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INT8_HUMAN
ID   INT8_HUMAN              Reviewed;         995 AA.
AC   Q75QN2; B2RN92; Q5RKZ3; Q6P1R5; Q7Z314; Q9NVS6; Q9NWY7;
DT   31-OCT-2006, integrated into UniProtKB/Swiss-Prot.
DT   05-JUL-2004, sequence version 1.
DT   03-AUG-2022, entry version 149.
DE   RecName: Full=Integrator complex subunit 8;
DE            Short=Int8;
DE   AltName: Full=Protein kaonashi-1;
GN   Name=INTS8; Synonyms=C8orf52;
OS   Homo sapiens (Human).
OC   Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia;
OC   Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae;
OC   Homo.
OX   NCBI_TaxID=9606;
RN   [1]
RP   NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 1).
RC   TISSUE=Brain;
RA   Atsushi S., Asakawa S., Shimizu N.;
RT   "Novel gene with no significant domain.";
RL   Submitted (FEB-2004) to the EMBL/GenBank/DDBJ databases.
RN   [2]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
RA   Mural R.J., Istrail S., Sutton G.G., Florea L., Halpern A.L., Mobarry C.M.,
RA   Lippert R., Walenz B., Shatkay H., Dew I., Miller J.R., Flanigan M.J.,
RA   Edwards N.J., Bolanos R., Fasulo D., Halldorsson B.V., Hannenhalli S.,
RA   Turner R., Yooseph S., Lu F., Nusskern D.R., Shue B.C., Zheng X.H.,
RA   Zhong F., Delcher A.L., Huson D.H., Kravitz S.A., Mouchard L., Reinert K.,
RA   Remington K.A., Clark A.G., Waterman M.S., Eichler E.E., Adams M.D.,
RA   Hunkapiller M.W., Myers E.W., Venter J.C.;
RL   Submitted (JUL-2005) to the EMBL/GenBank/DDBJ databases.
RN   [3]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 1).
RC   TISSUE=Brain, Testis, and Uterus;
RX   PubMed=15489334; DOI=10.1101/gr.2596504;
RG   The MGC Project Team;
RT   "The status, quality, and expansion of the NIH full-length cDNA project:
RT   the Mammalian Gene Collection (MGC).";
RL   Genome Res. 14:2121-2127(2004).
RN   [4]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 180-995 (ISOFORM 2).
RC   TISSUE=Rectum tumor;
RX   PubMed=17974005; DOI=10.1186/1471-2164-8-399;
RA   Bechtel S., Rosenfelder H., Duda A., Schmidt C.P., Ernst U.,
RA   Wellenreuther R., Mehrle A., Schuster C., Bahr A., Bloecker H., Heubner D.,
RA   Hoerlein A., Michel G., Wedler H., Koehrer K., Ottenwaelder B., Poustka A.,
RA   Wiemann S., Schupp I.;
RT   "The full-ORF clone resource of the German cDNA consortium.";
RL   BMC Genomics 8:399-399(2007).
RN   [5]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 307-995 (ISOFORM 1).
RC   TISSUE=Carcinoma, and Teratocarcinoma;
RX   PubMed=14702039; DOI=10.1038/ng1285;
RA   Ota T., Suzuki Y., Nishikawa T., Otsuki T., Sugiyama T., Irie R.,
RA   Wakamatsu A., Hayashi K., Sato H., Nagai K., Kimura K., Makita H.,
RA   Sekine M., Obayashi M., Nishi T., Shibahara T., Tanaka T., Ishii S.,
RA   Yamamoto J., Saito K., Kawai Y., Isono Y., Nakamura Y., Nagahari K.,
RA   Murakami K., Yasuda T., Iwayanagi T., Wagatsuma M., Shiratori A., Sudo H.,
RA   Hosoiri T., Kaku Y., Kodaira H., Kondo H., Sugawara M., Takahashi M.,
RA   Kanda K., Yokoi T., Furuya T., Kikkawa E., Omura Y., Abe K., Kamihara K.,
RA   Katsuta N., Sato K., Tanikawa M., Yamazaki M., Ninomiya K., Ishibashi T.,
RA   Yamashita H., Murakawa K., Fujimori K., Tanai H., Kimata M., Watanabe M.,
RA   Hiraoka S., Chiba Y., Ishida S., Ono Y., Takiguchi S., Watanabe S.,
RA   Yosida M., Hotuta T., Kusano J., Kanehori K., Takahashi-Fujii A., Hara H.,
RA   Tanase T.-O., Nomura Y., Togiya S., Komai F., Hara R., Takeuchi K.,
RA   Arita M., Imose N., Musashino K., Yuuki H., Oshima A., Sasaki N.,
RA   Aotsuka S., Yoshikawa Y., Matsunawa H., Ichihara T., Shiohata N., Sano S.,
RA   Moriya S., Momiyama H., Satoh N., Takami S., Terashima Y., Suzuki O.,
RA   Nakagawa S., Senoh A., Mizoguchi H., Goto Y., Shimizu F., Wakebe H.,
RA   Hishigaki H., Watanabe T., Sugiyama A., Takemoto M., Kawakami B.,
RA   Yamazaki M., Watanabe K., Kumagai A., Itakura S., Fukuzumi Y., Fujimori Y.,
RA   Komiyama M., Tashiro H., Tanigami A., Fujiwara T., Ono T., Yamada K.,
RA   Fujii Y., Ozaki K., Hirao M., Ohmori Y., Kawabata A., Hikiji T.,
RA   Kobatake N., Inagaki H., Ikema Y., Okamoto S., Okitani R., Kawakami T.,
RA   Noguchi S., Itoh T., Shigeta K., Senba T., Matsumura K., Nakajima Y.,
RA   Mizuno T., Morinaga M., Sasaki M., Togashi T., Oyama M., Hata H.,
RA   Watanabe M., Komatsu T., Mizushima-Sugano J., Satoh T., Shirai Y.,
RA   Takahashi Y., Nakagawa K., Okumura K., Nagase T., Nomura N., Kikuchi H.,
RA   Masuho Y., Yamashita R., Nakai K., Yada T., Nakamura Y., Ohara O.,
RA   Isogai T., Sugano S.;
RT   "Complete sequencing and characterization of 21,243 full-length human
RT   cDNAs.";
RL   Nat. Genet. 36:40-45(2004).
RN   [6]
RP   IDENTIFICATION BY MASS SPECTROMETRY, AND IDENTIFICATION IN THE INTEGRATOR
RP   COMPLEX.
RX   PubMed=16239144; DOI=10.1016/j.cell.2005.08.019;
RA   Baillat D., Hakimi M.-A., Naeaer A.M., Shilatifard A., Cooch N.,
RA   Shiekhattar R.;
RT   "Integrator, a multiprotein mediator of small nuclear RNA processing,
RT   associates with the C-terminal repeat of RNA polymerase II.";
RL   Cell 123:265-276(2005).
RN   [7]
RP   PHOSPHORYLATION [LARGE SCALE ANALYSIS] AT THR-18, AND IDENTIFICATION BY
RP   MASS SPECTROMETRY [LARGE SCALE ANALYSIS].
RC   TISSUE=Cervix carcinoma;
RX   PubMed=17081983; DOI=10.1016/j.cell.2006.09.026;
RA   Olsen J.V., Blagoev B., Gnad F., Macek B., Kumar C., Mortensen P., Mann M.;
RT   "Global, in vivo, and site-specific phosphorylation dynamics in signaling
RT   networks.";
RL   Cell 127:635-648(2006).
RN   [8]
RP   VARIANTS NEDCHS GLY-298 AND 973-GLU--LEU-975 DEL, CHARACTERIZATION OF
RP   VARIANTS NEDCHS GLY-298 AND 973-GLU--LEU-975 DEL, DEVELOPMENTAL STAGE, AND
RP   FUNCTION.
RX   PubMed=28542170; DOI=10.1371/journal.pgen.1006809;
RA   Oegema R., Baillat D., Schot R., van Unen L.M., Brooks A., Kia S.K.,
RA   Hoogeboom A.J.M., Xia Z., Li W., Cesaroni M., Lequin M.H.,
RA   van Slegtenhorst M., Dobyns W.B., de Coo I.F.M., Verheijen F.W., Kremer A.,
RA   van der Spek P.J., Heijsman D., Wagner E.J., Fornerod M., Mancini G.M.S.;
RT   "Human mutations in integrator complex subunits link transcriptome
RT   integrity to brain development.";
RL   PLoS Genet. 13:e1006809-e1006809(2017).
CC   -!- FUNCTION: Component of the Integrator complex, a complex involved in
CC       the small nuclear RNAs (snRNA) U1 and U2 transcription and in their 3'-
CC       box-dependent processing. The Integrator complex is associated with the
CC       C-terminal domain (CTD) of RNA polymerase II largest subunit (POLR2A)
CC       and is recruited to the U1 and U2 snRNAs genes.
CC       {ECO:0000269|PubMed:28542170}.
CC   -!- SUBUNIT: Belongs to the multiprotein complex Integrator, at least
CC       composed of INTS1, INTS2, INTS3, INTS4, INTS5, INTS6, INTS7, INTS8,
CC       INTS9/RC74, INTS10, INTS11/CPSF3L and INTS12.
CC       {ECO:0000269|PubMed:16239144}.
CC   -!- INTERACTION:
CC       Q75QN2; Q6P9B9: INTS5; NbExp=3; IntAct=EBI-2340089, EBI-7600112;
CC   -!- SUBCELLULAR LOCATION: Nucleus {ECO:0000305}.
CC   -!- ALTERNATIVE PRODUCTS:
CC       Event=Alternative splicing; Named isoforms=2;
CC       Name=1;
CC         IsoId=Q75QN2-1; Sequence=Displayed;
CC       Name=2;
CC         IsoId=Q75QN2-2; Sequence=VSP_021469;
CC   -!- DEVELOPMENTAL STAGE: Highly expressed in the brain in the ventricular
CC       and subventricular zones, caudal and lateral ganglionic eminences and
CC       cerebellar primordium at 16-21 postconceptional week.
CC       {ECO:0000269|PubMed:28542170}.
CC   -!- DISEASE: Neurodevelopmental disorder with cerebellar hypoplasia and
CC       spasticity (NEDCHS) [MIM:618572]: An autosomal recessive
CC       neurodevelopmental disorder characterized by global developmental
CC       delay, profound intellectual disability, seizures, absent speech,
CC       spasticity, facial and limb dysmorphism, and subtle structural brain
CC       abnormalities including cerebellar hypoplasia.
CC       {ECO:0000269|PubMed:28542170}. Note=The disease is caused by variants
CC       affecting the gene represented in this entry.
CC   -!- SIMILARITY: Belongs to the Integrator subunit 8 family. {ECO:0000305}.
CC   -!- SEQUENCE CAUTION:
CC       Sequence=AAH50536.1; Type=Frameshift; Evidence={ECO:0000305};
CC       Sequence=BAA91238.1; Type=Erroneous initiation; Note=Truncated N-terminus.; Evidence={ECO:0000305};
CC       Sequence=BAA91671.1; Type=Erroneous initiation; Note=Truncated N-terminus.; Evidence={ECO:0000305};
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DR   EMBL; AB161944; BAD10863.1; -; mRNA.
DR   EMBL; CH471060; EAW91726.1; -; Genomic_DNA.
DR   EMBL; BC050536; AAH50536.1; ALT_FRAME; mRNA.
DR   EMBL; BC064915; AAH64915.1; -; mRNA.
DR   EMBL; BC136754; AAI36755.1; -; mRNA.
DR   EMBL; BX538203; CAD98067.1; -; mRNA.
DR   EMBL; AK000537; BAA91238.1; ALT_INIT; mRNA.
DR   EMBL; AK001403; BAA91671.1; ALT_INIT; mRNA.
DR   EMBL; BK005731; DAA05731.1; -; mRNA.
DR   CCDS; CCDS34925.1; -. [Q75QN2-1]
DR   RefSeq; NP_060334.2; NM_017864.3. [Q75QN2-1]
DR   RefSeq; XP_016869108.1; XM_017013619.1.
DR   PDB; 7CUN; EM; 3.50 A; H=1-995.
DR   PDB; 7PKS; EM; 3.60 A; h=1-995.
DR   PDBsum; 7CUN; -.
DR   PDBsum; 7PKS; -.
DR   AlphaFoldDB; Q75QN2; -.
DR   SMR; Q75QN2; -.
DR   BioGRID; 120788; 46.
DR   ComplexPortal; CPX-6441; Integrator complex.
DR   CORUM; Q75QN2; -.
DR   IntAct; Q75QN2; 12.
DR   MINT; Q75QN2; -.
DR   STRING; 9606.ENSP00000430338; -.
DR   iPTMnet; Q75QN2; -.
DR   PhosphoSitePlus; Q75QN2; -.
DR   BioMuta; INTS8; -.
DR   DMDM; 74712892; -.
DR   EPD; Q75QN2; -.
DR   jPOST; Q75QN2; -.
DR   MassIVE; Q75QN2; -.
DR   MaxQB; Q75QN2; -.
DR   PaxDb; Q75QN2; -.
DR   PeptideAtlas; Q75QN2; -.
DR   PRIDE; Q75QN2; -.
DR   ProteomicsDB; 68647; -. [Q75QN2-1]
DR   ProteomicsDB; 68648; -. [Q75QN2-2]
DR   Antibodypedia; 25892; 47 antibodies from 17 providers.
DR   DNASU; 55656; -.
DR   Ensembl; ENST00000523731.6; ENSP00000430338.1; ENSG00000164941.14. [Q75QN2-1]
DR   GeneID; 55656; -.
DR   KEGG; hsa:55656; -.
DR   MANE-Select; ENST00000523731.6; ENSP00000430338.1; NM_017864.4; NP_060334.2.
DR   UCSC; uc003yhb.5; human. [Q75QN2-1]
DR   CTD; 55656; -.
DR   DisGeNET; 55656; -.
DR   GeneCards; INTS8; -.
DR   HGNC; HGNC:26048; INTS8.
DR   HPA; ENSG00000164941; Low tissue specificity.
DR   MalaCards; INTS8; -.
DR   MIM; 611351; gene.
DR   MIM; 618572; phenotype.
DR   neXtProt; NX_Q75QN2; -.
DR   OpenTargets; ENSG00000164941; -.
DR   PharmGKB; PA142672371; -.
DR   VEuPathDB; HostDB:ENSG00000164941; -.
DR   eggNOG; ENOG502QQS8; Eukaryota.
DR   GeneTree; ENSGT00390000007597; -.
DR   HOGENOM; CLU_012129_0_0_1; -.
DR   InParanoid; Q75QN2; -.
DR   OMA; YYSCIWD; -.
DR   OrthoDB; 461829at2759; -.
DR   PhylomeDB; Q75QN2; -.
DR   TreeFam; TF324241; -.
DR   PathwayCommons; Q75QN2; -.
DR   Reactome; R-HSA-6807505; RNA polymerase II transcribes snRNA genes.
DR   SignaLink; Q75QN2; -.
DR   SIGNOR; Q75QN2; -.
DR   BioGRID-ORCS; 55656; 685 hits in 1082 CRISPR screens.
DR   ChiTaRS; INTS8; human.
DR   GeneWiki; INTS8; -.
DR   GenomeRNAi; 55656; -.
DR   Pharos; Q75QN2; Tdark.
DR   PRO; PR:Q75QN2; -.
DR   Proteomes; UP000005640; Chromosome 8.
DR   RNAct; Q75QN2; protein.
DR   Bgee; ENSG00000164941; Expressed in secondary oocyte and 198 other tissues.
DR   ExpressionAtlas; Q75QN2; baseline and differential.
DR   Genevisible; Q75QN2; HS.
DR   GO; GO:0032039; C:integrator complex; IDA:HGNC-UCL.
DR   GO; GO:0005654; C:nucleoplasm; TAS:Reactome.
DR   GO; GO:0005634; C:nucleus; IC:ComplexPortal.
DR   GO; GO:0034243; P:regulation of transcription elongation from RNA polymerase II promoter; IC:ComplexPortal.
DR   GO; GO:0034472; P:snRNA 3'-end processing; IBA:GO_Central.
DR   GO; GO:0016180; P:snRNA processing; IDA:HGNC-UCL.
DR   InterPro; IPR038751; Int8.
DR   InterPro; IPR011990; TPR-like_helical_dom_sf.
DR   PANTHER; PTHR13350; PTHR13350; 1.
DR   SUPFAM; SSF48452; SSF48452; 1.
PE   1: Evidence at protein level;
KW   3D-structure; Alternative splicing; Disease variant;
KW   Intellectual disability; Nucleus; Phosphoprotein; Reference proteome;
KW   Repeat; TPR repeat.
FT   CHAIN           1..995
FT                   /note="Integrator complex subunit 8"
FT                   /id="PRO_0000259553"
FT   REPEAT          250..288
FT                   /note="TPR 1"
FT   REPEAT          320..356
FT                   /note="TPR 2"
FT   REPEAT          570..603
FT                   /note="TPR 3"
FT   REPEAT          833..866
FT                   /note="TPR 4"
FT   MOD_RES         18
FT                   /note="Phosphothreonine"
FT                   /evidence="ECO:0007744|PubMed:17081983"
FT   VAR_SEQ         879..895
FT                   /note="Missing (in isoform 2)"
FT                   /evidence="ECO:0000303|PubMed:17974005"
FT                   /id="VSP_021469"
FT   VARIANT         298
FT                   /note="D -> G (in NEDCHS; occurs in a splice site resulting
FT                   in altered splicing and probable nonsense-mediated mRNA
FT                   decay; dbSNP:rs1586479593)"
FT                   /evidence="ECO:0000269|PubMed:28542170"
FT                   /id="VAR_083358"
FT   VARIANT         973..975
FT                   /note="Missing (in NEDCHS; alters the assembly of the
FT                   Integrator complex)"
FT                   /evidence="ECO:0000269|PubMed:28542170"
FT                   /id="VAR_083359"
FT   CONFLICT        778
FT                   /note="V -> A (in Ref. 5; BAA91238)"
FT                   /evidence="ECO:0000305"
FT   CONFLICT        832
FT                   /note="N -> S (in Ref. 4; CAD98067)"
FT                   /evidence="ECO:0000305"
FT   HELIX           47..53
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   STRAND          56..60
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   HELIX           61..69
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   TURN            71..77
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   STRAND          79..82
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   HELIX           83..96
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   STRAND          103..105
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   HELIX           110..118
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   HELIX           137..156
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   HELIX           171..191
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   TURN            192..194
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   HELIX           195..206
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   HELIX           213..232
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   TURN            235..237
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   HELIX           242..258
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   STRAND          262..266
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   HELIX           269..282
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   HELIX           327..336
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   HELIX           340..347
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   HELIX           356..371
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   STRAND          372..374
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   HELIX           378..395
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   HELIX           401..407
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   HELIX           412..422
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   STRAND          424..427
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   HELIX           435..445
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   HELIX           446..448
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   HELIX           453..459
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   HELIX           462..464
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   HELIX           467..469
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   STRAND          470..472
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   HELIX           474..484
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   STRAND          503..505
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   HELIX           506..517
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   HELIX           522..535
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   HELIX           552..558
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   HELIX           564..582
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   HELIX           586..600
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   HELIX           605..625
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   HELIX           637..648
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   HELIX           657..669
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   STRAND          682..684
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   HELIX           689..701
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   HELIX           712..724
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   STRAND          736..738
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   HELIX           740..744
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   STRAND          750..752
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   HELIX           756..762
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   HELIX           767..781
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   STRAND          782..784
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   STRAND          786..788
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   TURN            806..808
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   HELIX           811..828
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   HELIX           833..845
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   HELIX           849..863
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   HELIX           865..867
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   TURN            873..875
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   HELIX           878..889
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   TURN            890..892
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   HELIX           894..900
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   STRAND          903..906
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   HELIX           909..916
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   HELIX           925..927
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   HELIX           929..931
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   HELIX           935..947
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   HELIX           951..961
FT                   /evidence="ECO:0007829|PDB:7CUN"
FT   HELIX           975..993
FT                   /evidence="ECO:0007829|PDB:7CUN"
SQ   SEQUENCE   995 AA;  113088 MW;  24D06E11821BD4D5 CRC64;
     MSAEAADREA ATSSRPCTPP QTCWFEFLLE ESLLEKHLRK PCPDPAPVQL IVQFLEQASK
     PSVNEQNQVQ PPPDNKRNRI LKLLALKVAA HLKWDLDILE KSLSVPVLNM LLNELLCISK
     VPPGTKHVDM DLATLPPTTA MAVLLYNRWA IRTIVQSSFP VKQAKPGPPQ LSVMNQMQQE
     KELTENILKV LKEQAADSIL VLEAALKLNK DLYVHTMRTL DLLAMEPGMV NGETESSTAG
     LKVKTEEMQC QVCYDLGAAY FQQGSTNSAV YENAREKFFR TKELIAEIGS LSLHCTIDEK
     RLAGYCQACD VLVPSSDSTS QQLTPYSQVH ICLRSGNYQE VIQIFIEDNL TLSLPVQFRQ
     SVLRELFKKA QQGNEALDEI CFKVCACNTV RDILEGRTIS VQFNQLFLRP NKEKIDFLLE
     VCSRSVNLEK ASESLKGNMA AFLKNVCLGL EDLQYVFMIS SHELFITLLK DEERKLLVDQ
     MRKRSPRVNL CIKPVTSFYD IPASASVNIG QLEHQLILSV DPWRIRQILI ELHGMTSERQ
     FWTVSNKWEV PSVYSGVILG IKDNLTRDLV YILMAKGLHC STVKDFSHAK QLFAACLELV
     TEFSPKLRQV MLNEMLLLDI HTHEAGTGQA GERPPSDLIS RVRGYLEMRL PDIPLRQVIA
     EECVAFMLNW RENEYLTLQV PAFLLQSNPY VKLGQLLAAT CKELPGPKES RRTAKDLWEV
     VVQICSVSSQ HKRGNDGRVS LIKQRESTLG IMYRSELLSF IKKLREPLVL TIILSLFVKL
     HNVREDIVND ITAEHISIWP SSIPNLQSVD FEAVAITVKE LVRYTLSINP NNHSWLIIQA
     DIYFATNQYS AALHYYLQAG AVCSDFFNKA VPPDVYTDQV IKRMIKCCSL LNCHTQVAIL
     CQFLREIDYK TAFKSLQEQN SHDAMDSYYD YIWDVTILEY LTYLHHKRGE TDKRQIAIKA
     IGQTELNASN PEEVLQLAAQ RRKKKFLQAM AKLYF
 
 
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