Q96M98 (PACRG_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
January 25, 2012.
Version 80.
History...
Names·Attributes·General annotation·Ontologies·Alt products·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order
Names·Attributes·General annotation·Ontologies·Alt products·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize orderNames and origin
| Protein names | Recommended name: Parkin coregulated gene protein Alternative name(s): Molecular chaperone/chaperonin-binding protein PARK2 coregulated gene protein | ||||
| Gene names |
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| Organism | Homo sapiens (Human) | ||||
| Taxonomic identifier | 9606 [NCBI] | ||||
| Taxonomic lineage | Eukaryota › Metazoa › Chordata › Craniata › Vertebrata › Euteleostomi › Mammalia › Eutheria › Euarchontoglires › Primates › Haplorrhini › Catarrhini › Hominidae › Homo |
Protein attributes
| Sequence length | 296 AA. |
| Sequence status | Complete. |
| Protein existence | Evidence at protein level |
General annotation (Comments)
| Function | Suppresses cell death induced by accumulation of unfolded Pael receptor (Pael-R, a substrate of Parkin). Facilitates the formation of inclusions consisting of Pael-R, molecular chaperones, protein degradation molecules and itself when proteasome is inhibited. May play an important role in the formation of Lewy bodies and protection of dopaminergic neurons against Parkinson disease. Ref.6 |
| Subunit structure | Forms a large molecular chaperone complex containing heat shock proteins 70 and 90 and chaperonin components. Interacts with STIP1, PARK2, GPR37, HSPA8, TCP1/CCT1, CCT2, CCT3, CCT4, CCT5, CCT6A, CCT7, CCT8. Interacts with MEIG1 By similarity. Ref.6 |
| Tissue specificity | Expressed in all immune tissues, spleen, lymph nodes, thymus, tonsils, leukocyte and bone marrow. Expressed also in heart, brain, skeletal muscle, kidney, lung and pancreas. Expressed in primary Schwann cells and very weakly by monocyte-derived macrophages the primary host cells of Mycobacterium leprae, the causative agent of leprosy. Component of Lewy bodies, intraneuronal inclusions found in the brain of Parkinson disease patients. |
| Polymorphism | Involved in susceptibility to leprosy (LPRS2) [MIM:607572]. LPRS2 is associated with polymorphisms in the 5'-regulatory region shared by the PARK2 gene. |
| Miscellaneous | Linked to PARK2 in a head-to-head arrangement on opposite DNA strands and share a common 5'-flanking promoter region. |
Ontologies
| Keywords | |
|---|---|
| Coding sequence diversity | Alternative splicing |
| Technical term | Complete proteome Reference proteome |
| Gene Ontology (GO) | |
| None. [Check GOA] | |
Alternative products
| This entry describes 2 isoforms produced by alternative splicing. [Align] [Select] | ||||||
| Isoform 1 (identifier: Q96M98-1) This isoform has been chosen as the 'canonical' sequence. All positional information in this entry refers to it. This is also the sequence that appears in the downloadable versions of the entry. | ||||||
| Note: No experimental confirmation available. | ||||||
| Isoform 2 (identifier: Q96M98-2) The sequence of this isoform differs from the canonical sequence as follows: 205-243: Missing. | ||||||
| Note: May be due to exon skipping. |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 296 | 296 | Parkin coregulated gene protein | PRO_0000058169 | |||||
Natural variations | |||||||||
| Alternative sequence | 205 – 243 | 39 | Missing in isoform 2. | VSP_010033 | |||||
Experimental info | |||||||||
| Sequence conflict | 93 | 1 | K → R in BAB71410. Ref.2 | ||||||
| Sequence conflict | 185 | 1 | A → T in AAH30642. Ref.5 | ||||||
Sequences
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References
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | AF546872 mRNA. Translation: AAN37911.1. AK057286 mRNA. Translation: BAB71410.1. AL354942 AP001576 Genomic DNA. Translation: CAI16054.1.AL137182 AP001576 Genomic DNA. Translation: CAI19951.1.AL031121 AP001576 Genomic DNA. Translation: CAI21557.1.AL078585 Genomic DNA. No translation available. AL590286 Genomic DNA. No translation available. AL603788 Genomic DNA. No translation available. CH471051 Genomic DNA. Translation: EAW47565.1. CH471051 Genomic DNA. Translation: EAW47566.1. BC030642 mRNA. Translation: AAH30642.1. BC044227 mRNA. Translation: AAH44227.1. BK001670 mRNA. Translation: DAA02134.1. |
| IPI | IPI00065440. IPI00410380. |
| RefSeq | NP_001073847.1. NM_001080378.1. NP_001073848.1. NM_001080379.1. NP_689623.2. NM_152410.2. |
| UniGene | Hs.25791. |
3D structure databases | |
| ProteinModelPortal | Q96M98. |
| ModBase | Search... |
Protein-protein interaction databases | |
| STRING | Q96M98. |
Polymorphism databases | |
| DMDM | 77416872. |
Proteomic databases | |
| PRIDE | Q96M98. |
Protocols and materials databases | |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000337019; ENSP00000337946; ENSG00000112530. |
| GeneID | 135138. |
| KEGG | hsa:135138. |
| UCSC | uc003qua.1. human. uc003qub.1. human. |
Organism-specific databases | |
| CTD | 135138. |
| GeneCards | GC06P163118. |
| HGNC | HGNC:19152. PACRG. |
| MIM | 607572. phenotype. 608427. gene. |
| neXtProt | NX_Q96M98. |
| Orphanet | 2828. Young adult-onset Parkinsonism. |
| PharmGKB | PA134909011. |
| GenAtlas | Search... |
Phylogenomic databases | |
| eggNOG | prNOG07653. |
| GeneTree | ENSGT00530000063549. |
| HOGENOM | HBG525259. |
| HOVERGEN | HBG053487. |
| InParanoid | Q96M98. |
| OMA | NLNSGDG. |
| OrthoDB | EOG4NCMD9. |
| PhylomeDB | Q96M98. |
Gene expression databases | |
| ArrayExpress | Q96M98. |
| Bgee | Q96M98. |
| CleanEx | HS_PACRG. |
| Genevestigator | Q96M98. |
| GermOnline | ENSG00000112530. Homo sapiens. |
Family and domain databases | |
| InterPro | IPR019399. Parkin_co-regulated_protein. [Graphical view] |
| Pfam | PF10274. ParcG. 2 hits. [Graphical view] |
| ProtoNet | Search... |
Other | |
| NextBio | 83453. |
| SOURCE | Search... |
Entry information
| Entry name | PACRG_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q96M98 Secondary accession number(s): E1P5B5 Q9H1V9 | ||||||||
| Entry history |
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| Entry status | Reviewed (UniProtKB/Swiss-Prot) | ||||||||
| Annotation program | Chordata Protein Annotation Program | ||||||||
| Disclaimer | Any medical or genetic information present in this entry is provided for research, educational and informational purposes only. It is not in any way intended to be used as a substitute for professional medical advice, diagnosis, treatment or care. | ||||||||
Relevant documents
| Human chromosome 6 Human chromosome 6: entries, gene names and cross-references to MIM |
| MIM cross-references Online Mendelian Inheritance in Man (MIM) cross-references in UniProtKB/Swiss-Prot |

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