O95744 (PM2P2_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
May 1, 2013.
Version 77.
History...
Names·Attributes·General annotation·Ontologies·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order
Names·Attributes·General annotation·Ontologies·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize orderNames and origin
| Protein names | Recommended name: Putative postmeiotic segregation increased 2-like protein 2 Alternative name(s): Postmeiotic segregation increased 2-like protein 14 Postmeiotic segregation increased protein 4 Putative postmeiotic segregation increased 2 pseudogene 2 | ||||
| Gene names |
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| Organism | Homo sapiens (Human) [Reference proteome] | ||||
| Taxonomic identifier | 9606 [NCBI] | ||||
| Taxonomic lineage | Eukaryota › Metazoa › Chordata › Craniata › Vertebrata › Euteleostomi › Mammalia › Eutheria › Euarchontoglires › Primates › Haplorrhini › Catarrhini › Hominidae › Homo![]() |
Protein attributes
| Sequence length | 297 AA. |
| Sequence status | Complete. |
| Protein existence | Uncertain |
General annotation (Comments)
| Tissue specificity | Highly expressed in kidney, spleen, adrenal gland, esophagus, duodenum, colon, bladder, ovary, cerebrum and cerebellum and to a lower extent in lung, liver, stomach, uterus and pancreas. Not expressed in heart. Ref.1 |
| Miscellaneous | Encoded by one of the numerous copies of postmeiotic segregation increased 2-like genes scattered in the q11-q22 region of the chromosome 7. |
| Sequence similarities | Belongs to the DNA mismatch repair MutL/HexB family. |
| Caution | Could be the product of a pseudogene. |
Ontologies
| Keywords | |
|---|---|
| Technical term | Complete proteome Reference proteome |
| Gene Ontology (GO) | |
| Biological_process | mismatch repair Inferred from Biological aspect of Ancestor. Source: RefGenome reciprocal meiotic recombinationInferred from Biological aspect of Ancestor. Source: RefGenome somatic hypermutation of immunoglobulin genesInferred from Biological aspect of Ancestor. Source: RefGenome |
| Cellular_component | MutLalpha complex Inferred from Biological aspect of Ancestor. Source: RefGenome |
| Molecular_function | ATP binding Inferred from electronic annotation. Source: InterPro ATPase activityInferred from Biological aspect of Ancestor. Source: RefGenome MutSalpha complex bindingInferred from Biological aspect of Ancestor. Source: RefGenome mismatched DNA bindingInferred from electronic annotation. Source: InterPro single-stranded DNA bindingInferred from Biological aspect of Ancestor. Source: RefGenome |
| Complete GO annotation... | |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||
Molecule processing | |||||||
|---|---|---|---|---|---|---|---|
| Chain | 1 – 297 | 297 | Putative postmeiotic segregation increased 2-like protein 2 | PRO_0000311099 | |||
Sequences
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References
| [1] | "The human PMS2L proteins do not interact with hMLH1, a major DNA mismatch repair protein." Kondo E., Horii A., Fukushige S. J. Biochem. 125:818-825(1999) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA], TISSUE SPECIFICITY. Tissue: Fetal brain. |
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | AB017005 mRNA. Translation: BAA74754.1. |
| IPI | IPI00032884. |
3D structure databases | |
| HSSP | HSSP built from PDB template 1H7U based on UniProtKB P54278. |
| ProteinModelPortal | O95744. |
| ModBase | Search... |
Protein-protein interaction databases | |
| STRING | 9606.ENSP00000369775. |
Proteomic databases | |
| PaxDb | O95744. |
| PRIDE | O95744. |
Protocols and materials databases | |
| StructuralBiologyKnowledgebase | Search... |
Organism-specific databases | |
| GeneCards | GC07M074880. |
| HGNC | HGNC:9127. PMS2P2. |
| neXtProt | NX_O95744. |
| GenAtlas | Search... |
Phylogenomic databases | |
| eggNOG | COG0323. |
| HOVERGEN | HBG108275. |
| InParanoid | O95744. |
Gene expression databases | |
| Genevestigator | O95744. |
Family and domain databases | |
| Gene3D | 3.30.565.10. 1 hit. |
| InterPro | IPR002099. DNA_mismatch_repair. IPR003594. HATPase_ATP-bd. [Graphical view] |
| PANTHER | PTHR10073. PTHR10073. 1 hit. |
| SUPFAM | SSF55874. ATP_bd_ATPase. 1 hit. |
| ProtoNet | Search... |
Entry information
| Entry name | PM2P2_HUMAN | ||||||||
| Accession | Primary (citable) accession number: O95744 | ||||||||
| 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 7 Human chromosome 7: entries, gene names and cross-references to MIM |
| SIMILARITY comments Index of protein domains and families |

Clusters with
