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Chlorine in PDB 6hyx: The Glic Pentameric Ligand-Gated Ion Channel Mutant Y197F-P250C

Protein crystallography data

The structure of The Glic Pentameric Ligand-Gated Ion Channel Mutant Y197F-P250C, PDB code: 6hyx was solved by H.D.Hu, M.Delarue, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 20.00 / 3.00
Space group C 1 2 1
Cell size a, b, c (Å), α, β, γ (°) 182.810, 134.230, 160.300, 90.00, 102.09, 90.00
R / Rfree (%) 20.9 / 22.4

Other elements in 6hyx:

The structure of The Glic Pentameric Ligand-Gated Ion Channel Mutant Y197F-P250C also contains other interesting chemical elements:

Sodium (Na) 7 atoms

Chlorine Binding Sites:

The binding sites of Chlorine atom in the The Glic Pentameric Ligand-Gated Ion Channel Mutant Y197F-P250C (pdb code 6hyx). This binding sites where shown within 5.0 Angstroms radius around Chlorine atom.
In total 5 binding sites of Chlorine where determined in the The Glic Pentameric Ligand-Gated Ion Channel Mutant Y197F-P250C, PDB code: 6hyx:
Jump to Chlorine binding site number: 1; 2; 3; 4; 5;

Chlorine binding site 1 out of 5 in 6hyx

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Chlorine binding site 1 out of 5 in the The Glic Pentameric Ligand-Gated Ion Channel Mutant Y197F-P250C


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 1 of The Glic Pentameric Ligand-Gated Ion Channel Mutant Y197F-P250C within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl401

b:58.5
occ:1.00
N A:PHE78 3.1 48.5 1.0
O A:PHE78 3.8 51.5 1.0
CB A:PHE78 3.8 50.0 1.0
CG2 A:VAL81 3.8 57.5 1.0
CA A:ARG77 3.9 46.2 1.0
CA A:PHE78 3.9 48.6 1.0
NH1 A:ARG85 3.9 56.9 1.0
CD2 A:PHE78 3.9 56.2 1.0
C A:ARG77 4.0 51.5 1.0
CB A:ARG77 4.1 45.2 1.0
N A:ARG85 4.2 79.5 1.0
CG A:ARG85 4.3 74.8 1.0
C A:PHE78 4.3 51.3 1.0
CG A:PHE78 4.4 52.7 1.0
CA A:ALA84 4.5 84.8 1.0
CG A:ARG77 4.7 47.1 1.0
CB A:ARG85 4.7 73.4 1.0
C A:ALA84 4.9 86.1 1.0
CZ A:ARG85 5.0 80.7 1.0

Chlorine binding site 2 out of 5 in 6hyx

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Chlorine binding site 2 out of 5 in the The Glic Pentameric Ligand-Gated Ion Channel Mutant Y197F-P250C


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 2 of The Glic Pentameric Ligand-Gated Ion Channel Mutant Y197F-P250C within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Cl402

b:63.1
occ:1.00
N B:PHE78 3.2 38.4 1.0
CD2 B:PHE78 3.6 45.6 1.0
CB B:PHE78 3.7 39.6 1.0
CG2 B:VAL81 3.7 40.4 1.0
NH1 B:ARG85 3.8 49.1 1.0
CA B:PHE78 3.9 38.1 1.0
CG B:ARG85 3.9 76.5 1.0
N B:ARG85 4.0 78.4 1.0
O B:PHE78 4.0 42.9 1.0
CA B:ARG77 4.1 37.0 1.0
C B:ARG77 4.1 42.0 1.0
CG B:PHE78 4.1 42.6 1.0
CB B:ARG85 4.4 73.8 1.0
CB B:ARG77 4.4 37.8 1.0
C B:PHE78 4.5 42.0 1.0
CA B:ALA84 4.5 81.0 1.0
CD B:ARG85 4.7 71.5 1.0
CE2 B:PHE78 4.7 49.2 1.0
C B:ALA84 4.7 84.1 1.0
CZ B:ARG85 4.8 71.4 1.0
CA B:ARG85 4.8 77.0 1.0
O B:ASN83 4.9 81.2 1.0
CB B:VAL81 4.9 39.9 1.0

Chlorine binding site 3 out of 5 in 6hyx

Go back to Chlorine Binding Sites List in 6hyx
Chlorine binding site 3 out of 5 in the The Glic Pentameric Ligand-Gated Ion Channel Mutant Y197F-P250C


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 3 of The Glic Pentameric Ligand-Gated Ion Channel Mutant Y197F-P250C within 5.0Å range:
probe atom residue distance (Å) B Occ
C:Cl401

b:59.9
occ:1.00
N C:PHE78 3.0 53.9 1.0
CB C:PHE78 3.7 55.4 1.0
O C:PHE78 3.7 56.3 1.0
CG2 C:VAL81 3.8 57.1 1.0
CA C:PHE78 3.8 53.7 1.0
CA C:ARG77 3.9 52.5 1.0
CD2 C:PHE78 3.9 61.6 1.0
C C:ARG77 3.9 57.1 1.0
NH1 C:ARG85 4.0 59.9 1.0
CB C:ARG77 4.1 52.4 1.0
C C:PHE78 4.3 55.7 1.0
CG C:PHE78 4.3 58.4 1.0
CG C:ARG85 4.3 69.3 1.0
N C:ARG85 4.3 81.8 1.0
CA C:ALA84 4.6 86.1 1.0
CG C:ARG77 4.7 57.5 1.0
CB C:ARG85 4.8 74.0 1.0
NH1 B:ARG105 4.9 96.9 1.0
CZ C:ARG85 5.0 85.9 1.0

Chlorine binding site 4 out of 5 in 6hyx

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Chlorine binding site 4 out of 5 in the The Glic Pentameric Ligand-Gated Ion Channel Mutant Y197F-P250C


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 4 of The Glic Pentameric Ligand-Gated Ion Channel Mutant Y197F-P250C within 5.0Å range:
probe atom residue distance (Å) B Occ
D:Cl401

b:61.3
occ:1.00
N D:PHE78 3.1 54.2 1.0
NH1 D:ARG85 3.7 60.0 1.0
CD2 D:PHE78 3.7 59.8 1.0
CB D:PHE78 3.8 54.9 1.0
CA D:ARG77 3.9 53.7 1.0
CG2 D:VAL81 3.9 62.1 1.0
CG D:ARG85 4.0 80.3 1.0
CA D:PHE78 4.0 53.9 1.0
C D:ARG77 4.0 57.7 1.0
O D:PHE78 4.0 59.2 1.0
N D:ARG85 4.0 87.0 1.0
CB D:ARG77 4.2 52.7 1.0
CG D:PHE78 4.2 57.3 1.0
CB D:ARG85 4.5 80.6 1.0
C D:PHE78 4.5 58.1 1.0
CA D:ALA84 4.5 89.7 1.0
CD D:ARG85 4.7 77.3 1.0
CZ D:ARG85 4.7 80.7 1.0
CG D:ARG77 4.8 59.9 1.0
CE2 D:PHE78 4.8 63.2 1.0
C D:ALA84 4.8 93.0 1.0
CA D:ARG85 4.9 85.5 1.0

Chlorine binding site 5 out of 5 in 6hyx

Go back to Chlorine Binding Sites List in 6hyx
Chlorine binding site 5 out of 5 in the The Glic Pentameric Ligand-Gated Ion Channel Mutant Y197F-P250C


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 5 of The Glic Pentameric Ligand-Gated Ion Channel Mutant Y197F-P250C within 5.0Å range:
probe atom residue distance (Å) B Occ
E:Cl401

b:68.3
occ:1.00
N E:PHE78 3.3 57.7 1.0
CG2 E:VAL81 3.8 67.2 1.0
CB E:PHE78 3.9 57.6 1.0
CD2 E:PHE78 3.9 62.0 1.0
NH1 E:ARG85 4.0 68.2 1.0
O E:PHE78 4.0 61.8 1.0
N E:ARG85 4.1 85.8 1.0
CA E:PHE78 4.1 57.0 1.0
CA E:ARG77 4.1 58.2 1.0
CG E:ARG85 4.2 79.7 1.0
C E:ARG77 4.2 61.9 1.0
CB E:ARG77 4.3 61.6 1.0
CA E:ALA84 4.4 91.7 1.0
CG E:PHE78 4.4 58.9 1.0
C E:PHE78 4.5 61.8 1.0
CB E:ARG85 4.6 78.5 1.0
C E:ALA84 4.8 92.6 1.0
CG E:ARG77 4.9 74.4 1.0
O E:ASN83 4.9 95.0 1.0
CD E:ARG85 4.9 78.0 1.0
CZ E:ARG85 5.0 90.8 1.0
CA E:ARG85 5.0 83.0 1.0

Reference:

H.Hu, K.Ataka, A.Menny, Z.Fourati, L.Sauguet, P.J.Corringer, P.Koehl, J.Heberle, M.Delarue. Electrostatics, Proton Sensor, and Networks Governing the Gating Transition in Glic, A Proton-Gated Pentameric Ion Channel. Proc. Natl. Acad. Sci. V. 115 12172 2018U.S.A..
ISSN: ESSN 1091-6490
PubMed: 30541892
DOI: 10.1073/PNAS.1813378116
Page generated: Sat Jul 12 15:32:53 2025

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