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Ligands
Code Name Style Show Link
CIY (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enal
EDO 1,2-ethanediol
FER 3-(4-hydroxy-3-methoxyphenyl)-2-propenoic acid
GJK (~{E})-4-(3-methoxy-4-oxidanyl-phenyl)but-3-en-2-one
SO4 Sulfate ion
V55 4-hydroxy-3-methoxybenzaldehyde
Non-standard Residues
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Code : 6HOP   PDBj   RCSB PDB   PDBe
Header : TRANSFERASE
Title : Human protein kinase CK2 alpha in complex with curcumin degradation products
Release Data : 2019-10-02
Compound :
mol_id molecule chains synonym
1 Casein kinase II subunit alpha A CK II alpha
ec: 2.7.11.1
fragment: kinase domain (residues 1-337)
Source :
mol_id organism_scientific organism_common expression_system
1 Homo sapiens  (taxid:9606) Human Escherichia coli  (taxid:562)
gene: CSNK2A1, CK2A1
Authors : Battistutta, R., Lolli, G.
Keywords : kinase domain, transferase
Exp. method : X-RAY DIFFRACTION ( 1.5500 Å )
Citation :

Biochemical and cellular mechanism of protein kinase CK2 inhibition by deceptive curcumin.

Cozza, G.,Zonta, F.,Dalle Vedove, A.  et al.
(2020)  Febs J.  287 : 1850 - 1864

PubMed: 31661600
DOI: 10.1111/febs.15111

Chain : A
UniProt : P68400 (CSK21_HUMAN)
Reaction: EC: Evidence:
Physiological Direction:
ATP + L-seryl-[protein] = ADP + H(+) + O-phospho-L-seryl- [protein] 2.7.11.1 PubMed:20545769, PubMed:20625391, PubMed:21482717, PubMed:22184066, PubMed:23123191, PubMed:30699359, PubMed:30898438, PubMed:31439799
left-to-right PubMed:20545769, PubMed:21482717, PubMed:23123191, PubMed:30699359, PubMed:30898438, PubMed:31439799, PubMed:35597237
ATP + L-threonyl-[protein] = ADP + H(+) + O-phospho-L- threonyl-[protein] 2.7.11.1 PubMed:20625391, PubMed:22325354, PubMed:31439799
left-to-right PubMed:31439799