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Iron in PDB 3fm3: Crystal Structure of An Encephalitozoon Cuniculi Methionine Aminopeptidase Type 2

Enzymatic activity of Crystal Structure of An Encephalitozoon Cuniculi Methionine Aminopeptidase Type 2

All present enzymatic activity of Crystal Structure of An Encephalitozoon Cuniculi Methionine Aminopeptidase Type 2:
3.4.11.18;

Protein crystallography data

The structure of Crystal Structure of An Encephalitozoon Cuniculi Methionine Aminopeptidase Type 2, PDB code: 3fm3 was solved by J.J.Alvarado, M.Russell, A.Zhang, J.Adams, R.Toro, S.K.Burley, L.M.Weiss, S.C.Almo, New York Sgx Research Center For Structural Genomics(Nysgxrc), with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 50.00 / 2.18
Space group P 1 21 1
Cell size a, b, c (Å), α, β, γ (°) 62.204, 94.274, 66.496, 90.00, 99.22, 90.00
R / Rfree (%) 18.7 / 24.2

Iron Binding Sites:

The binding sites of Iron atom in the Crystal Structure of An Encephalitozoon Cuniculi Methionine Aminopeptidase Type 2 (pdb code 3fm3). This binding sites where shown within 5.0 Angstroms radius around Iron atom.
In total 4 binding sites of Iron where determined in the Crystal Structure of An Encephalitozoon Cuniculi Methionine Aminopeptidase Type 2, PDB code: 3fm3:
Jump to Iron binding site number: 1; 2; 3; 4;

Iron binding site 1 out of 4 in 3fm3

Go back to Iron Binding Sites List in 3fm3
Iron binding site 1 out of 4 in the Crystal Structure of An Encephalitozoon Cuniculi Methionine Aminopeptidase Type 2


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 1 of Crystal Structure of An Encephalitozoon Cuniculi Methionine Aminopeptidase Type 2 within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe451

b:46.1
occ:1.00
OD2 A:ASP141 2.2 27.5 1.0
OE2 A:GLU339 2.2 24.3 1.0
NE2 A:HIS210 2.4 41.2 1.0
O A:HOH498 2.9 39.3 1.0
OE1 A:GLU243 2.9 36.9 1.0
FE A:FE452 3.1 30.5 1.0
CD A:GLU339 3.2 22.5 1.0
CG A:ASP141 3.3 23.5 1.0
CD2 A:HIS210 3.3 41.5 1.0
CD A:GLU243 3.4 35.9 1.0
OE1 A:GLU339 3.4 22.0 1.0
CE1 A:HIS210 3.5 41.2 1.0
OE2 A:GLU243 3.6 38.5 1.0
OD1 A:ASP141 3.7 22.9 1.0
CB A:ALA241 4.0 28.3 1.0
CB A:ASP141 4.5 21.0 1.0
CG A:HIS210 4.5 41.3 1.0
CG A:GLU243 4.5 32.2 1.0
CG A:GLU339 4.6 20.0 1.0
ND1 A:HIS210 4.6 41.3 1.0
CB A:GLU243 4.7 30.1 1.0
OD2 A:ASP130 5.0 19.9 1.0

Iron binding site 2 out of 4 in 3fm3

Go back to Iron Binding Sites List in 3fm3
Iron binding site 2 out of 4 in the Crystal Structure of An Encephalitozoon Cuniculi Methionine Aminopeptidase Type 2


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 2 of Crystal Structure of An Encephalitozoon Cuniculi Methionine Aminopeptidase Type 2 within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe452

b:30.5
occ:1.00
OD1 A:ASP141 2.0 22.9 1.0
OE1 A:GLU339 2.1 22.0 1.0
OD1 A:ASP130 2.2 18.9 1.0
OD2 A:ASP130 2.6 19.9 1.0
CG A:ASP130 2.7 17.6 1.0
CG A:ASP141 2.8 23.5 1.0
O A:HOH498 2.8 39.3 1.0
OD2 A:ASP141 2.9 27.5 1.0
CD A:GLU339 3.0 22.5 1.0
FE A:FE451 3.1 46.1 1.0
OE2 A:GLU339 3.3 24.3 1.0
CZ A:PHE97 3.6 21.5 1.0
OE2 A:GLU243 3.9 38.5 1.0
CE1 A:PHE97 4.2 22.3 1.0
CB A:ASP130 4.2 16.2 1.0
CB A:ASP141 4.2 21.0 1.0
O A:HOH497 4.4 37.7 1.0
CG A:GLU339 4.4 20.0 1.0
NE2 A:GLN337 4.4 14.7 1.0
CD A:GLU243 4.4 35.9 1.0
CE2 A:PHE97 4.5 21.0 1.0
N A:SER142 4.6 19.1 1.0
O A:HOH412 4.6 29.7 1.0
CB A:ALA143 4.7 17.6 1.0
C A:ASP141 4.7 19.9 1.0
CA A:ASP141 4.8 20.5 1.0
OE1 A:GLU243 4.8 36.9 1.0
CB A:GLU339 4.8 18.9 1.0
CA A:ASP130 4.9 16.2 1.0
O A:SER142 4.9 18.6 1.0
C A:SER142 5.0 18.9 1.0

Iron binding site 3 out of 4 in 3fm3

Go back to Iron Binding Sites List in 3fm3
Iron binding site 3 out of 4 in the Crystal Structure of An Encephalitozoon Cuniculi Methionine Aminopeptidase Type 2


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 3 of Crystal Structure of An Encephalitozoon Cuniculi Methionine Aminopeptidase Type 2 within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Fe551

b:35.6
occ:1.00
NE2 B:HIS210 2.2 30.7 1.0
OE2 B:GLU339 2.3 20.8 1.0
O B:HOH537 2.3 31.9 1.0
OD2 B:ASP141 2.3 23.0 1.0
OE2 B:GLU243 2.7 27.9 1.0
CD2 B:HIS210 3.2 30.1 1.0
FE B:FE552 3.2 26.4 1.0
CD B:GLU339 3.2 19.8 1.0
CG B:ASP141 3.3 19.0 1.0
CE1 B:HIS210 3.3 29.9 1.0
CD B:GLU243 3.3 27.0 1.0
OE1 B:GLU339 3.5 22.5 1.0
OD1 B:ASP141 3.6 22.8 1.0
OE1 B:GLU243 3.8 28.5 1.0
CB B:ALA241 3.9 18.1 1.0
CG B:GLU243 4.2 22.7 1.0
CG B:HIS210 4.4 28.6 1.0
ND1 B:HIS210 4.4 30.9 1.0
CB B:ASP141 4.5 15.6 1.0
CG B:GLU339 4.6 15.7 1.0
NE2 B:HIS218 4.9 39.8 1.0
CB B:GLU243 5.0 20.3 1.0
OD2 B:ASP130 5.0 15.5 1.0

Iron binding site 4 out of 4 in 3fm3

Go back to Iron Binding Sites List in 3fm3
Iron binding site 4 out of 4 in the Crystal Structure of An Encephalitozoon Cuniculi Methionine Aminopeptidase Type 2


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 4 of Crystal Structure of An Encephalitozoon Cuniculi Methionine Aminopeptidase Type 2 within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Fe552

b:26.4
occ:1.00
OE1 B:GLU339 1.9 22.5 1.0
OD1 B:ASP130 2.1 11.7 1.0
OD1 B:ASP141 2.1 22.8 1.0
O B:HOH537 2.3 31.9 1.0
OD2 B:ASP130 2.5 15.5 1.0
CG B:ASP130 2.6 13.2 1.0
CD B:GLU339 2.9 19.8 1.0
CG B:ASP141 3.0 19.0 1.0
OD2 B:ASP141 3.2 23.0 1.0
FE B:FE551 3.2 35.6 1.0
OE2 B:GLU339 3.3 20.8 1.0
CZ B:PHE97 3.6 23.0 1.0
CB B:ASP130 4.1 13.1 1.0
CE1 B:PHE97 4.2 22.0 1.0
CG B:GLU339 4.2 15.7 1.0
OE1 B:GLU243 4.3 28.5 1.0
CB B:ASP141 4.4 15.6 1.0
NE2 B:GLN337 4.4 8.7 1.0
CE2 B:PHE97 4.5 22.8 1.0
CB B:ALA143 4.6 11.7 1.0
N B:SER142 4.7 13.7 1.0
C B:ASP141 4.7 14.4 1.0
CD B:GLU243 4.7 27.0 1.0
OE2 B:GLU243 4.8 27.9 1.0
CB B:GLU339 4.8 15.0 1.0
O B:SER142 4.8 12.4 1.0
CA B:ASP141 4.8 15.1 1.0
CA B:ASP130 4.8 13.7 1.0
C B:SER142 4.9 12.7 1.0

Reference:

J.J.Alvarado, A.Nemkal, J.M.Sauder, M.Russell, D.E.Akiyoshi, W.Shi, S.C.Almo, L.M.Weiss. Structure of A Microsporidian Methionine Aminopeptidase Type 2 Complexed with Fumagillin and Tnp-470. Mol.Biochem.Parasitol. V. 168 158 2009.
ISSN: ISSN 0166-6851
PubMed: 19660503
DOI: 10.1016/J.MOLBIOPARA.2009.07.008
Page generated: Tue Aug 5 01:12:30 2025

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