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CFA91_HUMAN
ID   CFA91_HUMAN             Reviewed;         767 AA.
AC   Q7Z4T9; A0AVK2; A8K1J9; B3KP23; B4DG52; B4DZ14; C9JUG4; Q68DX2; Q8TD41;
AC   Q96A45; Q96JE8;
DT   19-JUL-2005, integrated into UniProtKB/Swiss-Prot.
DT   28-MAR-2018, sequence version 3.
DT   03-AUG-2022, entry version 144.
DE   RecName: Full=Cilia- and flagella-associated protein 91 {ECO:0000305};
DE            Short=CFAP91 {ECO:0000305};
DE   AltName: Full=AMY-1-associating protein expressed in testis 1 {ECO:0000303|PubMed:15863901};
DE            Short=AAT-1 {ECO:0000303|PubMed:15863901};
DE   AltName: Full=MYCBP/AMY-1-associated testis-expressed protein 1 {ECO:0000303|PubMed:12223483};
DE   AltName: Full=Protein MAATS1 {ECO:0000303|PubMed:12223483};
GN   Name=CFAP91 {ECO:0000312|HGNC:HGNC:24010};
GN   Synonyms=AAT1 {ECO:0000303|PubMed:15863901}, C3orf15, MAATS1;
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 5), NUCLEOTIDE SEQUENCE [MRNA] OF
RP   617-767 (ISOFORM 7), FUNCTION, INTERACTION WITH MYCBP AND AKAP1,
RP   PHOSPHORYLATION, AND SUBCELLULAR LOCATION.
RC   TISSUE=Testis;
RX   PubMed=12223483; DOI=10.1074/jbc.m206201200;
RA   Yukitake H., Furusawa M., Taira T., Iguchi-Ariga S.M.M., Ariga H.;
RT   "AAT-1, a novel testis-specific AMY-1-binding protein, forms a quaternary
RT   complex between AMY-1, A-kinase anchor protein 84 and a regulatory subunit
RT   of cAMP-dependent protein kinase and is phosphorylated by its kinase.";
RL   J. Biol. Chem. 277:45480-45492(2002).
RN   [2]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORMS 1 AND 2), AND VARIANT
RP   PRO-207.
RC   TISSUE=Lung;
RA   Guo J.H., Yu L.;
RL   Submitted (MAR-2002) to the EMBL/GenBank/DDBJ databases.
RN   [3]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORMS 6; 7 AND 8), AND VARIANT
RP   PRO-207.
RC   TISSUE=Amygdala, Corpus callosum, Lung, and 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   [4]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 3), AND VARIANT PRO-207.
RC   TISSUE=Testis;
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 GENOMIC DNA].
RX   PubMed=16641997; DOI=10.1038/nature04728;
RA   Muzny D.M., Scherer S.E., Kaul R., Wang J., Yu J., Sudbrak R., Buhay C.J.,
RA   Chen R., Cree A., Ding Y., Dugan-Rocha S., Gill R., Gunaratne P.,
RA   Harris R.A., Hawes A.C., Hernandez J., Hodgson A.V., Hume J., Jackson A.,
RA   Khan Z.M., Kovar-Smith C., Lewis L.R., Lozado R.J., Metzker M.L.,
RA   Milosavljevic A., Miner G.R., Morgan M.B., Nazareth L.V., Scott G.,
RA   Sodergren E., Song X.-Z., Steffen D., Wei S., Wheeler D.A., Wright M.W.,
RA   Worley K.C., Yuan Y., Zhang Z., Adams C.Q., Ansari-Lari M.A., Ayele M.,
RA   Brown M.J., Chen G., Chen Z., Clendenning J., Clerc-Blankenburg K.P.,
RA   Chen R., Chen Z., Davis C., Delgado O., Dinh H.H., Dong W., Draper H.,
RA   Ernst S., Fu G., Gonzalez-Garay M.L., Garcia D.K., Gillett W., Gu J.,
RA   Hao B., Haugen E., Havlak P., He X., Hennig S., Hu S., Huang W.,
RA   Jackson L.R., Jacob L.S., Kelly S.H., Kube M., Levy R., Li Z., Liu B.,
RA   Liu J., Liu W., Lu J., Maheshwari M., Nguyen B.-V., Okwuonu G.O.,
RA   Palmeiri A., Pasternak S., Perez L.M., Phelps K.A., Plopper F.J., Qiang B.,
RA   Raymond C., Rodriguez R., Saenphimmachak C., Santibanez J., Shen H.,
RA   Shen Y., Subramanian S., Tabor P.E., Verduzco D., Waldron L., Wang J.,
RA   Wang J., Wang Q., Williams G.A., Wong G.K.-S., Yao Z., Zhang J., Zhang X.,
RA   Zhao G., Zhou J., Zhou Y., Nelson D., Lehrach H., Reinhardt R.,
RA   Naylor S.L., Yang H., Olson M., Weinstock G., Gibbs R.A.;
RT   "The DNA sequence, annotation and analysis of human chromosome 3.";
RL   Nature 440:1194-1198(2006).
RN   [6]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 7), AND VARIANT PRO-207.
RC   TISSUE=Lung;
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   [7]
RP   ALTERNATIVE SPLICING, INTERACTION WITH MYCBP, TISSUE SPECIFICITY (ISOFORM
RP   1), SUBCELLULAR LOCATION (ISOFORM 7), AND SUBCELLULAR LOCATION.
RX   PubMed=15863901; DOI=10.1248/bpb.28.898;
RA   Matsuda E., Ishizaki R., Taira T., Iguchi-Ariga S.M.M., Ariga H.;
RT   "Structure and characterization of AAT-1 isoforms.";
RL   Biol. Pharm. Bull. 28:898-901(2005).
RN   [8]
RP   INVOLVEMENT IN SPGF51, AND FUNCTION.
RX   PubMed=32161152; DOI=10.1136/jmedgenet-2019-106775;
RA   Martinez G., Beurois J., Dacheux D., Cazin C., Bidart M., Kherraf Z.E.,
RA   Robinson D.R., Satre V., Le Gac G., Ka C., Gourlaouen I., Fichou Y.,
RA   Petre G., Dulioust E., Zouari R., Thierry-Mieg N., Toure A., Arnoult C.,
RA   Bonhivers M., Ray P., Coutton C.;
RT   "Biallelic variants in MAATS1 encoding CFAP91, a calmodulin-associated and
RT   spoke-associated complex protein, cause severe astheno-teratozoospermia and
RT   male infertility.";
RL   J. Med. Genet. 57:708-716(2020).
CC   -!- FUNCTION: Involved in sperm flagellum axonemal organization and
CC       function (PubMed:12223483, PubMed:32161152). May regulate cilium
CC       motility through its role in the assembly of the axonemal radial spokes
CC       (By similarity). {ECO:0000250|UniProtKB:A8IH47,
CC       ECO:0000269|PubMed:12223483, ECO:0000269|PubMed:32161152}.
CC   -!- SUBUNIT: Interacts with MYCBP and AKAP1. Part of a complex containing
CC       MYCBP, AKAP1 and PRKAR2B. {ECO:0000269|PubMed:12223483,
CC       ECO:0000269|PubMed:15863901}.
CC   -!- SUBUNIT: [Isoform 3]: Does not interact with MYCBP.
CC       {ECO:0000269|PubMed:15863901}.
CC   -!- INTERACTION:
CC       Q7Z4T9; Q9C005: DPY30; NbExp=3; IntAct=EBI-2119657, EBI-744973;
CC       Q7Z4T9-3; Q92667-2: AKAP1; NbExp=3; IntAct=EBI-17172567, EBI-2120060;
CC       Q7Z4T9-3; Q99417: MYCBP; NbExp=5; IntAct=EBI-17172567, EBI-716185;
CC   -!- SUBCELLULAR LOCATION: Mitochondrion {ECO:0000269|PubMed:12223483,
CC       ECO:0000269|PubMed:15863901}. Cytoplasm {ECO:0000269|PubMed:12223483,
CC       ECO:0000269|PubMed:15863901}. Cytoplasm, cytoskeleton, cilium axoneme
CC       {ECO:0000250|UniProtKB:A8IH47}. Note=Localized in the neck of the
CC       sperm.
CC   -!- SUBCELLULAR LOCATION: [Isoform 7]: Cytoplasm
CC       {ECO:0000269|PubMed:15863901}.
CC   -!- ALTERNATIVE PRODUCTS:
CC       Event=Alternative promoter usage, Alternative splicing; Named isoforms=7;
CC         Comment=Additional isoforms may exist.;
CC       Name=7; Synonyms=AAT-1L {ECO:0000303|PubMed:15863901};
CC         IsoId=Q7Z4T9-7; Sequence=Displayed;
CC       Name=1; Synonyms=AAT-1M {ECO:0000303|PubMed:15863901};
CC         IsoId=Q7Z4T9-1; Sequence=VSP_059500;
CC       Name=2;
CC         IsoId=Q7Z4T9-2; Sequence=VSP_014910, VSP_014911;
CC       Name=3;
CC         IsoId=Q7Z4T9-3; Sequence=VSP_014907;
CC       Name=6;
CC         IsoId=Q7Z4T9-6; Sequence=VSP_039503;
CC       Name=8;
CC         IsoId=Q7Z4T9-8; Sequence=VSP_039504;
CC       Name=5; Synonyms=AAT1-beta {ECO:0000303|PubMed:15863901};
CC         IsoId=Q7Z4T9-5; Sequence=VSP_059499;
CC   -!- TISSUE SPECIFICITY: [Isoform 1]: Strongly expressed in the liver.
CC   -!- TISSUE SPECIFICITY: [Isoform 7]: Widely expressed, but strongly
CC       expressed in all spermatogenesis-related tissues, including the testis,
CC       the epithelium of cauda and the corpus epididymis, as well as the
CC       spermatid and mature sperm. Also expressed in Leydig cells.
CC       {ECO:0000269|PubMed:15863901, ECO:0000269|PubMed:32161152}.
CC   -!- PTM: Phosphorylated by PKA. {ECO:0000269|PubMed:12223483}.
CC   -!- DISEASE: Spermatogenic failure 51 (SPGF51) [MIM:619177]: An autosomal
CC       recessive infertility disorder characterized by
CC       asthenoteratozoospermia. Spermatozoa exhibit multiple morphologic
CC       abnormalities, including absent, short, bent, coiled and irregular-
CC       caliber flagella. Abnormalities of the sperm head, base, and acrosome
CC       have also been observed. {ECO:0000269|PubMed:32161152}. Note=The
CC       disease is caused by variants affecting the gene represented in this
CC       entry.
CC   -!- MISCELLANEOUS: [Isoform 5]: May be produced by alternative promoter
CC       usage. {ECO:0000305}.
CC   -!- SIMILARITY: Belongs to the CFAP91 family.
CC   -!- SEQUENCE CAUTION:
CC       Sequence=BAB60902.1; Type=Erroneous initiation; Note=Truncated N-terminus.; Evidence={ECO:0000305};
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DR   EMBL; AB063296; BAB60902.1; ALT_INIT; mRNA.
DR   EMBL; AB063297; BAB60903.1; -; mRNA.
DR   EMBL; AB063298; BAB60904.1; -; mRNA.
DR   EMBL; AF440403; AAP97317.1; -; mRNA.
DR   EMBL; AF497717; AAM19218.1; -; mRNA.
DR   EMBL; AK055558; BAG51535.1; -; mRNA.
DR   EMBL; AK289914; BAF82603.1; -; mRNA.
DR   EMBL; AK294413; BAG57663.1; -; mRNA.
DR   EMBL; AK302699; BAG63926.1; -; mRNA.
DR   EMBL; CR749242; CAH18098.1; -; mRNA.
DR   EMBL; AC117466; -; NOT_ANNOTATED_CDS; Genomic_DNA.
DR   EMBL; AC069444; -; NOT_ANNOTATED_CDS; Genomic_DNA.
DR   EMBL; BC126394; AAI26395.1; -; mRNA.
DR   CCDS; CCDS2994.1; -. [Q7Z4T9-7]
DR   RefSeq; NP_001307245.1; NM_001320316.1.
DR   RefSeq; NP_001307246.1; NM_001320317.1. [Q7Z4T9-3]
DR   RefSeq; NP_001307247.1; NM_001320318.1. [Q7Z4T9-6]
DR   RefSeq; NP_203528.2; NM_033364.3. [Q7Z4T9-7]
DR   RefSeq; XP_011511579.1; XM_011513277.1. [Q7Z4T9-6]
DR   AlphaFoldDB; Q7Z4T9; -.
DR   SMR; Q7Z4T9; -.
DR   BioGRID; 124630; 7.
DR   IntAct; Q7Z4T9; 6.
DR   STRING; 9606.ENSP00000273390; -.
DR   iPTMnet; Q7Z4T9; -.
DR   PhosphoSitePlus; Q7Z4T9; -.
DR   BioMuta; MAATS1; -.
DR   DMDM; 300669603; -.
DR   MassIVE; Q7Z4T9; -.
DR   PaxDb; Q7Z4T9; -.
DR   PeptideAtlas; Q7Z4T9; -.
DR   PRIDE; Q7Z4T9; -.
DR   ProteomicsDB; 69234; -. [Q7Z4T9-1]
DR   ProteomicsDB; 69235; -. [Q7Z4T9-2]
DR   ProteomicsDB; 69236; -. [Q7Z4T9-3]
DR   ProteomicsDB; 69238; -. [Q7Z4T9-5]
DR   ProteomicsDB; 69239; -. [Q7Z4T9-6]
DR   ProteomicsDB; 69240; -. [Q7Z4T9-7]
DR   ProteomicsDB; 69241; -. [Q7Z4T9-8]
DR   Antibodypedia; 32764; 133 antibodies from 16 providers.
DR   DNASU; 89876; -.
DR   Ensembl; ENST00000273390.9; ENSP00000273390.5; ENSG00000183833.16. [Q7Z4T9-7]
DR   Ensembl; ENST00000463700.1; ENSP00000419489.1; ENSG00000183833.16. [Q7Z4T9-2]
DR   GeneID; 89876; -.
DR   KEGG; hsa:89876; -.
DR   MANE-Select; ENST00000273390.9; ENSP00000273390.5; NM_033364.4; NP_203528.3.
DR   UCSC; uc003edc.3; human. [Q7Z4T9-7]
DR   CTD; 89876; -.
DR   DisGeNET; 89876; -.
DR   GeneCards; CFAP91; -.
DR   HGNC; HGNC:24010; CFAP91.
DR   HPA; ENSG00000183833; Tissue enhanced (fallopian).
DR   MalaCards; CFAP91; -.
DR   MIM; 609910; gene.
DR   MIM; 619177; phenotype.
DR   neXtProt; NX_Q7Z4T9; -.
DR   OpenTargets; ENSG00000183833; -.
DR   VEuPathDB; HostDB:ENSG00000183833; -.
DR   eggNOG; ENOG502QRFI; Eukaryota.
DR   GeneTree; ENSGT00390000003024; -.
DR   HOGENOM; CLU_011633_0_0_1; -.
DR   InParanoid; Q7Z4T9; -.
DR   OMA; HLNAQWS; -.
DR   OrthoDB; 496618at2759; -.
DR   PhylomeDB; Q7Z4T9; -.
DR   TreeFam; TF328648; -.
DR   PathwayCommons; Q7Z4T9; -.
DR   SignaLink; Q7Z4T9; -.
DR   BioGRID-ORCS; 89876; 12 hits in 1076 CRISPR screens.
DR   ChiTaRS; MAATS1; human.
DR   GeneWiki; C3orf15; -.
DR   GenomeRNAi; 89876; -.
DR   Pharos; Q7Z4T9; Tbio.
DR   PRO; PR:Q7Z4T9; -.
DR   Proteomes; UP000005640; Chromosome 3.
DR   RNAct; Q7Z4T9; protein.
DR   Bgee; ENSG00000183833; Expressed in right uterine tube and 153 other tissues.
DR   ExpressionAtlas; Q7Z4T9; baseline and differential.
DR   Genevisible; Q7Z4T9; HS.
DR   GO; GO:0005930; C:axoneme; ISS:UniProtKB.
DR   GO; GO:0005739; C:mitochondrion; IEA:UniProtKB-SubCell.
DR   GO; GO:0031514; C:motile cilium; ISS:UniProtKB.
DR   GO; GO:1904158; P:axonemal central apparatus assembly; IMP:UniProtKB.
DR   GO; GO:0030154; P:cell differentiation; IEA:UniProtKB-KW.
DR   GO; GO:0003341; P:cilium movement; ISS:UniProtKB.
DR   GO; GO:0007283; P:spermatogenesis; IMP:UniProtKB.
DR   InterPro; IPR026720; CFAP91.
DR   InterPro; IPR032840; CFAP91_dom.
DR   PANTHER; PTHR22455; PTHR22455; 1.
DR   Pfam; PF14738; CFAP91; 1.
PE   1: Evidence at protein level;
KW   Alternative promoter usage; Alternative splicing; Cell projection;
KW   Cytoplasm; Cytoskeleton; Differentiation; Mitochondrion; Phosphoprotein;
KW   Reference proteome; Spermatogenesis.
FT   CHAIN           1..767
FT                   /note="Cilia- and flagella-associated protein 91"
FT                   /id="PRO_0000064417"
FT   REGION          1..29
FT                   /note="Disordered"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   COMPBIAS        1..22
FT                   /note="Polar residues"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   VAR_SEQ         1..736
FT                   /note="Missing (in isoform 5)"
FT                   /id="VSP_059499"
FT   VAR_SEQ         1..126
FT                   /note="Missing (in isoform 6)"
FT                   /evidence="ECO:0000303|PubMed:14702039"
FT                   /id="VSP_039503"
FT   VAR_SEQ         1..67
FT                   /note="MSHAVTIEEPQAQPQVSQTRYRERSRAGSHISSNRAYDFLYDPLFIVSSEKD
FT                   HTQANIQATLIRSRL -> MIFCT (in isoform 3)"
FT                   /evidence="ECO:0000303|PubMed:17974005"
FT                   /id="VSP_014907"
FT   VAR_SEQ         1..41
FT                   /note="MSHAVTIEEPQAQPQVSQTRYRERSRAGSHISSNRAYDFLY -> MIFCTVR
FT                   TAADLPLRPSPPRP (in isoform 8)"
FT                   /evidence="ECO:0000303|PubMed:14702039"
FT                   /id="VSP_039504"
FT   VAR_SEQ         229..238
FT                   /note="RGLPAGQAEV -> ELVNLLTIGR (in isoform 2)"
FT                   /evidence="ECO:0000303|Ref.2"
FT                   /id="VSP_014910"
FT   VAR_SEQ         239..767
FT                   /note="Missing (in isoform 2)"
FT                   /evidence="ECO:0000303|Ref.2"
FT                   /id="VSP_014911"
FT   VAR_SEQ         330..493
FT                   /note="Missing (in isoform 1)"
FT                   /id="VSP_059500"
FT   VARIANT         207
FT                   /note="A -> P (in dbSNP:rs6438544)"
FT                   /evidence="ECO:0000269|PubMed:14702039,
FT                   ECO:0000269|PubMed:15489334, ECO:0000269|PubMed:17974005,
FT                   ECO:0000269|Ref.2"
FT                   /id="VAR_030243"
FT   VARIANT         253
FT                   /note="S -> T (in dbSNP:rs9817771)"
FT                   /id="VAR_030244"
FT   VARIANT         320
FT                   /note="S -> C (in dbSNP:rs9819218)"
FT                   /id="VAR_030245"
FT   CONFLICT        311
FT                   /note="N -> D (in Ref. 3; BAG51535)"
FT                   /evidence="ECO:0000305"
FT   CONFLICT        362
FT                   /note="K -> R (in Ref. 3; BAF82603)"
FT                   /evidence="ECO:0000305"
FT   CONFLICT        508
FT                   /note="V -> I (in Ref. 2; AAP97317)"
FT                   /evidence="ECO:0000305"
FT   CONFLICT        624
FT                   /note="R -> C (in Ref. 3; BAG51535)"
FT                   /evidence="ECO:0000305"
FT   CONFLICT        636..637
FT                   /note="VK -> A (in Ref. 1; BAB60902)"
FT                   /evidence="ECO:0000305"
FT   CONFLICT        649
FT                   /note="D -> A (in Ref. 4; CAH18098)"
FT                   /evidence="ECO:0000305"
FT   CONFLICT        680
FT                   /note="E -> G (in Ref. 3; BAG63926)"
FT                   /evidence="ECO:0000305"
SQ   SEQUENCE   767 AA;  89955 MW;  7EBE6F798C496845 CRC64;
     MSHAVTIEEP QAQPQVSQTR YRERSRAGSH ISSNRAYDFL YDPLFIVSSE KDHTQANIQA
     TLIRSRLRKV PRFKTMFSNL IHYPRYSLYW SKSDPVPPFI SREWKGHKEK HREALRQLTT
     TDASFQMPKE VYEDPEVTGK NRYKYFERPF LPFFQQMPFN VVYAVSKAEP YTFPPTSTKH
     LSIPSKSTVG TQTDYRDADV QTDPYSAEYV VCQDSIPELL TLATLTWGRG LPAGQAEVEM
     IERAREKRAW EASLPALSDT SQFEKRRKMM NEMERKEWAF REQEIEKLQE IRLEVLKELL
     RKREENQNEV NMKHLNARWS KLQEGKEAKM AKIQRTHVST IRKLVGKRKN IEGKLERRNI
     IKDYSDYASQ VYGPLSRLGC FPDNNSEDFV VKNYYLNTYE GLVELESCLP DFVTQPQIRA
     PKPKVITTKA GFLKRAARLD YELAEVHKAL LDKKNKVLEV KKPPRFLQRN PIPQPRLPTP
     TLEMTSNEEE EMEMAVIYLQ KLLRGRVVQN MMFEGKEKRL ELIQELRTCH ALQEDEKLVK
     KAEKQVTLAL QRQRNLHEHK VSLVENHLAG LEGRALADMF DFLSKELVRL QEERRIHAFV
     MLAERQRRVR EAEESGRRQV EKQRLREEDE IFKEVVKVHH STISSYLEDI ILNTEANTAE
     EQARAEIEKM AEKINDIAYE MESRRTYLQS EEIVAELVYS FLIPEVQKYF VKEKVRNAQR
     KHILAAHQII HSYTESMVQK KLTEGEQDEA SNAAMLLEKE TQNENNS
 
 
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