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Atomistry » Zinc » PDB 1jao-1joe » 1jcs » |
Zinc in PDB 1jcs: Crystal Structure of Rat Protein Farnesyltransferase Complexed with the Peptide Substrate Tkcvfm and An Analog of Farnesyl DiphosphateProtein crystallography data
The structure of Crystal Structure of Rat Protein Farnesyltransferase Complexed with the Peptide Substrate Tkcvfm and An Analog of Farnesyl Diphosphate, PDB code: 1jcs
was solved by
S.B.Long,
P.J.Casey,
L.S.Beese,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Zinc Binding Sites:
The binding sites of Zinc atom in the Crystal Structure of Rat Protein Farnesyltransferase Complexed with the Peptide Substrate Tkcvfm and An Analog of Farnesyl Diphosphate
(pdb code 1jcs). This binding sites where shown within
5.0 Angstroms radius around Zinc atom.
In total only one binding site of Zinc was determined in the Crystal Structure of Rat Protein Farnesyltransferase Complexed with the Peptide Substrate Tkcvfm and An Analog of Farnesyl Diphosphate, PDB code: 1jcs: Zinc binding site 1 out of 1 in 1jcsGo back to Zinc Binding Sites List in 1jcs
Zinc binding site 1 out
of 1 in the Crystal Structure of Rat Protein Farnesyltransferase Complexed with the Peptide Substrate Tkcvfm and An Analog of Farnesyl Diphosphate
Mono view Stereo pair view
Reference:
S.B.Long,
P.J.Hancock,
A.M.Kral,
H.W.Hellinga,
L.S.Beese.
The Crystal Structure of Human Protein Farnesyltransferase Reveals the Basis For Inhibition By Caax Tetrapeptides and Their Mimetics. Proc.Natl.Acad.Sci.Usa V. 98 12948 2001.
Page generated: Wed Dec 16 02:53:47 2020
ISSN: ISSN 0027-8424 PubMed: 11687658 DOI: 10.1073/PNAS.241407898 |
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