Q9NV79 (PCMD2_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
May 1, 2013.
Version 91.
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: Protein-L-isoaspartate O-methyltransferase domain-containing protein 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 | 361 AA. |
| Sequence status | Complete. |
| Sequence processing | The displayed sequence is further processed into a mature form. |
| Protein existence | Evidence at transcript level |
General annotation (Comments)
| Subcellular location | Cytoplasm By similarity. |
| Sequence similarities | Belongs to the methyltransferase superfamily. L-isoaspartyl/D-aspartyl protein methyltransferase family. |
Ontologies
| Keywords | |
|---|---|
| Cellular component | Cytoplasm |
| Coding sequence diversity | Alternative splicing |
| PTM | Lipoprotein Myristate |
| Technical term | Complete proteome Reference proteome |
| Gene Ontology (GO) | |
| Cellular_component | cytoplasm Inferred from electronic annotation. Source: UniProtKB-SubCell |
| Molecular_function | protein-L-isoaspartate (D-aspartate) O-methyltransferase activity Inferred from electronic annotation. Source: InterPro |
| Complete GO annotation... | |
Alternative products
| This entry describes 3 isoforms produced by alternative splicing. [Align] [Select] | ||||||
| Isoform 1 (identifier: Q9NV79-1) 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. | ||||||
| Isoform 2 (identifier: Q9NV79-2) The sequence of this isoform differs from the canonical sequence as follows: 195-221: Missing. | ||||||
| Note: No experimental confirmation available. | ||||||
| Isoform 3 (identifier: Q9NV79-3) The sequence of this isoform differs from the canonical sequence as follows: 1-224: Missing. 225-236: SESGKSRLVQLP → MLRFCAGLSDFA | ||||||
| Note: No experimental confirmation available. |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Initiator methionine | 1 | 1 | Removed Potential | ||||||
| Chain | 2 – 361 | 360 | Protein-L-isoaspartate O-methyltransferase domain-containing protein 2 | PRO_0000111927 | |||||
Regions | |||||||||
| Compositional bias | 279 – 286 | 8 | Poly-Arg | ||||||
Sites | |||||||||
| Active site | 64 | 1 | By similarity | ||||||
Amino acid modifications | |||||||||
| Lipidation | 2 | 1 | N-myristoyl glycine Potential | ||||||
Natural variations | |||||||||
| Alternative sequence | 1 – 224 | 224 | Missing in isoform 3. | VSP_008546 | |||||
| Alternative sequence | 195 – 221 | 27 | Missing in isoform 2. | VSP_008547 | |||||
| Alternative sequence | 225 – 236 | 12 | SESGK…LVQLP → MLRFCAGLSDFA in isoform 3. | VSP_008548 | |||||
Experimental info | |||||||||
| Sequence conflict | 12 | 1 | D → E in BAA91877. Ref.1 | ||||||
Sequences
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References
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | AK001745 mRNA. Translation: BAA91877.1. AK126700 mRNA. Translation: BAC86648.1. AL121581 Genomic DNA. Translation: CAC17006.1. CH471077 Genomic DNA. Translation: EAW75152.1. CH471077 Genomic DNA. Translation: EAW75153.1. BC033665 mRNA. Translation: AAH33665.1. BC040945 mRNA. Translation: AAH40945.1. |
| IPI | IPI00217155. IPI00374720. IPI00884185. |
| RefSeq | NP_001098395.1. NM_001104925.1. NP_060727.2. NM_018257.2. |
| UniGene | Hs.741158. |
3D structure databases | |
| ProteinModelPortal | Q9NV79. |
| ModBase | Search... |
Protein-protein interaction databases | |
| IntAct | Q9NV79. 1 interaction. |
| STRING | 9606.ENSP00000307854. |
PTM databases | |
| PhosphoSite | Q9NV79. |
Polymorphism databases | |
| DMDM | 41688812. |
Proteomic databases | |
| PaxDb | Q9NV79. |
| PRIDE | Q9NV79. |
Protocols and materials databases | |
| DNASU | 55251. |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000266078; ENSP00000266078; ENSG00000203880. ENST00000308824; ENSP00000307854; ENSG00000203880. ENST00000369758; ENSP00000358773; ENSG00000203880. |
| GeneID | 55251. |
| KEGG | hsa:55251. |
| UCSC | uc002yil.4. human. uc002yim.4. human. |
Organism-specific databases | |
| CTD | 55251. |
| GeneCards | GC20P062887. |
| HGNC | HGNC:15882. PCMTD2. |
| neXtProt | NX_Q9NV79. |
| PharmGKB | PA25750. |
| GenAtlas | Search... |
Phylogenomic databases | |
| eggNOG | COG2518. |
| HOGENOM | HOG000038039. |
| HOVERGEN | HBG013478. |
| InParanoid | Q9NV79. |
| OrthoDB | EOG40GCRC. |
Gene expression databases | |
| ArrayExpress | Q9NV79. |
| Bgee | Q9NV79. |
| CleanEx | HS_PCMTD2. |
| Genevestigator | Q9NV79. |
| GermOnline | ENSG00000203880. Homo sapiens. |
Family and domain databases | |
| InterPro | IPR000682. PCMT. [Graphical view] |
| PANTHER | PTHR11579. PTHR11579. 1 hit. |
| Pfam | PF01135. PCMT. 1 hit. [Graphical view] |
| PROSITE | PS01279. PCMT. False negative. [Graphical view] |
| ProtoNet | Search... |
Other | |
| GenomeRNAi | 55251. |
| NextBio | 59314. |
Entry information
| Entry name | PCMD2_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q9NV79 Secondary accession number(s): E1P5H3, Q8IW60, Q9H4K2 | ||||||||
| 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 20 Human chromosome 20: entries, gene names and cross-references to MIM |
| SIMILARITY comments Index of protein domains and families |

Clusters with
