1. Gene
  2. PKM - pyruvate kinase M1/2 Gene

PKM - pyruvate kinase M1/2 Gene

Homo sapiens

Also known as PK3; TCB; p58; OIP3; PKM2; CTHBP; THBP1; HEL-S-30

Gene ID: 5315 | Gene type: protein coding

About PKM

Cytogenetic location: 15q23 Genomic coordinates (GRCh38): 15:72,199,029-72,231,591 (from NCBI)

This gene has 25 transcripts (splice variants), 294 orthologues and 1 paralogue. Ubiquitous expression in brain (RPKM 155.4), esophagus (RPKM 151.3) and 24 other tissues.

Summary

This gene encodes a protein involved in glycolysis. The encoded protein is a Pyruvate Kinase that catalyzes the transfer of a phosphoryl group from phosphoenolpyruvate to ADP, generating ATP and pyruvate. This protein has been shown to interact with thyroid hormone and may mediate cellular metabolic effects induced by thyroid Hormones. This protein has been found to bind Opa protein, a Bacterial outer membrane protein involved in gonococcal adherence to and invasion of human cells, suggesting a role of this protein in Bacterial pathogenesis. Several alternatively spliced transcript variants encoding a few distinct isoforms have been reported. [provided by RefSeq, May 2011]

PKM Products(18)

mRNA Protein Name
XM_047432666.1 XP_047288622.1 pyruvate kinase PKM isoform X8
XM_047432663.1 XP_047288619.1 pyruvate kinase PKM isoform X2
NM_001206797.3 NP_001193726.1 pyruvate kinase PKM isoform d
XM_006720570.2 XP_006720633.1 pyruvate kinase PKM isoform X3
XM_047432665.1 XP_047288621.1 pyruvate kinase PKM isoform X7
XM_047432664.1 XP_047288620.1 pyruvate kinase PKM isoform X6
NM_001206798.3 NP_001193727.1 pyruvate kinase PKM isoform e
NM_182470.4 NP_872270.1 pyruvate kinase PKM isoform b
XM_047432662.1 XP_047288618.1 pyruvate kinase PKM isoform X1
NM_001206799.2 NP_001193728.1 pyruvate kinase PKM isoform f
XM_005254443.2 XP_005254500.1 pyruvate kinase PKM isoform X4
XM_005254445.6 XP_005254502.1 pyruvate kinase PKM isoform X8
NM_182471.4 NP_872271.1 pyruvate kinase PKM isoform b
NM_001316318.2 NP_001303247.1 pyruvate kinase PKM isoform g
NM_001206796.3 NP_001193725.1 pyruvate kinase PKM isoform c
NM_002654.6 NP_002645.3 pyruvate kinase PKM isoform a
NM_001411081.1 NP_001398010.1 pyruvate kinase PKM
XM_011521670.2 XP_011519972.1 pyruvate kinase PKM isoform X5
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
NOT enables histone H3T11 kinase activity IDA
IDA: Inferred from direct assay
22901803 GOA
enables histone H3T11 kinase activity IDA
IDA: Inferred from direct assay
22901803 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
12620389 GOA
enables protein homodimerization activity IDA
IDA: Inferred from direct assay
22306293 GOA
enables protein tyrosine kinase activity IDA
IDA: Inferred from direct assay
22306293 GOA
enables pyruvate kinase activity IDA
IDA: Inferred from direct assay
20005212 GOA
enables transcription coactivator activity IDA
IDA: Inferred from direct assay
22056988 GOA
Biological Process GO Annotation Evidence Reference Source
involved in glycolytic process IDA
IDA: Inferred from direct assay
20847263 GOA
involved in positive regulation of sprouting angiogenesis IMP
IMP: Inferred from mutant phenotype
27199445 GOA
involved in positive regulation of transcription by RNA polymerase II IDA
IDA: Inferred from direct assay
22056988 GOA
involved in programmed cell death IDA
IDA: Inferred from direct assay
17308100 GOA
Cellular Component GO Annotation Evidence Reference Source
located in cytoplasm IDA
IDA: Inferred from direct assay
18298799 GOA
is active in nucleus IDA
IDA: Inferred from direct assay
22901803 GOA
located in nucleus IDA
IDA: Inferred from direct assay
17308100 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

PKM Protein Structure

PK

PK: Pyruvate kinase, barrel domain (43 - 395)

PK_C

PK_C: Pyruvate kinase, alpha/beta domain (409 - 529)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 500
  • 531 a.a.
Protein Preferred Names Protein Names

pyruvate kinase PKM

OPA-interacting protein 3

PK, muscle type

cytosolic thyroid hormone-binding protein

epididymis secretory protein Li 30

pyruvate kinase 2/3

pyruvate kinase isozymes M1/M2

pyruvate kinase muscle isozyme

pyruvate kinase, muscle

threonine-protein kinase PKM2

thyroid hormone-binding protein 1

thyroid hormone-binding protein, cytosolic

tumor M2-PK

tyrosine-protein kinase PKM2

Recombinant PKM Proteins

Cat. No. Product Name Accession Purity
HY-P7803 PKM2 Protein, Human (420 a.a, His) P14618-1 (L61-E480) ≥95%
HY-P70599 PKM2 Protein, Human (530a.a, His) P14618-1 (S2-P531) ≥95%

Related Diseases

Diseases Alias
Bilirubin Metabolic Disorder

Hyperbilirubinemia

Hereditary Hyperbilirubinemia

Hyperbilirubinemia, Hereditary

Hyperbilirubinaemia

Liver Carcinoma In Situ

Carcinoma In Situ Of Liver And Biliary System

Carcinoma In Situ Of Liver, Gallbladder And Bile Ducts

Meningioma, Familial

Meningioma

Familial Meningioma

Meningioma, Familial, Susceptibility To

Meningeal Neoplasm

Meningeal Neoplasms

Meningiomas

Meningioma, Nf2-Related, Somatic

Meningioma, Sis-Related

Meningothelial Cell Tumor

Neoplasm Of The Meninges

Primary Meningeal Tumor

Familial Multiple Meningioma

MNGMA

Meningioma, Benign, No Icd-O Subtype

Intracranial Meningioma

Meningothelial Cell Neoplasm

Supratentorial Meningioma

Primary Neoplasm Of Spinal Meninges

Benign Intracranial Meningioma

Benign Meningioma

Meningeal Tumours

Meningeal Sarcoma Of Unspecified Site

Meningothelial Sarcoma Of Unspecified Site

Colorectal Cancer

Colon Cancer

Colorectal Carcinoma

Colon Carcinoma

Colorectal Cancer, Susceptibility To

Carcinoma Of Colon

CRC

Colorectal Cancer With Chromosomal Instability, Somatic

Colon Cancer, Somatic

Colon Cancer, Susceptibility To

Colonic Neoplasms

Colorectal Neoplasms

Colorectal Cancer, Somatic

Colon Cancer, Advanced, Somatic

Colonic Carcinoma

Colorectal Carcinomas

Colon Cancers

Colorectal Cancers

Cancer, Colorectal, Somatic

Cancer, Colon

Cancer, Colorectal, Susceptibility To

Colorectal Neoplasm

Colonic Neoplasm

Malignant Tumor Of Colon

Pyruvate Kinase Deficiency Of Red Cells

Pyruvate Kinase Deficiency

Pk Deficiency

Pyruvate Kinase Deficiency Of Erythrocyte

Hemolytic Anemia Due To Red Cell Pyruvate Kinase Deficiency

Pyruvate Kinase Deficiency Of Erythrocytes

Pkd

PKRD

Hereditary Non-Spherocytic Hemolytic Anemia Due To Pyruvate Kinase Deficiency

Hnsha

Pyruvate Kinase-Deficient Hemolytic Anemia

Red Cell Pyruvate Kinase Deficiency

Deficiency Of Pyruvate Kinase

Anemia, Hemolytic, Congenital Nonspherocytic

Glycogen Storage Disease

Glycogenosis

Glycogenoses

Gsd

Storage Disease, Glycogen

Gsd - [Glycogen Storage Disease]

Glycogen Thesaurismosis

Diffuse Glycogenosis

Generalised Glycogen Storage Disease

Generalised Glycogenosis

Generalised Glycogen Storage Disease Of Infants

Glycogen Synthase Deficiency

Neonatal Jaundice

Neonatal Hyperbilirubinemia

Neonatal Icterus

Jaundice Neonatal

Jaundice, Neonatal

Hyperbilirubinemia, Neonatal

Blood Group Incompatibility
Anterior Dislocation Of Lens
Congenital Nonspherocytic Hemolytic Anemia

Hereditary Nonspherocytic Hemolytic Anemia

Hereditary Non-Spherocytic Hemolytic Anemia

Anemia, Hemolytic, Congenital Nonspherocytic

Congenital Nonspherocytic Hemolytic Anaemia

Hereditary Nonspherocytic Hemolytic Anaemia

Hnsha

Pigmentation Disease

Pigmentation Disorders

Skin Pigmentation Disorder

Renal Cell Carcinoma, Nonpapillary

Renal Cell Carcinoma

RCC

Nonpapillary Renal Cell Carcinoma

Clear Cell Renal Cell Carcinoma

Hypernephroma

Adenocarcinoma Of Kidney

Renal Carcinoma, Chromophobe, Somatic

Clear Cell Carcinoma Of Kidney

Clear-Cell Metastatic Renal Cell Carcinoma

Clear Cell Renal Carcinoma

Renal Cell Carcinoma, Somatic

Conventional Renal Cell Carcinoma

Conventional Renal Cell Carcinoma

Renal Clear Cell Carcinoma

Ccrcc

Hereditary Clear Cell Renal Cell Carcinoma

Carcinoma, Renal Cell

Renal Cell Carcinoma, Clear Cell, Somatic

Renal Cell Carcinoma, Clear Cell

Clear Cell Kidney Carcinoma

Clear Cell Rcc

Cystic-Multilocular Variant

Clear Cell Renal Cell Adenocarcinoma

Hereditary Clear Cell Renal Cell Adenocarcinoma

Common Renal Cell Carcinoma

Crcc

Renal Cell Carcinoma Non-Papillary

Carcinoma Renal Cell

Renal Cell Cancer

Carcinoma, Renal Cell, Nonpapillary

Pancreatic Cancer

Pancreatic Carcinoma

Familial Pancreatic Carcinoma

Pancreatic Neoplasm

Carcinoma Of Pancreas

Pancreatic Carcinoma, Familial

Malignant Neoplasm Of Pancreas

Pancreatic Acinar Carcinoma

Pancreatic Tumor

Familial Pancreatic Cancer

Neoplasm Of The Pancreas

Pancreatic Carcinoma, Somatic

Pancreatic Cancer, Somatic

Ca Body Of Pancreas

Ca Head Of Pancreas

Ca Tail Of Pancreas

Malignant Neoplasm Of Body Of Pancreas

Malignant Neoplasm Of Head Of Pancreas

Malignant Neoplasm Of Tail Of Pancreas

Pancreas Neoplasm

Exocrine Cancer

Exocrine Pancreas Carcinoma

Hereditary Pancreatic Cancer

Hereditary Pancreatic Carcinoma

PNCA

Cancer Of The Pancreas

Pancreatic Cancer, Susceptibility To

Carcinoma Of Head Of Pancreas

Pancreatic Neoplasms

Pancreatic Tumors

Cancer, Pancreatic

Cancer Of Pancreas

Mixed Islet Cell With Exocrine Carcinoma Of Unspecified Site

Kernicterus

Bilirubin Encephalopathy

Hyperbilirubinemic Encephalopathy

Kernicterus Spectrum Disorder

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Bos taurus PKM VGNC VGNC:55132
Rattus norvegicus PKM RGD RGD:3337
Mus musculus PKM MGD MGI:97591
Others PKM NCBI