Iron in PDB 2yl0: Cytochrome C Prime From Alcaligenes Xylosoxidans: As Isolated L16A Variant at 0.95 A Resolution

The structure of Cytochrome C Prime From Alcaligenes Xylosoxidans: As Isolated L16A Variant at 0.95 A Resolution, PDB code: 2yl0 was solved by S.V.Antonyuk, R.R.Eady, S.S.Hasnain, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å)	46.22 / 0.95
Space group	P 65 2 2
Cell size a, b, c (Å), α, β, γ (°)	53.400, 53.400, 181.250, 90.00, 90.00, 120.00
R / Rfree (%)	13.213 / 14.968

The binding sites of Iron atom in the Cytochrome C Prime From Alcaligenes Xylosoxidans: As Isolated L16A Variant at 0.95 A Resolution (pdb code 2yl0). 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 Prime From Alcaligenes Xylosoxidans: As Isolated L16A Variant at 0.95 A Resolution, PDB code: 2yl0:

Iron binding site 1 out of 1 in the Cytochrome C Prime From Alcaligenes Xylosoxidans: As Isolated L16A Variant at 0.95 A Resolution


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 1 of Cytochrome C Prime From Alcaligenes Xylosoxidans: As Isolated L16A Variant at 0.95 A Resolution within 5.0Å range: probe atom residue distance (Å) B Occ A:Fe128 b:7.4 occ:1.00 FE A:HEC128 0.0 7.4 1.0 C A:CMO155 1.8 7.9 0.5 NC A:HEC128 2.0 7.3 1.0 ND A:HEC128 2.0 7.8 1.0 NB A:HEC128 2.0 7.7 1.0 NA A:HEC128 2.0 7.8 1.0 NE2 A:HIS120 2.0 8.2 1.0 O A:HOH1056 2.1 9.0 0.5 O A:CMO155 2.9 9.2 0.5 CE1 A:HIS120 3.0 9.2 1.0 C1D A:HEC128 3.0 7.7 1.0 C4A A:HEC128 3.0 8.1 1.0 C1C A:HEC128 3.0 7.5 1.0 C1B A:HEC128 3.0 8.2 1.0 C4B A:HEC128 3.0 7.6 1.0 C1A A:HEC128 3.0 8.2 1.0 C4C A:HEC128 3.0 7.4 1.0 C4D A:HEC128 3.0 8.2 1.0 CD2 A:HIS120 3.1 8.4 1.0 HE1 A:HIS120 3.2 8.8 1.0 HD2 A:HIS120 3.3 8.2 1.0 CHD A:HEC128 3.4 7.7 1.0 CHC A:HEC128 3.4 7.5 1.0 CHB A:HEC128 3.4 8.3 1.0 CHA A:HEC128 3.4 8.5 1.0 HB3 A:ALA16 4.0 7.5 1.0 ND1 A:HIS120 4.1 9.9 1.0 HH11 A:ARG124 4.2 11.9 1.0 CG A:HIS120 4.2 9.5 1.0 C3A A:HEC128 4.3 8.3 1.0 C2A A:HEC128 4.3 8.7 1.0 C3B A:HEC128 4.3 8.0 1.0 C2C A:HEC128 4.3 7.6 1.0 C3C A:HEC128 4.3 7.6 1.0 C2D A:HEC128 4.3 8.0 1.0 C2B A:HEC128 4.3 8.2 1.0 C3D A:HEC128 4.3 8.6 1.0 HB1 A:ALA16 4.3 7.4 1.0 HHD A:HEC128 4.4 7.4 1.0 HHC A:HEC128 4.4 7.3 1.0 HHB A:HEC128 4.4 7.9 1.0 HHA A:HEC128 4.4 8.1 1.0 HH2 A:TRP56 4.4 9.2 1.0 O A:HOH2064 4.4 10.5 0.5 HD3 A:ARG124 4.5 11.4 1.0 CB A:ALA16 4.6 7.8 1.0 CE A:MET19 4.6 9.6 0.3 NH1 A:ARG124 4.6 12.2 1.0 HH12 A:ARG124 4.7 11.8 1.0 HD1 A:HIS120 4.9 9.4 1.0 HB3 A:CYS116 5.0 9.2 1.0

S.V.Antonyuk, N.Rustage, C.A.Petersen, J.L.Arnst, D.J.Heyes, R.Sharma, N.G.Berry, N.S.Scrutton, R.R.Eady, C.R.Andrew, S.S.Hasnain. Carbon Monoxide Poisoning Is Prevented By the Energy Costs of Conformational Changes in Gas- Binding Haemproteins. Proc.Natl.Acad.Sci.Usa V. 108 15780 2011.
ISSN: ISSN 0027-8424
PubMed: 21900609
DOI: 10.1073/PNAS.1109051108