Holmium in PDB 2olc: Crystal Structure of 5-Methylthioribose Kinase in Complex with Adp-2HO
Enzymatic activity of Crystal Structure of 5-Methylthioribose Kinase in Complex with Adp-2HO
All present enzymatic activity of Crystal Structure of 5-Methylthioribose Kinase in Complex with Adp-2HO:
2.7.1.100;
Protein crystallography data
The structure of Crystal Structure of 5-Methylthioribose Kinase in Complex with Adp-2HO, PDB code: 2olc
was solved by
S.Y.Ku,
G.D.Smith,
P.L.Howell,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
107.83 /
2.00
|
Space group
|
P 21 21 2
|
Cell size a, b, c (Å), α, β, γ (°)
|
215.200,
83.600,
51.600,
90.00,
90.00,
90.00
|
R / Rfree (%)
|
21.4 /
25
|
Holmium Binding Sites:
The binding sites of Holmium atom in the Crystal Structure of 5-Methylthioribose Kinase in Complex with Adp-2HO
(pdb code 2olc). This binding sites where shown within
5.0 Angstroms radius around Holmium atom.
In total 4 binding sites of Holmium where determined in the
Crystal Structure of 5-Methylthioribose Kinase in Complex with Adp-2HO, PDB code: 2olc:
Jump to Holmium binding site number:
1;
2;
3;
4;
Holmium binding site 1 out
of 4 in 2olc
Go back to
Holmium Binding Sites List in 2olc
Holmium binding site 1 out
of 4 in the Crystal Structure of 5-Methylthioribose Kinase in Complex with Adp-2HO
 Mono view
 Stereo pair view
|
A full contact list of Holmium with other atoms in the Ho binding
site number 1 of Crystal Structure of 5-Methylthioribose Kinase in Complex with Adp-2HO within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Ho400
b:44.8
occ:1.00
|
O
|
A:HOH1001
|
2.0
|
23.3
|
1.0
|
O
|
A:HOH1002
|
2.2
|
14.3
|
1.0
|
O2A
|
A:ADP999
|
2.2
|
29.9
|
1.0
|
O3B
|
A:ADP999
|
2.3
|
26.1
|
1.0
|
OD2
|
A:ASP250
|
2.6
|
17.6
|
1.0
|
PB
|
A:ADP999
|
3.4
|
25.6
|
1.0
|
PA
|
A:ADP999
|
3.5
|
28.5
|
1.0
|
CG
|
A:ASP250
|
3.6
|
20.6
|
1.0
|
O2B
|
A:ADP999
|
3.8
|
23.9
|
1.0
|
O3A
|
A:ADP999
|
3.9
|
26.8
|
1.0
|
HO
|
A:HO401
|
4.1
|
39.2
|
1.0
|
CB
|
A:ASP250
|
4.1
|
20.3
|
1.0
|
OD1
|
A:ASP40
|
4.4
|
45.6
|
1.0
|
O
|
A:GLY237
|
4.5
|
20.8
|
1.0
|
O1A
|
A:ADP999
|
4.5
|
29.3
|
1.0
|
OD1
|
A:ASP250
|
4.6
|
20.9
|
1.0
|
O5'
|
A:ADP999
|
4.6
|
27.7
|
1.0
|
OG
|
A:SER238
|
4.7
|
26.8
|
1.0
|
O1B
|
A:ADP999
|
4.8
|
26.7
|
1.0
|
C5'
|
A:ADP999
|
4.9
|
29.2
|
1.0
|
|
Holmium binding site 2 out
of 4 in 2olc
Go back to
Holmium Binding Sites List in 2olc
Holmium binding site 2 out
of 4 in the Crystal Structure of 5-Methylthioribose Kinase in Complex with Adp-2HO
 Mono view
 Stereo pair view
|
A full contact list of Holmium with other atoms in the Ho binding
site number 2 of Crystal Structure of 5-Methylthioribose Kinase in Complex with Adp-2HO within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Ho401
b:39.2
occ:1.00
|
OE1
|
A:GLU252
|
2.3
|
26.8
|
1.0
|
OD2
|
A:ASP250
|
2.3
|
17.6
|
1.0
|
O2B
|
A:ADP999
|
2.3
|
23.9
|
1.0
|
O
|
A:HOH1000
|
2.4
|
24.8
|
1.0
|
OD1
|
A:ASP250
|
2.5
|
20.9
|
1.0
|
CG
|
A:ASP250
|
2.7
|
20.6
|
1.0
|
O
|
A:HOH1001
|
2.9
|
23.3
|
1.0
|
CD
|
A:GLU252
|
3.4
|
23.4
|
1.0
|
PB
|
A:ADP999
|
3.6
|
25.6
|
1.0
|
CG
|
A:GLU252
|
3.9
|
23.7
|
1.0
|
O3B
|
A:ADP999
|
3.9
|
26.1
|
1.0
|
HO
|
A:HO400
|
4.1
|
44.8
|
1.0
|
CB
|
A:GLU252
|
4.2
|
23.2
|
1.0
|
ND2
|
A:ASN44
|
4.2
|
33.6
|
1.0
|
CB
|
A:ASP250
|
4.3
|
20.3
|
1.0
|
NZ
|
A:LYS61
|
4.3
|
24.9
|
1.0
|
OE2
|
A:GLU252
|
4.4
|
26.2
|
1.0
|
O3A
|
A:ADP999
|
4.5
|
26.8
|
1.0
|
O1B
|
A:ADP999
|
4.5
|
26.7
|
1.0
|
O
|
A:ASP250
|
4.7
|
22.6
|
1.0
|
O2A
|
A:ADP999
|
4.9
|
29.9
|
1.0
|
CE1
|
A:PHE253
|
4.9
|
20.3
|
1.0
|
|
Holmium binding site 3 out
of 4 in 2olc
Go back to
Holmium Binding Sites List in 2olc
Holmium binding site 3 out
of 4 in the Crystal Structure of 5-Methylthioribose Kinase in Complex with Adp-2HO
 Mono view
 Stereo pair view
|
A full contact list of Holmium with other atoms in the Ho binding
site number 3 of Crystal Structure of 5-Methylthioribose Kinase in Complex with Adp-2HO within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Ho400
b:41.9
occ:1.00
|
O2A
|
B:ADP999
|
2.2
|
27.3
|
1.0
|
O
|
B:HOH1000
|
2.3
|
24.5
|
1.0
|
O3B
|
B:ADP999
|
2.4
|
25.7
|
1.0
|
O
|
B:HOH1001
|
2.5
|
24.3
|
1.0
|
OD2
|
B:ASP250
|
2.5
|
19.5
|
1.0
|
PB
|
B:ADP999
|
3.5
|
26.2
|
1.0
|
CG
|
B:ASP250
|
3.6
|
20.0
|
1.0
|
PA
|
B:ADP999
|
3.6
|
26.8
|
1.0
|
O2B
|
B:ADP999
|
3.7
|
28.2
|
1.0
|
HO
|
B:HO401
|
3.9
|
40.0
|
1.0
|
O3A
|
B:ADP999
|
4.0
|
27.3
|
1.0
|
CB
|
B:ASP250
|
4.2
|
21.4
|
1.0
|
OD1
|
B:ASP250
|
4.4
|
21.0
|
1.0
|
O
|
B:GLY237
|
4.5
|
20.4
|
1.0
|
O1A
|
B:ADP999
|
4.6
|
27.7
|
1.0
|
O5'
|
B:ADP999
|
4.6
|
28.4
|
1.0
|
C5'
|
B:ADP999
|
4.8
|
29.2
|
1.0
|
O1B
|
B:ADP999
|
4.8
|
26.4
|
1.0
|
OD2
|
B:ASP40
|
4.9
|
45.2
|
1.0
|
|
Holmium binding site 4 out
of 4 in 2olc
Go back to
Holmium Binding Sites List in 2olc
Holmium binding site 4 out
of 4 in the Crystal Structure of 5-Methylthioribose Kinase in Complex with Adp-2HO
 Mono view
 Stereo pair view
|
A full contact list of Holmium with other atoms in the Ho binding
site number 4 of Crystal Structure of 5-Methylthioribose Kinase in Complex with Adp-2HO within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Ho401
b:40.0
occ:1.00
|
O
|
B:HOH1002
|
2.0
|
21.9
|
1.0
|
O2B
|
B:ADP999
|
2.3
|
28.2
|
1.0
|
OE1
|
B:GLU252
|
2.4
|
25.8
|
1.0
|
OD2
|
B:ASP250
|
2.4
|
19.5
|
1.0
|
OD1
|
B:ASP250
|
2.4
|
21.0
|
1.0
|
CG
|
B:ASP250
|
2.8
|
20.0
|
1.0
|
PB
|
B:ADP999
|
3.5
|
26.2
|
1.0
|
CD
|
B:GLU252
|
3.6
|
23.0
|
1.0
|
O3B
|
B:ADP999
|
3.8
|
25.7
|
1.0
|
O
|
B:HOH1001
|
3.8
|
24.3
|
1.0
|
HO
|
B:HO400
|
3.9
|
41.9
|
1.0
|
NZ
|
B:LYS61
|
4.2
|
26.5
|
1.0
|
CB
|
B:ASP250
|
4.3
|
21.4
|
1.0
|
CG
|
B:GLU252
|
4.3
|
22.8
|
1.0
|
CB
|
B:GLU252
|
4.3
|
23.0
|
1.0
|
ND2
|
B:ASN44
|
4.3
|
29.1
|
1.0
|
O1B
|
B:ADP999
|
4.4
|
26.4
|
1.0
|
O3A
|
B:ADP999
|
4.5
|
27.3
|
1.0
|
OE2
|
B:GLU252
|
4.5
|
23.5
|
1.0
|
O
|
B:ASP250
|
4.6
|
22.7
|
1.0
|
O2A
|
B:ADP999
|
4.6
|
27.3
|
1.0
|
PA
|
B:ADP999
|
5.0
|
26.8
|
1.0
|
|
Reference:
S.Y.Ku,
G.D.Smith,
P.L.Howell.
Adp-2HO As A Phasing Tool For Nucleotide-Containing Proteins. Acta Crystallogr.,Sect.D V. 63 493 2007.
ISSN: ISSN 0907-4449
PubMed: 17372354
DOI: 10.1107/S0907444907006592
Page generated: Sun Aug 11 09:14:18 2024
|