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Chlorine in PDB 5ldi: Crystal Structure of E.Coli Ligt in Apo Form

Protein crystallography data

The structure of Crystal Structure of E.Coli Ligt in Apo Form, PDB code: 5ldi was solved by M.Myllykoski, P.Kursula, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 36.60 / 2.10
Space group P 1 21 1
Cell size a, b, c (Å), α, β, γ (°) 63.390, 88.320, 73.840, 90.00, 115.01, 90.00
R / Rfree (%) 17.7 / 22.7

Chlorine Binding Sites:

The binding sites of Chlorine atom in the Crystal Structure of E.Coli Ligt in Apo Form (pdb code 5ldi). This binding sites where shown within 5.0 Angstroms radius around Chlorine atom.
In total 3 binding sites of Chlorine where determined in the Crystal Structure of E.Coli Ligt in Apo Form, PDB code: 5ldi:
Jump to Chlorine binding site number: 1; 2; 3;

Chlorine binding site 1 out of 3 in 5ldi

Go back to Chlorine Binding Sites List in 5ldi
Chlorine binding site 1 out of 3 in the Crystal Structure of E.Coli Ligt in Apo Form


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 1 of Crystal Structure of E.Coli Ligt in Apo Form within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl201

b:75.7
occ:1.00
HH22 A:ARG93 2.4 59.0 1.0
HH12 A:ARG93 2.9 57.2 1.0
NH2 A:ARG93 3.2 49.2 1.0
NH1 A:ARG93 3.6 47.7 1.0
O A:HOH408 3.7 52.4 1.0
HH21 A:ARG93 3.8 59.0 1.0
CZ A:ARG93 3.8 39.8 1.0
HH11 A:ARG93 4.3 57.2 1.0

Chlorine binding site 2 out of 3 in 5ldi

Go back to Chlorine Binding Sites List in 5ldi
Chlorine binding site 2 out of 3 in the Crystal Structure of E.Coli Ligt in Apo Form


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 2 of Crystal Structure of E.Coli Ligt in Apo Form within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Cl201

b:51.1
occ:1.00
HH22 B:ARG112 2.2 76.8 1.0
O B:HOH397 2.3 50.8 1.0
HE21 B:GLN109 2.6 41.2 1.0
NH2 B:ARG112 2.7 64.0 1.0
HH21 B:ARG112 2.7 76.8 1.0
HG2 B:GLN109 3.1 45.3 1.0
NE2 B:GLN109 3.4 34.3 1.0
HD22 B:LEU63 3.6 66.0 1.0
HG3 B:GLN109 3.7 45.3 1.0
CG B:GLN109 3.8 37.7 1.0
CZ B:ARG112 3.9 58.8 1.0
HE22 B:GLN109 4.0 41.2 1.0
CD B:GLN109 4.1 31.7 1.0
SD B:MET105 4.1 54.2 1.0
HH12 B:ARG112 4.1 0.1 1.0
NH1 B:ARG112 4.4 0.8 1.0
HE B:ARG66 4.4 96.2 1.0
O B:HOH418 4.5 53.1 1.0
CD2 B:LEU63 4.6 55.0 1.0
HH21 B:ARG66 4.8 72.1 1.0
HE B:ARG112 4.8 86.8 1.0
O B:HOH400 4.8 51.7 1.0
NE B:ARG112 4.8 72.3 1.0
HD23 B:LEU63 4.9 66.0 1.0
HB3 B:LEU63 4.9 42.4 1.0
HD21 B:LEU63 4.9 66.0 1.0
HA B:GLN109 5.0 41.6 1.0

Chlorine binding site 3 out of 3 in 5ldi

Go back to Chlorine Binding Sites List in 5ldi
Chlorine binding site 3 out of 3 in the Crystal Structure of E.Coli Ligt in Apo Form


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 3 of Crystal Structure of E.Coli Ligt in Apo Form within 5.0Å range:
probe atom residue distance (Å) B Occ
C:Cl201

b:77.8
occ:1.00
H C:THR75 2.5 33.7 1.0
HG2 C:MET92 2.6 64.5 1.0
HD3 C:PRO96 2.8 64.0 1.0
HB3 C:MET92 3.0 55.6 1.0
HG3 C:PRO96 3.2 58.3 1.0
N C:THR75 3.3 28.1 1.0
CG C:MET92 3.4 53.7 1.0
HA C:LEU74 3.4 40.9 1.0
HB C:THR75 3.5 40.8 1.0
O C:THR75 3.5 30.4 1.0
HA C:PRO95 3.6 55.6 1.0
CD C:PRO96 3.6 53.4 1.0
CB C:MET92 3.7 46.3 1.0
CG C:PRO96 3.8 48.6 1.0
SD C:MET92 3.9 81.6 1.0
O C:GLN94 3.9 48.8 1.0
HB2 C:MET92 4.1 55.6 1.0
CA C:THR75 4.1 28.9 1.0
C C:THR75 4.2 29.1 1.0
HG2 C:PRO96 4.2 58.3 1.0
CB C:THR75 4.2 34.0 1.0
O C:THR73 4.2 38.5 1.0
HG3 C:MET92 4.2 64.5 1.0
CA C:LEU74 4.2 34.1 1.0
C C:LEU74 4.3 32.1 1.0
O C:HOH341 4.3 29.5 1.0
HD2 C:PRO96 4.3 64.0 1.0
HD23 C:LEU74 4.3 61.5 1.0
N C:PRO96 4.4 39.4 1.0
O C:HOH304 4.4 63.9 1.0
HD22 C:LEU74 4.4 61.5 1.0
CA C:PRO95 4.5 46.3 1.0
C C:GLN94 4.7 42.7 1.0
C C:PRO95 4.8 39.8 1.0
OG1 C:THR75 4.8 32.0 1.0
CD2 C:LEU74 4.8 51.2 1.0
HA C:MET92 4.9 52.4 1.0
HB3 C:LEU74 4.9 51.0 1.0
CA C:MET92 4.9 43.6 1.0
N C:PRO95 4.9 40.7 1.0

Reference:

M.Myllykoski, P.Kursula. Structural Aspects of Nucleotide Ligand Binding By A Bacterial 2H Phosphoesterase. Plos One V. 12 70355 2017.
ISSN: ESSN 1932-6203
PubMed: 28141848
DOI: 10.1371/JOURNAL.PONE.0170355
Page generated: Fri Jul 26 11:19:55 2024

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