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Iron in PDB 5o64: From Macrocrystals to Microcrystals: A Strategy For Membrane Protein Serial Crystallography

Protein crystallography data

The structure of From Macrocrystals to Microcrystals: A Strategy For Membrane Protein Serial Crystallography, PDB code: 5o64 was solved by R.Dods, P.Baath, G.Branden, R.Neutze, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 46.39 / 3.30
Space group P 43 21 2
Cell size a, b, c (Å), α, β, γ (°) 226.600, 226.600, 113.800, 90.00, 90.00, 90.00
R / Rfree (%) 15.4 / 19.6

Other elements in 5o64:

The structure of From Macrocrystals to Microcrystals: A Strategy For Membrane Protein Serial Crystallography also contains other interesting chemical elements:

Magnesium (Mg) 4 atoms

Iron Binding Sites:

The binding sites of Iron atom in the From Macrocrystals to Microcrystals: A Strategy For Membrane Protein Serial Crystallography (pdb code 5o64). This binding sites where shown within 5.0 Angstroms radius around Iron atom.
In total 5 binding sites of Iron where determined in the From Macrocrystals to Microcrystals: A Strategy For Membrane Protein Serial Crystallography, PDB code: 5o64:
Jump to Iron binding site number: 1; 2; 3; 4; 5;

Iron binding site 1 out of 5 in 5o64

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Iron binding site 1 out of 5 in the From Macrocrystals to Microcrystals: A Strategy For Membrane Protein Serial Crystallography


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 1 of From Macrocrystals to Microcrystals: A Strategy For Membrane Protein Serial Crystallography within 5.0Å range:
probe atom residue distance (Å) B Occ
C:Fe401

b:0.5
occ:1.00
FE C:HEC401 0.0 0.5 1.0
NE2 C:HIS91 2.0 0.5 1.0
NB C:HEC401 2.0 0.3 1.0
NA C:HEC401 2.1 0.6 1.0
NC C:HEC401 2.1 0.2 1.0
ND C:HEC401 2.1 0.7 1.0
SD C:MET74 2.4 0.1 1.0
CD2 C:HIS91 3.0 0.3 1.0
CE1 C:HIS91 3.0 0.3 1.0
C4A C:HEC401 3.0 0.1 1.0
C1B C:HEC401 3.1 0.7 1.0
C1C C:HEC401 3.1 0.4 1.0
C4B C:HEC401 3.1 0.4 1.0
C1D C:HEC401 3.1 0.5 1.0
C1A C:HEC401 3.1 0.2 1.0
C4C C:HEC401 3.1 0.8 1.0
C4D C:HEC401 3.1 0.8 1.0
CHB C:HEC401 3.4 0.5 1.0
CHC C:HEC401 3.4 0.4 1.0
CHD C:HEC401 3.4 0.0 1.0
CHA C:HEC401 3.5 0.7 1.0
CE C:MET74 3.6 0.1 1.0
CG C:MET74 3.7 1.0 1.0
ND1 C:HIS91 4.1 0.9 1.0
CG C:HIS91 4.1 0.9 1.0
C3A C:HEC401 4.3 0.8 1.0
C3B C:HEC401 4.3 99.0 1.0
C2A C:HEC401 4.3 0.3 1.0
C2B C:HEC401 4.3 0.1 1.0
C2C C:HEC401 4.3 0.6 1.0
C2D C:HEC401 4.3 0.8 1.0
C3D C:HEC401 4.3 0.6 1.0
C3C C:HEC401 4.3 0.8 1.0
CB C:MET74 4.4 0.3 1.0

Iron binding site 2 out of 5 in 5o64

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Iron binding site 2 out of 5 in the From Macrocrystals to Microcrystals: A Strategy For Membrane Protein Serial Crystallography


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 2 of From Macrocrystals to Microcrystals: A Strategy For Membrane Protein Serial Crystallography within 5.0Å range:
probe atom residue distance (Å) B Occ
C:Fe402

b:0.1
occ:1.00
FE C:HEC402 0.0 0.1 1.0
NB C:HEC402 2.0 0.5 1.0
NC C:HEC402 2.1 0.1 1.0
NA C:HEC402 2.1 0.5 1.0
ND C:HEC402 2.1 1.0 1.0
NE2 C:HIS136 2.1 0.0 1.0
SD C:MET110 2.3 99.8 1.0
CE1 C:HIS136 3.0 0.1 1.0
C4B C:HEC402 3.0 98.7 1.0
C1B C:HEC402 3.0 95.5 1.0
C1C C:HEC402 3.0 0.1 1.0
C4A C:HEC402 3.1 100.0 1.0
C1A C:HEC402 3.1 0.7 1.0
C1D C:HEC402 3.1 1.0 1.0
C4C C:HEC402 3.1 0.9 1.0
C4D C:HEC402 3.1 1.0 1.0
CD2 C:HIS136 3.2 98.5 1.0
CG C:MET110 3.3 0.0 1.0
CHC C:HEC402 3.4 0.2 1.0
CHB C:HEC402 3.4 93.4 1.0
CHA C:HEC402 3.5 0.5 1.0
CHD C:HEC402 3.5 0.7 1.0
CE C:MET110 3.5 0.1 1.0
CB C:MET110 4.1 0.1 1.0
ND1 C:HIS136 4.1 95.2 1.0
C2B C:HEC402 4.2 91.5 1.0
C3B C:HEC402 4.2 97.1 1.0
CG C:HIS136 4.3 100.0 1.0
C3A C:HEC402 4.3 0.5 1.0
C2A C:HEC402 4.3 0.5 1.0
C2C C:HEC402 4.3 0.9 1.0
C2D C:HEC402 4.3 0.1 1.0
C3C C:HEC402 4.3 0.3 1.0
C3D C:HEC402 4.3 0.8 1.0

Iron binding site 3 out of 5 in 5o64

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Iron binding site 3 out of 5 in the From Macrocrystals to Microcrystals: A Strategy For Membrane Protein Serial Crystallography


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 3 of From Macrocrystals to Microcrystals: A Strategy For Membrane Protein Serial Crystallography within 5.0Å range:
probe atom residue distance (Å) B Occ
C:Fe403

b:93.8
occ:1.00
FE C:HEC403 0.0 93.8 1.0
NB C:HEC403 2.0 90.5 1.0
NA C:HEC403 2.1 92.1 1.0
NC C:HEC403 2.1 95.4 1.0
ND C:HEC403 2.1 87.6 1.0
NE2 C:HIS248 2.1 94.2 1.0
SD C:MET233 2.3 99.5 1.0
CE1 C:HIS248 2.8 0.5 1.0
C4B C:HEC403 3.0 90.0 1.0
C4A C:HEC403 3.0 91.2 1.0
C1B C:HEC403 3.0 89.5 1.0
C1C C:HEC403 3.1 90.1 1.0
C1D C:HEC403 3.1 93.5 1.0
C1A C:HEC403 3.1 94.9 1.0
C4C C:HEC403 3.1 96.6 1.0
C4D C:HEC403 3.1 86.0 1.0
CD2 C:HIS248 3.3 90.2 1.0
CHC C:HEC403 3.4 88.5 1.0
CHB C:HEC403 3.4 90.6 1.0
CG C:MET233 3.4 98.6 1.0
CHD C:HEC403 3.5 96.1 1.0
CHA C:HEC403 3.5 91.4 1.0
CE C:MET233 3.5 95.4 1.0
ND1 C:HIS248 4.1 0.3 1.0
CB C:MET233 4.3 95.1 1.0
C3B C:HEC403 4.3 87.2 1.0
C3A C:HEC403 4.3 92.1 1.0
C2B C:HEC403 4.3 89.0 1.0
C2C C:HEC403 4.3 92.0 1.0
C2A C:HEC403 4.3 94.5 1.0
C2D C:HEC403 4.3 93.5 1.0
C3C C:HEC403 4.3 96.3 1.0
CG C:HIS248 4.3 96.4 1.0
C3D C:HEC403 4.3 89.4 1.0

Iron binding site 4 out of 5 in 5o64

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Iron binding site 4 out of 5 in the From Macrocrystals to Microcrystals: A Strategy For Membrane Protein Serial Crystallography


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 4 of From Macrocrystals to Microcrystals: A Strategy For Membrane Protein Serial Crystallography within 5.0Å range:
probe atom residue distance (Å) B Occ
C:Fe404

b:97.0
occ:1.00
FE C:HEC404 0.0 97.0 1.0
NB C:HEC404 2.0 91.1 1.0
NC C:HEC404 2.0 97.2 1.0
NA C:HEC404 2.1 91.9 1.0
ND C:HEC404 2.1 97.9 1.0
NE2 C:HIS309 2.1 89.5 1.0
NE2 C:HIS124 2.2 1.0 1.0
C4B C:HEC404 3.0 93.3 1.0
CE1 C:HIS124 3.0 0.8 1.0
C1C C:HEC404 3.0 99.2 1.0
C1B C:HEC404 3.0 91.7 1.0
C4A C:HEC404 3.1 0.9 1.0
C1D C:HEC404 3.1 0.8 1.0
C4C C:HEC404 3.1 0.5 1.0
C1A C:HEC404 3.1 89.6 1.0
CE1 C:HIS309 3.1 87.1 1.0
C4D C:HEC404 3.1 1.0 1.0
CD2 C:HIS309 3.2 91.1 1.0
CD2 C:HIS124 3.3 0.8 1.0
CHC C:HEC404 3.3 0.3 1.0
CHB C:HEC404 3.4 0.7 1.0
CHD C:HEC404 3.4 0.1 1.0
CHA C:HEC404 3.4 0.0 1.0
ND1 C:HIS124 4.1 0.2 1.0
ND1 C:HIS309 4.2 91.3 1.0
C3B C:HEC404 4.3 92.7 1.0
C2B C:HEC404 4.3 89.5 1.0
C2C C:HEC404 4.3 96.5 1.0
CG C:HIS124 4.3 95.8 1.0
C3A C:HEC404 4.3 98.2 1.0
CG C:HIS309 4.3 93.6 1.0
C2D C:HEC404 4.3 0.2 1.0
C3C C:HEC404 4.3 0.4 1.0
C2A C:HEC404 4.3 94.0 1.0
C3D C:HEC404 4.4 0.2 1.0
CG C:PRO315 5.0 0.1 1.0

Iron binding site 5 out of 5 in 5o64

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Iron binding site 5 out of 5 in the From Macrocrystals to Microcrystals: A Strategy For Membrane Protein Serial Crystallography


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 5 of From Macrocrystals to Microcrystals: A Strategy For Membrane Protein Serial Crystallography within 5.0Å range:
probe atom residue distance (Å) B Occ
L:Fe306

b:97.4
occ:1.00
NE2 L:HIS190 2.2 97.2 1.0
OE2 M:GLU232 2.2 94.8 1.0
NE2 M:HIS217 2.3 97.0 1.0
NE2 L:HIS230 2.4 0.8 1.0
NE2 M:HIS264 2.4 0.6 1.0
OE1 M:GLU232 2.5 0.9 1.0
CD M:GLU232 2.7 0.5 1.0
CE1 L:HIS190 3.1 0.9 1.0
CE1 M:HIS217 3.1 94.3 1.0
CD2 L:HIS190 3.2 0.5 1.0
CE1 M:HIS264 3.3 98.4 1.0
CE1 L:HIS230 3.3 0.8 1.0
CD2 M:HIS217 3.4 98.5 1.0
CD2 L:HIS230 3.4 0.5 1.0
CD2 M:HIS264 3.5 0.5 1.0
CG M:GLU232 4.2 1.0 1.0
ND1 L:HIS190 4.3 1.0 1.0
ND1 M:HIS217 4.3 99.4 1.0
CG L:HIS190 4.3 96.9 1.0
CG1 M:ILE221 4.4 94.1 1.0
ND1 M:HIS264 4.4 93.2 1.0
ND1 L:HIS230 4.4 99.7 1.0
CG M:HIS217 4.5 0.7 1.0
CG1 L:ILE194 4.5 0.2 1.0
CG L:HIS230 4.5 99.1 1.0
CG M:HIS264 4.6 96.9 1.0
CD1 M:ILE221 5.0 95.4 1.0

Reference:

R.Dods, P.Bath, D.Arnlund, K.R.Beyerlein, G.Nelson, M.Liang, R.Harimoorthy, P.Berntsen, E.Malmerberg, L.Johansson, R.Andersson, R.Bosman, S.Carbajo, E.Claesson, C.E.Conrad, P.Dahl, G.Hammarin, M.S.Hunter, C.Li, S.Lisova, D.Milathianaki, J.Robinson, C.Safari, A.Sharma, G.Williams, C.Wickstrand, O.Yefanov, J.Davidsson, D.P.Deponte, A.Barty, G.Branden, R.Neutze. From Macrocrystals to Microcrystals: A Strategy For Membrane Protein Serial Crystallography. Structure V. 25 1461 2017.
ISSN: ISSN 1878-4186
PubMed: 28781082
DOI: 10.1016/J.STR.2017.07.002
Page generated: Wed Aug 6 00:13:39 2025

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