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Zinc in PDB 5l3u: Thermolysin in Complex with JC149 (Mpd Cryo Protectant)

Enzymatic activity of Thermolysin in Complex with JC149 (Mpd Cryo Protectant)

All present enzymatic activity of Thermolysin in Complex with JC149 (Mpd Cryo Protectant):
3.4.24.27;

Protein crystallography data

The structure of Thermolysin in Complex with JC149 (Mpd Cryo Protectant), PDB code: 5l3u was solved by S.G.Krimmer, J.Cramer, A.Heine, G.Klebe, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 38.42 / 1.23
Space group P 61 2 2
Cell size a, b, c (Å), α, β, γ (°) 92.793, 92.793, 131.074, 90.00, 90.00, 120.00
R / Rfree (%) 10.4 / 12.4

Other elements in 5l3u:

The structure of Thermolysin in Complex with JC149 (Mpd Cryo Protectant) also contains other interesting chemical elements:

Calcium (Ca) 4 atoms

Zinc Binding Sites:

The binding sites of Zinc atom in the Thermolysin in Complex with JC149 (Mpd Cryo Protectant) (pdb code 5l3u). This binding sites where shown within 5.0 Angstroms radius around Zinc atom.
In total only one binding site of Zinc was determined in the Thermolysin in Complex with JC149 (Mpd Cryo Protectant), PDB code: 5l3u:

Zinc binding site 1 out of 1 in 5l3u

Go back to Zinc Binding Sites List in 5l3u
Zinc binding site 1 out of 1 in the Thermolysin in Complex with JC149 (Mpd Cryo Protectant)


Mono view


Stereo pair view

A full contact list of Zinc with other atoms in the Zn binding site number 1 of Thermolysin in Complex with JC149 (Mpd Cryo Protectant) within 5.0Å range:
probe atom residue distance (Å) B Occ
E:Zn401

b:6.7
occ:1.00
OE2 E:GLU166 2.0 7.3 1.0
O14 E:6NG409 2.0 6.9 1.0
NE2 E:HIS146 2.0 6.3 1.0
NE2 E:HIS142 2.0 6.6 1.0
CD E:GLU166 2.8 6.9 1.0
CE1 E:HIS146 2.9 6.7 1.0
O15 E:6NG409 3.0 7.4 1.0
P13 E:6NG409 3.0 7.0 1.0
OE1 E:GLU166 3.0 7.2 1.0
CE1 E:HIS142 3.0 6.4 1.0
CD2 E:HIS142 3.0 6.2 1.0
HE1 E:HIS146 3.0 8.1 1.0
CD2 E:HIS146 3.1 7.0 1.0
HH E:TYR157 3.2 9.9 1.0
HD2 E:HIS142 3.2 7.4 1.0
HE1 E:HIS142 3.2 7.6 1.0
HE2 E:HIS231 3.3 9.1 1.0
HD2 E:HIS146 3.4 8.4 1.0
OH E:TYR157 3.8 8.2 1.0
HA E:GLU166 4.0 7.5 1.0
NE2 E:HIS231 4.0 7.6 1.0
HB2 E:SER169 4.0 8.1 1.0
ND1 E:HIS146 4.1 6.8 1.0
C17 E:6NG409 4.1 7.7 1.0
ND1 E:HIS142 4.1 6.4 1.0
N16 E:6NG409 4.1 8.4 1.0
CG E:HIS142 4.2 6.3 1.0
CG E:HIS146 4.2 6.6 1.0
HB3 E:SER169 4.2 8.1 1.0
CG E:GLU166 4.2 6.8 1.0
HD2 E:HIS231 4.3 8.7 1.0
C12 E:6NG409 4.4 8.8 1.0
HE1 E:TYR157 4.4 8.8 1.0
HG2 E:GLU166 4.4 8.2 1.0
CB E:SER169 4.5 6.7 1.0
C22 E:6NG409 4.6 8.0 1.0
CD2 E:HIS231 4.6 7.2 1.0
N11 E:6NG409 4.6 10.1 1.0
O23 E:6NG409 4.6 7.9 1.0
OG E:SER169 4.7 6.9 1.0
O E:HOH688 4.7 8.5 1.0
HG3 E:GLU166 4.8 8.2 1.0
CZ E:TYR157 4.8 7.9 1.0
HH12 E:ARG203 4.8 9.1 1.0
HD1 E:HIS146 4.8 8.2 1.0
CA E:GLU166 4.9 6.2 1.0
HD1 E:HIS142 4.9 7.7 1.0
OE1 E:GLU143 4.9 10.2 1.0
CE1 E:TYR157 5.0 7.3 1.0

Reference:

S.G.Krimmer, J.Cramer, M.Betz, V.Fridh, R.Karlsson, A.Heine, G.Klebe. Rational Design of Thermodynamic and Kinetic Binding Profiles By Optimizing Surface Water Networks Coating Protein-Bound Ligands. J. Med. Chem. V. 59 10530 2016.
ISSN: ISSN 1520-4804
PubMed: 27933956
DOI: 10.1021/ACS.JMEDCHEM.6B00998
Page generated: Wed Dec 16 06:28:15 2020

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