Entity Details

Primary name PAPS2_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionO95340
EntryNamePAPS2_HUMAN
FullNameBifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase 2
TaxID9606
Evidenceevidence at protein level
Length614
SequenceStatuscomplete
DateCreated2000-05-30
DateModified2021-06-02

Ontological Relatives

GenesPAPSS2

GO terms

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GOName
GO:0000103 sulfate assimilation
GO:0001501 skeletal system development
GO:0004020 adenylylsulfate kinase activity
GO:0004781 sulfate adenylyltransferase (ATP) activity
GO:0005524 ATP binding
GO:0005829 cytosol
GO:0016779 nucleotidyltransferase activity
GO:0050428 3'-phosphoadenosine 5'-phosphosulfate biosynthetic process

Subcellular Location

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Domains

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DomainNameCategoryType
IPR002650 Sulphate adenylyltransferaseDomainDomain
IPR002891 Adenylyl-sulfate kinaseFamilyFamily
IPR014729 Rossmann-like alpha/beta/alpha sandwich foldFamilyHomologous superfamily
IPR015947 PUA-like superfamilyFamilyHomologous superfamily
IPR024951 Sulphate adenylyltransferase catalytic domainDomainDomain
IPR025980 ATP-sulfurylase PUA-like domainDomainDomain
IPR027417 P-loop containing nucleoside triphosphate hydrolaseFamilyHomologous superfamily

Diseases

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Disease IDSourceNameDescription
612847 OMIMBrachyolmia type 4 with mild epiphyseal and metaphyseal changes (BCYM4)A form of brachyolmia, a clinically and genetically heterogeneous skeletal dysplasia primarily affecting the spine and characterized by a short trunk, short stature, and platyspondyly. BCYM4 is an autosomal recessive form with mild epiphyseal and metaphyseal changes. Clinical features include short stature evidenced at birth, short and bowed lower limbs, mild brachydactyly, kyphoscoliosis, abnormal gait, enlarged knee joints. Some BCYM4 patients may manifest premature pubarche and hyperandrogenism associated with skeletal dysplasia and short stature. The disease is caused by variants affecting the gene represented in this entry.

Interactions

5 interactions