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Calcium in PDB 2dur: Crystal Structure of VIP36 Exoplasmic/Lumenal Domain, CA2+/MAN2-Bound Form

Protein crystallography data

The structure of Crystal Structure of VIP36 Exoplasmic/Lumenal Domain, CA2+/MAN2-Bound Form, PDB code: 2dur was solved by T.Satoh, N.P.Cowieson, R.Kato, S.Wakatsuki, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 20.00 / 1.65
Space group C 1 2 1
Cell size a, b, c (Å), α, β, γ (°) 171.200, 45.500, 117.400, 90.00, 132.70, 90.00
R / Rfree (%) 19.9 / 22.8

Other elements in 2dur:

The structure of Crystal Structure of VIP36 Exoplasmic/Lumenal Domain, CA2+/MAN2-Bound Form also contains other interesting chemical elements:

Chlorine (Cl) 8 atoms

Calcium Binding Sites:

The binding sites of Calcium atom in the Crystal Structure of VIP36 Exoplasmic/Lumenal Domain, CA2+/MAN2-Bound Form (pdb code 2dur). This binding sites where shown within 5.0 Angstroms radius around Calcium atom.
In total 2 binding sites of Calcium where determined in the Crystal Structure of VIP36 Exoplasmic/Lumenal Domain, CA2+/MAN2-Bound Form, PDB code: 2dur:
Jump to Calcium binding site number: 1; 2;

Calcium binding site 1 out of 2 in 2dur

Go back to Calcium Binding Sites List in 2dur
Calcium binding site 1 out of 2 in the Crystal Structure of VIP36 Exoplasmic/Lumenal Domain, CA2+/MAN2-Bound Form


Mono view


Stereo pair view

A full contact list of Calcium with other atoms in the Ca binding site number 1 of Crystal Structure of VIP36 Exoplasmic/Lumenal Domain, CA2+/MAN2-Bound Form within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Ca1

b:17.7
occ:1.00
OD2 A:ASP193 2.4 16.7 1.0
O A:TYR164 2.4 19.6 1.0
OD1 A:ASN166 2.4 17.4 1.0
O A:HOH332 2.4 17.2 1.0
O A:HOH313 2.4 17.7 1.0
OD2 A:ASP162 2.5 17.6 1.0
OD1 A:ASP162 2.5 17.0 1.0
CG A:ASP162 2.9 17.4 1.0
CG A:ASP193 3.5 17.2 1.0
CG A:ASN166 3.5 18.3 1.0
C A:TYR164 3.6 20.3 1.0
N A:ASN166 3.9 19.7 1.0
CB A:ASP193 4.2 17.0 1.0
CB A:ASN166 4.2 19.1 1.0
CA A:TYR164 4.4 19.8 1.0
N A:TYR164 4.4 19.5 1.0
CB A:ASP162 4.4 16.3 1.0
CA A:ASP193 4.4 16.9 1.0
O A:HIS190 4.4 17.9 1.0
OD1 A:ASP193 4.5 18.2 1.0
CB A:TYR164 4.5 20.1 1.0
CE2 A:PHE174 4.5 24.4 1.0
CE1 A:HIS190 4.5 24.1 1.0
OH A:TYR188 4.6 17.6 1.0
N A:PRO165 4.6 21.4 1.0
ND2 A:ASN166 4.6 17.9 1.0
CA A:PRO165 4.6 21.2 1.0
CA A:ASN166 4.7 19.9 1.0
C A:PRO165 4.7 21.0 1.0
CD2 A:TYR164 4.8 20.2 1.0
OD2 A:ASP131 4.8 20.8 1.0
O A:ASP131 4.8 16.9 1.0
NE2 A:HIS190 4.9 24.4 1.0
ND1 A:HIS190 4.9 25.5 1.0
O A:HOH334 5.0 20.7 1.0
N A:ASP193 5.0 17.6 1.0

Calcium binding site 2 out of 2 in 2dur

Go back to Calcium Binding Sites List in 2dur
Calcium binding site 2 out of 2 in the Crystal Structure of VIP36 Exoplasmic/Lumenal Domain, CA2+/MAN2-Bound Form


Mono view


Stereo pair view

A full contact list of Calcium with other atoms in the Ca binding site number 2 of Crystal Structure of VIP36 Exoplasmic/Lumenal Domain, CA2+/MAN2-Bound Form within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Ca2

b:22.2
occ:1.00
O B:TYR164 2.3 22.0 1.0
OD1 B:ASN166 2.4 26.9 1.0
OD2 B:ASP193 2.4 25.3 1.0
O B:HOH323 2.4 21.7 1.0
O B:HOH324 2.5 24.6 1.0
OD1 B:ASP162 2.6 23.5 1.0
OD2 B:ASP162 2.6 24.0 1.0
CG B:ASP162 3.0 22.1 1.0
CG B:ASN166 3.5 25.4 1.0
CG B:ASP193 3.5 27.9 1.0
C B:TYR164 3.5 22.8 1.0
N B:ASN166 3.9 26.4 1.0
CB B:ASN166 4.1 27.8 1.0
CB B:ASP193 4.1 26.5 1.0
CA B:TYR164 4.3 22.0 1.0
CA B:ASP193 4.4 27.0 1.0
N B:TYR164 4.4 21.1 1.0
O B:HIS190 4.5 28.1 1.0
CB B:TYR164 4.5 22.0 1.0
CB B:ASP162 4.5 21.4 1.0
OD1 B:ASP193 4.5 26.9 1.0
N B:PRO165 4.6 23.6 1.0
ND2 B:ASN166 4.6 27.6 1.0
CE1 B:HIS190 4.6 28.6 1.0
CA B:ASN166 4.6 27.6 1.0
CA B:PRO165 4.6 24.5 1.0
OH B:TYR188 4.7 25.3 1.0
CE2 B:PHE174 4.7 28.8 1.0
C B:PRO165 4.7 25.2 1.0
OD2 B:ASP131 4.8 21.8 1.0
CD2 B:TYR164 4.8 21.9 1.0
NE2 B:HIS190 4.8 28.6 1.0
O B:ASP131 4.9 19.4 1.0
O B:HOH360 4.9 30.7 1.0
N B:ASP193 5.0 27.7 1.0

Reference:

T.Satoh, N.P.Cowieson, W.Hakamata, H.Ideo, K.Fukushima, M.Kurihara, R.Kato, K.Yamashita, S.Wakatsuki. Structural Basis For Recognition of High Mannose Type Glycoproteins By Mammalian Transport Lectin VIP36 J.Biol.Chem. V. 282 28246 2007.
ISSN: ISSN 0021-9258
PubMed: 17652092
DOI: 10.1074/JBC.M703064200
Page generated: Tue Jul 8 05:08:30 2025

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