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Atomistry » Magnesium » PDB 7nnk-7nv4 » 7ntr | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Atomistry » Magnesium » PDB 7nnk-7nv4 » 7ntr » |
Magnesium in PDB 7ntr: Crystal Structure of Human Cytosolic Branched-Chain Aminotransferase (BCAT1) in Complex with Plp and Substrate Mimic 3-PhenylpropionateEnzymatic activity of Crystal Structure of Human Cytosolic Branched-Chain Aminotransferase (BCAT1) in Complex with Plp and Substrate Mimic 3-Phenylpropionate
All present enzymatic activity of Crystal Structure of Human Cytosolic Branched-Chain Aminotransferase (BCAT1) in Complex with Plp and Substrate Mimic 3-Phenylpropionate:
2.6.1.42; Protein crystallography data
The structure of Crystal Structure of Human Cytosolic Branched-Chain Aminotransferase (BCAT1) in Complex with Plp and Substrate Mimic 3-Phenylpropionate, PDB code: 7ntr
was solved by
R.C.Hillig,
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 Human Cytosolic Branched-Chain Aminotransferase (BCAT1) in Complex with Plp and Substrate Mimic 3-Phenylpropionate
(pdb code 7ntr). This binding sites where shown within
5.0 Angstroms radius around Magnesium atom.
In total only one binding site of Magnesium was determined in the Crystal Structure of Human Cytosolic Branched-Chain Aminotransferase (BCAT1) in Complex with Plp and Substrate Mimic 3-Phenylpropionate, PDB code: 7ntr: Magnesium binding site 1 out of 1 in 7ntrGo back to Magnesium Binding Sites List in 7ntr
Magnesium binding site 1 out
of 1 in the Crystal Structure of Human Cytosolic Branched-Chain Aminotransferase (BCAT1) in Complex with Plp and Substrate Mimic 3-Phenylpropionate
Mono view Stereo pair view
Reference:
J.Gunther,
R.C.Hillig,
K.Zimmermann,
S.Kaulfuss,
C.Lemos,
D.Nguyen,
H.Rehwinkel,
M.Habgood,
C.Lechner,
R.Neuhaus,
U.Ganzer,
M.Drewes,
J.Chai,
L.Bouche.
Bay-069, A Novel (Trifluoromethyl)Pyrimidinedione-Based BCAT1/2 Inhibitor and Chemical Probe. J.Med.Chem. V. 65 14366 2022.
Page generated: Thu Oct 3 02:13:11 2024
ISSN: ISSN 0022-2623 PubMed: 36261130 DOI: 10.1021/ACS.JMEDCHEM.2C00441 |
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