Zinc in PDB 8h1f: Aquifex Aeolicus Mutl Endonuclease Domain Complexed with Zinc Ions After Soaking
Protein crystallography data
The structure of Aquifex Aeolicus Mutl Endonuclease Domain Complexed with Zinc Ions After Soaking, PDB code: 8h1f
was solved by
K.Fukui,
T.Yano,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
34.75 /
1.22
|
Space group
|
P 43 21 2
|
Cell size a, b, c (Å), α, β, γ (°)
|
35.529,
35.529,
167.288,
90,
90,
90
|
R / Rfree (%)
|
15.7 /
17.5
|
Other elements in 8h1f:
The structure of Aquifex Aeolicus Mutl Endonuclease Domain Complexed with Zinc Ions After Soaking also contains other interesting chemical elements:
Zinc Binding Sites:
The binding sites of Zinc atom in the Aquifex Aeolicus Mutl Endonuclease Domain Complexed with Zinc Ions After Soaking
(pdb code 8h1f). This binding sites where shown within
5.0 Angstroms radius around Zinc atom.
In total 5 binding sites of Zinc where determined in the
Aquifex Aeolicus Mutl Endonuclease Domain Complexed with Zinc Ions After Soaking, PDB code: 8h1f:
Jump to Zinc binding site number:
1;
2;
3;
4;
5;
Zinc binding site 1 out
of 5 in 8h1f
Go back to
Zinc Binding Sites List in 8h1f
Zinc binding site 1 out
of 5 in the Aquifex Aeolicus Mutl Endonuclease Domain Complexed with Zinc Ions After Soaking
Mono view
Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 1 of Aquifex Aeolicus Mutl Endonuclease Domain Complexed with Zinc Ions After Soaking within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Zn501
b:9.1
occ:1.00
|
OE1
|
A:GLU384
|
2.3
|
13.7
|
1.0
|
OE2
|
A:GLU384
|
2.4
|
13.5
|
1.0
|
CL
|
A:CL509
|
2.5
|
15.9
|
1.0
|
CL
|
A:CL510
|
2.5
|
13.6
|
1.0
|
CD
|
A:GLU384
|
2.7
|
13.1
|
1.0
|
CG
|
A:GLU384
|
4.3
|
14.1
|
1.0
|
O
|
A:HOH714
|
4.3
|
22.6
|
1.0
|
NE
|
A:ARG387
|
4.3
|
16.6
|
1.0
|
CG
|
A:GLU388
|
4.4
|
17.1
|
1.0
|
O
|
A:GLU384
|
4.7
|
13.7
|
1.0
|
CB
|
A:ARG387
|
4.8
|
14.3
|
1.0
|
NH2
|
A:ARG387
|
4.8
|
16.6
|
1.0
|
OE2
|
A:GLU388
|
4.9
|
18.3
|
1.0
|
|
Zinc binding site 2 out
of 5 in 8h1f
Go back to
Zinc Binding Sites List in 8h1f
Zinc binding site 2 out
of 5 in the Aquifex Aeolicus Mutl Endonuclease Domain Complexed with Zinc Ions After Soaking
Mono view
Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 2 of Aquifex Aeolicus Mutl Endonuclease Domain Complexed with Zinc Ions After Soaking within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Zn502
b:25.0
occ:1.00
|
O
|
A:HOH611
|
2.3
|
26.2
|
1.0
|
O
|
A:HOH605
|
2.4
|
30.0
|
1.0
|
OD2
|
A:ASP366
|
2.4
|
28.0
|
1.0
|
O
|
A:HOH687
|
2.6
|
25.6
|
1.0
|
O
|
A:HOH678
|
2.7
|
17.9
|
1.0
|
OD1
|
A:ASP366
|
2.7
|
22.3
|
1.0
|
CG
|
A:ASP366
|
2.9
|
24.1
|
1.0
|
ND2
|
A:ASN368
|
4.1
|
35.7
|
1.0
|
O
|
A:HOH602
|
4.2
|
27.2
|
1.0
|
CB
|
A:ASN368
|
4.3
|
23.1
|
1.0
|
N
|
A:LEU369
|
4.3
|
15.0
|
1.0
|
CB
|
A:ASP366
|
4.4
|
21.1
|
1.0
|
CB
|
A:LEU369
|
4.6
|
17.4
|
1.0
|
CG
|
A:ASN368
|
4.7
|
30.8
|
1.0
|
N
|
A:ASN368
|
5.0
|
17.9
|
1.0
|
CA
|
A:ASN368
|
5.0
|
17.6
|
1.0
|
|
Zinc binding site 3 out
of 5 in 8h1f
Go back to
Zinc Binding Sites List in 8h1f
Zinc binding site 3 out
of 5 in the Aquifex Aeolicus Mutl Endonuclease Domain Complexed with Zinc Ions After Soaking
Mono view
Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 3 of Aquifex Aeolicus Mutl Endonuclease Domain Complexed with Zinc Ions After Soaking within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Zn503
b:24.3
occ:1.00
|
O
|
A:HOH703
|
2.2
|
25.4
|
1.0
|
SG
|
A:CYS371
|
2.5
|
17.0
|
1.0
|
O
|
A:HOH688
|
2.5
|
19.4
|
1.0
|
O
|
A:HOH720
|
2.5
|
26.1
|
1.0
|
O
|
A:HOH718
|
2.8
|
20.2
|
1.0
|
O
|
A:HOH666
|
3.1
|
24.9
|
1.0
|
CB
|
A:CYS371
|
3.5
|
13.9
|
1.0
|
ZN
|
A:ZN505
|
3.7
|
11.1
|
1.0
|
O
|
A:HOH671
|
3.8
|
21.1
|
1.0
|
O
|
A:HOH620
|
4.5
|
24.0
|
1.0
|
CE1
|
A:HIS404
|
4.7
|
21.6
|
1.0
|
OE2
|
A:GLU357
|
4.8
|
16.9
|
1.0
|
CA
|
A:CYS371
|
4.9
|
13.3
|
1.0
|
|
Zinc binding site 4 out
of 5 in 8h1f
Go back to
Zinc Binding Sites List in 8h1f
Zinc binding site 4 out
of 5 in the Aquifex Aeolicus Mutl Endonuclease Domain Complexed with Zinc Ions After Soaking
Mono view
Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 4 of Aquifex Aeolicus Mutl Endonuclease Domain Complexed with Zinc Ions After Soaking within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Zn504
b:12.4
occ:1.00
|
OE1
|
A:GLU357
|
2.1
|
17.3
|
1.0
|
O
|
A:HOH675
|
2.2
|
21.8
|
1.0
|
ND1
|
A:HIS404
|
2.3
|
18.5
|
1.0
|
SG
|
A:CYS402
|
2.4
|
15.8
|
1.0
|
O
|
A:HOH663
|
2.4
|
18.1
|
1.0
|
CD
|
A:GLU357
|
3.0
|
14.9
|
1.0
|
OE2
|
A:GLU357
|
3.2
|
16.9
|
1.0
|
CE1
|
A:HIS404
|
3.2
|
21.6
|
1.0
|
CG
|
A:HIS404
|
3.3
|
19.5
|
1.0
|
CB
|
A:CYS402
|
3.4
|
15.1
|
1.0
|
CB
|
A:HIS404
|
3.6
|
20.6
|
1.0
|
CD2
|
A:LEU354
|
3.8
|
13.8
|
1.0
|
N
|
A:HIS404
|
3.9
|
20.6
|
1.0
|
ZN
|
A:ZN505
|
4.0
|
11.1
|
1.0
|
O
|
A:HOH688
|
4.2
|
19.4
|
1.0
|
CA
|
A:HIS404
|
4.4
|
21.0
|
1.0
|
CG
|
A:GLU357
|
4.4
|
13.4
|
1.0
|
NE2
|
A:HIS404
|
4.4
|
23.7
|
1.0
|
CD2
|
A:HIS404
|
4.4
|
22.5
|
1.0
|
CD
|
A:PRO403
|
4.4
|
17.8
|
1.0
|
N
|
A:PRO403
|
4.5
|
17.7
|
1.0
|
CG
|
A:PRO403
|
4.6
|
23.0
|
1.0
|
CA
|
A:CYS402
|
4.6
|
15.3
|
1.0
|
C
|
A:CYS402
|
4.7
|
16.3
|
1.0
|
CD
|
A:ARG406
|
4.9
|
28.0
|
1.0
|
|
Zinc binding site 5 out
of 5 in 8h1f
Go back to
Zinc Binding Sites List in 8h1f
Zinc binding site 5 out
of 5 in the Aquifex Aeolicus Mutl Endonuclease Domain Complexed with Zinc Ions After Soaking
Mono view
Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 5 of Aquifex Aeolicus Mutl Endonuclease Domain Complexed with Zinc Ions After Soaking within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Zn505
b:11.1
occ:1.00
|
O
|
A:HOH663
|
2.2
|
18.1
|
1.0
|
OE2
|
A:GLU357
|
2.3
|
16.9
|
1.0
|
NE2
|
A:HIS353
|
2.3
|
15.9
|
1.0
|
O
|
A:HOH671
|
2.4
|
21.1
|
1.0
|
SG
|
A:CYS371
|
2.5
|
17.0
|
1.0
|
O
|
A:HOH688
|
2.7
|
19.4
|
1.0
|
CE1
|
A:HIS353
|
3.2
|
14.2
|
1.0
|
CD
|
A:GLU357
|
3.4
|
14.9
|
1.0
|
CD2
|
A:HIS353
|
3.4
|
14.7
|
1.0
|
CB
|
A:CYS371
|
3.5
|
13.9
|
1.0
|
ZN
|
A:ZN503
|
3.7
|
24.3
|
1.0
|
OE1
|
A:GLU357
|
3.9
|
17.3
|
1.0
|
ZN
|
A:ZN504
|
4.0
|
12.4
|
1.0
|
CA
|
A:CYS371
|
4.2
|
13.3
|
1.0
|
O
|
A:HOH675
|
4.3
|
21.8
|
1.0
|
O
|
A:HOH720
|
4.3
|
26.1
|
1.0
|
ND1
|
A:HIS353
|
4.4
|
13.6
|
1.0
|
CE1
|
A:HIS404
|
4.4
|
21.6
|
1.0
|
CG
|
A:GLU357
|
4.4
|
13.4
|
1.0
|
CG
|
A:HIS353
|
4.5
|
12.3
|
1.0
|
O
|
A:HOH695
|
4.6
|
22.6
|
1.0
|
ND1
|
A:HIS404
|
4.6
|
18.5
|
1.0
|
CB
|
A:GLU357
|
4.9
|
12.2
|
1.0
|
C
|
A:CYS371
|
5.0
|
12.1
|
1.0
|
O
|
A:CYS371
|
5.0
|
13.5
|
1.0
|
|
Reference:
K.Fukui,
T.Yamamoto,
T.Murakawa,
S.Baba,
T.Kumasaka,
T.Yano.
Catalytic Mechanism of the Zinc-Dependent Mutl Endonuclease Reaction. Life Sci Alliance V. 6 2023.
ISSN: ESSN 2575-1077
PubMed: 37487639
DOI: 10.26508/LSA.202302001
Page generated: Thu Oct 31 06:54:04 2024
|