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Zinc in PDB 2fea: Crystal Structure of Mtnx Phosphatase From Bacillus Subtilis at 2.00 A Resolution

Protein crystallography data

The structure of Crystal Structure of Mtnx Phosphatase From Bacillus Subtilis at 2.00 A Resolution, PDB code: 2fea was solved by Joint Center For Structural Genomics (Jcsg), with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 22.95 / 2.00
Space group P 1 21 1
Cell size a, b, c (Å), α, β, γ (°) 59.013, 43.104, 109.553, 90.00, 98.91, 90.00
R / Rfree (%) 16 / 21.7

Other elements in 2fea:

The structure of Crystal Structure of Mtnx Phosphatase From Bacillus Subtilis at 2.00 A Resolution also contains other interesting chemical elements:

Magnesium (Mg) 2 atoms

Zinc Binding Sites:

The binding sites of Zinc atom in the Crystal Structure of Mtnx Phosphatase From Bacillus Subtilis at 2.00 A Resolution (pdb code 2fea). This binding sites where shown within 5.0 Angstroms radius around Zinc atom.
In total 2 binding sites of Zinc where determined in the Crystal Structure of Mtnx Phosphatase From Bacillus Subtilis at 2.00 A Resolution, PDB code: 2fea:
Jump to Zinc binding site number: 1; 2;

Zinc binding site 1 out of 2 in 2fea

Go back to Zinc Binding Sites List in 2fea
Zinc binding site 1 out of 2 in the Crystal Structure of Mtnx Phosphatase From Bacillus Subtilis at 2.00 A Resolution


Mono view


Stereo pair view

A full contact list of Zinc with other atoms in the Zn binding site number 1 of Crystal Structure of Mtnx Phosphatase From Bacillus Subtilis at 2.00 A Resolution within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Zn1302

b:40.4
occ:1.00
SG A:CYS139 2.2 38.7 1.0
SG A:CYS143 2.3 39.4 1.0
SG A:CYS150 2.4 39.6 1.0
SG A:CYS147 2.4 41.1 1.0
CB A:CYS150 3.2 35.8 1.0
CB A:CYS139 3.3 37.6 1.0
CB A:CYS143 3.3 38.0 1.0
CB A:CYS147 3.4 41.2 1.0
CA A:CYS139 3.9 36.5 1.0
CA A:CYS150 4.0 37.1 1.0
N A:CYS147 4.2 41.7 1.0
N A:ASN145 4.4 50.3 1.0
CA A:CYS147 4.4 40.8 1.0
N A:CYS139 4.5 39.4 1.0
CA A:CYS143 4.5 37.8 1.0
C A:CYS143 4.6 39.4 1.0
O A:HOH1334 4.6 34.2 1.0
CB A:ASN145 4.6 47.9 1.0
OG A:SER153 4.7 33.4 1.0
N A:GLN146 4.8 48.0 1.0
CA A:ASN145 4.8 49.3 1.0
O A:CYS143 4.9 38.0 1.0
C A:ASN145 4.9 48.4 1.0
C A:CYS150 4.9 36.7 1.0
N A:SER144 4.9 42.2 1.0
CD A:PRO152 5.0 39.5 1.0

Zinc binding site 2 out of 2 in 2fea

Go back to Zinc Binding Sites List in 2fea
Zinc binding site 2 out of 2 in the Crystal Structure of Mtnx Phosphatase From Bacillus Subtilis at 2.00 A Resolution


Mono view


Stereo pair view

A full contact list of Zinc with other atoms in the Zn binding site number 2 of Crystal Structure of Mtnx Phosphatase From Bacillus Subtilis at 2.00 A Resolution within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Zn2302

b:41.4
occ:1.00
SG B:CYS143 2.3 40.2 1.0
SG B:CYS139 2.4 38.3 1.0
SG B:CYS150 2.4 35.6 1.0
SG B:CYS147 2.4 40.7 1.0
CB B:CYS150 3.1 35.8 1.0
CB B:CYS143 3.2 40.0 1.0
CB B:CYS139 3.4 40.6 1.0
CB B:CYS147 3.4 37.9 1.0
OD1 B:ASN145 3.7 63.2 1.0
CA B:CYS139 3.9 37.1 1.0
CA B:CYS150 4.0 36.5 1.0
N B:CYS147 4.2 41.0 1.0
CA B:CYS147 4.4 39.0 1.0
CA B:CYS143 4.5 41.9 1.0
OG B:SER153 4.6 37.1 1.0
N B:CYS139 4.6 37.3 1.0
C B:CYS143 4.6 43.3 1.0
N B:ASN145 4.7 48.7 1.0
CG B:ASN145 4.7 53.4 1.0
O B:HOH2451 4.7 55.0 1.0
N B:GLN146 4.7 42.6 1.0
O B:CYS143 4.8 44.8 1.0
C B:CYS150 4.9 36.3 1.0
C B:ASN145 5.0 45.2 1.0
O B:HOH2360 5.0 39.9 1.0

Reference:

Q.Xu, K.S.Saikatendu, S.S.Krishna, D.Mcmullan, P.Abdubek, S.Agarwalla, E.Ambing, T.Astakhova, H.L.Axelrod, D.Carlton, H.J.Chiu, T.Clayton, M.Didonato, L.Duan, M.A.Elsliger, J.Feuerhelm, S.K.Grzechnik, J.Hale, E.Hampton, G.W.Han, J.Haugen, L.Jaroszewski, K.K.Jin, H.E.Klock, M.W.Knuth, E.Koesema, M.D.Miller, A.T.Morse, E.Nigoghossian, L.Okach, S.Oommachen, J.Paulsen, R.Reyes, C.L.Rife, R.Schwarzenbacher, H.Van Den Bedem, A.White, G.Wolf, K.O.Hodgson, J.Wooley, A.M.Deacon, A.Godzik, S.A.Lesley, I.A.Wilson. Crystal Structure of Mtnx Phosphatase From Bacillus Subtilis at 2.0 A Resolution Provides A Structural Basis For Bipartite Phosphomonoester Hydrolysis of 2-Hydroxy-3-Keto-5-Methylthiopentenyl-1-Phosphate. Proteins V. 69 433 2007.
ISSN: ISSN 0887-3585
PubMed: 17654724
DOI: 10.1002/PROT.21602
Page generated: Wed Oct 16 23:45:06 2024

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