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WormBase Tree Display for Gene: WBGene00010160

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Name Class

WBGene00010160SMapS_parentSequenceCHROMOSOME_I
IdentityVersion2
NameCGC_namepng-1Person_evidenceWBPerson114
Sequence_nameF56G4.5
Molecular_nameF56G4.5
F56G4.5.1
CE23786
Other_namebam-1
CELE_F56G4.5Accession_evidenceNDBBX284601
Public_namepng-1
DB_infoDatabase (13)
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:51WBPerson1971EventImportedInitial conversion from CDS class of WS125
215 Mar 2007 17:00:31WBPerson2970Name_changeCGC_namepng-1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classpng
Allele (152)
StrainWBStrain00001991
WBStrain00030529
WBStrain00032150
RNASeq_FPKM (74)
GO_annotation (25)
Contained_in_operonCEOP1652
Ortholog (35)
Paralog (15)
Structured_descriptionConcise_descriptionpng-1 encodes a peptide-N[4]-(N-acetyl-beta-D-glucosaminyl) asparagineamidase (i.e., peptide:N-glycanase or PNGase) orthologous to buddingyeast PNG1 and human NGLY1; PNG-1 is atypically organized, with anN-terminal thioredoxin-like domain, a central transglutaminase domain,and a C-terminal DUF750 domain, while lacking the PUB domain found inmammalian or insect PNGases; both in vitro and in vivo, PNG-1 shows bothprotein disulfide reductase and PNGase activities, which require itsN-terminal and central domains respectively; PNG-1 has PNGase activityon denatured but not natively folded RNAse B, and releases both highmannose- and sialo-complex-type N-glycans from glycopeptides anddenatured glycoproteins; in vivo, the png-1(cy8) mutation C251Y(predicted to destroy the PNGase active site) abolishes PNGase activitywhile leaving PNG-1's reductase activity intact; conversely, PNG-1'sreductase activity is abolished by the dual missense mutation C34S/C37S,which alters its predicted N-terminal active site; by orthology, PNG-1is expected to aid proteasomal degradation of misfolded proteins; PNG-1activity is inhibited by Zn(2+) and the caspase inhibitor z-VAD-fmk, butnot by EDTA; PNG-1 is expressed in renal gland cells and intestine;although W04G5.5 and Y50D4B.7 have some similarity to thetransglutaminase domain of PNG-1, they lack a predicted catalytic triadactive site.Paper_evidenceWBPaper00006525
WBPaper00029398
WBPaper00029436
Curator_confirmedWBPerson567
Date_last_updated05 Jun 2007 00:00:00
Automated_descriptionEnables peptide-N4-(N-acetyl-beta-glucosaminyl)asparagine amidase activity and protein-disulfide reductase (NAD(P)) activity. Involved in cell redox homeostasis; negative regulation of collateral sprouting; and ubiquitin-dependent ERAD pathway. Located in cytoplasm. Expressed in body wall musculature; gonad; neurons; pharynx; and vulva. Human ortholog(s) of this gene implicated in NGLY1-deficiency. Is an ortholog of human NGLY1 (N-glycanase 1).Paper_evidenceWBPaper00065943
Curator_confirmedWBPerson324
WBPerson37462
Inferred_automaticallyThis description was generated automatically by a script based on data from the WS291 version of WormBase
Date_last_updated29 Nov 2023 00:00:00
Disease_infoPotential_modelDOID:0060728Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:17646)
Molecular_infoCorresponding_CDSF56G4.5
Corresponding_transcriptF56G4.5.1
Other_sequenceEX539623.1
Acan_isotig11424
CBC00976_1
MAC00959_1
ACC06749_1
PT03448
SR04827
Dviv_isotig29313
MA01872
Associated_featureWBsf656941
WBsf985278
WBsf1010709
WBsf218531
Experimental_infoRNAi_resultWBRNAi00116961Inferred_automaticallyRNAi_primary
WBRNAi00076493Inferred_automaticallyRNAi_primary
WBRNAi00048764Inferred_automaticallyRNAi_primary
WBRNAi00032982Inferred_automaticallyRNAi_primary
WBRNAi00004720Inferred_automaticallyRNAi_primary
Expr_patternExpr6232
Expr8899
Expr8900
Expr1024009
Expr1034438
Expr1152511
Expr2014983
Expr2033218
Drives_constructWBCnstr00002775
WBCnstr00013592
WBCnstr00013594
Construct_productWBCnstr00013594
Microarray_results (21)
Expression_cluster (85)
Interaction (21)
Map_infoMapIPosition7.95669Error0.002444
PositivePositive_cloneF56G4Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
Reference (17)
RemarkMap position created from combination of previous interpolated map position (based on known location of sequence) and allele information. Therefore this is not a genetic map position based on recombination frequencies or genetic experiments. This was done on advice of the CGC.CGC_data_submission
MethodGene