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Copper in PDB 2hrf: Solution Structure of Cu(I) P174L HSCO1

Copper Binding Sites:

The binding sites of Copper atom in the Solution Structure of Cu(I) P174L HSCO1 (pdb code 2hrf). This binding sites where shown within 5.0 Angstroms radius around Copper atom.
In total only one binding site of Copper was determined in the Solution Structure of Cu(I) P174L HSCO1, PDB code: 2hrf:

Copper binding site 1 out of 1 in 2hrf

Go back to Copper Binding Sites List in 2hrf
Copper binding site 1 out of 1 in the Solution Structure of Cu(I) P174L HSCO1


Mono view


Stereo pair view

A full contact list of Copper with other atoms in the Cu binding site number 1 of Solution Structure of Cu(I) P174L HSCO1 within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cu302

b:0.0
occ:1.00
NE2 A:HIS260 2.0 0.0 1.0
HG13 A:VAL172 2.3 0.0 1.0
SG A:CYS173 2.4 0.0 1.0
SG A:CYS169 2.4 0.0 1.0
H A:CYS173 2.5 0.0 1.0
HG12 A:VAL172 2.6 0.0 1.0
CG1 A:VAL172 2.9 0.0 1.0
CE1 A:HIS260 3.0 0.0 1.0
CD2 A:HIS260 3.1 0.0 1.0
HE1 A:HIS260 3.2 0.0 1.0
HB2 A:CYS169 3.2 0.0 1.0
HB3 A:PHE166 3.3 0.0 1.0
HG11 A:VAL172 3.3 0.0 1.0
CB A:CYS169 3.3 0.0 1.0
N A:CYS173 3.4 0.0 1.0
HD2 A:HIS260 3.4 0.0 1.0
CB A:CYS173 3.5 0.0 1.0
HB3 A:CYS169 3.5 0.0 1.0
HB2 A:CYS173 3.6 0.0 1.0
H A:PHE166 3.6 0.0 1.0
CA A:CYS173 3.9 0.0 1.0
ND1 A:HIS260 4.1 0.0 1.0
CG A:HIS260 4.2 0.0 1.0
CB A:VAL172 4.2 0.0 1.0
HA A:CYS173 4.2 0.0 1.0
CB A:PHE166 4.2 0.0 1.0
C A:VAL172 4.3 0.0 1.0
O A:PHE166 4.3 0.0 1.0
N A:PHE166 4.3 0.0 1.0
HB2 A:PHE166 4.4 0.0 1.0
HB3 A:CYS173 4.5 0.0 1.0
H A:CYS169 4.5 0.0 1.0
HA2 A:GLY165 4.5 0.0 1.0
HD2 A:PHE166 4.5 0.0 1.0
CA A:VAL172 4.5 0.0 1.0
HH A:TYR216 4.6 0.0 1.0
H A:VAL172 4.6 0.0 1.0
N A:VAL172 4.6 0.0 1.0
CA A:PHE166 4.8 0.0 1.0
HG23 A:VAL172 4.8 0.0 1.0
CA A:CYS169 4.8 0.0 1.0
HB A:VAL172 4.9 0.0 1.0
C A:PHE166 5.0 0.0 1.0

Reference:

L.Banci, I.Bertini, S.Ciofi-Baffoni, I.Leontari, M.Martinelli, P.Palumaa, R.Sillard, S.Wang. Human SCO1 Functional Studies and Pathological Implications of the P174L Mutant. Proc.Natl.Acad.Sci.Usa V. 104 15 2007.
ISSN: ISSN 0027-8424
PubMed: 17182746
DOI: 10.1073/PNAS.0606189103
Page generated: Tue Jul 30 23:39:36 2024

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