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Magnesium in PDB 2hf9: Crystal Structure of Hypb From Methanocaldococcus Jannaschii in the Triphosphate Form

Protein crystallography data

The structure of Crystal Structure of Hypb From Methanocaldococcus Jannaschii in the Triphosphate Form, PDB code: 2hf9 was solved by R.Gasper, A.Scrima, A.Wittinghofer, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 19.96 / 1.90
Space group P 21 21 21
Cell size a, b, c (Å), α, β, γ (°) 43.463, 68.107, 155.840, 90.00, 90.00, 90.00
R / Rfree (%) 21.7 / 24.1

Other elements in 2hf9:

The structure of Crystal Structure of Hypb From Methanocaldococcus Jannaschii in the Triphosphate Form also contains other interesting chemical elements:

Zinc (Zn) 2 atoms

Magnesium Binding Sites:

The binding sites of Magnesium atom in the Crystal Structure of Hypb From Methanocaldococcus Jannaschii in the Triphosphate Form (pdb code 2hf9). This binding sites where shown within 5.0 Angstroms radius around Magnesium atom.
In total 2 binding sites of Magnesium where determined in the Crystal Structure of Hypb From Methanocaldococcus Jannaschii in the Triphosphate Form, PDB code: 2hf9:
Jump to Magnesium binding site number: 1; 2;

Magnesium binding site 1 out of 2 in 2hf9

Go back to Magnesium Binding Sites List in 2hf9
Magnesium binding site 1 out of 2 in the Crystal Structure of Hypb From Methanocaldococcus Jannaschii in the Triphosphate Form


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 1 of Crystal Structure of Hypb From Methanocaldococcus Jannaschii in the Triphosphate Form within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Mg301

b:9.1
occ:1.00
O3G A:GSP300 2.0 11.1 1.0
O A:HOH319 2.0 8.7 1.0
O2B A:GSP300 2.0 6.7 1.0
OG1 A:THR47 2.1 5.6 1.0
OD2 A:ASP75 2.1 9.2 1.0
OE2 A:GLU120 2.1 9.6 1.0
CG A:ASP75 2.9 11.4 1.0
CD A:GLU120 3.1 9.0 1.0
PG A:GSP300 3.2 11.1 1.0
PB A:GSP300 3.2 7.5 1.0
CB A:THR47 3.2 6.7 1.0
OD1 A:ASP75 3.3 11.8 1.0
OE1 A:GLU120 3.4 9.4 1.0
O3B A:GSP300 3.4 9.6 1.0
O A:HOH343 3.8 25.4 1.0
N A:THR47 3.8 7.0 1.0
O2G A:GSP300 4.0 11.1 1.0
NZ B:LYS153 4.0 20.9 1.0
CA A:THR47 4.1 6.8 1.0
CB A:ASP75 4.1 11.7 1.0
O2A A:GSP300 4.2 7.3 1.0
O1B A:GSP300 4.3 7.0 1.0
O3A A:GSP300 4.3 7.9 1.0
CG2 A:THR47 4.3 7.0 1.0
O A:HOH303 4.3 12.9 1.0
CG A:GLU120 4.5 9.5 1.0
S1G A:GSP300 4.5 14.6 1.0
PA A:GSP300 4.6 8.4 1.0
O1A A:GSP300 4.7 7.6 1.0
CB A:LYS46 4.8 7.5 1.0
O A:HOH306 4.8 19.4 1.0
C A:LYS46 4.9 7.0 1.0
CE A:LYS46 5.0 10.9 1.0

Magnesium binding site 2 out of 2 in 2hf9

Go back to Magnesium Binding Sites List in 2hf9
Magnesium binding site 2 out of 2 in the Crystal Structure of Hypb From Methanocaldococcus Jannaschii in the Triphosphate Form


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 2 of Crystal Structure of Hypb From Methanocaldococcus Jannaschii in the Triphosphate Form within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Mg301

b:11.1
occ:1.00
O3G B:GSP300 2.0 11.5 1.0
OE2 B:GLU120 2.0 9.5 1.0
OG1 B:THR47 2.1 7.8 1.0
O2B B:GSP300 2.1 8.3 1.0
OD2 B:ASP75 2.1 13.1 1.0
O B:HOH318 2.1 13.4 1.0
CG B:ASP75 3.0 15.3 1.0
CD B:GLU120 3.1 9.9 1.0
PB B:GSP300 3.2 9.3 1.0
PG B:GSP300 3.2 12.5 1.0
CB B:THR47 3.3 7.9 1.0
OD1 B:ASP75 3.4 12.8 1.0
OE1 B:GLU120 3.4 10.0 1.0
O3B B:GSP300 3.4 9.3 1.0
N B:THR47 3.9 8.4 1.0
O2G B:GSP300 4.1 11.5 1.0
CA B:THR47 4.1 8.1 1.0
CB B:ASP75 4.1 16.3 1.0
NZ A:LYS153 4.2 22.9 1.0
O1B B:GSP300 4.2 9.4 1.0
O B:HOH303 4.3 20.0 1.0
O2A B:GSP300 4.3 8.6 1.0
O B:HOH387 4.3 18.9 1.0
CG2 B:THR47 4.4 7.9 1.0
O3A B:GSP300 4.4 8.9 1.0
CG B:GLU120 4.4 9.2 1.0
S1G B:GSP300 4.5 14.5 1.0
PA B:GSP300 4.7 10.1 1.0
CB B:LYS46 4.7 9.1 1.0
O1A B:GSP300 4.8 9.2 1.0
CE B:LYS46 4.8 11.5 1.0
C B:LYS46 4.9 8.5 1.0

Reference:

R.Gasper, A.Scrima, A.Wittinghofer. Structural Insights Into Hypb, A Gtp-Binding Protein That Regulates Metal Binding. J.Biol.Chem. V. 281 27492 2006.
ISSN: ISSN 0021-9258
PubMed: 16807243
DOI: 10.1074/JBC.M600809200
Page generated: Tue Aug 13 23:50:33 2024

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