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Chlorine in PDB 1xrl: Crystal Structure of Active Site F1-Mutant Y205F Complex with Inhibitor Pck

Enzymatic activity of Crystal Structure of Active Site F1-Mutant Y205F Complex with Inhibitor Pck

All present enzymatic activity of Crystal Structure of Active Site F1-Mutant Y205F Complex with Inhibitor Pck:
3.4.11.5;

Protein crystallography data

The structure of Crystal Structure of Active Site F1-Mutant Y205F Complex with Inhibitor Pck, PDB code: 1xrl was solved by P.Goettig, H.Brandstetter, M.Groll, W.Goehring, P.V.Konarev, D.I.Svergun, R.Huber, J.-S.Kim, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 19.40 / 1.82
Space group P 21 21 21
Cell size a, b, c (Å), α, β, γ (°) 57.330, 61.850, 80.770, 90.00, 90.00, 90.00
R / Rfree (%) 24.1 / 27.9

Chlorine Binding Sites:

The binding sites of Chlorine atom in the Crystal Structure of Active Site F1-Mutant Y205F Complex with Inhibitor Pck (pdb code 1xrl). This binding sites where shown within 5.0 Angstroms radius around Chlorine atom.
In total only one binding site of Chlorine was determined in the Crystal Structure of Active Site F1-Mutant Y205F Complex with Inhibitor Pck, PDB code: 1xrl:

Chlorine binding site 1 out of 1 in 1xrl

Go back to Chlorine Binding Sites List in 1xrl
Chlorine binding site 1 out of 1 in the Crystal Structure of Active Site F1-Mutant Y205F Complex with Inhibitor Pck


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 1 of Crystal Structure of Active Site F1-Mutant Y205F Complex with Inhibitor Pck within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl300

b:23.5
occ:1.00
CL A:PHK300 0.0 23.5 1.0
C1 A:PHK300 1.8 20.6 1.0
OG A:SER105 2.8 30.0 1.0
C A:PHK300 2.9 24.2 1.0
O A:PHK300 3.1 20.7 1.0
OH A:TYR44 3.3 13.9 1.0
SD A:MET40 3.5 33.9 1.0
CB A:SER105 3.6 19.7 1.0
NE2 A:HIS271 3.7 22.9 1.0
CZ A:TYR44 3.8 12.9 1.0
CD2 A:HIS271 3.9 22.4 1.0
N A:GLY37 4.0 16.4 1.0
CA A:PHK300 4.1 22.7 1.0
CA A:GLY36 4.1 16.6 1.0
CE2 A:TYR44 4.3 15.5 1.0
OG A:SER104 4.4 20.2 1.0
C A:GLY36 4.4 14.6 1.0
N A:PHK300 4.4 19.3 1.0
CE1 A:TYR44 4.5 15.8 1.0
CD2 A:LEU272 4.5 21.2 1.0
CE A:MET40 4.5 33.2 1.0
N A:GLY36 4.6 15.3 1.0
O A:SER104 4.7 17.5 1.0
OE2 A:GLU213 4.8 20.6 1.0
CA A:GLY37 4.9 16.5 1.0
CA A:SER105 4.9 17.0 1.0
CE1 A:HIS271 5.0 22.3 1.0

Reference:

P.Goettig, H.Brandstetter, M.Groll, W.Goehring, P.V.Konarev, D.I.Svergun, R.Huber, J.-S.Kim. X-Ray Snapshots of Peptide Processing in Mutants of Tricorn-Interacting Factor F1 From Thermoplasma Acidophilum J.Biol.Chem. V. 280 33387 2005.
ISSN: ISSN 0021-9258
PubMed: 15994304
DOI: 10.1074/JBC.M505030200
Page generated: Sat Jul 20 04:03:06 2024

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