CAND1 (cullin associated and neddylation dissociated 1)

symbol:
CAND1
locus group:
protein-coding gene
location:
12q14.3-q15
gene_family:
alias symbol:
TIP120A|DKFZp434M1414|KIAA0829|TIP120
alias name:
TBP interacting protein
entrez id:
55832
ensembl gene id:
ENSG00000111530
ucsc gene id:
uc001stn.3
refseq accession:
NM_018448
hgnc_id:
HGNC:30688
approved reserved:
2005-05-24
12q14.3-q15

CAND1(Cullin-associated and neddylation-dissociated 1)是一个重要的调控蛋白,属于CAND蛋白家族,主要参与泛素-蛋白酶体系统的调控。CAND1的核心功能是与Cullin-RING泛素连接酶(CRLs)复合物相互作用,通过阻止Cullin蛋白的neddylation修饰来调控CRLs的组装和活性。CRLs是细胞内最大的泛素连接酶家族,负责靶向特定底物蛋白进行泛素化标记,进而通过蛋白酶体降解这些蛋白,从而调控多种细胞过程如细胞周期、信号转导和DNA修复等。CAND1通过结合未neddylated的Cullin蛋白,阻止其与底物适配器(如F-box蛋白或SOCS-box蛋白)的结合,从而负调控CRLs的活性。这种动态平衡对维持细胞内蛋白质稳态至关重要。CAND1的突变或表达异常可能导致CRLs功能紊乱,进而影响细胞增殖、分化或凋亡。例如,CAND1功能缺失可能导致CRLs过度激活,引发某些底物蛋白的异常降解,与肿瘤发生、神经退行性疾病或免疫失调相关。研究表明,CAND1在某些癌症中表达下调,可能通过破坏CRLs的正常调控促进肿瘤发展。相反,CAND1过表达可能抑制CRLs活性,导致细胞周期调控蛋白积累,影响细胞分裂。CAND1属于CAND基因家族,该家族成员通常含有TPR(tetratricopeptide repeat)结构域,介导蛋白质相互作用,并在CRLs调控中发挥类似功能。CAND1的TPR结构域是其与Cullin蛋白结合的关键区域,突变可能破坏这种相互作用,导致CRLs调控失衡。此外,CAND1的表达受细胞状态和环境信号影响,如DNA损伤或氧化应激可调节其水平,进一步影响CRLs的活性。总之,CAND1是CRLs动态组装和功能的重要调节因子,其表达或功能异常与多种疾病相关,尤其在癌症和神经退行性疾病中具有潜在的研究价值。

ChineseEnglish

None

Nucleotide sequence of CAND1:[NCBI]
Loading Gene Browser...
Protein Sequence
1MASASYHISN LLEKMTSSDK DFRFMATNDL MTELQKDSIK
41LDDDSERKVV KMILKLLEDK NGEVQNLAVK CLGPLVSKVK
81 EYQVETIVD TLCTNMLSDK EQLRDISSIG LKTVIGELPP
121ASSGSALAAN VCKKITGRLT SAIAKQEDVS VQLEALDIMA
161D MLSRQGGL LVNFHPSILT CLLPQLTSPR LAVRKRTIIA
201LGHLVMSCGN IVFVDLIEHL LSELSKNDSM STTRTYIQCI
241AA ISRQAGH RIGEYLEKII PLVVKFCNVD DDELREYCIQ
281AFESFVRRCP KEVYPHVSTI INICLKYLTY DPNYNYDDED
321EDE NAMDAD GGDDDDQGSD DEYSDDDDMS WKVRRAAAKC
361LDAVVSTRHE MLPEFYKTVS PALISRFKER EENVKADVFH
401AYLS LLKQT RPVQSWLCDP DAMEQGETPL TMLQSQVPNI
441VKALHKQMKE KSVKTRQCCF NMLTELVNVL PGALTQHIPV
481LVPGI IFSL NDKSSSSNLK IDALSCLYVI LCNHSPQVFH
521PHVQALVPPV VACVGDPFYK ITSEALLVTQ QLVKVIRPLD
561QPSSFD ATP YIKDLFTCTI KRLKAADIDQ EVKERAISCM
601GQIICNLGDN LGSDLPNTLQ IFLERLKNEI TRLTTVKALT
641LIAGSPL KI DLRPVLGEGV PILASFLRKN QRALKLGTLS
681ALDILIKNYS DSLTAAMIDA VLDELPPLIS ESDMHVSQMA
721ISFLTTLA K VYPSSLSKIS GSILNELIGL VRSPLLQGGA
761LSAMLDFFQA LVVTGTNNLG YMDLLRMLTG PVYSQSTALT
801HKQSYYSIA KCVAALTRAC PKEGPAVVGQ FIQDVKNSRS
841TDSIRLLALL SLGEVGHHID LSGQLELKSV ILEAFSSPSE
881EVKSAASYAL GSISVGNLP EYLPFVLQEI TSQPKRQYLL
921LHSLKEIISS ASVVGLKPYV ENIWALLLKH CECAEEGTRN
961VVAECLGKLT L IDPETLLP RLKGYLISGS SYARSSVVTA
1001VKFTISDHPQ PIDPLLKNCI GDFLKTLEDP DLNVRRVALV
1041TFNSAAHNKP SL IRDLLDT VLPHLYNETK VRKELIREVE
1081MGPFKHTVDD GLDIRKAAFE CMYTLLDSCL DRLDIFEFLN
1121HVEDGLKDHY DIK MLTFLM LVRLSTLCPS AVLQRLDRLV
1161EPLRATCTTK VKANSVKQEF EKQDELKRSA MRAVAALLTI
1201PEAEKSPLMS EFQS QISSN PELAAIFESI QKDSSSTNLE
1241SMDTS
结构预测来自 AlphaFold DB(UniProt: Q86VP6),颜色表示 pLDDT 置信度(深蓝高、黄橙低)。
SNP variants of CAND1:           Showing partial SNPs
rs710621       rs710622       rs710623       rs710629       rs710630       rs775306       rs775308       rs775309       rs775310       rs775311       rs775312       rs775625       rs775627       rs775628       rs775657       rs775658       rs775659      

Tissue expression of CAND1:    [UniProt]

Gene expression across tissues
Forward Primer
Forward Tm
Reverse Primer
Reverse Tm
Score
GATATCAGGCTCATCATATGCC
59
ATCAATAGGTTGTGGATGGTC
58
CAGAAAGATTCCATCAAGTTGG
58
CTAAAGGACCAAGACATTTGAC
57
GATATGTTGAGCAGGCAAGG
59
GTCTAGGGCTGGTCAACTG
60
CTGTCAAATGTCTTGGTCCT
58
AAAGCATGTTAGTGCAGAGG
59
AAGTTGGCTATGTGACCCT
59
ACAATGTTGGGAACCTGAC
58
CAAGGACTTTAGGTTTATGGCT
59
AGCTAAATTCTGTACCTCTCCA
59
TACCCTCTGCACTAACATGC
60
CTAATGCAGAGCCACTGGA
60
GGACTTTAGTTCCTCTTGTCAG
59
TTAAGATCCAGCAATCCACC
58
TTTGGTTCCTCCAGTGGTG
60
TATGATGAGCTTTGACAAGCTG
59
TGATATCAGGCTCATCATATGC
58
TCAATAGGTTGTGGATGGTC
57
      No data available

Subcellular localization of CAND1 (and its protein):

[UniProt]     [GenomeNet]

" d="M482.414,245.296c3.539,4.293,4.455,10.009,0.202,11 c-4.244,0.996-4.983-10.983-8.293-8.438c-5.271,4.08,9.834,12.271,5.144,17.287c-3.717,3.607-6.172-5.75-10.839-1.976 c-4.673,3.776,6.781,7.299,2.831,11.326c-4.354,4.045-6.979-1.449-9.837-5.517c-1.193-1.742-2.059-3.851-3.595-2.748 c-1.516,1.078-1.854,1.795-0.938,3.666c2.374,4.854,9.235,10.119,5.156,12.535c-5.636,3.346-5.044-8.871-9.426-7.574 c-4.388,1.291,2.557,10.66-1.245,11.141c-4.089,0.545-3.483-10.239-6.979-8.575c-2.522,1.206-0.929,3.071-0.938,4.899 c0.004,1.32-0.964,3.6-2.372,4.062c-3.593,1.171-8.544-1.065-10.251-3.59c-6.04-8.93,0.396-15.997,4.639-7.015 c3.023,4.642,5.182,0.834,2.839-2.219c-1.032-1.354-4.309-5.901-0.781-7.252c2.904-1.113,4.271,1.941,5.985,4.592 c2.61,4.016,5.485,0.117,3.031-3.414c-1.828-2.633-2.74-3.803,3.156-7.42c6.405-4.369,6.52,3.869,10.077,0.646 c2.309-1.832-4.783-5.149,0.06-8.995c2.896-2.293,5.18,6.207,7.961,3.516c3.523-2.737-7.717-7.369,0.117-11.736 C473.413,240.77,480.519,242.891,482.414,245.296z"/> Extracellular space Cytosol Plasma membrane Cytoskeleton Lysosome Endosome Peroxisome ER Golgi Apparatus Nucleus Mitochondrion 0 1 2 3 4 5 Confidence
  • plasma membrane
  • cytoplasm
  • extracellular
  • golgi
  • vesicle
  • cytoskeleton
  • endoplasmic reticulum
  • nucleus
  • endosome
  • lysosome
  • mitochondrion

Gene Ontology (GO) terms for CAND1:

GO ID
Protein
Source DB
GO:0000151
Q86VP6 (UniProtKB)
IDA
GO:0005515
Q86VP6 (UniProtKB)
IPI
GO:0005515
Q86VP6 (UniProtKB)
IPI
GO:0005515
Q86VP6 (UniProtKB)
IPI
GO:0005515
Q86VP6 (UniProtKB)
IPI
GO:0005515
Q86VP6 (UniProtKB)
IPI
GO:0005515
Q86VP6 (UniProtKB)
IPI
GO:0005515
Q86VP6 (UniProtKB)
IPI
GO:0005515
Q86VP6 (UniProtKB)
IPI
GO:0005515
Q86VP6 (UniProtKB)
IPI
GO:0005515
Q86VP6 (UniProtKB)
IPI
GO:0005515
Q86VP6 (UniProtKB)
IPI
GO:0005515
Q86VP6 (UniProtKB)
IPI
GO:0005515
Q86VP6 (UniProtKB)
IPI
GO:0005515
Q86VP6 (UniProtKB)
IPI
GO:0005515
Q86VP6 (UniProtKB)
IPI
GO:0005634
Q86VP6 (UniProtKB)
IDA
GO:0005634
Q86VP6 (UniProtKB)
IDA
GO:0005634
Q86VP6 (UniProtKB)
IDA
GO:0005654
Q86VP6 (UniProtKB)
IDA
GO:0005737
Q86VP6 (UniProtKB)
IDA
GO:0005737
Q86VP6 (UniProtKB)
IDA
GO:0005794
Q86VP6 (UniProtKB)
IDA
GO:0010265
Q86VP6 (UniProtKB)
IDA
GO:0010265
Q86VP6 (UniProtKB)
IDA
GO:0016020
Q86VP6 (UniProtKB)
IDA
GO:0016567
Q86VP6 (UniProtKB)
IDA
GO:0016567
Q86VP6 (UniProtKB)
IDA
GO:0016567
Q86VP6 (UniProtKB)
IDA
GO:0017025
Q86VP6 (UniProtKB)
IEA
GO:0030154
Q86VP6 (UniProtKB)
IDA
GO:0031461
Q86VP6 (UniProtKB)
IDA
GO:0031461
Q86VP6 (UniProtKB)
IDA
GO:0031461
Q86VP6 (UniProtKB)
IDA
GO:0043086
Q86VP6 (UniProtKB)
IDA
GO:0045899
Q86VP6 (UniProtKB)
IEA
GO:0070062
Q86VP6 (UniProtKB)
IDA
GO:0070062
Q86VP6 (UniProtKB)
IDA
GO:0070062
Q86VP6 (UniProtKB)
IDA

microRNAs potentially regulating CAND1:     

BioGrid
IntAct
mentha
MINT
Loading…
Interacting Gene Interaction Source/Score
Disease Score NofPmids NofSnps Source
Disease Score NofPmids NofSnps Source
Osteoporosis 0.002367032 1 1 GAD
Prostatic Neoplasms 0.000271442 1 0 BeFree
Malignant neoplasm of prostate 0.000271442 1 0 BeFree
Adenocarcinoma 0.000271442 1 0 BeFree
Prostate carcinoma 0.000271442 1 0 BeFree
Carcinogenesis 0.000271442 1 0 BeFree
Identification of Candidate Genes Associated with Growth Traits in Procambarus clarkii Using Whole-Genome Resequencing.
Li J, Hu P, Zhang H, Luo Y, Huang X, Wang D, Li J, Wang Z, Wang Y, Liu S Int J Mol Sci IF: 3.226 2026-08-29
Proximal Proteomics Reveals Potential Regulators of Programmed Death-Ligand 1 in Human Cancer.
Shi F, Liu D, Liu Y, Li F, Zhang CZ, Li Q, Tian QH ACS Omega IF: 5.2 2026-08-25
CAND1 drives intestinal ischemia/reperfusion injury via SCFFBXO6-PKM2-mediated mitochondrial fission and apoptosis.
Qiang M, Zhao Y, Wang G, Chen Z, Zhang F, Wang Z, Wang G, Zhuang C, Ning S, Yao J, Tian X Free Radic Biol Med IF: 8.0 2026-10-00
Identification of CAND1 as a DNA-dependent protein kinase-regulated coactivator of androgen receptor and the ARv7 splice variant.
Hamilton RA, Paul B, Yi P, Rajapakshe K, Panigrahi AK, Grimm SL, Coarfa C, Malovannaya A, Weigel NL, Lonard DM, Foulds CE PLoS One IF: 2.6 None
Integrated molecular mechanisms of salinity response in Apostichopus japonicus: focus on miRNA-driven core pathways and target gene regulation.
Chen J, Zhao Y, Li N, Wang H, Wu X, Wang B, Wei X, Chang Y, Tian Y Mar Biotechnol (NY) IF: 2.8 2026-08-10
Early regulatory networks driving somatic embryogenesis in Saccharum spp. L. revealed by time-resolved proteomics.
da Paschoa RP, Xavier LR, Corrêa CCG, Vieira KDS, Pacheco DDR, Gomes LDES, da Silva CEA, Alves LEO, Pinto VB, Santa-Catarina C, Silveira V J Proteomics IF: 3.1 2026-04-20
Characterisation of the Cullin-3 mutation that causes a severe form of familial hypertension and hyperkalaemia.
Schumacher Frances-Rose, Siew Keith, Zhang Jinwei, Johnson Clare, Wood Nicola, Cleary Sarah E, Al Maskari Raya S, Ferryman James T, Hardege Iris, Yasmin, Figg Nichola L, Enchev Radoslav, Knebel Axel, O'Shaughnessy Kevin M, Kurz Thimo EMBO Mol Med IF: 7.9 2016-07-11

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