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Atomistry » Calcium » PDB 5afp-5b4x » 5b3p | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Atomistry » Calcium » PDB 5afp-5b4x » 5b3p » |
Calcium in PDB 5b3p: NQO5 of the Trypsin-Resistant Fragment (1-134) in P212121 FormEnzymatic activity of NQO5 of the Trypsin-Resistant Fragment (1-134) in P212121 Form
All present enzymatic activity of NQO5 of the Trypsin-Resistant Fragment (1-134) in P212121 Form:
1.6.5.11; Protein crystallography data
The structure of NQO5 of the Trypsin-Resistant Fragment (1-134) in P212121 Form, PDB code: 5b3p
was solved by
Y.Hanazono,
K.Takeda,
K.Miki,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Calcium Binding Sites:
The binding sites of Calcium atom in the NQO5 of the Trypsin-Resistant Fragment (1-134) in P212121 Form
(pdb code 5b3p). This binding sites where shown within
5.0 Angstroms radius around Calcium atom.
In total 3 binding sites of Calcium where determined in the NQO5 of the Trypsin-Resistant Fragment (1-134) in P212121 Form, PDB code: 5b3p: Jump to Calcium binding site number: 1; 2; 3; Calcium binding site 1 out of 3 in 5b3pGo back to Calcium Binding Sites List in 5b3p
Calcium binding site 1 out
of 3 in the NQO5 of the Trypsin-Resistant Fragment (1-134) in P212121 Form
Mono view Stereo pair view
Calcium binding site 2 out of 3 in 5b3pGo back to Calcium Binding Sites List in 5b3p
Calcium binding site 2 out
of 3 in the NQO5 of the Trypsin-Resistant Fragment (1-134) in P212121 Form
Mono view Stereo pair view
Calcium binding site 3 out of 3 in 5b3pGo back to Calcium Binding Sites List in 5b3p
Calcium binding site 3 out
of 3 in the NQO5 of the Trypsin-Resistant Fragment (1-134) in P212121 Form
Mono view Stereo pair view
Reference:
Y.Hanazono,
K.Takeda,
K.Miki.
Characterization of the NQO5 Subunit of Bacterial Complex I in the Isolated State Febs Open Bio V. 6 687 2016.
Page generated: Sun Jul 14 16:44:19 2024
ISSN: ESSN 2211-5463 PubMed: 27398308 DOI: 10.1002/2211-5463.12070 |
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