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Chlorine in PDB 3i59: Crystal Structure of Mtbcrp in Complex with N6-Camp

Protein crystallography data

The structure of Crystal Structure of Mtbcrp in Complex with N6-Camp, PDB code: 3i59 was solved by M.C.Reddy, S.K.Palaninathan, J.B.Bruning, C.Thurman, D.Smith, J.C.Sacchettini, Tb Structural Genomics Consortium (Tbsgc), with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 19.48 / 2.29
Space group C 1 2 1
Cell size a, b, c (Å), α, β, γ (°) 113.732, 75.716, 63.639, 90.00, 110.91, 90.00
R / Rfree (%) 23.4 / 28.4

Chlorine Binding Sites:

The binding sites of Chlorine atom in the Crystal Structure of Mtbcrp in Complex with N6-Camp (pdb code 3i59). This binding sites where shown within 5.0 Angstroms radius around Chlorine atom.
In total only one binding site of Chlorine was determined in the Crystal Structure of Mtbcrp in Complex with N6-Camp, PDB code: 3i59:

Chlorine binding site 1 out of 1 in 3i59

Go back to Chlorine Binding Sites List in 3i59
Chlorine binding site 1 out of 1 in the Crystal Structure of Mtbcrp in Complex with N6-Camp


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 1 of Crystal Structure of Mtbcrp in Complex with N6-Camp within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl302

b:70.9
occ:1.00
NH2 A:ARG133 2.9 65.9 1.0
NH2 A:ARG129 3.5 57.5 1.0
NH1 A:ARG160 3.5 66.4 1.0
NH2 A:ARG130 3.6 47.2 1.0
NE A:ARG130 3.6 61.4 1.0
O A:HOH234 4.0 80.4 1.0
CZ A:ARG133 4.0 66.9 1.0
NE A:ARG129 4.1 69.5 1.0
CZ A:ARG130 4.1 51.7 1.0
CZ A:ARG129 4.3 67.8 1.0
NH1 A:ARG133 4.3 68.8 1.0
CZ A:ARG160 4.5 67.1 1.0
NH2 A:ARG160 4.6 65.9 1.0
CG A:ARG130 4.7 56.8 1.0
CG1 A:VAL126 4.7 43.0 1.0
CD A:ARG130 4.7 58.3 1.0
OD1 A:ASP76 4.8 42.2 1.0

Reference:

M.C.Reddy, S.K.Palaninathan, J.B.Bruning, C.Thurman, D.Smith, J.C.Sacchettini. Structural Insights Into the Mechanism of the Allosteric Transitions of Mycobacterium Tuberculosis Camp Receptor Protein. J.Biol.Chem. V. 284 36581 2009.
ISSN: ISSN 0021-9258
PubMed: 19740754
DOI: 10.1074/JBC.M109.041343
Page generated: Sat Jul 20 21:17:20 2024

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