Zinc in PDB 2hvw: Crystal Structure of Dcmp Deaminase From Streptococcus Mutans
Enzymatic activity of Crystal Structure of Dcmp Deaminase From Streptococcus Mutans
All present enzymatic activity of Crystal Structure of Dcmp Deaminase From Streptococcus Mutans:
3.5.4.12;
Protein crystallography data
The structure of Crystal Structure of Dcmp Deaminase From Streptococcus Mutans, PDB code: 2hvw
was solved by
H.F.Hou,
Z.Q.Gao,
L.F.Li,
Y.H.Liang,
X.D.Su,
Y.H.Dong,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
16.00 /
1.67
|
Space group
|
C 2 2 21
|
Cell size a, b, c (Å), α, β, γ (°)
|
95.498,
99.657,
141.388,
90.00,
90.00,
90.00
|
R / Rfree (%)
|
14.9 /
17.9
|
Other elements in 2hvw:
The structure of Crystal Structure of Dcmp Deaminase From Streptococcus Mutans also contains other interesting chemical elements:
Zinc Binding Sites:
The binding sites of Zinc atom in the Crystal Structure of Dcmp Deaminase From Streptococcus Mutans
(pdb code 2hvw). This binding sites where shown within
5.0 Angstroms radius around Zinc atom.
In total 6 binding sites of Zinc where determined in the
Crystal Structure of Dcmp Deaminase From Streptococcus Mutans, PDB code: 2hvw:
Jump to Zinc binding site number:
1;
2;
3;
4;
5;
6;
Zinc binding site 1 out
of 6 in 2hvw
Go back to
Zinc Binding Sites List in 2hvw
Zinc binding site 1 out
of 6 in the Crystal Structure of Dcmp Deaminase From Streptococcus Mutans
Mono view
Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 1 of Crystal Structure of Dcmp Deaminase From Streptococcus Mutans within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Zn1001
b:16.0
occ:0.85
|
ND1
|
A:HIS59
|
2.2
|
17.5
|
1.0
|
SG
|
A:CYS54
|
2.3
|
18.1
|
1.0
|
SG
|
A:CYS66
|
2.4
|
16.6
|
1.0
|
SG
|
A:CYS24
|
2.4
|
16.5
|
1.0
|
CE1
|
A:HIS59
|
3.1
|
18.8
|
1.0
|
CB
|
A:CYS54
|
3.2
|
17.4
|
1.0
|
CG
|
A:HIS59
|
3.2
|
19.7
|
1.0
|
CB
|
A:CYS66
|
3.3
|
16.6
|
1.0
|
CB
|
A:CYS24
|
3.3
|
16.5
|
1.0
|
CB
|
A:HIS59
|
3.6
|
18.3
|
1.0
|
CA
|
A:HIS59
|
3.8
|
18.8
|
1.0
|
CA
|
A:CYS24
|
4.1
|
16.5
|
1.0
|
NE2
|
A:HIS59
|
4.2
|
19.6
|
1.0
|
CD2
|
A:HIS59
|
4.3
|
19.0
|
1.0
|
CG2
|
A:THR69
|
4.3
|
13.3
|
1.0
|
O3'
|
A:DDN1301
|
4.5
|
16.1
|
1.0
|
CD
|
A:ARG26
|
4.6
|
18.5
|
1.0
|
CA
|
A:CYS54
|
4.6
|
17.8
|
1.0
|
N
|
A:HIS59
|
4.7
|
18.8
|
1.0
|
CA
|
A:CYS66
|
4.7
|
16.3
|
1.0
|
CB
|
A:ARG68
|
4.8
|
15.2
|
1.0
|
C
|
A:CYS24
|
4.8
|
17.5
|
1.0
|
N
|
A:GLU60
|
4.9
|
18.8
|
1.0
|
C
|
A:HIS59
|
4.9
|
19.1
|
1.0
|
CG
|
A:ARG26
|
5.0
|
18.2
|
1.0
|
|
Zinc binding site 2 out
of 6 in 2hvw
Go back to
Zinc Binding Sites List in 2hvw
Zinc binding site 2 out
of 6 in the Crystal Structure of Dcmp Deaminase From Streptococcus Mutans
Mono view
Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 2 of Crystal Structure of Dcmp Deaminase From Streptococcus Mutans within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Zn1002
b:14.1
occ:0.90
|
O4
|
A:DDN1301
|
2.0
|
15.7
|
1.0
|
ND1
|
A:HIS71
|
2.0
|
15.1
|
1.0
|
SG
|
A:CYS102
|
2.3
|
13.1
|
1.0
|
SG
|
A:CYS99
|
2.3
|
13.7
|
1.0
|
CE1
|
A:HIS71
|
3.0
|
15.0
|
1.0
|
CG
|
A:HIS71
|
3.0
|
12.9
|
1.0
|
C4
|
A:DDN1301
|
3.1
|
14.9
|
1.0
|
CB
|
A:CYS102
|
3.2
|
13.4
|
1.0
|
CB
|
A:CYS99
|
3.4
|
13.9
|
1.0
|
N3
|
A:DDN1301
|
3.4
|
15.6
|
1.0
|
CB
|
A:HIS71
|
3.4
|
12.4
|
1.0
|
C5
|
A:DDN1301
|
3.5
|
14.3
|
1.0
|
O
|
A:HOH1443
|
3.7
|
16.7
|
1.0
|
OE2
|
A:GLU73
|
3.7
|
14.8
|
1.0
|
N
|
A:CYS99
|
3.8
|
13.9
|
1.0
|
C2
|
A:DDN1301
|
4.0
|
16.2
|
1.0
|
NE2
|
A:HIS71
|
4.1
|
14.5
|
1.0
|
N
|
A:CYS102
|
4.1
|
13.6
|
1.0
|
CD2
|
A:HIS71
|
4.1
|
14.9
|
1.0
|
CA
|
A:CYS99
|
4.1
|
13.7
|
1.0
|
C6
|
A:DDN1301
|
4.1
|
14.3
|
1.0
|
CA
|
A:CYS102
|
4.2
|
12.9
|
1.0
|
CD
|
A:GLU73
|
4.3
|
14.0
|
1.0
|
OE1
|
A:GLU73
|
4.3
|
14.2
|
1.0
|
N1
|
A:DDN1301
|
4.4
|
14.6
|
1.0
|
O
|
A:HOH1456
|
4.6
|
18.7
|
1.0
|
O
|
A:HOH1431
|
4.7
|
16.2
|
1.0
|
C
|
A:CYS99
|
4.7
|
13.5
|
1.0
|
O
|
A:CYS99
|
4.8
|
12.6
|
1.0
|
O2
|
A:DDN1301
|
4.8
|
14.1
|
1.0
|
C
|
A:PRO98
|
4.8
|
14.1
|
1.0
|
CA
|
A:HIS71
|
4.9
|
12.2
|
1.0
|
CA
|
A:PRO98
|
5.0
|
14.4
|
1.0
|
|
Zinc binding site 3 out
of 6 in 2hvw
Go back to
Zinc Binding Sites List in 2hvw
Zinc binding site 3 out
of 6 in the Crystal Structure of Dcmp Deaminase From Streptococcus Mutans
Mono view
Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 3 of Crystal Structure of Dcmp Deaminase From Streptococcus Mutans within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Zn1003
b:15.1
occ:0.90
|
ND1
|
B:HIS59
|
2.1
|
16.3
|
1.0
|
SG
|
B:CYS54
|
2.3
|
15.5
|
1.0
|
SG
|
B:CYS24
|
2.4
|
14.2
|
1.0
|
SG
|
B:CYS66
|
2.4
|
15.6
|
1.0
|
CE1
|
B:HIS59
|
3.0
|
17.4
|
1.0
|
CG
|
B:HIS59
|
3.2
|
17.9
|
1.0
|
CB
|
B:CYS54
|
3.2
|
16.0
|
1.0
|
CB
|
B:CYS66
|
3.3
|
15.1
|
1.0
|
CB
|
B:CYS24
|
3.3
|
15.5
|
1.0
|
CB
|
B:HIS59
|
3.6
|
17.3
|
1.0
|
CA
|
B:HIS59
|
3.8
|
16.9
|
1.0
|
CA
|
B:CYS24
|
4.1
|
15.2
|
1.0
|
NE2
|
B:HIS59
|
4.2
|
18.8
|
1.0
|
CD2
|
B:HIS59
|
4.3
|
18.4
|
1.0
|
CG2
|
B:THR69
|
4.4
|
13.4
|
1.0
|
O3'
|
B:DDN1302
|
4.6
|
12.9
|
1.0
|
CA
|
B:CYS54
|
4.6
|
15.9
|
1.0
|
CD
|
B:ARG26
|
4.6
|
16.0
|
1.0
|
N
|
B:HIS59
|
4.6
|
16.5
|
1.0
|
CA
|
B:CYS66
|
4.7
|
14.7
|
1.0
|
CB
|
B:ARG68
|
4.8
|
13.6
|
1.0
|
C
|
B:CYS24
|
4.8
|
16.0
|
1.0
|
N
|
B:GLU60
|
4.9
|
16.3
|
1.0
|
CG
|
B:ARG26
|
4.9
|
16.3
|
1.0
|
C
|
B:HIS59
|
4.9
|
17.0
|
1.0
|
|
Zinc binding site 4 out
of 6 in 2hvw
Go back to
Zinc Binding Sites List in 2hvw
Zinc binding site 4 out
of 6 in the Crystal Structure of Dcmp Deaminase From Streptococcus Mutans
Mono view
Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 4 of Crystal Structure of Dcmp Deaminase From Streptococcus Mutans within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Zn1004
b:12.5
occ:0.85
|
O4
|
B:DDN1302
|
2.1
|
13.9
|
1.0
|
ND1
|
B:HIS71
|
2.1
|
14.7
|
1.0
|
SG
|
B:CYS102
|
2.3
|
12.6
|
1.0
|
SG
|
B:CYS99
|
2.3
|
13.5
|
1.0
|
CE1
|
B:HIS71
|
3.0
|
12.9
|
1.0
|
CG
|
B:HIS71
|
3.1
|
12.5
|
1.0
|
C4
|
B:DDN1302
|
3.1
|
13.4
|
1.0
|
CB
|
B:CYS102
|
3.2
|
12.1
|
1.0
|
CB
|
B:HIS71
|
3.4
|
11.4
|
1.0
|
CB
|
B:CYS99
|
3.4
|
13.2
|
1.0
|
N3
|
B:DDN1302
|
3.4
|
12.5
|
1.0
|
C5
|
B:DDN1302
|
3.6
|
13.8
|
1.0
|
O
|
B:HOH1418
|
3.6
|
19.2
|
1.0
|
OE2
|
B:GLU73
|
3.7
|
13.2
|
1.0
|
N
|
B:CYS99
|
3.8
|
13.5
|
1.0
|
C2
|
B:DDN1302
|
4.1
|
15.2
|
1.0
|
N
|
B:CYS102
|
4.1
|
13.0
|
1.0
|
NE2
|
B:HIS71
|
4.1
|
13.3
|
1.0
|
CA
|
B:CYS99
|
4.1
|
13.0
|
1.0
|
CD2
|
B:HIS71
|
4.2
|
13.4
|
1.0
|
C6
|
B:DDN1302
|
4.2
|
14.2
|
1.0
|
CA
|
B:CYS102
|
4.2
|
12.1
|
1.0
|
CD
|
B:GLU73
|
4.3
|
13.6
|
1.0
|
OE1
|
B:GLU73
|
4.4
|
14.8
|
1.0
|
N1
|
B:DDN1302
|
4.4
|
15.0
|
1.0
|
O
|
B:HOH1431
|
4.6
|
18.9
|
1.0
|
C
|
B:CYS99
|
4.7
|
13.3
|
1.0
|
O
|
B:HOH1478
|
4.8
|
15.9
|
1.0
|
O
|
B:CYS99
|
4.8
|
12.1
|
1.0
|
C
|
B:PRO98
|
4.8
|
13.6
|
1.0
|
O2
|
B:DDN1302
|
4.8
|
12.4
|
1.0
|
CA
|
B:HIS71
|
4.9
|
11.4
|
1.0
|
CA
|
B:PRO98
|
5.0
|
13.9
|
1.0
|
|
Zinc binding site 5 out
of 6 in 2hvw
Go back to
Zinc Binding Sites List in 2hvw
Zinc binding site 5 out
of 6 in the Crystal Structure of Dcmp Deaminase From Streptococcus Mutans
Mono view
Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 5 of Crystal Structure of Dcmp Deaminase From Streptococcus Mutans within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Zn1005
b:16.8
occ:0.90
|
ND1
|
C:HIS59
|
2.2
|
18.7
|
1.0
|
SG
|
C:CYS54
|
2.3
|
16.8
|
1.0
|
SG
|
C:CYS66
|
2.3
|
16.6
|
1.0
|
SG
|
C:CYS24
|
2.4
|
16.4
|
1.0
|
CE1
|
C:HIS59
|
3.1
|
21.0
|
1.0
|
CB
|
C:CYS54
|
3.2
|
17.5
|
1.0
|
CG
|
C:HIS59
|
3.2
|
20.4
|
1.0
|
CB
|
C:CYS66
|
3.3
|
16.1
|
1.0
|
CB
|
C:CYS24
|
3.4
|
17.3
|
1.0
|
CB
|
C:HIS59
|
3.6
|
19.3
|
1.0
|
CA
|
C:HIS59
|
3.8
|
19.0
|
1.0
|
CA
|
C:CYS24
|
4.2
|
17.2
|
1.0
|
NE2
|
C:HIS59
|
4.2
|
21.1
|
1.0
|
CD2
|
C:HIS59
|
4.3
|
20.7
|
1.0
|
CG2
|
C:THR69
|
4.4
|
14.0
|
1.0
|
O3'
|
C:DDN1303
|
4.5
|
14.0
|
1.0
|
CD
|
C:ARG26
|
4.6
|
18.2
|
1.0
|
CA
|
C:CYS54
|
4.6
|
17.9
|
1.0
|
N
|
C:HIS59
|
4.7
|
18.9
|
1.0
|
CA
|
C:CYS66
|
4.7
|
15.4
|
1.0
|
CB
|
C:ARG68
|
4.8
|
15.1
|
1.0
|
N
|
C:GLU60
|
4.8
|
18.4
|
1.0
|
C
|
C:CYS24
|
4.9
|
17.7
|
1.0
|
C
|
C:HIS59
|
4.9
|
19.0
|
1.0
|
CG
|
C:ARG26
|
4.9
|
18.0
|
1.0
|
|
Zinc binding site 6 out
of 6 in 2hvw
Go back to
Zinc Binding Sites List in 2hvw
Zinc binding site 6 out
of 6 in the Crystal Structure of Dcmp Deaminase From Streptococcus Mutans
Mono view
Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 6 of Crystal Structure of Dcmp Deaminase From Streptococcus Mutans within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Zn1006
b:13.3
occ:0.85
|
ND1
|
C:HIS71
|
2.0
|
15.6
|
1.0
|
O4
|
C:DDN1303
|
2.0
|
16.0
|
1.0
|
SG
|
C:CYS102
|
2.3
|
13.8
|
1.0
|
SG
|
C:CYS99
|
2.3
|
14.2
|
1.0
|
CE1
|
C:HIS71
|
3.0
|
15.1
|
1.0
|
CG
|
C:HIS71
|
3.0
|
13.2
|
1.0
|
C4
|
C:DDN1303
|
3.1
|
14.3
|
1.0
|
CB
|
C:CYS102
|
3.2
|
13.3
|
1.0
|
CB
|
C:CYS99
|
3.4
|
13.1
|
1.0
|
CB
|
C:HIS71
|
3.4
|
13.3
|
1.0
|
N3
|
C:DDN1303
|
3.4
|
14.3
|
1.0
|
C5
|
C:DDN1303
|
3.5
|
14.4
|
1.0
|
O
|
C:HOH1452
|
3.6
|
18.1
|
1.0
|
OE2
|
C:GLU73
|
3.7
|
14.9
|
1.0
|
N
|
C:CYS99
|
3.7
|
13.7
|
1.0
|
C2
|
C:DDN1303
|
4.0
|
15.4
|
1.0
|
NE2
|
C:HIS71
|
4.0
|
14.6
|
1.0
|
N
|
C:CYS102
|
4.1
|
13.7
|
1.0
|
CD2
|
C:HIS71
|
4.1
|
13.9
|
1.0
|
CA
|
C:CYS99
|
4.1
|
13.6
|
1.0
|
C6
|
C:DDN1303
|
4.2
|
13.8
|
1.0
|
CA
|
C:CYS102
|
4.2
|
13.2
|
1.0
|
CD
|
C:GLU73
|
4.3
|
14.4
|
1.0
|
OE1
|
C:GLU73
|
4.3
|
13.9
|
1.0
|
N1
|
C:DDN1303
|
4.4
|
15.3
|
1.0
|
O
|
C:HOH1426
|
4.6
|
22.4
|
1.0
|
C
|
C:CYS99
|
4.7
|
13.4
|
1.0
|
O
|
C:CYS99
|
4.7
|
12.9
|
1.0
|
O
|
C:HOH1443
|
4.8
|
15.8
|
1.0
|
O2
|
C:DDN1303
|
4.8
|
14.1
|
1.0
|
C
|
C:PRO98
|
4.8
|
13.7
|
1.0
|
CA
|
C:HIS71
|
4.9
|
12.5
|
1.0
|
CA
|
C:PRO98
|
5.0
|
14.2
|
1.0
|
|
Reference:
H.F.Hou,
Y.H.Liang,
L.F.Li,
X.D.Su,
Y.H.Dong.
Crystal Structures of Streptococcus Mutans 2'-Deoxycytidylate Deaminase and Its Complex with Substrate Analog and Allosteric Regulator Dctp X MG2+. J.Mol.Biol. V. 377 220 2008.
ISSN: ISSN 0022-2836
PubMed: 18255096
DOI: 10.1016/J.JMB.2007.12.064
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