======= YME1L1 ======= == Gene Information == * **Official Symbol**: YME1L1 * **Official Name**: YME1 like 1 ATPase * **Aliases and Previous Symbols**: N/A * **Entrez ID**: [[https://www.ncbi.nlm.nih.gov/gene/?term=10730|10730]] * **UniProt**: [[https://www.uniprot.org/uniprot/Q96TA2|Q96TA2]] * **Interactions**: [[https://thebiogrid.org/search.php?search=YME1L1&organism=9606|BioGRID]] * **PubMed articles**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20YME1L1|Open PubMed]] * **OMIM**: [[https://omim.org/entry/607472|Open OMIM]] == Function Summary == * **Entrez Summary**: The protein encoded by this gene is the human ortholog of yeast mitochondrial AAA metalloprotease, Yme1p. It is localized in the mitochondria and can functionally complement a yme1 disruptant yeast strain. It is proposed that this gene plays a role in mitochondrial protein metabolism and could be involved in mitochondrial pathologies. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]. * **UniProt Summary**: ATP-dependent metalloprotease that catalyzes the degradation of folded and unfolded proteins with a suitable degron sequence in the mitochondrial intermembrane region (PubMed:26923599, PubMed:27786171). Plays an important role in regulating mitochondrial morphology and function by cleaving OPA1 at position S2, giving rise to a form of OPA1 that promotes maintenance of normal mitochondrial structure and mitochondrial protein metabolism (PubMed:18076378, PubMed:26923599, PubMed:27495975). Ensures cell proliferation, maintains normal cristae morphology and complex I respiration activity, promotes antiapoptotic activity and protects mitochondria from the accumulation of oxidatively damaged membrane proteins (PubMed:22262461). Required for normal, constitutive degradation of PRELID1 (PubMed:27495975). Catalyzes the degradation of OMA1 in response to membrane depolarization (PubMed:26923599). Required to control the accumulation of nonassembled respiratory chain subunits (NDUFB6, OX4 and ND1) (PubMed:22262461). {ECO:0000269|PubMed:18076378, ECO:0000269|PubMed:22262461, ECO:0000269|PubMed:26923599, ECO:0000269|PubMed:27495975, ECO:0000269|PubMed:27786171}. |Peptidase M41| |AAA| |ATP-dependent peptidase activity| |mitochondrial protein catabolic process| |mitochondrial protein processing| |protein hexamerization| |mitochondrial calcium ion transmembrane transport| |protein quality control for misfolded or incompletely synthesized proteins| |metalloendopeptidase activity| |protein processing| |calcium ion transmembrane transport| |protein maturation| |calcium ion transport| |nuclear body| |divalent metal ion transport| |divalent inorganic cation transport| |mitochondrial inner membrane| |mitochondrion organization| |protein complex oligomerization| |cell population proliferation| |inorganic cation transmembrane transport| |proteolysis involved in cellular protein catabolic process| |cation transmembrane transport| |cellular protein catabolic process| |metal ion transport| |inorganic ion transmembrane transport| |protein catabolic process| |cation transport| |negative regulation of apoptotic process| |negative regulation of programmed cell death| |cellular macromolecule catabolic process| |ion transmembrane transport| |negative regulation of cell death| |macromolecule catabolic process| |organonitrogen compound catabolic process| |mitochondrion| |proteolysis| |transmembrane transport| |ion transport| |ATP binding| |regulation of apoptotic process| |protein-containing complex assembly| |regulation of programmed cell death| |regulation of cell death| |organic substance catabolic process| |cellular catabolic process| |protein-containing complex subunit organization| |membrane| |gene expression| \\ === CRISPR Data === ^Screen^Score^ |[[:results:exp359|FK-506 30μM R07 exp359]]|-1.74| |[[:results:exp191|Hypoxia 5%O2 R04 exp191]]|1.72| |[[:results:exp356|Docosahexaenoic-acid 50μM R07 exp356]]|1.76| |[[:results:exp143|Phenformin 20μM R03 exp143]]|1.79| |[[:results:exp292|Menadione 5μM R06 exp292]]|1.81| |[[:results:exp520|Rucaparib 6.5μM R08 exp520]]|1.82| |[[:results:exp499|LY2090314 0.003μM R08 exp499]]|1.89| |[[:results:exp54|Taxol 0.002μM R01 exp54]]|1.89| |[[:results:exp295|Pyronaridine 1μM R06 exp295]]|1.93| |[[:results:exp357|Dorsomorphin 5μM R07 exp357]]|2.05| |[[:results:exp106|UM131593 0.2μM R03 exp106]]|2.06| |[[:results:exp135|MS023 7μM R03 exp135]]|2.09| |[[:results:exp45|Docetaxel 0.002μM R01 exp45]]|2.15| |[[:results:exp299|Talazoparib 0.006μM R06 exp299]]|2.17| |[[:results:exp291|LLY-284 2.6μM R06 exp291]]|2.2| |[[:results:exp460|BML-284 0.09μM R08 exp460]]|2.21| |[[:results:exp517|Quercetin 20μM R08 exp517]]|2.21| |[[:results:exp21|MLN-4924 0.2μM R00 exp21]]|2.51| |[[:results:exp47|Lapatinib 5μM R01 exp47]]|2.78| |[[:results:exp287|HMS-I2 5μM R06 exp287]]|2.89| ^Gene^Correlation^ |[[:human genes:c:clpb|CLPB]]|0.417| Global Fraction of Cell Lines Where Essential: 8/739 ^Tissue^Fraction Of Cell Lines Where Essential^ |1290807.0|0/1| |909776.0|0/1| |bile duct|0/28| |blood|1/28| |bone|1/26| |breast|0/33| |central nervous system|1/56| |cervix|0/4| |colorectal|0/17| |esophagus|0/13| |fibroblast|0/1| |gastric|0/16| |kidney|0/21| |liver|0/20| |lung|0/75| |lymphocyte|0/16| |ovary|1/26| |pancreas|0/24| |peripheral nervous system|0/16| |plasma cell|0/15| |prostate|0/1| |skin|0/24| |soft tissue|0/9| |thyroid|0/2| |upper aerodigestive|1/22| |urinary tract|0/29| |uterus|0/5| == Essentiality in NALM6 == * **Essentiality Rank**: 1546 * **Expression level (log2 read counts)**: 7.92 {{:chemogenomics:nalm6 dist.png?nolink |}}