PLB1
Phospholipase B1, membrane-associated
Also known as: FLJ30866, PLB, PLB1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q6P1J6
- Gene
- PLB1
- Ensembl
- ENSG00000163803
- Chromosome
- 2
- Canonical length
- 1458 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted intracellular proteins, Predicted membrane proteins
OverviewNCBI Gene
This gene encodes a membrane-associated phospholipase that displays lysophospholipase and phospholipase A2 activities through removal of sn-1 and sn-2 fatty acids of glycerophospholipids. In addition, it displays lipase and retinyl ester hydrolase activities. The encoded protein is highly conserved and is composed of a large, glycosylated extracellular domain composed of four tandem homologous domains, followed by a hydrophobic segment that anchors the enzyme to the membrane and a short C-terminal cytoplasmic tail. This gene has been identified as a candidate rheumatoid arthritis risk gene. [provided by RefSeq, Jul 2016]
Canonical amino-acid sequenceUniProt
1458 residues, UniProt reviewed canonical sequence.
>Q6P1J6|PLB1
1 MGLRPGIFLL ELLLLLGQGT PQIHTSPRKS TLEGQLWPET LKNSPFPCNP NKLGVNMPSK
61 SVHSLKPSDI KFVAAIGNLE IPPDPGTGDL EKQDWTERPQ QVCMGVMTVL SDIIRYFSPS
121 VPMPVCHTGK RVIPHDGAED LWIQAQELVR NMKENLQLDF QFDWKLINVF FSNASQCYLC
181 PSAQQNGLAA GGVDELMGVL DYLQQEVPRA FVNLVDLSEV AEVSRQYHGT WLSPAPEPCN
241 CSEETTRLAK VVMQWSYQEA WNSLLASSRY SEQESFTVVF QPFFYETTPS LHSEDPRLQD
301 STTLAWHLWN RMMEPAGEKD EPLSVKHGRP MKCPSQESPY LFSYRNSNYL TRLQKPQDKL
361 EVREGAEIRC PDKDPSDTVP TSVHRLKPAD INVIGALGDS LTAGNGAGST PGNVLDVLTQ
421 YRGLSWSVGG DENIGTVTTL ANILREFNPS LKGFSVGTGK ETSPNAFLNQ AVAGGRAEDL
481 PVQARRLVDL MKNDTRIHFQ EDWKIITLFI GGNDLCDFCN DLVHYSPQNF TDNIGKALDI
541 LHAEVPRAFV NLVTVLEIVN LRELYQEKKV YCPRMILRSL CPCVLKFDDN STELATLIEF
601 NKKFQEKTHQ LIESGRYDTR EDFTVVVQPF FENVDMPKTS EGLPDNSFFA PDCFHFSSKS
661 HSRAASALWN NMLEPVGQKT TRHKFENKIN ITCPNQVQPF LRTYKNSMQG HGTWLPCRDR
721 APSALHPTSV HALRPADIQV VAALGDSLTA GNGIGSKPDD LPDVTTQYRG LSYSAGGDGS
781 LENVTTLPNI LREFNRNLTG YAVGTGDAND TNAFLNQAVP GAKAEDLMSQ VQTLMQKMKD
841 DHRVNFHEDW KVITVLIGGS DLCDYCTDSN LYSAANFVHH LRNALDVLHR EVPRVLVNLV
901 DFLNPTIMRQ VFLGNPDKCP VQQASVLCNC VLTLRENSQE LARLEAFSRA YRSSMRELVG
961 SGRYDTQEDF SVVLQPFFQN IQLPVLADGL PDTSFFAPDC IHPNQKFHSQ LARALWTNML
1021 EPLGSKTETL DLRAEMPITC PTQNEPFLRT PRNSNYTYPI KPAIENWGSD FLCTEWKASN
1081 SVPTSVHQLR PADIKVVAAL GDSLTTAVGA RPNNSSDLPT SWRGLSWSIG GDGNLETHTT
1141 LPNILKKFNP YLLGFSTSTW EGTAGLNVAA EGARARDMPA QAWDLVERMK NSPDINLEKD
1201 WKLVTLFIGV NDLCHYCENP EAHLATEYVQ HIQQALDILS EELPRAFVNV VEVMELASLY
1261 QGQGGKCAML AAQNNCTCLR HSQSSLEKQE LKKVNWNLQH GISSFSYWHQ YTQREDFAVV
1321 VQPFFQNTLT PLNERGDTDL TFFSEDCFHF SDRGHAEMAI ALWNNMLEPV GRKTTSNNFT
1381 HSRAKLKCPS PESPYLYTLR NSRLLPDQAE EAPEVLYWAV PVAAGVGLVV GIIGTVVWRC
1441 RRGGRREDPP MSLRTVALLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PLB1 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Cell surface
- Secreted
- No
- Transmembrane segments
- 1
- Mean surface accessibility (rSASA)
- 0.25
- Highest tissue expression
- 37 nTPM
Expression across tissuesHPA
Tissue
- small intestine: 37 nTPM
- skin: 7.4 nTPM
- adrenal gland: 5.2 nTPM
- bone marrow: 4.7 nTPM
- choroid plexus: 4.5 nTPM
- spleen: 4 nTPM
Single-cell type
- neutrophils: 337 nCPM
- enterocytes: 314 nCPM
- neutrophil progenitors: 67 nCPM
- kupffer cells: 67 nCPM
- epicardial cells: 64 nCPM
- extravillous trophoblasts: 61 nCPM
Immune cell
- neutrophil: 8.9 nTPM
- myeloid DC: 5.7 nTPM
- non-classical monocyte: 5 nTPM
- intermediate monocyte: 4.4 nTPM
- classical monocyte: 3 nTPM
- eosinophil: 3 nTPM
Brain region
- amygdala: 6.2 nTPM
- basal ganglia: 6.2 nTPM
- hypothalamus: 5.6 nTPM
- hippocampal formation: 5.1 nTPM
- spinal cord: 4.9 nTPM
- cerebral cortex: 4.7 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about PLB1.
Disease | AutoantibodyPubMed
Conditions in which antibodies against PLB1 are reported. Each links to that disease's full target list.
- Glomerulonephritis, Membranous 173
- Proteinuria 25
- Nephrotic Syndrome 20
- Kidney Failure, Chronic 6
- Anti-Glomerular Basement Membrane Disease 3
- Glomerulonephritis 3
Showing 6 of 7 — disease pages carrying at least 10 antigens.
ReferencesPubMed · IEDB
Publications for PLB1 from three distinct lines of evidence, kept separate because they answer different questions: whether antibodies are directed at the protein, whether a B-cell epitope has been mapped on it, and whether a T-cell epitope has. Each is labelled with its source.
Reference: AutoantibodyPubMed
204 publications
- Thrombospondin type-1 domain-containing 7A in idiopathic membranous nephropathy.
2014 · N Engl J Med · RCR 23.7 · 706 citations - Membranous nephropathy: new pathogenic mechanisms and their clinical implications.
2022 · Nat Rev Nephrol · RCR 11.2 · 128 citations - Altered glycosylation of IgG4 promotes lectin complement pathway activation in anti-PLA2R1-associated membranous nephropathy.
2021 · J Clin Invest · RCR 10.8 · 153 citations - Anti-Phospholipase A2 Receptor Antibody Titer Predicts Post-Rituximab Outcome of Membranous Nephropathy.
2015 · J Am Soc Nephrol · RCR 10.8 · 291 citations - Anti-phospholipase A2 receptor antibody in membranous nephropathy.
2011 · J Am Soc Nephrol · RCR 10.7 · 334 citations
Show 20 more of 204 total
- Phospholipase A2 receptor autoantibodies and clinical outcome in patients with primary membranous nephropathy.
2014 · J Am Soc Nephrol · RCR 9 · 261 citations - Anti-PLA2R antibodies measured by ELISA predict long-term outcome in a prevalent population of patients with idiopathic membranous nephropathy.
2013 · Kidney Int · RCR 9 · 272 citations - Antiphospholipase A2 receptor antibody titer and subclass in idiopathic membranous nephropathy.
2012 · J Am Soc Nephrol · RCR 8.2 · 260 citations - Noninvasive diagnosis of primary membranous nephropathy using phospholipase A2 receptor antibodies.
2019 · Kidney Int · RCR 7.7 · 141 citations - Ofatumumab in Rituximab-Resistant and Rituximab-Intolerant Patients With Primary Membranous Nephropathy: A Case Series.
2024 · Am J Kidney Dis · RCR 5.4 · 30 citations - Association of anti-PLA₂R antibodies with outcomes after immunosuppressive therapy in idiopathic membranous nephropathy.
2014 · Clin J Am Soc Nephrol · RCR 5 · 145 citations - Mechanisms of Primary Membranous Nephropathy.
2021 · Biomolecules · RCR 5 · 67 citations - Identification of the immunodominant epitope region in phospholipase A2 receptor-mediating autoantibody binding in idiopathic membranous nephropathy.
2015 · J Am Soc Nephrol · RCR 4.3 · 119 citations - Membranous nephropathy: recent travels and new roads ahead.
2010 · Kidney Int · RCR 4.3 · 144 citations - Membranous nephropathy: a review on the pathogenesis, diagnosis, and treatment.
2015 · J Formos Med Assoc · RCR 4.2 · 106 citations - Phase 1b/2a Study Assessing the Safety and Efficacy of Felzartamab in Anti-Phospholipase A2 Receptor Autoantibody-Positive Primary Membranous Nephropathy.
2024 · Kidney Int Rep · RCR 4.2 · 23 citations - Noninvasive Diagnosis of PLA2R-Associated Membranous Nephropathy: A Validation Study.
2021 · Clin J Am Soc Nephrol · RCR 4.2 · 54 citations - The diagnosis accuracy of PLA2R-AB in the diagnosis of idiopathic membranous nephropathy: a meta-analysis.
2014 · PLoS One · RCR 4 · 108 citations - Development of a standardized ELISA for the determination of autoantibodies against human M-type phospholipase A2 receptor in primary membranous nephropathy.
2013 · Clin Chim Acta · RCR 4 · 119 citations - Autoantibodies against phospholipase A2 receptor in Korean patients with membranous nephropathy.
2013 · PLoS One · RCR 3.9 · 102 citations - Novel ELISA for thrombospondin type 1 domain-containing 7A autoantibodies in membranous nephropathy.
2019 · Kidney Int · RCR 3.7 · 68 citations - Detection of PLA2R Autoantibodies before the Diagnosis of Membranous Nephropathy.
2020 · J Am Soc Nephrol · RCR 3.6 · 64 citations - Tacrolimus combined with corticosteroids versus Modified Ponticelli regimen in treatment of idiopathic membranous nephropathy: Randomized control trial.
2016 · Nephrology (Carlton) · RCR 3.5 · 77 citations - Clinical Relevance of Domain-Specific Phospholipase A2 Receptor 1 Antibody Levels in Patients with Membranous Nephropathy.
2020 · J Am Soc Nephrol · RCR 3.4 · 62 citations - Autoantibodies specific for the phospholipase A2 receptor in recurrent and De Novo membranous nephropathy.
2011 · Am J Transplant · RCR 3.4 · 106 citations
Sources: PubMed — antigen-level antibody evidence from a custom retrieval. Records matching a controlled set of autoantibody terms (the MeSH descriptors Autoantibodies and Autoantigens, with title and abstract term variants) were obtained through NCBI E-utilities, and their titles and abstracts parsed for constructions that direct an antibody at a named protein rather than for co-occurrence. Captured names were resolved against UniProt nomenclature and each antigen adjudicated individually against the source text. Bibliographic records from PubMed and MeSH, U.S. National Library of Medicine; citation metrics from NIH iCite (Hutchins et al., PLoS Biology 2016). Titles link to PubMed; abstracts are not reproduced here. The NLM does not endorse this analysis.
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 1.23
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.59
- DepMap mean gene effect
- -0.06
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- diacylglycerol catabolic process
- phosphatidylcholine acyl-chain remodeling
- phosphatidylcholine catabolic process
- phosphatidylethanolamine catabolic process
- phosphatidylglycerol catabolic process
- phospholipid metabolic process
- positive regulation of acrosome reaction
- retinoid metabolic process
- triglyceride catabolic process
Molecular functions
- calcium-independent phospholipase A2 activity
- phosphatidylcholine lysophospholipase activity
- phospholipase A2 activity
- retinyl-palmitate esterase activity
- triacylglycerol lipase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
- GDSL lipase/esterase
- SGNH hydrolase superfamily
- GDSL-like Lipase/Acylhydrolase
- Lipase, GDSL, active site
- Phospholipase B
- Phospholipase B1, membrane-associated
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads PLB1 as an antibody target. Whether an autoantibody or antibody against PLB1 could matter depends on whether native PLB1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PLB1 is annotated at the cell surface, where native PLB1 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label PLB1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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