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ALDH4A1
HPA
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  • ALDH4A1
PROTEIN SUMMARY GENE INFORMATION RNA DATA ANTIBODY DATA
GENERAL INFORMATIONi

General description of the gene and the encoded protein(s) using information from HGNC and Ensembl, as well as predictions made by the Human Protein Atlas project.

Gene namei

Official gene symbol, which is typically a short form of the gene name, according to HGNC.

ALDH4A1
Synonyms ALDH4, P5CDh
Gene descriptioni

Full gene name according to HGNC.

Aldehyde dehydrogenase 4 family member A1
Protein classi

Assigned HPA protein class(es) for the encoded protein(s).

Disease related genes
Enzymes
Human disease related genes
Metabolic proteins
Plasma proteins
Potential drug targets
Predicted locationi

All transcripts of all genes have been analyzed regarding the location(s) of corresponding protein based on prediction methods for signal peptides and transmembrane regions.

  • Genes with at least one transcript predicted to encode a secreted protein, according to prediction methods or to UniProt location data, have been further annotated and classified with the aim to determine if the corresponding protein(s) are secreted or actually retained in intracellular locations or membrane-attached.

  • Remaining genes, with no transcript predicted to encode a secreted protein, will be assigned the prediction-based location(s).

The annotated location overrules the predicted location, so that a gene encoding a predicted secreted protein that has been annotated as intracellular will have intracellular as the final location.

Intracellular
Protein evidence Evidence at protein level (all genes)
GENE INFORMATIONi

Gene information from Ensembl and Entrez, as well as links to available gene identifiers are displayed here. Information was retrieved from Ensembl if not indicated otherwise.

Chromosome 1
Cytoband p36.13
Chromosome location (bp) 18871430 - 18902724
Number of transcriptsi

Number of protein-coding transcripts from the gene as defined by Ensembl.

5
Ensembl ENSG00000159423 (version 109)
Entrez gene 8659
HGNC HGNC:406
UniProt P30038 (UniProt - Evidence at protein level)
neXtProt NX_P30038
GeneCards ALDH4A1
Antibodypedia ALDH4A1 antibodies


PROTEIN FUNCTION
Protein function (UniProt)i

Useful information about the protein provided by UniProt.

Irreversible conversion of delta-1-pyrroline-5-carboxylate (P5C), derived either from proline or ornithine, to glutamate. This is a necessary step in the pathway interconnecting the urea and tricarboxylic acid cycles. The preferred substrate is glutamic gamma-semialdehyde, other substrates include succinic, glutaric and adipic semialdehydes.... show less
Molecular function (UniProt)i

Keywords assigned by UniProt to proteins due to their particular molecular function.

Oxidoreductase
Biological process (UniProt)i

Keywords assigned by UniProt to proteins because they are involved in a particular biological process.

Proline metabolism
Ligand (UniProt)i

Keywords assigned by UniProt to proteins because they bind, are associated with, or whose activity is dependent of some molecule.

NAD
Gene summary (Entrez)i

Useful information about the gene from Entrez

This protein belongs to the aldehyde dehydrogenase family of proteins. This enzyme is a mitochondrial matrix NAD-dependent dehydrogenase which catalyzes the second step of the proline degradation pathway, converting pyrroline-5-carboxylate to glutamate. Deficiency of this enzyme is associated with type II hyperprolinemia, an autosomal recessive disorder characterized by accumulation of delta-1-pyrroline-5-carboxylate (P5C) and proline. Alternatively spliced transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Jun 2009]... show less
PROTEIN INFORMATIONi

The protein information section displays alternative protein-coding transcripts (splice variants) encoded by this gene according to the Ensembl database.

The Splice variant identifier links to the Ensembl website protein summary for the selected splice variant. The data in the Swissprot and TrEMBL columns links to corresponding pages in the UniProt database.

The protein classes assigned to this protein are shown if expanding the data in the protein class column. Parent protein classes are in bold font and subclasses are listed under the parent class.

The length of the protein (amino acid residues according to Ensembl), molecular mass (kDalton), predicted signal peptide and number of predicted transmembrane region(s) according to in-house majority decision methods based on sets of predictors are also reported.
Splice variant SwissProt TrEMBL Protein class Gene ontology Length & mass Signal peptide
(predicted)
Transmembrane regions
(predicted)
ALDH4A1-201
ENSP00000290597
ENST00000290597
P30038
[Direct mapping] Delta-1-pyrroline-5-carboxylate dehydrogenase, mitochondrial
Show all
A0A024RAC7
[Target identity:100%; Query identity:100%] Multifunctional fusion protein L-glutamate gamma-semialdehyde dehydrogenase Delta-1-pyrroline-5-carboxylate dehydrogenase
Show all
Enzymes
   ENZYME proteins
   Oxidoreductases
Metabolic proteins
   MEMSAT-SVM predicted membrane proteins
   SPOCTOPUS predicted membrane proteins
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Plasma proteins
Disease related genes
Potential drug targets
Human disease related genes
   Congenital disorders of metabolism
   Congenital disorders of amino acid metabolism
Mapped to neXtProt
   neXtProt - Evidence at protein level
Protein evidence (Kim et al 2014)
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0003842 [1-pyrroline-5-carboxylate dehydrogenase activity]
GO:0004029 [aldehyde dehydrogenase (NAD+) activity]
GO:0005515 [protein binding]
GO:0005739 [mitochondrion]
GO:0005759 [mitochondrial matrix]
GO:0005829 [cytosol]
GO:0006560 [proline metabolic process]
GO:0006562 [proline catabolic process]
GO:0009055 [electron transfer activity]
GO:0010133 [proline catabolic process to glutamate]
GO:0016491 [oxidoreductase activity]
GO:0016620 [oxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor]
GO:0019470 [4-hydroxyproline catabolic process]
GO:0022900 [electron transport chain]
GO:0042802 [identical protein binding]
Show all
563 aa
61.7 kDa
No 0
ALDH4A1-202
ENSP00000364490
ENST00000375341
P30038
[Direct mapping] Delta-1-pyrroline-5-carboxylate dehydrogenase, mitochondrial
Show all
A0A024RAC7
[Target identity:100%; Query identity:100%] Multifunctional fusion protein L-glutamate gamma-semialdehyde dehydrogenase Delta-1-pyrroline-5-carboxylate dehydrogenase
Show all
Enzymes
   ENZYME proteins
   Oxidoreductases
Metabolic proteins
   MEMSAT-SVM predicted membrane proteins
   SPOCTOPUS predicted membrane proteins
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Plasma proteins
Disease related genes
Potential drug targets
Human disease related genes
   Congenital disorders of metabolism
   Congenital disorders of amino acid metabolism
Mapped to neXtProt
   neXtProt - Evidence at protein level
Protein evidence (Kim et al 2014)
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0003842 [1-pyrroline-5-carboxylate dehydrogenase activity]
GO:0004029 [aldehyde dehydrogenase (NAD+) activity]
GO:0005515 [protein binding]
GO:0005739 [mitochondrion]
GO:0005759 [mitochondrial matrix]
GO:0005829 [cytosol]
GO:0006560 [proline metabolic process]
GO:0006562 [proline catabolic process]
GO:0009055 [electron transfer activity]
GO:0010133 [proline catabolic process to glutamate]
GO:0016491 [oxidoreductase activity]
GO:0016620 [oxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor]
GO:0019470 [4-hydroxyproline catabolic process]
GO:0022900 [electron transport chain]
GO:0042802 [identical protein binding]
Show all
563 aa
61.7 kDa
No 0
ALDH4A1-203
ENSP00000393209
ENST00000432718
Q5TF55
[Direct mapping] Delta-1-pyrroline-5-carboxylate dehydrogenase, mitochondrial
Show all
Metabolic proteins
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Human disease related genes
   Congenital disorders of metabolism
   Congenital disorders of amino acid metabolism
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0005739 [mitochondrion]
GO:0005829 [cytosol]
GO:0016491 [oxidoreductase activity]
Show all
214 aa
23.1 kDa
No 0
ALDH4A1-205
ENSP00000442988
ENST00000538309
P30038
[Direct mapping] Delta-1-pyrroline-5-carboxylate dehydrogenase, mitochondrial
Show all
Enzymes
   ENZYME proteins
   Oxidoreductases
Metabolic proteins
   MEMSAT-SVM predicted membrane proteins
   SPOCTOPUS predicted membrane proteins
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Plasma proteins
Disease related genes
Potential drug targets
Human disease related genes
   Congenital disorders of metabolism
   Congenital disorders of amino acid metabolism
Mapped to neXtProt
   neXtProt - Evidence at protein level
Protein evidence (Kim et al 2014)
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0003842 [1-pyrroline-5-carboxylate dehydrogenase activity]
GO:0004029 [aldehyde dehydrogenase (NAD+) activity]
GO:0005515 [protein binding]
GO:0005739 [mitochondrion]
GO:0005759 [mitochondrial matrix]
GO:0005829 [cytosol]
GO:0006560 [proline metabolic process]
GO:0006562 [proline catabolic process]
GO:0009055 [electron transfer activity]
GO:0010133 [proline catabolic process to glutamate]
GO:0016491 [oxidoreductase activity]
GO:0016620 [oxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor]
GO:0019470 [4-hydroxyproline catabolic process]
GO:0022900 [electron transport chain]
GO:0042802 [identical protein binding]
Show all
503 aa
55.1 kDa
No 0
ALDH4A1-206
ENSP00000446071
ENST00000538839
P30038
[Direct mapping] Delta-1-pyrroline-5-carboxylate dehydrogenase, mitochondrial
Show all
Enzymes
   ENZYME proteins
   Oxidoreductases
Metabolic proteins
   MEMSAT-SVM predicted membrane proteins
   SPOCTOPUS predicted membrane proteins
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Plasma proteins
Disease related genes
Potential drug targets
Human disease related genes
   Congenital disorders of metabolism
   Congenital disorders of amino acid metabolism
Mapped to neXtProt
   neXtProt - Evidence at protein level
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0003842 [1-pyrroline-5-carboxylate dehydrogenase activity]
GO:0004029 [aldehyde dehydrogenase (NAD+) activity]
GO:0005515 [protein binding]
GO:0005739 [mitochondrion]
GO:0005759 [mitochondrial matrix]
GO:0005829 [cytosol]
GO:0006560 [proline metabolic process]
GO:0006562 [proline catabolic process]
GO:0009055 [electron transfer activity]
GO:0010133 [proline catabolic process to glutamate]
GO:0016491 [oxidoreductase activity]
GO:0016620 [oxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor]
GO:0019470 [4-hydroxyproline catabolic process]
GO:0022900 [electron transport chain]
GO:0042802 [identical protein binding]
Show all
512 aa
56 kDa
No 0

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