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Atomistry » Magnesium » PDB 7uer-7us2 » 7uir » |
Magnesium in PDB 7uir: Cocrystal Structure of Human Camkii-Alpha (CAMK2A)Kinase Domain and TIAM1 in Complex with AtpEnzymatic activity of Cocrystal Structure of Human Camkii-Alpha (CAMK2A)Kinase Domain and TIAM1 in Complex with Atp
All present enzymatic activity of Cocrystal Structure of Human Camkii-Alpha (CAMK2A)Kinase Domain and TIAM1 in Complex with Atp:
2.7.11.17; Protein crystallography data
The structure of Cocrystal Structure of Human Camkii-Alpha (CAMK2A)Kinase Domain and TIAM1 in Complex with Atp, PDB code: 7uir
was solved by
C.Ozden,
M.M.Stratton,
S.C.Garman,
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 Cocrystal Structure of Human Camkii-Alpha (CAMK2A)Kinase Domain and TIAM1 in Complex with Atp
(pdb code 7uir). This binding sites where shown within
5.0 Angstroms radius around Magnesium atom.
In total 2 binding sites of Magnesium where determined in the Cocrystal Structure of Human Camkii-Alpha (CAMK2A)Kinase Domain and TIAM1 in Complex with Atp, PDB code: 7uir: Jump to Magnesium binding site number: 1; 2; Magnesium binding site 1 out of 2 in 7uirGo back to Magnesium Binding Sites List in 7uir
Magnesium binding site 1 out
of 2 in the Cocrystal Structure of Human Camkii-Alpha (CAMK2A)Kinase Domain and TIAM1 in Complex with Atp
Mono view Stereo pair view
Magnesium binding site 2 out of 2 in 7uirGo back to Magnesium Binding Sites List in 7uir
Magnesium binding site 2 out
of 2 in the Cocrystal Structure of Human Camkii-Alpha (CAMK2A)Kinase Domain and TIAM1 in Complex with Atp
Mono view Stereo pair view
Reference:
C.Ozden,
R.Sloutsky,
T.Mitsugi,
N.Santos,
E.Agnello,
C.Gaubitz,
J.Foster,
E.Lapinskas,
E.A.Esposito,
T.Saneyoshi,
B.A.Kelch,
S.C.Garman,
Y.Hayashi,
M.M.Stratton.
Camkii Binds Both Substrates and Activators at the Active Site. Cell Rep V. 40 11064 2022.
Page generated: Thu Oct 3 10:00:43 2024
ISSN: ESSN 2211-1247 PubMed: 35830796 DOI: 10.1016/J.CELREP.2022.111064 |
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