Details for: TXNL4A
Associated with
Other Information
Genular Protein ID: 2374307508
Symbol: TXN4A_HUMAN
Name: Thioredoxin-like protein 4A
UniProtKB Accession Codes:
Database IDs:
Citations:
PubMed ID: 10610776
Title: Identification, characterization and crystal structure analysis of the human spliceosomal U5 snRNP-specific 15kD protein.
PubMed ID: 10610776
PubMed ID: 14702039
Title: Complete sequencing and characterization of 21,243 full-length human cDNAs.
PubMed ID: 14702039
DOI: 10.1038/ng1285
PubMed ID: 15489334
Title: The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
PubMed ID: 15489334
DOI: 10.1101/gr.2596504
PubMed ID: 11054566
Title: Evidence that Dim1 associates with proteins involved in pre-mRNA splicing, and delineation of residues essential for Dim1 interactions with hnRNP F and Npw38/PQBP-1.
PubMed ID: 11054566
PubMed ID: 16723661
Title: The network of protein-protein interactions within the human U4/U6.U5 tri-snRNP.
PubMed ID: 16723661
DOI: 10.1261/rna.55406
PubMed ID: 18669648
Title: A quantitative atlas of mitotic phosphorylation.
PubMed ID: 18669648
PubMed ID: 19690332
Title: Quantitative phosphoproteomic analysis of T cell receptor signaling reveals system-wide modulation of protein-protein interactions.
PubMed ID: 19690332
PubMed ID: 20858735
Title: Interactions of ErbB4 and Kap1 connect the growth factor and DNA damage response pathways.
PubMed ID: 20858735
PubMed ID: 21269460
Title: Initial characterization of the human central proteome.
PubMed ID: 21269460
PubMed ID: 25434003
Title: Compound heterozygosity of low-frequency promoter deletions and rare loss-of-function mutations in TXNL4A causes Burn-McKeown syndrome.
PubMed ID: 25434003
PubMed ID: 11015569
Title: The evolutionarily conserved Dim1 protein defines a novel branch of the thioredoxin fold superfamily.
PubMed ID: 11015569
PubMed ID: 12911302
Title: Structure, stability, and function of hDim1 investigated by NMR, circular dichroism, and mutational analysis.
PubMed ID: 12911302
DOI: 10.1021/bi034486i
PubMed ID: 17467737
Title: Structural basis for the bifunctionality of the U5 snRNP 52K protein (CD2BP2).
PubMed ID: 17467737
PubMed ID: 24781215
Title: Mutations in the PQBP1 gene prevent its interaction with the spliceosomal protein U5-15 kD.
PubMed ID: 24781215
DOI: 10.1038/ncomms4822
PubMed ID: 26912367
Title: Molecular architecture of the human U4/U6.U5 tri-snRNP.
PubMed ID: 26912367
PubMed ID: 28781166
Title: Cryo-EM Structure of a Pre-catalytic Human Spliceosome Primed for Activation.
PubMed ID: 28781166
Sequence Information:
- Length: 142
- Mass: 16786
- Checksum: EDDDAD7ADAEE87F3
- Sequence:
MSYMLPHLHN GWQVDQAILS EEDRVVVIRF GHDWDPTCMK MDEVLYSIAE KVKNFAVIYL VDITEVPDFN KMYELYDPCT VMFFFRNKHI MIDLGTGNNN KINWAMEDKQ EMVDIIETVY RGARKGRGLV VSPKDYSTKY RY
Genular Protein ID: 3696430537
Symbol: K7ESL1_HUMAN
Name: N/A
UniProtKB Accession Codes:
Database IDs:
Citations:
PubMed ID: 16177791
Title: DNA sequence and analysis of human chromosome 18.
PubMed ID: 16177791
DOI: 10.1038/nature03983
PubMed ID: 18669648
Title: A quantitative atlas of mitotic phosphorylation.
PubMed ID: 18669648
PubMed ID: 19690332
Title: Quantitative phosphoproteomic analysis of T cell receptor signaling reveals system-wide modulation of protein-protein interactions.
PubMed ID: 19690332
PubMed ID: 21269460
Title: Initial characterization of the human central proteome.
PubMed ID: 21269460
Sequence Information:
- Length: 71
- Mass: 8463
- Checksum: ECE068B4B93C20CC
- Sequence:
MYELYDPCTV MFFFRNKHIM IDLGTGNNNK INWAMEDKQE MVDIIETVYR GARKGRGLVV SPKDYSTKYR Y
Database document:
This is a preview of the gene's schema. Only a few entries are kept for 'singleCellExpressions,' 'mRNAExpressions,' and other large data arrays for visualization purposes. You can zoom in with the mouse wheel for a closer view, and the text will adjust automatically if necessary. For the full schema, download it here.