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Ligands
Code Name Style Show Link
9JS 4-({5-[(3-hydroxy-4-methylphenyl)amino]-4-oxo-4h-1,2,6-thiadiazin-3-yl}amino)benzamide
MG Magnesium ion
Non-standard Residues
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Glycosylation
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Code : 5VT1   PDBj   RCSB PDB   PDBe
Header : Transferase/Transferase Inhibitor
Title : Crystal Structure of the Human CAMKK2B bound to a thiadiazinone benzamide inhibitor
Release Data : 2017-05-24
Compound :
mol_id molecule chains synonym
1 Calcium/calmodulin-dependent protein kinase kinase 2 A CaMKK 2,Calcium/calmodulin-dependent protein kinase kinase beta,CaMKK beta
ec: 2.7.11.17
fragment: UNP residues 161-449
Source :
mol_id organism_scientific organism_common expression_system
1 Homo sapiens  (taxid:9606) Human Escherichia coli  (taxid:469008)
gene: CAMKK2, CAMKKB, KIAA0787
expression_system_strain: BL21(DE3)
expression_system_variant: R3
expression_system_vector_type: plasmid
Authors : Counago, R.M., Asquith, C.R.M., Arruda, P., Edwards, A.M., Gileadi, O., Kalogirou, A.S., Koutentis, P.A., Structural Genomics Consortium (SGC)
Keywords : transferase, protein kinase domain, Structural Genomics, Structural Genomics Consortium, SGC, Transferase-Transferase Inhibitor Complex
Exp. method : X-RAY DIFFRACTION ( 1.90 Å )
Citation :

1,2,6-Thiadiazinones as Novel Narrow Spectrum Calcium/Calmodulin-Dependent Protein Kinase Kinase 2 (CaMKK2) Inhibitors.

Asquith, C.R.M.,Godoi, P.H.,Counago, R.M.  et al.
(2018)  Molecules  23

PubMed: 29783765
DOI: 10.3390/molecules23051221

Chain : A
UniProt : Q96RR4 (KKCC2_HUMAN)
Reaction: EC: Evidence:
Physiological Direction:
ATP + L-seryl-[protein] = ADP + H(+) + O-phospho-L-seryl- [protein] 2.7.11.17 -
-
ATP + L-threonyl-[protein] = ADP + H(+) + O-phospho-L- threonyl-[protein] 2.7.11.17 -
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