Search Database

Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
A0A7I2V3Z0 PFKP ATP-dependent 6-phosphofructokinase (ATP-PFK) (Phosphofructokinase) (EC … Homo sapiens (Human) 746 aa

Protein Details: A0A7I2V3Z0 (PFKP)

Protein Information
Accession A0A7I2V3Z0
Protein Names ATP-dependent 6-phosphofructokinase (ATP-PFK) (Phosphofructokinase) (EC 2.7.1.11) (Phosphohexokinase)
Gene Symbol PFKP
Organism Homo sapiens (Human)
Length 746 aa
Isoforms No isoforms
Related PMIDs 19137006 32944167
Database Sources No database sources
These studies detected palmitoylation of this protein in the samples.
Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 0.625
Bubble Size: Positive Samples Count Color Intensity: Positive Ratio
5
Jurkat T cells
Specificity: 0.625
5/25 (20.0%)
3
PC3 cells
Specificity: 0.375
3/4 (75.0%)
0
U937 cells
Specificity: 0.000
0/1 (0.0%)
0
DU145 cells
Specificity: 0.000
0/2 (0.0%)
0
HeLa cells
Specificity: 0.000
0/1 (0.0%)
0
LNCaP cells
Specificity: 0.000
0/46 (0.0%)
0
T cells
Specificity: 0.000
0/4 (0.0%)
0
HAP1 cells
Specificity: 0.000
0/10 (0.0%)
0
293T cells
Specificity: 0.000
0/10 (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
1-501MNAAVRAVVR11MGIYVGAKVY21FIYEGYQGMV31DGGSNIAEAD41WESVSSILQV
51-10051GGTIIGSARC61QAFRTREGRL71KAACNLLQRG81ITNLCVIGGD91GSLTGANLFR
101-150101KEWSGLLEEL111ARNGQIDKEA121VQKYAYLNVV131GMVGSIDNDF141CGTDMTIGTD
151-200151SALHRIIEVV161DAIMTTAQSH171QRTFVLEVMG181RHCGYLALVS191ALACGADWVF
201-250201LPESPPEEGW211EEQMCVKLSE221NRARKKRLNI231IIVAEGAIDT241QNKPITSEKI
251-300251KELVVTQLGY261DTRVTILGHV271QRGGTPSAFD281RILASRMGVE291AVIALLEATP
301-350301DTPACVVSLN311GNHAVRLPLM321ECVQMTQDVQ331KAMDERRFQD341AVRLRGRSFA
351-400351GNLNTYKRLA361IKLPDDQIPK371TNCNVAVINV381GAPAAGMNAA391VRSAVRVGIA
401-450401DGHRMLAIYD411GFDGFAKGQI421KEIGWTDVGG431WTGQGGSILG441TKRVLPGKYL
451-500451EEIATQMRTH461SINALLIIGG471FEAYLGLLEL481SAAREKHEEF491CVPMVMVPAT
501-550501VSNNVPGSDF511SIGADTALNT521ITDTCDRIKQ531SASGTKRRVF541IIETMGGYCG
551-600551YLANMGGLAA561GADAAYIFEE571PFDIRDLQSN581VEHLTEKMKT591TIQRGLVLRN
601-650601ESCSENYTTD611FIYQLYSEEG621KGVFDCRKNV631LGHMQQGGAP641SPFDRNFGTK
651-700651ISARAMEWIT661AKLKEARGRG671KKFTTDDSIC681VLGISKRNVI691FQPVAELKKQ
701-746701TDFEHRIPKE711QWWLKLRPLM721KILAKYKASY731DVSDSGQLEH741VQPWSV
Palmitoylation Sites Details
Position Sources Domains Experimental PMIDs
60 Prediction (Medium) - -
74 Prediction (High) - -
85 Prediction (Medium) - -
141 Prediction (Low) - -
183 Prediction (Low) - -
322 Prediction (Medium) - -
525 Prediction (Medium) - -
549 Prediction (Low) - -
603 Prediction (Low) - -
680 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
44 R → C 0.002506 SNP Missense Mutation COAD
44 R → C 0.002141 SNP Missense Mutation SKCM
48 R → C 0.002288 SNP Missense Mutation STAD
48 R → C 0.002506 SNP Missense Mutation COAD
48 R → C 0.001887 SNP Missense Mutation UCEC
117 R → C 0.002288 SNP Missense Mutation STAD
118 G → C 0.002033 SNP Missense Mutation LUSC
343 C → C 0.004577 SNP Silent STAD
354 R → C 0.002288 SNP Missense Mutation STAD
354 R → C 0.001887 SNP Missense Mutation UCEC
440 G → C 0.001887 SNP Missense Mutation UCEC
563 C → C 0.001887 SNP Silent UCEC
576 R → C 0.002288 SNP Missense Mutation STAD