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Atomistry » Zinc » PDB 4ixj-4jea » 4je7 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Atomistry » Zinc » PDB 4ixj-4jea » 4je7 » |
Zinc in PDB 4je7: Crystal Structure of A Human-Like Mitochondrial Peptide Deformylase in Complex with ActinoninEnzymatic activity of Crystal Structure of A Human-Like Mitochondrial Peptide Deformylase in Complex with Actinonin
All present enzymatic activity of Crystal Structure of A Human-Like Mitochondrial Peptide Deformylase in Complex with Actinonin:
3.5.1.88; Protein crystallography data
The structure of Crystal Structure of A Human-Like Mitochondrial Peptide Deformylase in Complex with Actinonin, PDB code: 4je7
was solved by
S.Fieulaine,
T.Meinnel,
C.Giglione,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Zinc Binding Sites:
The binding sites of Zinc atom in the Crystal Structure of A Human-Like Mitochondrial Peptide Deformylase in Complex with Actinonin
(pdb code 4je7). This binding sites where shown within
5.0 Angstroms radius around Zinc atom.
In total 2 binding sites of Zinc where determined in the Crystal Structure of A Human-Like Mitochondrial Peptide Deformylase in Complex with Actinonin, PDB code: 4je7: Jump to Zinc binding site number: 1; 2; Zinc binding site 1 out of 2 in 4je7Go back to![]() ![]()
Zinc binding site 1 out
of 2 in the Crystal Structure of A Human-Like Mitochondrial Peptide Deformylase in Complex with Actinonin
![]() Mono view ![]() Stereo pair view
Zinc binding site 2 out of 2 in 4je7Go back to![]() ![]()
Zinc binding site 2 out
of 2 in the Crystal Structure of A Human-Like Mitochondrial Peptide Deformylase in Complex with Actinonin
![]() Mono view ![]() Stereo pair view
Reference:
S.Fieulaine,
M.Desmadril,
T.Meinnel,
C.Giglione.
Understanding the Highly Efficient Catalysis of Prokaryotic Peptide Deformylases By Shedding Light on the Determinants Specifying the Low Activity of the Human Counterpart. Acta Crystallogr.,Sect.D V. 70 242 2014.
Page generated: Sun Oct 27 01:10:06 2024
ISSN: ISSN 0907-4449 PubMed: 24531459 DOI: 10.1107/S1399004713026461 |
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