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The following sections contain reference sequences that belong to a
specific genome build. Explain
This section includes genomic Reference
Sequences (RefSeqs) from all assemblies on which this gene is annotated, such as
RefSeqs for chromosomes and scaffolds (contigs) from both reference and alternate
assemblies. Model RNAs and proteins are also reported here.
Reference Zm-B73-REFERENCE-NAM-5.0 Primary Assembly
Genomic
-
NC_050101.1 Reference Zm-B73-REFERENCE-NAM-5.0 Primary Assembly
- Range
-
55493697..55497576 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
mRNA and Protein(s)
-
XM_008649484.4 → XP_008647706.1 uncharacterized protein LOC100279212 isoform X1
- UniProtKB/TrEMBL
-
A0A804PSF0
- Conserved Domains (4) summary
-
- PLN02972
Location:138 → 890
- PLN02972; Histidyl-tRNA synthetase
- cd00773
Location:469 → 784
- HisRS-like_core; Class II Histidinyl-tRNA synthetase (HisRS)-like catalytic core domain. HisRS is a homodimer. It is responsible for the attachment of histidine to the 3' OH group of ribose of the appropriate tRNA. This domain is primarily responsible for ATP-dependent ...
- cd00859
Location:797 → 885
- HisRS_anticodon; HisRS Histidyl-anticodon binding domain. HisRS belongs to class II aminoacyl-tRNA synthetases (aaRS). This alignment contains the anticodon binding domain, which is responsible for specificity in tRNA-binding, so that the activated amino acid is ...
- cl00013
Location:145 → 282
- Lyase_I_like; Lyase class I_like superfamily: contains the lyase class I family, histidine ammonia-lyase and phenylalanine ammonia-lyase, which catalyze similar beta-elimination reactions
The following Reference Sequences have been suppressed. Explain
These RefSeqs were suppressed for the
cited reason(s). Suppressed RefSeqs do not appear in BLAST databases, related
sequence links, or BLAST links (BLink), but may still be retrieved by clicking on
their accession.version below.
-
NM_001152236.1: Suppressed sequence
- Description
- NM_001152236.1: This RefSeq was removed because currently there is insufficient support for the transcript and the protein.