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IMPDH2

IMPDH2

Protein-coding gene in the species Homo sapiens

known as IMP dehydrogenase 2, is an enzyme that in humans is encoded by the IMPDH2 gene. IMP dehydrogenase 2 is the rate-limiting enzyme in the de novo guanine

IMPDH2

Inosine-5′-monophosphate dehydrogenase

Class of enzymes

two distinct isozymes of IMPDH encoded by two distinct genes, IMPDH1 and IMPDH2. Both isozymes contain 514 residues, have an 84% similarity in peptide sequence

Inosine-5′-monophosphate dehydrogenase

Inosine-5′-monophosphate_dehydrogenase

List of genetic disorders

CC2D2A, OFD1, TMEM138, TCTN3, ZNF423, AMRC9 Juvenile-onset dystonia ACTB, IMPDH2 dominant Juvenile primary lateral sclerosis (JPLS) ALS2 Keloid disorder

List of genetic disorders

List_of_genetic_disorders

Tetrameric protein

Quaternary-structure protein with 4 subunits

ion transporters such as CorA. lectins such as Concanavalin A IMPDH and IMPDH2 Examples of heterotetramers include haemoglobin (pictured), the NMDA receptor

Tetrameric protein

Tetrameric_protein

Juvenile-onset dystonia

Medical condition

of juvenile-onset dystonia. Another gene associated with the disorder is IMPDH2. "Dystonia, juvenile-onset". www.uniprot.org. Retrieved 2022-05-15. "Search

Juvenile-onset dystonia

Juvenile-onset_dystonia

IMPDH1

Protein-coding gene in the species Homo sapiens

Sasaki T, et al. (2009). "Genetic variations in the HGPRT, ITPA, IMPDH1, IMPDH2, and GMPS genes in Japanese individuals". Drug Metab. Pharmacokinet. 24

IMPDH1

List of human protein-coding genes 4

O14732 7655 IMPACT HGNC:20387; Q9P2X3 7656 IMPDH1 HGNC:6052; P20839 7657 IMPDH2 HGNC:6053; P12268 7658 IMPG1 HGNC:6055; Q17R60 7659 IMPG2 HGNC:18362; Q9BZV3

List of human protein-coding genes 4

List_of_human_protein-coding_genes_4