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Chlorine in PDB 2ga2: H-METAP2 Complexed with A193400

Enzymatic activity of H-METAP2 Complexed with A193400

All present enzymatic activity of H-METAP2 Complexed with A193400:
3.4.11.18;

Protein crystallography data

The structure of H-METAP2 Complexed with A193400, PDB code: 2ga2 was solved by C.Park, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 15.79 / 1.95
Space group C 2 2 21
Cell size a, b, c (Å), α, β, γ (°) 89.731, 98.793, 101.213, 90.00, 90.00, 90.00
R / Rfree (%) n/a / n/a

Other elements in 2ga2:

The structure of H-METAP2 Complexed with A193400 also contains other interesting chemical elements:

Bromine (Br) 1 atom
Manganese (Mn) 2 atoms

Chlorine Binding Sites:

The binding sites of Chlorine atom in the H-METAP2 Complexed with A193400 (pdb code 2ga2). 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 H-METAP2 Complexed with A193400, PDB code: 2ga2:

Chlorine binding site 1 out of 1 in 2ga2

Go back to Chlorine Binding Sites List in 2ga2
Chlorine binding site 1 out of 1 in the H-METAP2 Complexed with A193400


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 1 of H-METAP2 Complexed with A193400 within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl482

b:46.4
occ:1.00
CL1 A:A19482 0.0 46.4 1.0
C2 A:A19482 1.7 46.1 1.0
C3 A:A19482 2.7 46.0 1.0
C7 A:A19482 2.7 46.0 1.0
CD2 A:LEU328 3.0 19.9 1.0
CB A:ALA230 3.4 15.8 1.0
CZ A:PHE366 3.5 15.6 1.0
CD1 A:LEU328 3.7 19.8 1.0
CE2 A:PHE366 3.8 15.7 1.0
CG A:LEU328 3.9 20.1 1.0
CD1 A:LEU447 4.0 18.4 1.0
C4 A:A19482 4.0 45.9 1.0
C6 A:A19482 4.0 45.9 1.0
CE1 A:PHE366 4.3 15.3 1.0
CB A:LEU328 4.4 20.3 1.0
C5 A:A19482 4.5 45.8 1.0
NE2 A:HIS231 4.6 17.3 1.0
O20 A:A19482 4.7 44.1 1.0
CD2 A:PHE366 4.7 15.4 1.0
CE1 A:HIS231 4.7 17.1 1.0
CA A:ALA230 4.9 15.7 1.0
OE2 A:GLU364 4.9 18.1 1.0
CD2 A:HIS231 5.0 17.2 1.0

Reference:

M.Kawai, N.Y.Bamaung, S.D.Fidanze, S.A.Erickson, J.S.Tedrow, W.J.Sanders, A.Vasudevan, C.Park, C.Hutchins, K.M.Comess, D.Kalvin, J.Wang, Q.Zhang, P.Lou, L.Tucker-Garcia, J.Bouska, R.L.Bell, R.Lesniewski, J.Henkin, G.S.Sheppard. Development of Sulfonamide Compounds As Potent Methionine Aminopeptidase Type II Inhibitors with Antiproliferative Properties. Bioorg.Med.Chem.Lett. V. 16 3574 2006.
ISSN: ISSN 0960-894X
PubMed: 16632353
DOI: 10.1016/J.BMCL.2006.03.085
Page generated: Thu Jul 10 22:19:23 2025

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