Potassium in PDB 1egv: Crystal Structure of the Diol Dehydratase-Adeninylpentylcobalamin Complex From Klebsella Oxytoca Under the Illuminated Condition.
Enzymatic activity of Crystal Structure of the Diol Dehydratase-Adeninylpentylcobalamin Complex From Klebsella Oxytoca Under the Illuminated Condition.
All present enzymatic activity of Crystal Structure of the Diol Dehydratase-Adeninylpentylcobalamin Complex From Klebsella Oxytoca Under the Illuminated Condition.:
4.2.1.28;
Protein crystallography data
The structure of Crystal Structure of the Diol Dehydratase-Adeninylpentylcobalamin Complex From Klebsella Oxytoca Under the Illuminated Condition., PDB code: 1egv
was solved by
J.Masuda,
N.Shibata,
T.Toraya,
Y.Morimoto,
N.Yasuoka,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
30.00 /
1.75
|
Space group
|
P 21 21 21
|
Cell size a, b, c (Å), α, β, γ (°)
|
73.380,
121.400,
207.600,
90.00,
90.00,
90.00
|
R / Rfree (%)
|
15.5 /
21.4
|
Other elements in 1egv:
The structure of Crystal Structure of the Diol Dehydratase-Adeninylpentylcobalamin Complex From Klebsella Oxytoca Under the Illuminated Condition. also contains other interesting chemical elements:
Potassium Binding Sites:
The binding sites of Potassium atom in the Crystal Structure of the Diol Dehydratase-Adeninylpentylcobalamin Complex From Klebsella Oxytoca Under the Illuminated Condition.
(pdb code 1egv). This binding sites where shown within
5.0 Angstroms radius around Potassium atom.
In total 4 binding sites of Potassium where determined in the
Crystal Structure of the Diol Dehydratase-Adeninylpentylcobalamin Complex From Klebsella Oxytoca Under the Illuminated Condition., PDB code: 1egv:
Jump to Potassium binding site number:
1;
2;
3;
4;
Potassium binding site 1 out
of 4 in 1egv
Go back to
Potassium Binding Sites List in 1egv
Potassium binding site 1 out
of 4 in the Crystal Structure of the Diol Dehydratase-Adeninylpentylcobalamin Complex From Klebsella Oxytoca Under the Illuminated Condition.
Mono view
Stereo pair view
|
A full contact list of Potassium with other atoms in the K binding
site number 1 of Crystal Structure of the Diol Dehydratase-Adeninylpentylcobalamin Complex From Klebsella Oxytoca Under the Illuminated Condition. within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:K603
b:9.8
occ:1.00
|
OE1
|
A:GLU221
|
2.2
|
10.5
|
1.0
|
OE1
|
A:GLU170
|
2.3
|
11.4
|
1.0
|
OE1
|
A:GLN296
|
2.4
|
7.3
|
1.0
|
O
|
A:SER362
|
2.4
|
7.7
|
1.0
|
O2
|
A:PGO602
|
2.4
|
10.9
|
1.0
|
OE1
|
A:GLN141
|
2.4
|
11.9
|
1.0
|
O1
|
A:PGO602
|
2.5
|
10.8
|
1.0
|
CD
|
A:GLU221
|
3.3
|
14.7
|
1.0
|
C2
|
A:PGO602
|
3.3
|
19.5
|
1.0
|
CD
|
A:GLU170
|
3.3
|
8.3
|
1.0
|
C1
|
A:PGO602
|
3.3
|
11.3
|
1.0
|
CD
|
A:GLN296
|
3.4
|
12.2
|
1.0
|
C
|
A:SER362
|
3.4
|
8.8
|
1.0
|
CD
|
A:GLN141
|
3.6
|
13.1
|
1.0
|
OE2
|
A:GLU221
|
3.7
|
13.4
|
1.0
|
OE2
|
A:GLU170
|
3.7
|
10.0
|
1.0
|
NE2
|
A:GLN296
|
3.7
|
12.3
|
1.0
|
CB
|
A:SER362
|
3.9
|
10.7
|
1.0
|
NE2
|
A:HIS143
|
4.0
|
10.2
|
1.0
|
NE2
|
A:GLN141
|
4.1
|
8.9
|
1.0
|
OD2
|
A:ASP335
|
4.2
|
11.3
|
1.0
|
CA
|
A:SER362
|
4.2
|
8.4
|
1.0
|
OG
|
A:SER362
|
4.2
|
10.3
|
1.0
|
NE2
|
A:GLN200
|
4.2
|
8.3
|
1.0
|
CD2
|
A:HIS143
|
4.4
|
12.8
|
1.0
|
N
|
A:GLY363
|
4.4
|
10.3
|
1.0
|
CG
|
A:GLU221
|
4.5
|
11.2
|
1.0
|
CA
|
A:GLY363
|
4.5
|
7.7
|
1.0
|
CG
|
A:GLU170
|
4.6
|
8.5
|
1.0
|
C3
|
A:PGO602
|
4.7
|
12.6
|
1.0
|
CG
|
A:GLN296
|
4.7
|
14.4
|
1.0
|
CB
|
A:GLU170
|
4.7
|
5.6
|
1.0
|
CG
|
A:GLN141
|
4.9
|
8.6
|
1.0
|
|
Potassium binding site 2 out
of 4 in 1egv
Go back to
Potassium Binding Sites List in 1egv
Potassium binding site 2 out
of 4 in the Crystal Structure of the Diol Dehydratase-Adeninylpentylcobalamin Complex From Klebsella Oxytoca Under the Illuminated Condition.
Mono view
Stereo pair view
|
A full contact list of Potassium with other atoms in the K binding
site number 2 of Crystal Structure of the Diol Dehydratase-Adeninylpentylcobalamin Complex From Klebsella Oxytoca Under the Illuminated Condition. within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:K604
b:12.5
occ:1.00
|
OE1
|
A:GLU265
|
2.6
|
8.7
|
1.0
|
O
|
A:GLY261
|
2.8
|
11.2
|
1.0
|
O
|
A:HOH625
|
2.8
|
11.6
|
1.0
|
OE1
|
A:GLU280
|
2.8
|
13.8
|
1.0
|
O
|
A:HOH727
|
3.0
|
12.3
|
1.0
|
OG
|
A:SER264
|
3.0
|
10.7
|
1.0
|
OE2
|
A:GLU265
|
3.3
|
13.2
|
1.0
|
CD
|
A:GLU265
|
3.3
|
12.0
|
1.0
|
SG
|
A:CYS283
|
3.4
|
11.3
|
1.0
|
C
|
A:GLY261
|
3.4
|
11.0
|
1.0
|
N
|
A:GLY261
|
3.8
|
7.4
|
1.0
|
CA
|
A:GLU280
|
4.0
|
6.8
|
1.0
|
CD
|
A:GLU280
|
4.1
|
12.3
|
1.0
|
N
|
A:SER262
|
4.1
|
8.4
|
1.0
|
CB
|
A:SER264
|
4.1
|
8.2
|
1.0
|
CB
|
A:GLU280
|
4.2
|
7.2
|
1.0
|
CA
|
A:SER262
|
4.2
|
8.7
|
1.0
|
CA
|
A:GLY261
|
4.3
|
6.3
|
1.0
|
N
|
A:SER264
|
4.4
|
9.2
|
1.0
|
N
|
A:GLU280
|
4.4
|
9.3
|
1.0
|
CB
|
A:CYS283
|
4.5
|
4.7
|
1.0
|
N
|
A:GLY263
|
4.6
|
8.6
|
1.0
|
O
|
A:LEU279
|
4.6
|
14.7
|
1.0
|
C
|
A:SER262
|
4.6
|
11.7
|
1.0
|
CB
|
A:SER260
|
4.6
|
10.9
|
1.0
|
N
|
A:GLY227
|
4.7
|
5.6
|
1.0
|
C
|
A:LEU279
|
4.7
|
10.1
|
1.0
|
CG
|
A:GLU265
|
4.7
|
11.9
|
1.0
|
CG
|
A:GLU280
|
4.7
|
9.3
|
1.0
|
C
|
A:SER260
|
4.8
|
10.5
|
1.0
|
CA
|
A:SER264
|
4.9
|
9.8
|
1.0
|
OE2
|
A:GLU280
|
5.0
|
9.4
|
1.0
|
|
Potassium binding site 3 out
of 4 in 1egv
Go back to
Potassium Binding Sites List in 1egv
Potassium binding site 3 out
of 4 in the Crystal Structure of the Diol Dehydratase-Adeninylpentylcobalamin Complex From Klebsella Oxytoca Under the Illuminated Condition.
Mono view
Stereo pair view
|
A full contact list of Potassium with other atoms in the K binding
site number 3 of Crystal Structure of the Diol Dehydratase-Adeninylpentylcobalamin Complex From Klebsella Oxytoca Under the Illuminated Condition. within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
L:K603
b:12.7
occ:1.00
|
OE1
|
L:GLU170
|
2.2
|
13.7
|
1.0
|
O
|
L:SER362
|
2.3
|
13.1
|
1.0
|
OE1
|
L:GLU221
|
2.4
|
16.2
|
1.0
|
OE1
|
L:GLN141
|
2.4
|
13.1
|
1.0
|
O2
|
L:PGO602
|
2.4
|
15.6
|
1.0
|
OE1
|
L:GLN296
|
2.4
|
11.2
|
1.0
|
O1
|
L:PGO602
|
2.5
|
11.2
|
1.0
|
CD
|
L:GLU170
|
3.2
|
19.1
|
1.0
|
C2
|
L:PGO602
|
3.3
|
21.8
|
1.0
|
C
|
L:SER362
|
3.3
|
14.4
|
1.0
|
C1
|
L:PGO602
|
3.4
|
17.6
|
1.0
|
CD
|
L:GLU221
|
3.4
|
14.1
|
1.0
|
CD
|
L:GLN296
|
3.4
|
14.0
|
1.0
|
CD
|
L:GLN141
|
3.5
|
9.3
|
1.0
|
OE2
|
L:GLU170
|
3.6
|
12.8
|
1.0
|
NE2
|
L:GLN296
|
3.7
|
14.7
|
1.0
|
OE2
|
L:GLU221
|
3.7
|
10.0
|
1.0
|
CB
|
L:SER362
|
4.0
|
9.6
|
1.0
|
NE2
|
L:GLN141
|
4.1
|
10.0
|
1.0
|
NE2
|
L:HIS143
|
4.1
|
9.4
|
1.0
|
OG
|
L:SER362
|
4.2
|
9.9
|
1.0
|
CA
|
L:SER362
|
4.2
|
10.1
|
1.0
|
OD2
|
L:ASP335
|
4.2
|
11.4
|
1.0
|
NE2
|
L:GLN200
|
4.2
|
10.8
|
1.0
|
N
|
L:GLY363
|
4.3
|
10.9
|
1.0
|
CA
|
L:GLY363
|
4.5
|
9.2
|
1.0
|
CD2
|
L:HIS143
|
4.5
|
11.2
|
1.0
|
CG
|
L:GLU170
|
4.5
|
14.8
|
1.0
|
CG
|
L:GLU221
|
4.6
|
13.3
|
1.0
|
CB
|
L:GLU170
|
4.7
|
16.6
|
1.0
|
C3
|
L:PGO602
|
4.7
|
10.8
|
1.0
|
CG
|
L:GLN296
|
4.7
|
8.2
|
1.0
|
CG
|
L:GLN141
|
4.8
|
12.2
|
1.0
|
|
Potassium binding site 4 out
of 4 in 1egv
Go back to
Potassium Binding Sites List in 1egv
Potassium binding site 4 out
of 4 in the Crystal Structure of the Diol Dehydratase-Adeninylpentylcobalamin Complex From Klebsella Oxytoca Under the Illuminated Condition.
Mono view
Stereo pair view
|
A full contact list of Potassium with other atoms in the K binding
site number 4 of Crystal Structure of the Diol Dehydratase-Adeninylpentylcobalamin Complex From Klebsella Oxytoca Under the Illuminated Condition. within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
L:K604
b:16.3
occ:1.00
|
OE1
|
L:GLU265
|
2.7
|
11.5
|
1.0
|
OE1
|
L:GLU280
|
2.8
|
11.6
|
1.0
|
O
|
L:GLY261
|
2.8
|
11.5
|
1.0
|
O
|
L:HOH624
|
2.8
|
13.0
|
1.0
|
OG
|
L:SER264
|
3.0
|
10.4
|
1.0
|
O
|
L:HOH606
|
3.0
|
9.5
|
1.0
|
CD
|
L:GLU265
|
3.4
|
13.4
|
1.0
|
SG
|
L:CYS283
|
3.4
|
13.9
|
1.0
|
OE2
|
L:GLU265
|
3.4
|
8.2
|
1.0
|
C
|
L:GLY261
|
3.4
|
11.2
|
1.0
|
N
|
L:GLY261
|
3.7
|
16.0
|
1.0
|
CD
|
L:GLU280
|
4.0
|
15.2
|
1.0
|
CA
|
L:GLU280
|
4.0
|
14.2
|
1.0
|
N
|
L:SER262
|
4.0
|
15.5
|
1.0
|
CB
|
L:SER264
|
4.1
|
9.4
|
1.0
|
CA
|
L:GLY261
|
4.2
|
11.2
|
1.0
|
CA
|
L:SER262
|
4.2
|
13.9
|
1.0
|
CB
|
L:GLU280
|
4.3
|
9.7
|
1.0
|
N
|
L:GLU280
|
4.3
|
10.7
|
1.0
|
N
|
L:SER264
|
4.4
|
14.1
|
1.0
|
CB
|
L:CYS283
|
4.5
|
6.7
|
1.0
|
CB
|
L:SER260
|
4.5
|
12.5
|
1.0
|
C
|
L:SER262
|
4.6
|
17.9
|
1.0
|
N
|
L:GLY263
|
4.6
|
12.2
|
1.0
|
O
|
L:LEU279
|
4.6
|
11.8
|
1.0
|
N
|
L:GLY227
|
4.6
|
10.8
|
1.0
|
C
|
L:LEU279
|
4.7
|
17.2
|
1.0
|
CG
|
L:GLU280
|
4.7
|
12.3
|
1.0
|
C
|
L:SER260
|
4.7
|
16.6
|
1.0
|
CG
|
L:GLU265
|
4.8
|
11.6
|
1.0
|
CA
|
L:SER264
|
4.8
|
16.5
|
1.0
|
OE2
|
L:GLU280
|
4.9
|
12.1
|
1.0
|
|
Reference:
J.Masuda,
N.Shibata,
Y.Morimoto,
T.Toraya,
N.Yasuoka.
How A Protein Generates A Catalytic Radical From Coenzyme B(12): X-Ray Structure of A Diol-Dehydratase-Adeninylpentylcobalamin Complex. Structure Fold.Des. V. 8 775 2000.
ISSN: ISSN 0969-2126
PubMed: 10903944
DOI: 10.1016/S0969-2126(00)00164-7
Page generated: Mon Aug 12 04:26:24 2024
|