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Chlorine in PDB 4eta: Lysozyme, Room Temperature, 400 Kgy Dose

Enzymatic activity of Lysozyme, Room Temperature, 400 Kgy Dose

All present enzymatic activity of Lysozyme, Room Temperature, 400 Kgy Dose:
3.2.1.17;

Protein crystallography data

The structure of Lysozyme, Room Temperature, 400 Kgy Dose, PDB code: 4eta was solved by S.Boutet, L.Lomb, G.Williams, T.Barends, A.Aquila, R.B.Doak, U.Weierstall, D.Deponte, J.Steinbrener, R.Shoeman, M.Messerschmidt, A.Barty, T.White, S.Kassemeyer, R.Kirian, M.Seibert, P.Montanez, C.Kenney, R.Herbst, P.Hart, J.Pines, G.Haller, S.Gruner, H.Philllip, M.Tate, M.Hromalik, L.Koerner, N.Van Bakel, J.Morse, W.Ghonsalves, D.Arnlund, M.Bogan, C.Calemann, R.Fromme, C.Hampton, M.Hunter, L.Johansson, G.Katona, C.Kupitz, M.Liang, A.Martin, K.Nass, L.Redecke, F.Stellato, N.Timneanu, D.Wang, N.Zatsepin, D.Schafer, K.Defever, R.Neutze, P.Fromme, J.Spence, H.Chapman, I.Schlichting, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 35.46 / 1.91
Space group P 43 21 2
Cell size a, b, c (Å), α, β, γ (°) 79.300, 79.300, 38.200, 90.00, 90.00, 90.00
R / Rfree (%) 16 / 18

Chlorine Binding Sites:

The binding sites of Chlorine atom in the Lysozyme, Room Temperature, 400 Kgy Dose (pdb code 4eta). 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 Lysozyme, Room Temperature, 400 Kgy Dose, PDB code: 4eta:

Chlorine binding site 1 out of 1 in 4eta

Go back to Chlorine Binding Sites List in 4eta
Chlorine binding site 1 out of 1 in the Lysozyme, Room Temperature, 400 Kgy Dose


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 1 of Lysozyme, Room Temperature, 400 Kgy Dose within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl201

b:22.5
occ:1.00
OH A:TYR23 3.0 12.7 1.0
CZ A:TYR23 3.7 13.2 1.0
CE2 A:TYR23 3.7 14.0 1.0
CA A:GLY104 4.1 13.4 1.0
O A:ARG21 4.6 17.2 1.0
O A:HOH312 4.7 23.1 1.0
N A:GLY104 4.7 12.8 1.0
CE1 A:TYR23 4.9 12.7 1.0
CD2 A:TYR23 4.9 12.5 1.0

Reference:

S.Boutet, L.Lomb, G.J.Williams, T.R.Barends, A.Aquila, R.B.Doak, U.Weierstall, D.P.Deponte, J.Steinbrener, R.L.Shoeman, M.Messerschmidt, A.Barty, T.A.White, S.Kassemeyer, R.A.Kirian, M.M.Seibert, P.A.Montanez, C.Kenney, R.Herbst, P.Hart, J.Pines, G.Haller, S.M.Gruner, H.T.Philipp, M.W.Tate, M.Hromalik, L.J.Koerner, N.Van Bakel, J.Morse, W.Ghonsalves, D.Arnlund, M.J.Bogan, C.Caleman, R.Fromme, C.Y.Hampton, M.S.Hunter, L.C.Johansson, G.Katona, C.Kupitz, M.Liang, A.V.Martin, K.Nass, L.Redecke, F.Stellato, N.Timneanu, D.Wang, N.A.Zatsepin, D.Schafer, J.Defever, R.Neutze, P.Fromme, J.C.Spence, H.N.Chapman, I.Schlichting. High-Resolution Protein Structure Determination By Serial Femtosecond Crystallography. Science V. 337 362 2012.
ISSN: ISSN 0036-8075
PubMed: 22653729
DOI: 10.1126/SCIENCE.1217737
Page generated: Sun Jul 21 13:16:29 2024

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