Reviewed,
UniProtKB/Swiss-Prot Q9P2N2 (RHG28_HUMAN)
Last modified
November 24, 2009.
Version 55.
History...
Clusters with 100%,
90%,
50% identity |
Documents (5) |
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Names and origin
| Protein names | Recommended name: Rho GTPase-activating protein 28 Alternative name(s): Rho-type GTPase-activating protein 28 | ||||
| Gene names |
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| Organism | Homo sapiens (Human) [Complete 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 | 729 AA. |
| Sequence status | Complete. |
| Sequence processing | The displayed sequence is not processed. |
| Protein existence | Evidence at transcript level. |
General annotation (Comments)
| Function | GTPase activator for the Rho-type GTPases by converting them to an inactive GDP-bound state By similarity. |
| Tissue specificity | Expressed in testis. Expressed at moderate level in kidney and ovary, and weakly expressed in spleen and skeletal muscle. Ref.1 |
| Post-translational modification | Phosphorylated upon DNA damage, probably by ATM or ATR By similarity. |
| Sequence similarities | Contains 1 Rho-GAP domain. |
Ontologies
| Keywords | |
|---|---|
| Coding sequence diversity | Alternative splicing Polymorphism |
| Molecular function | GTPase activation |
| PTM | Phosphoprotein |
| Technical term | Complete proteome |
| Gene Ontology (GO) | |
| Biological process | signal transduction Inferred from electronic annotation. Source: InterPro |
| Cellular component | intracellular Inferred from electronic annotation. Source: InterPro |
| Molecular function | GTPase activator activity Inferred from electronic annotation. Source: UniProtKB-KW |
| Complete GO annotation... | |
Alternative products
| This entry describes 4 isoforms produced by alternative splicing. [Align] [Select] | ||||||
| Isoform 1 (identifier: Q9P2N2-1) 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: Q9P2N2-2) The sequence of this isoform differs from the canonical sequence as follows: 1-52: Missing. 677-729: SHGSSECIKI...EWVIKPQPSS → RILHWQRAAL...LFTIGLDIST | ||||||
| Isoform 3 (identifier: Q9P2N2-3) The sequence of this isoform differs from the canonical sequence as follows: 1-177: Missing. 178-181: SESP → MNEL 677-729: SHGSSECIKI...EWVIKPQPSS → RILHWQRAAL...LFTIGLDIST | ||||||
| Note: No experimental confirmation available. | ||||||
| Isoform 4 (identifier: Q9P2N2-4) The sequence of this isoform differs from the canonical sequence as follows: 677-729: SHGSSECIKI...EWVIKPQPSS → RILHWQRAAL...LFTIGLDIST | ||||||
| Note: No experimental confirmation available. |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 729 | 729 | Rho GTPase-activating protein 28 | PRO_0000280476 | |||||
Regions | |||||||||
| Domain | 380 – 577 | 198 | Rho-GAP | ||||||
Amino acid modifications | |||||||||
| Modified residue | 155 | 1 | Phosphothreonine By similarity | ||||||
| Modified residue | 157 | 1 | Phosphothreonine By similarity | ||||||
| Modified residue | 159 | 1 | Phosphothreonine By similarity | ||||||
Natural variations | |||||||||
| Alternative sequence | 1 – 177 | 177 | Missing in isoform 3. | VSP_023725 | |||||
| Alternative sequence | 1 – 52 | 52 | Missing in isoform 2. | VSP_023726 | |||||
| Alternative sequence | 178 – 181 | 4 | SESP → MNEL in isoform 3. | VSP_023727 | |||||
| Alternative sequence | 677 – 729 | 53 | SHGSS…PQPSS → RILHWQRAALSFLNGKWVKK EREESTETNRSPKHVFLFTI GLDIST in isoform 2, isoform 3 and isoform 4. | VSP_023728 | |||||
| Natural variant | 168 | 1 | I → V: dbSNP rs2303978. | VAR_055833 | |||||
| Natural variant | 190 | 1 | T → S: dbSNP rs6506448. | VAR_031155 | |||||
| Natural variant | 727 | 1 | P → Q: dbSNP rs1056408. Ref.2 | VAR_031156 | |||||
Sequences
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References
| [1] | "Prediction of the coding sequences of unidentified human genes. XVI. The complete sequences of 150 new cDNA clones from brain which code for large proteins in vitro." Nagase T., Kikuno R., Ishikawa K., Hirosawa M., Ohara O. DNA Res. 7:65-73(2000) [PubMed: 10718198] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 2), TISSUE SPECIFICITY. Tissue: Brain. |
| [2] | "DNA sequence and analysis of human chromosome 18." Nusbaum C., Zody M.C., Borowsky M.L., Kamal M., Kodira C.D., Taylor T.D., Whittaker C.A., Chang J.L., Cuomo C.A., Dewar K., FitzGerald M.G., Yang X., Abouelleil A., Allen N.R., Anderson S., Bloom T., Bugalter B., Butler J. Lander E.S.Nature 437:551-555(2005) [PubMed: 16177791] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA], VARIANT GLN-727. |
| [3] | "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)." The MGC Project Team Genome Res. 14:2121-2127(2004) [PubMed: 15489334] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 3), NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 334-729 (ISOFORM 1). Tissue: Brain and Skin. |
| [4] | "Complete sequencing and characterization of 21,243 full-length human cDNAs." Ota T., Suzuki Y., Nishikawa T., Otsuki T., Sugiyama T., Irie R., Wakamatsu A., Hayashi K., Sato H., Nagai K., Kimura K., Makita H., Sekine M., Obayashi M., Nishi T., Shibahara T., Tanaka T., Ishii S. Sugano S.Nat. Genet. 36:40-45(2004) [PubMed: 14702039] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 298-729. |
Cross-references
Sequence databases | |
|---|---|
| AB037735 mRNA. Translation: BAA92552.1. Different initiation. AP005205 Genomic DNA. No translation available. AP005210 Genomic DNA. No translation available. BC033668 mRNA. Translation: AAH33668.2. BC065274 mRNA. Translation: AAH65274.1. AK001174 mRNA. Translation: BAA91533.1. Different initiation. | |
| IPI | IPI00002392. IPI00296793. IPI00743001. IPI00830014. |
| PIR | E59436. |
| RefSeq | NP_001010000.1. NP_109597.2. |
| UniGene | Hs.183114 |
3D structure databases | |
| ModBase | Search... |
Protein-protein interaction databases | |
| STRING | Q9P2N2. |
PTM databases | |
| PhosphoSite | Q9P2N2. |
Genome annotation databases | |
| Ensembl | ENST00000419673; ENSP00000392660; ENSG00000088756; Homo sapiens. [Genome view] |
| GeneID | 79822. |
| KEGG | hsa:79822. |
| UCSC | uc002knf.1. human. |
Organism-specific databases | |
| CTD | 79822. |
| GeneCards | GC18P006781. |
| HGNC | HGNC:25509. ARHGAP28. |
| MIM | 610592. gene. |
| PharmGKB | PA134915320. |
| HUGE | Search... |
| GenAtlas | Search... |
Phylogenomic databases | |
| HOVERGEN | Q9P2N2. |
| OMA | SSRRMSD |
| OrthoDB | EOG9FXTSW |
Enzyme and pathway databases | |
| Reactome | REACT_11044. Signaling by Rho GTPases. |
Gene expression databases | |
| ArrayExpress | Q9P2N2. |
| Bgee | Q9P2N2. |
| CleanEx | HS_ARHGAP28. |
| Genevestigator | Q9P2N2. |
Family and domain databases | |
| InterPro | IPR008936. Rho_GTPase_activation_prot. IPR000198. RhoGAP. [Graphical view] |
| Gene3D | G3DSA:1.10.555.10. RhoGAP. 1 hit. |
| Pfam | PF00620. RhoGAP. 1 hit. [Graphical view] |
| SMART | SM00324. RhoGAP. 1 hit. [Graphical view] |
| PROSITE | PS50238. RHOGAP. 1 hit. [Graphical view] |
| ProtoNet | Search... |
Other Resources | |
| NextBio | 69444. |
| SOURCE | Search... |
Entry information
| Entry name | RHG28_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q9P2N2 Secondary accession number(s): Q6P160, Q8N4T3, Q9NW53 | ||||||||
| Entry history |
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| Entry status | Reviewed (UniProtKB/Swiss-Prot) | ||||||||
| Annotation project | HPI (Human Proteome Initiative) | ||||||||
| 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 18 Human chromosome 18: 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 |
| MIM cross-references Online Mendelian Inheritance in Man (MIM) cross-references in UniProtKB/Swiss-Prot |
| SIMILARITY comments Index of protein domains and families |

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