ID   IQCN_HUMAN              Reviewed;        1180 AA.
AC   Q9H0B3; B4DYH2; E9PDE0; E9PH54; Q2KHR5; Q8N4G8; Q96M14; Q9C0I0;
DT   30-AUG-2005, integrated into UniProtKB/Swiss-Prot.
DT   01-MAR-2001, sequence version 1.
DT   24-JAN-2024, entry version 169.
DE   RecName: Full=IQ domain-containing protein N {ECO:0000312|HGNC:HGNC:29350};
GN   Name=IQCN {ECO:0000312|HGNC:HGNC:29350}; Synonyms=KIAA1683;
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 [LARGE SCALE MRNA] (ISOFORM 1).
RC   TISSUE=Testis;
RX   PubMed=11230166; DOI=10.1101/gr.gr1547r;
RA   Wiemann S., Weil B., Wellenreuther R., Gassenhuber J., Glassl S.,
RA   Ansorge W., Boecher M., Bloecker H., Bauersachs S., Blum H., Lauber J.,
RA   Duesterhoeft A., Beyer A., Koehrer K., Strack N., Mewes H.-W.,
RA   Ottenwaelder B., Obermaier B., Tampe J., Heubner D., Wambutt R., Korn B.,
RA   Klein M., Poustka A.;
RT   "Towards a catalog of human genes and proteins: sequencing and analysis of
RT   500 novel complete protein coding human cDNAs.";
RL   Genome Res. 11:422-435(2001).
RN   [2]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORMS 2 AND 5), AND VARIANTS
RP   PRO-44; VAL-235; THR-285; THR-359; PRO-610; PHE-648 AND HIS-908.
RC   TISSUE=Testis;
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   [3]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
RX   PubMed=15057824; DOI=10.1038/nature02399;
RA   Grimwood J., Gordon L.A., Olsen A.S., Terry A., Schmutz J., Lamerdin J.E.,
RA   Hellsten U., Goodstein D., Couronne O., Tran-Gyamfi M., Aerts A.,
RA   Altherr M., Ashworth L., Bajorek E., Black S., Branscomb E., Caenepeel S.,
RA   Carrano A.V., Caoile C., Chan Y.M., Christensen M., Cleland C.A.,
RA   Copeland A., Dalin E., Dehal P., Denys M., Detter J.C., Escobar J.,
RA   Flowers D., Fotopulos D., Garcia C., Georgescu A.M., Glavina T., Gomez M.,
RA   Gonzales E., Groza M., Hammon N., Hawkins T., Haydu L., Ho I., Huang W.,
RA   Israni S., Jett J., Kadner K., Kimball H., Kobayashi A., Larionov V.,
RA   Leem S.-H., Lopez F., Lou Y., Lowry S., Malfatti S., Martinez D.,
RA   McCready P.M., Medina C., Morgan J., Nelson K., Nolan M., Ovcharenko I.,
RA   Pitluck S., Pollard M., Popkie A.P., Predki P., Quan G., Ramirez L.,
RA   Rash S., Retterer J., Rodriguez A., Rogers S., Salamov A., Salazar A.,
RA   She X., Smith D., Slezak T., Solovyev V., Thayer N., Tice H., Tsai M.,
RA   Ustaszewska A., Vo N., Wagner M., Wheeler J., Wu K., Xie G., Yang J.,
RA   Dubchak I., Furey T.S., DeJong P., Dickson M., Gordon D., Eichler E.E.,
RA   Pennacchio L.A., Richardson P., Stubbs L., Rokhsar D.S., Myers R.M.,
RA   Rubin E.M., Lucas S.M.;
RT   "The DNA sequence and biology of human chromosome 19.";
RL   Nature 428:529-535(2004).
RN   [4]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORMS 3 AND 4), AND VARIANTS
RP   PRO-44; ARG-197; VAL-235; THR-285; THR-359; PRO-610; PHE-648; ARG-823;
RP   LEU-835 AND HIS-908.
RC   TISSUE=Brain, and Skin;
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   [5]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 873-1180, AND VARIANT HIS-908.
RC   TISSUE=Brain;
RX   PubMed=11214970; DOI=10.1093/dnares/7.6.347;
RA   Nagase T., Kikuno R., Hattori A., Kondo Y., Okumura K., Ohara O.;
RT   "Prediction of the coding sequences of unidentified human genes. XIX. The
RT   complete sequences of 100 new cDNA clones from brain which code for large
RT   proteins in vitro.";
RL   DNA Res. 7:347-355(2000).
RN   [6]
RP   INVOLVEMENT IN SPGF78, FUNCTION, AND VARIANT SPGF78 304-GLN--ILE-1180 DEL.
RX   PubMed=36321563; DOI=10.15252/emmm.202216501;
RA   Dai J., Li Q., Zhou Q., Zhang S., Chen J., Wang Y., Guo J., Gu Y., Gong F.,
RA   Tan Y., Lu G., Zheng W., Lin G.;
RT   "IQCN disruption causes fertilization failure and male infertility due to
RT   manchette assembly defect.";
RL   EMBO Mol. Med. 14:e16501-e16501(2022).
CC   -!- FUNCTION: Essential for spermiogenesis and fertilization
CC       (PubMed:36321563). May be required for manchette assembly in elongating
CC       spermatids (By similarity). {ECO:0000250|UniProtKB:A0A1D5RMD1,
CC       ECO:0000269|PubMed:36321563}.
CC   -!- SUBUNIT: Interacts with calmodulin. {ECO:0000250|UniProtKB:A0A1D5RMD1}.
CC   -!- INTERACTION:
CC       Q9H0B3; B4DJ51: CALM1; NbExp=5; IntAct=EBI-745878, EBI-10171450;
CC       Q9H0B3; P62158: CALM3; NbExp=4; IntAct=EBI-745878, EBI-397435;
CC       Q9H0B3; P27482: CALML3; NbExp=4; IntAct=EBI-745878, EBI-747537;
CC       Q9H0B3; Q9BRK4: LZTS2; NbExp=3; IntAct=EBI-745878, EBI-741037;
CC       Q9H0B3; Q9UJV3-2: MID2; NbExp=3; IntAct=EBI-745878, EBI-10172526;
CC       Q9H0B3; Q9UHX1: PUF60; NbExp=3; IntAct=EBI-745878, EBI-1053259;
CC       Q9H0B3; Q96I25: RBM17; NbExp=3; IntAct=EBI-745878, EBI-740272;
CC       Q9H0B3; Q8IUQ4: SIAH1; NbExp=3; IntAct=EBI-745878, EBI-747107;
CC       Q9H0B3; P14373: TRIM27; NbExp=3; IntAct=EBI-745878, EBI-719493;
CC   -!- ALTERNATIVE PRODUCTS:
CC       Event=Alternative splicing; Named isoforms=5;
CC       Name=1;
CC         IsoId=Q9H0B3-1; Sequence=Displayed;
CC       Name=2;
CC         IsoId=Q9H0B3-2; Sequence=VSP_015474, VSP_015476;
CC       Name=3;
CC         IsoId=Q9H0B3-3; Sequence=VSP_015473, VSP_015475;
CC       Name=4;
CC         IsoId=Q9H0B3-4; Sequence=VSP_045714;
CC       Name=5;
CC         IsoId=Q9H0B3-5; Sequence=VSP_045713;
CC   -!- DISEASE: Spermatogenic failure 78 (SPGF78) [MIM:620170]: An autosomal
CC       recessive, male infertility disorder characterized by a high proportion
CC       of sperm head anomalies, primarily tapered and microcephalic heads, and
CC       an abnormal acrosome structure. {ECO:0000269|PubMed:36321563}. Note=The
CC       disease is caused by variants affecting the gene represented in this
CC       entry.
CC   -!- SEQUENCE CAUTION:
CC       Sequence=BAB21774.1; Type=Erroneous translation; Note=Wrong choice of frame.; Evidence={ECO:0000305};
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DR   EMBL; AL136867; CAB66801.1; -; mRNA.
DR   EMBL; AK057466; BAB71500.1; -; mRNA.
DR   EMBL; AK302431; BAG63734.1; -; mRNA.
DR   EMBL; AC008397; -; NOT_ANNOTATED_CDS; Genomic_DNA.
DR   EMBL; BC034327; AAH34327.1; -; mRNA.
DR   EMBL; BC112932; AAI12933.1; -; mRNA.
DR   EMBL; AB051470; BAB21774.1; ALT_SEQ; mRNA.
DR   CCDS; CCDS32958.1; -. [Q9H0B3-1]
DR   CCDS; CCDS46017.1; -. [Q9H0B3-4]
DR   CCDS; CCDS46018.1; -. [Q9H0B3-5]
DR   RefSeq; NP_001138776.1; NM_001145304.1. [Q9H0B3-4]
DR   RefSeq; NP_001138777.1; NM_001145305.1. [Q9H0B3-5]
DR   RefSeq; NP_079525.1; NM_025249.3. [Q9H0B3-1]
DR   RefSeq; XP_005260141.1; XM_005260084.1. [Q9H0B3-4]
DR   AlphaFoldDB; Q9H0B3; -.
DR   BioGRID; 123276; 72.
DR   IntAct; Q9H0B3; 60.
DR   MINT; Q9H0B3; -.
DR   STRING; 9606.ENSP00000376213; -.
DR   GlyGen; Q9H0B3; 1 site, 1 O-linked glycan (1 site).
DR   iPTMnet; Q9H0B3; -.
DR   PhosphoSitePlus; Q9H0B3; -.
DR   BioMuta; KIAA1683; -.
DR   DMDM; 73920083; -.
DR   jPOST; Q9H0B3; -.
DR   MassIVE; Q9H0B3; -.
DR   MaxQB; Q9H0B3; -.
DR   PeptideAtlas; Q9H0B3; -.
DR   ProteomicsDB; 19643; -.
DR   ProteomicsDB; 20458; -.
DR   ProteomicsDB; 80240; -. [Q9H0B3-1]
DR   ProteomicsDB; 80241; -. [Q9H0B3-2]
DR   ProteomicsDB; 80242; -. [Q9H0B3-3]
DR   Antibodypedia; 51823; 37 antibodies from 11 providers.
DR   DNASU; 80726; -.
DR   Ensembl; ENST00000392413.5; ENSP00000376213.2; ENSG00000130518.18. [Q9H0B3-4]
DR   Ensembl; ENST00000600328.7; ENSP00000470780.1; ENSG00000130518.18. [Q9H0B3-1]
DR   Ensembl; ENST00000600359.7; ENSP00000472912.1; ENSG00000130518.18. [Q9H0B3-5]
DR   GeneID; 80726; -.
DR   KEGG; hsa:80726; -.
DR   MANE-Select; ENST00000392413.5; ENSP00000376213.2; NM_001145304.2; NP_001138776.1. [Q9H0B3-4]
DR   UCSC; uc002nin.3; human. [Q9H0B3-1]
DR   AGR; HGNC:29350; -.
DR   CTD; 80726; -.
DR   DisGeNET; 80726; -.
DR   GeneCards; IQCN; -.
DR   HGNC; HGNC:29350; IQCN.
DR   HPA; ENSG00000130518; Tissue enriched (testis).
DR   MalaCards; IQCN; -.
DR   MIM; 620160; gene.
DR   MIM; 620170; phenotype.
DR   neXtProt; NX_Q9H0B3; -.
DR   OpenTargets; ENSG00000130518; -.
DR   PharmGKB; PA134952902; -.
DR   VEuPathDB; HostDB:ENSG00000130518; -.
DR   eggNOG; ENOG502SCUX; Eukaryota.
DR   GeneTree; ENSGT00940000156018; -.
DR   HOGENOM; CLU_008587_0_0_1; -.
DR   InParanoid; Q9H0B3; -.
DR   OMA; ITAKHQP; -.
DR   OrthoDB; 4641432at2759; -.
DR   PhylomeDB; Q9H0B3; -.
DR   TreeFam; TF337595; -.
DR   PathwayCommons; Q9H0B3; -.
DR   SignaLink; Q9H0B3; -.
DR   BioGRID-ORCS; 80726; 20 hits in 1143 CRISPR screens.
DR   ChiTaRS; KIAA1683; human.
DR   GeneWiki; KIAA1683; -.
DR   GenomeRNAi; 80726; -.
DR   Pharos; Q9H0B3; Tdark.
DR   PRO; PR:Q9H0B3; -.
DR   Proteomes; UP000005640; Chromosome 19.
DR   RNAct; Q9H0B3; Protein.
DR   Bgee; ENSG00000130518; Expressed in sural nerve and 105 other cell types or tissues.
DR   ExpressionAtlas; Q9H0B3; baseline and differential.
DR   GO; GO:0005739; C:mitochondrion; IDA:LIFEdb.
DR   GO; GO:0005634; C:nucleus; HDA:UniProtKB.
DR   GO; GO:0007286; P:spermatid development; IMP:UniProtKB.
DR   Gene3D; 1.20.5.190; -; 3.
DR   InterPro; IPR000048; IQ_motif_EF-hand-BS.
DR   InterPro; IPR027417; P-loop_NTPase.
DR   PANTHER; PTHR22590:SF2; IQ DOMAIN-CONTAINING PROTEIN N; 1.
DR   PANTHER; PTHR22590; UNCHARACTERIZED; 1.
DR   Pfam; PF00612; IQ; 6.
DR   SMART; SM00015; IQ; 6.
DR   SUPFAM; SSF52540; P-loop containing nucleoside triphosphate hydrolases; 2.
DR   PROSITE; PS50096; IQ; 6.
DR   Genevisible; Q9H0B3; HS.
PE   1: Evidence at protein level;
KW   Alternative splicing; Developmental protein; Disease variant;
KW   Reference proteome; Repeat.
FT   CHAIN           1..1180
FT                   /note="IQ domain-containing protein N"
FT                   /id="PRO_0000050801"
FT   DOMAIN          103..132
FT                   /note="IQ 1"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00116"
FT   DOMAIN          926..955
FT                   /note="IQ 2"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00116"
FT   DOMAIN          956..978
FT                   /note="IQ 3"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00116"
FT   DOMAIN          979..1001
FT                   /note="IQ 4"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00116"
FT   DOMAIN          1113..1142
FT                   /note="IQ 5"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00116"
FT   DOMAIN          1143..1165
FT                   /note="IQ 6"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00116"
FT   REGION          34..78
FT                   /note="Disordered"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   REGION          283..324
FT                   /note="Disordered"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   REGION          476..496
FT                   /note="Disordered"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   REGION          786..820
FT                   /note="Disordered"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   COMPBIAS        50..67
FT                   /note="Basic and acidic residues"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   VAR_SEQ         1..736
FT                   /note="Missing (in isoform 3)"
FT                   /evidence="ECO:0000303|PubMed:15489334"
FT                   /id="VSP_015473"
FT   VAR_SEQ         1..46
FT                   /note="Missing (in isoform 5)"
FT                   /evidence="ECO:0000303|PubMed:14702039"
FT                   /id="VSP_045713"
FT   VAR_SEQ         440..1053
FT                   /note="Missing (in isoform 2)"
FT                   /evidence="ECO:0000303|PubMed:14702039"
FT                   /id="VSP_015474"
FT   VAR_SEQ         737..872
FT                   /note="TCLTKTQSRGQPITDITTCLIPAHQAADLSSNTHSQVLLTGSKVSNHACQRL
FT                   GGLSAPPWAKPEDRQTQPQPHGHVPGKTTQGGPCPAACEVQGMLVPPMAPTGHSTCNVE
FT                   SWGDNGATRAQPSMPGQAVPCQEDT -> MAPSSRWDAMGPKNSYRSVHGRIVPELLES
FT                   SVARVRPLQYVQRQPSQASARSGANPTHRPSAEVRPVIRTGEMTHSSVIPPLAPGVRRV
FT                   SLGYESSPSGSLPPLFNQESPWRRQDSYSPQNPAVSHKASLNSTILQ (in isoform
FT                   3)"
FT                   /evidence="ECO:0000303|PubMed:15489334"
FT                   /id="VSP_015475"
FT   VAR_SEQ         872
FT                   /note="T -> TVGSLLASLCAEVAGVLASQEDLRTLLAKALSQGEVWAALNQALSKE
FT                   VLGATVTKALPQSMLSMALVKALSWSELRLTLSRALSRGELRAELTKVMQGKLAEVLSK
FT                   ALTEEEWVALSQALCQGELGALLSQSWCRVALRTGTILPKAASKSTGSGVTKTPALVKV
FT                   ACRRSPSAAWGPSLGPVRPQTSK (in isoform 4)"
FT                   /evidence="ECO:0000303|PubMed:15489334"
FT                   /id="VSP_045714"
FT   VAR_SEQ         1148..1180
FT                   /note="RGHHTRSCLKNTEALLGPADPSASSRHMHWPGI -> HLGPWLPAVGTSWEA
FT                   LMALWV (in isoform 2)"
FT                   /evidence="ECO:0000303|PubMed:14702039"
FT                   /id="VSP_015476"
FT   VARIANT         44
FT                   /note="L -> P (in dbSNP:rs1469023)"
FT                   /evidence="ECO:0000269|PubMed:14702039,
FT                   ECO:0000269|PubMed:15489334"
FT                   /id="VAR_023418"
FT   VARIANT         50
FT                   /note="A -> V (in dbSNP:rs3810431)"
FT                   /id="VAR_049520"
FT   VARIANT         197
FT                   /note="C -> R (in dbSNP:rs12609001)"
FT                   /evidence="ECO:0000269|PubMed:15489334"
FT                   /id="VAR_049521"
FT   VARIANT         235
FT                   /note="L -> V (in dbSNP:rs8103906)"
FT                   /evidence="ECO:0000269|PubMed:14702039,
FT                   ECO:0000269|PubMed:15489334"
FT                   /id="VAR_023419"
FT   VARIANT         285
FT                   /note="S -> T (in dbSNP:rs8104533)"
FT                   /evidence="ECO:0000269|PubMed:14702039,
FT                   ECO:0000269|PubMed:15489334"
FT                   /id="VAR_023420"
FT   VARIANT         304..1180
FT                   /note="Missing (in SPGF78)"
FT                   /evidence="ECO:0000269|PubMed:36321563"
FT                   /id="VAR_087804"
FT   VARIANT         359
FT                   /note="M -> T (in dbSNP:rs3746186)"
FT                   /evidence="ECO:0000269|PubMed:14702039,
FT                   ECO:0000269|PubMed:15489334"
FT                   /id="VAR_023421"
FT   VARIANT         524
FT                   /note="T -> A (in dbSNP:rs12462974)"
FT                   /id="VAR_049522"
FT   VARIANT         610
FT                   /note="T -> P (in dbSNP:rs2277922)"
FT                   /evidence="ECO:0000269|PubMed:14702039,
FT                   ECO:0000269|PubMed:15489334"
FT                   /id="VAR_049523"
FT   VARIANT         614
FT                   /note="A -> V (in dbSNP:rs16982285)"
FT                   /id="VAR_049524"
FT   VARIANT         648
FT                   /note="Y -> F (in dbSNP:rs8110972)"
FT                   /evidence="ECO:0000269|PubMed:14702039,
FT                   ECO:0000269|PubMed:15489334"
FT                   /id="VAR_034042"
FT   VARIANT         823
FT                   /note="P -> R (in dbSNP:rs12608777)"
FT                   /evidence="ECO:0000269|PubMed:15489334"
FT                   /id="VAR_034043"
FT   VARIANT         835
FT                   /note="P -> L (in dbSNP:rs2277921)"
FT                   /evidence="ECO:0000269|PubMed:15489334"
FT                   /id="VAR_049525"
FT   VARIANT         908
FT                   /note="P -> H (in dbSNP:rs999813)"
FT                   /evidence="ECO:0000269|PubMed:11214970,
FT                   ECO:0000269|PubMed:14702039, ECO:0000269|PubMed:15489334"
FT                   /id="VAR_023422"
FT   CONFLICT        381
FT                   /note="M -> V (in Ref. 2; BAB71500)"
FT                   /evidence="ECO:0000305"
SQ   SEQUENCE   1180 AA;  127693 MW;  A81A2824C2794AC3 CRC64;
     MTLQGRADLS GNQGNAAGRL ATVHEPVVTQ WAVHPPAPAH PSLLDKMEKA PPQPQHEGLK
     SKEHLPQQPA EGKTASRRVP RLRAVVESQA FKNILVDEMD MMHARAATLI QANWRGYWLR
     QKLISQMMAA KAIQEAWRRF NKRHILHSSK SLVKKTRAEE GDIPYHAPQQ VRFQHPEENR
     LLSPPIMVNK ETQFPSCDNL VLCRPQSSPL LQPPAAQGTP EPCVQGPHAA RVRGLAFLPH
     QTVTIRFPCP VSLDAKCQPC LLTRTIRSTC LVHIEGDSVK TKRVSARTNK ARAPETPLSR
     RYDQAVTRPS RAQTQGPVKA ETPKAPFQIC PGPMITKTLL QTYPVVSVTL PQTYPASTMT
     TTPPKTSPVP KVTIIKTPAQ MYPGPTVTKT APHTCPMPTM TKIQVHPTAS RTGTPRQTCP
     ATITAKNRPQ VSLLASIMKS LPQVCPGPAM AKTPPQMHPV TTPAKNPLQT CLSATMSKTS
     SQRSPVGVTK PSPQTRLPAM ITKTPAQLRS VATILKTLCL ASPTVANVKA PPQVAVAAGT
     PNTSGSIHEN PPKAKATVNV KQAAKVVKAS SPSYLAEGKI RCLAQPHPGT GVPRAAAELP
     LEAEKIKTGT QKQAKTDMAF KTSVAVEMAG APSWTKVAEE GDKPPHVYVP VDMAVTLPRG
     QLAAPLTNAS SQRHPPCLSQ RPLAAPLTKA SSQGHLPTEL TKTPSLAHLD TCLSKMHSQT
     HLATGAVKVQ SQAPLATCLT KTQSRGQPIT DITTCLIPAH QAADLSSNTH SQVLLTGSKV
     SNHACQRLGG LSAPPWAKPE DRQTQPQPHG HVPGKTTQGG PCPAACEVQG MLVPPMAPTG
     HSTCNVESWG DNGATRAQPS MPGQAVPCQE DTGPADAGVV GGQSWNRAWE PARGAASWDT
     WRNKAVVPPR RSGEPMVSMQ AAEEIRILAV ITIQAGVRGY LARRRIRLWH RGAMVIQATW
     RGYRVRRNLA HLCRATTTIQ SAWRGYSTRR DQARHWQMLH PVTWVELGSR AGVMSDRSWF
     QDGRARTVSD HRCFQSCQAH ACSVCHSLSS RIGSPPSVVM LVGSSPRTCH TCGRTQPTRV
     VQGMGQGTEG PGAVSWASAY QLAALSPRQP HRQDKAATAI QSAWRGFKIR QQMRQQQMAA
     KIVQATWRGH HTRSCLKNTE ALLGPADPSA SSRHMHWPGI
//