Entity Details

Primary name CLPP_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ16740
EntryNameCLPP_HUMAN
FullNameATP-dependent Clp protease proteolytic subunit, mitochondrial
TaxID9606
Evidenceevidence at protein level
Length277
SequenceStatuscomplete
DateCreated1998-07-15
DateModified2021-06-02

Ontological Relatives

GenesCLPP

GO terms

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GOName
GO:0004175 endopeptidase activity
GO:0004176 ATP-dependent peptidase activity
GO:0004252 serine-type endopeptidase activity
GO:0005739 mitochondrion
GO:0005759 mitochondrial matrix
GO:0006515 protein quality control for misfolded or incompletely synthesized proteins
GO:0008233 peptidase activity
GO:0009368 endopeptidase Clp complex
GO:0033619 membrane protein proteolysis
GO:0042802 identical protein binding
GO:0051117 ATPase binding
GO:0051603 proteolysis involved in cellular protein catabolic process

Subcellular Location

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Subcellular Location
Mitochondrion matrix

Domains

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DomainNameCategoryType
IPR001907 ATP-dependent Clp protease proteolytic subunitFamilyFamily
IPR018215 ClpP, Ser active siteSiteActive site
IPR023562 Clp protease proteolytic subunit /Translocation-enhancing protein TepAFamilyFamily
IPR029045 ClpP/crotonase-like domain superfamilyFamilyHomologous superfamily
IPR033135 ClpP, histidine active siteSiteActive site

Diseases

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Disease IDSourceNameDescription
614129 OMIMPerrault syndrome 3 (PRLTS3)A sex-influenced disorder characterized by sensorineural deafness in both males and females, and ovarian dysgenesis in females. Affected females have primary amenorrhea, streak gonads, and infertility, whereas affected males show normal pubertal development and are fertile. A spectrum of additional clinical features, including cerebellar ataxia, learning disability, and peripheral neuropathy, have been described in some PRLTS3 affected individuals. The disease is caused by variants affecting the gene represented in this entry.

Drugs

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DrugNameSourceType
DB04464 N-FormylmethionineDrugbanksmall molecule

Interactions

33 interactions

InteractorPartnerSourcesPublicationsLink
CLPP_HUMANPLS4_HUMANBioGRID, IntAct32296183 details
CLPP_HUMANCLPX_HUMANBioGRID, HPRD, IntAct11923310 26058080 details
CLPP_HUMANRBPMS_HUMANBioGRID, IntAct32296183 details
CLPP_HUMANCN119_HUMANBioGRID, IntAct32296183 details
CLPP_HUMANWFS1_HUMANIntAct32814053 details
CLPP_HUMANPP2AA_HUMANBioGRID, IntAct32296183 details
CLPP_HUMANP4HA3_HUMANBioGRID, IntAct32296183 details
CLPP_HUMANGDAP1_HUMANIntAct32814053 details
CLPP_HUMANFBLN4_HUMANBioGRID, IntAct32296183 details
CLPP_HUMANTNPO3_HUMANBioGRID, IntAct32296183 details
CLPP_HUMANJPH3_HUMANIntAct32814053 details
CLPP_HUMANFBLN3_HUMANBioGRID, IntAct32296183 details
CLPP_HUMANATX3_HUMANIntAct32814053 details
CLPP_HUMANPSB1_HUMANBioGRID, IntAct32296183 details
CLPP_HUMANDTX2_HUMANBioGRID, IntAct32296183 details
CLPP_HUMANCLPP_HUMANBioGRID, DIP, HPRD16115876 20637416 31056398 details
CLPP_HUMANABI2_HUMANBioGRID, IntAct32296183 details
CLPP_HUMANGRN_HUMANBioGRID, IntAct32296183 details
CLPP_HUMANNTF2_HUMANBioGRID, IntAct32296183 details
CLPP_HUMANTRI54_HUMANBioGRID, IntAct31391242 details
CLPP_HUMANSYUA_HUMANBioGRID, IntAct30877431 32814053 details
CLPP_HUMANDYN2_HUMANIntAct32814053 details
CLPP_HUMANA4_HUMANIntAct32814053 details
CLPP_HUMANKR101_HUMANBioGRID32296183 details
CLPP_HUMANHD_HUMANIntAct32814053 details
CLPP_HUMANMIC19_HUMANBioGRID30877431 31056398 details
CLPP_HUMANTADBP_HUMANIntAct32814053 details
CLPP_HUMANHLAB_HUMANIntAct17353931 details
CLPP_HUMANRCAF1_HUMANIntAct17353931 details
CLPP_HUMANRBM47_HUMANBioGRID29395067 details
CLPP_HUMANSAP18_HUMANIntAct17353931 details
CLPP_HUMANGRSF1_HUMANBioGRID29395067 31056398 details
CLPP_HUMANSOMA_HUMANIntAct17353931 details