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Atomistry » Sodium » PDB 6f1r-6fmp » 6fgb » |
Sodium in PDB 6fgb: Human Fcrn Extra-Cellular Domain Complexed with Fab Fragment of RozanolixizumabProtein crystallography data
The structure of Human Fcrn Extra-Cellular Domain Complexed with Fab Fragment of Rozanolixizumab, PDB code: 6fgb
was solved by
K.Sarkar,
T.Ceska,
C.Meier,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Other elements in 6fgb:
The structure of Human Fcrn Extra-Cellular Domain Complexed with Fab Fragment of Rozanolixizumab also contains other interesting chemical elements:
Sodium Binding Sites:
The binding sites of Sodium atom in the Human Fcrn Extra-Cellular Domain Complexed with Fab Fragment of Rozanolixizumab
(pdb code 6fgb). This binding sites where shown within
5.0 Angstroms radius around Sodium atom.
In total 2 binding sites of Sodium where determined in the Human Fcrn Extra-Cellular Domain Complexed with Fab Fragment of Rozanolixizumab, PDB code: 6fgb: Jump to Sodium binding site number: 1; 2; Sodium binding site 1 out of 2 in 6fgbGo back to Sodium Binding Sites List in 6fgb
Sodium binding site 1 out
of 2 in the Human Fcrn Extra-Cellular Domain Complexed with Fab Fragment of Rozanolixizumab
Mono view Stereo pair view
Sodium binding site 2 out of 2 in 6fgbGo back to Sodium Binding Sites List in 6fgb
Sodium binding site 2 out
of 2 in the Human Fcrn Extra-Cellular Domain Complexed with Fab Fragment of Rozanolixizumab
Mono view Stereo pair view
Reference:
B.Smith,
A.Kiessling,
R.Lledo-Garcia,
K.L.Dixon,
L.Christodoulou,
M.C.Catley,
P.Atherfold,
L.E.D'hooghe,
H.Finney,
K.Greenslade,
H.Hailu,
L.Kevorkian,
D.Lightwood,
C.Meier,
R.Munro,
O.Qureshi,
K.Sarkar,
S.P.Shaw,
R.Tewari,
A.Turner,
K.Tyson,
S.West,
S.Shaw,
F.R.Brennan.
Generation and Characterization of A High Affinity Anti-Human Fcrn Antibody, Rozanolixizumab, and the Effects of Different Molecular Formats on the Reduction of Plasma Igg Concentration. Mabs V. 10 1111 2018.
Page generated: Tue Oct 8 08:45:23 2024
ISSN: ESSN 1942-0870 PubMed: 30130439 DOI: 10.1080/19420862.2018.1505464 |
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