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Iron in PDB 2eut: Cytochrome C Peroxidase (Ccp) in Complex with 2-Amino-4- Picoline

Enzymatic activity of Cytochrome C Peroxidase (Ccp) in Complex with 2-Amino-4- Picoline

All present enzymatic activity of Cytochrome C Peroxidase (Ccp) in Complex with 2-Amino-4- Picoline:
1.11.1.5;

Protein crystallography data

The structure of Cytochrome C Peroxidase (Ccp) in Complex with 2-Amino-4- Picoline, PDB code: 2eut 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 / 1.12
Space group P 21 21 21
Cell size a, b, c (Å), α, β, γ (°) 43.600, 73.530, 104.630, 90.00, 90.00, 90.00
R / Rfree (%) 14.3 / 15.2

Iron Binding Sites:

The binding sites of Iron atom in the Cytochrome C Peroxidase (Ccp) in Complex with 2-Amino-4- Picoline (pdb code 2eut). 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 (Ccp) in Complex with 2-Amino-4- Picoline, PDB code: 2eut:

Iron binding site 1 out of 1 in 2eut

Go back to Iron Binding Sites List in 2eut
Iron binding site 1 out of 1 in the Cytochrome C Peroxidase (Ccp) in Complex with 2-Amino-4- Picoline


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 (Ccp) in Complex with 2-Amino-4- Picoline within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe295

b:8.7
occ:1.00
FE A:HEM295 0.0 8.7 1.0
NC A:HEM295 2.0 13.5 1.0
NA A:HEM295 2.0 13.5 1.0
NB A:HEM295 2.0 13.5 1.0
ND A:HEM295 2.1 13.5 1.0
NE2 A:HIS175 2.1 9.6 1.0
C1C A:HEM295 3.0 8.6 1.0
C1A A:HEM295 3.0 8.7 1.0
C4C A:HEM295 3.0 7.8 1.0
C4B A:HEM295 3.1 9.2 1.0
C1D A:HEM295 3.1 8.6 1.0
C1B A:HEM295 3.1 9.1 1.0
C4A A:HEM295 3.1 9.4 1.0
C4D A:HEM295 3.1 8.7 1.0
CD2 A:HIS175 3.1 9.2 1.0
CE1 A:HIS175 3.1 9.3 1.0
CHD A:HEM295 3.4 8.7 1.0
CHC A:HEM295 3.4 8.9 1.0
CHA A:HEM295 3.4 8.7 1.0
CHB A:HEM295 3.4 10.0 1.0
NE1 A:TRP51 4.0 11.2 1.0
NE A:ARG48 4.1 15.3 1.0
O A:HOH495 4.2 15.8 1.0
ND1 A:HIS175 4.2 8.9 1.0
CG A:HIS175 4.2 8.8 1.0
C2C A:HEM295 4.3 8.3 1.0
C2B A:HEM295 4.3 9.6 1.0
C2A A:HEM295 4.3 9.4 1.0
C3B A:HEM295 4.3 9.2 1.0
C3C A:HEM295 4.3 8.7 1.0
C2D A:HEM295 4.3 9.0 1.0
C3A A:HEM295 4.3 9.5 1.0
C3D A:HEM295 4.3 9.2 1.0
NH2 A:ARG48 4.5 14.5 1.0
CD1 A:TRP51 4.6 10.8 1.0
C1 A:BVF401 4.7 10.9 1.0
CZ A:ARG48 4.8 15.4 1.0
C2 A:BVF401 4.9 11.2 1.0
CD A:ARG48 5.0 12.6 1.0
CG A:ARG48 5.0 10.9 1.0

Reference:

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
Page generated: Sun Dec 13 14:43:47 2020

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