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Atomistry » Silicon » PDB 1fuq-7zpw » 1fv2 » |
Silicon in PDB 1fv2: The Hc Fragment of Tetanus Toxin Complexed with An Analogue of Its Ganglioside Receptor GT1BEnzymatic activity of The Hc Fragment of Tetanus Toxin Complexed with An Analogue of Its Ganglioside Receptor GT1B
All present enzymatic activity of The Hc Fragment of Tetanus Toxin Complexed with An Analogue of Its Ganglioside Receptor GT1B:
3.4.24.68; Protein crystallography data
The structure of The Hc Fragment of Tetanus Toxin Complexed with An Analogue of Its Ganglioside Receptor GT1B, PDB code: 1fv2
was solved by
C.Fotinou,
P.Emsley,
I.Black,
H.Ando,
H.Ishida,
M.Kiso,
K.A.Sinha,
N.F.Fairweather,
N.W.Isaacs,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Silicon Binding Sites:
The binding sites of Silicon atom in the The Hc Fragment of Tetanus Toxin Complexed with An Analogue of Its Ganglioside Receptor GT1B
(pdb code 1fv2). This binding sites where shown within
5.0 Angstroms radius around Silicon atom.
In total 2 binding sites of Silicon where determined in the The Hc Fragment of Tetanus Toxin Complexed with An Analogue of Its Ganglioside Receptor GT1B, PDB code: 1fv2: Jump to Silicon binding site number: 1; 2; Silicon binding site 1 out of 2 in 1fv2Go back to Silicon Binding Sites List in 1fv2
Silicon binding site 1 out
of 2 in the The Hc Fragment of Tetanus Toxin Complexed with An Analogue of Its Ganglioside Receptor GT1B
Mono view Stereo pair view
Silicon binding site 2 out of 2 in 1fv2Go back to Silicon Binding Sites List in 1fv2
Silicon binding site 2 out
of 2 in the The Hc Fragment of Tetanus Toxin Complexed with An Analogue of Its Ganglioside Receptor GT1B
Mono view Stereo pair view
Reference:
C.Fotinou,
P.Emsley,
I.Black,
H.Ando,
H.Ishida,
M.Kiso,
K.A.Sinha,
N.F.Fairweather,
N.W.Isaacs.
The Crystal Structure of Tetanus Toxin Hc Fragment Complexed with A Synthetic GT1B Analogue Suggests Cross-Linking Between Ganglioside Receptors and the Toxin. J.Biol.Chem. V. 276 32274 2001.
Page generated: Thu Oct 10 13:20:47 2024
ISSN: ISSN 0021-9258 PubMed: 11418600 DOI: 10.1074/JBC.M103285200 |
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