This subsection of the ‘Names and taxonomy’ section indicates the name(s) of the gene(s) that code for the protein sequence(s) described in the entry. Association of Tri C/CCT with target proteins during biosynthesis. Cooperation of PDCL (Ph LP1) and TRi C/CCT in G-protein beta folding.

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This study explored the potential critical gene targets of EWSR1/FLI1 knockdown in Ewing sarcoma cells on the gene expression profile based on online dataset, performed Limma algorithm for differentially expressed genes identification, constructed the transcriptional factor (TF)-gene regulatory network based on integrate transcriptional regulatory element database (TRED).

The data showed up- and down-regulation of differentially expressed genes over time and peaked at 72 h after EWSR1/FLI1 knockdown in Ewing sarcoma cells.

Ewing sarcoma breakpoint region 1 (EWSR1) fusion with Friend leukemia integration 1 transcription factor (FLI1) induced by a translocation of chromosome 11 with 22 contributes to Ewing sarcoma development.

To date, the precise molecular mechanisms about EWSR1/FLI1 involving in Ewing sarcoma development remains to be defined.

Cyclic redundancy and other checksums Numerical recipes in C 2nd ed., pp896-902, Cambridge University Press (1993)) 10 20 30 40 50MMDSQLVAGV AFKKTFSYAG FEMQPKKYHN PKIALLNVEL ELKAEKDNAE 60 70 80 90 100IRVHTVEDYQ AIVDAEWNIL YDKLEKIHHS GAKVVLSKLP IGDVATQYFA 110 120 130 140 150DRDMFCAGRV PEEDLKRTMM ACGGSIQTSV NALSADVLGR CQVFEETQIG 160 170 180 190 200GERYNFFTGC PKAKTCTFIL RGGAEQFMEE TERSLHDAIM IVRRAIKNDS 210 220 230 240 250VVAGGGAIEM ELSKYLRDYS RTIPGKQQLL IGAYAKALEI IPRQLCDNAG 260 270 280 290 300FDATNILNKL RARHAQGGTW YGVDINNEDI ADNFEAFVWE PAMVRINALT 310 320 330 AASEAACLIV SVDETIKNPR STVDAPTAAG RGRGRGRPH The checksum is a form of redundancy check that is calculated from the sequence. It should be noted that while, in theory, two different sequences could have the same checksum value, the likelihood that this would happen is extremely low. The checksum is computed as the sequence 64-bit Cyclic Redundancy Check value (CRC64) using the generator polynomial: x x 1. The information stored in this subsection is used to automatically construct alternative protein sequence(s) for display.

However Uni Prot KB may contain entries with identical sequences in case of multiple genes (paralogs). The algorithm is described in the ISO 3309 standard. The changes in the amino acid sequence may be due to alternative splicing, alternative promoter usage, alternative initiation, or ribosomal frameshifting.

Cyclic redundancy and other checksums Numerical recipes in C 2nd ed., pp896-902, Cambridge University Press (1993)) 10 20 30 40 50MDKLIVDGRG KATISNDGAT ILKLLDVVHP AAKTLVDIAK SQDAEVGDGT 60 70 80 90 100TSVTLLAAEF LKQVKPYVEE GLHPQIIIRA FRTATQLAVN KIKEIAVTVK 110 120 130 140 150KADKVEQRKL LEKCAMTALS SKLISQQKAF FAKMVVDAVM MLDDLLQLKM 160 170 180 190 200IGIKKVQGGA LEDSQLVAGV AFKKTFSYAG FEMQPKKYHN PKIALLNVEL 210 220 230 240 250ELKAEKDNAE IRVHTVEDYQ AIVDAEWNIL YDKLEKIHHS GAKVVLSKLP 260 270 280 290 300IGDVATQYFA DRDMFCAGRV PEEDLKRTMM ACGGSIQTSV NALSADVLGR 310 320 330 340 350CQVFEETQIG GERYNFFTGC PKAKTCTFIL RGGAEQFMEE TERSLHDAIM 360 370 380 390 400IVRRAIKNDS VVAGGGAIEM ELSKYLRDYS RTIPGKQQLL IGAYAKALEI 410 420 430 440 450IPRQLCDNAG FDATNILNKL RARHAQGGTW YGVDINNEDI ADNFEAFVWE 460 470 480 490 PAMVRINALT AASEAACLIV SVDETIKNPR STVDAPTAAG RGRGRGRPH The checksum is a form of redundancy check that is calculated from the sequence. It should be noted that while, in theory, two different sequences could have the same checksum value, the likelihood that this would happen is extremely low. The checksum is computed as the sequence 64-bit Cyclic Redundancy Check value (CRC64) using the generator polynomial: x x 1. The information stored in this subsection is used to automatically construct alternative protein sequence(s) for display. This subsection of the ‘Sequence’ section describes the sequence of naturally occurring alternative protein isoform(s).

However Uni Prot KB may contain entries with identical sequences in case of multiple genes (paralogs). The changes in the amino acid sequence may be due to alternative splicing, alternative promoter usage, alternative initiation, or ribosomal frameshifting.

Cyclic redundancy and other checksums Numerical recipes in C 2nd ed., pp896-902, Cambridge University Press (1993)) 10 20 30 40 50MMVGDGTTSV TLLAAEFLKQ VKPYVEEGLH PQIIIRAFRT ATQLAVNKIK 60 70 80 90 100EIAVTVKKAD KVEQRKLLEK CAMTALSSKL ISQQKAFFAK MVVDAVMMLD 110 120 130 140 150DLLQLKMIGI KKVQGGALED SQLVAGVAFK KTFSYAGFEM QPKKYHNPKI 160 170 180 190 200ALLNVELELK AEKDNAEIRV HTVEDYQAIV DAEWNILYDK LEKIHHSGAK 210 220 230 240 250VVLSKLPIGD VATQYFADRD MFCAGRVPEE DLKRTMMACG GSIQTSVNAL 260 270 280 290 300SADVLGRCQV FEETQIGGER YNFFTGCPKA KTCTFILRGG AEQFMEETER 310 320 330 340 350SLHDAIMIVR RAIKNDSVVA GGGAIEMELS KYLRDYSRTI PGKQQLLIGA 360 370 380 390 400YAKALEIIPR QLCDNAGFDA TNILNKLRAR HAQGGTWYGV DINNEDIADN 410 420 430 440 450FEAFVWEPAM VRINALTAAS EAACLIVSVD ETIKNPRSTV DAPTAAGRGR GRGRPH The checksum is a form of redundancy check that is calculated from the sequence. It should be noted that while, in theory, two different sequences could have the same checksum value, the likelihood that this would happen is extremely low. The information stored in this subsection is used to automatically construct alternative protein sequence(s) for display. This subsection of the ‘Sequence’ section describes the sequence of naturally occurring alternative protein isoform(s).

These various submissions may originate from different sequencing projects, different types of experiments, or different biological samples. These various submissions may originate from different sequencing projects, different types of experiments, or different biological samples. These various submissions may originate from different sequencing projects, different types of experiments, or different biological samples. These various submissions may originate from different sequencing projects, different types of experiments, or different biological samples. These various submissions may originate from different sequencing projects, different types of experiments, or different biological samples. These various submissions may originate from different sequencing projects, different types of experiments, or different biological samples. These various submissions may originate from different sequencing projects, different types of experiments, or different biological samples. The changes in the amino acid sequence may be due to alternative splicing, alternative promoter usage, alternative initiation, or ribosomal frameshifting.

Cyclic redundancy and other checksums Numerical recipes in C 2nd ed., pp896-902, Cambridge University Press (1993)) This subsection of the ‘Sequence’ section reports difference(s) between the canonical sequence (displayed by default in the entry) and the different sequence submissions merged in the entry. This subsection of the ‘Sequence’ section reports difference(s) between the canonical sequence (displayed by default in the entry) and the different sequence submissions merged in the entry. This subsection of the ‘Sequence’ section reports difference(s) between the canonical sequence (displayed by default in the entry) and the different sequence submissions merged in the entry. This subsection of the ‘Sequence’ section reports difference(s) between the canonical sequence (displayed by default in the entry) and the different sequence submissions merged in the entry. This subsection of the ‘Sequence’ section reports difference(s) between the canonical sequence (displayed by default in the entry) and the different sequence submissions merged in the entry. This subsection of the ‘Sequence’ section reports difference(s) between the canonical sequence (displayed by default in the entry) and the different sequence submissions merged in the entry. This subsection of the ‘Sequence’ section reports difference(s) between the canonical sequence (displayed by default in the entry) and the different sequence submissions merged in the entry. This subsection of the ‘Sequence’ section describes the sequence of naturally occurring alternative protein isoform(s).