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Magnesium in PDB 7nkj: Mycobacterium Smegmatis Atp Synthase F1 State 3

Enzymatic activity of Mycobacterium Smegmatis Atp Synthase F1 State 3

All present enzymatic activity of Mycobacterium Smegmatis Atp Synthase F1 State 3:
7.1.2.2;

Magnesium Binding Sites:

The binding sites of Magnesium atom in the Mycobacterium Smegmatis Atp Synthase F1 State 3 (pdb code 7nkj). This binding sites where shown within 5.0 Angstroms radius around Magnesium atom.
In total 5 binding sites of Magnesium where determined in the Mycobacterium Smegmatis Atp Synthase F1 State 3, PDB code: 7nkj:
Jump to Magnesium binding site number: 1; 2; 3; 4; 5;

Magnesium binding site 1 out of 5 in 7nkj

Go back to Magnesium Binding Sites List in 7nkj
Magnesium binding site 1 out of 5 in the Mycobacterium Smegmatis Atp Synthase F1 State 3


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 1 of Mycobacterium Smegmatis Atp Synthase F1 State 3 within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Mg601

b:29.6
occ:1.00
O2G A:ATP600 2.2 30.9 1.0
OG1 A:THR179 2.2 28.7 1.0
O A:HOH811 2.2 28.4 1.0
O A:HOH783 2.2 28.8 1.0
O2B A:ATP600 2.2 30.9 1.0
O A:HOH767 2.2 29.5 1.0
HB A:THR179 3.0 28.7 1.0
CB A:THR179 3.2 28.7 1.0
H A:THR179 3.3 28.7 1.0
PG A:ATP600 3.3 30.9 1.0
PB A:ATP600 3.4 30.9 1.0
O3B A:ATP600 3.4 30.9 1.0
OD2 A:ASP272 3.8 27.5 1.0
N A:THR179 4.0 28.7 1.0
O3G A:ATP600 4.0 30.9 1.0
OD1 A:ASP272 4.0 27.5 1.0
O A:HOH808 4.0 32.3 1.0
HG21 A:THR179 4.0 28.7 1.0
CA A:THR179 4.1 28.7 1.0
O A:HOH711 4.2 30.0 1.0
O A:HOH745 4.2 31.5 1.0
CG2 A:THR179 4.2 28.7 1.0
HB2 A:LYS178 4.3 28.8 1.0
O3A A:ATP600 4.3 30.9 1.0
O2A A:ATP600 4.3 30.9 1.0
CG A:ASP272 4.4 27.5 1.0
O A:HOH816 4.4 33.3 1.0
O1B A:ATP600 4.4 30.9 1.0
HE2 A:LYS178 4.4 28.8 1.0
HA A:THR179 4.5 28.7 1.0
O1G A:ATP600 4.5 30.9 1.0
O A:HOH708 4.5 29.9 1.0
O A:HOH817 4.5 32.4 1.0
PA A:ATP600 4.7 30.9 1.0
O1A A:ATP600 4.8 30.9 1.0
HG23 A:THR179 4.8 28.7 1.0
HZ3 A:LYS178 4.8 28.8 1.0
HG22 A:THR179 4.9 28.7 1.0
HG21 A:ILE329 5.0 27.3 1.0

Magnesium binding site 2 out of 5 in 7nkj

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Magnesium binding site 2 out of 5 in the Mycobacterium Smegmatis Atp Synthase F1 State 3


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 2 of Mycobacterium Smegmatis Atp Synthase F1 State 3 within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Mg601

b:33.8
occ:1.00
O2B B:ATP600 2.2 36.2 1.0
O2G B:ATP600 2.2 36.2 1.0
O B:HOH752 2.2 33.3 1.0
OG1 B:THR179 2.2 33.0 1.0
O B:HOH756 2.2 31.7 1.0
O B:HOH711 2.2 31.2 1.0
HB B:THR179 3.1 33.0 1.0
CB B:THR179 3.2 33.0 1.0
PB B:ATP600 3.3 36.2 1.0
O3B B:ATP600 3.4 36.2 1.0
PG B:ATP600 3.4 36.2 1.0
H B:THR179 3.4 33.0 1.0
OD2 B:ASP272 3.7 29.6 1.0
O B:HOH765 3.9 34.0 1.0
HG21 B:THR179 4.0 33.0 1.0
OD1 B:ASP272 4.0 29.6 1.0
N B:THR179 4.1 33.0 1.0
O3G B:ATP600 4.2 36.2 1.0
CG2 B:THR179 4.2 33.0 1.0
CA B:THR179 4.2 33.0 1.0
O1A B:ATP600 4.3 36.2 1.0
O3A B:ATP600 4.3 36.2 1.0
CG B:ASP272 4.3 29.6 1.0
OE1 B:GLN211 4.3 31.7 1.0
O1B B:ATP600 4.4 36.2 1.0
HB2 B:LYS178 4.4 32.7 1.0
O1G B:ATP600 4.4 36.2 1.0
O B:HOH705 4.5 32.7 1.0
HE2 B:LYS178 4.5 32.7 1.0
O B:HOH771 4.5 35.7 1.0
HA B:THR179 4.6 33.0 1.0
PA B:ATP600 4.6 36.2 1.0
O2A B:ATP600 4.8 36.2 1.0
HG23 B:THR179 4.8 33.0 1.0
HG22 B:THR179 4.8 33.0 1.0
HZ3 B:LYS178 4.9 32.7 1.0
HZ1 B:LYS178 5.0 32.7 1.0

Magnesium binding site 3 out of 5 in 7nkj

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Magnesium binding site 3 out of 5 in the Mycobacterium Smegmatis Atp Synthase F1 State 3


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 3 of Mycobacterium Smegmatis Atp Synthase F1 State 3 within 5.0Å range:
probe atom residue distance (Å) B Occ
C:Mg601

b:28.2
occ:1.00
O2G C:ATP600 2.2 31.2 1.0
O C:HOH763 2.2 29.3 1.0
OG1 C:THR179 2.2 29.1 1.0
O C:HOH789 2.2 29.6 1.0
O C:HOH725 2.2 27.7 1.0
O2B C:ATP600 2.2 31.2 1.0
HB C:THR179 3.0 29.1 1.0
CB C:THR179 3.2 29.1 1.0
H C:THR179 3.3 29.1 1.0
PB C:ATP600 3.4 31.2 1.0
PG C:ATP600 3.4 31.2 1.0
O3B C:ATP600 3.4 31.2 1.0
HG21 C:THR179 4.0 29.1 1.0
N C:THR179 4.0 29.1 1.0
OD2 C:ASP272 4.0 28.8 1.0
OD1 C:ASP272 4.0 28.8 1.0
O C:HOH722 4.1 31.7 1.0
CA C:THR179 4.2 29.1 1.0
CG2 C:THR179 4.2 29.1 1.0
O1A C:ATP600 4.2 31.2 1.0
O3G C:ATP600 4.2 31.2 1.0
O C:HOH756 4.3 32.3 1.0
HB2 C:LYS178 4.3 29.5 1.0
O3A C:ATP600 4.3 31.2 1.0
O1B C:ATP600 4.4 31.2 1.0
O1G C:ATP600 4.5 31.2 1.0
O C:HOH709 4.5 32.0 1.0
CG C:ASP272 4.5 28.8 1.0
HA C:THR179 4.5 29.1 1.0
HE2 C:LYS178 4.6 29.5 1.0
PA C:ATP600 4.6 31.2 1.0
O2A C:ATP600 4.7 31.2 1.0
HG23 C:THR179 4.7 29.1 1.0
O C:HOH712 4.8 32.0 1.0
HG22 C:THR179 4.8 29.1 1.0
HZ3 C:LYS178 4.8 29.5 1.0
HZ1 C:LYS178 4.9 29.5 1.0
HD13 C:ILE329 4.9 28.3 1.0
HG21 C:ILE329 4.9 28.3 1.0

Magnesium binding site 4 out of 5 in 7nkj

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Magnesium binding site 4 out of 5 in the Mycobacterium Smegmatis Atp Synthase F1 State 3


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 4 of Mycobacterium Smegmatis Atp Synthase F1 State 3 within 5.0Å range:
probe atom residue distance (Å) B Occ
D:Mg601

b:31.2
occ:1.00
OG1 D:THR167 2.2 30.4 1.0
O D:HOH713 2.2 31.8 1.0
O2B D:ADP600 2.2 30.7 1.0
O D:HOH703 2.2 30.8 1.0
O D:HOH702 2.2 31.7 1.0
O D:HOH743 2.2 31.6 1.0
HB D:THR167 3.0 30.4 1.0
CB D:THR167 3.1 30.4 1.0
HH12 D:ARG193 3.1 30.8 1.0
PB D:ADP600 3.3 30.7 1.0
H D:THR167 3.4 30.4 1.0
O3B D:ADP600 3.5 30.7 1.0
HH11 D:ARG193 3.7 30.8 1.0
NH1 D:ARG193 3.8 30.8 1.0
HH11 C:ARG376 3.8 30.4 1.0
HH12 C:ARG376 3.9 30.4 1.0
O2A D:ADP600 3.9 30.7 1.0
N D:THR167 3.9 30.4 1.0
OE2 D:GLU196 3.9 31.7 1.0
OE1 D:GLU192 3.9 31.6 1.0
HG21 D:THR167 4.1 30.4 1.0
O3A D:ADP600 4.1 30.7 1.0
CA D:THR167 4.1 30.4 1.0
HB2 D:LYS166 4.1 28.9 1.0
OE1 D:GLU196 4.1 31.7 1.0
NH1 C:ARG376 4.2 30.4 1.0
OD2 D:ASP254 4.2 30.2 1.0
CG2 D:THR167 4.2 30.4 1.0
PA D:ADP600 4.3 30.7 1.0
OD1 D:ASP254 4.3 30.2 1.0
HA D:THR167 4.3 30.4 1.0
O1A D:ADP600 4.4 30.7 1.0
CD D:GLU196 4.4 31.7 1.0
CD D:GLU192 4.4 31.6 1.0
HE2 D:LYS166 4.5 28.9 1.0
O1B D:ADP600 4.6 30.7 1.0
HZ3 D:LYS166 4.7 28.9 1.0
HZ1 D:LYS166 4.7 28.9 1.0
CG D:ASP254 4.7 30.2 1.0
OE2 D:GLU192 4.7 31.6 1.0
HG3 D:GLU192 4.8 31.6 1.0
HG23 D:THR167 4.8 30.4 1.0
HG22 D:THR167 4.8 30.4 1.0
O D:HOH783 4.9 31.5 1.0
HD22 D:ASN255 5.0 28.6 1.0
C D:LYS166 5.0 28.9 1.0
CZ D:ARG193 5.0 30.8 1.0
CB D:LYS166 5.0 28.9 1.0

Magnesium binding site 5 out of 5 in 7nkj

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Magnesium binding site 5 out of 5 in the Mycobacterium Smegmatis Atp Synthase F1 State 3


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 5 of Mycobacterium Smegmatis Atp Synthase F1 State 3 within 5.0Å range:
probe atom residue distance (Å) B Occ
F:Mg601

b:29.2
occ:1.00
OG1 F:THR167 2.2 29.3 1.0
O2B F:ATP600 2.2 30.6 1.0
O2G F:ATP600 2.2 30.6 1.0
O F:HOH701 2.2 29.6 1.0
O F:HOH761 2.2 28.1 1.0
O F:HOH708 2.2 28.1 1.0
HB F:THR167 3.0 29.3 1.0
CB F:THR167 3.1 29.3 1.0
HH12 F:ARG193 3.2 29.9 1.0
PB F:ATP600 3.4 30.6 1.0
O3B F:ATP600 3.4 30.6 1.0
PG F:ATP600 3.4 30.6 1.0
OE1 F:GLU192 3.5 30.6 1.0
H F:THR167 3.5 29.3 1.0
NH1 F:ARG193 3.8 29.9 1.0
HH11 F:ARG193 3.8 29.9 1.0
HE2 F:LYS166 3.9 28.5 1.0
HG21 F:THR167 4.0 29.3 1.0
N F:THR167 4.0 29.3 1.0
HB2 F:LYS166 4.0 28.5 1.0
OE2 F:GLU196 4.0 31.4 1.0
O F:HOH750 4.0 29.9 1.0
O2A F:ATP600 4.1 30.6 1.0
OD2 F:ASP254 4.1 29.1 1.0
CA F:THR167 4.1 29.3 1.0
OE1 F:GLU196 4.1 31.4 1.0
HH12 B:ARG376 4.1 32.9 1.0
CG2 F:THR167 4.2 29.3 1.0
O3A F:ATP600 4.3 30.6 1.0
O1G F:ATP600 4.3 30.6 1.0
O3G F:ATP600 4.4 30.6 1.0
O F:HOH702 4.4 29.6 1.0
HA F:THR167 4.4 29.3 1.0
O1B F:ATP600 4.4 30.6 1.0
CD F:GLU196 4.5 31.4 1.0
OD1 F:ASP254 4.5 29.1 1.0
CD F:GLU192 4.6 30.6 1.0
HG3 F:GLU192 4.6 30.6 1.0
PA F:ATP600 4.6 30.6 1.0
HG23 F:THR167 4.8 29.3 1.0
CG F:ASP254 4.8 29.1 1.0
HG22 F:THR167 4.8 29.3 1.0
NH1 B:ARG376 4.8 32.9 1.0
CE F:LYS166 4.8 28.5 1.0
HZ1 F:LYS166 4.9 28.5 1.0
HH11 B:ARG376 4.9 32.9 1.0
O1A F:ATP600 4.9 30.6 1.0
CB F:LYS166 4.9 28.5 1.0
HH22 F:ARG193 5.0 29.9 1.0
CZ F:ARG193 5.0 29.9 1.0

Reference:

J.Petri, M.G.Montgomery, T.J.Spikes, G.M.Cook, J.E.Walker. Structure of the Atp Synthase From Mycobacterium Smegmatis To Be Published.
Page generated: Thu Oct 3 02:08:44 2024

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