Manganese in PDB 5l9x: Human Dna Polymerase Eta-Dna Ternary Complex: Reaction with 10 Mm MN2+ For 60S
Enzymatic activity of Human Dna Polymerase Eta-Dna Ternary Complex: Reaction with 10 Mm MN2+ For 60S
All present enzymatic activity of Human Dna Polymerase Eta-Dna Ternary Complex: Reaction with 10 Mm MN2+ For 60S:
2.7.7.7;
Protein crystallography data
The structure of Human Dna Polymerase Eta-Dna Ternary Complex: Reaction with 10 Mm MN2+ For 60S, PDB code: 5l9x
was solved by
Y.Gao,
W.Yang,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
19.94 /
1.90
|
Space group
|
P 61
|
Cell size a, b, c (Å), α, β, γ (°)
|
98.290,
98.290,
82.050,
90.00,
90.00,
120.00
|
R / Rfree (%)
|
16.5 /
21.4
|
Other elements in 5l9x:
The structure of Human Dna Polymerase Eta-Dna Ternary Complex: Reaction with 10 Mm MN2+ For 60S also contains other interesting chemical elements:
Manganese Binding Sites:
The binding sites of Manganese atom in the Human Dna Polymerase Eta-Dna Ternary Complex: Reaction with 10 Mm MN2+ For 60S
(pdb code 5l9x). This binding sites where shown within
5.0 Angstroms radius around Manganese atom.
In total 3 binding sites of Manganese where determined in the
Human Dna Polymerase Eta-Dna Ternary Complex: Reaction with 10 Mm MN2+ For 60S, PDB code: 5l9x:
Jump to Manganese binding site number:
1;
2;
3;
Manganese binding site 1 out
of 3 in 5l9x
Go back to
Manganese Binding Sites List in 5l9x
Manganese binding site 1 out
of 3 in the Human Dna Polymerase Eta-Dna Ternary Complex: Reaction with 10 Mm MN2+ For 60S
Mono view
Stereo pair view
|
A full contact list of Manganese with other atoms in the Mn binding
site number 1 of Human Dna Polymerase Eta-Dna Ternary Complex: Reaction with 10 Mm MN2+ For 60S within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Mn501
b:13.9
occ:0.90
|
OP1
|
P:DA9
|
2.1
|
15.3
|
0.2
|
OD1
|
A:ASP115
|
2.1
|
10.5
|
1.0
|
OE2
|
A:GLU116
|
2.2
|
15.0
|
1.0
|
OD2
|
A:ASP13
|
2.2
|
17.8
|
1.0
|
O
|
P:HOH214
|
2.2
|
13.3
|
1.0
|
O1A
|
A:DTP507
|
2.3
|
15.5
|
0.8
|
O3'
|
P:DT8
|
2.4
|
13.8
|
0.8
|
O3'
|
P:DT8
|
2.4
|
16.3
|
0.2
|
P
|
P:DA9
|
2.8
|
18.2
|
0.2
|
CG
|
A:ASP115
|
3.1
|
13.8
|
1.0
|
CD
|
A:GLU116
|
3.2
|
18.4
|
1.0
|
CG
|
A:ASP13
|
3.2
|
17.0
|
1.0
|
C3'
|
P:DT8
|
3.3
|
22.8
|
0.8
|
OD2
|
A:ASP115
|
3.3
|
13.6
|
1.0
|
C3'
|
P:DT8
|
3.4
|
21.5
|
0.2
|
MN
|
A:MN503
|
3.5
|
16.7
|
0.3
|
CA
|
A:CA502
|
3.5
|
16.7
|
0.7
|
PA
|
A:DTP507
|
3.6
|
15.6
|
0.8
|
OD1
|
A:ASP13
|
3.7
|
13.5
|
1.0
|
OG
|
A:SER113
|
3.8
|
18.0
|
1.0
|
OE1
|
A:GLU116
|
3.8
|
18.7
|
1.0
|
OP2
|
P:DA9
|
3.9
|
17.3
|
0.2
|
O5'
|
P:DA9
|
3.9
|
16.8
|
0.2
|
C4'
|
P:DT8
|
4.0
|
20.7
|
0.2
|
O5'
|
A:DTP507
|
4.0
|
16.8
|
0.8
|
O2A
|
A:DTP507
|
4.0
|
16.4
|
0.8
|
C4'
|
P:DT8
|
4.1
|
20.1
|
0.8
|
CB
|
A:GLU116
|
4.1
|
15.5
|
1.0
|
CG
|
A:GLU116
|
4.1
|
17.6
|
1.0
|
C5'
|
A:DTP507
|
4.2
|
16.1
|
0.8
|
C5'
|
P:DA9
|
4.2
|
16.1
|
0.2
|
NZ
|
A:LYS224
|
4.3
|
14.6
|
0.6
|
O
|
A:HOH715
|
4.3
|
23.1
|
1.0
|
C2'
|
P:DT8
|
4.4
|
20.4
|
0.2
|
C5'
|
P:DT8
|
4.5
|
24.5
|
0.2
|
CB
|
A:ASP13
|
4.5
|
13.4
|
1.0
|
O
|
P:HOH204
|
4.5
|
13.7
|
0.7
|
CB
|
A:ASP115
|
4.5
|
11.2
|
1.0
|
C
|
A:ASP115
|
4.6
|
16.2
|
1.0
|
O
|
A:ASP115
|
4.6
|
13.3
|
1.0
|
C2'
|
P:DT8
|
4.6
|
21.4
|
0.8
|
C5'
|
P:DT8
|
4.7
|
24.2
|
0.8
|
N
|
A:GLU116
|
4.8
|
10.2
|
1.0
|
O5
|
A:DPO508
|
4.8
|
14.7
|
0.2
|
O3A
|
A:DTP507
|
4.9
|
17.2
|
0.8
|
O1G
|
A:DTP507
|
4.9
|
14.2
|
0.8
|
CB
|
A:SER113
|
5.0
|
16.9
|
1.0
|
CA
|
A:ASP115
|
5.0
|
12.9
|
1.0
|
|
Manganese binding site 2 out
of 3 in 5l9x
Go back to
Manganese Binding Sites List in 5l9x
Manganese binding site 2 out
of 3 in the Human Dna Polymerase Eta-Dna Ternary Complex: Reaction with 10 Mm MN2+ For 60S
Mono view
Stereo pair view
|
A full contact list of Manganese with other atoms in the Mn binding
site number 2 of Human Dna Polymerase Eta-Dna Ternary Complex: Reaction with 10 Mm MN2+ For 60S within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Mn503
b:16.7
occ:0.35
|
CA
|
A:CA502
|
0.0
|
16.7
|
0.7
|
O5
|
A:DPO508
|
2.2
|
14.7
|
0.2
|
O1G
|
A:DTP507
|
2.3
|
14.2
|
0.8
|
O1A
|
A:DTP507
|
2.3
|
15.5
|
0.8
|
O1B
|
A:DTP507
|
2.3
|
14.1
|
0.8
|
OD1
|
A:ASP13
|
2.3
|
13.5
|
1.0
|
OD2
|
A:ASP115
|
2.3
|
13.6
|
1.0
|
O1
|
A:DPO508
|
2.4
|
14.5
|
0.2
|
O
|
A:MET14
|
2.4
|
12.1
|
1.0
|
OP1
|
P:DA9
|
2.5
|
15.3
|
0.2
|
CG
|
A:ASP13
|
3.1
|
17.0
|
1.0
|
OD2
|
A:ASP13
|
3.2
|
17.8
|
1.0
|
PB
|
A:DTP507
|
3.3
|
16.1
|
0.8
|
CG
|
A:ASP115
|
3.4
|
13.8
|
1.0
|
P2
|
A:DPO508
|
3.5
|
17.8
|
0.2
|
PG
|
A:DTP507
|
3.5
|
18.0
|
0.8
|
P1
|
A:DPO508
|
3.5
|
16.1
|
0.2
|
PA
|
A:DTP507
|
3.5
|
15.6
|
0.8
|
C
|
A:MET14
|
3.5
|
13.3
|
1.0
|
MN
|
A:MN501
|
3.5
|
13.9
|
0.9
|
O3A
|
A:DTP507
|
3.6
|
17.2
|
0.8
|
O3B
|
A:DTP507
|
3.8
|
14.6
|
0.8
|
O2
|
A:DPO508
|
3.8
|
17.1
|
0.2
|
OD1
|
A:ASP115
|
3.8
|
10.5
|
1.0
|
O
|
A:HOH715
|
3.9
|
23.1
|
1.0
|
O4
|
A:DPO508
|
3.9
|
14.7
|
0.2
|
P
|
P:DA9
|
4.0
|
18.2
|
0.2
|
O7
|
A:DPO508
|
4.0
|
13.2
|
0.2
|
O2G
|
A:DTP507
|
4.0
|
12.8
|
0.8
|
N
|
A:MET14
|
4.0
|
11.5
|
1.0
|
NZ
|
A:LYS231
|
4.0
|
16.5
|
0.5
|
C5'
|
A:DTP507
|
4.1
|
16.1
|
0.8
|
C5'
|
P:DA9
|
4.2
|
16.1
|
0.2
|
C
|
A:ASP13
|
4.3
|
9.8
|
1.0
|
O5'
|
A:DTP507
|
4.3
|
16.8
|
0.8
|
O
|
P:HOH214
|
4.3
|
13.3
|
1.0
|
CA
|
A:MET14
|
4.3
|
14.4
|
1.0
|
N
|
A:CYS16
|
4.4
|
12.4
|
1.0
|
CB
|
A:ASP13
|
4.4
|
13.4
|
1.0
|
O5'
|
P:DA9
|
4.4
|
16.8
|
0.2
|
N
|
A:ASP15
|
4.5
|
10.6
|
1.0
|
CA
|
A:ASP15
|
4.6
|
12.3
|
1.0
|
O
|
A:HOH765
|
4.6
|
14.3
|
0.5
|
O2B
|
A:DTP507
|
4.6
|
15.5
|
0.8
|
O6
|
A:DPO508
|
4.6
|
16.5
|
0.2
|
CB
|
A:ASP115
|
4.7
|
11.2
|
1.0
|
C
|
A:ASP15
|
4.7
|
16.4
|
1.0
|
O
|
A:ASP13
|
4.7
|
11.6
|
1.0
|
O3G
|
A:DTP507
|
4.7
|
16.7
|
0.8
|
O2A
|
A:DTP507
|
4.8
|
16.4
|
0.8
|
N
|
A:PHE17
|
4.8
|
9.4
|
1.0
|
O3
|
A:DPO508
|
4.8
|
15.6
|
0.2
|
CB
|
A:MET14
|
4.8
|
12.0
|
1.0
|
OP2
|
P:DA9
|
4.8
|
17.3
|
0.2
|
CA
|
A:ASP13
|
4.9
|
15.1
|
1.0
|
O3'
|
P:DT8
|
4.9
|
16.3
|
0.2
|
CB
|
A:PHE17
|
5.0
|
9.7
|
1.0
|
|
Manganese binding site 3 out
of 3 in 5l9x
Go back to
Manganese Binding Sites List in 5l9x
Manganese binding site 3 out
of 3 in the Human Dna Polymerase Eta-Dna Ternary Complex: Reaction with 10 Mm MN2+ For 60S
Mono view
Stereo pair view
|
A full contact list of Manganese with other atoms in the Mn binding
site number 3 of Human Dna Polymerase Eta-Dna Ternary Complex: Reaction with 10 Mm MN2+ For 60S within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
P:Mn101
b:18.6
occ:0.20
|
O2A
|
A:DTP507
|
1.8
|
16.4
|
0.8
|
OP2
|
P:DA9
|
2.0
|
17.3
|
0.2
|
O
|
A:HOH606
|
2.2
|
22.7
|
0.1
|
O3A
|
A:DTP507
|
2.3
|
17.2
|
0.8
|
O2
|
A:DPO508
|
2.3
|
17.1
|
0.2
|
PA
|
A:DTP507
|
2.5
|
15.6
|
0.8
|
NH1
|
A:ARG61
|
2.6
|
23.8
|
0.8
|
O
|
A:HOH642
|
2.8
|
18.0
|
1.0
|
O
|
P:HOH217
|
2.8
|
16.0
|
0.1
|
O
|
A:HOH899
|
3.1
|
34.6
|
1.0
|
P
|
P:DA9
|
3.2
|
18.2
|
0.2
|
O
|
A:HOH715
|
3.4
|
23.1
|
1.0
|
O1A
|
A:DTP507
|
3.5
|
15.5
|
0.8
|
CZ
|
A:ARG61
|
3.6
|
28.5
|
0.8
|
OP1
|
P:DA9
|
3.6
|
15.3
|
0.2
|
NH2
|
A:ARG61
|
3.7
|
20.2
|
0.8
|
P1
|
A:DPO508
|
3.8
|
16.1
|
0.2
|
O5'
|
A:DTP507
|
3.8
|
16.8
|
0.8
|
PB
|
A:DTP507
|
3.8
|
16.1
|
0.8
|
O5'
|
P:DA9
|
3.9
|
16.8
|
0.2
|
NH2
|
A:ARG61
|
3.9
|
27.7
|
0.2
|
O
|
A:HOH771
|
4.0
|
27.6
|
0.6
|
O5
|
A:DPO508
|
4.0
|
14.7
|
0.2
|
O6
|
A:DPO508
|
4.0
|
16.5
|
0.2
|
O3B
|
A:DTP507
|
4.1
|
14.6
|
0.8
|
O
|
A:HOH701
|
4.1
|
18.9
|
0.1
|
O1G
|
A:DTP507
|
4.1
|
14.2
|
0.8
|
O4
|
A:DPO508
|
4.2
|
14.7
|
0.2
|
O3G
|
A:DTP507
|
4.3
|
16.7
|
0.8
|
O
|
A:HOH921
|
4.3
|
25.5
|
1.0
|
P2
|
A:DPO508
|
4.3
|
17.8
|
0.2
|
O
|
P:HOH214
|
4.4
|
13.3
|
1.0
|
NE
|
A:ARG61
|
4.4
|
25.5
|
0.2
|
PG
|
A:DTP507
|
4.4
|
18.0
|
0.8
|
O
|
P:HOH215
|
4.4
|
27.9
|
1.0
|
O3'
|
P:DT8
|
4.5
|
16.3
|
0.2
|
CZ
|
A:ARG61
|
4.6
|
25.3
|
0.2
|
C2'
|
P:DT8
|
4.6
|
21.4
|
0.8
|
O2B
|
A:DTP507
|
4.6
|
15.5
|
0.8
|
O1
|
A:DPO508
|
4.6
|
14.5
|
0.2
|
C3'
|
P:DT8
|
4.7
|
21.5
|
0.2
|
O3
|
A:DPO508
|
4.7
|
15.6
|
0.2
|
C3'
|
P:DT8
|
4.7
|
22.8
|
0.8
|
O
|
P:HOH220
|
4.7
|
32.1
|
1.0
|
NE
|
A:ARG61
|
4.8
|
28.2
|
0.8
|
O1B
|
A:DTP507
|
4.8
|
14.1
|
0.8
|
C8
|
A:DTP507
|
5.0
|
20.2
|
0.8
|
O3'
|
P:DT8
|
5.0
|
13.8
|
0.8
|
C5'
|
A:DTP507
|
5.0
|
16.1
|
0.8
|
|
Reference:
Y.Gao,
W.Yang.
Capture of A Third MG2+ Is Essential For Catalyzing Dna Synthesis. Science V. 352 1334 2016.
ISSN: ESSN 1095-9203
PubMed: 27284197
DOI: 10.1126/SCIENCE.AAD9633
Page generated: Sun Oct 6 01:49:27 2024
|