Q59FS0 (Q59FS0_HUMAN) Unreviewed, UniProtKB/TrEMBL

Names and origin

Protein names	Submitted name: GTF2I repeat domain containing 1 isoform 2 variant EMBL BAD92626.1
Organism	Homo sapiens (Human) EMBL BAD92626.1
Taxonomic identifier	9606 [NCBI]
Taxonomic lineage	cellular organisms › Eukaryota › Opisthokonta › Metazoa › Eumetazoa › Bilateria › Deuterostomia › Chordata › Craniata › Vertebrata › Gnathostomata › Teleostomi › Euteleostomi › Sarcopterygii › Tetrapoda › Amniota › Mammalia › Theria › Eutheria › Euarchontoglires › Primates › Haplorrhini › Simiiformes › Catarrhini › Hominoidea › Hominidae › Homininae › Homo

Protein attributes

Sequence length	967 AA.
Sequence status	Fragment.
Protein existence	Evidence at transcript level

Ontologies

Gene Ontology (GO)
Cellular_component	cytoplasm Inferred from direct assay. Source: HPA nucleus Inferred from direct assay. Source: HPA
Complete GO annotation...

Sequence annotation (Features)

	Feature key	Position(s)	Length	Description	Graphical view	Feature identifier
Experimental info
	Non-terminal residue	1	1	EMBL BAD92626.1

Sequences

	Sequence		Length	Mass (Da)
	Q59FS0 [UniParc]. Last modified April 26, 2005. Version 1. Checksum: F5B74BAF487B83B2	FASTA	967	106,680
	10 20 30 40 50 60 GTGDQATMAL LGKRCDVPTN GCGPDRWNSA FTRKDEIITS LVSALDSMCS ALSKLNAEVA 70 80 90 100 110 120 CVAVHDESAF VVGTEKGRMF LNARKELQSD FLRFCRGPPW KDPEAEHPKK VQRGEGGGRS 130 140 150 160 170 180 LPRSSLEHGS DVYLLRKMVE EVFDVLYSEA LGRASVVPLP YERLLREPGL LAVQGLPEGL 190 200 210 220 230 240 AFRRPAEYDP KALMAILEHS HRIRFKLKRP LEDGGRDSKA LVELNGVSLI PKGSRDCGLH 250 260 270 280 290 300 GQAPKVPPQD LPPTATSSSM ASFLYSTALP NHAIRELKQE APSCPLAPSD LGLSRPMPEP 310 320 330 340 350 360 KATGAQDFSD CCGQKPTGPG GPLIQNVHAS KRILFSIVHD KSEKWDAFIK ETEDINTLRE 370 380 390 400 410 420 CVQILFNSRY AEALGLDHMV PVPYRKIACD PEAVEIVGIP DKIPFKRPCT YGVPKLKRIL 430 440 450 460 470 480 EERHSIHFII KRMFDERIFT GNKFTKDTTK LEPASPPEDT SAEVSRATVL DLAGNARSDK 490 500 510 520 530 540 GSMSEDCGPG TSGELGGLRP IKIEPEDLDI IQVTVPDPSP TSEEMTDSMP GHLPSEDSGY 550 560 570 580 590 600 GMEMLTDKGL SEDARPEERP VEDSHGDVIR PLRKQVELLF NTRYAKAIGI SEPVKVPYSK 610 620 630 640 650 660 FLMHPEELFV VGLPEGISLR RPNCFGIAKL RKILEASNSI QFVIKRPELL TEGVKEPIMD 670 680 690 700 710 720 SQERDSGDPL VDESLKRQGF QENYDARLSR IDIANTLREQ VQDLFNKKYG EALGIKYPVQ 730 740 750 760 770 780 VPYKRIKSNP GSVIIEGLPP GIPFRKPCTF GSQNLERILA VADKIKFTVT RPFQGLIPKP 790 800 810 820 830 840 DEDDANRLGE KVILREQVKE LFNEKYGEAL GLNRPVLVPY KLIRDSPDAV EVTGLPDDIP 850 860 870 880 890 900 FRNPNTYDIH RLEKILKARE HVRMVIINQL QPFAEICNDA KVPAKDSSIP KRKRKRVSEG 910 920 930 940 950 960 NSVSSSSSSS SSSSSNPDSV ASANQISLVV KLHRFGLRHS SLWPSPLCLA GPSTLGCGPR GRGGTGL

References

[1]	"Homo sapiens protein coding cDNA." Totoki Y., Toyoda A., Takeda T., Sakaki Y., Tanaka A., Yokoyama S., Ohara O., Nagase T., Kikuno R.F. Submitted (MAR-2005) to the EMBL/GenBank/DDBJ databases Cited for: NUCLEOTIDE SEQUENCE. Tissue: Brain EMBL BAD92626.1.
+	Additional computationally mapped references.

Cross-references

Sequence databases
EMBL GenBank DDBJ	AB209389 mRNA. Translation: BAD92626.1.
IPI	IPI00454912.
UniGene	Hs.647056.
3D structure databases
ProteinModelPortal	Q59FS0.
ModBase	Search...
Proteomic databases
PRIDE	Q59FS0.
Protocols and materials databases
StructuralBiologyKnowledgebase	Search...
Phylogenomic databases
HOGENOM	HOG000112829.
HOVERGEN	HBG051855.
Gene expression databases
ArrayExpress	Q59FS0.
Bgee	Q59FS0.
Family and domain databases
Gene3D	3.90.1460.10. 5 hits.
InterPro	IPR004212. GTF2I. IPR016659. TF_II-I. [Graphical view]
Pfam	PF02946. GTF2I. 5 hits. [Graphical view]
PIRSF	PIRSF016441. TF_II-I. 1 hit.
SUPFAM	SSF117773. SSF117773. 5 hits.
PROSITE	PS51139. GTF2I. 5 hits. [Graphical view]
ProtoNet	Search...

Entry information

Entry name

Q59FS0_HUMAN

Accession

Primary (citable) accession number: Q59FS0

Entry history

Integrated into UniProtKB/TrEMBL:	April 26, 2005
Last sequence update:	April 26, 2005
Last modified:	May 29, 2013
This is version 49 of the entry and version 1 of the sequence. [Complete history]

Entry status

Unreviewed (UniProtKB/TrEMBL)

Disclaimer

Any medical or genetic information present in this entry is provided for research, educational and informational purposes only. It is not in any way intended to be used as a substitute for professional medical advice, diagnosis, treatment or care.