Magnesium in PDB 7o0c: Human Phosphomannomutase 2 (PMM2) Wild-Type in Apo State
Enzymatic activity of Human Phosphomannomutase 2 (PMM2) Wild-Type in Apo State
All present enzymatic activity of Human Phosphomannomutase 2 (PMM2) Wild-Type in Apo State:
5.4.2.8;
Protein crystallography data
The structure of Human Phosphomannomutase 2 (PMM2) Wild-Type in Apo State, PDB code: 7o0c
was solved by
S.Ramon-Maiques,
A.Briso-Montiano,
F.Del Cano-Ochoa,
A.Vilas,
B.Perez,
V.Rubio,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
39.40 /
2.80
|
Space group
|
P 65 2 2
|
Cell size a, b, c (Å), α, β, γ (°)
|
70.582,
70.582,
360.801,
90,
90,
120
|
R / Rfree (%)
|
21.7 /
26.8
|
Other elements in 7o0c:
The structure of Human Phosphomannomutase 2 (PMM2) Wild-Type in Apo State also contains other interesting chemical elements:
Magnesium Binding Sites:
The binding sites of Magnesium atom in the Human Phosphomannomutase 2 (PMM2) Wild-Type in Apo State
(pdb code 7o0c). This binding sites where shown within
5.0 Angstroms radius around Magnesium atom.
In total 4 binding sites of Magnesium where determined in the
Human Phosphomannomutase 2 (PMM2) Wild-Type in Apo State, PDB code: 7o0c:
Jump to Magnesium binding site number:
1;
2;
3;
4;
Magnesium binding site 1 out
of 4 in 7o0c
Go back to
Magnesium Binding Sites List in 7o0c
Magnesium binding site 1 out
of 4 in the Human Phosphomannomutase 2 (PMM2) Wild-Type in Apo State
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 1 of Human Phosphomannomutase 2 (PMM2) Wild-Type in Apo State within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Mg301
b:62.0
occ:1.00
|
OD1
|
A:ASP12
|
1.9
|
62.2
|
1.0
|
O
|
A:ASP14
|
1.9
|
64.6
|
1.0
|
O
|
A:HOH409
|
2.0
|
66.2
|
1.0
|
O
|
A:HOH401
|
2.1
|
72.9
|
1.0
|
OD1
|
A:ASP209
|
2.6
|
62.2
|
1.0
|
O
|
A:HOH405
|
2.6
|
69.5
|
1.0
|
CG
|
A:ASP12
|
2.8
|
59.5
|
1.0
|
OD2
|
A:ASP12
|
3.0
|
60.6
|
1.0
|
C
|
A:ASP14
|
3.0
|
62.4
|
1.0
|
CG
|
A:ASP209
|
3.5
|
59.3
|
1.0
|
N
|
A:ASP14
|
3.7
|
63.1
|
1.0
|
CA
|
A:ASP14
|
3.7
|
60.3
|
1.0
|
OG1
|
A:THR16
|
3.7
|
56.6
|
1.0
|
OD2
|
A:ASP209
|
3.8
|
58.5
|
1.0
|
CB
|
A:ASP14
|
3.9
|
66.4
|
1.0
|
ND2
|
A:ASN216
|
4.1
|
73.2
|
1.0
|
N
|
A:GLY15
|
4.1
|
59.8
|
1.0
|
CB
|
A:ASP12
|
4.2
|
52.6
|
1.0
|
OD2
|
A:ASP217
|
4.3
|
66.2
|
1.0
|
N
|
A:THR16
|
4.4
|
56.4
|
1.0
|
C
|
A:VAL13
|
4.4
|
62.7
|
1.0
|
CA
|
A:GLY15
|
4.4
|
59.1
|
1.0
|
N
|
A:VAL13
|
4.6
|
55.6
|
1.0
|
OD1
|
A:ASP217
|
4.7
|
63.6
|
1.0
|
N
|
A:ASP209
|
4.7
|
64.3
|
1.0
|
NZ
|
A:LYS189
|
4.7
|
64.2
|
1.0
|
CB
|
A:ASP209
|
4.7
|
53.0
|
1.0
|
C
|
A:GLY15
|
4.7
|
55.1
|
1.0
|
CB
|
A:THR16
|
4.8
|
58.7
|
1.0
|
O
|
A:VAL13
|
4.9
|
54.9
|
1.0
|
OD1
|
A:ASN216
|
4.9
|
88.3
|
1.0
|
O
|
A:HOH412
|
4.9
|
40.1
|
1.0
|
CG
|
A:ASP217
|
4.9
|
63.8
|
1.0
|
C
|
A:ASP12
|
4.9
|
57.8
|
1.0
|
CG
|
A:ASN216
|
4.9
|
67.7
|
1.0
|
|
Magnesium binding site 2 out
of 4 in 7o0c
Go back to
Magnesium Binding Sites List in 7o0c
Magnesium binding site 2 out
of 4 in the Human Phosphomannomutase 2 (PMM2) Wild-Type in Apo State
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 2 of Human Phosphomannomutase 2 (PMM2) Wild-Type in Apo State within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Mg302
b:60.5
occ:1.00
|
O
|
A:THR226
|
2.0
|
64.3
|
1.0
|
O
|
A:ASP223
|
2.2
|
58.4
|
1.0
|
O
|
A:PHE221
|
2.5
|
63.7
|
1.0
|
OG1
|
A:THR226
|
2.6
|
60.4
|
1.0
|
O
|
A:HOH414
|
2.8
|
67.3
|
1.0
|
C
|
A:THR226
|
3.1
|
57.0
|
1.0
|
C
|
A:ASP223
|
3.3
|
65.2
|
1.0
|
N
|
A:ASP223
|
3.6
|
61.5
|
1.0
|
C
|
A:PHE221
|
3.6
|
60.8
|
1.0
|
CB
|
A:THR226
|
3.7
|
59.7
|
1.0
|
CA
|
A:THR226
|
3.7
|
58.3
|
1.0
|
C
|
A:THR222
|
3.8
|
59.4
|
1.0
|
N
|
A:THR226
|
3.8
|
59.2
|
1.0
|
N
|
A:GLY228
|
3.9
|
61.0
|
1.0
|
CA
|
A:ASP223
|
4.0
|
59.2
|
1.0
|
N
|
A:MET227
|
4.1
|
56.2
|
1.0
|
CA
|
A:THR222
|
4.2
|
58.0
|
1.0
|
O
|
A:ILE220
|
4.3
|
61.9
|
1.0
|
N
|
A:PRO224
|
4.3
|
70.0
|
1.0
|
N
|
A:THR222
|
4.3
|
63.0
|
1.0
|
O
|
A:THR222
|
4.4
|
63.7
|
1.0
|
CA
|
A:MET227
|
4.4
|
60.3
|
1.0
|
CA
|
A:PRO224
|
4.4
|
64.2
|
1.0
|
CA
|
A:GLY228
|
4.5
|
52.8
|
1.0
|
C
|
A:MET227
|
4.6
|
60.9
|
1.0
|
C
|
A:PRO224
|
4.6
|
63.9
|
1.0
|
CA
|
A:PHE221
|
4.6
|
58.8
|
1.0
|
CB
|
A:ASP223
|
4.7
|
76.3
|
1.0
|
O
|
A:PRO224
|
4.7
|
59.3
|
1.0
|
CG2
|
A:THR226
|
4.9
|
61.1
|
1.0
|
|
Magnesium binding site 3 out
of 4 in 7o0c
Go back to
Magnesium Binding Sites List in 7o0c
Magnesium binding site 3 out
of 4 in the Human Phosphomannomutase 2 (PMM2) Wild-Type in Apo State
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 3 of Human Phosphomannomutase 2 (PMM2) Wild-Type in Apo State within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Mg301
b:67.7
occ:1.00
|
OD1
|
B:ASP12
|
1.9
|
67.7
|
1.0
|
O
|
B:ASP14
|
2.1
|
64.7
|
1.0
|
O
|
B:HOH409
|
2.2
|
80.4
|
1.0
|
O
|
B:HOH401
|
2.2
|
66.2
|
1.0
|
O
|
B:HOH414
|
2.2
|
73.9
|
1.0
|
OD1
|
B:ASP209
|
2.3
|
76.7
|
1.0
|
CG
|
B:ASP12
|
2.9
|
66.3
|
1.0
|
CG
|
B:ASP209
|
3.1
|
69.7
|
1.0
|
C
|
B:ASP14
|
3.3
|
63.8
|
1.0
|
OD2
|
B:ASP209
|
3.3
|
67.0
|
1.0
|
OD2
|
B:ASP12
|
3.4
|
72.9
|
1.0
|
OD1
|
B:ASP217
|
4.0
|
64.5
|
1.0
|
CA
|
B:ASP14
|
4.1
|
68.3
|
1.0
|
CB
|
B:ASP14
|
4.1
|
67.2
|
1.0
|
ND2
|
B:ASN216
|
4.1
|
59.2
|
1.0
|
CB
|
B:ASP12
|
4.2
|
56.9
|
1.0
|
N
|
B:ASP14
|
4.2
|
68.4
|
1.0
|
N
|
B:GLY15
|
4.3
|
61.9
|
1.0
|
CA
|
B:GLY15
|
4.5
|
67.1
|
1.0
|
OD1
|
B:ASN216
|
4.5
|
77.7
|
1.0
|
CB
|
B:ASP209
|
4.6
|
62.5
|
1.0
|
CG
|
B:LYS210
|
4.6
|
56.6
|
1.0
|
OD2
|
B:ASP217
|
4.7
|
68.1
|
1.0
|
CG
|
B:ASN216
|
4.8
|
61.0
|
1.0
|
N
|
B:ASP209
|
4.8
|
64.2
|
1.0
|
CG
|
B:ASP217
|
4.8
|
63.6
|
1.0
|
N
|
B:THR16
|
4.8
|
56.9
|
1.0
|
|
Magnesium binding site 4 out
of 4 in 7o0c
Go back to
Magnesium Binding Sites List in 7o0c
Magnesium binding site 4 out
of 4 in the Human Phosphomannomutase 2 (PMM2) Wild-Type in Apo State
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 4 of Human Phosphomannomutase 2 (PMM2) Wild-Type in Apo State within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Mg302
b:70.3
occ:1.00
|
O
|
B:THR226
|
1.9
|
62.0
|
1.0
|
O
|
B:ASP223
|
2.1
|
56.0
|
1.0
|
OG1
|
B:THR226
|
2.4
|
60.6
|
1.0
|
O
|
B:HOH413
|
2.6
|
69.7
|
1.0
|
O
|
B:HOH411
|
2.8
|
66.8
|
1.0
|
O
|
B:PHE221
|
2.8
|
69.4
|
1.0
|
C
|
B:THR226
|
2.8
|
56.8
|
1.0
|
C
|
B:ASP223
|
3.2
|
63.0
|
1.0
|
CA
|
B:THR226
|
3.3
|
54.2
|
1.0
|
CB
|
B:THR226
|
3.4
|
57.9
|
1.0
|
N
|
B:THR226
|
3.4
|
62.2
|
1.0
|
N
|
B:ASP223
|
3.6
|
59.2
|
1.0
|
C
|
B:PHE221
|
3.8
|
62.9
|
1.0
|
CA
|
B:ASP223
|
3.9
|
58.7
|
1.0
|
C
|
B:THR222
|
4.0
|
59.1
|
1.0
|
N
|
B:MET227
|
4.0
|
62.3
|
1.0
|
O
|
B:ILE220
|
4.0
|
60.5
|
1.0
|
N
|
B:GLY228
|
4.2
|
52.7
|
1.0
|
N
|
B:PRO224
|
4.3
|
61.4
|
1.0
|
O
|
B:THR222
|
4.4
|
67.3
|
1.0
|
CG2
|
B:THR226
|
4.4
|
54.4
|
1.0
|
CA
|
B:PRO224
|
4.5
|
60.0
|
1.0
|
CA
|
B:MET227
|
4.5
|
63.1
|
1.0
|
C
|
B:PRO224
|
4.5
|
59.6
|
1.0
|
CB
|
B:ASP223
|
4.5
|
57.2
|
1.0
|
CA
|
B:THR222
|
4.6
|
59.9
|
1.0
|
CA
|
B:PHE221
|
4.6
|
62.4
|
1.0
|
N
|
B:THR222
|
4.6
|
59.2
|
1.0
|
C
|
B:ARG225
|
4.7
|
59.9
|
1.0
|
C
|
B:MET227
|
4.8
|
62.8
|
1.0
|
N
|
B:ARG225
|
4.8
|
54.3
|
1.0
|
O
|
B:PRO224
|
4.8
|
65.3
|
1.0
|
CA
|
B:GLY228
|
4.8
|
52.0
|
1.0
|
|
Reference:
A.Briso-Montiano,
F.Del Cano-Ochoa,
A.Vilas,
A.Velazquez-Campoy,
V.Rubio,
B.Perez,
S.Ramon-Maiques.
Insight on Molecular Pathogenesis and Pharmacochaperoning Potential in Phosphomannomutase 2 Deficiency, Provided By Novel Human Phosphomannomutase 2 Structures. J Inherit Metab Dis V. 45 318 2022.
ISSN: ISSN 1573-2665
PubMed: 34859900
DOI: 10.1002/JIMD.12461
Page generated: Thu Oct 3 02:21:57 2024
|