NOXRED1 | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Aliases | NOXRED1 , C14orf148, NADP-dependent oxidoreductase domain containing 1, NADP dependent oxidoreductase domain containing 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||
External IDs | MGI: 1918525 HomoloGene: 51388 GeneCards: NOXRED1 | ||||||||||||||||||||||||||||||||||||||||||||||||||
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NADP-dependent oxidoreductase domain-containing protein 1 is a protein that in humans is encoded by the NOXRED1 gene. An alias of this gene is Chromosome 14 Open Reading Frame 148 (c14orf148) [5] . This gene is located on chromosome 14, at 14q24.3. [5] [6] NOXRED1 is predicted to be involved in pyrroline-5-carboxylate reductase activity as part of the L-proline biosynthetic pathway. [5] It is expressed in a wide variety of tissues at a relatively low level, including the testes, thyroid, skin, small intestine, brain, kidney, colon, and more. [5]
NOXRED1 is coded on the minus strand of the human Chromosome 14 from nucleotides 77,394,021-77,423,523. [6] It has a total of 9 exons and 8 introns, and it spans a total of 29,502 bases. [6]
The gene neighborhood of NOXRED1 includes Transmembrane p24 TraffickingProtein Family Member 8 (TMED8), Sterile Alpha Motif Domain 15 (SAMD15), VPS33B Interacting Protein (VIPAS39), and Activator of HSP90 ATPase Activity 1 (AHSA1).
NOXRED1 has three known mRNA isoforms (table 2). [7] The primary isoform is 2324 bases in length and is composed of 6 exons. [8] Isoform 2 [9] and Isoform 3 [10] are 1773 and 1770 nucleotides long, respectively.
NADP-dependent oxidoreductase domain-containing protein 1 (NOXRED1) is a protein which in humans is encoded by the gene NOXRED1. [11] It is 359 residues long and has a molecular weight of ~39.9 kDa. [11] This protein is enriched in leucine residues, in comparison to other human proteins. [12] NOXRED1 is predicted to localize in the cytoplasm and perform functions involving pyrroline-5-carboxylate reductase. [7] From residues 78-189, NOXRED1 contains the conserved protein domain family pyrroline-5-carboxylate reductase (ProC). [11]
NOXRED1 has three known protein isoforms (Table 2). [11] [13] [14] Isoform 1 is the largest and most abundant. [11]
Isoform | Accession Number | mRNA Length (nucleotides) | Accession Number | Protein Length (amino acids) | Molecular Weight (kDa) |
1 | NM_001113475.3 | 2324 | NP_001106946.1 | 359 | 39.9 |
2 | NM_001394980.1 | 1773 | XP_011534731.1 | 269 | 29.8 |
3 | XM_011536429.4 | 1770 | XP_016876458.1 | 234 | 25.9 |
Isoforms of NOXRED1. Information obtained from NCBI Nucleotide [15] and NCBI Protein [16] databases.
ThermoFisher Scientific has developed a human polyclonal antibody targeting NOXRED1. [17] It can be used for a variety of different functions, including immunocytochemistry, immunohistochemistry, immunoprecipitation, and western blotting. [17] Additionally, the Human Protein Atlas database shows immunocytochemistry produced images of NOXRED1 within the A549, MCF-7, and U2OS cell lines [18]
The Allen Brain Institute shows that NOXRED1 is expressed at a moderate level throughout the Mus musculus brain [19]
Some predicted proteins that interact with the human NOXRED1 are Delta-1-pyrroline-5-carboxylate synthase and ornithine aminotransferase. [20] Delta-1-pyrroline-5-carboxylate synthase catalyzes the conversion of glutamate to delta-1-pyrroline-5-carboxylate synthase. [21] Ornithine aminotransferase is an enzyme that converts arginine and ornithine into glutamate and GABA. [22] Both of these proteins are involved in the proline biosynthesis pathway. [21] [22]
NOXRED1 has three orthologs. Pyrroline-5-carboxylate reductase 1 (PYCR1), pyrroline-5-carboxylate reductase 2 (PYCR2), and pyrroline-5-carboxylate reductase 3 (PYCR3) all are also involved in the synthesis of proline from pyrroline-5-carboxylate. [23] [24] [25] PYCR1 is located at 17q25.3, [23] PYCR2 is located at 1q42.12, [24] and PYCR3 is located at 8q24.3. [25]
Gene | Genus and Species | Protein Accession Number | Sequence Length (aa) | % Sequence Identity to Human Protein | % Sequence Similarity to Human Protein |
NOXRED1 | Homo sapiens | NP_001106946.1 | 359 | 100 | 100 |
PYCR2 | Homo sapiens | NP_037460.2 | 320 | 15.4 | 23.3 |
PYCR3 | Homo sapiens | NP_075566.3 | 274 | 13.6 | 23.8 |
PYCR1 | Homo sapiens | NP_008838.2 | 319 | 13.2 | 20.6 |
Paralogs of NOXRED1. Percent sequence identity and similarity were calculated using EMBOSS Needle [26] .
NOXRED1 was found to be highly conserved throughout history—there are existing orthologs within mammals, aves, reptiles, amphibians, bony fish, cartilaginous fish, trichoplaxes, and some invertebrates. [27] [28] Interestingly, orthologs were not able to be found in one of the three orders of amphibians—Urodela. [27] Additionally, orthologs were not able to be found in insects, fungi, protists, plants, bacteria, or archaea25. [27] Listed in a table are a list of 20 different NOXRED1 protein orthologs from a diverse array of species, including mammals, aves, reptiles, amphibians, different classes of fish, and invertebrates.
Genus and Species | Common Name | Taxonomic Class | Taxonomic Order | DOD (MYA) | Accession Number | AA Sequence Length | % Sequence Identity to Human Protein | % Sequence Similarity to Human Protein |
Homo sapiens | Human | Mammalia | Primata | 0 | NP_001106946.1 | 359 | 100 | 100 |
Mus musculus | Mouse | Mammalia | Rodentia | 87 | NP_082020.1 | 366 | 60.6 | 76.9 |
Felis catus | Cat | Mammalia | Carnivora | 94 | XP_019688936.1 | 381 | 72 | 79.3 |
Elephas maximus indicus | Indian Elephant | Mammalia | Proboscidea | 99 | XP_049755695.1 | 384 | 69.4 | 77.2 |
Struthio camelus australis | Southern Ostrich | Aves | Struthioniformes | 319 | XP_009673940.1 | 345 | 44 | 60.4 |
Oxyura jamaicensis | Ruddy Duck | Aves | Anseriformes | 319 | XP_035184255.1 | 392 | 43.8 | 56.8 |
Pygoscelis adeliae | Adélie penguin | Aves | Spheniscoformes | 319 | XP_009317781.1 | 323 | 34.4 | 48.8 |
Mauremys mutica | Yellow Pond Turtle | Reptilia | Testudines | 319 | XP_044872068.1 | 372 | 47.5 | 65.3 |
Protobothrops mucrosquamatus | Brown Spotted Pit Viper | Reptilia | Serpentes | 319 | XP_029139298.1 | 388 | 39.8 | 58.8 |
Gekko japonicus | Japanese Gecko | Reptilia | Squamata | 319 | XP_015273827.1 | 403 | 37.6 | 56.6 |
Geotrypetes seraphini | Gaboon Caecilian | Amphibia | Gymnophiona | 353 | XP_033807528.1 | 371 | 45.2 | 59.7 |
Xenopus tropicalus | Western Clawed Frog | Amphibia | Anura | 353 | NP_001072734.1 | 344 | 40.9 | 56.5 |
Rana temporaria | Common Frog | Amphibia | Anura | 353 | XP_040189126.1 | 367 | 36.2 | 52.4 |
Polypterus senegalus | Gray bichir | Actinopterygii | Polypteriformes | 431 | XP_039598035.1 | 364 | 39.8 | 57.3 |
Danio rerio | Zebrafish | Actinopterygii | Cypriniformes | 431 | XP_005169929.1 | 333 | 36.8 | 53.8 |
Rhincodon typus | Whale Shark | Chondrichthyes | Orectolobiformes | 464 | XP_020369405.1 | 365 | 33.3 | 50.6 |
Petromyzon marinus | Sea Lampray | Hyperoartia | Petromyzontiformes | 599 | XP_032812106.1 | 359 | 25.7 | 37 |
Strongylocentrotus purpuratus | Pacific Purple Sea Urchin | Echinoidea | Echinoida | 619 | XP_011675891.2 | 380 | 28.3 | 47.3 |
Trichoplax sp. H2 | Trichoplax H2 | Trichoplax | - | 661 | RDD44387.1 | 382 | 28.2 | 46.1 |
Crassostrea gigas | Sea Oyster | Bivalvia | Ostreida | 694 | XP_011447367.2 | 366 | 31.6 | 49.7 |
Table 1. Orthologs of NOXRED1. Orthologs are grouped by taxonomic class and then sorted first by increasing date of divergence (MYA) and second by percent sequence identity to the human protein. Date of divergence was calculated using the pairwise divergence median time from Timetree.org. [29] Percent sequence identity and similarity were calculated using EMBOSS Needle. [26]
The human NOXRED1 protein is predicted to play a role in the L-proline biosynthesis pathway. [11]
NOXRED1 has a few clinically significant associations. Chen et al., 2020 found that the variant rs8012548 (an intron variant) within NOXRED1 is significantly associated withcutaneous melanoma specific survival, meaning that patients with cutaneous melanoma who have carry rs8012548 are less likely to perish due to the disease. [30] Tabe-Bordbar et al., 2020 found that rs12890411 within intron 5 of NOXRED1 lies within an Estrogen Receptor Alpha (Erα) enhancer region. [31] This variant is an eQTL for breast cancer, and it at least partially decreases the binding affinity of the transcription factor RELA. [31] Yuan et al., 2021 predicted that NOXRED1 influences the pathogenesis of Alzheimer's disease and mild cognitive impairment by increasing oxidative stress within the limbic region. [32] Nacita et al., 2015 reported that a patient with the interstitial deletion of 14q24-14q32 exhibits developmental and neurological delays, face dysmorphology, and epilepsy. [33] Relating to the transcript, MacNair et al., 2016 found that NOXRED1 is downregulated in the motor neurons in mice with a TDP-43 mutation related to amyotrophic lateral sclerosis (ALS). [34] Relating to the protein, Vandenbrouck et al., 2016 found that NOXRED1 is found within the proteome of human spermatozoa. [35]
Chromosome 16 open reading frame 95 (C16orf95) is a gene which in humans encodes the protein C16orf95. It has orthologs in mammals, and is expressed at a low level in many tissues. C16orf95 evolves quickly compared to other proteins.
The coiled-coil domain containing 142 (CCDC142) is a gene which in humans encodes the CCDC142 protein. The CCDC142 gene is located on chromosome 2, spans 4339 base pairs and contains 9 exons. The gene codes for the coiled-coil domain containing protein 142 (CCDC142), whose function is not yet well understood. There are two known isoforms of CCDC142. CCDC142 proteins produced from these transcripts range in size from 743 to 665 amino acids and contain signals suggesting protein movement between the cytosol and nucleus. Homologous CCDC142 genes are found in many animals including vertebrates and invertebrates but not fungus, plants, protists, archea, or bacteria. Although the function of this protein is not well understood, it contains a coiled-coil domain and a RINT1_TIP1 motif located within the coiled-coil domain.
PRR29 is a protein encoded by the PRR29 gene located in humans on chromosome 17 at 17q23.
BEND2 is a protein that in humans is encoded by the BEND2 gene. It is also found in other vertebrates, including mammals, birds, and reptiles. The expression of BEND2 in Homo sapiens is regulated and occurs at high levels in the skeletal muscle tissue of the male testis and in the bone marrow. The presence of the BEN domains in the BEND2 protein indicates that this protein may be involved in chromatin modification and regulation.
CRACD-like protein. previously known as KIAA1211L is a protein that in humans is encoded by the CRACDL gene. It is highly expressed in the cerebral cortex of the brain. Furthermore, it is localized to the microtubules and the centrosomes and is subcellularly located in the nucleus. Finally, CRACDL is associated with certain mental disorders and various cancers.
C17orf53 is a gene in humans that encodes a protein known as C17orf53, uncharacterized protein C17orf53. It has been shown to target the nucleus, with minor localization in the cytoplasm. Based on current findings C17orf53 is predicted to perform functions of transport, however further research into the protein could provide more specific evidence regarding its function.
Chromosome 21 Open Reading Frame 58 (C21orf58) is a protein that in humans is encoded by the C21orf58 gene.
C1orf122 is a gene in the human genome that encodes the cytosolic protein ALAESM.. ALAESM is present in all tissue cells and highly up-regulated in the brain, spinal cord, adrenal gland and kidney. This gene can be expressed up to 2.5 times the average gene in its highly expressed tissues. Although the function of C1orf122 is unknown, it is predicted to be used for mitochondria localization.
TMEM275 is a protein that in humans is encoded by the TMEM275 gene. TMEM275 has two, highly-conserved, helical trans-membrane regions. It is predicted to reside within the plasma membrane or the endoplasmic reticulum's membrane.
Chromosome 9 open reading frame 85, commonly known as C9orf85, is a protein in Homo sapiens encoded by the C9orf85 gene. The gene is located at 9q21.13. When spliced, four different isoforms are formed. C9orf85 has a predicted molecular weight of 20.17 kdal. Isoelectric point was found to be 9.54. The function of the gene has not yet been confirmed, however it has been found to show high levels of expression in cells of high differentiation.
Family with sequence 98, member C or FAM98C is a gene that encodes for FAM98C has two aliases FLJ44669 and hypothetical protein LOC147965. FAM98C has two paralogs in humans FAM98A and FAM98B. FAM98C can be characterized for being a Leucine-rich protein. The function of FAM98C is still not defined. FAM98C has orthologs in mammals, reptiles, and amphibians and has a distant orhtologs in Rhinatrema bivittatum and Nanorana parkeri.
Family with Sequence Similarity 166, member C (FAM166C), is a protein encoded by the FAM166C gene. The protein FAM166C is localized in the nucleus. It has a calculated molecular weight of 23.29 kDa. It also contains DUF2475, a protein of unknown function from amino acid 19–85. The FAM166C protein is nominally expressed in the testis, stomach, and thyroid.
Chromosome 12 Open Reading Frame 50 (C12orf50) is a protein-encoding gene which in humans encodes for the C12orf50 protein. The accession id for this gene is NM_152589. The location of C12orf50 is 12q21.32. It covers 55.42 kb, from 88429231 to 88373811, on the reverse strand. Some of the neighboring genes to C12orf50 are RPS4XP15, LOC107984542, and C12orf29. RPS4XP15 is upstream C12orf50 and is on the same strand. LOC107984542 and C12orf29 are both downstream. LOC107984542 is on the opposite strand while C12orf29 is on the same strand. C12orf50 has six isoforms. This page is focusing on isoform X1. C12orf50 isoform X1 is 1711 nucleotides long and has a protein with a length of 414 aa.
Chromosome 4 open reading frame 50 is a protein that in humans is encoded by the C4orf50 gene. The protein localizes in the nucleus. C4orf50 has orthologs in vertebrates but not invertebrates
TEKTIP1, also known as tektin-bundle interacting protein 1, is a protein that in humans is encoded by the TEKTIP1 gene.
THAP domain-containing protein 3 (THAP3) is a protein that, in Homo sapiens (humans), is encoded by the THAP3 gene. The THAP3 protein is as known as MGC33488, LOC90326, and THAP domain-containing, apoptosis associated protein 3. This protein contains the Thanatos-associated protein (THAP) domain and a host-cell factor 1C binding motif. These domains allow THAP3 to influence a variety of processes, including transcription and neuronal development. THAP3 is ubiquitously expressed in H. sapiens, though expression is highest in the kidneys.
Chromosome 13 Open Reading Frame 46 is a protein which in humans is encoded by the C13orf46 gene. In humans, C13orf46 is ubiquitously expressed at low levels in tissues, including the lungs, stomach, prostate, spleen, and thymus. This gene encodes eight alternatively spliced mRNA transcript, which produce five different protein isoforms.
Transmembrane protein 248, also known as C7orf42, is a gene that in humans encodes the TMEM248 protein. This gene contains multiple transmembrane domains and is composed of seven exons.TMEM248 is predicted to be a component of the plasma membrane and be involved in vesicular trafficking. It has low tissue specificity, meaning it is ubiquitously expressed in tissues throughout the human body. Orthology analyses determined that TMEM248 is highly conserved, having homology with vertebrates and invertebrates. TMEM248 may play a role in cancer development. It was shown to be more highly expressed in cases of colon, breast, lung, ovarian, brain, and renal cancers.
Secernin-3 (SCRN3) is a protein that is encoded by the human SCRN3 gene. SCRN3 belongs to the peptidase C69 family and the secernin subfamily. As a part of this family, the protein is predicted to enable cysteine-type exopeptidase activity and dipeptidase activity, as well as be involved in proteolysis. It is ubiquitously expressed in the brain, thyroid, and 25 other tissues. Additionally, SCRN3 is conserved in a variety of species, including mammals, birds, fish, amphibians, and invertebrates. SCRN3 is predicted to be an integral component of the cytoplasm.
Leucine-rich repeat-containing protein 74A (LRRC74A), is a protein encoded by the LRRC74A gene. The protein LRRC74A is localized in the cytoplasm. It has a calculated molecular weight of approximately 55 kDa. The LRRC74A protein is nominally expressed in the testis, salivary gland, and pancreas.