Magnesium in PDB 7zz8: Cryo-Em Structure of Lactococcus Lactis Pyruvate Carboxylase with Acetyl-Coa and Cyclic Di-Amp

Enzymatic activity of Cryo-Em Structure of Lactococcus Lactis Pyruvate Carboxylase with Acetyl-Coa and Cyclic Di-Amp

All present enzymatic activity of Cryo-Em Structure of Lactococcus Lactis Pyruvate Carboxylase with Acetyl-Coa and Cyclic Di-Amp:
6.4.1.1;

Other elements in 7zz8:

The structure of Cryo-Em Structure of Lactococcus Lactis Pyruvate Carboxylase with Acetyl-Coa and Cyclic Di-Amp also contains other interesting chemical elements:

Manganese (Mn) 4 atoms

Magnesium Binding Sites:

The binding sites of Magnesium atom in the Cryo-Em Structure of Lactococcus Lactis Pyruvate Carboxylase with Acetyl-Coa and Cyclic Di-Amp (pdb code 7zz8). This binding sites where shown within 5.0 Angstroms radius around Magnesium atom.
In total 8 binding sites of Magnesium where determined in the Cryo-Em Structure of Lactococcus Lactis Pyruvate Carboxylase with Acetyl-Coa and Cyclic Di-Amp, PDB code: 7zz8:
Jump to Magnesium binding site number: 1; 2; 3; 4; 5; 6; 7; 8;

Magnesium binding site 1 out of 8 in 7zz8

Go back to Magnesium Binding Sites List in 7zz8
Magnesium binding site 1 out of 8 in the Cryo-Em Structure of Lactococcus Lactis Pyruvate Carboxylase with Acetyl-Coa and Cyclic Di-Amp


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 1 of Cryo-Em Structure of Lactococcus Lactis Pyruvate Carboxylase with Acetyl-Coa and Cyclic Di-Amp within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Mg1201

b:74.2
occ:1.00
O A:THR522 2.1 77.3 1.0
OD1 A:ASP753 2.8 84.8 1.0
O A:VAL519 3.0 79.3 1.0
C A:THR522 3.3 74.9 1.0
NH2 A:ARG783 3.3 65.4 1.0
CA A:THR522 4.0 76.4 1.0
N A:THR522 4.0 78.9 1.0
CG A:ASP753 4.0 82.6 1.0
O A:GLU524 4.1 77.4 1.0
O A:LYS520 4.1 77.6 1.0
CB A:THR522 4.1 74.7 1.0
C A:VAL519 4.2 76.5 1.0
C A:LYS520 4.3 77.6 1.0
N A:LYS523 4.3 68.0 1.0
O A:LYS523 4.4 74.6 1.0
CA A:LYS520 4.5 77.5 1.0
CZ A:ARG783 4.5 64.2 1.0
C A:LYS523 4.5 73.7 1.0
CA A:LYS523 4.6 69.2 1.0
CB A:ASP753 4.6 75.6 1.0
CA A:ASP753 4.7 70.4 1.0
N A:LYS520 4.8 77.2 1.0
CG2 A:THR522 4.9 71.0 1.0
OD2 A:ASP753 4.9 81.4 1.0
C A:GLU524 5.0 72.6 1.0

Magnesium binding site 2 out of 8 in 7zz8

Go back to Magnesium Binding Sites List in 7zz8
Magnesium binding site 2 out of 8 in the Cryo-Em Structure of Lactococcus Lactis Pyruvate Carboxylase with Acetyl-Coa and Cyclic Di-Amp


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 2 of Cryo-Em Structure of Lactococcus Lactis Pyruvate Carboxylase with Acetyl-Coa and Cyclic Di-Amp within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Mg1204

b:88.9
occ:1.00
OE1 A:GLU274 2.1 67.0 1.0
O3A A:ADP1203 2.1 108.9 1.0
OE1 A:GLU286 2.4 66.5 1.0
OE2 A:GLU274 2.6 53.4 1.0
CD A:GLU274 2.6 63.6 1.0
O1A A:ADP1203 2.8 95.8 1.0
PA A:ADP1203 2.9 112.8 1.0
PB A:ADP1203 3.3 109.1 1.0
O1B A:ADP1203 3.3 98.9 1.0
O5' A:ADP1203 3.5 100.7 1.0
CD A:GLU286 3.6 63.9 1.0
O3B A:ADP1203 3.9 98.9 1.0
NE2 A:HIS207 4.0 52.8 1.0
CG A:GLU274 4.1 57.5 1.0
OD1 A:ASN288 4.3 52.6 1.0
CB A:GLU286 4.3 56.9 1.0
O2A A:ADP1203 4.3 102.6 1.0
OE2 A:GLU286 4.4 62.8 1.0
CE1 A:HIS207 4.4 49.3 1.0
O2B A:ADP1203 4.5 97.6 1.0
CG A:GLU286 4.5 58.3 1.0
CB A:GLU274 4.7 42.7 1.0
C5' A:ADP1203 4.8 97.0 1.0

Magnesium binding site 3 out of 8 in 7zz8

Go back to Magnesium Binding Sites List in 7zz8
Magnesium binding site 3 out of 8 in the Cryo-Em Structure of Lactococcus Lactis Pyruvate Carboxylase with Acetyl-Coa and Cyclic Di-Amp


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 3 of Cryo-Em Structure of Lactococcus Lactis Pyruvate Carboxylase with Acetyl-Coa and Cyclic Di-Amp within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Mg1201

b:62.2
occ:1.00
O B:THR522 2.1 65.2 1.0
OD1 B:ASP753 2.4 83.7 1.0
O B:VAL519 2.9 60.8 1.0
C B:THR522 3.3 66.8 1.0
NH2 B:ARG783 3.5 59.7 1.0
CG B:ASP753 3.7 79.9 1.0
O B:LYS520 3.9 61.3 1.0
N B:THR522 4.0 73.7 1.0
CA B:THR522 4.0 70.0 1.0
C B:VAL519 4.1 60.9 1.0
C B:LYS520 4.2 61.1 1.0
CB B:THR522 4.2 64.0 1.0
O B:GLU524 4.3 74.7 1.0
CA B:LYS520 4.3 58.7 1.0
N B:LYS523 4.3 68.0 1.0
OD2 B:ASP753 4.5 77.5 1.0
CB B:ASP753 4.5 69.9 1.0
CA B:ASP753 4.6 65.7 1.0
CA B:LYS523 4.6 71.8 1.0
CZ B:ARG783 4.6 60.8 1.0
N B:LYS520 4.7 60.1 1.0
C B:LYS523 4.8 76.6 1.0
N B:ASN521 5.0 59.7 1.0
O B:VAL752 5.0 65.7 1.0

Magnesium binding site 4 out of 8 in 7zz8

Go back to Magnesium Binding Sites List in 7zz8
Magnesium binding site 4 out of 8 in the Cryo-Em Structure of Lactococcus Lactis Pyruvate Carboxylase with Acetyl-Coa and Cyclic Di-Amp


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 4 of Cryo-Em Structure of Lactococcus Lactis Pyruvate Carboxylase with Acetyl-Coa and Cyclic Di-Amp within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Mg1204

b:95.1
occ:1.00
O1B B:ADP1203 2.1 124.4 1.0
OE1 B:GLU274 2.1 90.1 1.0
CD B:GLU274 2.9 89.8 1.0
OE2 B:GLU274 3.0 87.8 1.0
OE1 B:GLU286 3.1 89.0 1.0
PB B:ADP1203 3.4 131.5 1.0
O2B B:ADP1203 3.8 124.7 1.0
C5' B:ADP1203 3.9 125.6 1.0
NE2 B:HIS207 4.0 69.5 1.0
O1A B:ADP1203 4.1 125.1 1.0
CD B:GLU286 4.3 88.1 1.0
O3B B:ADP1203 4.3 125.5 1.0
CG B:GLU274 4.3 85.0 1.0
CB B:GLU286 4.4 83.4 1.0
O3A B:ADP1203 4.5 128.9 1.0
CE1 B:HIS207 4.7 69.6 1.0
O5' B:ADP1203 4.7 128.4 1.0
PA B:ADP1203 4.7 134.8 1.0
CB B:GLU274 4.8 75.6 1.0
C3' B:ADP1203 4.9 123.5 1.0
CG B:GLU286 5.0 85.5 1.0
C4' B:ADP1203 5.0 124.1 1.0

Magnesium binding site 5 out of 8 in 7zz8

Go back to Magnesium Binding Sites List in 7zz8
Magnesium binding site 5 out of 8 in the Cryo-Em Structure of Lactococcus Lactis Pyruvate Carboxylase with Acetyl-Coa and Cyclic Di-Amp


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 5 of Cryo-Em Structure of Lactococcus Lactis Pyruvate Carboxylase with Acetyl-Coa and Cyclic Di-Amp within 5.0Å range:
probe atom residue distance (Å) B Occ
C:Mg1202

b:87.9
occ:1.00
O C:THR522 2.1 73.9 1.0
O C:VAL519 2.5 76.5 1.0
C C:THR522 3.0 68.4 1.0
N C:THR522 3.4 74.2 1.0
CB C:THR522 3.4 70.7 1.0
CA C:THR522 3.4 71.2 1.0
C C:VAL519 3.7 72.1 1.0
NH2 C:ARG783 3.9 64.9 1.0
C C:LYS520 4.0 74.7 1.0
O C:LYS520 4.0 74.6 1.0
O C:GLU524 4.0 74.4 1.0
OG1 C:THR522 4.2 75.1 1.0
CA C:LYS520 4.2 73.2 1.0
N C:LYS523 4.3 62.9 1.0
N C:LYS520 4.4 74.0 1.0
OD2 C:ASP753 4.5 87.2 1.0
N C:ASN521 4.5 67.2 1.0
C C:ASN521 4.5 70.2 1.0
CG2 C:THR522 4.5 70.5 1.0
C C:LYS523 4.8 71.4 1.0
CA C:LYS523 4.8 68.0 1.0
CA C:VAL519 4.8 68.0 1.0
O C:LYS523 4.8 72.0 1.0
CG1 C:VAL519 5.0 70.0 1.0

Magnesium binding site 6 out of 8 in 7zz8

Go back to Magnesium Binding Sites List in 7zz8
Magnesium binding site 6 out of 8 in the Cryo-Em Structure of Lactococcus Lactis Pyruvate Carboxylase with Acetyl-Coa and Cyclic Di-Amp


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 6 of Cryo-Em Structure of Lactococcus Lactis Pyruvate Carboxylase with Acetyl-Coa and Cyclic Di-Amp within 5.0Å range:
probe atom residue distance (Å) B Occ
C:Mg1205

b:88.7
occ:1.00
OE1 C:GLU274 2.1 68.1 1.0
O3A C:ADP1204 2.4 107.8 1.0
OE2 C:GLU286 2.5 71.4 1.0
O2A C:ADP1204 2.6 97.7 1.0
CD C:GLU274 2.9 65.5 1.0
OE2 C:GLU274 3.0 60.6 1.0
PA C:ADP1204 3.0 112.0 1.0
CD C:GLU286 3.6 69.5 1.0
O5' C:ADP1204 3.7 102.1 1.0
PB C:ADP1204 3.7 109.7 1.0
O3B C:ADP1204 3.8 100.0 1.0
CG C:GLU286 4.0 65.5 1.0
O2B C:ADP1204 4.2 96.1 1.0
C5' C:ADP1204 4.3 97.8 1.0
CE1 C:HIS207 4.3 52.7 1.0
CG C:GLU274 4.3 58.7 1.0
O1A C:ADP1204 4.4 101.5 1.0
OD1 C:ASN288 4.6 56.8 1.0
OE1 C:GLU286 4.6 68.5 1.0
O1B C:ADP1204 4.8 99.7 1.0
NE2 C:HIS207 4.8 56.4 1.0
CB C:GLU274 4.9 45.2 1.0
NZ C:LYS236 5.0 58.9 1.0

Magnesium binding site 7 out of 8 in 7zz8

Go back to Magnesium Binding Sites List in 7zz8
Magnesium binding site 7 out of 8 in the Cryo-Em Structure of Lactococcus Lactis Pyruvate Carboxylase with Acetyl-Coa and Cyclic Di-Amp


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 7 of Cryo-Em Structure of Lactococcus Lactis Pyruvate Carboxylase with Acetyl-Coa and Cyclic Di-Amp within 5.0Å range:
probe atom residue distance (Å) B Occ
D:Mg1201

b:57.6
occ:1.00
O D:THR522 2.1 67.8 1.0
OD1 D:ASP753 2.7 79.5 1.0
O D:VAL519 2.8 57.5 1.0
OG1 D:THR522 3.0 67.2 1.0
C D:THR522 3.2 62.8 1.0
NH2 D:ARG783 3.4 64.0 1.0
N D:THR522 3.7 69.0 1.0
CA D:THR522 3.8 65.2 1.0
CB D:THR522 3.9 65.1 1.0
CG D:ASP753 4.0 76.5 1.0
C D:VAL519 4.0 56.0 1.0
O D:GLU524 4.1 75.1 1.0
C D:LYS520 4.3 60.0 1.0
O D:LYS520 4.3 66.0 1.0
N D:LYS523 4.4 60.3 1.0
CA D:LYS520 4.4 58.5 1.0
CZ D:ARG783 4.5 63.3 1.0
N D:LYS520 4.7 58.2 1.0
CA D:LYS523 4.7 68.1 1.0
C D:LYS523 4.7 68.4 1.0
N D:ASN521 4.7 57.5 1.0
O D:LYS523 4.8 65.0 1.0
CB D:ASP753 4.8 67.2 1.0
CA D:ASP753 4.8 61.5 1.0
OD2 D:ASP753 4.8 74.8 1.0
C D:ASN521 4.9 64.2 1.0

Magnesium binding site 8 out of 8 in 7zz8

Go back to Magnesium Binding Sites List in 7zz8
Magnesium binding site 8 out of 8 in the Cryo-Em Structure of Lactococcus Lactis Pyruvate Carboxylase with Acetyl-Coa and Cyclic Di-Amp


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 8 of Cryo-Em Structure of Lactococcus Lactis Pyruvate Carboxylase with Acetyl-Coa and Cyclic Di-Amp within 5.0Å range:
probe atom residue distance (Å) B Occ
D:Mg1204

b:111.2
occ:1.00
OE1 D:GLU274 2.1 84.4 1.0
O3A D:ADP1203 2.2 121.0 1.0
O2A D:ADP1203 2.3 116.0 1.0
OE2 D:GLU286 2.7 88.5 1.0
OE2 D:GLU274 2.7 79.0 1.0
PA D:ADP1203 2.7 124.6 1.0
CD D:GLU274 2.7 83.5 1.0
O5' D:ADP1203 3.3 117.4 1.0
PB D:ADP1203 3.7 121.8 1.0
CD D:GLU286 3.7 86.8 1.0
O3B D:ADP1203 3.9 114.6 1.0
CE1 D:HIS207 4.0 68.0 1.0
CG D:GLU286 4.1 83.8 1.0
C5' D:ADP1203 4.1 115.6 1.0
O1A D:ADP1203 4.1 114.0 1.0
O2B D:ADP1203 4.1 112.9 1.0
CG D:GLU274 4.2 79.2 1.0
NE2 D:HIS207 4.3 72.1 1.0
O1B D:ADP1203 4.7 113.5 1.0
OE2 D:GLU209 4.7 77.3 1.0
CB D:GLU274 4.8 71.4 1.0
OE1 D:GLU286 4.8 85.0 1.0
OD1 D:ASN288 4.9 74.4 1.0
C3' D:ADP1203 4.9 113.2 1.0

Reference:

J.P.Lopez-Alonso, M.Lazaro, D.Gil-Carton, P.H.Choi, L.Tong, M.Valle. Cryoem Structural Exploration of Catalytically Active Enzyme Pyruvate Carboxylase. Nat Commun V. 13 6185 2022.
ISSN: ESSN 2041-1723
PubMed: 36261450
DOI: 10.1038/S41467-022-33987-2
Page generated: Fri Apr 7 05:03:53 2023

Last articles

Zn in 8WB0
Zn in 8WAX
Zn in 8WAU
Zn in 8WAZ
Zn in 8WAY
Zn in 8WAV
Zn in 8WAW
Zn in 8WAT
Zn in 8W7M
Zn in 8WD3
© Copyright 2008-2020 by atomistry.com
Home   |    Site Map   |    Copyright   |    Contact us   |    Privacy