Cobalt in PDB 5yr5: Human Methionine Aminopeptidase Type 1B (F309L Mutant) in Complex with Ovalicin
Enzymatic activity of Human Methionine Aminopeptidase Type 1B (F309L Mutant) in Complex with Ovalicin
All present enzymatic activity of Human Methionine Aminopeptidase Type 1B (F309L Mutant) in Complex with Ovalicin:
3.4.11.18;
Protein crystallography data
The structure of Human Methionine Aminopeptidase Type 1B (F309L Mutant) in Complex with Ovalicin, PDB code: 5yr5
was solved by
V.Pillalamarri,
T.Arya,
A.Addlagatta,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
31.24 /
1.60
|
Space group
|
P 1 21 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
47.392,
77.339,
47.464,
90.00,
87.95,
90.00
|
R / Rfree (%)
|
17.7 /
20.1
|
Other elements in 5yr5:
The structure of Human Methionine Aminopeptidase Type 1B (F309L Mutant) in Complex with Ovalicin also contains other interesting chemical elements:
Cobalt Binding Sites:
The binding sites of Cobalt atom in the Human Methionine Aminopeptidase Type 1B (F309L Mutant) in Complex with Ovalicin
(pdb code 5yr5). This binding sites where shown within
5.0 Angstroms radius around Cobalt atom.
In total 3 binding sites of Cobalt where determined in the
Human Methionine Aminopeptidase Type 1B (F309L Mutant) in Complex with Ovalicin, PDB code: 5yr5:
Jump to Cobalt binding site number:
1;
2;
3;
Cobalt binding site 1 out
of 3 in 5yr5
Go back to
Cobalt Binding Sites List in 5yr5
Cobalt binding site 1 out
of 3 in the Human Methionine Aminopeptidase Type 1B (F309L Mutant) in Complex with Ovalicin
 Mono view
 Stereo pair view
|
A full contact list of Cobalt with other atoms in the Co binding
site number 1 of Human Methionine Aminopeptidase Type 1B (F309L Mutant) in Complex with Ovalicin within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Co401
b:18.1
occ:1.00
|
O
|
A:HOH455
|
2.0
|
18.5
|
1.0
|
NE2
|
A:HIS303
|
2.0
|
16.3
|
1.0
|
OE2
|
A:GLU367
|
2.0
|
16.5
|
1.0
|
OD2
|
A:ASP240
|
2.0
|
16.6
|
1.0
|
OE1
|
A:GLU336
|
2.2
|
18.3
|
1.0
|
CE1
|
A:HIS303
|
2.9
|
18.8
|
1.0
|
CG
|
A:ASP240
|
2.9
|
17.7
|
1.0
|
CD
|
A:GLU367
|
3.0
|
19.1
|
1.0
|
CD
|
A:GLU336
|
3.0
|
17.6
|
1.0
|
CD2
|
A:HIS303
|
3.1
|
20.0
|
1.0
|
CO
|
A:CO402
|
3.2
|
18.4
|
1.0
|
OE2
|
A:GLU336
|
3.3
|
18.9
|
1.0
|
OE1
|
A:GLU367
|
3.3
|
16.7
|
1.0
|
OD1
|
A:ASP240
|
3.4
|
17.1
|
1.0
|
O11
|
A:OVA405
|
3.5
|
20.3
|
1.0
|
O
|
A:HOH438
|
3.6
|
20.8
|
1.0
|
OG1
|
A:THR334
|
3.6
|
17.1
|
1.0
|
CG2
|
A:THR334
|
3.9
|
17.8
|
1.0
|
ND1
|
A:HIS303
|
4.1
|
19.4
|
1.0
|
CB
|
A:THR334
|
4.1
|
17.2
|
1.0
|
CB
|
A:ASP240
|
4.1
|
18.0
|
1.0
|
CG
|
A:HIS303
|
4.2
|
18.4
|
1.0
|
O
|
A:HOH447
|
4.2
|
19.5
|
1.0
|
CG
|
A:GLU367
|
4.3
|
18.8
|
1.0
|
CG
|
A:GLU336
|
4.4
|
15.7
|
1.0
|
C1
|
A:OVA405
|
4.7
|
19.2
|
1.0
|
C5
|
A:OVA405
|
4.7
|
20.6
|
1.0
|
CB
|
A:GLU336
|
4.9
|
16.1
|
1.0
|
OD2
|
A:ASP229
|
4.9
|
18.6
|
1.0
|
C6
|
A:OVA405
|
5.0
|
19.5
|
1.0
|
|
Cobalt binding site 2 out
of 3 in 5yr5
Go back to
Cobalt Binding Sites List in 5yr5
Cobalt binding site 2 out
of 3 in the Human Methionine Aminopeptidase Type 1B (F309L Mutant) in Complex with Ovalicin
 Mono view
 Stereo pair view
|
A full contact list of Cobalt with other atoms in the Co binding
site number 2 of Human Methionine Aminopeptidase Type 1B (F309L Mutant) in Complex with Ovalicin within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Co402
b:18.4
occ:1.00
|
OD1
|
A:ASP240
|
2.0
|
17.1
|
1.0
|
O
|
A:HOH455
|
2.1
|
18.5
|
1.0
|
O
|
A:HOH447
|
2.1
|
19.5
|
1.0
|
OE1
|
A:GLU367
|
2.1
|
16.7
|
1.0
|
OD2
|
A:ASP229
|
2.2
|
18.6
|
1.0
|
OD1
|
A:ASP229
|
2.3
|
18.3
|
1.0
|
CG
|
A:ASP229
|
2.5
|
16.0
|
1.0
|
CG
|
A:ASP240
|
2.9
|
17.7
|
1.0
|
CD
|
A:GLU367
|
3.1
|
19.1
|
1.0
|
CO
|
A:CO401
|
3.2
|
18.1
|
1.0
|
OD2
|
A:ASP240
|
3.2
|
16.6
|
1.0
|
OE2
|
A:GLU367
|
3.3
|
16.5
|
1.0
|
O
|
A:HOH438
|
3.8
|
20.8
|
1.0
|
CB
|
A:ASP229
|
4.0
|
15.7
|
1.0
|
O
|
A:HOH493
|
4.0
|
23.9
|
0.8
|
OE2
|
A:GLU336
|
4.1
|
18.9
|
1.0
|
ND2
|
A:ASN242
|
4.1
|
15.5
|
1.0
|
CG2
|
A:THR231
|
4.1
|
19.2
|
0.7
|
OG1
|
A:THR231
|
4.2
|
19.6
|
0.3
|
O
|
A:HOH430
|
4.2
|
18.6
|
1.0
|
O11
|
A:OVA405
|
4.3
|
20.3
|
1.0
|
CB
|
A:ASP240
|
4.3
|
18.0
|
1.0
|
CG
|
A:GLU367
|
4.5
|
18.8
|
1.0
|
O
|
A:HOH506
|
4.5
|
22.8
|
1.0
|
O
|
A:LEU241
|
4.5
|
16.4
|
1.0
|
OE1
|
A:GLU336
|
4.6
|
18.3
|
1.0
|
N
|
A:LEU241
|
4.6
|
15.9
|
1.0
|
CD
|
A:GLU336
|
4.7
|
17.6
|
1.0
|
C
|
A:LEU241
|
4.8
|
17.9
|
1.0
|
C
|
A:ASP240
|
4.9
|
16.5
|
1.0
|
CA
|
A:ASP240
|
4.9
|
18.1
|
1.0
|
CA
|
A:ASP229
|
4.9
|
15.3
|
1.0
|
CB
|
A:ASN242
|
4.9
|
16.7
|
1.0
|
CB
|
A:GLU367
|
5.0
|
16.5
|
1.0
|
O
|
A:ILE230
|
5.0
|
15.5
|
1.0
|
|
Cobalt binding site 3 out
of 3 in 5yr5
Go back to
Cobalt Binding Sites List in 5yr5
Cobalt binding site 3 out
of 3 in the Human Methionine Aminopeptidase Type 1B (F309L Mutant) in Complex with Ovalicin
 Mono view
 Stereo pair view
|
A full contact list of Cobalt with other atoms in the Co binding
site number 3 of Human Methionine Aminopeptidase Type 1B (F309L Mutant) in Complex with Ovalicin within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Co403
b:36.4
occ:0.40
|
OE1
|
A:GLU128
|
1.8
|
41.1
|
0.4
|
O
|
A:HOH613
|
2.0
|
29.3
|
0.4
|
OH
|
A:TYR195
|
2.0
|
31.8
|
1.0
|
O
|
A:HOH612
|
2.3
|
36.0
|
0.4
|
NE2
|
A:HIS310
|
2.3
|
35.7
|
1.0
|
O
|
A:HOH612
|
2.4
|
30.6
|
0.5
|
OE1
|
A:GLU128
|
2.7
|
46.4
|
0.6
|
CD
|
A:GLU128
|
2.8
|
39.9
|
0.4
|
CZ
|
A:TYR195
|
3.2
|
29.5
|
1.0
|
CD2
|
A:HIS310
|
3.2
|
33.5
|
1.0
|
OE2
|
A:GLU128
|
3.3
|
38.4
|
0.4
|
CE1
|
A:HIS310
|
3.4
|
33.9
|
1.0
|
CE1
|
A:TYR196
|
3.6
|
27.5
|
0.2
|
CE1
|
A:TYR196
|
3.7
|
42.8
|
0.8
|
CE2
|
A:TYR195
|
3.7
|
25.5
|
1.0
|
CD
|
A:GLU128
|
3.8
|
41.3
|
0.6
|
CG
|
A:GLU128
|
4.1
|
36.6
|
0.4
|
CE1
|
A:TYR195
|
4.2
|
29.8
|
1.0
|
CD1
|
A:TYR196
|
4.2
|
27.1
|
0.2
|
CZ
|
A:TYR196
|
4.3
|
27.5
|
0.2
|
OE2
|
A:GLU128
|
4.3
|
35.1
|
0.6
|
CD1
|
A:TYR196
|
4.4
|
37.9
|
0.8
|
CZ
|
A:TYR196
|
4.4
|
39.9
|
0.8
|
CG
|
A:HIS310
|
4.4
|
27.1
|
1.0
|
OH
|
A:TYR196
|
4.4
|
27.6
|
0.2
|
OH
|
A:TYR196
|
4.4
|
50.6
|
0.8
|
ND1
|
A:HIS310
|
4.5
|
34.3
|
1.0
|
O
|
A:HOH611
|
4.8
|
30.1
|
0.8
|
|
Reference:
V.Pillalamarri,
T.Arya,
N.Haque,
S.C.Bala,
A.K.Marapaka,
A.Addlagatta.
Discovery of Natural Product Ovalicin Sensitive Type 1 Methionine Aminopeptidases: Molecular and Structural Basis. Biochem. J. V. 476 991 2019.
ISSN: ESSN 1470-8728
PubMed: 30837307
DOI: 10.1042/BCJ20180874
Page generated: Tue Jul 30 18:21:09 2024
|