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Chlorine in PDB 9h44: Jumonji Domain-Containing Protein 2B with Crown Ether and Crystallization Epitope Mutations L916G:R917A:A918D

Enzymatic activity of Jumonji Domain-Containing Protein 2B with Crown Ether and Crystallization Epitope Mutations L916G:R917A:A918D

All present enzymatic activity of Jumonji Domain-Containing Protein 2B with Crown Ether and Crystallization Epitope Mutations L916G:R917A:A918D:
1.14.11.66;

Protein crystallography data

The structure of Jumonji Domain-Containing Protein 2B with Crown Ether and Crystallization Epitope Mutations L916G:R917A:A918D, PDB code: 9h44 was solved by M.Fairhead, C.Strain-Damerell, M.Ye, S.R.Mackinnon, D.Pinkas, E.M.Maclean, L.Koekemoer, D.Damerell, T.Krojer, W.Yue, N.Burgess-Brown, B.Marsden, F.Von Delft, Structural Genomics Consortium (Sgc), with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 32.31 / 1.74
Space group H 3 2
Cell size a, b, c (Å), α, β, γ (°) 87.93, 87.93, 142.91, 90, 90, 120
R / Rfree (%) 20.3 / 22.5

Chlorine Binding Sites:

The binding sites of Chlorine atom in the Jumonji Domain-Containing Protein 2B with Crown Ether and Crystallization Epitope Mutations L916G:R917A:A918D (pdb code 9h44). 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 Jumonji Domain-Containing Protein 2B with Crown Ether and Crystallization Epitope Mutations L916G:R917A:A918D, PDB code: 9h44:

Chlorine binding site 1 out of 1 in 9h44

Go back to Chlorine Binding Sites List in 9h44
Chlorine binding site 1 out of 1 in the Jumonji Domain-Containing Protein 2B with Crown Ether and Crystallization Epitope Mutations L916G:R917A:A918D


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 1 of Jumonji Domain-Containing Protein 2B with Crown Ether and Crystallization Epitope Mutations L916G:R917A:A918D within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl1102

b:33.9
occ:0.49
 OAO A:O4B1101 2.5 112.9 0.6
OAM A:O4B1101 2.8 85.4 0.6
OAP A:O4B1101 2.9 38.0 0.6
CAC A:O4B1101 2.9 96.8 0.6
CAD A:O4B1101 3.0 104.8 0.6
OAN A:O4B1101 3.0 39.4 0.6
OAR A:O4B1101 3.1 53.5 0.6
O A:HOH1201 3.1 34.2 1.0
CAJ A:O4B1101 3.3 49.2 0.6
CAG A:O4B1101 3.4 106.7 0.6
CAA A:O4B1101 3.5 56.6 0.5
CAI A:O4B1101 3.5 39.8 0.6
CAF A:O4B1101 3.8 38.5 0.6
CAB A:O4B1101 3.9 43.3 0.6
CAL A:O4B1101 3.9 72.3 0.6
CAE A:O4B1101 4.0 39.0 0.6
CAK A:O4B1101 4.1 88.1 0.6
CAH A:O4B1101 4.3 105.2 0.6
OD2 A:ASP954 4.5 34.1 1.0
O A:HOH1202 4.7 44.4 1.0
OAQ A:O4B1101 4.8 102.5 0.6

Reference:

M.Fairhead, C.Strain-Damerell, M.Ye, S.R.Mackinnon, D.Pinkas, E.M.Maclean, L.Koekemoer, D.Damerell, T.Krojer, W.Yue, N.Burgess-Brown, B.Marsden, F.Von Delft. A Fast, Parallel Method For Efficiently Exploring Crystallization Behaviour of Large Numbers of Protein Variants To Be Published.
Page generated: Tue Dec 10 19:31:45 2024

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