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Magnesium in PDB 1m15: Transition State Structure of Arginine Kinase

Enzymatic activity of Transition State Structure of Arginine Kinase

All present enzymatic activity of Transition State Structure of Arginine Kinase:
2.7.3.3;

Protein crystallography data

The structure of Transition State Structure of Arginine Kinase, PDB code: 1m15 was solved by M.S.Yousef, F.Fabiola, J.L.Gattis, T.Somasundaram, M.S.Chapman, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 6.00 / 1.20
Space group P 21 21 21
Cell size a, b, c (Å), α, β, γ (°) 65.393, 70.312, 80.319, 90.00, 90.00, 90.00
R / Rfree (%) 12.5 / 14

Magnesium Binding Sites:

The binding sites of Magnesium atom in the Transition State Structure of Arginine Kinase (pdb code 1m15). This binding sites where shown within 5.0 Angstroms radius around Magnesium atom.
In total only one binding site of Magnesium was determined in the Transition State Structure of Arginine Kinase, PDB code: 1m15:

Magnesium binding site 1 out of 1 in 1m15

Go back to Magnesium Binding Sites List in 1m15
Magnesium binding site 1 out of 1 in the Transition State Structure of Arginine Kinase


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 1 of Transition State Structure of Arginine Kinase within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Mg408

b:11.6
occ:1.00
O1B A:ADP400 2.0 9.6 1.0
O A:HOH1297 2.0 10.5 1.0
O1A A:ADP400 2.1 9.6 1.0
O A:HOH1296 2.1 9.8 1.0
O1 A:NO3405 2.1 10.8 1.0
O A:HOH1298 2.1 10.0 1.0
N A:NO3405 3.1 10.4 1.0
PB A:ADP400 3.3 9.2 1.0
PA A:ADP400 3.3 9.0 1.0
O3 A:NO3405 3.4 10.9 1.0
O3A A:ADP400 3.5 8.8 1.0
O A:HOH1215 3.9 10.8 1.0
O3B A:ADP400 4.1 9.8 1.0
NH1 A:ARG229 4.1 9.7 1.0
OE2 A:GLU314 4.1 9.8 1.0
OE2 A:GLU224 4.2 10.4 1.0
O A:HOH1223 4.2 12.7 1.0
NH2 A:ARG403 4.3 9.8 1.0
O2A A:ADP400 4.3 9.6 1.0
O2B A:ADP400 4.3 9.0 1.0
O2 A:NO3405 4.4 11.5 1.0
CZ3 A:TRP221 4.4 9.6 1.0
OE2 A:GLU225 4.4 10.6 1.0
O5' A:ADP400 4.4 8.9 1.0
OE1 A:GLU224 4.4 10.0 1.0
C5' A:ADP400 4.5 9.0 1.0
O A:HOH1214 4.5 10.8 1.0
CH2 A:TRP221 4.6 10.1 1.0
CD A:GLU314 4.8 10.2 1.0
CD A:GLU224 4.8 10.1 1.0
NH1 A:ARG309 4.8 9.8 1.0
NH2 A:ARG229 4.9 10.1 1.0
CG A:GLU314 4.9 11.0 1.0
CZ A:ARG229 4.9 9.1 1.0

Reference:

M.S.Yousef, F.Fabiola, J.L.Gattis, T.Somasundaram, M.S.Chapman. Refinement of the Arginine Kinase Transition-State Analogue Complex at 1.2 A Resolution: Mechanistic Insights. Acta Crystallogr.,Sect.D V. 58 2009 2002.
ISSN: ISSN 0907-4449
PubMed: 12454458
DOI: 10.1107/S0907444902014683
Page generated: Mon Dec 14 06:23:46 2020

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