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Chlorine in PDB 6mps: Tagt Bound to Liia-Wta

Protein crystallography data

The structure of Tagt Bound to Liia-Wta, PDB code: 6mps was solved by T.W.Owens, K.Schaefer, D.Kahne, S.Walker, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 60.36 / 1.86
Space group P 41 21 2
Cell size a, b, c (Å), α, β, γ (°) 66.373, 66.373, 145.060, 90.00, 90.00, 90.00
R / Rfree (%) 21.6 / 23.5

Other elements in 6mps:

The structure of Tagt Bound to Liia-Wta also contains other interesting chemical elements:

Magnesium (Mg) 1 atom

Chlorine Binding Sites:

The binding sites of Chlorine atom in the Tagt Bound to Liia-Wta (pdb code 6mps). 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 Tagt Bound to Liia-Wta, PDB code: 6mps:

Chlorine binding site 1 out of 1 in 6mps

Go back to Chlorine Binding Sites List in 6mps
Chlorine binding site 1 out of 1 in the Tagt Bound to Liia-Wta


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 1 of Tagt Bound to Liia-Wta within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl403

b:36.0
occ:1.00
H A:LYS182 2.3 40.7 1.0
H A:SER183 2.9 51.1 1.0
O A:HOH656 3.0 45.6 1.0
HG13 A:VAL181 3.1 37.9 1.0
HA A:VAL181 3.1 37.6 1.0
O A:HOH625 3.2 45.9 1.0
N A:LYS182 3.2 33.7 1.0
HB3 A:SER183 3.3 53.0 1.0
HE1 A:TYR215 3.4 38.4 1.0
N A:SER183 3.5 42.5 1.0
HG21 A:VAL186 3.7 46.4 1.0
HB2 A:LYS182 3.7 42.9 1.0
HG11 A:VAL186 3.8 38.8 1.0
OH A:TYR215 3.8 31.3 1.0
HB A:VAL186 3.8 40.9 1.0
CG1 A:VAL181 3.9 31.4 1.0
CA A:VAL181 3.9 31.2 1.0
HB2 A:SER183 4.0 53.0 1.0
HG12 A:VAL181 4.0 37.9 1.0
CB A:SER183 4.0 44.0 1.0
CA A:LYS182 4.0 30.8 1.0
C A:VAL181 4.0 33.7 1.0
C A:LYS182 4.2 38.4 1.0
CE1 A:TYR215 4.2 31.9 1.0
HG3 A:LYS182 4.2 46.6 1.0
CB A:LYS182 4.3 35.6 1.0
CA A:SER183 4.3 42.2 1.0
CB A:VAL186 4.4 33.9 1.0
HG22 A:VAL181 4.4 42.8 1.0
HH A:TYR215 4.4 37.8 1.0
CG2 A:VAL186 4.4 38.5 1.0
CB A:VAL181 4.5 29.1 1.0
CG1 A:VAL186 4.5 32.2 1.0
CZ A:TYR215 4.5 31.5 1.0
HG11 A:VAL181 4.7 37.9 1.0
O A:THR180 4.7 33.0 1.0
HG23 A:VAL186 4.7 46.4 1.0
HD3 A:ARG230 4.8 42.4 1.0
HG12 A:VAL186 4.8 38.8 1.0
CG A:LYS182 4.8 38.7 1.0
O A:SER183 4.8 34.1 1.0
HA A:LYS182 4.9 37.2 1.0
CG2 A:VAL181 5.0 35.5 1.0

Reference:

K.Schaefer, T.W.Owens, D.Kahne, S.Walker. Substrate Preferences Establish the Order of Cell Wall Assembly in Staphylococcus Aureus. J. Am. Chem. Soc. V. 140 2442 2018.
ISSN: ESSN 1520-5126
PubMed: 29402087
DOI: 10.1021/JACS.7B13551
Page generated: Sun Jul 28 03:20:53 2024

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