CKB - creatine kinase B Gene

Also Known as BCK; B-CK; CKBB; CPK-B; HEL-211; HEL-S-29

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 1152

About CKB

Cytogenetic location: 14q32.33 Genomic coordinates (GRCh38): 14:103,519,667-103,522,830 (from NCBI)

This gene has 18 transcripts (splice variants), 214 orthologues and 4 paralogues. Broad expression in colon (RPKM 268.3), prostate (RPKM 227.9) and 18 other tissues.

Summary

The protein encoded by this gene is a cytoplasmic enzyme involved in energy homeostasis. The encoded protein reversibly catalyzes the transfer of phosphate between ATP and various phosphogens such as creatine phosphate. It acts as a homodimer in brain as well as in Other tissues, and as a heterodimer with a similar muscle isozyme in heart. The encoded protein is a member of the ATP:guanido phosphotransferase protein family. A pseudogene of this gene has been characterized. [provided by RefSeq, Jul 2008]

CKB Products (2)

mRNA Protein Name
NM_001362531.2 NP_001349460.1 creatine kinase B-type isoform 2
NM_001823.5 NP_001814.2 creatine kinase B-type isoform 1
Molecular Function GO Annotation Evidence References Source
enables creatine kinase activity IDA
IDA: Inferred from direct assay
8186255 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
16189514 GOA
enables ubiquitin protein ligase binding IPI
IPI: Inferred from physical interaction
19725078 GOA
Biological Process GO Annotation Evidence References Source
involved in phosphocreatine biosynthetic process IDA
IDA: Inferred from direct assay
8186255 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

CKB Protein Structure

ATP-gua_PtransN

ATP-gua_PtransN: ATP:guanido phosphotransferase, N-terminal domain (21 - 100)

ATP-gua_Ptrans

ATP-gua_Ptrans: ATP:guanido phosphotransferase, C-terminal catalytic domain (121 - 366)

  • 0
  • 100
  • 200
  • 300
  • 381 a.a.
Protein Preferred Names Protein Names

creatine kinase B-type

  • brain creatine kinase

CKB Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
CKB P12277 CKM Homo sapiens P06732 35271311
Intra
CKB P12277 CKM Homo sapiens P06732 33961781
Intra
CKB P12277 CKM Homo sapiens P06732 28514442
Intra
CKB P12277 ASB9 Homo sapiens Q96DX5 16189514
Intra
CKB P12277 ASB9 Homo sapiens Q96DX5 32296183
Intra
CKB P12277 ASB9 Homo sapiens Q96DX5 25416956
Intra
CKB P12277 ASB9 Homo sapiens Q96DX5 25416956
Cross
CKB P12277 Q03463-PRO_0000278738 Hepatitis C virus Q03463-PRO_0000278738 19264780
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant CKB Proteins

Cat. No. Product Name Accession Purity
HY-P7897 Creatine kinase B-type/CKB Protein, Human (His) P12277 (M1-K381) ≥ 90%, as determined by reducing SDS-PAGE.

CKB Antibodies

Cat. No. Product Name Application Reactivity
HY-P80629 Creatine Kinase B type Antibody (YA492) WB, IHC-P Human, Mouse, Rat
HY-P80629A Creatine Kinase B type Antibody (YA492)(PBS only) WB, IHC-P Human, Mouse, Rat

Related Diseases

Diseases Alias
Subendocardial Myocardial Infarction
Neonatal Hypoxic And Ischemic Brain Injury
  • Perinatal Asphyxia

  • Hypoxic-Ischemic Encephalopathy

  • Perinatal Hypoxia

  • Hie

  • Hypoxic And Ischemic Brain Injury In The Newborn

  • Encephalopathy, Hypoxic Ischemic

  • Encephalopathies Hypoxic-Ischemic

  • Hypoxic Ischemic Encephalopathy

  • Hypoxic Ischaemic Brain Injury

  • Brain Hypoxia

  • Cerebral Hypoxia

  • Hypoxic Encephalopathy

  • Hypoxic Brain Damage

  • Hypoxic Brain Injury

  • Brainstem Hypoxia

  • Hypoxic Brainstem Damage

Acute Myocardial Infarction
  • Cardiac Attack

  • Heart Attack

Cardiac Arrest
  • Cardiopulmonary Arrest

  • Circulatory Arrest

  • Heart Arrest

Bacterial Meningitis
  • Meningitis, Bacterial

  • Meningitis Bacterial

  • Bm - [Bacterial Meningitis]

  • Leptomeningitis Bacterial

  • Pachymeningitis Bacterial

  • Arachnoiditis Bacterial

Prostate Rhabdomyosarcoma
  • Rhabdomyosarcoma Of The Prostate

Myocardial Infarction
  • Heart Attack

  • Myocardial Infarction, Susceptibility To

  • Myocardial Infarction 1

  • Myocardial Infarction, Protection Against

  • Myocardial Infarction, Decreased Susceptibility To

  • Myocardial Infarction, Decreased

  • Myocardial Infarct

  • MCI1

  • Premature Myocardial Infarction

  • Myocardial Infarction, Susceptibility To, Type 1

Small Cell Cancer Of The Lung
  • Small Cell Lung Cancer

  • Small Cell Lung Carcinoma

  • Sclc

  • Small-Cell Cancer Of Lung

  • Lung Small Cell Carcinoma

  • Sclc1

  • Sccl

  • Cancer, Lung, Small Cell

  • Small Cell Carcinoma Of Lung

  • Carcinoma, Small Cell

Mitral Valve Insufficiency
  • Mitral Regurgitation

  • Congenital Insufficiency Of Mitral Valve

  • Congenital Mitral Insufficiency

  • Congenital Mitral Regurgitation

  • Mitral Valve Incompetence

  • Mitral Valve Regurgitation

  • Mr - [Mitral Regurgitation]

  • Mi - [Mitral Incompetence]

  • Mitral Valve Annular Incompetency

  • Congenital Mitral Valve Incompetence

  • Congenital Mitral Valve Insufficiency

  • Congenital Mitral Valve Regurgitation

  • Congenital Mitral Incompetence

Osteopetrosis
  • Marble Bone Disease

  • Albers-Schonberg Disease

  • Osteopetroses

  • Marble Bones

  • Osteopetrosis And Related Disorders

  • Congenital Osteopetrosis

  • Marble Bone

  • Albers-Schoenberg Disease

  • Albers-Schonberg Osteopetrosis

  • Osteosclerosis Fragilis

  • Ivory Bones

Huntington Disease
  • Huntington'S Disease

  • Huntington Chorea

  • Huntington'S Chorea

  • HD

  • Huntington Chronic Progressive Hereditary Chorea

  • Juvenile Huntington Disease

  • Chronic Progressive Chorea

  • Chronic Progressive Hereditary Chorea

  • Hc - [Huntington Chorea]

  • Hereditary Chorea

  • Progressive Hereditary Chorea

Heart Disease
  • Heart Failure

  • Congenital Heart Disease

  • Heart Diseases

  • Congenital Heart Defects

  • Congenital Heart Defect

  • Heart Malformation

  • Congenital Anomaly Of Heart

  • Heart Defect

  • Heart-Congenital Defect

  • Congenital Heart Disorder

  • Heart Defects Congenital

  • Heart Defects, Congenital

  • Heart Defects

  • Heart Disease, Congenital

  • Disease, Heart, Congenital

  • Congestive Heart Failure

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
Macaca mulatta CKB VGNC VGNC:108291
Mus musculus CKB MGD MGI:88407
Bos taurus CKB VGNC VGNC:27384
Rattus norvegicus CKB RGD RGD:2357
Felis catus CKB VGNC VGNC:60913
Others CKB NCBI