Gene: Medtr1g099620

General Information

Structural Information

  • Species Medicago truncatula
  • Gene Identifier Medtr1g099620
  • Transcript Identifier Medtr1g099620.1
  • Gene Type Coding gene
  • Location chr1 : 44997526-44998536 : negative

Gene Family Information

  • ID HOM05D002465
  • #Genes/#Species 275/100
  • Phylogenetic origin

Gene Duplication Information

Labels

Identifiers

  • pacid 31100753
  • id Medtr1g099620.JCVIMt4.0v1

Descriptions

  • Description ornithine cyclodeaminase/mu-crystallin
  • Loading (ortholog descriptions from ath)...

Functional Annotation

Biological Process

GO termEvidence(s)Provider(s)DescriptionSource(s)
GO:0009627
ISO
PLAZA Integrative Orthologysystemic acquired resistance AT5G52810
GO:1901672
ISO
PLAZA Integrative Orthologypositive regulation of systemic acquired resistance AT5G52810
GO:0062034
ISO
PLAZA Integrative OrthologyL-pipecolic acid biosynthetic process AT5G52810
GO:0042276
ISO
PLAZA Homology (enrichment)error-prone translesion synthesis HOM05D002465

Molecular Function

GO termEvidence(s)Provider(s)DescriptionSource(s)
GO:0062046
ISO
PLAZA Integrative Orthologydehydropipecolic acid reductase AT5G52810
GO:0003896
ISO
PLAZA Homology (enrichment)DNA primase activity HOM05D002465
GO:0003887
ISO
PLAZA Homology (enrichment)DNA-directed DNA polymerase activity HOM05D002465
GO:0008473
ISO
PLAZA Integrative Orthologyornithine cyclodeaminase activity AT5G52810

Cellular Component

GO termEvidence(s)Provider(s)DescriptionSource(s)
GO:0009507
ISO
PLAZA Integrative Orthologychloroplast AT5G52810
GO:0009536
ISO
PLAZA Integrative Orthologyplastid AT5G52810

Color Legend

Experimental Evidence
Computational Reviewed Evidence
Electronic Evidence
GO Sources: Primary Orthology Homology
Show redundant parents:
InterPro Description
IPR023401 Ornithine cyclodeaminase, N-terminal
IPR003462 Ornithine cyclodeaminase/mu-crystallin
IPR036291 NAD(P)-binding domain superfamily
Mapman id Description
26.9.3.1.5.2 External stimuli response.pathogen.defense mechanisms.systemic acquired resistance (SAR).pipecolic acid metabolism.cyclodeaminase (SARD4)