Atomistry » Magnesium » PDB 5y4j-5yls » 5yfm
Atomistry »
  Magnesium »
    PDB 5y4j-5yls »
      5yfm »

Magnesium in PDB 5yfm: Human Isocitrate Dehydrogenase 1 Bound with Nadp

Enzymatic activity of Human Isocitrate Dehydrogenase 1 Bound with Nadp

All present enzymatic activity of Human Isocitrate Dehydrogenase 1 Bound with Nadp:
1.1.1.42;

Protein crystallography data

The structure of Human Isocitrate Dehydrogenase 1 Bound with Nadp, PDB code: 5yfm was solved by P.Nordlund, D.Chen, A.Jansson, A.Larsson, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 100.50 / 2.40
Space group C 1 2 1
Cell size a, b, c (Å), α, β, γ (°) 203.020, 85.580, 86.070, 90.00, 98.08, 90.00
R / Rfree (%) 17.3 / 23.9

Magnesium Binding Sites:

The binding sites of Magnesium atom in the Human Isocitrate Dehydrogenase 1 Bound with Nadp (pdb code 5yfm). This binding sites where shown within 5.0 Angstroms radius around Magnesium atom.
In total 3 binding sites of Magnesium where determined in the Human Isocitrate Dehydrogenase 1 Bound with Nadp, PDB code: 5yfm:
Jump to Magnesium binding site number: 1; 2; 3;

Magnesium binding site 1 out of 3 in 5yfm

Go back to Magnesium Binding Sites List in 5yfm
Magnesium binding site 1 out of 3 in the Human Isocitrate Dehydrogenase 1 Bound with Nadp


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 1 of Human Isocitrate Dehydrogenase 1 Bound with Nadp within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Mg502

b:24.2
occ:1.00
OD1 A:ASP275 2.1 14.3 1.0
OD2 A:ASP279 2.3 15.7 1.0
O A:ASP275 2.4 17.1 1.0
OD2 B:ASP252 2.4 15.6 1.0
CG A:ASP279 3.2 16.2 1.0
CG A:ASP275 3.2 15.0 1.0
C A:ASP275 3.3 15.5 1.0
CG B:ASP252 3.4 16.4 1.0
OD1 A:ASP279 3.4 16.1 1.0
CA A:ASP275 3.7 15.0 1.0
CB B:ASP252 3.9 15.1 1.0
CB A:ASP275 4.0 14.7 1.0
OD2 A:ASP275 4.0 13.8 1.0
OD1 B:ASP252 4.4 16.2 1.0
CB A:ASP279 4.5 16.1 1.0
N A:VAL276 4.5 15.1 1.0
NH1 A:ARG132 4.9 14.8 1.0
OG A:SER278 4.9 16.8 1.0
CA A:VAL276 5.0 15.8 1.0

Magnesium binding site 2 out of 3 in 5yfm

Go back to Magnesium Binding Sites List in 5yfm
Magnesium binding site 2 out of 3 in the Human Isocitrate Dehydrogenase 1 Bound with Nadp


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 2 of Human Isocitrate Dehydrogenase 1 Bound with Nadp within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Mg502

b:33.2
occ:1.00
OD1 B:ASP275 2.3 12.8 1.0
OD2 A:ASP252 2.3 16.7 1.0
OD2 B:ASP279 2.3 14.4 1.0
O B:ASP275 2.9 17.4 1.0
CG A:ASP252 3.2 14.7 1.0
CG B:ASP279 3.3 14.7 1.0
CG B:ASP275 3.4 13.8 1.0
OD1 B:ASP279 3.5 14.2 1.0
CB A:ASP252 3.6 14.3 1.0
C B:ASP275 4.0 16.1 1.0
OD2 B:ASP275 4.1 12.3 1.0
OD1 A:ASP252 4.2 14.7 1.0
CA B:ASP275 4.5 14.3 1.0
CB B:ASP275 4.5 13.8 1.0
CB B:ASP279 4.6 14.7 1.0
NZ A:LYS212 4.8 11.8 1.0
CA A:ASP252 4.9 14.1 1.0

Magnesium binding site 3 out of 3 in 5yfm

Go back to Magnesium Binding Sites List in 5yfm
Magnesium binding site 3 out of 3 in the Human Isocitrate Dehydrogenase 1 Bound with Nadp


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 3 of Human Isocitrate Dehydrogenase 1 Bound with Nadp within 5.0Å range:
probe atom residue distance (Å) B Occ
C:Mg502

b:32.8
occ:1.00
OD1 C:ASP275 2.2 27.9 1.0
OD2 C:ASP279 2.2 25.1 1.0
O C:ASP275 3.0 25.9 1.0
CG C:ASP279 3.1 24.3 1.0
O C:HOH669 3.2 32.2 1.0
OD1 C:ASP279 3.3 25.9 1.0
CG C:ASP275 3.4 24.0 1.0
C C:ASP275 3.7 21.5 1.0
CA C:ASP275 4.0 21.2 1.0
OD2 C:ASP275 4.1 25.0 1.0
CB C:ASP275 4.3 22.4 1.0
CB C:ASP279 4.4 23.8 1.0
O C:HOH683 4.8 22.7 1.0
N C:VAL276 4.8 20.0 1.0

Reference:

P.Nordlund, D.Chen, A.Jansson, A.Larsson. Human Isocitrate Dehydrogenase 1 Bound with Nadp To Be Published.
Page generated: Mon Sep 30 11:07:03 2024

Last articles

Zn in 9JYW
Zn in 9IR4
Zn in 9IR3
Zn in 9GMX
Zn in 9GMW
Zn in 9JEJ
Zn in 9ERF
Zn in 9ERE
Zn in 9EGV
Zn in 9EGW
© Copyright 2008-2020 by atomistry.com
Home   |    Site Map   |    Copyright   |    Contact us   |    Privacy