|
Minichromosome Maintenance Proteins
|
D064110 |
[A family of proteins that were originally identified in SACCHAROMYCES CEREVISIAE as being essential for maintaining the structure of minichromosomes00. They form into a protein complex that has helicase activity and is involved in a variety of DNA-related functions including replication elongation, RNA transcription, chromatin remodeling, and genome stability.
] |
|
Thing
|
Thing |
|
|
Minichromosome Maintenance Complex Component 2
|
D064111 |
[A minichromosome maintenance protein that is a key component of the six member MCM protein complex. It contains a NUCLEAR LOCALIZATION SIGNAL which may provide targeting of the protein complex and an extended N-terminus which is rich in SERINE residues.
] |
|
Clustered Regularly Interspaced Short Palindromic Repeats
|
D064112 |
[Repetitive nucleic acid sequences that are principal components of the archaeal and bacterial CRISPR-CAS SYSTEMS, which function as adaptive antiviral defense systems.
] |
|
technetium 99m diethylenetriaminepentaacetate-deoxyglucose
|
C509840 |
|
|
CRISPR-Cas Systems
|
D064113 |
[Adaptive antiviral defense mechanisms, in archaea and bacteria, based on DNA repeat arrays called CLUSTERED REGULARLY INTERSPACED SHORT PALINDROMIC REPEATS (CRISPR elements) that function in conjunction with CRISPR-ASSOCIATED PROTEINS (Cas proteins). Several types have been distinguished, including Type I, Type II, and Type III, based on signature motifs of CRISPR-ASSOCIATED PROTEINS.
] |
|
N-(2-methoxybenzyl)-3-phenylacrylamidine
|
C509841 |
|
|
6-(1-hydroxyimino-4-methylpentyl)-5,8-dimethoxy-1,4-naphthoquinone
|
C509842 |
|
|
HY52 compound
|
C509843 |
|
|
KIAA1009 protein, human
|
C509844 |
|
|
PRUNE2 protein, human
|
C509845 |
|
|
YY2 protein, rat
|
C509846 |
|
|
Mcm7 protein, Xenopus
|
C509836 |
|
|
6,6'-bisbenzothiazole-2,2'-diamine
|
C509837 |
|
|
Dpo4 protein, E coli
|
C509838 |
|
|
IMB 10
|
C509839 |
|
|
Muscular Dystrophy, Oculopharyngeal
|
D039141 |
[An autosomal dominant hereditary disease that presents in late in life and is characterized by DYSPHAGIA and progressive ptosis of the eyelids. Mutations in the gene for POLY(A)-BINDING PROTEIN II have been associated with oculopharyngeal muscular dystrophy.
] |
|
Viscoseal
|
C509830 |
|
|
VP2 protein, infectious pancreatic necrosis virus
|
C509831 |
|
|
Rab20 protein, human
|
C509832 |
|
