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HAM2_CAEEL
ID   HAM2_CAEEL              Reviewed;         392 AA.
AC   H2KYH4; A3RMS1; A3RMS3;
DT   07-OCT-2020, integrated into UniProtKB/Swiss-Prot.
DT   21-MAR-2012, sequence version 1.
DT   03-AUG-2022, entry version 73.
DE   RecName: Full=Zinc finger protein ham-2 {ECO:0000305};
DE   AltName: Full=HSN abnormal migration protein 2 {ECO:0000312|WormBase:C07A12.1b};
GN   Name=ham-2 {ECO:0000312|WormBase:C07A12.1b};
GN   ORFNames=C07A12.1 {ECO:0000312|WormBase:C07A12.1b};
OS   Caenorhabditis elegans.
OC   Eukaryota; Metazoa; Ecdysozoa; Nematoda; Chromadorea; Rhabditida;
OC   Rhabditina; Rhabditomorpha; Rhabditoidea; Rhabditidae; Peloderinae;
OC   Caenorhabditis.
OX   NCBI_TaxID=6239 {ECO:0000312|Proteomes:UP000001940};
RN   [1] {ECO:0000312|Proteomes:UP000001940}
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
RC   STRAIN=Bristol N2 {ECO:0000312|Proteomes:UP000001940};
RX   PubMed=9851916; DOI=10.1126/science.282.5396.2012;
RG   The C. elegans sequencing consortium;
RT   "Genome sequence of the nematode C. elegans: a platform for investigating
RT   biology.";
RL   Science 282:2012-2018(1998).
RN   [2] {ECO:0000305}
RP   FUNCTION, SUBCELLULAR LOCATION, DEVELOPMENTAL STAGE, AND MUTAGENESIS OF
RP   SER-30 AND HIS-39.
RX   PubMed=10049362; DOI=10.1101/gad.13.4.472;
RA   Baum P.D., Guenther C., Frank C.A., Pham B.V., Garriga G.;
RT   "The Caenorhabditis elegans gene ham-2 links Hox patterning to migration of
RT   the HSN motor neuron.";
RL   Genes Dev. 13:472-483(1999).
CC   -!- FUNCTION: Probable transcription factor that acts downstream of egl-15,
CC       to promote migration of the HSN motor neurons from the tail to the
CC       gonad primordium during HSN cell differentiation (PubMed:10049362).
CC       {ECO:0000269|PubMed:10049362}.
CC   -!- SUBCELLULAR LOCATION: Nucleus {ECO:0000269|PubMed:10049362}.
CC   -!- ALTERNATIVE PRODUCTS:
CC       Event=Alternative splicing; Named isoforms=3;
CC       Name=b {ECO:0000312|WormBase:C07A12.1b};
CC         IsoId=H2KYH4-1; Sequence=Displayed;
CC       Name=c {ECO:0000312|WormBase:C07A12.1c};
CC         IsoId=H2KYH4-2; Sequence=VSP_060687;
CC       Name=a {ECO:0000312|WormBase:C07A12.1a};
CC         IsoId=H2KYH4-3; Sequence=VSP_060688;
CC   -!- DEVELOPMENTAL STAGE: During embryogenesis, expressed in HSN motor
CC       neurons (at protein level) (PubMed:10049362). Expressed in HSNs both
CC       before and during cell migration (at protein level) (PubMed:10049362).
CC       {ECO:0000269|PubMed:10049362}.
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DR   EMBL; BX284606; CCD63271.1; -; Genomic_DNA.
DR   EMBL; BX284606; CCD63272.1; -; Genomic_DNA.
DR   EMBL; BX284606; CCD63273.1; -; Genomic_DNA.
DR   RefSeq; NP_001024363.2; NM_001029192.4. [H2KYH4-3]
DR   RefSeq; NP_001024364.2; NM_001029193.3. [H2KYH4-1]
DR   RefSeq; NP_001294827.1; NM_001307898.1. [H2KYH4-2]
DR   AlphaFoldDB; H2KYH4; -.
DR   IntAct; H2KYH4; 51.
DR   STRING; 6239.C07A12.1b; -.
DR   EPD; H2KYH4; -.
DR   PaxDb; H2KYH4; -.
DR   EnsemblMetazoa; C07A12.1a.1; C07A12.1a.1; WBGene00001821. [H2KYH4-3]
DR   EnsemblMetazoa; C07A12.1b.1; C07A12.1b.1; WBGene00001821. [H2KYH4-1]
DR   EnsemblMetazoa; C07A12.1c.1; C07A12.1c.1; WBGene00001821. [H2KYH4-2]
DR   GeneID; 180727; -.
DR   KEGG; cel:CELE_C07A12.1; -.
DR   UCSC; C07A12.1b; c. elegans.
DR   CTD; 180727; -.
DR   WormBase; C07A12.1a; CE39669; WBGene00001821; ham-2.
DR   WormBase; C07A12.1b; CE07992; WBGene00001821; ham-2.
DR   WormBase; C07A12.1c; CE39670; WBGene00001821; ham-2.
DR   eggNOG; KOG1721; Eukaryota.
DR   GeneTree; ENSGT00970000196410; -.
DR   HOGENOM; CLU_704449_0_0_1; -.
DR   InParanoid; H2KYH4; -.
DR   OMA; IHISHDQ; -.
DR   OrthoDB; 858046at2759; -.
DR   PhylomeDB; H2KYH4; -.
DR   SignaLink; H2KYH4; -.
DR   Proteomes; UP000001940; Chromosome X.
DR   Bgee; WBGene00001821; Expressed in anatomical system and 4 other tissues.
DR   ExpressionAtlas; H2KYH4; baseline and differential.
DR   GO; GO:0005634; C:nucleus; IDA:WormBase.
DR   GO; GO:0003700; F:DNA-binding transcription factor activity; ISS:WormBase.
DR   GO; GO:0000981; F:DNA-binding transcription factor activity, RNA polymerase II-specific; IBA:GO_Central.
DR   GO; GO:0046872; F:metal ion binding; IEA:UniProtKB-KW.
DR   GO; GO:0043565; F:sequence-specific DNA binding; IBA:GO_Central.
DR   GO; GO:0001709; P:cell fate determination; IMP:WormBase.
DR   GO; GO:0016477; P:cell migration; IMP:WormBase.
DR   GO; GO:0045664; P:regulation of neuron differentiation; IMP:WormBase.
DR   GO; GO:0006357; P:regulation of transcription by RNA polymerase II; IBA:GO_Central.
DR   GO; GO:0006355; P:regulation of transcription, DNA-templated; ISS:WormBase.
DR   InterPro; IPR036236; Znf_C2H2_sf.
DR   InterPro; IPR013087; Znf_C2H2_type.
DR   Pfam; PF00096; zf-C2H2; 1.
DR   SMART; SM00355; ZnF_C2H2; 3.
DR   SUPFAM; SSF57667; SSF57667; 2.
DR   PROSITE; PS00028; ZINC_FINGER_C2H2_1; 2.
DR   PROSITE; PS50157; ZINC_FINGER_C2H2_2; 2.
PE   1: Evidence at protein level;
KW   Alternative splicing; Metal-binding; Nucleus; Reference proteome; Repeat;
KW   Transcription; Zinc; Zinc-finger.
FT   CHAIN           1..392
FT                   /note="Zinc finger protein ham-2"
FT                   /id="PRO_0000450750"
FT   ZN_FING         16..39
FT                   /note="C2H2-type 1"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00042"
FT   ZN_FING         43..66
FT                   /note="C2H2-type 2"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00042"
FT   ZN_FING         72..95
FT                   /note="C2H2-type 3; degenerate"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00042"
FT   REGION          106..130
FT                   /note="Disordered"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   REGION          278..303
FT                   /note="Disordered"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   COMPBIAS        110..128
FT                   /note="Polar residues"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   COMPBIAS        281..303
FT                   /note="Polar residues"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   VAR_SEQ         1..61
FT                   /note="Missing (in isoform c)"
FT                   /evidence="ECO:0000305"
FT                   /id="VSP_060687"
FT   VAR_SEQ         112..113
FT                   /note="Missing (in isoform a)"
FT                   /evidence="ECO:0000305"
FT                   /id="VSP_060688"
FT   MUTAGEN         30
FT                   /note="S->F: In gm16; causes arrest at the L1 larval stage,
FT                   defects in hermaphrodite-specific neuron migration, and
FT                   impairs pharynx attachment to the nose."
FT                   /evidence="ECO:0000269|PubMed:10049362"
FT   MUTAGEN         39
FT                   /note="H->Y: In gm48; in some mutants, causes arrest at the
FT                   L1 larval stage and defects in hermaphrodite-specific
FT                   neuron migration."
FT                   /evidence="ECO:0000269|PubMed:10049362"
SQ   SEQUENCE   392 AA;  43672 MW;  EC027C509321EA9C CRC64;
     MPYRAELKRP DLKGSFPCSI CQKVFCHSSS LSRHRMQAHF KSYTCTTCNN EIPSNDTLRS
     HMYRVHNITR MFMCRCCNWA FPDKTSLHIH MQSMLKNGTP GEAAVLAKSS DVVDSTSESG
     SPRQSPPFSP DLLMQKRMLQ VAANNNNIGS IFPTLLKSPD SKSMFPLDLS NMGPSQFLSA
     WLANNPINTA ALNLAAQQTP SKDSIQSSNI SDYDDLEVQT TEEDIKFEVE SSDVSPRSVI
     VKTEPTFKRE LEHDADIDVE GDDGEPPLKM TIDDKNIHIS HDQPSPTVSD SHISGGSSSH
     SGESLKCFDC QVARGKLVAV EDKCRAYEKT IRELQVQVDF LRKIQPNPMP PVMLPPPMMP
     MPSPGPNNLF QNPAMRMLLN NLIHMNRPSV VP
 
 
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