ID:CXL11_HUMAN DESCRIPTION: RecName: Full=C-X-C motif chemokine 11; AltName: Full=Beta-R1; AltName: Full=H174; AltName: Full=Interferon gamma-inducible protein 9; Short=IP-9; AltName: Full=Interferon-inducible T-cell alpha chemoattractant; Short=I-TAC; AltName: Full=Small-inducible cytokine B11; Flags: Precursor; FUNCTION: Chemotactic for interleukin-activated T-cells but not unstimulated T-cells, neutrophils or monocytes. Induces calcium release in activated T-cells. Binds to CXCR3. May play an important role in CNS diseases which involve T-cell recruitment. May play a role in skin immune responses. SUBCELLULAR LOCATION: Secreted. TISSUE SPECIFICITY: High levels in peripheral blood leukocytes, pancreas and liver astrocytes. Moderate levels in thymus, spleen and lung. Low levels in placenta, prostate and small intestine. Also found in epidermal basal layer keratinocytes in skin disorders. INDUCTION: By IFNG/IFN-gamma and IFNB1/IFN-beta. Induction by IFNG/IFN-gamma is enhanced by TNF in monocytes, dermal fibroblasts and endothelial cells, and by IL1/interleukin-1 in astrocytes. MASS SPECTROMETRY: Mass=8303; Method=MALDI; Range=22-94; Source=PubMed:10233762; SIMILARITY: Belongs to the intercrine alpha (chemokine CxC) family. SEQUENCE CAUTION: Sequence=AAB17374.1; Type=Erroneous initiation; WEB RESOURCE: Name=Wikipedia; Note=CXCL11 entry; URL="http://en.wikipedia.org/wiki/CXCL11";
The RNAfold program from the Vienna RNA Package is used to perform the secondary structure predictions and folding calculations. The estimated folding energy is in kcal/mol. The more negative the energy, the more secondary structure the RNA is likely to have.
ModBase Predicted Comparative 3D Structure on O14625
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Orthologous Genes in Other Species
Orthologies between human, mouse, and rat are computed by taking the best BLASTP hit, and filtering out non-syntenic hits. For more distant species reciprocal-best BLASTP hits are used. Note that the absence of an ortholog in the table below may reflect incomplete annotations in the other species rather than a true absence of the orthologous gene.