Iron in PDB 2as6: Cytochrome C Peroxidase in Complex with Cyclopentylamine

All present enzymatic activity of Cytochrome C Peroxidase in Complex with Cyclopentylamine:
1.11.1.5;

The structure of Cytochrome C Peroxidase in Complex with Cyclopentylamine, PDB code: 2as6 was solved by R.Brenk, S.W.Vetter, S.E.Boyce, D.B.Goodin, B.K.Shoichet, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å)	10.00 / 1.45
Space group	P 21 21 21
Cell size a, b, c (Å), α, β, γ (°)	51.132, 75.717, 106.905, 90.00, 90.00, 90.00
R / Rfree (%)	n/a / 18.3

The binding sites of Iron atom in the Cytochrome C Peroxidase in Complex with Cyclopentylamine (pdb code 2as6). This binding sites where shown within 5.0 Angstroms radius around Iron atom.
In total only one binding site of Iron was determined in the Cytochrome C Peroxidase in Complex with Cyclopentylamine, PDB code: 2as6:

Iron binding site 1 out of 1 in the Cytochrome C Peroxidase in Complex with Cyclopentylamine


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 1 of Cytochrome C Peroxidase in Complex with Cyclopentylamine within 5.0Å range: probe atom residue distance (Å) B Occ A:Fe400 b:11.6 occ:1.00 FE A:HEM400 0.0 11.6 1.0 O A:HOH1415 2.0 35.5 1.0 NC A:HEM400 2.0 11.1 1.0 NA A:HEM400 2.0 12.2 1.0 ND A:HEM400 2.1 12.5 1.0 NE2 A:HIS175 2.1 12.7 1.0 NB A:HEM400 2.1 12.7 1.0 C1C A:HEM400 3.0 10.9 1.0 CE1 A:HIS175 3.0 12.2 1.0 C1A A:HEM400 3.0 12.0 1.0 C4B A:HEM400 3.1 13.3 1.0 C4A A:HEM400 3.1 12.8 1.0 C4D A:HEM400 3.1 13.5 1.0 C4C A:HEM400 3.1 11.1 1.0 C1D A:HEM400 3.1 10.8 1.0 C1B A:HEM400 3.1 11.4 1.0 CD2 A:HIS175 3.1 12.7 1.0 CHC A:HEM400 3.4 10.4 1.0 CHA A:HEM400 3.4 13.1 1.0 CHD A:HEM400 3.4 11.1 1.0 CHB A:HEM400 3.4 11.8 1.0 NE1 A:TRP51 4.0 14.0 1.0 NE A:ARG48 4.1 20.6 1.0 ND1 A:HIS175 4.2 12.7 1.0 O A:HOH1200 4.2 19.7 1.0 C2A A:HEM400 4.2 12.8 1.0 CG A:HIS175 4.2 12.6 1.0 C3A A:HEM400 4.2 12.2 1.0 C3B A:HEM400 4.2 12.0 1.0 C2C A:HEM400 4.2 12.2 1.0 C3C A:HEM400 4.2 11.1 1.0 C3D A:HEM400 4.3 10.9 1.0 C2D A:HEM400 4.3 10.0 1.0 C2B A:HEM400 4.3 11.4 1.0 CD1 A:TRP51 4.6 15.0 1.0 NH2 A:ARG48 4.6 16.0 1.0 CZ A:ARG48 4.9 18.3 1.0 CD A:ARG48 4.9 19.5 1.0 CG A:ARG48 5.0 13.1 1.0

R.Brenk, S.W.Vetter, S.E.Boyce, D.B.Goodin, B.K.Shoichet. Probing Molecular Docking in A Charged Model Binding Site. J.Mol.Biol. V. 357 1449 2006.
ISSN: ISSN 0022-2836
PubMed: 16490206
DOI: 10.1016/J.JMB.2006.01.034