Modomics - A Database of RNA Modifications

ID Card:

Full name: nucleophosmin 1
Synonym: B23,NPM
GI: 114762
UniProt: P06748
Structures: | 2LLH | 2P1B | 2VXD | 5EHD | 7OBG | 7OBH |
Alpha Fold Predicted Structure: AF-P06748-F1


PDB Structures:


2LLH

Structure Description:

Title:
Classification:
Technique:

Abstract of the PDB Structure's related Publication:

Nucleophosmin (NPM1) is a nucleocytoplasmic shuttling protein, mainly localized at nucleoli, that plays a key role in several cellular functions, including ribosome maturation and export, centrosome duplication, and response to stress stimuli. More than 50 mutations at the terminal exon of the NPM1 gene have been identified so far in acute myeloid leukemia; the mutated proteins are aberrantly and stably localized in the cytoplasm due to high destabilization of the NPM1 C-terminal domain and the appearance of a new nuclear export signal. We have shown previously that the 70-residue NPM1 C-terminal domain (NPM1-C70) is able to bind with high affinity a specific region at the c-MYC gene promoter characterized by parallel G-quadruplex structure. Here we present the solution structure of the NPM1-C70 domain and NMR analysis of its interaction with a c-MYC-derived G-quadruplex. These data were used to calculate an experimentally restrained molecular docking model for the complex. The NPM1-C70 terminal three-helix bundle binds the G-quadruplex DNA at the interface between helices H1 and H2 through electrostatic interactions with the G-quadruplex phosphate backbone. Furthermore, we show that the 17-residue lysine-rich sequence at the N terminus of the three-helix bundle is disordered and, although necessary, does not participate directly in the contact surface in the complex.

Download RCSB-PDB Structures:

Pdb Files   2LLH.pdb   2P1B.pdb   2VXD.pdb   5EHD.pdb   7OBG.pdb   7OBH.pdb  
Pdbx/mmCIF Files   2LLH.cif   2P1B.cif   2VXD.cif   5EHD.cif   7OBG.cif   7OBH.cif  


Protein sequence:

MEDSMDMDMSPLRPQNYLFGCELKADKDYHFKVDNDENEHQLSLRTVSLGAGAKDELHIVEAEAMNYEGSPIKVTLATLKMSVQPTVSLGGFEITPPVVLRLKCGSGPVHISGQHLVAVEEDAESEDEEEEDVKLLSISGKRSAPGGGSKVPQKKVKLAADEDDDDDDEEDDDEDDDDDDFDDEEAEEKAPVKKSIRDTPAKNAQKSNQNGKDSKPSSTPRSKGQESFKKQEKTPKTPKGPSSVEDIKAKMQASIEKGGSLPKVEAKFINYVKNCFRMTDQEAIQDLWQWRKSL

Comments:

None





Alpha Fold Predicted Structure:






Clear Selection and Reset Camera

Protein sequence:

M E D S M D M D M S P L R P Q N Y L F G C E L K A D K D Y H F K V D N D E N E H Q L S L R T V S L G A G A K D E L H I V E A E A M N Y E G S P I K V T L A T L K M S V Q P T V S L G G F E I T P P V V L R L K C G S G P V H I S G Q H L V A V E E D A E S E D E E E E D V K L L S I S G K R S A P G G G S K V P Q K K V K L A A D E D D D D D D E E D D D E D D D D D D F D D E E A E E K A P V K K S I R D T P A K N A Q K S N Q N G K D S K P S S T P R S K G Q E S F K K Q E K T P K T P K G P S S V E D I K A K M Q A S I E K G G S L P K V E A K F I N Y V K N C F R M T D Q E A I Q D L W Q W R K S L

Secondary Structure Alphabet

  • G: 3-turn helix (310helix)
  • H: α-helix
  • I: 𝝅-helix (5 - turn helix)
  • T: Hydrogen Bonded Turn
  • B: β-sheet
  • S: Bend
  • C: Coil (residues not present in any of the above conformations)
  • N: Not assigned

Download PDB Structures & DSSP Secondary Structures:

Alpha Fold Pdb Files   AF-P06748-F1.pdb  
Alpha Fold Pdbx/mmCIF Files   AF-P06748-F1.cif  
DSSP Secondary Structures   P06748.dssp  





Diseases connected to this enzyme:

Description Reaction Disease Name
2′-O-Me-regulated translation is important for cellular growth, differentiation, and hematopoietic stem cell maintenance. Aberrant 2'O-Me is induced by mutations in NPM1 observed in patients with dyskeratosis congenita. N:Nm
Dyskeratosis Congenita

Publications:

Title Authors Journal Details PubMed Id DOI