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Atomistry » Magnesium » PDB 6s43-6ses » 6s6a | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Atomistry » Magnesium » PDB 6s43-6ses » 6s6a » |
Magnesium in PDB 6s6a: Crystal Structure of Raga-Q66L/Ragc-T90N Gtpase Heterodimer ComplexProtein crystallography data
The structure of Crystal Structure of Raga-Q66L/Ragc-T90N Gtpase Heterodimer Complex, PDB code: 6s6a
was solved by
M.Anandapadamanaban,
G.R.Masson,
O.Perisic,
J.Kaufman,
R.L.Williams,
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 Crystal Structure of Raga-Q66L/Ragc-T90N Gtpase Heterodimer Complex
(pdb code 6s6a). This binding sites where shown within
5.0 Angstroms radius around Magnesium atom.
In total 2 binding sites of Magnesium where determined in the Crystal Structure of Raga-Q66L/Ragc-T90N Gtpase Heterodimer Complex, PDB code: 6s6a: Jump to Magnesium binding site number: 1; 2; Magnesium binding site 1 out of 2 in 6s6aGo back to Magnesium Binding Sites List in 6s6a
Magnesium binding site 1 out
of 2 in the Crystal Structure of Raga-Q66L/Ragc-T90N Gtpase Heterodimer Complex
Mono view Stereo pair view
Magnesium binding site 2 out of 2 in 6s6aGo back to Magnesium Binding Sites List in 6s6a
Magnesium binding site 2 out
of 2 in the Crystal Structure of Raga-Q66L/Ragc-T90N Gtpase Heterodimer Complex
Mono view Stereo pair view
Reference:
M.Anandapadamanaban,
G.R.Masson,
O.Perisic,
A.Berndt,
J.Kaufman,
C.M.Johnson,
B.Santhanam,
K.B.Rogala,
D.M.Sabatini,
R.L.Williams.
Architecture of Human Rag Gtpase Heterodimers and Their Complex with MTORC1. Science V. 366 203 2019.
Page generated: Tue Oct 1 17:46:46 2024
ISSN: ESSN 1095-9203 PubMed: 31601764 DOI: 10.1126/SCIENCE.AAX3939 |
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