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Entry version 149 (29 Sep 2021)
Sequence version 1 (01 Dec 2001)
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Protein

ATP synthase membrane subunit K, mitochondrial

Gene

ATP5MK

Organism
Homo sapiens (Human)
Status
Reviewed-Annotation score:

Annotation score:5 out of 5

<p>The annotation score provides a heuristic measure of the annotation content of a UniProtKB entry or proteome. This score <strong>cannot</strong> be used as a measure of the accuracy of the annotation as we cannot define the 'correct annotation' for any given protein.<p><a href='/help/annotation_score' target='_top'>More...</a></p>
-Experimental evidence at protein leveli <p>This indicates the type of evidence that supports the existence of the protein. Note that the 'protein existence' evidence does not give information on the accuracy or correctness of the sequence(s) displayed.<p><a href='/help/protein_existence' target='_top'>More...</a></p>

<p>This section provides any useful information about the protein, mostly biological knowledge.<p><a href='/help/function_section' target='_top'>More...</a></p>Functioni

Mitochondrial membrane ATP synthase (F1F0 ATP synthase or Complex V) produces ATP from ADP in the presence of a proton gradient across the membrane which is generated by electron transport complexes of the respiratory chain. F-type ATPases consist of two structural domains, F1 - containing the extramembraneous catalytic core and F0 - containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F1 is coupled via a rotary mechanism of the central stalk subunits to proton translocation (PubMed:29917077).

ATP5MK is a minor subunit of the mitochondrial membrane ATP synthase required for dimerization of the ATP synthase complex and as such regulates ATP synthesis in the mitochondria (PubMed:21345788, PubMed:29917077).

1 Publication2 Publications

Enzyme and pathway databases

Pathway Commons web resource for biological pathway data

More...
PathwayCommonsi
Q96IX5

<p>This section provides information about the protein and gene name(s) and synonym(s) and about the organism that is the source of the protein sequence.<p><a href='/help/names_and_taxonomy_section' target='_top'>More...</a></p>Names & Taxonomyi

<p>This subsection of the <a href="http://www.uniprot.org/help/names_and_taxonomy_section">Names and taxonomy</a> section provides an exhaustive list of all names of the protein, from commonly used to obsolete, to allow unambiguous identification of a protein.<p><a href='/help/protein_names' target='_top'>More...</a></p>Protein namesi
Recommended name:
ATP synthase membrane subunit K, mitochondrialCurated
Alternative name(s):
ATP synthase membrane subunit DAPIT, mitochondrialCurated
Diabetes-associated protein in insulin-sensitive tissues
HCV F-transactivated protein 2
Up-regulated during skeletal muscle growth protein 5Curated
<p>This subsection of the <a href="http://www.uniprot.org/help/names_and_taxonomy_section">Names and taxonomy</a> section indicates the name(s) of the gene(s) that code for the protein sequence(s) described in the entry. Four distinct tokens exist: 'Name', 'Synonyms', 'Ordered locus names' and 'ORF names'.<p><a href='/help/gene_name' target='_top'>More...</a></p>Gene namesi
Name:ATP5MKImported
Synonyms:ATP5MD, DAPIT, HCVFTP2, USMG5
ORF Names:PD04912
<p>This subsection of the <a href="http://www.uniprot.org/help/names_and_taxonomy_section">Names and taxonomy</a> section provides information on the name(s) of the organism that is the source of the protein sequence.<p><a href='/help/organism-name' target='_top'>More...</a></p>OrganismiHomo sapiens (Human)
<p>This subsection of the <a href="http://www.uniprot.org/help/names_and_taxonomy_section">Names and taxonomy</a> section shows the unique identifier assigned by the NCBI to the source organism of the protein. This is known as the 'taxonomic identifier' or 'taxid'.<p><a href='/help/taxonomic_identifier' target='_top'>More...</a></p>Taxonomic identifieri9606 [NCBI]
<p>This subsection of the <a href="http://www.uniprot.org/help/names_and_taxonomy_section">Names and taxonomy</a> section contains the taxonomic hierarchical classification lineage of the source organism. It lists the nodes as they appear top-down in the taxonomic tree, with the more general grouping listed first.<p><a href='/help/taxonomic_lineage' target='_top'>More...</a></p>Taxonomic lineageiEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo
<p>This subsection of the <a href="http://www.uniprot.org/help/names_and_taxonomy_section">Names and taxonomy</a> section is present for entries that are part of a <a href="http://www.uniprot.org/proteomes">proteome</a>, i.e. of a set of proteins thought to be expressed by organisms whose genomes have been completely sequenced.<p><a href='/help/proteomes_manual' target='_top'>More...</a></p>Proteomesi
  • UP000005640 <p>A UniProt <a href="http://www.uniprot.org/manual/proteomes_manual">proteome</a> can consist of several components.<br></br>The component name refers to the genomic component encoding a set of proteins.<p><a href='/help/proteome_component' target='_top'>More...</a></p> Componenti: Chromosome 10

Organism-specific databases

Human Gene Nomenclature Database

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HGNCi
HGNC:30889, ATP5MK

Online Mendelian Inheritance in Man (OMIM)

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MIMi
615204, gene

neXtProt; the human protein knowledge platform

More...
neXtProti
NX_Q96IX5

Eukaryotic Pathogen, Vector and Host Database Resources

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VEuPathDBi
HostDB:ENSG00000173915

<p>This section provides information on the location and the topology of the mature protein in the cell.<p><a href='/help/subcellular_location_section' target='_top'>More...</a></p>Subcellular locationi

Topology

Feature keyPosition(s)DescriptionActionsGraphical viewLength
<p>This subsection of the <a href="http://www.uniprot.org/help/subcellular_location_section">'Subcellular location'</a> section describes the extent of a membrane-spanning region of the protein. It denotes the presence of both alpha-helical transmembrane regions and the membrane spanning regions of beta-barrel transmembrane proteins.<p><a href='/help/transmem' target='_top'>More...</a></p>Transmembranei23 – 45HelicalSequence analysisAdd BLAST23

<p>UniProtKB Keywords constitute a <a href="http://www.uniprot.org/keywords">controlled vocabulary</a> with a hierarchical structure. Keywords summarise the content of a UniProtKB entry and facilitate the search for proteins of interest.<p><a href='/help/keywords' target='_top'>More...</a></p>Keywords - Cellular componenti

Membrane, Mitochondrion

<p>This section provides information on the disease(s) and phenotype(s) associated with a protein.<p><a href='/help/pathology_and_biotech_section' target='_top'>More...</a></p>Pathology & Biotechi

<p>This subsection of the 'Pathology and Biotech' section provides information on the disease(s) associated with genetic variations in a given protein. The information is extracted from the scientific literature and diseases that are also described in the <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?db=omim">OMIM</a> database are represented with a <a href="http://www.uniprot.org/diseases">controlled vocabulary</a> in the following way:<p><a href='/help/involvement_in_disease' target='_top'>More...</a></p>Involvement in diseasei

Mitochondrial complex V deficiency, nuclear type 6 (MC5DN6)1 Publication
The disease is caused by variants affecting the gene represented in this entry.
Disease descriptionAn autosomal recessive mitochondrial disorder characterized by gross motor developmental delay manifesting in the first years of life, and subsequent episodic developmental regression. The episodes are associated with metabolic stress, including fever, illness, and general anesthesia. Patients develop gait difficulties or loss of ambulation, as well as other variable abnormalities, including abnormal movements, hemiplegia, and persistent lethargy. Brain imaging shows degenerative features in the basal ganglia and brainstem consistent with a diagnosis of Leigh syndrome.
Related information in OMIM

Keywords - Diseasei

Primary mitochondrial disease

Organism-specific databases

DisGeNET

More...
DisGeNETi
84833

MalaCards human disease database

More...
MalaCardsi
ATP5MD
MIMi618683, phenotype

Open Targets

More...
OpenTargetsi
ENSG00000173915

Orphanet; a database dedicated to information on rare diseases and orphan drugs

More...
Orphaneti
254913, Isolated ATP synthase deficiency

The Pharmacogenetics and Pharmacogenomics Knowledge Base

More...
PharmGKBi
PA134968209

Miscellaneous databases

Pharos NIH Druggable Genome Knowledgebase

More...
Pharosi
Q96IX5, Tbio

Genetic variation databases

BioMuta curated single-nucleotide variation and disease association database

More...
BioMutai
USMG5

<p>This section describes post-translational modifications (PTMs) and/or processing events.<p><a href='/help/ptm_processing_section' target='_top'>More...</a></p>PTM / Processingi

Molecule processing

Feature keyPosition(s)DescriptionActionsGraphical viewLength
<p>This subsection of the <a href="http://www.uniprot.org/help/ptm_processing_section">PTM / Processing</a> section indicates that the initiator methionine is cleaved from the mature protein.<p><a href='/help/init_met' target='_top'>More...</a></p>Initiator methionineiRemovedCombined sources
<p>This subsection of the 'PTM / Processing' section describes the extent of a polypeptide chain in the mature protein following processing or proteolytic cleavage.<p><a href='/help/chain' target='_top'>More...</a></p>ChainiPRO_00002315782 – 58ATP synthase membrane subunit K, mitochondrialAdd BLAST57

Amino acid modifications

Feature keyPosition(s)DescriptionActionsGraphical viewLength
<p>This subsection of the 'PTM / Processing' section specifies the position and type of each modified residue excluding <a href="http://www.uniprot.org/manual/lipid">lipids</a>, <a href="http://www.uniprot.org/manual/carbohyd">glycans</a> and <a href="http://www.uniprot.org/manual/crosslnk">protein cross-links</a>.<p><a href='/help/mod_res' target='_top'>More...</a></p>Modified residuei16N6-acetyllysineBy similarity1
Modified residuei17N6-acetyllysineBy similarity1

Keywords - PTMi

Acetylation

Proteomic databases

Encyclopedia of Proteome Dynamics

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EPDi
Q96IX5

jPOST - Japan Proteome Standard Repository/Database

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jPOSTi
Q96IX5

MassIVE - Mass Spectrometry Interactive Virtual Environment

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MassIVEi
Q96IX5

MaxQB - The MaxQuant DataBase

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MaxQBi
Q96IX5

PaxDb, a database of protein abundance averages across all three domains of life

More...
PaxDbi
Q96IX5

PeptideAtlas

More...
PeptideAtlasi
Q96IX5

PRoteomics IDEntifications database

More...
PRIDEi
Q96IX5

ProteomicsDB: a multi-organism proteome resource

More...
ProteomicsDBi
76865

Consortium for Top Down Proteomics

More...
TopDownProteomicsi
Q96IX5

PTM databases

GlyGen: Computational and Informatics Resources for Glycoscience

More...
GlyGeni
Q96IX5, 1 site, 1 O-linked glycan (1 site)

iPTMnet integrated resource for PTMs in systems biology context

More...
iPTMneti
Q96IX5

Comprehensive resource for the study of protein post-translational modifications (PTMs) in human, mouse and rat.

More...
PhosphoSitePlusi
Q96IX5

SwissPalm database of S-palmitoylation events

More...
SwissPalmi
Q96IX5

<p>This section provides information on the expression of a gene at the mRNA or protein level in cells or in tissues of multicellular organisms.<p><a href='/help/expression_section' target='_top'>More...</a></p>Expressioni

<p>This subsection of the 'Expression' section reports the experimentally proven effects of inducers and repressors (usually chemical compounds or environmental factors) on the level of protein (or mRNA) expression (up-regulation, down-regulation, constitutive expression).<p><a href='/help/induction' target='_top'>More...</a></p>Inductioni

Transactivated by SBP1.1 Publication

Gene expression databases

Bgee dataBase for Gene Expression Evolution

More...
Bgeei
ENSG00000173915, Expressed in caudate nucleus and 119 other tissues

Genevisible search portal to normalized and curated expression data from Genevestigator

More...
Genevisiblei
Q96IX5, HS

Organism-specific databases

Human Protein Atlas

More...
HPAi
ENSG00000173915, Low tissue specificity

<p>This section provides information on the quaternary structure of a protein and on interaction(s) with other proteins or protein complexes.<p><a href='/help/interaction_section' target='_top'>More...</a></p>Interactioni

<p>This subsection of the <a href="http://www.uniprot.org/help/interaction_section">'Interaction'</a> section provides information about the protein quaternary structure and interaction(s) with other proteins or protein complexes (with the exception of physiological receptor-ligand interactions which are annotated in the <a href="http://www.uniprot.org/help/function_section">'Function'</a> section).<p><a href='/help/subunit_structure' target='_top'>More...</a></p>Subunit structurei

Component of the ATP synthase complex/complex V which is composed of ATP5PB, ATP5MC1, ATP5F1E, ATP5PD, ATP5ME, ATP5PF, ATP5MF, MT-ATP6, MT-ATP8, ATP5F1A, ATP5F1B, ATP5F1D, ATP5F1C, ATP5PO, ATP5MG, ATP5MK and ATP5MJ (By similarity). The ATP synthase complex/complex V exists as a monomeric and a dimeric supercomplex that helps shape mitochondrial cristae to optimize proton flow (PubMed:29917077).

By similarity1 Publication

Protein-protein interaction databases

The Biological General Repository for Interaction Datasets (BioGRID)

More...
BioGRIDi
124287, 93 interactors

ComplexPortal: manually curated resource of macromolecular complexes

More...
ComplexPortali
CPX-6151, Mitochondrial proton-transporting ATP synthase complex

Protein interaction database and analysis system

More...
IntActi
Q96IX5, 62 interactors

Molecular INTeraction database

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MINTi
Q96IX5

STRING: functional protein association networks

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STRINGi
9606.ENSP00000358840

Miscellaneous databases

RNAct, Protein-RNA interaction predictions for model organisms.

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RNActi
Q96IX5, protein

<p>This section provides information on the tertiary and secondary structure of a protein.<p><a href='/help/structure_section' target='_top'>More...</a></p>Structurei

3D structure databases

SWISS-MODEL Repository - a database of annotated 3D protein structure models

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SMRi
Q96IX5

Database of comparative protein structure models

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ModBasei
Search...

<p>This section provides information on sequence similarities with other proteins and the domain(s) present in a protein.<p><a href='/help/family_and_domains_section' target='_top'>More...</a></p>Family & Domainsi

Keywords - Domaini

Transmembrane, Transmembrane helix

Phylogenomic databases

evolutionary genealogy of genes: Non-supervised Orthologous Groups

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eggNOGi
ENOG502S82X, Eukaryota

Ensembl GeneTree

More...
GeneTreei
ENSGT00390000015489

The HOGENOM Database of Homologous Genes from Fully Sequenced Organisms

More...
HOGENOMi
CLU_209345_1_0_1

InParanoid: Eukaryotic Ortholog Groups

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InParanoidi
Q96IX5

Identification of Orthologs from Complete Genome Data

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OMAi
RYFNSYT

Database of Orthologous Groups

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OrthoDBi
1629213at2759

Database for complete collections of gene phylogenies

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PhylomeDBi
Q96IX5

TreeFam database of animal gene trees

More...
TreeFami
TF324671

Family and domain databases

Integrated resource of protein families, domains and functional sites

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InterProi
View protein in InterPro
IPR009125, ATPMK

The PANTHER Classification System

More...
PANTHERi
PTHR34038, PTHR34038, 1 hit

Pfam protein domain database

More...
Pfami
View protein in Pfam
PF14960, ATP_synth_reg, 1 hit

Protein Motif fingerprint database; a protein domain database

More...
PRINTSi
PR01821, DAPIT

<p>This section displays by default the canonical protein sequence and upon request all isoforms described in the entry. It also includes information pertinent to the sequence(s), including <a href="http://www.uniprot.org/help/sequence_length">length</a> and <a href="http://www.uniprot.org/help/sequences">molecular weight</a>. The information is filed in different subsections. The current subsections and their content are listed below:<p><a href='/help/sequences_section' target='_top'>More...</a></p>Sequencei

<p>This subsection of the <a href="http://www.uniprot.org/help/sequences_section">Sequence</a> section indicates if the <a href="http://www.uniprot.org/help/canonical_and_isoforms">canonical sequence</a> displayed by default in the entry is complete or not.<p><a href='/help/sequence_status' target='_top'>More...</a></p>Sequence statusi: Complete.

<p>This subsection of the <a href="http://www.uniprot.org/help/sequences_section">Sequence</a> section indicates if the <a href="http://www.uniprot.org/help/canonical_and_isoforms">canonical sequence</a> displayed by default in the entry is in its mature form or if it represents the precursor.<p><a href='/help/sequence_processing' target='_top'>More...</a></p>Sequence processingi: The displayed sequence is further processed into a mature form.

Q96IX5-1 [UniParc]FASTAAdd to basket
« Hide
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MAGPESDAQY QFTGIKKYFN SYTLTGRMNC VLATYGSIAL IVLYFKLRSK

KTPAVKAT
Length:58
Mass (Da):6,458
Last modified:December 1, 2001 - v1
<p>The checksum is a form of redundancy check that is calculated from the sequence. It is useful for tracking sequence updates.</p> <p>It should be noted that while, in theory, two different sequences could have the same checksum value, the likelihood that this would happen is extremely low.</p> <p>However UniProtKB may contain entries with identical sequences in case of multiple genes (paralogs).</p> <p>The checksum is computed as the sequence 64-bit Cyclic Redundancy Check value (CRC64) using the generator polynomial: x<sup>64</sup> + x<sup>4</sup> + x<sup>3</sup> + x + 1. The algorithm is described in the ISO 3309 standard. </p> <p class="publication">Press W.H., Flannery B.P., Teukolsky S.A. and Vetterling W.T.<br /> <strong>Cyclic redundancy and other checksums</strong><br /> <a href="http://www.nrbook.com/b/bookcpdf.php">Numerical recipes in C 2nd ed., pp896-902, Cambridge University Press (1993)</a>)</p> Checksum:i3BFC4C9E2920B126
GO

Sequence databases

Select the link destinations:

EMBL nucleotide sequence database

More...
EMBLi

GenBank nucleotide sequence database

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GenBanki

DNA Data Bank of Japan; a nucleotide sequence database

More...
DDBJi
Links Updated
AY740522 mRNA Translation: AAU89079.1
AJ272056 mRNA Translation: CAC81243.1
AK311888 mRNA Translation: BAG34829.1
AL591408 Genomic DNA No translation available.
CH471066 Genomic DNA Translation: EAW49642.1
CH471066 Genomic DNA Translation: EAW49643.1
CH471066 Genomic DNA Translation: EAW49644.1
BC007087 mRNA Translation: AAH07087.1
BC072683 mRNA Translation: AAH72683.1
BC091507 mRNA Translation: AAH91507.1

The Consensus CDS (CCDS) project

More...
CCDSi
CCDS7548.1

NCBI Reference Sequences

More...
RefSeqi
NP_001193355.1, NM_001206426.1
NP_001193356.1, NM_001206427.1
NP_116136.1, NM_032747.3

Genome annotation databases

Ensembl eukaryotic genome annotation project

More...
Ensembli
ENST00000309579; ENSP00000311245; ENSG00000173915
ENST00000337003; ENSP00000337705; ENSG00000173915
ENST00000369811; ENSP00000358826; ENSG00000173915
ENST00000369815; ENSP00000358830; ENSG00000173915
ENST00000369825; ENSP00000358840; ENSG00000173915

Database of genes from NCBI RefSeq genomes

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GeneIDi
84833

KEGG: Kyoto Encyclopedia of Genes and Genomes

More...
KEGGi
hsa:84833

UCSC genome browser

More...
UCSCi
uc001kww.4, human

<p>This section provides links to proteins that are similar to the protein sequence(s) described in this entry at different levels of sequence identity thresholds (100%, 90% and 50%) based on their membership in UniProt Reference Clusters (<a href="http://www.uniprot.org/help/uniref">UniRef</a>).<p><a href='/help/similar_proteins_section' target='_top'>More...</a></p>Similar proteinsi

<p>This section is used to point to information related to entries and found in data collections other than UniProtKB.<p><a href='/help/cross_references_section' target='_top'>More...</a></p>Cross-referencesi

Sequence databases

Select the link destinations:
EMBLi
GenBanki
DDBJi
Links Updated
AY740522 mRNA Translation: AAU89079.1
AJ272056 mRNA Translation: CAC81243.1
AK311888 mRNA Translation: BAG34829.1
AL591408 Genomic DNA No translation available.
CH471066 Genomic DNA Translation: EAW49642.1
CH471066 Genomic DNA Translation: EAW49643.1
CH471066 Genomic DNA Translation: EAW49644.1
BC007087 mRNA Translation: AAH07087.1
BC072683 mRNA Translation: AAH72683.1
BC091507 mRNA Translation: AAH91507.1
CCDSiCCDS7548.1
RefSeqiNP_001193355.1, NM_001206426.1
NP_001193356.1, NM_001206427.1
NP_116136.1, NM_032747.3

3D structure databases

SMRiQ96IX5
ModBaseiSearch...

Protein-protein interaction databases

BioGRIDi124287, 93 interactors
ComplexPortaliCPX-6151, Mitochondrial proton-transporting ATP synthase complex
IntActiQ96IX5, 62 interactors
MINTiQ96IX5
STRINGi9606.ENSP00000358840

PTM databases

GlyGeniQ96IX5, 1 site, 1 O-linked glycan (1 site)
iPTMnetiQ96IX5
PhosphoSitePlusiQ96IX5
SwissPalmiQ96IX5

Genetic variation databases

BioMutaiUSMG5

Proteomic databases

EPDiQ96IX5
jPOSTiQ96IX5
MassIVEiQ96IX5
MaxQBiQ96IX5
PaxDbiQ96IX5
PeptideAtlasiQ96IX5
PRIDEiQ96IX5
ProteomicsDBi76865
TopDownProteomicsiQ96IX5

Protocols and materials databases

Antibodypedia a portal for validated antibodies

More...
Antibodypediai
46057, 75 antibodies

The DNASU plasmid repository

More...
DNASUi
84833

Genome annotation databases

EnsembliENST00000309579; ENSP00000311245; ENSG00000173915
ENST00000337003; ENSP00000337705; ENSG00000173915
ENST00000369811; ENSP00000358826; ENSG00000173915
ENST00000369815; ENSP00000358830; ENSG00000173915
ENST00000369825; ENSP00000358840; ENSG00000173915
GeneIDi84833
KEGGihsa:84833
UCSCiuc001kww.4, human

Organism-specific databases

Comparative Toxicogenomics Database

More...
CTDi
84833
DisGeNETi84833

GeneCards: human genes, protein and diseases

More...
GeneCardsi
ATP5MD
HGNCiHGNC:30889, ATP5MK
HPAiENSG00000173915, Low tissue specificity
MalaCardsiATP5MD
MIMi615204, gene
618683, phenotype
neXtProtiNX_Q96IX5
OpenTargetsiENSG00000173915
Orphaneti254913, Isolated ATP synthase deficiency
PharmGKBiPA134968209
VEuPathDBiHostDB:ENSG00000173915

GenAtlas: human gene database

More...
GenAtlasi
Search...

Phylogenomic databases

eggNOGiENOG502S82X, Eukaryota
GeneTreeiENSGT00390000015489
HOGENOMiCLU_209345_1_0_1
InParanoidiQ96IX5
OMAiRYFNSYT
OrthoDBi1629213at2759
PhylomeDBiQ96IX5
TreeFamiTF324671

Enzyme and pathway databases

PathwayCommonsiQ96IX5

Miscellaneous databases

BioGRID ORCS database of CRISPR phenotype screens

More...
BioGRID-ORCSi
84833, 12 hits in 880 CRISPR screens

ChiTaRS: a database of human, mouse and fruit fly chimeric transcripts and RNA-sequencing data

More...
ChiTaRSi
USMG5, human

Database of phenotypes from RNA interference screens in Drosophila and Homo sapiens

More...
GenomeRNAii
84833
PharosiQ96IX5, Tbio

Protein Ontology

More...
PROi
PR:Q96IX5
RNActiQ96IX5, protein

The Stanford Online Universal Resource for Clones and ESTs

More...
SOURCEi
Search...

Gene expression databases

BgeeiENSG00000173915, Expressed in caudate nucleus and 119 other tissues
GenevisibleiQ96IX5, HS

Family and domain databases

InterProiView protein in InterPro
IPR009125, ATPMK
PANTHERiPTHR34038, PTHR34038, 1 hit
PfamiView protein in Pfam
PF14960, ATP_synth_reg, 1 hit
PRINTSiPR01821, DAPIT

MobiDB: a database of protein disorder and mobility annotations

More...
MobiDBi
Search...

<p>This section provides general information on the entry.<p><a href='/help/entry_information_section' target='_top'>More...</a></p>Entry informationi

<p>This subsection of the 'Entry information' section provides a mnemonic identifier for a UniProtKB entry, but it is not a stable identifier. Each reviewed entry is assigned a unique entry name upon integration into UniProtKB/Swiss-Prot.<p><a href='/help/entry_name' target='_top'>More...</a></p>Entry nameiATPMK_HUMAN
<p>This subsection of the 'Entry information' section provides one or more accession number(s). These are stable identifiers and should be used to cite UniProtKB entries. Upon integration into UniProtKB, each entry is assigned a unique accession number, which is called 'Primary (citable) accession number'.<p><a href='/help/accession_numbers' target='_top'>More...</a></p>AccessioniPrimary (citable) accession number: Q96IX5
Secondary accession number(s): B2R4N2, D3DR92
<p>This subsection of the 'Entry information' section shows the date of integration of the entry into UniProtKB, the date of the last sequence update and the date of the last annotation modification ('Last modified'). The version number for both the entry and the <a href="http://www.uniprot.org/help/canonical_and_isoforms">canonical sequence</a> are also displayed.<p><a href='/help/entry_history' target='_top'>More...</a></p>Entry historyiIntegrated into UniProtKB/Swiss-Prot: April 4, 2006
Last sequence update: December 1, 2001
Last modified: September 29, 2021
This is version 149 of the entry and version 1 of the sequence. See complete history.
<p>This subsection of the 'Entry information' section indicates whether the entry has been manually annotated and reviewed by UniProtKB curators or not, in other words, if the entry belongs to the Swiss-Prot section of UniProtKB (<strong>reviewed</strong>) or to the computer-annotated TrEMBL section (<strong>unreviewed</strong>).<p><a href='/help/entry_status' target='_top'>More...</a></p>Entry statusiReviewed (UniProtKB/Swiss-Prot)
Annotation programChordata Protein Annotation Program
DisclaimerAny medical or genetic information present in this entry is provided for research, educational and informational purposes only. It is not in any way intended to be used as a substitute for professional medical advice, diagnosis, treatment or care.

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Keywords - Technical termi

Reference proteome

Documents

  1. Human chromosome 10
    Human chromosome 10: entries, gene names and cross-references to MIM
  2. MIM cross-references
    Online Mendelian Inheritance in Man (MIM) cross-references in UniProtKB/Swiss-Prot
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