.0 occ:1.00 O A:HOH534 1.9 32.2 1.0 NE2 A:HIS448 2.0 15.9 1.0 NE2 A:HIS499 2.0 17.2 1.0 NE2 A:HIS143 2.0 19.0 1.0 CE1 A:HIS448 2.9 18.6 1.0 CD2 A:HIS499 3.0 18.4 1.0 CE1 A:HIS499 3.0 19.8 1.0 CD2 A:HIS448 3.0 17.6 1.0 CE1 A:HIS143 3.0 23.6 1.0 CD2 A:HIS143 3.0 19.9 1.0 CD2 A:HIS446 3.7 16.6 1.0 O A:HOH933 3.8 31.2 1.0 CU A:CU603 3.9 19.9 1.0 ND1 A:HIS448 4.0 18.6 1.0 ND1 A:HIS499 4.1 18.9 1.0 CG A:HIS499 4.1 16.9 1.0 CG A:HIS448 4.1 17.2 1.0 ND1 A:HIS143 4.1 20.6 1.0 CD2 A:HIS101 4.1 16.1 1.0 CG A:HIS143 4.2 18.7 1.0 NE2 A:HIS101 4.2 16.9 1.0 NE2 A:HIS446 4.2 15.3 1.0 CB A:MET497 4.4 16.1 1.0 CU A:CU602 4.8 19.7 1.0 OE2 A:GLU506 4.8 33.6 1.0 CG A:MET497 4.9 18.1 1.0 CE1 A:HIS101 4.9 19.6 1.0 CG A:HIS101 4.9 17.1 1.0 CG A:HIS446 4.9 14.5 1.0

S.K.Singh, S.A.Roberts, S.F.Mcdevitt, A.Weichsel, G.F.Wildner, G.B.Grass, C.Rensing, W.R.Montfort. Crystal Structures of Multicopper Oxidase Cueo Bound to Copper(I) and Silver(I): Functional Role of A Methionine-Rich Sequence. J. Biol. Chem. V. 286 37849 2011.
ISSN: ESSN 1083-351X
PubMed: 21903583
DOI: 10.1074/JBC.M111.293589