P16220

PTMD Annotation Information


※ Protein Information

Tag Content
UniProt Accession CREB1_HUMAN; P16220;
Entrez ID 1385
GenBank Protein ID NM_004379.4; NM_134442.4; XM_011510645.1; XM_011510647.2;
GenBank Nucleotide ID NP_004370.1; NP_604391.1; XP_011508947.1; XP_011508949.1;
Protein Name Cyclic AMP-responsive element-binding protein 1 (CREB-1) (cAMP-responsive element-binding protein 1)
Gene Name CREB1
Organism Homo sapiens
NCBI Taxa ID 9606
Functional DescriptionPhosphorylation-dependent transcription factor that stimulates transcription upon binding to the DNA cAMP response element (CRE), a sequence present in many viral and cellular promoters. Transcription activation is enhanced by the TORC coactivators which act independently of Ser-133 phosphorylation. Involved in different cellular processes including the synchronization of circadian rhythmicity and the differentiation of adipose cells.
Sequence
(Fasta)
MTMESGAENQ QSGDAAVTEA ENQQMTVQAQ PQIATLAQVS MPAAHATSSA PTVTLVQLPN 60
GQTVQVHGVI QAAQPSVIQS PQVQTVQSSC KDLKRLFSGT QISTIAESED SQESVDSVTD 120
SQKRREILSR RPSYRKILND LSSDAPGVPR IEEEKSEEET SAPAITTVTV PTPIYQTSSG 180
QYIAITQGGA IQLANNGTDG VQGLQTLTMT NAAATQPGTT ILQYAQTTDG QQILVPSNQV 240
VVQAASGDVQ TYQIRTAPTS TIAPGVVMAS SPALPTQPAE EAARKREVRL MKNREAAREC 300
RRKKKEYVKC LENRVAVLEN QNKTLIEELK ALKDLYCHKS D 342

※ PTM-Disease Association

NumPTMDiseaseCell TypeTypePTM SitePMID
1PhosphorylationAlzheimer's diseaseP24523906
[Reference]: These data suggest that NaHS may preferentially suppress AC activity when it was stimulated. In conclusion, H2S attenuated HENECA induced A42 production in SH-SY5Y neuroblastoma cells through inhibiting -secretase via a cAMP dependent pathway.
2PhosphorylationNeuroblastomaP10366032
[Reference]: We report here that chronic, but not acute treatment with lithium chloride in human neuroblastoma SH-SY5Y cells, inhibits phosphorylation of cyclic AMP responsive element binding protein and cyclic AMP responsive element DNA binding induced by the adenylyl cyclase activator forskolin, but has no effect on constitutive expression of cyclic AMP responsive element binding protein.
3Serine PhosphorylationProstate cancer/carcinoma/adenocarcinomaUS12912900420
[Reference]: This study also demonstrated for the first time that expression of constitutively active GSK-3betadelta9 results in the phosphorylation of CRE-binding protein on serine 129 and enhancement of CRE-mediated transcription in intact cell nuclei.
4Serine PhosphorylationAlzheimer's diseaseDS13323266915
[Reference]: We found that 17-estradiol protected PC12 cells from A1?
5Serine PhosphorylationProstate cancer/carcinoma/adenocarcinomaPS13322710715
[Reference]: Decreased tumorigenicity correlated with decreased expression of CREB and its targets, including Bcl-2 and cyclin A1
6Serine PhosphorylationDuodenal cancerPS13312220644
[Reference]: Here, we demonstrated hGRP-R activation stimulated sustained cyclic AMP response element binding protein (CREB) phosphorylation and transactivation in duodenal cancer cells through a protein kinase C and partially p38 mitogen-activated protein kinase-dependent pathway.

※ Disease Cross-ref Annotation

DatabaseAnnotation
Cancer Gene Census
clear cell sarcoma, angiomatoid fibrous histiocytoma
CTD (Curated)
(count: 5)
MESH:D019970 ; Cocaine-Related Disorders
MESH:C563181 ; Histiocytoma, Angiomatoid Fibrous
MESH:D009021 ; Morphine Dependence
MESH:D009203 ; Myocardial Infarction
MESH:D013375 ; Substance Withdrawal Syndrome
DisGeNet (Curated)
(count: 16)
(view all)
C0001973; Alcoholic Intoxication, Chronic
C0005586; Bipolar Disorder
C0011570; Mental Depression
C0011581; Depressive disorder
C0026552; Morphine Dependence
C0027051; Myocardial Infarction
HGMD
(count: 1)
CR083279; Increased promoter activity, association with; Regulatory
GWASdb
(count: 2)
rs2254137; Opioid sensitivity; drug dependence
rs1806584; Type 2 diabetes and 6 quantitative traits; type 2 diabetes mellitus

※ PTM Sites

PTM Modification Sites
Phosphorylation
(count: 17)
(view all)
100       LKRLFSGTQISTIAE     dbPAF
108       QISTIAESEDSQESV     dbPAF
111       TIAESEDSQESVDSV     dbPAF
114       ESEDSQESVDSVTDS     dbPAF
117       DSQESVDSVTDSQKR     dbPAF
119       QESVDSVTDSQKRRE     dbPAF
Acetylation
(count: 3)
136       SRRPSYRKILNDLSS     PLMD
91        QTVQSSCKDLKRLFS     PLMD
94        QSSCKDLKRLFSGTQ     PLMD
Ubiquitination
(count: 7)
(view all)
136       SRRPSYRKILNDLSS     PLMD
304       ARECRRKKKEYVKCL     PLMD
309       RKKKEYVKCLENRVA     PLMD
323       AVLENQNKTLIEELK     PLMD
330       KTLIEELKALKDLYC     PLMD
333       IEELKALKDLYCHKS     PLMD
Sumoylation
(count: 2)
285       PAEEAARKREVRLMK     PLMD
304       ARECRRKKKEYVKCL     PLMD

※ Protein-Protein Interaction

NetworkInteraction
ABSource
E9PG89P16220HPRD
H0YFA3P16220IntAct
O00470P16220IntAct
O60264P16220HPRD; MINT
O60869P16220HPRD
O75582P16220HPRD
O75676P16220HPRD
O75925P16220IntAct
O94762P16220HPRD; IntAct; MINT
O94842P16220IntAct
P00519P16220HPRD
P03165P16220MINT
P04150P16220HPRD
P08670P16220HPRD; IntAct; MINT
P0CG20P16220MINT
P10070P16220HPRD
P10827P16220HPRD
P11831P16220HPRD
P13984P16220HPRD
P16220P17676HPRD
P16220P18846HPRD
P16220P18850IntAct
P16220P31749HPRD
P16220P38398MINT
P16220P48436HPRD
P16220P49137HPRD
P16220P49841HPRD
P16220P50748BioGRID
P16220P51532MINT
P16220P51812HPRD
P16220P52655IntAct
P16220P52945HPRD
P16220P62820HPRD; IntAct; MINT
P16220P63279IntAct
P16220P68104BioGRID
P16220Q03060HPRD
P16220Q09472MINT
P16220Q12772IntAct
P16220Q12873IntAct; MINT
P16220Q13315HPRD
P16220Q13535IntAct
P16220Q13627HPRD
P16220Q13976HPRD
P16220Q15349HPRD
P16220Q15418IntAct;HPRD
P16220Q16539HPRD
P16220Q4LE28HPRD; DIP; MINT
P16220Q5HYC2IntAct
P16220Q5TD97HPRD
P16220Q6SA08HPRD; IntAct
P16220Q6UUV9IntAct
P16220Q6ZNA4IntAct
P16220Q7Z3K3IntAct
P16220Q86YV9HPRD; IntAct; MINT
P16220Q8IYT8IntAct
P16220Q92793IntAct
P16220Q92993HPRD
P16220Q96RG2MINT
P16220Q96RN5IntAct
P16220Q9H422IntAct
P16220Q9HBD4HPRD
P16220Q9HCK8IntAct
P16220Q9UBW7IntAct
P16220Q9UKR5HPRD; IntAct; MINT
P16220Q9UKY1IntAct
P16220Q9Y2W7HPRD
P16220Q9Y4E5IntAct