ID.9

235AA LONG HYPOTHETICAL BIOTIN--[ACETYL-COA-CARBOXYLASE] LIGASE


PDB

The ligand-free form

2hni_AB [Alignment: 1 2]

The ligand-bound form

2dth_AB[Alignment: 1 2]


View

Animations of

the structural change



Using Jmol


Function

EC*1

CSA distance*2

6.3.4.15

2.6

*1 Enzyme commission number.
*2 The distance between the active site annotated in CSA23 and the ligand-binding sites.


Ligand

PDB*1

Full name

2xADP,2xBTN

2x(ADENOSINE-5'-DIPHOSPHATE),2x(BIOTIN)

*1 Ligand name designated by the PDB identifiers.


Segments

Component No.

Fixed*1

Moving*1

Motion type

Ligand binding

Coupled motion type

1

D1(3A-4A,10A-12A,5B-110B,112B-233B)

D2(5A-9A,13A-48A,54A-110A,112A-235A,1B-4B)

Domain

Independent

2

D1

L3(227B-233B)

Local

Independent

3

D2

L4(48A-54A)

Local

Coupled

Closure

*1 The location of the fixed and moving segments indicated by the residue number assigned in the ligand-bound form. The background color of characters indicates the corresponding segment in the structure. The colored segments not described in the Table are: 1) a part of component in which the motion is small (< 1.0 A), or, 2) a part of a protomer of homodimers, for which a corresponding part of the other protomer is shown in the Table.


Displacement and disorder

Component No.

RMSD*1

Displacement*2

Disorder-order transition*3

Disorder residue*4

Helix-Coil*5

1

1.4

2

5.5

3

Yes

+5

*1 The root-mean-square displacement of a component of motion calculated for the domain motions.
*2 The mean displacement of a component of motion calculated for the local motions.
*3 Order-disorder transition: Whether the open form contains the disordered structure.
*4 The number of disordered residues.
*5 The number of residues exhibiting the alpha-helix to coil transition.


Crystal environment

Component No.

Open state*1

Crystal packing*2

1

Free

Coupled

2

Bound

Coupled

3

*1 Distinction between the open state and the closed state required for examining the influence of the crystal environment.
*2 Crystal packing: Whether the change in the crystal environment is coupled with the structural change.


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