A4D1S0 (KLRG2_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
April 3, 2013.
Version 51.
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: Killer cell lectin-like receptor subfamily G member 2 Alternative name(s): C-type lectin domain family 15 member B | ||||
| 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 | 409 AA. |
| Sequence status | Complete. |
| Protein existence | Evidence at transcript level |
General annotation (Comments)
| Subcellular location | Membrane; Single-pass membrane protein Potential. |
| Sequence similarities | Contains 1 C-type lectin domain. |
Ontologies
| Keywords | |
|---|---|
| Cellular component | Membrane |
| Coding sequence diversity | Alternative splicing Polymorphism |
| Domain | Transmembrane Transmembrane helix |
| Ligand | Lectin |
| PTM | Disulfide bond |
| Technical term | Complete proteome Reference proteome |
| Gene Ontology (GO) | |
| Cellular_component | integral to membrane Inferred from electronic annotation. Source: UniProtKB-KW |
| Molecular_function | carbohydrate binding Inferred from electronic annotation. Source: InterPro |
| Complete GO annotation... | |
Alternative products
| This entry describes 2 isoforms produced by alternative splicing. [Align] [Select] | ||||||
| Isoform 1 (identifier: A4D1S0-1) 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: A4D1S0-2) The sequence of this isoform differs from the canonical sequence as follows: 253-312: GLPMYVKSLY...HCYYFSAEAQ → DSLRTARTIW...DAAPPTGEAS 313-409: Missing. |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||||
Molecule processing | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 409 | 409 | Killer cell lectin-like receptor subfamily G member 2 | PRO_0000316792 | |||||||
Regions | |||||||||||
| Transmembrane | 263 – 283 | 21 | Helical; Potential | ||||||||
| Domain | 300 – 405 | 106 | C-type lectin | ||||||||
| Compositional bias | 18 – 159 | 142 | Pro-rich | ||||||||
Amino acid modifications | |||||||||||
| Disulfide bond | 321 ↔ 404 | By similarity | |||||||||
| Disulfide bond | 383 ↔ 396 | By similarity | |||||||||
Natural variations | |||||||||||
| Alternative sequence | 253 – 312 | 60 | GLPMY…SAEAQ → DSLRTARTIWISTVGPWRKA RWWLQTAALQDPGSVPRGPS DLGSAWSSACQADAAPPTGE AS in isoform 2. | VSP_030779 | |||||||
| Alternative sequence | 313 – 409 | 97 | Missing in isoform 2. | VSP_030780 | |||||||
| Natural variant | 152 | 1 | K → T. Ref.3 Corresponds to variant rs1860150 [ dbSNP | Ensembl ]. | VAR_038396 | |||||||
| Natural variant | 339 | 1 | G → A. Corresponds to variant rs17160911 [ dbSNP | Ensembl ]. | VAR_038397 | |||||||
Experimental info | |||||||||||
| Sequence conflict | 109 | 1 | A → V in EAL24036. Ref.3 | ||||||||
Sequences
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References
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | AK126174 mRNA. Translation: BAC86473.1. AC005531 Genomic DNA. No translation available. CH236950 Genomic DNA. Translation: EAL24036.1. BC104963 mRNA. Translation: AAI04964.1. BC104965 mRNA. Translation: AAI04966.1. BC110858 mRNA. Translation: AAI10859.1. |
| IPI | IPI00394851. IPI00719758. |
| RefSeq | NP_940910.1. NM_198508.2. |
| UniGene | Hs.741701. |
3D structure databases | |
| ProteinModelPortal | A4D1S0. |
| SMR | A4D1S0. Positions 293-406. |
| ModBase | Search... |
Protein family/group databases | |
| MEROPS | I63.002. |
Proteomic databases | |
| PaxDb | A4D1S0. |
| PRIDE | A4D1S0. |
Protocols and materials databases | |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000340940; ENSP00000339356; ENSG00000188883. ENST00000393039; ENSP00000376759; ENSG00000188883. |
| GeneID | 346689. |
| KEGG | hsa:346689. |
| UCSC | uc003vvb.3. human. uc010lnc.3. human. |
Organism-specific databases | |
| CTD | 346689. |
| GeneCards | GC07M139137. |
| HGNC | HGNC:24778. KLRG2. |
| HPA | HPA018199. |
| neXtProt | NX_A4D1S0. |
| PharmGKB | PA162393624. |
| GenAtlas | Search... |
Phylogenomic databases | |
| eggNOG | NOG239548. |
| HOGENOM | HOG000168488. |
| HOVERGEN | HBG108069. |
| InParanoid | A4D1S0. |
| OMA | CSAYHAT. |
| OrthoDB | EOG4894MZ. |
| PhylomeDB | A4D1S0. |
Gene expression databases | |
| Bgee | A4D1S0. |
| CleanEx | HS_KLRG2. |
| Genevestigator | A4D1S0. |
Family and domain databases | |
| Gene3D | 3.10.100.10. 1 hit. |
| InterPro | IPR001304. C-type_lectin. IPR016186. C-type_lectin-like. IPR016187. C-type_lectin_fold. [Graphical view] |
| SMART | SM00034. CLECT. 1 hit. [Graphical view] |
| SUPFAM | SSF56436. C-type_lectin_fold. 1 hit. |
| PROSITE | PS00615. C_TYPE_LECTIN_1. False negative. PS50041. C_TYPE_LECTIN_2. 1 hit. [Graphical view] |
| ProtoNet | Search... |
Other | |
| ChiTaRS | KLRG2. human. |
| GenomeRNAi | 346689. |
| NextBio | 99004. |
Entry information
| Entry name | KLRG2_HUMAN | ||||||||
| Accession | Primary (citable) accession number: A4D1S0 Secondary accession number(s): Q2NL79, Q6ZTV6 | ||||||||
| 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 |
| Human entries with polymorphisms or disease mutations List of human entries with polymorphisms or disease mutations |
| Human polymorphisms and disease mutations Index of human polymorphisms and disease mutations |
| SIMILARITY comments Index of protein domains and families |

Clusters with
