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Mercury in PDB 5awg: Crystal Structure of Hg-Bound Sufb-Sufc-Sufd Complex From Escherichia Coli

Protein crystallography data

The structure of Crystal Structure of Hg-Bound Sufb-Sufc-Sufd Complex From Escherichia Coli, PDB code: 5awg was solved by K.Hirabayashi, K.Wada, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 43.94 / 4.28
Space group P 1 21 1
Cell size a, b, c (Å), α, β, γ (°) 119.848, 139.379, 124.414, 90.00, 113.55, 90.00
R / Rfree (%) 29.5 / 34

Mercury Binding Sites:

The binding sites of Mercury atom in the Crystal Structure of Hg-Bound Sufb-Sufc-Sufd Complex From Escherichia Coli (pdb code 5awg). This binding sites where shown within 5.0 Angstroms radius around Mercury atom.
In total 4 binding sites of Mercury where determined in the Crystal Structure of Hg-Bound Sufb-Sufc-Sufd Complex From Escherichia Coli, PDB code: 5awg:
Jump to Mercury binding site number: 1; 2; 3; 4;

Mercury binding site 1 out of 4 in 5awg

Go back to Mercury Binding Sites List in 5awg
Mercury binding site 1 out of 4 in the Crystal Structure of Hg-Bound Sufb-Sufc-Sufd Complex From Escherichia Coli


Mono view


Stereo pair view

A full contact list of Mercury with other atoms in the Hg binding site number 1 of Crystal Structure of Hg-Bound Sufb-Sufc-Sufd Complex From Escherichia Coli within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Hg600

b:0.5
occ:1.00
SG A:CYS405 2.5 0.8 1.0
O A:CYS405 2.6 96.1 1.0
OG1 A:THR418 2.7 0.7 1.0
CG2 A:THR418 3.2 93.2 1.0
CB A:CYS405 3.4 93.1 1.0
CB A:THR418 3.4 95.0 1.0
OG A:SER407 3.4 83.2 1.0
C A:CYS405 3.5 86.0 1.0
CB A:ALA435 4.0 88.9 1.0
CA A:CYS405 4.1 87.2 1.0
N A:ASP406 4.5 86.5 1.0
CB A:SER407 4.7 94.4 1.0
CA A:ASP406 4.8 83.4 1.0
C A:ASP406 4.8 84.6 1.0
CA A:THR418 4.8 81.2 1.0
N A:SER407 4.8 82.5 1.0
CA A:ALA435 4.9 81.9 1.0

Mercury binding site 2 out of 4 in 5awg

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Mercury binding site 2 out of 4 in the Crystal Structure of Hg-Bound Sufb-Sufc-Sufd Complex From Escherichia Coli


Mono view


Stereo pair view

A full contact list of Mercury with other atoms in the Hg binding site number 2 of Crystal Structure of Hg-Bound Sufb-Sufc-Sufd Complex From Escherichia Coli within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Hg600

b:0.8
occ:1.00
N B:SER359 2.5 0.4 1.0
SG B:CYS358 2.5 0.3 1.0
C B:CYS358 2.7 0.9 1.0
CB B:CYS358 2.8 0.0 1.0
CD2 B:LEU349 2.8 0.2 1.0
CA B:SER359 3.1 99.7 1.0
CD1 B:LEU349 3.2 88.4 1.0
CA B:CYS358 3.2 0.3 1.0
C B:SER359 3.3 88.3 1.0
O B:CYS358 3.4 0.5 1.0
O B:GLY328 3.5 92.0 1.0
O B:SER359 3.5 94.1 1.0
CG B:LEU349 3.6 0.3 1.0
N B:HIS360 4.1 84.0 1.0
C B:GLY328 4.5 84.2 1.0
N B:CYS358 4.5 88.2 1.0
CB B:SER359 4.5 88.9 1.0
CB B:LEU349 4.6 0.9 1.0
CB B:HIS360 4.9 81.7 1.0
CD2 B:HIS360 4.9 82.5 1.0
CA B:HIS360 5.0 76.6 1.0

Mercury binding site 3 out of 4 in 5awg

Go back to Mercury Binding Sites List in 5awg
Mercury binding site 3 out of 4 in the Crystal Structure of Hg-Bound Sufb-Sufc-Sufd Complex From Escherichia Coli


Mono view


Stereo pair view

A full contact list of Mercury with other atoms in the Hg binding site number 3 of Crystal Structure of Hg-Bound Sufb-Sufc-Sufd Complex From Escherichia Coli within 5.0Å range:
probe atom residue distance (Å) B Occ
E:Hg600

b:0.4
occ:1.00
O E:CYS405 2.3 99.0 1.0
OG1 E:THR418 2.4 0.6 1.0
OG E:SER407 2.8 0.5 1.0
SG E:CYS405 2.9 0.1 1.0
C E:CYS405 3.1 97.8 1.0
CB E:THR418 3.4 0.3 1.0
CG2 E:THR418 3.5 0.3 1.0
N E:ASP406 3.6 0.3 1.0
CA E:ASP406 3.6 0.4 1.0
C E:ASP406 3.7 0.1 1.0
CB E:CYS405 3.8 95.9 1.0
N E:SER407 3.8 0.8 1.0
CA E:CYS405 4.1 96.8 1.0
CB E:SER407 4.1 0.8 1.0
CB E:ALA435 4.2 96.5 1.0
O E:ASP406 4.3 0.6 1.0
CA E:SER407 4.5 0.3 1.0
CA E:THR418 4.7 94.4 1.0
CD1 F:LEU349 4.9 0.6 1.0

Mercury binding site 4 out of 4 in 5awg

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Mercury binding site 4 out of 4 in the Crystal Structure of Hg-Bound Sufb-Sufc-Sufd Complex From Escherichia Coli


Mono view


Stereo pair view

A full contact list of Mercury with other atoms in the Hg binding site number 4 of Crystal Structure of Hg-Bound Sufb-Sufc-Sufd Complex From Escherichia Coli within 5.0Å range:
probe atom residue distance (Å) B Occ
F:Hg600

b:0.4
occ:0.94
SG F:CYS358 2.6 97.2 1.0
CD1 F:LEU349 2.6 0.6 1.0
N F:SER359 2.8 0.9 1.0
CG F:LEU349 3.1 0.7 1.0
CB F:CYS358 3.1 96.6 1.0
C F:CYS358 3.1 0.9 1.0
CD2 F:LEU349 3.2 0.5 1.0
CA F:SER359 3.3 0.7 1.0
C F:SER359 3.4 0.9 1.0
CA F:CYS358 3.6 0.8 1.0
O F:SER359 3.6 0.9 1.0
O F:CYS358 3.6 0.6 1.0
O F:GLY328 3.9 89.8 1.0
N F:HIS360 4.0 0.3 1.0
CB F:HIS360 4.2 0.7 1.0
CD1 F:ILE317 4.5 87.9 1.0
CB F:LEU349 4.6 0.4 1.0
CG F:HIS360 4.6 0.7 1.0
CA F:HIS360 4.8 97.6 1.0
CB F:SER359 4.8 86.7 1.0
N F:CYS358 4.9 0.7 1.0
C F:GLY328 4.9 91.5 1.0

Reference:

K.Hirabayashi, E.Yuda, N.Tanaka, S.Katayama, K.Iwasaki, T.Matsumoto, G.Kurisu, F.W.Outten, K.Fukuyama, Y.Takahashi, K.Wada. Functional Dynamics Revealed By the Structure of the Sufbcd Complex, A Novel Atp-Binding Cassette (Abc) Protein That Serves As A Scaffold For Iron-Sulfur Cluster Biogenesis J.Biol.Chem. V. 290 29717 2015.
ISSN: ESSN 1083-351X
PubMed: 26472926
DOI: 10.1074/JBC.M115.680934
Page generated: Sun Dec 13 19:12:16 2020

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