Details for: PNKD
Associated with
Other Information
Genular Protein ID: 3680217716
Symbol: PNKD_HUMAN
Name: Probable hydrolase PNKD
UniProtKB Accession Codes:
Database IDs:
Citations:
PubMed ID: 15188056
Title: Characterization of MR-1, a novel myofibrillogenesis regulator in human muscle.
PubMed ID: 15188056
PubMed ID: 15188498
Title: Transactivating effect of hepatitis C virus core protein: a suppression subtractive hybridization study.
PubMed ID: 15188498
PubMed ID: 12975309
Title: The secreted protein discovery initiative (SPDI), a large-scale effort to identify novel human secreted and transmembrane proteins: a bioinformatics assessment.
PubMed ID: 12975309
DOI: 10.1101/gr.1293003
PubMed ID: 14702039
Title: Complete sequencing and characterization of 21,243 full-length human cDNAs.
PubMed ID: 14702039
DOI: 10.1038/ng1285
PubMed ID: 17974005
Title: The full-ORF clone resource of the German cDNA consortium.
PubMed ID: 17974005
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: 10574461
Title: Characterization of cDNA clones selected by the GeneMark analysis from size-fractionated cDNA libraries from human brain.
PubMed ID: 10574461
PubMed ID: 16717228
Title: Genetic heterogeneity in paroxysmal nonkinesigenic dyskinesia.
PubMed ID: 16717228
PubMed ID: 17525332
Title: ATM and ATR substrate analysis reveals extensive protein networks responsive to DNA damage.
PubMed ID: 17525332
PubMed ID: 18691976
Title: Kinase-selective enrichment enables quantitative phosphoproteomics of the kinome across the cell cycle.
PubMed ID: 18691976
PubMed ID: 21269460
Title: Initial characterization of the human central proteome.
PubMed ID: 21269460
PubMed ID: 24275569
Title: An enzyme assisted RP-RPLC approach for in-depth analysis of human liver phosphoproteome.
PubMed ID: 24275569
PubMed ID: 15262732
Title: Myofibrillogenesis regulator 1 gene mutations cause paroxysmal dystonic choreoathetosis.
PubMed ID: 15262732
PubMed ID: 15496428
Title: The gene for paroxysmal non-kinesigenic dyskinesia encodes an enzyme in a stress response pathway.
PubMed ID: 15496428
DOI: 10.1093/hmg/ddh330
PubMed ID: 15824259
Title: Presence of alanine-to-valine substitutions in myofibrillogenesis regulator 1 in paroxysmal nonkinesigenic dyskinesia: confirmation in 2 kindreds.
PubMed ID: 15824259
PubMed ID: 16972263
Title: Clinical characteristics of paroxysmal nonkinesigenic dyskinesia in Serbian family with Myofibrillogenesis regulator 1 gene mutation.
PubMed ID: 16972263
DOI: 10.1002/mds.21095
PubMed ID: 16632198
Title: Myofibrillogenesis regulator 1 gene (MR-1) mutation in an Omani family with paroxysmal nonkinesigenic dyskinesia.
PubMed ID: 16632198
Sequence Information:
- Length: 385
- Mass: 42876
- Checksum: A4D631D3A4319A2C
- Sequence:
MAAVVAATAL KGRGARNARV LRGILAGATA NKASHNRTRA LQSHSSPEGK EEPEPLSPEL EYIPRKRGKN PMKAVGLAWY SLYTRTWLGY LFYRQQLRRA RNRYPKGHSK TQPRLFNGVK VLPIPVLSDN YSYLIIDTQA QLAVAVDPSD PRAVQASIEK EGVTLVAILC THKHWDHSGG NRDLSRRHRD CRVYGSPQDG IPYLTHPLCH QDVVSVGRLQ IRALATPGHT QGHLVYLLDG EPYKGPSCLF SGDLLFLSGC GRTFEGNAET MLSSLDTVLG LGDDTLLWPG HEYAEENLGF AGVVEPENLA RERKMQWVQR QRLERKGTCP STLGEERSYN PFLRTHCLAL QEALGPGPGP TGDDDYSRAQ LLEELRRLKD MHKSK
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.