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Atomistry » Iron » PDB 4m71-4n0k » 4m74 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Atomistry » Iron » PDB 4m71-4n0k » 4m74 » |
Iron in PDB 4m74: Mutant Structure of Methyltransferase From Streptomyces HygroscopicusProtein crystallography data
The structure of Mutant Structure of Methyltransferase From Streptomyces Hygroscopicus, PDB code: 4m74
was solved by
Y.C.Liu,
X.W.Zou,
H.C.Chan,
C.J.Huang,
T.L.Li,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Other elements in 4m74:
The structure of Mutant Structure of Methyltransferase From Streptomyces Hygroscopicus also contains other interesting chemical elements:
Iron Binding Sites:
The binding sites of Iron atom in the Mutant Structure of Methyltransferase From Streptomyces Hygroscopicus
(pdb code 4m74). This binding sites where shown within
5.0 Angstroms radius around Iron atom.
In total 2 binding sites of Iron where determined in the Mutant Structure of Methyltransferase From Streptomyces Hygroscopicus, PDB code: 4m74: Jump to Iron binding site number: 1; 2; Iron binding site 1 out of 2 in 4m74Go back to![]() ![]()
Iron binding site 1 out
of 2 in the Mutant Structure of Methyltransferase From Streptomyces Hygroscopicus
![]() Mono view ![]() Stereo pair view
Iron binding site 2 out of 2 in 4m74Go back to![]() ![]()
Iron binding site 2 out
of 2 in the Mutant Structure of Methyltransferase From Streptomyces Hygroscopicus
![]() Mono view ![]() Stereo pair view
Reference:
X.W.Zou,
Y.C.Liu,
N.S.Hsu,
C.J.Huang,
S.Y.Lyu,
H.C.Chan,
C.Y.Chang,
H.W.Yeh,
K.H.Lin,
C.J.Wu,
M.D.Tsai,
T.L.Li.
Structure and Mechanism of A Nonhaem-Iron Sam-Dependent C-Methyltransferase and Its Engineering to A Hydratase and An O-Methyltransferase Acta Crystallogr.,Sect.D V. 70 1549 2014.
Page generated: Tue Aug 5 12:43:59 2025
ISSN: ISSN 0907-4449 PubMed: 24914966 DOI: 10.1107/S1399004714005239 |
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