Overview
| Uniprot ID | Q53ET0 |
| Protein Name | CREB-regulated transcription coactivator 2 |
| Gene Name | CRTC2 |
| Organism | Homo sapiens |
Kla Sites from experimental identification
| Position |
Flanking peptide |
| 25 |
NPRKFSEKIALQKQR |
| 56 |
STRLQAQKLRLAYTR |
Function
Transcriptional coactivator for CREB1 which activates transcription through both consensus and variant cAMP response element (CRE) sites. Acts as a coactivator, in the SIK/TORC signaling pathway, being active when dephosphorylated and acts independently of CREB1 'Ser-133' phosphorylation. Enhances the interaction of CREB1 with TAF4. Regulates gluconeogenesis as a component of the LKB1/AMPK/TORC2 signaling pathway. Regulates the expression of specific genes such as the steroidogenic gene, StAR. Potent coactivator of PPARGC1A and inducer of mitochondrial biogenesis in muscle cells. Also coactivator for TAX activation of the human T-cell leukemia virus type 1 (HTLV-1) long terminal repeats (LTR)
Protein Sequence
10
MATSGANGPG
20
SATASASNPR
30
KFSEKIALQK
40
QRQAEETAAF
50
EEVMMDIGST
60
RLQAQKLRLA
70
YTRSSHYGGS
80
LPNVNQIGSG
90
LAEFQSPLHS
100
PLDSSRSTRH
110
HGLVERVQRD
120
PRRMVSPLRR
130
YTRHIDSSPY
140
SPAYLSPPPE
150
SSWRRTMAWG
160
NFPAEKGQLF
170
RLPSALNRTS
180
SDSALHTSVM
190
NPSPQDTYPG
200
PTPPSILPSR
210
RGGILDGEMD
220
PKVPAIEENL
230
LDDKHLLKPW
240
DAKKLSSSSS
250
RPRSCEVPGI
260
NIFPSPDQPA
270
NVPVLPPAMN
280
TGGSLPDLTN
290
LHFPPPLPTP
300
LDPEETAYPS
310
LSGGNSTSNL
320
THTMTHLGIS
330
RGMGLGPGYD
340
APGLHSPLSH
350
PSLQSSLSNP
360
NLQASLSSPQ
370
PQLQGSHSHP
380
SLPASSLARH
390
VLPTTSLGHP
400
SLSAPALSSS
410
SSSSSTSSPV
420
LGAPSYPAST
430
PGASPHHRRV
440
PLSPLSLLAG
450
PADARRSQQQ
460
LPKQFSPTMS
470
PTLSSITQGV
480
PLDTSKLSTD
490
QRLPPYPYSS
500
PSLVLPTQPH
510
TPKSLQQPGL
520
PSQSCSVQSS
530
GGQPPGRQSH
540
YGTPYPPGPS
550
GHGQQSYHRP
560
MSDFNLGNLE
570
QFSMESPSAS
580
LVLDPPGFSE
590
GPGFLGGEGP
600
MGGPQDPHTF
610
NHQNLTHCSR
620
HGSGPNIILT
630
GDSSPGFSKE
640
IAAALAGVPG
650
FEVSAAGLEL
660
GLGLEDELRM
670
EPLGLEGLNM
680
LSDPCALLPD
690
PAVEESFRSD
RLQ
Gene Ontology
| Classification |
GO ID |
Description |
| Cellular Component |
GO:0005737 |
cytoplasm |
| Cellular Component |
GO:0070062 |
extracellular exosome |
| Cellular Component |
GO:0005654 |
nucleoplasm |
| Cellular Component |
GO:0005634 |
nucleus |
| Molecular Function |
GO:0008140 |
cAMP response element binding protein binding |
| Molecular Function |
GO:0003713 |
transcription coactivator activity |
| Biological Process |
GO:0071320 |
cellular response to cAMP |
| Biological Process |
GO:0006351 |
DNA-templated transcription |
| Biological Process |
GO:0006094 |
gluconeogenesis |
| Biological Process |
GO:0042593 |
glucose homeostasis |
| Biological Process |
GO:0045944 |
positive regulation of transcription by RNA polymerase II |
| Biological Process |
GO:0051289 |
protein homotetramerization |
Reference
[1] Wu Q, Li Z, Gong T, Zheng X, Zhou X et al.. Porphyromonas gingivalis infection induces lysine lactylation reprogramming in human umbilical vein endothelial cells.. Front Cell Infect Microbiol 16:1706727. 2026. PMID: 41696360.