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Magnesium in PDB 4kfs: Structure of the Genome Packaging Ntpase B204 From Sulfolobus Turreted Icosahedral Virus 2 in Complex with Amp

Protein crystallography data

The structure of Structure of the Genome Packaging Ntpase B204 From Sulfolobus Turreted Icosahedral Virus 2 in Complex with Amp, PDB code: 4kfs was solved by L.J.Happonen, E.Oksanen, T.Kajander, A.Goldman, S.Butcher, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 46.29 / 1.95
Space group P 1 21 1
Cell size a, b, c (Å), α, β, γ (°) 46.600, 61.015, 70.004, 90.00, 96.57, 90.00
R / Rfree (%) 19.7 / 23.8

Other elements in 4kfs:

The structure of Structure of the Genome Packaging Ntpase B204 From Sulfolobus Turreted Icosahedral Virus 2 in Complex with Amp also contains other interesting chemical elements:

Zinc (Zn) 1 atom

Magnesium Binding Sites:

The binding sites of Magnesium atom in the Structure of the Genome Packaging Ntpase B204 From Sulfolobus Turreted Icosahedral Virus 2 in Complex with Amp (pdb code 4kfs). This binding sites where shown within 5.0 Angstroms radius around Magnesium atom.
In total 2 binding sites of Magnesium where determined in the Structure of the Genome Packaging Ntpase B204 From Sulfolobus Turreted Icosahedral Virus 2 in Complex with Amp, PDB code: 4kfs:
Jump to Magnesium binding site number: 1; 2;

Magnesium binding site 1 out of 2 in 4kfs

Go back to Magnesium Binding Sites List in 4kfs
Magnesium binding site 1 out of 2 in the Structure of the Genome Packaging Ntpase B204 From Sulfolobus Turreted Icosahedral Virus 2 in Complex with Amp


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 1 of Structure of the Genome Packaging Ntpase B204 From Sulfolobus Turreted Icosahedral Virus 2 in Complex with Amp within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Mg301

b:32.6
occ:1.00
O B:HOH428 2.1 34.3 1.0
O B:HOH429 2.1 29.9 1.0
OB1 B:FLC303 2.1 34.7 1.0
O B:HOH458 2.1 31.5 1.0
OHB B:FLC303 2.2 35.9 1.0
OA2 B:FLC303 2.6 37.4 1.0
CBC B:FLC303 2.9 41.0 1.0
CB B:FLC303 3.1 39.1 1.0
ND2 B:ASN194 3.5 28.0 1.0
CAC B:FLC303 3.6 39.9 1.0
CA B:FLC303 3.9 45.1 1.0
OD1 B:ASP192 4.0 24.1 1.0
OD2 B:ASP192 4.1 31.0 1.0
O B:HOH453 4.1 37.5 1.0
OB2 B:FLC303 4.1 43.5 1.0
OD2 B:ASP5 4.3 26.8 1.0
CG B:ASP192 4.4 28.1 1.0
O B:ASP152 4.4 17.6 1.0
OD1 B:ASN2 4.4 39.4 1.0
CB B:ASP152 4.4 18.2 1.0
CG B:ASN194 4.4 32.9 1.0
CB B:ASN194 4.5 27.4 1.0
OD1 B:ASP5 4.5 26.0 1.0
CD2 B:LEU153 4.6 22.0 1.0
OA1 B:FLC303 4.7 41.4 1.0
CG B:ASP5 4.7 29.2 1.0
C B:ASP152 4.9 17.8 1.0
CG B:LEU153 5.0 26.3 1.0

Magnesium binding site 2 out of 2 in 4kfs

Go back to Magnesium Binding Sites List in 4kfs
Magnesium binding site 2 out of 2 in the Structure of the Genome Packaging Ntpase B204 From Sulfolobus Turreted Icosahedral Virus 2 in Complex with Amp


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 2 of Structure of the Genome Packaging Ntpase B204 From Sulfolobus Turreted Icosahedral Virus 2 in Complex with Amp within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Mg302

b:37.3
occ:1.00
OA1 B:FLC304 1.9 36.2 1.0
O B:HOH449 2.1 36.3 1.0
O B:HOH448 2.1 35.0 1.0
OB1 B:FLC304 2.1 36.1 1.0
O B:HOH450 2.1 32.2 1.0
OHB B:FLC304 2.3 34.0 1.0
CBC B:FLC304 2.8 39.4 1.0
CB B:FLC304 3.0 31.6 1.0
CAC B:FLC304 3.0 37.9 1.0
CA B:FLC304 3.5 37.0 1.0
O B:GLN150 4.0 17.6 1.0
OD1 B:ASN126 4.0 20.5 1.0
OB2 B:FLC304 4.0 37.7 1.0
OG1 B:FLC304 4.0 26.1 1.0
OA2 B:FLC304 4.0 41.1 1.0
OD1 B:ASP152 4.3 26.3 1.0
CG B:FLC304 4.4 30.9 1.0
O B:LEU123 4.4 17.6 1.0
OD2 B:ASP152 4.4 21.3 1.0
NH2 B:ARG127 4.5 24.0 1.0
CD1 B:ILE6 4.5 17.6 1.0
NE B:ARG127 4.6 24.2 1.0
OE1 B:GLN150 4.6 24.9 1.0
CGC B:FLC304 4.7 27.9 1.0
CG B:ASP152 4.7 23.1 1.0
O B:HOH467 4.9 27.9 1.0
CZ B:ARG127 4.9 29.2 1.0

Reference:

L.J.Happonen, E.Oksanen, L.Liljeroos, A.Goldman, T.Kajander, S.J.Butcher. The Structure of the Ntpase That Powers Dna Packaging Into Sulfolobus Turreted Icosahedral Virus 2. J.Virol. V. 87 8388 2013.
ISSN: ISSN 0022-538X
PubMed: 23698307
DOI: 10.1128/JVI.00831-13
Page generated: Sat Aug 17 03:35:00 2024

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