Metabolite Card

Formula: C4H10N3O5P (211.0358)
SMILES: CN(CC(O)=O)C(=N)NP(O)(O)=O

Synonyms [en]

Phosphocreatine; CREATINE PHOSPHATE; N-phosphocreatine; N-(N-Phosphonoamido)sarcosine; N(omega)-Phosphonocreatine; phosphorylcreatine

Reviewed

Last reviewed on 2024-06-28.

Cite this Page

Phosphocreatine. 数据之源,洞见之始. SMRUCC genomics institute, a synthetic life researcher from China. https://biocad_registry.innovation.ac.cn/s/(-)-arctiin (retrieved 2026-01-03) (CAD Registry RN: BioCAD00000016242). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

Note

Phosphocreatine, also known as creatine phosphate (CP) or PCr (Pcr), is a phosphorylated creatine molecule that serves as a rapidly mobilizable reserve of high-energy phosphates in skeletal muscle, myocardium and the brain to recycle adenosine triphosphate, the energy currency of the cell. Phosphocreatine undergoes irreversible cyclization and dehydration to form creatinine at a fractional rate of 0.026 per day, thus forming approximately 2 g creatinine/day in an adult male. This is the amount of creatine that must be provided either from dietary sources or by endogenous synthesis to maintain the body pool of (creatine and) phosphocreatine. Creatine is an amino acid that plays a vital role as phosphocreatine in regenerating adenosine triphosphate in skeletal muscle to energize muscle contraction. Creatine is phosphorylated to phosphocreatine in muscle in a reaction that is catalyzed by the enzyme creatine kinase. This enzyme is in highest concentration in muscle and nerve. Oral administration increases muscle stores. During the past decade, creatine has assumed prominence as an ergogenic (and legal) aid for professional and elite athletes. Most (~ 95%) of the total body creatine-phosphocreatine pool is in muscle (more in skeletal muscle than in smooth muscle) and amounts to 120 g (or 925 mmol) in a 70 kg adult male. Approximately 60-67% of the content in resting muscle is in the phosphorylated form. This generates enough ATP at the myofibrillar apparatus to power about 4 seconds of muscle contraction in exercise. Phosphocreatine reacts with ADP to yield ATP and creatine; the reversible reaction is catalyzed by creatine kinase. phosphocreatine is the chief store of high-energy phosphates in muscle. Thus, this reaction, which permits the rephosphorylation of ADP to ATP, is the immediate source of energy in muscle contraction. During rest, metabolic processes regenerate phosphocreatine stores. In normal muscle, ATP that is broken down to ADP is immediately rephosphorylated to ATP. Thus, phosphocreatine serves as a reservoir of ATP-synthesizing potential. phosphocreatine is the only fuel available to precipitously regenerate ATP during episodes of rapid fluctuations in demand. The availability of phosphocreatine likely limits muscle performance during brief, high-power exercise, i.e., maximal exercise of short duration. With near maximal isometric contraction, the rate of utilization of phosphocreatine declines after 1-2 seconds of contraction, prior to the glycolysis peak at approximately 3 seconds (PMID:10079702).

Entity Information

DBLinks

Other DBLinks
  • CAS Registry Number: 19333-65-4
  • CAS Registry Number: 67-07-2
  • CAS Registry Number: 71519-72-7
  • CAS Registry Number: 922-32-7
  • PubChem: 587
  • PubChem: 9548602
  • ChEBI: ChEBI:17287
  • HMDB: HMDB0001511
  • KEGG: C02305
  • BioCyc: CREATINE-P
  • NCBI MeSH: Phosphocreatine
  • Wikipedia: Phosphocreatine
  • DrugBank: DB13191
  • RefMet: RM0009827
  • MoNA: BAF_UVA_POS000045
  • MoNA: BAF_UVA_POS000105
  • MoNA: CCMSLIB00000578001
  • MoNA: CCMSLIB00000578042
  • MoNA: CCMSLIB00005464354
  • MoNA: CCMSLIB00005464356
  • MoNA: CCMSLIB00005464372
  • MoNA: CCMSLIB00005720442
  • MoNA: EMBL-MCF_spec124367
  • MoNA: EMBL-MCF_spec134496
  • MoNA: EMBL-MCF_spec52920
  • MoNA: EMBL-MCF_spec63933
  • MoNA: EMBL_MCF_2_0_HRMS_Library000021
  • MoNA: EMBL_MCF_2_0_HRMS_Library000242
  • MoNA: HMDB0001511_ms_ms_1616
  • MoNA: HMDB0001511_ms_ms_1617
  • MoNA: HMDB0001511_ms_ms_1618
  • MoNA: KO003848
  • MoNA: KO003849
  • MoNA: KO003850
  • MoNA: KO003851
  • MoNA: KO003852
  • MoNA: KO009218
  • MoNA: KO009219
  • MoNA: KO009220
  • MoNA: MoNA011261
  • MoNA: MoNA011262
  • MoNA: MoNA011263
  • MoNA: MoNA011264
  • MoNA: MoNA023992
  • MoNA: MoNA024034
  • Metlin: METLIN_326
  • Coconut NaturalProduct: CNP0262318.0
  • Coconut NaturalProduct: CNP0537820.0

Class / Ontology

Metabolic Network
ID EC Number Name
KEGG:R01881 2.7.3.2 ATP:creatine N-phosphotransferase
KEGG:R01882 3.9.1.1 N-phosphocreatine hydrolase
KEGG:R07420 C02305<=>C00791 + C00009
BioCyc:PHOSPHOAMIDASE-RXN 3.9.1.1 WATER + CREATINE-P --> Pi + CREATINE
BioCyc:RXN-22062 CREATINE-P --> CPD-10788 + WATER
BioCyc:CREATINE-KINASE-RXN 2.7.3.2 CREATINE + ATP<=>PROTON + CREATINE-P + ADP
BioCyc:RXN-22061 CREATINE-P --> CREATININE + Pi
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Organism Source

Taxonomy Source

  1. Cyprinus carpio [ncbi taxid: 7962]
  2. Homo sapiens [ncbi taxid: 9606]
  3. Mus musculus [ncbi taxid: 10090]
  4. Rana nigromaculata [ncbi taxid: ]
  5. Homo sapiens [ncbi taxid: 9606]

Pathway Synthetic

pathway id name
PathBank:SMP0120710 Guanidinoacetate Methyltransferase Deficiency (GAMT Deficiency)
PathBank:SMP0120758 Ornithine Aminotransferase Deficiency (OAT Deficiency)
PathBank:SMP0120790 Hyperornithinemia-Hyperammonemia-Homocitrullinuria [HHH-syndrome]
PathBank:SMP0120569 Creatine Deficiency, Guanidinoacetate Methyltransferase Deficiency
PathBank:SMP0000020 Arginine and Proline Metabolism
PathBank:SMP0000362 Arginine: Glycine Amidinotransferase Deficiency (AGAT Deficiency)
PathBank:SMP0000188 Guanidinoacetate Methyltransferase Deficiency (GAMT Deficiency)
PathBank:SMP0000504 Creatine Deficiency, Guanidinoacetate Methyltransferase Deficiency
PathBank:SMP0063596 Arginine and Proline Metabolism
PathBank:SMP0120721 Hyperprolinemia Type II
PathBank:SMP0120761 Prolidase Deficiency (PD)
PathBank:SMP0120789 Hyperornithinemia with Gyrate Atrophy (HOGA)
PathBank:SMP0120499 Hyperprolinemia Type I
PathBank:SMP0120539 Prolinemia Type II
PathBank:SMP0120572 L-Arginine:Glycine Amidinotransferase Deficiency
PathBank:SMP0000207 Prolidase Deficiency (PD)
PathBank:SMP0000208 Prolinemia Type II
PathBank:SMP0000507 L-Arginine:Glycine Amidinotransferase Deficiency
PathBank:SMP0120788 Creatine Deficiency, Guanidinoacetate Methyltransferase Deficiency
PathBank:SMP0120501 Hyperprolinemia Type II
View All Pathways