Iron in PDB 3bj2: Met-Perch Hemoglobin at pH 6.3

The structure of Met-Perch Hemoglobin at pH 6.3, PDB code: 3bj2 was solved by R.Aranda Iv, H.Cai, E.J.Levin, M.P.Richards, G.N.Phillips Jr., with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å)	70.00 / 2.00
Space group	P 21 21 21
Cell size a, b, c (Å), α, β, γ (°)	57.636, 85.022, 123.227, 90.00, 90.00, 90.00
R / Rfree (%)	18.4 / 23.2

The binding sites of Iron atom in the Met-Perch Hemoglobin at pH 6.3 (pdb code 3bj2). This binding sites where shown within 5.0 Angstroms radius around Iron atom.
In total 4 binding sites of Iron where determined in the Met-Perch Hemoglobin at pH 6.3, PDB code: 3bj2:
Jump to Iron binding site number: 1; 2; 3; 4;

Iron binding site 1 out of 4 in the Met-Perch Hemoglobin at pH 6.3


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 1 of Met-Perch Hemoglobin at pH 6.3 within 5.0Å range: probe atom residue distance (Å) B Occ A:Fe143 b:34.3 occ:1.00 FE A:HEM143 0.0 34.3 1.0 NB A:HEM143 1.9 29.7 1.0 ND A:HEM143 2.0 32.6 1.0 O A:HOH144 2.0 31.1 1.0 NC A:HEM143 2.1 32.2 1.0 NA A:HEM143 2.1 33.7 1.0 NE2 A:HIS88 2.2 16.7 1.0 C4B A:HEM143 2.9 30.5 1.0 C4D A:HEM143 3.0 35.9 1.0 C1B A:HEM143 3.0 30.5 1.0 C1D A:HEM143 3.0 35.2 1.0 C1C A:HEM143 3.0 28.9 1.0 CE1 A:HIS88 3.1 17.6 1.0 C1A A:HEM143 3.1 32.7 1.0 C4A A:HEM143 3.1 30.1 1.0 C4C A:HEM143 3.1 32.2 1.0 CHC A:HEM143 3.3 31.2 1.0 CD2 A:HIS88 3.4 20.2 1.0 CHA A:HEM143 3.4 32.7 1.0 CHB A:HEM143 3.5 31.8 1.0 CHD A:HEM143 3.5 32.8 1.0 CD1 A:ILE63 4.1 27.0 1.0 C3B A:HEM143 4.2 31.4 1.0 C2B A:HEM143 4.2 30.6 1.0 C3D A:HEM143 4.2 36.9 1.0 ND1 A:HIS88 4.2 19.5 1.0 C2D A:HEM143 4.3 35.3 1.0 C2C A:HEM143 4.3 31.2 1.0 C2A A:HEM143 4.3 37.3 1.0 C3A A:HEM143 4.3 33.7 1.0 NE2 A:HIS59 4.3 24.8 1.0 C3C A:HEM143 4.4 30.2 1.0 CG A:HIS88 4.4 19.9 1.0 CE1 A:HIS59 4.6 26.3 1.0

Iron binding site 2 out of 4 in the Met-Perch Hemoglobin at pH 6.3


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 2 of Met-Perch Hemoglobin at pH 6.3 within 5.0Å range: probe atom residue distance (Å) B Occ B:Fe148 b:26.6 occ:1.00 FE B:HEM148 0.0 26.6 1.0 NB B:HEM148 2.0 25.3 1.0 ND B:HEM148 2.0 26.0 1.0 NA B:HEM148 2.0 27.5 1.0 NC B:HEM148 2.0 23.9 1.0 NE2 B:HIS92 2.1 15.2 1.0 O B:HOH150 2.1 29.8 1.0 C4B B:HEM148 3.0 25.4 1.0 C1D B:HEM148 3.0 26.5 1.0 C4D B:HEM148 3.0 30.0 1.0 C4C B:HEM148 3.1 23.6 1.0 C1A B:HEM148 3.1 27.9 1.0 C1C B:HEM148 3.1 26.2 1.0 C1B B:HEM148 3.1 25.3 1.0 CE1 B:HIS92 3.1 14.2 1.0 C4A B:HEM148 3.1 26.2 1.0 CD2 B:HIS92 3.1 16.6 1.0 CHC B:HEM148 3.4 25.8 1.0 CHD B:HEM148 3.4 26.7 1.0 CHA B:HEM148 3.4 27.4 1.0 CHB B:HEM148 3.5 25.8 1.0 NE2 B:HIS63 4.0 27.8 1.0 ND1 B:HIS92 4.2 15.5 1.0 C3B B:HEM148 4.2 25.8 1.0 CG B:HIS92 4.3 16.3 1.0 C3D B:HEM148 4.3 29.9 1.0 C2D B:HEM148 4.3 31.1 1.0 C2A B:HEM148 4.3 27.1 1.0 C3C B:HEM148 4.3 26.7 1.0 C2B B:HEM148 4.3 23.4 1.0 C2C B:HEM148 4.3 26.9 1.0 C3A B:HEM148 4.3 28.2 1.0 CE1 B:HIS63 4.5 28.8 1.0 CG1 B:ILE67 4.9 17.3 1.0

Iron binding site 3 out of 4 in the Met-Perch Hemoglobin at pH 6.3


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 3 of Met-Perch Hemoglobin at pH 6.3 within 5.0Å range: probe atom residue distance (Å) B Occ C:Fe143 b:31.2 occ:1.00 FE C:HEM143 0.0 31.2 1.0 ND C:HEM143 2.0 31.1 1.0 NB C:HEM143 2.0 29.2 1.0 NA C:HEM143 2.1 29.0 1.0 NC C:HEM143 2.1 27.2 1.0 O C:HOH145 2.1 31.0 1.0 NE2 C:HIS88 2.1 18.0 1.0 C4D C:HEM143 3.0 34.3 1.0 C4B C:HEM143 3.0 32.1 1.0 C1A C:HEM143 3.0 31.1 1.0 C1D C:HEM143 3.1 31.4 1.0 CE1 C:HIS88 3.1 20.2 1.0 C1C C:HEM143 3.1 29.4 1.0 C1B C:HEM143 3.1 30.1 1.0 C4C C:HEM143 3.1 28.8 1.0 C4A C:HEM143 3.1 27.4 1.0 CD2 C:HIS88 3.1 18.6 1.0 CHA C:HEM143 3.3 31.9 1.0 CHC C:HEM143 3.4 29.8 1.0 CHD C:HEM143 3.5 28.9 1.0 CHB C:HEM143 3.5 30.5 1.0 CD1 C:ILE63 4.2 22.0 1.0 ND1 C:HIS88 4.2 19.4 1.0 C3D C:HEM143 4.2 35.0 1.0 C3B C:HEM143 4.3 30.2 1.0 CG C:HIS88 4.3 18.3 1.0 NE2 C:HIS59 4.3 23.7 1.0 C2D C:HEM143 4.3 32.9 1.0 C2B C:HEM143 4.3 29.7 1.0 C2A C:HEM143 4.3 31.5 1.0 C3A C:HEM143 4.3 29.5 1.0 C2C C:HEM143 4.3 28.2 1.0 C3C C:HEM143 4.4 26.8 1.0 CE1 C:HIS59 4.8 27.0 1.0

Iron binding site 4 out of 4 in the Met-Perch Hemoglobin at pH 6.3


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 4 of Met-Perch Hemoglobin at pH 6.3 within 5.0Å range: probe atom residue distance (Å) B Occ D:Fe148 b:27.8 occ:1.00 FE D:HEM148 0.0 27.8 1.0 NC D:HEM148 2.0 28.6 1.0 ND D:HEM148 2.1 27.2 1.0 NB D:HEM148 2.1 24.8 1.0 NE2 D:HIS92 2.1 12.3 1.0 NA D:HEM148 2.1 27.2 1.0 O D:HOH201 2.2 34.7 1.0 C4B D:HEM148 3.0 24.6 1.0 C1C D:HEM148 3.0 27.8 1.0 CE1 D:HIS92 3.0 14.4 1.0 C4D D:HEM148 3.1 28.7 1.0 C1D D:HEM148 3.1 26.7 1.0 C4C D:HEM148 3.1 25.9 1.0 C1A D:HEM148 3.1 27.3 1.0 CD2 D:HIS92 3.2 11.1 1.0 C1B D:HEM148 3.2 24.1 1.0 C4A D:HEM148 3.2 26.6 1.0 CHC D:HEM148 3.3 26.4 1.0 CHA D:HEM148 3.4 27.6 1.0 CHD D:HEM148 3.5 24.9 1.0 CHB D:HEM148 3.6 26.6 1.0 NE2 D:HIS63 4.1 24.6 1.0 ND1 D:HIS92 4.2 15.7 1.0 C2C D:HEM148 4.2 29.0 1.0 C3B D:HEM148 4.3 24.2 1.0 C3C D:HEM148 4.3 28.0 1.0 CG D:HIS92 4.3 14.3 1.0 C2D D:HEM148 4.3 27.9 1.0 C3D D:HEM148 4.3 28.1 1.0 C2A D:HEM148 4.4 28.5 1.0 C2B D:HEM148 4.4 23.6 1.0 C3A D:HEM148 4.4 28.1 1.0 CE1 D:HIS63 4.7 25.9 1.0 CG1 D:ILE67 4.7 14.8 1.0 CD1 D:ILE67 5.0 18.9 1.0

R.Aranda, H.Cai, C.E.Worley, E.J.Levin, R.Li, J.S.Olson, G.N.Phillips, M.P.Richards. Structural Analysis of Fish Versus Mammalian Hemoglobins: Effect of the Heme Pocket Environment on Autooxidation and Hemin Loss. Proteins V. 75 217 2008.
ISSN: ISSN 0887-3585
PubMed: 18831041
DOI: 10.1002/PROT.22236