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Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
P33991 MCM4; CDC21 DNA replication licensing factor MCM4 … Homo sapiens (Human) 863 aa

Protein Details: P33991 (MCM4)

Protein Information
Accession P33991
Protein Names DNA replication licensing factor MCM4 (EC 3.6.4.12) (CDC21 homolog) (P1-CDC21)
Gene Symbol MCM4; CDC21
Organism Homo sapiens (Human)
Length 863 aa
Isoforms No isoforms
Related PMIDs 19137006 29733200 31251020 31382980
Database Sources No database sources
These studies detected palmitoylation of this protein in the samples.
Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 0.261
Bubble Size: Positive Samples Count Color Intensity: Positive Ratio
6
Jurkat T cells
Specificity: 0.261
6/25 (24.0%)
6
LNCaP cells
Specificity: 0.261
6/46 (13.0%)
6
HAP1 cells
Specificity: 0.261
6/10 (60.0%)
4
293T cells
Specificity: 0.174
4/10 (40.0%)
1
U937 cells
Specificity: 0.043
1/1 (100.0%)
0
DU145 cells
Specificity: 0.000
0/2 (0.0%)
0
HeLa cells
Specificity: 0.000
0/1 (0.0%)
0
PC3 cells
Specificity: 0.000
0/4 (0.0%)
0
T cells
Specificity: 0.000
0/4 (0.0%)
0
CEMx174 cells
Specificity: 0.000
0/3 (0.0%)
0
Endothelial cells
Specificity: 0.000
0/2 (0.0%)
0
Prefrontal cortex
Specificity: 0.000
0/1 (0.0%)
0
Cerebral cortex
Specificity: 0.000
0/4 (0.0%)
0
Liver membrane
Specificity: 0.000
0/1 (0.0%)
Palmitoylation Distribution by Study and Tissue/Cell Line
Chart Explanation: Each bar represents a study (PMID). The colored bottom segment shows palmitoylated samples, while the gray top segment shows non-palmitoylated samples. Bars are grouped by tissue/cell line for easy comparison.
Protein Sequence
Single Types:
Experimental Database High Prediction Medium Prediction Low Prediction
Combined Types:
All Three Exp + DB Exp + High Pred Exp + Med Pred Exp + Low Pred DB + High Pred DB + Med Pred DB + Low Pred Cysteine
1-501MSSPASTPSR11RGSRRGRATP21AQTPRSEDAR31SSPSQRRRGE41DSTSTGELQP
51-10051MPTSPGVDLQ61SPAAQDVLFS71SPPQMHSSAI81PLDFDVSSPL91TYGTPSSRVE
101-150101GTPRSGVRGT111PVRQRPDLGS121AQKGLQVDLQ131SDGAAAEDIV141ASEQSLGQKL
151-200151VIWGTDVNVA161ACKENFQRFL171QRFIDPLAKE181EENVGIDITE191PLYMQRLGEI
201-250201NVIGEPFLNV211NCEHIKSFDK221NLYRQLISYP231QEVIPTFDMA241VNEIFFDRYP
251-300251DSILEHQIQV261RPFNALKTKN271MRNLNPEDID281QLITISGMVI291RTSQLIPEMQ
301-350301EAFFQCQVCA311HTTRVEMDRG321RIAEPSVCGR331CHTTHSMALI341HNRSLFSDKQ
351-400351MIKLQESPED361MPAGQTPHTV371ILFAHNDLVD381KVQPGDRVNV391TGIYRAVPIR
401-450401VNPRVSNVKS411VYKTHIDVIH421YRKTDAKRLH431GLDEEAEQKL441FSEKRVELLK
451-500451ELSRKPDIYE461RLASALAPSI471YEHEDIKKGI481LLQLFGGTRK491DFSHTGRGKF
501-550501RAEINILLCG511DPGTSKSQLL521QYVYNLVPRG531QYTSGKGSSA541VGLTAYVMKD
551-600551PETRQLVLQT561GALVLSDNGI571CCIDEFDKMN581ESTRSVLHEV591MEQQTLSIAK
601-650601AGIICQLNAR611TSVLAAANPI621ESQWNPKKTT631IENIQLPHTL641LSRFDLIFLL
651-700651LDPQDEAYDR661RLAHHLVALY671YQSEEQAEEE681LLDMAVLKDY691IAYAHSTIMP
701-750701RLSEEASQAL711IEAYVDMRKI721GSSRGMVSAY731PRQLESLIRL741AEAHAKVRLS
751-800751NKVEAIDVEE761AKRLHREALK771QSATDPRTGI781VDISILTTGM791SATSRKRKEE
801-850801LAEALKKLIL811SKGKTPALKY821QQLFEDIRGQ831SDIAITKDMF841EEALRALADD
851-863851DFLTVTGKTV861RLL
Palmitoylation Sites Details
Position Sources Domains Experimental PMIDs
162 Prediction (Medium) - -
212 Prediction (Low) - -
328 Prediction (Medium) - -
509 Prediction (High) - -
571 Prediction (Low) - -
605 Prediction (Medium) - -
Conservation Scores
PhyloP
PhastCons
TCGA Cysteine Mutation Information

Note: Mutations indicate amino acid changes that may create potential palmitoylation sites.

Position Amino Acid Change Frequency Type Function Cancer Type
32 S → C 0.002427 SNP Missense Mutation BLCA
39 G → C 0.001887 SNP Missense Mutation UCEC
92 Y → C 0.002427 SNP Missense Mutation BLCA
172 R → C 0.001887 SNP Missense Mutation UCEC
328 C → C 0.004577 SNP Silent STAD
328 C → C 0.002506 SNP Silent COAD
330 R → C 0.001887 SNP Missense Mutation UCEC
343 R → C 0.002506 SNP Missense Mutation COAD
571 C → F 0.001764 SNP Missense Mutation LUAD
741 A → delinsVLGFFVCFFET 0.002294 INS In Frame Ins OV
772 S → C 0.001014 SNP Missense Mutation BRCA
861 R → C 0.002288 SNP Missense Mutation STAD
571* C → ? 0.001969 SNP Nonsense Mutation LGG