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Chlorine in PDB 4qxi: Crystal Structure of Human Ar Complexed with Nadp+ and AK198

Enzymatic activity of Crystal Structure of Human Ar Complexed with Nadp+ and AK198

All present enzymatic activity of Crystal Structure of Human Ar Complexed with Nadp+ and AK198:
1.1.1.21;

Protein crystallography data

The structure of Crystal Structure of Human Ar Complexed with Nadp+ and AK198, PDB code: 4qxi was solved by A.Cousido-Siah, A.Mitschler, F.X.Ruiz, J.Fanfrlik, P.Hobza, A.D.Podjarny, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 27.59 / 0.87
Space group P 1 21 1
Cell size a, b, c (Å), α, β, γ (°) 49.403, 66.542, 47.311, 90.00, 92.34, 90.00
R / Rfree (%) 13.4 / 14.5

Other elements in 4qxi:

The structure of Crystal Structure of Human Ar Complexed with Nadp+ and AK198 also contains other interesting chemical elements:

Fluorine (F) 1 atom

Chlorine Binding Sites:

The binding sites of Chlorine atom in the Crystal Structure of Human Ar Complexed with Nadp+ and AK198 (pdb code 4qxi). 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 Human Ar Complexed with Nadp+ and AK198, PDB code: 4qxi:

Chlorine binding site 1 out of 1 in 4qxi

Go back to Chlorine Binding Sites List in 4qxi
Chlorine binding site 1 out of 1 in the Crystal Structure of Human Ar Complexed with Nadp+ and AK198


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 Human Ar Complexed with Nadp+ and AK198 within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl402

b:6.2
occ:0.56
CL4 A:I98402 0.0 6.2 0.6
C8 A:I98402 1.8 5.3 0.6
C16 A:I98402 2.7 6.0 0.6
C9 A:I98402 2.7 5.6 0.6
O A:VAL47 3.1 5.6 1.0
O A:HOH591 3.5 11.9 1.0
O A:HOH525 3.6 7.7 1.0
NE1 A:TRP20 3.7 6.2 1.0
C A:VAL47 3.7 4.8 1.0
CD1 A:TYR48 3.8 5.0 1.0
CD1 A:TRP20 3.9 5.7 1.0
CG1 A:VAL47 3.9 5.5 1.0
C10 A:I98402 4.0 6.0 0.6
C12 A:I98402 4.0 5.5 0.6
CG2 A:VAL47 4.0 5.9 1.0
CA A:TYR48 4.0 5.0 1.0
N A:TYR48 4.2 4.5 1.0
CB A:VAL47 4.4 5.3 1.0
CE1 A:TYR48 4.4 5.3 1.0
C14 A:I98402 4.5 5.8 0.6
O A:HOH606 4.6 10.5 1.0
O A:HOH513 4.6 9.3 1.0
CA A:VAL47 4.7 4.9 1.0
CE2 A:TRP20 4.8 6.2 1.0
O A:HOH724 4.8 19.6 1.0
CG A:TYR48 4.8 4.9 1.0
C A:TYR48 5.0 4.9 1.0
CB A:TYR48 5.0 5.0 1.0

Reference:

J.Fanfrlik, F.X.Ruiz, A.Kadlcikova, J.Rezac, A.Cousido-Siah, A.Mitschler, S.Haldar, M.Lepsik, M.H.Kolar, P.Majer, A.D.Podjarny, P.Hobza. The Effect of Halogen-to-Hydrogen Bond Substitution on Human Aldose Reductase Inhibition Acs Chem.Biol. 2015.
ISSN: ESSN 1554-8937
PubMed: 25919404
DOI: 10.1021/ACSCHEMBIO.5B00151
Page generated: Sat Dec 12 11:09:24 2020

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