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Atomistry » Magnesium » PDB 5t2v-5tfb » 5tes | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Atomistry » Magnesium » PDB 5t2v-5tfb » 5tes » |
Magnesium in PDB 5tes: Tev Cleaved Human Atp Citrate Lyase Bound to Citrate and AdpEnzymatic activity of Tev Cleaved Human Atp Citrate Lyase Bound to Citrate and Adp
All present enzymatic activity of Tev Cleaved Human Atp Citrate Lyase Bound to Citrate and Adp:
2.3.3.8; Protein crystallography data
The structure of Tev Cleaved Human Atp Citrate Lyase Bound to Citrate and Adp, PDB code: 5tes
was solved by
J.Hu,
M.E.Fraser,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Magnesium Binding Sites:
The binding sites of Magnesium atom in the Tev Cleaved Human Atp Citrate Lyase Bound to Citrate and Adp
(pdb code 5tes). This binding sites where shown within
5.0 Angstroms radius around Magnesium atom.
In total 2 binding sites of Magnesium where determined in the Tev Cleaved Human Atp Citrate Lyase Bound to Citrate and Adp, PDB code: 5tes: Jump to Magnesium binding site number: 1; 2; Magnesium binding site 1 out of 2 in 5tesGo back to Magnesium Binding Sites List in 5tes
Magnesium binding site 1 out
of 2 in the Tev Cleaved Human Atp Citrate Lyase Bound to Citrate and Adp
Mono view Stereo pair view
Magnesium binding site 2 out of 2 in 5tesGo back to Magnesium Binding Sites List in 5tes
Magnesium binding site 2 out
of 2 in the Tev Cleaved Human Atp Citrate Lyase Bound to Citrate and Adp
Mono view Stereo pair view
Reference:
J.Hu,
A.Komakula,
M.E.Fraser.
Binding of Hydroxycitrate to Human Atp-Citrate Lyase. Acta Crystallogr D Struct V. 73 660 2017BIOL.
Page generated: Mon Sep 30 04:49:54 2024
ISSN: ISSN 2059-7983 PubMed: 28777081 DOI: 10.1107/S2059798317009871 |
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