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Atomistry » Chlorine » PDB 3r41-3rcg » 3rbf | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Atomistry » Chlorine » PDB 3r41-3rcg » 3rbf » |
Chlorine in PDB 3rbf: Crystal Structure of Human Aromatic L-Amino Acid Decarboxylase (Aadc) in the Apo FormEnzymatic activity of Crystal Structure of Human Aromatic L-Amino Acid Decarboxylase (Aadc) in the Apo Form
All present enzymatic activity of Crystal Structure of Human Aromatic L-Amino Acid Decarboxylase (Aadc) in the Apo Form:
4.1.1.28; Protein crystallography data
The structure of Crystal Structure of Human Aromatic L-Amino Acid Decarboxylase (Aadc) in the Apo Form, PDB code: 3rbf
was solved by
G.Giardina,
R.Montioli,
S.Gianni,
B.Cellini,
A.Paiardini,
C.Borrivoltattorni,
F.Cutruzzola,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Chlorine Binding Sites:
The binding sites of Chlorine atom in the Crystal Structure of Human Aromatic L-Amino Acid Decarboxylase (Aadc) in the Apo Form
(pdb code 3rbf). This binding sites where shown within
5.0 Angstroms radius around Chlorine atom.
In total 2 binding sites of Chlorine where determined in the Crystal Structure of Human Aromatic L-Amino Acid Decarboxylase (Aadc) in the Apo Form, PDB code: 3rbf: Jump to Chlorine binding site number: 1; 2; Chlorine binding site 1 out of 2 in 3rbfGo back to![]() ![]()
Chlorine binding site 1 out
of 2 in the Crystal Structure of Human Aromatic L-Amino Acid Decarboxylase (Aadc) in the Apo Form
![]() Mono view ![]() Stereo pair view
Chlorine binding site 2 out of 2 in 3rbfGo back to![]() ![]()
Chlorine binding site 2 out
of 2 in the Crystal Structure of Human Aromatic L-Amino Acid Decarboxylase (Aadc) in the Apo Form
![]() Mono view ![]() Stereo pair view
Reference:
G.Giardina,
R.Montioli,
S.Gianni,
B.Cellini,
A.Paiardini,
C.B.Voltattorni,
F.Cutruzzola.
Open Conformation of Human Dopa Decarboxylase Reveals the Mechanism of Plp Addition to Group II Decarboxylases. Proc.Natl.Acad.Sci.Usa V. 108 20514 2011.
Page generated: Sun Jul 21 03:33:56 2024
ISSN: ISSN 0027-8424 PubMed: 22143761 DOI: 10.1073/PNAS.1111456108 |
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