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Atomistry » Cobalt » PDB 3bbk-3ger » 3fqw | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Atomistry » Cobalt » PDB 3bbk-3ger » 3fqw » |
Cobalt in PDB 3fqw: Phosphorylation of Self-Peptides Alters Human Leukocyte Antigen Class I-Restricted Antigen Presentation and Generates Tumor Specific EpitopesProtein crystallography data
The structure of Phosphorylation of Self-Peptides Alters Human Leukocyte Antigen Class I-Restricted Antigen Presentation and Generates Tumor Specific Epitopes, PDB code: 3fqw
was solved by
J.Petersen,
J.Rossjohn,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Other elements in 3fqw:
The structure of Phosphorylation of Self-Peptides Alters Human Leukocyte Antigen Class I-Restricted Antigen Presentation and Generates Tumor Specific Epitopes also contains other interesting chemical elements:
Cobalt Binding Sites:
The binding sites of Cobalt atom in the Phosphorylation of Self-Peptides Alters Human Leukocyte Antigen Class I-Restricted Antigen Presentation and Generates Tumor Specific Epitopes
(pdb code 3fqw). This binding sites where shown within
5.0 Angstroms radius around Cobalt atom.
In total only one binding site of Cobalt was determined in the Phosphorylation of Self-Peptides Alters Human Leukocyte Antigen Class I-Restricted Antigen Presentation and Generates Tumor Specific Epitopes, PDB code: 3fqw: Cobalt binding site 1 out of 1 in 3fqwGo back to![]() ![]()
Cobalt binding site 1 out
of 1 in the Phosphorylation of Self-Peptides Alters Human Leukocyte Antigen Class I-Restricted Antigen Presentation and Generates Tumor Specific Epitopes
![]() Mono view ![]() Stereo pair view
Reference:
J.Petersen,
S.J.Wurzbacher,
N.A.Williamson,
S.H.Ramarathinam,
H.H.Reid,
A.K.Nair,
A.Y.Zhao,
R.Nastovska,
G.Rudge,
J.Rossjohn,
A.W.Purcell.
Phosphorylated Self-Peptides Alter Human Leukocyte Antigen Class I-Restricted Antigen Presentation and Generate Tumor-Specific Epitopes Proc.Natl.Acad.Sci.Usa V. 106 2776 2009.
Page generated: Sun Jul 13 18:51:21 2025
ISSN: ISSN 0027-8424 PubMed: 19196958 DOI: 10.1073/PNAS.0812901106 |
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