Calcium in PDB 2fhf: Crystal Structure Analysis of Klebsiella Pneumoniae Pullulanase Complexed with Maltotetraose
Enzymatic activity of Crystal Structure Analysis of Klebsiella Pneumoniae Pullulanase Complexed with Maltotetraose
All present enzymatic activity of Crystal Structure Analysis of Klebsiella Pneumoniae Pullulanase Complexed with Maltotetraose:
3.2.1.41;
Protein crystallography data
The structure of Crystal Structure Analysis of Klebsiella Pneumoniae Pullulanase Complexed with Maltotetraose, PDB code: 2fhf
was solved by
B.Mikami,
H.Iwamoto,
Y.Katsuya,
H.-J.Yoon,
E.Demirkan-Sarikaya,
D.Malle,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
14.98 /
1.65
|
Space group
|
C 1 2 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
150.159,
60.509,
134.664,
90.00,
111.87,
90.00
|
R / Rfree (%)
|
17.8 /
20.6
|
Calcium Binding Sites:
The binding sites of Calcium atom in the Crystal Structure Analysis of Klebsiella Pneumoniae Pullulanase Complexed with Maltotetraose
(pdb code 2fhf). This binding sites where shown within
5.0 Angstroms radius around Calcium atom.
In total 5 binding sites of Calcium where determined in the
Crystal Structure Analysis of Klebsiella Pneumoniae Pullulanase Complexed with Maltotetraose, PDB code: 2fhf:
Jump to Calcium binding site number:
1;
2;
3;
4;
5;
Calcium binding site 1 out
of 5 in 2fhf
Go back to
Calcium Binding Sites List in 2fhf
Calcium binding site 1 out
of 5 in the Crystal Structure Analysis of Klebsiella Pneumoniae Pullulanase Complexed with Maltotetraose
Mono view
Stereo pair view
|
A full contact list of Calcium with other atoms in the Ca binding
site number 1 of Crystal Structure Analysis of Klebsiella Pneumoniae Pullulanase Complexed with Maltotetraose within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Ca2401
b:16.6
occ:1.00
|
O
|
A:HOH1493
|
2.3
|
16.6
|
1.0
|
O
|
A:TYR555
|
2.4
|
15.2
|
1.0
|
O
|
A:ALA550
|
2.4
|
16.3
|
1.0
|
OD2
|
A:ASP893
|
2.4
|
18.2
|
1.0
|
OD1
|
A:ASP553
|
2.4
|
16.6
|
1.0
|
O
|
A:HOH1492
|
2.5
|
18.6
|
1.0
|
O
|
A:HOH1271
|
2.6
|
17.8
|
1.0
|
C
|
A:ALA550
|
3.4
|
17.8
|
1.0
|
CG
|
A:ASP553
|
3.5
|
17.8
|
1.0
|
C
|
A:TYR555
|
3.5
|
13.2
|
1.0
|
CG
|
A:ASP893
|
3.6
|
17.1
|
1.0
|
OD2
|
A:ASP553
|
3.9
|
16.6
|
1.0
|
CA
|
A:ALA550
|
3.9
|
16.4
|
1.0
|
OD1
|
A:ASP893
|
4.2
|
19.6
|
1.0
|
CB
|
A:ALA550
|
4.2
|
16.7
|
1.0
|
CA
|
A:TYR555
|
4.2
|
13.0
|
1.0
|
N
|
A:TYR555
|
4.2
|
15.1
|
1.0
|
O
|
A:ASP553
|
4.5
|
17.1
|
1.0
|
O
|
A:HOH1617
|
4.5
|
30.8
|
1.0
|
CB
|
A:TYR555
|
4.6
|
14.0
|
1.0
|
N
|
A:ASN556
|
4.6
|
14.8
|
1.0
|
ND2
|
A:ASN556
|
4.6
|
16.9
|
1.0
|
N
|
A:ASP553
|
4.6
|
14.3
|
1.0
|
N
|
A:GLN551
|
4.6
|
16.2
|
1.0
|
CB
|
A:ASN556
|
4.7
|
14.9
|
1.0
|
O
|
A:ASP893
|
4.7
|
16.1
|
1.0
|
C
|
A:ASP553
|
4.8
|
15.3
|
1.0
|
O
|
A:THR484
|
4.8
|
18.8
|
1.0
|
CB
|
A:ASP893
|
4.8
|
15.7
|
1.0
|
CB
|
A:ASP553
|
4.8
|
17.0
|
1.0
|
CA
|
A:ASP893
|
4.8
|
16.0
|
1.0
|
O
|
A:HOH1593
|
4.8
|
25.5
|
1.0
|
CA
|
A:ASN556
|
4.9
|
15.6
|
1.0
|
CA
|
A:ASP553
|
5.0
|
15.3
|
1.0
|
|
Calcium binding site 2 out
of 5 in 2fhf
Go back to
Calcium Binding Sites List in 2fhf
Calcium binding site 2 out
of 5 in the Crystal Structure Analysis of Klebsiella Pneumoniae Pullulanase Complexed with Maltotetraose
Mono view
Stereo pair view
|
A full contact list of Calcium with other atoms in the Ca binding
site number 2 of Crystal Structure Analysis of Klebsiella Pneumoniae Pullulanase Complexed with Maltotetraose within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Ca2402
b:35.9
occ:1.00
|
OE1
|
A:GLN1070
|
2.0
|
29.2
|
1.0
|
O
|
A:ASP1003
|
2.1
|
25.6
|
1.0
|
O
|
A:HOH1521
|
2.1
|
25.6
|
1.0
|
OD2
|
A:ASP994
|
2.1
|
22.1
|
1.0
|
OG
|
A:SER1001
|
2.1
|
31.0
|
1.0
|
O
|
A:VAL1006
|
2.2
|
26.8
|
1.0
|
C
|
A:ASP1003
|
3.1
|
27.5
|
1.0
|
CD
|
A:GLN1070
|
3.1
|
32.0
|
1.0
|
CB
|
A:SER1001
|
3.3
|
30.6
|
1.0
|
CG
|
A:ASP994
|
3.3
|
24.2
|
1.0
|
C
|
A:VAL1006
|
3.4
|
25.7
|
1.0
|
NE2
|
A:GLN1070
|
3.7
|
31.4
|
1.0
|
N
|
A:ASP1003
|
3.8
|
26.9
|
1.0
|
CA
|
A:ASP1003
|
4.0
|
27.7
|
1.0
|
CA
|
A:SER1001
|
4.0
|
30.3
|
1.0
|
N
|
A:SER1004
|
4.1
|
28.1
|
1.0
|
CB
|
A:ASP994
|
4.1
|
24.4
|
1.0
|
O
|
A:ASP994
|
4.1
|
25.5
|
1.0
|
N
|
A:VAL1006
|
4.2
|
28.0
|
1.0
|
N
|
A:ASP1007
|
4.2
|
25.3
|
1.0
|
OD1
|
A:ASP1007
|
4.2
|
25.9
|
1.0
|
OD1
|
A:ASP994
|
4.2
|
23.5
|
1.0
|
CA
|
A:ASP1007
|
4.2
|
25.1
|
1.0
|
CA
|
A:SER1004
|
4.2
|
29.4
|
1.0
|
CG
|
A:GLN1070
|
4.3
|
30.9
|
1.0
|
O
|
A:HOH2036
|
4.4
|
43.9
|
1.0
|
CA
|
A:VAL1006
|
4.4
|
27.1
|
1.0
|
CB
|
A:ASP1003
|
4.4
|
27.4
|
1.0
|
C
|
A:SER1001
|
4.4
|
30.4
|
1.0
|
C
|
A:SER1004
|
4.5
|
30.3
|
1.0
|
N
|
A:LEU1002
|
4.5
|
29.5
|
1.0
|
CB
|
A:GLN1070
|
4.7
|
32.5
|
1.0
|
N
|
A:ARG1005
|
4.8
|
30.7
|
1.0
|
O
|
A:SER1004
|
4.8
|
30.0
|
1.0
|
C
|
A:ASP994
|
4.9
|
25.2
|
1.0
|
|
Calcium binding site 3 out
of 5 in 2fhf
Go back to
Calcium Binding Sites List in 2fhf
Calcium binding site 3 out
of 5 in the Crystal Structure Analysis of Klebsiella Pneumoniae Pullulanase Complexed with Maltotetraose
Mono view
Stereo pair view
|
A full contact list of Calcium with other atoms in the Ca binding
site number 3 of Crystal Structure Analysis of Klebsiella Pneumoniae Pullulanase Complexed with Maltotetraose within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Ca2403
b:30.5
occ:1.00
|
O
|
A:HOH1424
|
2.1
|
17.2
|
1.0
|
O
|
A:HOH1738
|
2.1
|
17.8
|
1.0
|
O
|
A:HOH1737
|
2.1
|
20.8
|
1.0
|
O
|
A:HOH1252
|
2.2
|
17.5
|
1.0
|
O
|
A:HOH1246
|
2.2
|
21.7
|
1.0
|
O
|
A:HOH1736
|
2.2
|
16.5
|
1.0
|
NE
|
A:ARG715
|
4.0
|
17.4
|
1.0
|
OE1
|
A:GLU639
|
4.0
|
22.1
|
1.0
|
OE1
|
A:GLU633
|
4.1
|
22.3
|
1.0
|
OD2
|
A:ASP714
|
4.2
|
22.1
|
1.0
|
NH2
|
A:ARG715
|
4.2
|
18.9
|
1.0
|
OE1
|
A:GLN712
|
4.2
|
20.5
|
1.0
|
O
|
A:HOH1947
|
4.2
|
35.2
|
1.0
|
O
|
A:HOH1526
|
4.3
|
18.6
|
1.0
|
OD1
|
A:ASP714
|
4.3
|
21.8
|
1.0
|
OE2
|
A:GLU639
|
4.3
|
20.8
|
1.0
|
O
|
A:HOH1917
|
4.4
|
40.2
|
1.0
|
NE2
|
A:GLN712
|
4.4
|
18.4
|
1.0
|
OE2
|
A:GLU633
|
4.5
|
20.9
|
1.0
|
CZ
|
A:ARG715
|
4.6
|
19.6
|
1.0
|
CD
|
A:GLU639
|
4.6
|
21.7
|
1.0
|
O
|
A:ASN711
|
4.7
|
21.9
|
1.0
|
CG
|
A:ASP714
|
4.7
|
22.1
|
1.0
|
CD
|
A:GLN712
|
4.7
|
20.5
|
1.0
|
CD
|
A:GLU633
|
4.7
|
20.9
|
1.0
|
|
Calcium binding site 4 out
of 5 in 2fhf
Go back to
Calcium Binding Sites List in 2fhf
Calcium binding site 4 out
of 5 in the Crystal Structure Analysis of Klebsiella Pneumoniae Pullulanase Complexed with Maltotetraose
Mono view
Stereo pair view
|
A full contact list of Calcium with other atoms in the Ca binding
site number 4 of Crystal Structure Analysis of Klebsiella Pneumoniae Pullulanase Complexed with Maltotetraose within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Ca2404
b:18.5
occ:1.00
|
OD1
|
A:ASP481
|
2.2
|
14.4
|
1.0
|
O
|
A:HOH1253
|
2.2
|
15.4
|
1.0
|
OE2
|
A:GLU487
|
2.3
|
15.3
|
1.0
|
O
|
A:HOH1494
|
2.3
|
15.6
|
1.0
|
O
|
A:LEU482
|
2.3
|
15.5
|
1.0
|
OE2
|
A:GLU568
|
2.3
|
16.4
|
1.0
|
CD
|
A:GLU568
|
3.2
|
16.4
|
1.0
|
CD
|
A:GLU487
|
3.2
|
17.1
|
1.0
|
CG
|
A:ASP481
|
3.4
|
15.4
|
1.0
|
OE1
|
A:GLU568
|
3.4
|
15.8
|
1.0
|
C
|
A:LEU482
|
3.5
|
16.0
|
1.0
|
N
|
A:LEU482
|
3.7
|
16.2
|
1.0
|
CG
|
A:GLU487
|
3.9
|
17.5
|
1.0
|
OD2
|
A:ASP481
|
4.0
|
14.2
|
1.0
|
OG
|
A:SER388
|
4.1
|
16.3
|
1.0
|
OE1
|
A:GLU487
|
4.2
|
17.2
|
1.0
|
C
|
A:ASP481
|
4.2
|
15.1
|
1.0
|
CA
|
A:LEU482
|
4.2
|
16.5
|
1.0
|
O
|
A:HOH1351
|
4.2
|
16.8
|
1.0
|
N
|
A:GLY569
|
4.3
|
14.5
|
1.0
|
CA
|
A:ASP481
|
4.3
|
14.8
|
1.0
|
O
|
A:HOH1129
|
4.4
|
16.3
|
1.0
|
CB
|
A:ASP481
|
4.4
|
15.6
|
1.0
|
N
|
A:ALA483
|
4.5
|
15.2
|
1.0
|
CG
|
A:LEU482
|
4.5
|
17.2
|
1.0
|
CG
|
A:GLU568
|
4.6
|
16.6
|
1.0
|
O
|
A:VAL485
|
4.6
|
17.8
|
1.0
|
CA
|
A:ALA483
|
4.7
|
16.8
|
1.0
|
CA
|
A:GLU568
|
4.8
|
14.8
|
1.0
|
O
|
A:ASP481
|
4.9
|
15.5
|
1.0
|
CB
|
A:LEU482
|
4.9
|
17.4
|
1.0
|
|
Calcium binding site 5 out
of 5 in 2fhf
Go back to
Calcium Binding Sites List in 2fhf
Calcium binding site 5 out
of 5 in the Crystal Structure Analysis of Klebsiella Pneumoniae Pullulanase Complexed with Maltotetraose
Mono view
Stereo pair view
|
A full contact list of Calcium with other atoms in the Ca binding
site number 5 of Crystal Structure Analysis of Klebsiella Pneumoniae Pullulanase Complexed with Maltotetraose within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Ca2405
b:61.0
occ:1.00
|
O
|
A:ASP162
|
2.3
|
47.8
|
0.8
|
O
|
A:HOH2275
|
2.3
|
34.2
|
1.0
|
OD2
|
A:ASP162
|
2.4
|
49.7
|
0.8
|
OD1
|
A:ASP148
|
2.5
|
53.3
|
0.8
|
O
|
A:THR150
|
2.5
|
46.0
|
0.8
|
OD2
|
A:ASP148
|
2.7
|
54.2
|
0.8
|
CG
|
A:ASP148
|
2.9
|
53.7
|
0.8
|
CG
|
A:ASP162
|
3.3
|
50.3
|
0.8
|
C
|
A:ASP162
|
3.4
|
48.1
|
0.8
|
C
|
A:THR150
|
3.6
|
46.4
|
0.8
|
CB
|
A:THR150
|
3.7
|
46.8
|
0.8
|
CA
|
A:ASP162
|
4.0
|
49.0
|
0.8
|
OD1
|
A:ASP162
|
4.0
|
51.0
|
0.8
|
CA
|
A:THR150
|
4.1
|
46.7
|
0.8
|
O
|
A:HOH2119
|
4.2
|
40.2
|
1.0
|
CB
|
A:ASP162
|
4.2
|
49.6
|
0.8
|
O
|
A:HOH2223
|
4.2
|
45.3
|
1.0
|
N
|
A:THR150
|
4.3
|
47.9
|
0.8
|
CB
|
A:ASP148
|
4.3
|
53.5
|
0.8
|
CG2
|
A:THR150
|
4.3
|
46.0
|
0.8
|
N
|
A:SER163
|
4.6
|
47.0
|
0.8
|
OE1
|
A:GLU45
|
4.6
|
43.9
|
1.0
|
OG1
|
A:THR150
|
4.7
|
46.0
|
0.8
|
OE1
|
A:GLN48
|
4.7
|
55.0
|
0.8
|
N
|
A:VAL151
|
4.8
|
46.3
|
0.8
|
CA
|
A:SER163
|
4.9
|
46.1
|
0.8
|
|
Reference:
B.Mikami,
H.Iwamoto,
D.Malle,
H.-J.Yoon,
E.Demirkan-Sarikaya,
Y.Mezaki,
Y.Katsuya.
Crystal Structure of Pullulanase: Evidence For Parallel Binding of Oligosaccharides in the Active Site J.Mol.Biol. V. 359 690 2006.
ISSN: ISSN 0022-2836
PubMed: 16650854
DOI: 10.1016/J.JMB.2006.03.058
Page generated: Fri Jul 12 10:29:34 2024
|