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A0A1L9T9C0 | Ipi1_N domain-containing protein. (364 aa) | ||||
A0A1L9U131 | Uncharacterized protein; Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family. (309 aa) | ||||
A0A1L9U0K8 | Nucleolar complex-associated protein 3; Required for synthesis of 60S ribosomal subunits and the transport of pre-ribosomes from the nucleoplasm to the cytoplasm. Belongs to the CBF/MAK21 family. (691 aa) | ||||
A0A1L9U023 | SCD domain-containing protein. (1208 aa) | ||||
A0A1L9TZC4 | Uncharacterized protein. (166 aa) | ||||
A0A1L9TYD8 | Uncharacterized protein. (115 aa) | ||||
A0A1L9TY73 | Uncharacterized protein. (1053 aa) | ||||
A0A1L9TY10 | Chromo domain-containing protein. (264 aa) | ||||
A0A1L9TWN5 | Uncharacterized protein. (864 aa) | ||||
A0A1L9TVU8 | Uncharacterized protein. (673 aa) | ||||
A0A1L9TVN1 | Origin recognition complex subunit 1; Component of the origin recognition complex (ORC) that binds origins of replication. DNA-binding is ATP-dependent, however specific DNA sequences that define origins of replication have not been identified so far. ORC is required to assemble the pre-replication complex necessary to initiate DNA replication. (797 aa) | ||||
A0A1L9TVM1 | SLD3 domain-containing protein. (932 aa) | ||||
A0A1L9TVL1 | CBFD_NFYB_HMF domain-containing protein. (270 aa) | ||||
A0A1L9TVH4 | Uncharacterized protein. (1517 aa) | ||||
A0A1L9TVB0 | Protein HIR; Required for replication-independent chromatin assembly and for the periodic repression of histone gene transcription during the cell cycle; Belongs to the WD repeat HIR1 family. (1066 aa) | ||||
A0A1L9TUS7 | Uncharacterized protein. (1621 aa) | ||||
A0A1L9TUL2 | Uncharacterized protein. (1268 aa) | ||||
A0A1L9TT17 | Uncharacterized protein. (108 aa) | ||||
A0A1L9TS74 | Chromo domain-containing protein. (980 aa) | ||||
A0A1L9TRL9 | Uncharacterized protein; Belongs to the iron/ascorbate-dependent oxidoreductase family. (1085 aa) | ||||
A0A1L9TRG9 | Transcription initiation factor TFIID subunit 10; Functions as a component of the DNA-binding general transcription factor complex TFIID and the transcription regulatory histone acetylation (HAT) complexes SAGA and SLIK. Binding of TFIID to a promoter (with or without TATA element) is the initial step in preinitiation complex (PIC) formation. TFIID plays a key role in the regulation of gene expression by RNA polymerase II through different activities such as transcription activator interaction, core promoter recognition and selectivity, TFIIA and TFIIB interaction, chromatin modificati [...] (274 aa) | ||||
A0A1L9TR82 | WD_REPEATS_REGION domain-containing protein. (366 aa) | ||||
A0A1L9TQP7 | Transcription elongation factor Spt6; Plays a role in maintenance of chromatin structure during RNA polymerase II transcription elongation thereby repressing transcription initiation from cryptic promoters. Mediates the reassembly of nucleosomes onto the promoters of at least a selected set of genes during repression; the nucleosome reassembly is essential for transcriptional repression; Belongs to the SPT6 family. (1418 aa) | ||||
A0A1L9TQG1 | Uncharacterized protein; Belongs to the DEAD box helicase family. (419 aa) | ||||
A0A1L9TQE2 | Uncharacterized protein. (885 aa) | ||||
A0A1L9TPR9 | WD_REPEATS_REGION domain-containing protein. (572 aa) | ||||
A0A1L9TPI6 | H15 domain-containing protein. (95 aa) | ||||
A0A1L9TPE9 | Uncharacterized protein. (823 aa) | ||||
A0A1L9TPD3 | Myb-like domain-containing protein. (835 aa) | ||||
A0A1L9TNF7 | Uncharacterized protein. (162 aa) | ||||
A0A1L9TNF1 | PHD-type domain-containing protein. (902 aa) | ||||
A0A1L9TNA4 | Uncharacterized protein. (607 aa) | ||||
A0A1L9TMZ4 | Uncharacterized protein. (1111 aa) | ||||
A0A1L9TMD8 | Uncharacterized protein; Belongs to the actin family. (550 aa) | ||||
A0A1L9TKP8 | Uncharacterized protein. (699 aa) | ||||
A0A1L9TJA0 | Uncharacterized protein. (229 aa) | ||||
A0A1L9TJ59 | Uncharacterized protein. (1109 aa) | ||||
A0A1L9THJ9 | TPR_REGION domain-containing protein. (865 aa) | ||||
A0A1L9TGV3 | Uncharacterized protein. (491 aa) | ||||
A0A1L9TGU2 | Structural maintenance of chromosomes protein. (1179 aa) | ||||
A0A1L9TGP7 | SANT domain-containing protein. (754 aa) | ||||
A0A1L9TGJ2 | DNA polymerase. (1946 aa) | ||||
A0A1L9TF08 | Sister chromatid cohesion protein. (1777 aa) | ||||
A0A1L9TEI8 | Uncharacterized protein. (591 aa) | ||||
A0A1L9TEH1 | Uncharacterized protein; Belongs to the actin family. (472 aa) | ||||
A0A1L9TED5 | Condensin complex subunit 2; Regulatory subunit of the condensin complex, a complex required for conversion of interphase chromatin into mitotic-like condense chromosomes. (871 aa) | ||||
A0A1L9TEA0 | PHD-type domain-containing protein. (744 aa) | ||||
A0A1L9TDL1 | Uncharacterized protein. (872 aa) | ||||
A0A1L9TCU2 | Uncharacterized protein. (1698 aa) | ||||
A0A1L9TB46 | Histone H2A; Belongs to the histone H2A family. (138 aa) | ||||
A0A1L9TB28 | Cleavage and polyadenylation specificity factor subunit 5; Component of the cleavage factor Im (CFIm) complex that functions as an activator of the pre-mRNA 3'-end cleavage and polyadenylation processing required for the maturation of pre-mRNA into functional mRNAs. CFIm contributes to the recruitment of multiprotein complexes on specific sequences on the pre-mRNA 3'-end, so called cleavage and polyadenylation signals (pA signals). Most pre-mRNAs contain multiple pA signals, resulting in alternative cleavage and polyadenylation (APA) producing mRNAs with variable 3'-end formation. The [...] (277 aa) | ||||
A0A1L9TB12 | Cnd3 domain-containing protein. (310 aa) | ||||
A0A1L9TAY2 | Cnd3 domain-containing protein. (692 aa) | ||||
A0A1L9TAI1 | Uncharacterized protein. (364 aa) | ||||
A0A1L9TA71 | WD_REPEATS_REGION domain-containing protein. (839 aa) | ||||
A0A1L9TA54 | Uncharacterized protein. (1028 aa) | ||||
A0A1L9T9W4 | Uncharacterized protein. (143 aa) | ||||
A0A1L9T8K2 | Uncharacterized protein; Belongs to the actin family. (469 aa) | ||||
A0A1L9T8E9 | Uncharacterized protein. (172 aa) | ||||
A0A1L9T8A2 | Brr6_like_C_C domain-containing protein. (446 aa) | ||||
A0A1L9T7C9 | Uncharacterized protein; Belongs to the nucleosome assembly protein (NAP) family. (410 aa) | ||||
A0A1L9T6X2 | FACT complex subunit POB3; Component of the FACT complex, a general chromatin factor that acts to reorganize nucleosomes. The FACT complex is involved in multiple processes that require DNA as a template such as mRNA elongation, DNA replication and DNA repair. During transcription elongation the FACT complex acts as a histone chaperone that both destabilizes and restores nucleosomal structure. It facilitates the passage of RNA polymerase II and transcription by promoting the dissociation of one histone H2A-H2B dimer from the nucleosome, then subsequently promotes the reestablishment of [...] (576 aa) | ||||
A0A1L9T6U5 | FHA domain-containing protein. (515 aa) | ||||
A0A1L9T355 | Uncharacterized protein; Belongs to the nucleosome assembly protein (NAP) family. (351 aa) | ||||
A0A1L9T1K2 | Uncharacterized protein. (696 aa) | ||||
A0A1L9T1E2 | Uncharacterized protein. (1479 aa) | ||||
KAE1 | tRNA N6-adenosine threonylcarbamoyltransferase; Component of the EKC/KEOPS complex that is required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine. The complex is probably involved in the transfer of the threonylcarbamoyl moiety of threonylcarbamoyl-AMP (TC-AMP) to the N6 group of A37. KAE1 likely plays a direct catalytic role in this reaction, but requires other protein(s) of the complex to fulfill this activity. The EKC/KEOPS complex also promotes both telomere uncapping and telomere elongation. Th [...] (367 aa) |