Chlorine in PDB 8ixt: Rat Transcobalamin in Complex with Glutathionylcobalamin
Protein crystallography data
The structure of Rat Transcobalamin in Complex with Glutathionylcobalamin, PDB code: 8ixt
was solved by
M.Bokhove,
T.Kumasaka,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
37.45 /
1.20
|
Space group
|
P 21 21 21
|
Cell size a, b, c (Å), α, β, γ (°)
|
51.1,
55.06,
143.67,
90,
90,
90
|
R / Rfree (%)
|
16.1 /
17.1
|
Other elements in 8ixt:
The structure of Rat Transcobalamin in Complex with Glutathionylcobalamin also contains other interesting chemical elements:
Chlorine Binding Sites:
The binding sites of Chlorine atom in the Rat Transcobalamin in Complex with Glutathionylcobalamin
(pdb code 8ixt). This binding sites where shown within
5.0 Angstroms radius around Chlorine atom.
In total 2 binding sites of Chlorine where determined in the
Rat Transcobalamin in Complex with Glutathionylcobalamin, PDB code: 8ixt:
Jump to Chlorine binding site number:
1;
2;
Chlorine binding site 1 out
of 2 in 8ixt
Go back to
Chlorine Binding Sites List in 8ixt
Chlorine binding site 1 out
of 2 in the Rat Transcobalamin in Complex with Glutathionylcobalamin
Mono view
Stereo pair view
|
A full contact list of Chlorine with other atoms in the Cl binding
site number 1 of Rat Transcobalamin in Complex with Glutathionylcobalamin within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Cl503
b:12.0
occ:1.00
|
HE21
|
A:GLN407
|
2.4
|
17.2
|
1.0
|
H
|
A:ASN286
|
2.4
|
13.7
|
1.0
|
H331
|
A:B12501
|
2.5
|
12.8
|
1.0
|
H
|
A:GLN285
|
2.5
|
13.8
|
1.0
|
HH
|
A:TYR247
|
2.7
|
16.3
|
1.0
|
H
|
A:PHE284
|
3.1
|
13.4
|
1.0
|
HB2
|
A:ASN286
|
3.1
|
14.1
|
1.0
|
HA
|
A:PHE284
|
3.1
|
13.6
|
1.0
|
HB3
|
A:ASN286
|
3.2
|
14.1
|
1.0
|
N
|
A:GLN285
|
3.2
|
11.5
|
1.0
|
N
|
A:ASN286
|
3.2
|
11.4
|
1.0
|
HG2
|
A:GLN407
|
3.2
|
14.9
|
1.0
|
NE2
|
A:GLN407
|
3.2
|
14.4
|
1.0
|
N33
|
A:B12501
|
3.4
|
10.7
|
1.0
|
HB2
|
A:GLN285
|
3.4
|
16.4
|
1.0
|
OH
|
A:TYR247
|
3.4
|
13.6
|
1.0
|
CB
|
A:ASN286
|
3.5
|
11.8
|
1.0
|
HE1
|
A:TYR247
|
3.5
|
14.3
|
1.0
|
N
|
A:PHE284
|
3.6
|
11.2
|
1.0
|
HE22
|
A:GLN407
|
3.7
|
17.2
|
1.0
|
CA
|
A:PHE284
|
3.7
|
11.3
|
1.0
|
H332
|
A:B12501
|
3.7
|
12.8
|
1.0
|
CZ
|
A:TYR247
|
3.7
|
12.2
|
1.0
|
CE1
|
A:TYR247
|
3.8
|
11.9
|
1.0
|
HB3
|
A:ASP411
|
3.8
|
14.2
|
1.0
|
C
|
A:PHE284
|
3.9
|
11.1
|
1.0
|
CA
|
A:GLN285
|
4.0
|
12.4
|
1.0
|
CA
|
A:ASN286
|
4.0
|
11.2
|
1.0
|
CG
|
A:GLN407
|
4.0
|
12.4
|
1.0
|
C
|
A:GLN285
|
4.1
|
11.9
|
1.0
|
CB
|
A:GLN285
|
4.1
|
13.7
|
1.0
|
CD
|
A:GLN407
|
4.1
|
12.5
|
1.0
|
HG3
|
A:MET289
|
4.1
|
14.2
|
1.0
|
HB2
|
A:MET289
|
4.2
|
12.3
|
1.0
|
HG2
|
A:GLN285
|
4.3
|
17.4
|
1.0
|
C32
|
A:B12501
|
4.4
|
9.9
|
1.0
|
CB
|
A:ASP411
|
4.5
|
11.9
|
1.0
|
HG3
|
A:GLN407
|
4.5
|
14.9
|
1.0
|
HB2
|
A:ASP411
|
4.6
|
14.2
|
1.0
|
HA
|
A:ASN286
|
4.6
|
13.4
|
1.0
|
CE2
|
A:TYR247
|
4.6
|
12.0
|
1.0
|
O34
|
A:B12501
|
4.6
|
10.2
|
1.0
|
HA
|
A:ALA283
|
4.6
|
15.5
|
1.0
|
O
|
A:HOH757
|
4.7
|
11.3
|
1.0
|
CD1
|
A:TYR247
|
4.7
|
10.5
|
1.0
|
C
|
A:ALA283
|
4.7
|
11.2
|
1.0
|
CG
|
A:GLN285
|
4.7
|
14.5
|
1.0
|
CG
|
A:ASP411
|
4.8
|
11.4
|
1.0
|
CB
|
A:MET289
|
4.9
|
10.2
|
1.0
|
CG
|
A:MET289
|
4.9
|
11.9
|
1.0
|
HA
|
A:GLN285
|
4.9
|
14.9
|
1.0
|
CG
|
A:ASN286
|
4.9
|
12.1
|
1.0
|
HB3
|
A:GLN407
|
4.9
|
13.5
|
1.0
|
HB3
|
A:GLN285
|
4.9
|
16.4
|
1.0
|
HB3
|
A:MET289
|
4.9
|
12.3
|
1.0
|
HE2
|
A:TYR247
|
5.0
|
14.4
|
1.0
|
OD2
|
A:ASP411
|
5.0
|
11.4
|
1.0
|
|
Chlorine binding site 2 out
of 2 in 8ixt
Go back to
Chlorine Binding Sites List in 8ixt
Chlorine binding site 2 out
of 2 in the Rat Transcobalamin in Complex with Glutathionylcobalamin
Mono view
Stereo pair view
|
A full contact list of Chlorine with other atoms in the Cl binding
site number 2 of Rat Transcobalamin in Complex with Glutathionylcobalamin within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Cl504
b:18.6
occ:1.00
|
HG
|
A:SER383
|
2.2
|
18.6
|
0.4
|
H
|
A:GLY386
|
2.2
|
21.5
|
1.0
|
HG
|
A:SER383
|
2.3
|
16.2
|
0.6
|
HG1
|
A:THR369
|
2.4
|
22.3
|
1.0
|
HA
|
A:TYR370
|
2.9
|
13.8
|
1.0
|
OG
|
A:SER383
|
3.0
|
15.5
|
0.4
|
N
|
A:GLY386
|
3.1
|
17.9
|
1.0
|
O
|
A:HOH957
|
3.2
|
22.7
|
1.0
|
OG
|
A:SER383
|
3.2
|
13.5
|
0.6
|
OG1
|
A:THR369
|
3.2
|
18.6
|
1.0
|
HA2
|
A:GLY386
|
3.2
|
26.7
|
1.0
|
HB2
|
A:SER383
|
3.2
|
15.7
|
0.6
|
HB3
|
A:SER383
|
3.3
|
17.8
|
0.4
|
H
|
A:LEU385
|
3.4
|
16.6
|
1.0
|
HB
|
A:THR369
|
3.5
|
20.5
|
1.0
|
CA
|
A:TYR370
|
3.5
|
11.5
|
1.0
|
N
|
A:LEU385
|
3.6
|
13.8
|
1.0
|
CA
|
A:GLY386
|
3.6
|
22.2
|
1.0
|
CB
|
A:SER383
|
3.7
|
14.8
|
0.4
|
N
|
A:TYR370
|
3.7
|
12.0
|
1.0
|
HA
|
A:VAL384
|
3.7
|
13.6
|
1.0
|
CB
|
A:SER383
|
3.7
|
13.1
|
0.6
|
C
|
A:THR369
|
3.8
|
13.5
|
1.0
|
C
|
A:TYR370
|
3.8
|
13.0
|
1.0
|
C
|
A:SER383
|
3.8
|
12.1
|
0.4
|
CB
|
A:THR369
|
3.8
|
17.1
|
1.0
|
N
|
A:VAL384
|
3.9
|
11.7
|
1.0
|
C
|
A:VAL384
|
3.9
|
13.6
|
1.0
|
O
|
A:THR369
|
3.9
|
12.8
|
1.0
|
C
|
A:SER383
|
3.9
|
12.1
|
0.6
|
O
|
A:SER383
|
3.9
|
11.7
|
0.4
|
O
|
A:SER383
|
4.0
|
11.7
|
0.6
|
CA
|
A:VAL384
|
4.0
|
11.3
|
1.0
|
H
|
A:GLY371
|
4.0
|
15.2
|
1.0
|
N
|
A:GLY371
|
4.0
|
12.7
|
1.0
|
H
|
A:TYR370
|
4.1
|
14.4
|
1.0
|
C
|
A:LEU385
|
4.1
|
16.2
|
1.0
|
H
|
A:VAL384
|
4.2
|
14.1
|
1.0
|
CA
|
A:LEU385
|
4.2
|
15.2
|
1.0
|
HA
|
A:LEU385
|
4.3
|
18.2
|
1.0
|
H
|
A:LYS387
|
4.3
|
19.7
|
1.0
|
O
|
A:TYR370
|
4.3
|
13.8
|
1.0
|
CA
|
A:SER383
|
4.4
|
13.1
|
0.4
|
HA3
|
A:GLY386
|
4.4
|
26.7
|
1.0
|
CA
|
A:SER383
|
4.4
|
13.2
|
0.6
|
C
|
A:GLY386
|
4.5
|
23.7
|
1.0
|
CA
|
A:THR369
|
4.5
|
15.1
|
1.0
|
HB2
|
A:SER383
|
4.5
|
17.8
|
0.4
|
HB3
|
A:SER383
|
4.5
|
15.7
|
0.6
|
O
|
A:VAL384
|
4.5
|
14.1
|
1.0
|
HA3
|
A:GLY371
|
4.6
|
15.2
|
1.0
|
O
|
A:HOH1020
|
4.6
|
31.5
|
1.0
|
N
|
A:LYS387
|
4.7
|
16.4
|
1.0
|
HA
|
A:SER383
|
4.9
|
15.8
|
0.4
|
CB
|
A:TYR370
|
4.9
|
11.7
|
1.0
|
CA
|
A:GLY371
|
4.9
|
12.7
|
1.0
|
O
|
A:HOH922
|
5.0
|
21.2
|
1.0
|
|
Reference:
M.Bokhove,
T.Kawamura,
H.Okumura,
S.Goto,
Y.Kawano,
S.Werner,
F.Jarczowski,
V.Klimyuk,
A.Saito,
T.Kumasaka.
The Structure of the Rat Vitamin B 12 Transporter Tc and Its Complex with Glutathionylcobalamin. J.Biol.Chem. V. 300 07289 2024.
ISSN: ESSN 1083-351X
PubMed: 38636663
DOI: 10.1016/J.JBC.2024.107289
Page generated: Tue Jul 30 10:52:27 2024
|