Chlorine in PDB 4l9o: Crystal Structure of the SEC13-SEC16 Blade-Inserted Complex From Pichia Pastoris
Protein crystallography data
The structure of Crystal Structure of the SEC13-SEC16 Blade-Inserted Complex From Pichia Pastoris, PDB code: 4l9o
was solved by
C.Mcmahon,
P.D.Jeffrey,
F.M.Hughson,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
44.42 /
1.60
|
Space group
|
P 1 21 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
70.509,
49.320,
90.904,
90.00,
111.70,
90.00
|
R / Rfree (%)
|
17.3 /
20.5
|
Other elements in 4l9o:
The structure of Crystal Structure of the SEC13-SEC16 Blade-Inserted Complex From Pichia Pastoris also contains other interesting chemical elements:
Chlorine Binding Sites:
The binding sites of Chlorine atom in the Crystal Structure of the SEC13-SEC16 Blade-Inserted Complex From Pichia Pastoris
(pdb code 4l9o). This binding sites where shown within
5.0 Angstroms radius around Chlorine atom.
In total 2 binding sites of Chlorine where determined in the
Crystal Structure of the SEC13-SEC16 Blade-Inserted Complex From Pichia Pastoris, PDB code: 4l9o:
Jump to Chlorine binding site number:
1;
2;
Chlorine binding site 1 out
of 2 in 4l9o
Go back to
Chlorine Binding Sites List in 4l9o
Chlorine binding site 1 out
of 2 in the Crystal Structure of the SEC13-SEC16 Blade-Inserted Complex From Pichia Pastoris
Mono view
Stereo pair view
|
A full contact list of Chlorine with other atoms in the Cl binding
site number 1 of Crystal Structure of the SEC13-SEC16 Blade-Inserted Complex From Pichia Pastoris within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Cl2403
b:18.8
occ:1.00
|
H
|
A:TRP2072
|
2.3
|
10.8
|
1.0
|
HH12
|
A:ARG1052
|
2.5
|
19.5
|
1.0
|
HH22
|
A:ARG1052
|
2.6
|
29.6
|
1.0
|
HA
|
A:ALA2071
|
2.8
|
11.2
|
1.0
|
HG21
|
A:VAL2027
|
2.9
|
19.1
|
1.0
|
O
|
A:HOH2563
|
3.1
|
20.4
|
1.0
|
N
|
A:TRP2072
|
3.1
|
9.0
|
1.0
|
HD1
|
A:TRP2072
|
3.3
|
12.7
|
1.0
|
NH1
|
A:ARG1052
|
3.3
|
16.2
|
1.0
|
NH2
|
A:ARG1052
|
3.4
|
24.7
|
1.0
|
HB2
|
A:TRP2072
|
3.4
|
12.1
|
1.0
|
HB1
|
A:ALA2071
|
3.5
|
15.6
|
1.0
|
CA
|
A:ALA2071
|
3.6
|
9.3
|
1.0
|
CG2
|
A:VAL2027
|
3.8
|
15.9
|
1.0
|
CZ
|
A:ARG1052
|
3.8
|
23.9
|
1.0
|
C
|
A:ALA2071
|
3.9
|
11.4
|
1.0
|
HG22
|
A:VAL2027
|
3.9
|
19.1
|
1.0
|
HH11
|
A:ARG1052
|
4.0
|
19.5
|
1.0
|
O
|
A:HOH2518
|
4.0
|
16.8
|
1.0
|
CB
|
A:ALA2071
|
4.0
|
13.0
|
1.0
|
HH21
|
A:ARG1052
|
4.1
|
29.6
|
1.0
|
CD1
|
A:TRP2072
|
4.1
|
10.5
|
1.0
|
O
|
A:TRP2072
|
4.1
|
11.2
|
1.0
|
OH
|
A:TYR2030
|
4.1
|
25.7
|
1.0
|
CB
|
A:TRP2072
|
4.1
|
10.1
|
1.0
|
CA
|
A:TRP2072
|
4.1
|
11.1
|
1.0
|
HG23
|
A:VAL2027
|
4.2
|
19.1
|
1.0
|
HG11
|
A:VAL2027
|
4.2
|
24.8
|
1.0
|
HB2
|
A:ALA2071
|
4.2
|
15.6
|
1.0
|
CG
|
A:TRP2072
|
4.5
|
7.6
|
1.0
|
HH
|
A:TYR2030
|
4.6
|
30.9
|
1.0
|
C
|
A:TRP2072
|
4.6
|
11.6
|
1.0
|
CZ
|
A:TYR2030
|
4.6
|
21.7
|
1.0
|
O
|
A:VAL2070
|
4.7
|
11.9
|
1.0
|
HE2
|
A:TYR2030
|
4.7
|
22.9
|
1.0
|
HD1
|
A:TRP2118
|
4.8
|
13.6
|
1.0
|
CB
|
A:VAL2027
|
4.8
|
15.2
|
1.0
|
N
|
A:ALA2071
|
4.8
|
9.3
|
1.0
|
CG1
|
A:VAL2027
|
4.9
|
20.7
|
1.0
|
HB3
|
A:ALA2071
|
4.9
|
15.6
|
1.0
|
CE2
|
A:TYR2030
|
4.9
|
19.1
|
1.0
|
O
|
A:HOH2613
|
4.9
|
30.1
|
1.0
|
O
|
A:HOH2573
|
4.9
|
20.4
|
1.0
|
HB3
|
A:TRP2072
|
4.9
|
12.1
|
1.0
|
HA
|
A:TRP2072
|
4.9
|
13.3
|
1.0
|
O
|
A:HOH2509
|
4.9
|
18.6
|
1.0
|
HG13
|
A:VAL2027
|
5.0
|
24.8
|
1.0
|
|
Chlorine binding site 2 out
of 2 in 4l9o
Go back to
Chlorine Binding Sites List in 4l9o
Chlorine binding site 2 out
of 2 in the Crystal Structure of the SEC13-SEC16 Blade-Inserted Complex From Pichia Pastoris
Mono view
Stereo pair view
|
A full contact list of Chlorine with other atoms in the Cl binding
site number 2 of Crystal Structure of the SEC13-SEC16 Blade-Inserted Complex From Pichia Pastoris within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Cl2404
b:21.3
occ:1.00
|
H
|
A:TRP2265
|
2.4
|
12.1
|
1.0
|
HB1
|
A:ALA2214
|
2.9
|
15.2
|
1.0
|
HA
|
A:SER2264
|
2.9
|
11.9
|
1.0
|
HD1
|
A:TRP2265
|
3.0
|
13.4
|
1.0
|
O
|
A:HOH2605
|
3.1
|
23.3
|
1.0
|
N
|
A:TRP2265
|
3.2
|
10.1
|
1.0
|
O
|
A:HOH2562
|
3.3
|
25.6
|
1.0
|
HB2
|
A:TRP2265
|
3.3
|
14.6
|
1.0
|
HB2
|
A:SER2264
|
3.5
|
23.8
|
1.0
|
CA
|
A:SER2264
|
3.7
|
9.9
|
1.0
|
CB
|
A:ALA2214
|
3.8
|
12.7
|
1.0
|
CD1
|
A:TRP2265
|
3.8
|
11.2
|
1.0
|
HD3
|
A:PRO2217
|
3.9
|
23.6
|
1.0
|
HB2
|
A:ALA2214
|
4.0
|
15.2
|
1.0
|
C
|
A:SER2264
|
4.0
|
12.0
|
1.0
|
CB
|
A:TRP2265
|
4.0
|
12.2
|
1.0
|
CB
|
A:SER2264
|
4.1
|
19.8
|
1.0
|
HA
|
A:ALA2214
|
4.1
|
13.3
|
1.0
|
CA
|
A:TRP2265
|
4.2
|
12.7
|
1.0
|
O
|
A:TRP2215
|
4.2
|
15.0
|
1.0
|
O
|
A:HOH2537
|
4.3
|
20.2
|
1.0
|
O
|
A:TRP2265
|
4.3
|
12.1
|
1.0
|
H
|
A:TRP2215
|
4.3
|
12.8
|
1.0
|
CG
|
A:TRP2265
|
4.3
|
10.4
|
1.0
|
CA
|
A:ALA2214
|
4.5
|
11.1
|
1.0
|
HB3
|
A:ALA2214
|
4.5
|
15.2
|
1.0
|
HA
|
A:SER2216
|
4.5
|
15.2
|
1.0
|
O
|
A:HOH2612
|
4.5
|
43.9
|
1.0
|
HB3
|
A:SER2264
|
4.6
|
23.8
|
1.0
|
N
|
A:TRP2215
|
4.6
|
10.7
|
1.0
|
O
|
A:HOH2557
|
4.7
|
26.6
|
1.0
|
O
|
A:ALA2263
|
4.7
|
13.3
|
1.0
|
C
|
A:TRP2265
|
4.7
|
12.0
|
1.0
|
C
|
A:ALA2214
|
4.7
|
12.2
|
1.0
|
CD
|
A:PRO2217
|
4.8
|
19.7
|
1.0
|
C
|
A:TRP2215
|
4.8
|
11.9
|
1.0
|
HB3
|
A:TRP2265
|
4.9
|
14.6
|
1.0
|
N
|
A:SER2264
|
4.9
|
10.5
|
1.0
|
HD2
|
A:PRO2217
|
4.9
|
23.6
|
1.0
|
O
|
A:HOH2597
|
5.0
|
27.1
|
1.0
|
NE1
|
A:TRP2265
|
5.0
|
13.4
|
1.0
|
|
Reference:
N.Bharucha,
Y.Liu,
E.Papanikou,
C.Mcmahon,
M.Esaki,
P.D.Jeffrey,
F.M.Hughson,
B.S.Glick.
SEC16 Influences Transitional Er Sites By Regulating Rather Than Organizing Copii. Mol Biol Cell V. 24 3406 2013.
PubMed: 24006484
DOI: 10.1091/MBC.E13-04-0185
Page generated: Sun Jul 21 18:45:32 2024
|