Nickel in PDB 2v4b: Crystal Structure of Human Adamts-1 Catalytic Domain and Cysteine- Rich Domain (Apo-Form)
Protein crystallography data
The structure of Crystal Structure of Human Adamts-1 Catalytic Domain and Cysteine- Rich Domain (Apo-Form), PDB code: 2v4b
was solved by
S.Gerhardt,
G.Hassall,
P.Hawtin,
E.Mccall,
L.Flavell,
C.Minshull,
D.Hargreaves,
A.Ting,
R.A.Pauptit,
A.E.Parker,
W.M.Abbott,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
40.26 /
2.00
|
Space group
|
P 1 21 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
51.579,
64.396,
113.524,
90.00,
90.91,
90.00
|
R / Rfree (%)
|
22 /
26.3
|
Other elements in 2v4b:
The structure of Crystal Structure of Human Adamts-1 Catalytic Domain and Cysteine- Rich Domain (Apo-Form) also contains other interesting chemical elements:
Nickel Binding Sites:
Pages:
>>> Page 1 <<<
Page 2, Binding sites: 11 -
14;
Binding sites:
The binding sites of Nickel atom in the Crystal Structure of Human Adamts-1 Catalytic Domain and Cysteine- Rich Domain (Apo-Form)
(pdb code 2v4b). This binding sites where shown within
5.0 Angstroms radius around Nickel atom.
In total 14 binding sites of Nickel where determined in the
Crystal Structure of Human Adamts-1 Catalytic Domain and Cysteine- Rich Domain (Apo-Form), PDB code: 2v4b:
Jump to Nickel binding site number:
1;
2;
3;
4;
5;
6;
7;
8;
9;
10;
Nickel binding site 1 out
of 14 in 2v4b
Go back to
Nickel Binding Sites List in 2v4b
Nickel binding site 1 out
of 14 in the Crystal Structure of Human Adamts-1 Catalytic Domain and Cysteine- Rich Domain (Apo-Form)
Mono view
Stereo pair view
|
A full contact list of Nickel with other atoms in the Ni binding
site number 1 of Crystal Structure of Human Adamts-1 Catalytic Domain and Cysteine- Rich Domain (Apo-Form) within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Ni1555
b:40.2
occ:1.00
|
NE2
|
B:HIS313
|
2.2
|
47.1
|
1.0
|
O
|
B:HOH2007
|
2.3
|
45.0
|
1.0
|
OE1
|
A:GLU494
|
2.5
|
48.3
|
1.0
|
O
|
A:HOH2106
|
2.5
|
37.2
|
1.0
|
O
|
B:HOH2003
|
2.6
|
48.4
|
1.0
|
OE2
|
A:GLU494
|
2.6
|
49.0
|
1.0
|
CD
|
A:GLU494
|
2.9
|
46.1
|
1.0
|
CD2
|
B:HIS313
|
2.9
|
46.4
|
1.0
|
CE1
|
B:HIS313
|
3.4
|
47.5
|
1.0
|
O
|
A:HOH2107
|
4.1
|
53.8
|
1.0
|
CG
|
B:HIS313
|
4.2
|
47.5
|
1.0
|
ND1
|
B:HIS313
|
4.3
|
47.2
|
1.0
|
CG
|
A:GLU494
|
4.4
|
43.1
|
1.0
|
CB
|
B:ALA271
|
4.6
|
39.6
|
1.0
|
O
|
B:GLY275
|
4.7
|
37.0
|
1.0
|
O
|
B:ALA271
|
4.7
|
39.2
|
1.0
|
C
|
B:GLY275
|
4.9
|
36.9
|
1.0
|
|
Nickel binding site 2 out
of 14 in 2v4b
Go back to
Nickel Binding Sites List in 2v4b
Nickel binding site 2 out
of 14 in the Crystal Structure of Human Adamts-1 Catalytic Domain and Cysteine- Rich Domain (Apo-Form)
Mono view
Stereo pair view
|
A full contact list of Nickel with other atoms in the Ni binding
site number 2 of Crystal Structure of Human Adamts-1 Catalytic Domain and Cysteine- Rich Domain (Apo-Form) within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Ni1556
b:26.0
occ:1.00
|
O
|
B:HOH2057
|
1.8
|
48.3
|
1.0
|
O
|
A:HOH2013
|
2.1
|
34.7
|
1.0
|
OD1
|
B:ASP483
|
2.1
|
36.3
|
1.0
|
ND1
|
A:HIS280
|
2.2
|
27.8
|
1.0
|
CE1
|
A:HIS280
|
3.0
|
30.8
|
1.0
|
CG
|
B:ASP483
|
3.1
|
35.4
|
1.0
|
CG
|
A:HIS280
|
3.3
|
30.3
|
1.0
|
OD2
|
B:ASP483
|
3.3
|
35.4
|
1.0
|
CB
|
A:HIS280
|
3.7
|
27.9
|
1.0
|
O
|
B:HOH2056
|
4.2
|
46.0
|
1.0
|
NE2
|
A:HIS280
|
4.2
|
33.4
|
1.0
|
CA
|
A:HIS280
|
4.3
|
28.0
|
1.0
|
CD2
|
A:HIS280
|
4.3
|
31.7
|
1.0
|
CG
|
B:ARG486
|
4.4
|
31.2
|
1.0
|
CB
|
B:ASP483
|
4.5
|
33.5
|
1.0
|
ND2
|
B:ASN485
|
4.5
|
35.5
|
1.0
|
CB
|
B:ASN485
|
4.5
|
31.8
|
1.0
|
CD
|
B:ARG486
|
4.8
|
33.2
|
1.0
|
|
Nickel binding site 3 out
of 14 in 2v4b
Go back to
Nickel Binding Sites List in 2v4b
Nickel binding site 3 out
of 14 in the Crystal Structure of Human Adamts-1 Catalytic Domain and Cysteine- Rich Domain (Apo-Form)
Mono view
Stereo pair view
|
A full contact list of Nickel with other atoms in the Ni binding
site number 3 of Crystal Structure of Human Adamts-1 Catalytic Domain and Cysteine- Rich Domain (Apo-Form) within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Ni1557
b:28.2
occ:1.00
|
O
|
A:HOH2089
|
2.2
|
33.9
|
1.0
|
OE1
|
A:GLU261
|
2.3
|
31.6
|
1.0
|
OD1
|
A:ASP465
|
2.4
|
39.5
|
1.0
|
O
|
A:CYS462
|
2.4
|
32.7
|
1.0
|
OD2
|
A:ASP351
|
2.6
|
34.3
|
1.0
|
OD1
|
A:ASP351
|
2.6
|
31.4
|
1.0
|
OD2
|
A:ASP344
|
2.6
|
50.6
|
1.0
|
CG
|
A:ASP351
|
3.0
|
31.8
|
1.0
|
CD
|
A:GLU261
|
3.3
|
34.2
|
1.0
|
CG
|
A:ASP344
|
3.4
|
49.9
|
1.0
|
OD1
|
A:ASP344
|
3.4
|
48.4
|
1.0
|
CG
|
A:ASP465
|
3.4
|
36.9
|
1.0
|
C
|
A:CYS462
|
3.6
|
33.1
|
1.0
|
OD2
|
A:ASP465
|
3.7
|
34.1
|
1.0
|
CD
|
A:CD1553
|
4.0
|
38.0
|
1.0
|
CG
|
A:GLU261
|
4.0
|
32.4
|
1.0
|
CA
|
A:LEU463
|
4.3
|
33.1
|
1.0
|
OE2
|
A:GLU261
|
4.3
|
38.3
|
1.0
|
O
|
A:TYR259
|
4.3
|
34.5
|
1.0
|
N
|
A:LEU463
|
4.3
|
33.0
|
1.0
|
CB
|
A:GLU261
|
4.4
|
32.6
|
1.0
|
CB
|
A:ASP351
|
4.4
|
31.7
|
1.0
|
O
|
A:ASP465
|
4.5
|
37.2
|
1.0
|
CA
|
A:CYS462
|
4.6
|
33.2
|
1.0
|
CB
|
A:CYS462
|
4.6
|
33.5
|
1.0
|
O
|
A:HOH2047
|
4.7
|
35.9
|
1.0
|
O
|
A:HOH2087
|
4.7
|
44.0
|
1.0
|
C
|
A:LEU463
|
4.8
|
33.5
|
1.0
|
CB
|
A:ASP465
|
4.8
|
36.5
|
1.0
|
N
|
A:ASP465
|
4.9
|
35.9
|
1.0
|
CB
|
A:ASP344
|
4.9
|
49.0
|
1.0
|
|
Nickel binding site 4 out
of 14 in 2v4b
Go back to
Nickel Binding Sites List in 2v4b
Nickel binding site 4 out
of 14 in the Crystal Structure of Human Adamts-1 Catalytic Domain and Cysteine- Rich Domain (Apo-Form)
Mono view
Stereo pair view
|
A full contact list of Nickel with other atoms in the Ni binding
site number 4 of Crystal Structure of Human Adamts-1 Catalytic Domain and Cysteine- Rich Domain (Apo-Form) within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Ni1558
b:37.8
occ:1.00
|
O
|
A:HOH2009
|
2.4
|
43.0
|
1.0
|
O
|
A:HOH2006
|
2.4
|
46.1
|
1.0
|
NE2
|
A:HIS313
|
2.4
|
36.8
|
1.0
|
O
|
A:HOH2024
|
2.5
|
36.1
|
1.0
|
CD2
|
A:HIS313
|
3.1
|
36.4
|
1.0
|
OE2
|
B:GLU494
|
3.5
|
50.2
|
1.0
|
CE1
|
A:HIS313
|
3.6
|
34.9
|
1.0
|
CD
|
B:GLU494
|
3.7
|
46.5
|
1.0
|
OE1
|
B:GLU494
|
4.1
|
49.0
|
1.0
|
CG
|
B:GLU494
|
4.2
|
43.5
|
1.0
|
O
|
B:HOH2062
|
4.3
|
39.4
|
1.0
|
CG
|
A:HIS313
|
4.3
|
35.6
|
1.0
|
O
|
B:HOH2004
|
4.3
|
47.7
|
1.0
|
O
|
A:GLY275
|
4.4
|
34.7
|
1.0
|
ND1
|
A:HIS313
|
4.5
|
37.1
|
1.0
|
O
|
A:ALA271
|
4.6
|
35.5
|
1.0
|
CB
|
A:ALA271
|
4.6
|
34.6
|
1.0
|
C
|
A:GLY275
|
4.7
|
33.9
|
1.0
|
CB
|
B:GLU494
|
4.9
|
41.2
|
1.0
|
CA
|
A:GLY275
|
4.9
|
33.9
|
1.0
|
|
Nickel binding site 5 out
of 14 in 2v4b
Go back to
Nickel Binding Sites List in 2v4b
Nickel binding site 5 out
of 14 in the Crystal Structure of Human Adamts-1 Catalytic Domain and Cysteine- Rich Domain (Apo-Form)
Mono view
Stereo pair view
|
A full contact list of Nickel with other atoms in the Ni binding
site number 5 of Crystal Structure of Human Adamts-1 Catalytic Domain and Cysteine- Rich Domain (Apo-Form) within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Ni1559
b:59.6
occ:1.00
|
OE2
|
A:GLU320
|
2.3
|
37.3
|
1.0
|
O
|
A:HOH2027
|
3.1
|
35.4
|
1.0
|
CD
|
A:GLU320
|
3.2
|
37.5
|
1.0
|
OE1
|
A:GLU320
|
3.3
|
39.6
|
1.0
|
CD
|
A:CD1554
|
3.8
|
35.4
|
1.0
|
OE1
|
A:GLU315
|
4.5
|
34.0
|
1.0
|
CG
|
A:GLU320
|
4.6
|
34.5
|
1.0
|
O
|
A:HOH2031
|
4.7
|
28.9
|
1.0
|
|
Nickel binding site 6 out
of 14 in 2v4b
Go back to
Nickel Binding Sites List in 2v4b
Nickel binding site 6 out
of 14 in the Crystal Structure of Human Adamts-1 Catalytic Domain and Cysteine- Rich Domain (Apo-Form)
Mono view
Stereo pair view
|
A full contact list of Nickel with other atoms in the Ni binding
site number 6 of Crystal Structure of Human Adamts-1 Catalytic Domain and Cysteine- Rich Domain (Apo-Form) within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Ni1561
b:34.3
occ:1.00
|
O
|
A:HOH2075
|
1.9
|
22.5
|
1.0
|
NE2
|
A:HIS428
|
2.3
|
39.3
|
1.0
|
CE1
|
A:HIS428
|
3.2
|
39.0
|
1.0
|
CD2
|
A:HIS428
|
3.3
|
39.3
|
1.0
|
ND1
|
A:HIS428
|
4.3
|
38.7
|
1.0
|
CG
|
A:HIS428
|
4.4
|
38.3
|
1.0
|
OG
|
A:SER427
|
4.5
|
40.1
|
1.0
|
CD
|
A:PRO445
|
4.6
|
36.7
|
1.0
|
|
Nickel binding site 7 out
of 14 in 2v4b
Go back to
Nickel Binding Sites List in 2v4b
Nickel binding site 7 out
of 14 in the Crystal Structure of Human Adamts-1 Catalytic Domain and Cysteine- Rich Domain (Apo-Form)
Mono view
Stereo pair view
|
A full contact list of Nickel with other atoms in the Ni binding
site number 7 of Crystal Structure of Human Adamts-1 Catalytic Domain and Cysteine- Rich Domain (Apo-Form) within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Ni1562
b:53.0
occ:1.00
|
OD1
|
A:ASP495
|
2.7
|
41.9
|
1.0
|
OE2
|
A:GLU494
|
3.0
|
49.0
|
1.0
|
CE1
|
B:HIS313
|
3.4
|
47.5
|
1.0
|
CG
|
A:ASP495
|
3.7
|
41.2
|
1.0
|
CD
|
A:GLU494
|
3.8
|
46.1
|
1.0
|
CG
|
A:GLU494
|
3.8
|
43.1
|
1.0
|
OD2
|
A:ASP495
|
4.0
|
43.7
|
1.0
|
NZ
|
B:LYS279
|
4.1
|
39.2
|
1.0
|
ND1
|
B:HIS313
|
4.2
|
47.2
|
1.0
|
NE2
|
B:HIS313
|
4.3
|
47.1
|
1.0
|
O
|
A:HOH2107
|
4.7
|
53.8
|
1.0
|
CE
|
B:LYS279
|
4.8
|
36.3
|
1.0
|
N
|
A:ASP495
|
4.9
|
38.9
|
1.0
|
CB
|
A:ASP495
|
4.9
|
39.3
|
1.0
|
OE1
|
A:GLU494
|
5.0
|
48.3
|
1.0
|
|
Nickel binding site 8 out
of 14 in 2v4b
Go back to
Nickel Binding Sites List in 2v4b
Nickel binding site 8 out
of 14 in the Crystal Structure of Human Adamts-1 Catalytic Domain and Cysteine- Rich Domain (Apo-Form)
Mono view
Stereo pair view
|
A full contact list of Nickel with other atoms in the Ni binding
site number 8 of Crystal Structure of Human Adamts-1 Catalytic Domain and Cysteine- Rich Domain (Apo-Form) within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Ni1563
b:48.7
occ:1.00
|
ND1
|
A:HIS498
|
2.4
|
39.9
|
1.0
|
O
|
A:HOH2109
|
2.8
|
42.5
|
1.0
|
CE1
|
A:HIS498
|
3.2
|
41.7
|
1.0
|
CG
|
A:HIS498
|
3.5
|
38.5
|
1.0
|
CB
|
A:HIS498
|
3.9
|
37.7
|
1.0
|
CG
|
A:PRO500
|
4.2
|
43.0
|
1.0
|
O
|
A:HOH2100
|
4.3
|
39.9
|
1.0
|
NE2
|
A:HIS498
|
4.4
|
41.9
|
1.0
|
CD2
|
A:HIS498
|
4.5
|
41.0
|
1.0
|
CB
|
A:ALA484
|
4.5
|
31.6
|
1.0
|
OD1
|
A:ASN485
|
4.8
|
31.3
|
1.0
|
CB
|
A:PRO500
|
4.9
|
43.6
|
1.0
|
O
|
A:HOH2099
|
5.0
|
30.7
|
1.0
|
|
Nickel binding site 9 out
of 14 in 2v4b
Go back to
Nickel Binding Sites List in 2v4b
Nickel binding site 9 out
of 14 in the Crystal Structure of Human Adamts-1 Catalytic Domain and Cysteine- Rich Domain (Apo-Form)
Mono view
Stereo pair view
|
A full contact list of Nickel with other atoms in the Ni binding
site number 9 of Crystal Structure of Human Adamts-1 Catalytic Domain and Cysteine- Rich Domain (Apo-Form) within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Ni1564
b:68.0
occ:1.00
|
NE2
|
A:HIS525
|
2.5
|
43.5
|
1.0
|
CD2
|
A:HIS525
|
3.3
|
43.0
|
1.0
|
CE1
|
A:HIS525
|
3.7
|
43.9
|
1.0
|
O
|
A:THR523
|
4.3
|
35.6
|
1.0
|
CG
|
A:HIS525
|
4.5
|
41.1
|
1.0
|
ND1
|
A:HIS525
|
4.7
|
43.8
|
1.0
|
|
Nickel binding site 10 out
of 14 in 2v4b
Go back to
Nickel Binding Sites List in 2v4b
Nickel binding site 10 out
of 14 in the Crystal Structure of Human Adamts-1 Catalytic Domain and Cysteine- Rich Domain (Apo-Form)
Mono view
Stereo pair view
|
A full contact list of Nickel with other atoms in the Ni binding
site number 10 of Crystal Structure of Human Adamts-1 Catalytic Domain and Cysteine- Rich Domain (Apo-Form) within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Ni1555
b:49.8
occ:1.00
|
O
|
A:HOH2012
|
2.2
|
48.2
|
1.0
|
OE2
|
B:GLU494
|
2.6
|
50.2
|
1.0
|
OD1
|
B:ASP495
|
2.8
|
42.1
|
1.0
|
OE1
|
B:GLU494
|
2.9
|
49.0
|
1.0
|
CD
|
B:GLU494
|
3.0
|
46.5
|
1.0
|
CE1
|
A:HIS313
|
3.1
|
34.9
|
1.0
|
CG
|
B:ASP495
|
3.7
|
42.3
|
1.0
|
O
|
B:HOH2063
|
3.8
|
57.5
|
1.0
|
ND1
|
A:HIS313
|
3.9
|
37.1
|
1.0
|
OD2
|
B:ASP495
|
4.0
|
44.6
|
1.0
|
NZ
|
A:LYS279
|
4.0
|
43.4
|
1.0
|
NE2
|
A:HIS313
|
4.1
|
36.8
|
1.0
|
O
|
A:HOH2023
|
4.3
|
50.2
|
1.0
|
CG
|
B:GLU494
|
4.4
|
43.5
|
1.0
|
O
|
B:HOH2062
|
4.7
|
39.4
|
1.0
|
CE
|
A:LYS279
|
4.8
|
40.7
|
1.0
|
CB
|
A:VAL311
|
4.8
|
33.4
|
1.0
|
CB
|
B:ASP495
|
5.0
|
40.0
|
1.0
|
|
Reference:
S.Gerhardt,
G.Hassall,
P.Hawtin,
E.Mccall,
L.Flavell,
C.Minshull,
D.Hargreaves,
A.Ting,
R.A.Pauptit,
A.E.Parker,
W.M.Abbott.
Crystal Structures of Human Adamts-1 Reveal A Conserved Catalytic Domain and A Disintegrin-Like Domain with A Fold Homologous to Cysteine-Rich Domains. J.Mol.Biol. V. 373 891 2007.
ISSN: ISSN 0022-2836
PubMed: 17897672
DOI: 10.1016/J.JMB.2007.07.047
Page generated: Wed Oct 9 16:59:17 2024
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