1sxe
From Proteopedia
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{{STRUCTURE_1sxe| PDB=1sxe | SCENE= }} | {{STRUCTURE_1sxe| PDB=1sxe | SCENE= }} | ||
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===The solution structure of the Pointed (PNT) domain from the transcrition factor Erg=== | ===The solution structure of the Pointed (PNT) domain from the transcrition factor Erg=== | ||
| + | {{ABSTRACT_PUBMED_15351649}} | ||
| - | + | ==Disease== | |
| + | [[http://www.uniprot.org/uniprot/ERG_HUMAN ERG_HUMAN]] Defects in ERG are a cause of Ewing sarcoma (ES) [MIM:[http://omim.org/entry/612219 612219]]. A highly malignant, metastatic, primitive small round cell tumor of bone and soft tissue that affects children and adolescents. It belongs to the Ewing sarcoma family of tumors, a group of morphologically heterogeneous neoplasms that share the same cytogenetic features. They are considered neural tumors derived from cells of the neural crest. Ewing sarcoma represents the less differentiated form of the tumors. Note=A chromosomal aberration involving ERG is found in patients with Erwing sarcoma. Translocation t(21;22)(q22;q12) with EWSR1. Note=Chromosomal aberrations involving ERG have been found in acute myeloid leukemia (AML). Translocation t(16;21)(p11;q22) with FUS. Translocation t(X;21)(q25-26;q22) with ELF4. | ||
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| + | ==Function== | ||
| + | [[http://www.uniprot.org/uniprot/ERG_HUMAN ERG_HUMAN]] Transcriptional regulator. May participate in transcriptional regulation through the recruitment of SETDB1 histone methyltransferase and subsequent modification of local chromatin structure. | ||
==About this Structure== | ==About this Structure== | ||
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==Reference== | ==Reference== | ||
| - | <ref group="xtra">PMID:015351649</ref><references group="xtra"/> | + | <ref group="xtra">PMID:015351649</ref><references group="xtra"/><references/> |
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Gentile, L N.]] | [[Category: Gentile, L N.]] | ||
Revision as of 05:12, 25 March 2013
Contents |
The solution structure of the Pointed (PNT) domain from the transcrition factor Erg
Template:ABSTRACT PUBMED 15351649
Disease
[ERG_HUMAN] Defects in ERG are a cause of Ewing sarcoma (ES) [MIM:612219]. A highly malignant, metastatic, primitive small round cell tumor of bone and soft tissue that affects children and adolescents. It belongs to the Ewing sarcoma family of tumors, a group of morphologically heterogeneous neoplasms that share the same cytogenetic features. They are considered neural tumors derived from cells of the neural crest. Ewing sarcoma represents the less differentiated form of the tumors. Note=A chromosomal aberration involving ERG is found in patients with Erwing sarcoma. Translocation t(21;22)(q22;q12) with EWSR1. Note=Chromosomal aberrations involving ERG have been found in acute myeloid leukemia (AML). Translocation t(16;21)(p11;q22) with FUS. Translocation t(X;21)(q25-26;q22) with ELF4.
Function
[ERG_HUMAN] Transcriptional regulator. May participate in transcriptional regulation through the recruitment of SETDB1 histone methyltransferase and subsequent modification of local chromatin structure.
About this Structure
1sxe is a 1 chain structure with sequence from Homo sapiens. Full experimental information is available from OCA.
Reference
- Mackereth CD, Scharpf M, Gentile LN, MacIntosh SE, Slupsky CM, McIntosh LP. Diversity in structure and function of the Ets family PNT domains. J Mol Biol. 2004 Sep 24;342(4):1249-64. PMID:15351649 doi:10.1016/j.jmb.2004.07.094
