MICAL1
[F-actin]-monooxygenase MICAL1
Also known as: DKFZp434B1517, FLJ11937, FLJ21739, MICA1_HUMAN, MICAL, NICAL
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8TDZ2
- Gene
- MICAL1
- Ensembl
- ENSG00000135596
- Chromosome
- 6
- Canonical length
- 1067 aa
- Protein class
- Enzymes, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Plasma membrane,Primary cilium,Basal body,Cytosol
OverviewNCBI Gene
This gene encodes an enzyme that oxidizes methionine residues on actin, thereby promoting depolymerization of actin filaments. This protein interacts with and regulates signalling by NEDD9/CAS-L (neural precursor cell expressed, developmentally down-regulated 9). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2015]
Canonical amino-acid sequenceUniProt
1067 residues, UniProt reviewed canonical sequence.
>Q8TDZ2|MICAL1
1 MASPTSTNPA HAHFESFLQA QLCQDVLSSF QELCGALGLE PGGGLPQYHK IKDQLNYWSA
61 KSLWTKLDKR AGQPVYQQGR ACTSTKCLVV GAGPCGLRVA VELALLGARV VLVEKRTKFS
121 RHNVLHLWPF TIHDLRALGA KKFYGRFCTG TLDHISIRQL QLLLLKVALL LGVEIHWGVT
181 FTGLQPPPRK GSGWRAQLQP NPPAQLANYE FDVLISAAGG KFVPEGFKVR EMRGKLAIGI
241 TANFVNGRTV EETQVPEISG VARIYNQSFF QSLLKATGID LENIVYYKDD THYFVMTAKK
301 QCLLRLGVLR QDWPDTNRLL GSANVVPEAL QRFTRAAADF ATHGKLGKLE FAQDAHGQPD
361 VSAFDFTSMM RAESSARVQE KHGARLLLGL VGDCLVEPFW PLGTGVARGF LAAFDAAWMV
421 KRWAEGAESL EVLAERESLY QLLSQTSPEN MHRNVAQYGL DPATRYPNLN LRAVTPNQVR
481 DLYDVLAKEP VQRNNDKTDT GMPATGSAGT QEELLRWCQE QTAGYPGVHV SDLSSSWADG
541 LALCALVYRL QPGLLEPSEL QGLGALEATA WALKVAENEL GITPVVSAQA VVAGSDPLGL
601 IAYLSHFHSA FKSMAHSPGP VSQASPGTSS AVLFLSKLQR TLQRSRAKEN AEDAGGKKLR
661 LEMEAETPST EVPPDPEPGV PLTPPSQHQE AGAGDLCALC GEHLYVLERL CVNGHFFHRS
721 CFRCHTCEAT LWPGGYEQHP GDGHFYCLQH LPQTDHKAEG SDRGPESPEL PTPSENSMPP
781 GLSTPTASQE GAGPVPDPSQ PTRRQIRLSS PERQRLSSLN LTPDPEMEPP PKPPRSCSAL
841 ARHALESSFV GWGLPVQSPQ ALVAMEKEEK ESPFSSEEEE EDVPLDSDVE QALQTFAKTS
901 GTMNNYPTWR RTLLRRAKEE EMKRFCKAQT IQRRLNEIEA ALRELEAEGV KLELALRRQS
961 SSPEQQKKLW VGQLLQLVDK KNSLVAEEAE LMITVQELNL EEKQWQLDQE LRGYMNREEN
1021 LKTAADRQAE DQVLRKLVDL VNQRDALIRF QEERRLSELA LGTGAQGLocalizationUniProt · AlphaFold · HPA
Whether an antibody against MICAL1 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
- Other membrane
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.36
- Highest tissue expression
- 74 nTPM
Expression across tissuesHPA
Tissue
- urinary bladder: 74 nTPM
- bone marrow: 62 nTPM
- spleen: 59 nTPM
- blood vessel: 48 nTPM
- small intestine: 44 nTPM
- fallopian tube: 39 nTPM
Single-cell type
- neutrophils: 86 nCPM
- neutrophil progenitors: 85 nCPM
- smooth muscle cells: 67 nCPM
- decidual stromal cells: 62 nCPM
- pdcs: 60 nCPM
- vascular smooth muscle cells: 58 nCPM
Immune cell
- basophil: 15 nTPM
- plasmacytoid DC: 14 nTPM
- non-classical monocyte: 14 nTPM
- eosinophil: 14 nTPM
- intermediate monocyte: 13 nTPM
- myeloid DC: 13 nTPM
Brain region
- white matter: 26 nTPM
- medulla oblongata: 23 nTPM
- pons: 22 nTPM
- thalamus: 22 nTPM
- hypothalamus: 21 nTPM
- cerebral cortex: 19 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about MICAL1.
Disease | GeneticClinVar
4 pathogenic / likely-pathogenic of 1,306 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
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)
- 0.92
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.24
- DepMap mean gene effect
- 0.01
- DepMap dependency class
- none
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
- actin filament bundle assembly
- actin filament depolymerization
- cytoskeleton organization
- negative regulation of apoptotic process
- regulation of regulated secretory pathway
- signal transduction
- sulfur oxidation
Molecular functions
- actin binding
- actin filament binding
- F-actin monooxygenase activity
- FAD binding
- metal ion binding
- monooxygenase activity
- NAD(P)H oxidase H2O2-forming activity
- oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen
- protein kinase binding
- SH3 domain binding
- small GTPase binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Calponin homology domain
- Zinc finger, LIM-type
- FAD-binding domain
- bMERB domain
- FAD/NAD(P)-binding domain superfamily
- CH domain superfamily
- F-actin Monooxygenase Mical
- [F-actin]-monooxygenase MICAL1-3-like, Rossman domain
- Calponin homology (CH) domain
- LIM domain
- FAD binding domain
- Bivalent Mical/EHBP Rab binding domain
- Mical, Rossman domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of MICAL1 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads MICAL1 as an antibody target. Whether an autoantibody or antibody against MICAL1 could matter depends on whether native MICAL1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
MICAL1 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label MICAL1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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