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Iodine in PDB 4m71: Mutant Structure of Methyltransferase From Streptomyces Hygroscopicus Complexed with S-Adenosyl-L-Homocysteine and Methylphenylpyruvic Acid

Protein crystallography data

The structure of Mutant Structure of Methyltransferase From Streptomyces Hygroscopicus Complexed with S-Adenosyl-L-Homocysteine and Methylphenylpyruvic Acid, PDB code: 4m71 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:

Resolution Low / High (Å) 28.95 / 2.21
Space group P 21 21 21
Cell size a, b, c (Å), α, β, γ (°) 60.833, 93.693, 137.375, 90.00, 90.00, 90.00
R / Rfree (%) 15.8 / 22.9

Other elements in 4m71:

The structure of Mutant Structure of Methyltransferase From Streptomyces Hygroscopicus Complexed with S-Adenosyl-L-Homocysteine and Methylphenylpyruvic Acid also contains other interesting chemical elements:

Iron (Fe) 2 atoms
Calcium (Ca) 14 atoms

Iodine Binding Sites:

The binding sites of Iodine atom in the Mutant Structure of Methyltransferase From Streptomyces Hygroscopicus Complexed with S-Adenosyl-L-Homocysteine and Methylphenylpyruvic Acid (pdb code 4m71). This binding sites where shown within 5.0 Angstroms radius around Iodine atom.
In total only one binding site of Iodine was determined in the Mutant Structure of Methyltransferase From Streptomyces Hygroscopicus Complexed with S-Adenosyl-L-Homocysteine and Methylphenylpyruvic Acid, PDB code: 4m71:

Iodine binding site 1 out of 1 in 4m71

Go back to Iodine Binding Sites List in 4m71
Iodine binding site 1 out of 1 in the Mutant Structure of Methyltransferase From Streptomyces Hygroscopicus Complexed with S-Adenosyl-L-Homocysteine and Methylphenylpyruvic Acid


Mono view


Stereo pair view

A full contact list of Iodine with other atoms in the I binding site number 1 of Mutant Structure of Methyltransferase From Streptomyces Hygroscopicus Complexed with S-Adenosyl-L-Homocysteine and Methylphenylpyruvic Acid within 5.0Å range:
probe atom residue distance (Å) B Occ
A:I414

b:37.1
occ:1.00
OG1 A:THR220 3.5 20.1 1.0
O A:HOH555 3.6 31.3 1.0
O A:HOH709 3.6 42.6 1.0
N A:ASP217 3.7 18.2 1.0
O A:HOH589 4.1 34.1 1.0
CG2 A:VAL224 4.1 25.7 1.0
CB A:ASP217 4.2 18.4 1.0
OE1 A:GLN223 4.2 34.0 1.0
O A:HOH722 4.2 51.8 1.0
CB A:GLN223 4.2 22.4 1.0
CA A:GLY216 4.2 20.9 1.0
O A:THR220 4.3 15.4 1.0
NH2 A:ARG215 4.4 52.3 1.0
C A:GLY216 4.5 19.6 1.0
CA A:ASP217 4.5 18.8 1.0
C A:GLN223 4.6 21.5 1.0
O A:GLN223 4.7 18.2 1.0
O A:ASP217 4.7 15.3 1.0
N A:VAL224 4.7 22.3 1.0
CB A:THR220 4.8 19.7 1.0
CA A:VAL224 4.9 21.8 1.0

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.
ISSN: ISSN 0907-4449
PubMed: 24914966
DOI: 10.1107/S1399004714005239
Page generated: Sun Dec 13 19:34:43 2020

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