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Manganese in PDB 3wzh: Crystal Structure of AFCSX3

Protein crystallography data

The structure of Crystal Structure of AFCSX3, PDB code: 3wzh was solved by Y.A.Yuan, X.Yan, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 22.88 / 3.31
Space group P 32 2 1
Cell size a, b, c (Å), α, β, γ (°) 86.726, 86.726, 112.529, 90.00, 90.00, 120.00
R / Rfree (%) 22.1 / 25.7

Manganese Binding Sites:

The binding sites of Manganese atom in the Crystal Structure of AFCSX3 (pdb code 3wzh). This binding sites where shown within 5.0 Angstroms radius around Manganese atom.
In total 5 binding sites of Manganese where determined in the Crystal Structure of AFCSX3, PDB code: 3wzh:
Jump to Manganese binding site number: 1; 2; 3; 4; 5;

Manganese binding site 1 out of 5 in 3wzh

Go back to Manganese Binding Sites List in 3wzh
Manganese binding site 1 out of 5 in the Crystal Structure of AFCSX3


Mono view


Stereo pair view

A full contact list of Manganese with other atoms in the Mn binding site number 1 of Crystal Structure of AFCSX3 within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Mn201

b:33.1
occ:1.00
NZ A:LYS58 3.1 31.1 1.0
OE2 B:GLU85 3.4 26.5 1.0
NE2 A:HIS57 3.5 30.2 1.0
CD2 A:HIS57 4.4 28.3 1.0
CE1 A:HIS57 4.4 31.4 1.0
CD B:GLU85 4.4 25.7 1.0
CE A:LYS58 4.5 29.4 1.0
OE1 B:GLU85 4.6 28.0 1.0
CD A:LYS58 4.8 28.7 1.0

Manganese binding site 2 out of 5 in 3wzh

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Manganese binding site 2 out of 5 in the Crystal Structure of AFCSX3


Mono view


Stereo pair view

A full contact list of Manganese with other atoms in the Mn binding site number 2 of Crystal Structure of AFCSX3 within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Mn202

b:60.2
occ:1.00
CE1 A:HIS80 3.6 56.1 1.0
NE2 A:HIS80 3.7 53.1 1.0
ND1 A:HIS60 3.9 37.0 1.0
NE2 B:HIS60 3.9 38.0 1.0
CE1 B:HIS57 4.0 31.7 1.0
CD2 B:HIS60 4.3 35.5 1.0
O A:HIS60 4.3 36.9 1.0
CE1 B:HIS60 4.5 36.6 1.0
OE1 A:GLN78 4.7 36.7 1.0
ND1 B:HIS57 4.7 29.5 1.0
ND1 A:HIS80 4.7 56.6 1.0
CE1 A:HIS60 4.8 37.8 1.0
CB A:HIS60 4.8 32.4 1.0
CG A:HIS60 4.8 33.8 1.0
CD2 A:HIS80 4.9 51.5 1.0
NE2 B:HIS57 5.0 31.7 1.0

Manganese binding site 3 out of 5 in 3wzh

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Manganese binding site 3 out of 5 in the Crystal Structure of AFCSX3


Mono view


Stereo pair view

A full contact list of Manganese with other atoms in the Mn binding site number 3 of Crystal Structure of AFCSX3 within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Mn201

b:44.2
occ:1.00
NH1 B:ARG84 3.5 30.3 1.0
CD B:ARG84 3.8 25.6 1.0
N B:GLU85 3.8 21.1 1.0
CD B:GLU85 3.9 25.7 1.0
OE1 B:GLU85 3.9 28.0 1.0
CB B:GLU85 4.0 22.7 1.0
CG B:GLU85 4.0 22.8 1.0
OE2 B:GLU85 4.3 26.5 1.0
CA B:ARG84 4.3 21.9 1.0
CB B:ARG84 4.3 23.1 1.0
CZ B:ARG84 4.4 29.8 1.0
NE B:ARG84 4.5 27.6 1.0
CA B:GLU85 4.6 20.9 1.0
C B:ARG84 4.6 20.6 1.0
CG B:ARG84 4.7 24.0 1.0
OG B:SER79 5.0 27.0 1.0

Manganese binding site 4 out of 5 in 3wzh

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Manganese binding site 4 out of 5 in the Crystal Structure of AFCSX3


Mono view


Stereo pair view

A full contact list of Manganese with other atoms in the Mn binding site number 4 of Crystal Structure of AFCSX3 within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Mn202

b:49.6
occ:1.00
NZ B:LYS58 3.2 35.2 1.0
NE2 B:HIS57 3.8 31.7 1.0
CE B:LYS58 4.5 33.0 1.0
CE1 B:HIS57 4.6 31.7 1.0
CD2 B:HIS57 4.7 29.5 1.0
CD B:LYS58 4.9 30.5 1.0

Manganese binding site 5 out of 5 in 3wzh

Go back to Manganese Binding Sites List in 3wzh
Manganese binding site 5 out of 5 in the Crystal Structure of AFCSX3


Mono view


Stereo pair view

A full contact list of Manganese with other atoms in the Mn binding site number 5 of Crystal Structure of AFCSX3 within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Mn203

b:61.6
occ:1.00
CE1 B:HIS80 3.4 42.3 1.0
O B:HOH312 3.6 8.4 1.0
NE2 B:HIS80 3.6 40.6 1.0
CE1 A:HIS60 3.7 37.8 1.0
CD2 B:HIS60 3.9 35.5 1.0
CE1 A:HIS57 4.0 31.4 1.0
ND1 A:HIS60 4.2 37.0 1.0
O B:HIS60 4.2 31.4 1.0
NE2 A:HIS60 4.4 35.5 1.0
ND1 B:HIS80 4.6 41.6 1.0
CG B:HIS60 4.6 33.1 1.0
ND1 A:HIS57 4.6 30.2 1.0
CB B:HIS60 4.6 30.2 1.0
NE2 B:GLN78 4.8 29.6 1.0
CD2 B:HIS80 4.9 38.6 1.0
NE2 B:HIS60 5.0 38.0 1.0

Reference:

X.Yan, W.Guo, Y.A.Yuan. Crystal Structures of Crispr-Associated CSX3 Reveal A Manganese-Dependent Deadenylation Exoribonuclease Rna Biol. 2015.
ISSN: ESSN 1555-8584
PubMed: 26106927
DOI: 10.1080/15476286.2015.1051300
Page generated: Sat Oct 5 18:31:09 2024

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