9EMY | pdb_00009emy

P. falciparum FIKK13 in complex with ATPgammaS


Experimental Data Snapshot

  • Method: X-RAY DIFFRACTION
  • Resolution: 2.81 Å
  • R-Value Free: 
    0.286 (Depositor), 0.286 (DCC) 
  • R-Value Work: 
    0.242 (Depositor), 0.242 (DCC) 

Starting Model: in silico
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wwPDB Validation   3D Report Full Report


Ligand Structure Quality Assessment 


This is version 1.0 of the entry. See complete history


Literature

Evolution and inhibition of the FIKK effector kinase family in P. falciparum

Purkiss, A.G.Ogrodowicz, R.W.Christodoulou, E.Kjaer, S.Belda, H.Bradley, D.Nofal, S.D.Broncel, M.Jones, D.A.Davies, H.Bertran, M.T.Joshi, D.OReilly, N.Walport, L.Claessens, A.Powell, A.J.House, D.Landry, C.R.

To be published.

Macromolecules
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Entity ID: 1
MoleculeChains Sequence LengthOrganismDetailsImage
non-specific serine/threonine protein kinase
A, B, G, H
413Plasmodium falciparumMutation(s): 0 
Gene Names: CK202_4380CYL21_5595
EC: 2.7.11.1
UniProt
Find proteins for A0A2I0BRS6 (Plasmodium falciparum (isolate NF54))
Explore A0A2I0BRS6 
Go to UniProtKB:  A0A2I0BRS6
Entity Groups  
Sequence Clusters30% Identity50% Identity70% Identity90% Identity95% Identity100% Identity
UniProt GroupA0A2I0BRS6
Sequence Annotations
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  • Reference Sequence
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Entity ID: 2
MoleculeChains Sequence LengthOrganismDetailsImage
Nanobody 9F10
C, D, I, J
136Lama glamaMutation(s): 0 
Entity Groups  
Sequence Clusters30% Identity50% Identity70% Identity90% Identity95% Identity100% Identity
Sequence Annotations
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  • Reference Sequence
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Entity ID: 3
MoleculeChains Sequence LengthOrganismDetailsImage
Nanobody 2G9
E, F, K, L
134Lama glamaMutation(s): 0 
Entity Groups  
Sequence Clusters30% Identity50% Identity70% Identity90% Identity95% Identity100% Identity
Sequence Annotations
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  • Reference Sequence
Experimental Data & Validation

Experimental Data

  • Method: X-RAY DIFFRACTION
  • Resolution: 2.81 Å
  • R-Value Free:  0.286 (Depositor), 0.286 (DCC) 
  • R-Value Work:  0.242 (Depositor), 0.242 (DCC) 
Space Group: P 1 21 1
Unit Cell:
Length ( Å )Angle ( ˚ )
a = 82.397α = 90
b = 121.657β = 90.02
c = 151.059γ = 90
Software Package:
Software NamePurpose
REFMACrefinement
DIALSdata reduction
Aimlessdata scaling
PHASERphasing

Structure Validation

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Ligand Structure Quality Assessment 


Entry History & Funding Information

Deposition Data


Funding OrganizationLocationGrant Number
The Francis Crick InstituteUnited Kingdom--

Revision History  (Full details and data files)

  • Version 1.0: 2025-03-26
    Type: Initial release