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Atomistry » Calcium » PDB 5day-5dzv » 5dlw » |
Calcium in PDB 5dlw: Crystal Structure of Autotaxin (ENPP2) with Tauroursodeoxycholic Acid (Tudca) and Lysophosphatidic Acid (Lpa)Enzymatic activity of Crystal Structure of Autotaxin (ENPP2) with Tauroursodeoxycholic Acid (Tudca) and Lysophosphatidic Acid (Lpa)
All present enzymatic activity of Crystal Structure of Autotaxin (ENPP2) with Tauroursodeoxycholic Acid (Tudca) and Lysophosphatidic Acid (Lpa):
3.1.4.39; Protein crystallography data
The structure of Crystal Structure of Autotaxin (ENPP2) with Tauroursodeoxycholic Acid (Tudca) and Lysophosphatidic Acid (Lpa), PDB code: 5dlw
was solved by
W.J.Keune,
T.Heidebrecht,
R.P.Joosten,
A.Perrakis,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Other elements in 5dlw:
The structure of Crystal Structure of Autotaxin (ENPP2) with Tauroursodeoxycholic Acid (Tudca) and Lysophosphatidic Acid (Lpa) also contains other interesting chemical elements:
Calcium Binding Sites:
The binding sites of Calcium atom in the Crystal Structure of Autotaxin (ENPP2) with Tauroursodeoxycholic Acid (Tudca) and Lysophosphatidic Acid (Lpa)
(pdb code 5dlw). This binding sites where shown within
5.0 Angstroms radius around Calcium atom.
In total only one binding site of Calcium was determined in the Crystal Structure of Autotaxin (ENPP2) with Tauroursodeoxycholic Acid (Tudca) and Lysophosphatidic Acid (Lpa), PDB code: 5dlw: Calcium binding site 1 out of 1 in 5dlwGo back to
Calcium binding site 1 out
of 1 in the Crystal Structure of Autotaxin (ENPP2) with Tauroursodeoxycholic Acid (Tudca) and Lysophosphatidic Acid (Lpa)
![]() Mono view ![]() Stereo pair view
Reference:
W.J.Keune,
J.Hausmann,
R.Bolier,
D.Tolenaars,
A.Kremer,
T.Heidebrecht,
R.P.Joosten,
M.Sunkara,
A.J.Morris,
E.Matas-Rico,
W.H.Moolenaar,
R.P.Oude Elferink,
A.Perrakis.
Steroid Binding to Autotaxin Links Bile Salts and Lysophosphatidic Acid Signalling. Nat Commun V. 7 11248 2016.
Page generated: Wed Jul 9 05:11:43 2025
ISSN: ESSN 2041-1723 PubMed: 27075612 DOI: 10.1038/NCOMMS11248 |
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