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Chlorine in PDB 8tsn: Pseudomonas Fluorescens G150T Isocyanide Hydratase at 298 K Xfel Data, Thioimidate Intermediate

Protein crystallography data

The structure of Pseudomonas Fluorescens G150T Isocyanide Hydratase at 298 K Xfel Data, Thioimidate Intermediate, PDB code: 8tsn was solved by M.A.Wilson, N.Smith, M.Dasgupta, C.Dolamore, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 21.98 / 1.30
Space group C 1 2 1
Cell size a, b, c (Å), α, β, γ (°) 72.136, 59.761, 56.11, 90, 115.88, 90
R / Rfree (%) 15.5 / 18.4

Chlorine Binding Sites:

The binding sites of Chlorine atom in the Pseudomonas Fluorescens G150T Isocyanide Hydratase at 298 K Xfel Data, Thioimidate Intermediate (pdb code 8tsn). 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 Pseudomonas Fluorescens G150T Isocyanide Hydratase at 298 K Xfel Data, Thioimidate Intermediate, PDB code: 8tsn:

Chlorine binding site 1 out of 1 in 8tsn

Go back to Chlorine Binding Sites List in 8tsn
Chlorine binding site 1 out of 1 in the Pseudomonas Fluorescens G150T Isocyanide Hydratase at 298 K Xfel Data, Thioimidate Intermediate


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 1 of Pseudomonas Fluorescens G150T Isocyanide Hydratase at 298 K Xfel Data, Thioimidate Intermediate within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl302

b:31.2
occ:1.00
HG1 A:THR153 2.2 22.8 0.6
HH21 A:ARG139 2.2 32.3 0.6
H A:THR153 2.3 16.3 0.6
HG1 A:THR153 2.7 18.8 0.4
HA3 A:GLY151 2.9 19.2 0.4
HA3 A:GLY151 2.9 18.5 0.6
OG1 A:THR153 3.0 15.6 0.4
HE A:ARG139 3.0 31.0 0.6
OG1 A:THR153 3.0 18.9 0.6
NH2 A:ARG139 3.1 26.9 0.6
N A:THR153 3.2 13.6 0.6
H A:ILE152 3.2 16.7 0.6
H A:THR153 3.3 15.4 0.4
N A:ILE152 3.4 13.9 0.6
C A:GLY151 3.6 14.8 0.6
CA A:GLY151 3.6 15.4 0.6
HG23 A:THR153 3.6 21.8 0.6
HH22 A:ARG139 3.6 32.3 0.6
NE A:ARG139 3.7 25.8 0.6
H A:ALA154 3.7 19.6 0.6
CA A:GLY151 3.7 16.0 0.4
CB A:THR153 3.8 17.1 0.6
CZ A:ARG139 3.9 26.4 0.6
CA A:THR153 3.9 15.4 0.6
HA2 A:GLY151 3.9 19.2 0.4
HA2 A:GLY151 4.0 18.5 0.6
O A:HOH518 4.0 24.6 1.0
HG13 A:ILE152 4.1 22.8 0.6
N A:THR153 4.1 12.8 0.4
N A:ALA154 4.1 16.3 0.6
C A:ILE152 4.2 15.9 0.6
CB A:THR153 4.2 14.4 0.4
CG2 A:THR153 4.2 18.2 0.6
C A:GLY151 4.2 14.9 0.4
O A:GLY151 4.3 15.3 0.6
C A:THR153 4.3 16.1 0.6
H A:ALA154 4.3 14.0 0.4
HG12 A:ILE152 4.3 22.8 0.6
CA A:ILE152 4.3 15.8 0.6
C A:THR153 4.4 12.3 0.4
N A:ALA154 4.4 11.7 0.4
O A:THR150 4.4 18.2 1.0
CA A:THR153 4.4 13.1 0.4
H A:ILE152 4.6 17.3 0.4
N A:ILE152 4.6 14.4 0.4
HG21 A:THR153 4.6 21.8 0.6
CG1 A:ILE152 4.6 19.0 0.6
HA A:ALA154 4.7 13.3 0.4
HG22 A:ILE152 4.7 16.8 0.4
HB2 A:ALA154 4.7 21.5 0.6
HB A:THR153 4.7 20.5 0.6
HA A:THR153 4.8 18.5 0.6
HB A:THR153 4.8 17.3 0.4
O A:GLY151 4.8 16.3 0.4
N A:GLY151 4.8 13.5 0.6
HG23 A:THR153 4.8 17.3 0.4
N A:GLY151 4.9 15.1 0.4
O A:THR153 4.9 13.4 0.4

Reference:

N.Smith, M.Dasgupta, D.C.Wych, C.Dolamore, R.G.Sierra, S.Lisova, D.Marchany-Rivera, A.E.Cohen, S.Boutet, M.S.Hunter, C.Kupitz, F.Poitevin, F.R.Moss, A.S.Brewster, N.K.Sauter, I.D.Young, A.M.Wolff, V.K.Tiwari, N.Kumar, D.B.Berkowitz, R.G.Hadt, M.C.Thompson, A.H.Follmer, M.E.Wall, M.A.Wilson. Changes in An Enzyme Ensemble During Catalysis Observed By High Resolution Xfel Crystallography. Biorxiv 2023.
ISSN: ISSN 2692-8205
PubMed: 37645800
DOI: 10.1101/2023.08.15.553460
Page generated: Thu Dec 28 03:33:15 2023

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