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Bromine in PDB 1eet: Hiv-1 Reverse Transcriptase in Complex with the Inhibitor MSC204

Enzymatic activity of Hiv-1 Reverse Transcriptase in Complex with the Inhibitor MSC204

All present enzymatic activity of Hiv-1 Reverse Transcriptase in Complex with the Inhibitor MSC204:
2.7.7.49;

Protein crystallography data

The structure of Hiv-1 Reverse Transcriptase in Complex with the Inhibitor MSC204, PDB code: 1eet was solved by M.Hogberg, C.Sahlberg, P.Engelhardt, R.Noreen, J.Kangasmetsa, N.G.Johansson, B.Oberg, L.Vrang, H.Zhang, B.L.Sahlberg, T.Unge, S.Lovgren, K.Fridborg, K.Backbro, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 47.50 / 2.73
Space group C 2 2 21
Cell size a, b, c (Å), α, β, γ (°) 119.570, 156.450, 156.350, 90.00, 90.00, 90.00
R / Rfree (%) 21.3 / 27.1

Other elements in 1eet:

The structure of Hiv-1 Reverse Transcriptase in Complex with the Inhibitor MSC204 also contains other interesting chemical elements:

Fluorine (F) 1 atom

Bromine Binding Sites:

The binding sites of Bromine atom in the Hiv-1 Reverse Transcriptase in Complex with the Inhibitor MSC204 (pdb code 1eet). This binding sites where shown within 5.0 Angstroms radius around Bromine atom.
In total only one binding site of Bromine was determined in the Hiv-1 Reverse Transcriptase in Complex with the Inhibitor MSC204, PDB code: 1eet:

Bromine binding site 1 out of 1 in 1eet

Go back to Bromine Binding Sites List in 1eet
Bromine binding site 1 out of 1 in the Hiv-1 Reverse Transcriptase in Complex with the Inhibitor MSC204


Mono view


Stereo pair view

A full contact list of Bromine with other atoms in the Br binding site number 1 of Hiv-1 Reverse Transcriptase in Complex with the Inhibitor MSC204 within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Br2000

b:56.9
occ:1.00
BR A:BFU2000 0.0 56.9 1.0
C2 A:BFU2000 1.8 42.2 1.0
C3 A:BFU2000 2.8 39.8 1.0
C7 A:BFU2000 2.8 39.9 1.0
CG1 A:VAL106 3.5 47.4 1.0
O A:LEU234 3.6 41.3 1.0
O A:HIS235 3.8 43.2 1.0
C A:LEU234 3.9 39.9 1.0
CB A:LEU234 3.9 36.3 1.0
C A:HIS235 3.9 42.7 1.0
CB A:PRO225 3.9 69.5 1.0
CD2 A:PHE227 3.9 61.7 1.0
N4 A:BFU2000 4.1 37.0 1.0
C6 A:BFU2000 4.1 34.3 1.0
N A:PRO236 4.2 43.2 1.0
CG2 A:VAL106 4.2 40.3 1.0
CG A:PRO225 4.2 70.0 1.0
N A:HIS235 4.3 40.9 1.0
CB A:VAL106 4.3 45.9 1.0
CA A:HIS235 4.4 42.0 1.0
CA A:PRO236 4.4 44.7 1.0
OH A:TYR318 4.5 32.2 1.0
CA A:LEU234 4.6 39.2 1.0
C5 A:BFU2000 4.6 34.3 1.0
CE2 A:PHE227 4.7 65.0 1.0
C26 A:BFU2000 4.7 35.9 1.0
CB A:PHE227 4.7 55.5 1.0
CG A:PHE227 4.8 58.8 1.0
O24 A:BFU2000 4.8 34.7 1.0
CD A:PRO225 4.9 70.8 1.0
CD A:PRO236 4.9 41.9 1.0

Reference:

M.Hogberg, C.Sahlberg, P.Engelhardt, R.Noreen, J.Kangasmetsa, N.G.Johansson, B.Oberg, L.Vrang, H.Zhang, B.L.Sahlberg, T.Unge, S.Lovgren, K.Fridborg, K.Backbro. Urea-Pett Compounds As A New Class of Hiv-1 Reverse Transcriptase Inhibitors. 3. Synthesis and Further Structure-Activity Relationship Studies of Pett Analogues. J.Med.Chem. V. 42 4150 1999.
ISSN: ISSN 0022-2623
PubMed: 10514285
DOI: 10.1021/JM990572Y
Page generated: Sat Dec 12 02:00:24 2020

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