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Calcium in PDB 1wc0: Soluble Adenylyl Cyclase Cyac From S. Platensis in Complex with Alpha,Beta-Methylene-Atp

Enzymatic activity of Soluble Adenylyl Cyclase Cyac From S. Platensis in Complex with Alpha,Beta-Methylene-Atp

All present enzymatic activity of Soluble Adenylyl Cyclase Cyac From S. Platensis in Complex with Alpha,Beta-Methylene-Atp:
4.6.1.1;

Protein crystallography data

The structure of Soluble Adenylyl Cyclase Cyac From S. Platensis in Complex with Alpha,Beta-Methylene-Atp, PDB code: 1wc0 was solved by C.Steegborn, T.N.Litvin, L.R.Levin, J.Buck, H.Wu, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 14.88 / 2.4
Space group P 21 21 21
Cell size a, b, c (Å), α, β, γ (°) 53.672, 71.539, 99.572, 90.00, 90.00, 90.00
R / Rfree (%) 21.9 / 27.1

Calcium Binding Sites:

The binding sites of Calcium atom in the Soluble Adenylyl Cyclase Cyac From S. Platensis in Complex with Alpha,Beta-Methylene-Atp (pdb code 1wc0). This binding sites where shown within 5.0 Angstroms radius around Calcium atom.
In total 2 binding sites of Calcium where determined in the Soluble Adenylyl Cyclase Cyac From S. Platensis in Complex with Alpha,Beta-Methylene-Atp, PDB code: 1wc0:
Jump to Calcium binding site number: 1; 2;

Calcium binding site 1 out of 2 in 1wc0

Go back to Calcium Binding Sites List in 1wc0
Calcium binding site 1 out of 2 in the Soluble Adenylyl Cyclase Cyac From S. Platensis in Complex with Alpha,Beta-Methylene-Atp


Mono view


Stereo pair view

A full contact list of Calcium with other atoms in the Ca binding site number 1 of Soluble Adenylyl Cyclase Cyac From S. Platensis in Complex with Alpha,Beta-Methylene-Atp within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Ca2100

b:22.5
occ:1.00
O1B A:APC1500 2.1 37.2 1.0
O A:HOH2070 2.3 22.9 1.0
OD1 A:ASP1017 2.4 34.8 1.0
OD1 A:ASP1061 2.5 28.4 1.0
O A:ILE1018 2.5 31.7 1.0
OD2 A:ASP1017 2.9 33.4 1.0
O3G A:APC1500 2.9 44.1 1.0
CG A:ASP1017 2.9 33.6 1.0
CG A:ASP1061 3.3 25.0 1.0
OD2 A:ASP1061 3.3 30.1 1.0
PB A:APC1500 3.4 36.8 1.0
C A:ILE1018 3.7 34.0 1.0
PG A:APC1500 3.8 41.8 1.0
O1A A:APC1500 3.9 29.4 1.0
O3B A:APC1500 4.0 39.5 1.0
N A:ILE1018 4.1 32.8 1.0
C3A A:APC1500 4.2 34.1 1.0
O1G A:APC1500 4.3 41.9 1.0
CB A:ASP1017 4.4 31.4 1.0
CA A:ILE1018 4.6 32.5 1.0
O2B A:APC1500 4.6 38.5 1.0
CG2 A:VAL1019 4.6 38.1 1.0
CB A:ASP1061 4.6 22.6 1.0
N A:VAL1019 4.7 37.3 1.0
PA A:APC1500 4.7 35.0 1.0
O A:HOH2068 4.7 30.1 1.0
CA A:VAL1019 4.7 39.5 1.0
C A:ASP1017 4.8 32.1 1.0
CG1 A:ILE1018 5.0 28.5 1.0
CA A:ASP1017 5.0 30.9 1.0

Calcium binding site 2 out of 2 in 1wc0

Go back to Calcium Binding Sites List in 1wc0
Calcium binding site 2 out of 2 in the Soluble Adenylyl Cyclase Cyac From S. Platensis in Complex with Alpha,Beta-Methylene-Atp


Mono view


Stereo pair view

A full contact list of Calcium with other atoms in the Ca binding site number 2 of Soluble Adenylyl Cyclase Cyac From S. Platensis in Complex with Alpha,Beta-Methylene-Atp within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Ca2100

b:21.7
occ:1.00
O1B B:APC1500 2.0 45.7 1.0
O B:HOH2070 2.3 10.3 1.0
OD1 B:ASP1017 2.3 29.6 1.0
O B:ILE1018 2.4 30.1 1.0
OD2 B:ASP1061 2.6 24.8 1.0
O3G B:APC1500 2.6 49.9 1.0
OD2 B:ASP1017 2.8 29.0 1.0
CG B:ASP1017 2.9 28.6 1.0
CG B:ASP1061 3.4 25.1 1.0
PB B:APC1500 3.4 43.1 1.0
OD1 B:ASP1061 3.5 31.2 1.0
C B:ILE1018 3.5 31.7 1.0
PG B:APC1500 3.7 47.6 1.0
O3B B:APC1500 3.9 45.4 1.0
N B:ILE1018 3.9 25.9 1.0
O1A B:APC1500 4.1 37.6 1.0
O1G B:APC1500 4.2 49.2 1.0
O B:HOH2018 4.3 17.0 1.0
CA B:ILE1018 4.3 29.9 1.0
C3A B:APC1500 4.4 40.0 1.0
CB B:ASP1017 4.4 24.8 1.0
O2B B:APC1500 4.4 44.5 1.0
N B:VAL1019 4.4 35.2 1.0
CA B:VAL1019 4.6 39.0 1.0
CG2 B:VAL1019 4.6 40.1 1.0
CG1 B:ILE1018 4.7 30.2 1.0
C B:ASP1017 4.7 23.6 1.0
CB B:ASP1061 4.7 22.7 1.0
O B:HOH2015 4.8 18.2 1.0
O B:ASP1061 4.8 19.2 1.0
O B:HOH2068 4.9 42.7 1.0
CA B:ASP1017 4.9 22.0 1.0
PA B:APC1500 4.9 40.8 1.0
C B:ASP1061 4.9 16.4 1.0
O2G B:APC1500 5.0 47.8 1.0

Reference:

C.Steegborn, T.N.Litvin, L.R.Levin, J.Buck, H.Wu. Bicarbonate Activation of Adenylyl Cyclase Via Promotion of Catalytic Active Site Closure and Metal Recruitment Nat.Struct.Mol.Biol. V. 12 32 2005.
ISSN: ISSN 1545-9993
PubMed: 15619637
DOI: 10.1038/NSMB880
Page generated: Fri Jul 12 07:09:32 2024

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