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Center for Computational Systems Medicine
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Protein Summary

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AS Summary

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Protein Functional Features

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Gene Isoform Structures and Expression Levels

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Protein Structures

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pLDDT Score Distribution

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Ramachandran Plot of Protein Structures

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Potential Active Site Information

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Protein Structure and Feature Comparision

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Protein-Protein Interaction

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Related Drugs

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Related Diseases

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Clinically Important Variants

Protein:FNTA

Protein Summary

check button Gene summary
Gene name: FNTA
ASpdb.0 ID: 2339
Gene
Gene symbol

FNTA

Gene ID

2339

Gene namefarnesyltransferase, CAAX box, subunit alpha
SynonymsFPTA|PGGT1A|PTAR2
Cytomap

8p11.21

Type of geneprotein-coding
Descriptionprotein farnesyltransferase/geranylgeranyltransferase type-1 subunit alphaFTase-alphaGGTase-I-alphafarnesyl-protein transferase alpha-subunitfarnesyltransferase, CAAX box, alphaprotein prenyltransferase alpha subunit repeat containing 2ras proteins
Modification date20240313
UniProtAcc

P49354


check button Gene ontology of this gene with evidence of Inferred from Direct Assay (IDA) from Entrez
PartnerGeneGO IDGO termPubMed ID
GeneFNTA

GO:0004660

protein farnesyltransferase activity

19228685

GeneFNTA

GO:0004660

protein farnesyltransferase activity

16893176

GeneFNTA

GO:0004661

protein geranylgeranyltransferase activity

16893176

GeneFNTA

GO:0005875

microtubule associated complex

19228685

GeneFNTA

GO:0005953

CAAX-protein geranylgeranyltransferase complex

16893176

GeneFNTA

GO:0005965

protein farnesyltransferase complex

16893176

GeneFNTA

GO:0008017

microtubule binding

19228685

GeneFNTA

GO:0018343

protein farnesylation

16893176|19228685

GeneFNTA

GO:0018344

protein geranylgeranylation

16893176

GeneFNTA

GO:0043014

alpha-tubulin binding

19228685

GeneFNTA

GO:0090044

positive regulation of tubulin deacetylation

19228685

GeneFNTA

GO:0090045

positive regulation of deacetylase activity

19228685



AS Summary

check button Information of the canonical protein with experimentally identified structure from PDB (2023).
UniProt AccFile namePDB IDMethodResolutionChainStartEnd
P49354-1P49354-1_1tn6_A.pdb1TN6X-ray1.8A55369

check button ASpdb's canonical and alternatively spliced isoform information.
accession_idgene_namecanonical_idalternative_idcanonical_lengthalternative_lengthcanonical_startcanonical_endtypeoriginalSEQvariationSEQalternative_startalternative_end
P49354FNTAP49354-1P49354-237931268134Deletionnonenone6767

check buttonMultiple sequence alignment of our canonical and alternatively spliced FNTA

check button Matched gene isoform IDs with Ensembl and RefSeq of our canonical and alternative spliced genes of FNTA
UniProt-idENSGENSTENSP
P49354-1ENSG00000168522.13ENST00000302279.8ENSP00000303423.3

UniProt-idNM IDNP ID
P49354-1NM_002027.2NP_002018.1

check buttonAmino acid sequences of our canonical and alternatively spliced FNTA
accession_idProtein sequence
P49354-1MAATEGVGEAAQGGEPGQPAQPPPQPHPPPPQQQHKEEMAAEAGEAVASPMDDGFVSLDSPSYVLYRDRAEWADIDPVPQNDGPNPVVQI
IYSDKFRDVYDYFRAVLQRDERSERAFKLTRDAIELNAANYTVWHFRRVLLKSLQKDLHEEMNYITAIIEEQPKNYQVWHHRRVLVEWLR
DPSQELEFIADILNQDAKNYHAWQHRQWVIQEFKLWDNELQYVDQLLKEDVRNNSVWNQRYFVISNTTGYNDRAVLEREVQYTLEMIKLV
PHNESAWNYLKGILQDRGLSKYPNLLNQLLDLQPSHSSPYLIAFLVDIYEDMLENQCDNKEDILNKALELCEILAKEKDTIRKEYWRYIG
P49354-2MAATEGVGEAAQGGEPGQPAQPPPQPHPPPPQQQHKEEMAAEAGEAVASPMDDGFVSLDSPSYVLYRHFRRVLLKSLQKDLHEEMNYITA
IIEEQPKNYQVWHHRRVLVEWLRDPSQELEFIADILNQDAKNYHAWQHRQWVIQEFKLWDNELQYVDQLLKEDVRNNSVWNQRYFVISNT
TGYNDRAVLEREVQYTLEMIKLVPHNESAWNYLKGILQDRGLSKYPNLLNQLLDLQPSHSSPYLIAFLVDIYEDMLENQCDNKEDILNKA

Protein Functional Features

check buttonMain function of this protein. (from UniProt)
FNTA (go to UniProt):P49354

check buttonRetention analysis result of protein across 39 protein features of UniProt such as six molecule processing features, 13 region features, four site features, six amino acid modification features, two natural variation features, five experimental info features, and 3 secondary structure features. Here, because of limited space for viewing, we only show the protein feature retention information belong to the 13 regional features. All retention annotation result can be downloaded at

download page

* Minus value of BPloci means that the break pointn is located before the CDS.
- Retained protein feature among the 13 regional features.
Accession_idSubsectionStartEndFuncitonal featureSplicing information
P49354Repeat112146Note=PFTA 1Type=Deletion;Start=68;End=134


Gene Isoform Structures and Expression Levels for FNTA

check buttonGene structures of our canonical and alternative spliced genes of FNTA
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
gene isoform structure of FNTA

check button Expression levels of gene isoforms across GTEx.
gtex expression

check button Expression levels of gene isoforms across TCGA.
tcga expression


Protein Structures

check button PDB and CIF files of the predicted protein structures
* Here we show the 3D structure of the proteins using Mol*. AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100. Model confidence is shown from the pLDDT values per residue. pLDDT corresponds to the model’s prediction of its score on the local Distance Difference Test. It is a measure of local accuracy (from AlphfaFold website). To color code individual residues, we transformed individual PDB files into CIF format.
3D view using mol* of P49354-1
3D view using mol* of P49354-2


pLDDT Score Distribution

check button pLDDT score distribution of the predicted protein structures from AlphaFold2
* AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100.
pLDDT distribution across the protein length of P49354-1
all structure
pLDDT distribution across the protein length of P49354-2
all structure


Ramachandran Plot of Protein Structures


check button Ramachandran plot of the torsional angles - phi (φ)and psi (ψ) - of the residues (amino acids) contained in this protein peptide.
Ramachandran plot of P49354-1
all structure
Ramachandran plot of P49354-2
all structure

Potential Active Site Information


check button The potential binding sites of these proteins were identified using SiteMap, a module of the Schrodinger suite.
UniProt-idSite scoreSizeD scoreVolumeExposureEnclosureContactPhobicPhilicBalanceDon/AccResidues
P49354-10.882660.888200.3120.6270.6780.8360.4170.8670.4811.341274,277,278,281,285,289,310,313,314,317,320,321,32
4,352,355,356,359
P49354-21.031741.084458.9340.5430.6710.8570.8630.7931.0871.71339,42,43,46,47,49,50,51,52,53,54,55,56,58,62,63,65
,66,67,69,70,73,74,77,79,80,83,84,87,91,94,95

Protein Structure and Feature Comparision


check button Protein Structure Comparision Using Template Modeling Scores (TM-score).
all structure

check button Protein Structure Comparision Visualization with mol*. between Canonical predicted structure (AF2)(orange) vs Canonical validated structure (PDB)(green)
3D view using mol* of P49354-1_P49354-1_1tn6_A.pdb

check button Protein Structure Comparision Visualization with mol*. between Canonical validated structure (PDB)(orange) vs Alternative predicted structure (AF2)(green)
3D view using mol* of P49354-1_1tn6_A_P49354-2.pdb

check button Protein Structure Comparision Visualization with mol*. between Canonical predicted structure (AF2)(orange) vs Alternative predicted structure (AF2)(green)
3D view using mol* of P49354-1_P49354-2.pdb

check button Protein Feature Comparison of the protein sequendary structures among the protiens.
./stats/secondary_structure/figure/P49354-1_vs_P49354-2.png
all structure<

check button Protein Feature Comparison of the relative accessible surface area (ASA) among the protiens.
./stats/relative_asa/P49354-1_vs_P49354-2.png
all structure<


Protein-Protein Interaction


check button Interactors from UniProt.
Accession_idSubsectionStartEndFuncitonal featureSplicing information


check button Interactors from STRING.
Gene nameInteractors


Related Drugs to FNTA


check button Drugs targeting this gene/protein.
(DrugBank)
UniProt accessionGene nameDrugBank IDDrug nameDrug groupActions
P49354FNTADB08676(20S)-19,20,22,23-TETRAHYDRO-19-OXO-5H,21H-18,20-ETHANO-12,14-ETHENO-6,10-METHENOBENZ[D]IMIDAZO[4,3-L][1,6,9,13]OXATRIAZACYCLONOADECOSINE-9-CARBONITRILEexperimental
P49354FNTADB07216(11S)-8-CHLORO-11-[1-(METHYLSULFONYL)PIPERIDIN-4-YL]-6-PIPERAZIN-1-YL-11H-BENZO[5,6]CYCLOHEPTA[1,2-B]PYRIDINEexperimental
P49354FNTADB04893AZD3409investigational
P49354FNTADB081802-[METHYL-(5-GERANYL-4-METHYL-PENT-3-ENYL)-AMINO]-ETHYL-DIPHOSPHATEexperimental
P49354FNTADB08674(20S)-19,20,21,22-TETRAHYDRO-19-OXO-5H-18,20-ETHANO-12,14-ETHENO-6,10-METHENO-18H-BENZ[D]IMIDAZO[4,3-K][1,6,9,12]OXATRIAZA-CYCLOOCTADECOSINE-9-CARBONITRILEexperimental
P49354FNTADB06448Lonafarnibapproved, investigationalinhibitor
P49354FNTADB07227L-778123experimental
P49354FNTADB07895ALPHA-HYDROXYFARNESYLPHOSPHONIC ACIDexperimental
P49354FNTADB07780Farnesyl diphosphateexperimental
P49354FNTADB069532-CHLORO-5-(3-CHLORO-PHENYL)-6-[(4-CYANO-PHENYL)-(3-METHYL-3H-IMIDAZOL-4-YL)- METHOXYMETHYL]-NICOTINONITRILEexperimental
P49354FNTADB07841Geranylgeranyl diphosphateexperimental
P49354FNTADB07771[(3,7,11-TRIMETHYL-DODECA-2,6,10-TRIENYLOXYCARBAMOYL)-METHYL]-PHOSPHONIC ACIDexperimental

Related Diseases to FNTA


check button Previous studies relating to the alternative splicing of FNTA and disease information from the MeSH term (PubMed)
GenePMIDTitleAbstractMeSH IDMeSH term
FNTA20403997Genetic variation in 3-hydroxy-3-methylglutaryl CoA reductase modifies the chemopreventive activity of statins for colorectal cancer.Genetic variation in 3-hydroxy-3-methylglutaryl CoA reductase (HMGCR), the rate-limiting enzyme in cholesterol synthesis, modifies the effect of statins on serum cholesterol levels. Long-term use of statins is associated with a reduced risk of colorectal cancer (CRC) in some, but not all, studies. We genotyped variants in 40 candidate genes important for cholesterol synthesis and metabolism in a population-based case-control study of CRC involving 2,138 incident cases and 2,049 population-based controls. We identified a single-nucleotide polymorphism in the HMGCR gene that significantly modified the protective association between statins and CRC risk. Compared with nonusers, the unadjusted odds ratio of CRC among statin users with the A/A genotype of rs12654264 in HMGCR was 0.3 (95% confidence interval, 0.18-0.51) and among statin users with the T/T genotype was 0.66 (95% confidence interval, 0.41-1.06; P-interaction = 0.0012). This genetic variant (A/A genotype of rs12654264) also was associated with lower serum levels of low-density lipoprotein among all cases and controls. In colon cancer cell lines, the reduction in cholesterol levels after statin treatment was substantially stronger in cells carrying the A/A genotype, and this difference was related to alternative splicing involving the HMGCR statin-binding domain. We anticipate that these data may advance the development of personalized statin use for reducing the risk of cancer as well as cardiovascular disease among the approximately 25 million people currently using statins worldwide.D015179Colorectal Neoplasms


Clinically important variants in FNTA


check button (ClinVar, 04/20/2024)
accession_iduniprot_idgene_nameTypeVariantClinical_significance