Protein Information

Cytoscape View


UniProt AC / UniProt ID Q9H6R4 / NOL6_HUMAN
Protein Name Nucleolar protein 6
Gene Name Name: NOL6
Organism Homo sapiens (Human)

PRO ID PR:Q9H6R4
DAG View
PRO Name nucleolar protein 6 (human)
Definition A nucleolar protein 6 that is encoded in the genome of human.
Short Label hNOL6
Category organism-gene

Interactive Sequence View

Select/align proteoforms across species


Q9H6R4 (NOL6) as Substrate



Site PTM Type PTM Enzyme Score Source PMID
T27 Phosphorylation PhosphoSitePlus
T40 Phosphorylation PhosphoSitePlus
K47 Ubiquitination PhosphoSitePlus
K54 Ubiquitination PhosphoSitePlus
S56 Phosphorylation PhosphoSitePlus   UniProt 23186163
K62 Ubiquitination PhosphoSitePlus
K93 Ubiquitination PhosphoSitePlus
K149 Ubiquitination PhosphoSitePlus
K192 Ubiquitination PhosphoSitePlus
S283 Phosphorylation PhosphoSitePlus   UniProt 23186163
S289 Phosphorylation PhosphoSitePlus   UniProt 23186163
T294 Phosphorylation PhosphoSitePlus
T367 Phosphorylation PhosphoSitePlus
K490 Sumoylation PhosphoSitePlus
K611 Ubiquitination PhosphoSitePlus
C633 Methylation IEDB 31844290
K726 Ubiquitination PhosphoSitePlus
K788 Ubiquitination PhosphoSitePlus
K807 Ubiquitination PhosphoSitePlus
S811 Phosphorylation phospho.ELM   PhosphoSitePlus   UniProt 21406692, 23186163, 16565220, ...18669648, 20068231
T821 Phosphorylation PhosphoSitePlus
S824 Phosphorylation PhosphoSitePlus
S908 Phosphorylation PhosphoSitePlus
S1028 Phosphorylation PhosphoSitePlus
S1032 Phosphorylation PhosphoSitePlus
S1044 Phosphorylation PhosphoSitePlus
K1097 Methylation PhosphoSitePlus
Site PTM Type PTM Enzyme Score Source PMID
S283 Phosphorylation HPRD 19007248, 18452278, 19664995, ...19691289
S289 Phosphorylation HPRD 19413330, 19007248, 19691289
T294 Phosphorylation HPRD 18452278
S811 Phosphorylation HPRD 18669648, 16565220, 19691289, ...20068231, 19007248
Site PTM Type PTM Enzyme Score Source PMID
S283 Phosphorylation HPRD 19007248, 18452278, 19664995, ...19691289
S289 Phosphorylation HPRD 19413330, 19007248, 19691289
T294 Phosphorylation HPRD 18452278


PTM sites affected in variants

Site Variant Source PMID Disease [Sample source]
K62 T62 Biomuta DOID:5041 / esophageal cancer [ cosmic ]
S811 N811 Biomuta DOID:3571 / liver cancer [ cosmic, icgc ]
S824 F824 Biomuta DOID:4159 / skin cancer [ cosmic ]