P00846 · ATP6_HUMAN
- ProteinATP synthase subunit a
- GeneMT-ATP6
- StatusUniProtKB reviewed (Swiss-Prot)
- Organism
- Amino acids226 (go to sequence)
- Protein existenceEvidence at protein level
- Annotation score5/5
Function
function
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. Key component of the proton channel; it may play a direct role in the translocation of protons across the membrane.
GO annotations
all annotations | all molecular function | virus receptor activity | dna binding | rna binding | cytoskeletal motor activity | catalytic activity | gtpase activity | structural molecule activity | transporter activity | cytoskeletal protein binding | lipid binding | cyclase activity | antioxidant activity | oxidoreductase activity | transferase activity | hydrolase activity | lyase activity | isomerase activity | ligase activity | protein tag activity | cargo receptor activity | histone binding | protein folding chaperone | translation regulator activity | nutrient reservoir activity | receptor ligand activity | molecular transducer activity | molecular adaptor activity | toxin activity | cell adhesion mediator activity | molecular function regulator activity | virus coreceptor activity | catalytic activity, acting on a protein | catalytic activity, acting on dna | catalytic activity, acting on rna | molecular carrier activity | transcription regulator activity | general transcription initiation factor activity | molecular sensor activity | molecular sequestering activity | atp-dependent activity | other molecular function | all biological process | mitotic cell cycle | cytokinesis | cytoplasmic translation | immune system process | muscle system process | circulatory system process | renal system process | respiratory system process | carbohydrate metabolic process | generation of precursor metabolites and energy | dna replication | dna repair | dna recombination | chromatin organization | dna-templated transcription | regulation of dna-templated transcription | trna metabolic process | protein folding | protein glycosylation | amino acid metabolic process | modified amino acid metabolic process | lipid metabolic process | vitamin metabolic process | sulfur compound metabolic process | intracellular protein transport | nucleocytoplasmic transport | autophagy | inflammatory response | mitochondrion organization | cytoskeleton organization | microtubule-based movement | peroxisome organization | lysosome organization | chromosome segregation | cell adhesion | establishment or maintenance of cell polarity | programmed cell death | photosynthesis | mrna metabolic process | snrna metabolic process | vesicle-mediated transport | reproductive process | digestive system process | signaling | cell differentiation | protein catabolic process | extracellular matrix organization | regulatory ncrna-mediated gene silencing | telomere organization | cell junction organization | wound healing | ribosome biogenesis | cilium organization | anatomical structure development | cell motility | nervous system process | endocrine process | protein maturation | transmembrane transport | nucleobase-containing small molecule metabolic process | hepaticobiliary system process | membrane organization | protein-containing complex assembly | cell wall organization or biogenesis | nitrogen cycle metabolic process | protein localization to plasma membrane | defense response to other organism | detoxification | meiotic nuclear division | mitotic nuclear division | mitochondrial gene expression | carbohydrate derivative metabolic process | other biological process | all cellular component | nuclear chromosome | extracellular region | extracellular space | cell wall | nucleus | nuclear envelope | nucleoplasm | chromosome | nucleolus | mitochondrion | lysosome | endosome | vacuole | peroxisome | endoplasmic reticulum | golgi apparatus | lipid droplet | microtubule organizing center | cytosol | ribosome | cytoskeleton | plasma membrane | cilium | plastid | thylakoid | external encapsulating structure | extracellular matrix | cytoplasmic vesicle | organelle | other cellular component | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Aspect | Term | |
---|---|---|
Cellular Component | mitochondrial inner membrane | |
Cellular Component | mitochondrial proton-transporting ATP synthase complex | |
Cellular Component | mitochondrion | |
Cellular Component | proton-transporting ATP synthase complex | |
Cellular Component | proton-transporting ATP synthase complex, coupling factor F(o) | |
Molecular Function | proton transmembrane transporter activity | |
Biological Process | proton motive force-driven ATP synthesis | |
Biological Process | proton motive force-driven mitochondrial ATP synthesis | |
Biological Process | response to hyperoxia |
Keywords
- Biological process
Enzyme and pathway databases
Protein family/group databases
Names & Taxonomy
Protein names
- Recommended nameATP synthase subunit a
- Alternative names
Gene names
Encoded on
- Mitochondrion
Organism names
- Organism
- Taxonomic lineageEukaryota > Metazoa > Chordata > Craniata > Vertebrata > Euteleostomi > Mammalia > Eutheria > Euarchontoglires > Primates > Haplorrhini > Catarrhini > Hominidae > Homo
Accessions
- Primary accessionP00846
- Secondary accessions
Proteomes
Organism-specific databases
Subcellular Location
UniProt Annotation
GO Annotation
Mitochondrion inner membrane ; Multi-pass membrane protein
Features
Showing features for transmembrane.
Type | ID | Position(s) | Description | |||
---|---|---|---|---|---|---|
Transmembrane | 6-26 | Helical | ||||
Sequence: FASFIAPTILGLPAAVLIILF | ||||||
Transmembrane | 68-88 | Helical | ||||
Sequence: WSLMLVSLIIFIATTNLLGLL | ||||||
Transmembrane | 97-117 | Helical | ||||
Sequence: QLSMNLAMAIPLWAGTVIMGF | ||||||
Transmembrane | 138-158 | Helical | ||||
Sequence: IPMLVIIETISLLIQPMALAV | ||||||
Transmembrane | 164-184 | Helical | ||||
Sequence: ITAGHLLMHLIGSATLAMSTI | ||||||
Transmembrane | 189-209 | Helical | ||||
Sequence: TLIIFTILILLTILEIAVALI |
Keywords
- Cellular component
Disease & Variants
Involvement in disease
Neuropathy, ataxia, and retinitis pigmentosa (NARP)
- Note
- DescriptionA syndrome characterized by variable combination of developmental delay, psychomotor retardation, hearing loss, optic atrophy and retinitis pigmentosa, dementia, seizures, ataxia, proximal neurogenic muscle weakness, and sensory neuropathy.
- See alsoMIM:551500
Natural variants in NARP
Variant ID | Position(s) | Change | Description | |
---|---|---|---|---|
VAR_000793 | 156 | L>R | in NARP and LS; dbSNP:rs199476133 |
Leber hereditary optic neuropathy (LHON)
- Note
- DescriptionA maternally inherited form of Leber hereditary optic neuropathy, a mitochondrial disease resulting in bilateral painless loss of central vision due to selective degeneration of the retinal ganglion cells and their axons. The disorder shows incomplete penetrance and male predominance. Cardiac conduction defects and neurological defects have also been described in some LHON patients. LHON results from primary mitochondrial DNA mutations affecting the respiratory chain complexes.
- See alsoMIM:535000
Natural variants in LHON
Variant ID | Position(s) | Change | Description | |
---|---|---|---|---|
VAR_000795 | 192 | I>T | in LHON; possible rate primary mutation; dbSNP:rs199476134 |
Leigh syndrome (LS)
- Note
- DescriptionAn early-onset progressive neurodegenerative disorder characterized by the presence of focal, bilateral lesions in one or more areas of the central nervous system including the brainstem, thalamus, basal ganglia, cerebellum and spinal cord. Clinical features depend on which areas of the central nervous system are involved and include subacute onset of psychomotor retardation, hypotonia, ataxia, weakness, vision loss, eye movement abnormalities, seizures, and dysphagia.
- See alsoMIM:256000
Natural variants in LS
Variant ID | Position(s) | Change | Description | |
---|---|---|---|---|
VAR_000794 | 156 | L>P | in LS, MC5DM1 and APAO; dbSNP:rs199476133 | |
VAR_000793 | 156 | L>R | in NARP and LS; dbSNP:rs199476133 | |
VAR_000797 | 217 | L>P | in LS and MIBSN; dbSNP:rs199476135 | |
VAR_073700 | 220 | L>P | in LS; dbSNP:rs199476138 |
Mitochondrial infantile bilateral striatal necrosis (MIBSN)
- Note
- DescriptionBilateral striatal necrosis is a neurological disorder resembling Leigh syndrome.
- See alsoMIM:500003
Natural variants in MIBSN
Variant ID | Position(s) | Change | Description | |
---|---|---|---|---|
VAR_000797 | 217 | L>P | in LS and MIBSN; dbSNP:rs199476135 |
Mitochondrial complex V deficiency, mitochondrial 1 (MC5DM1)
- Note
- DescriptionA mitochondrial disorder with heterogeneous clinical manifestations including neuropathy, ataxia, hypertrophic cardiomyopathy. Hypertrophic cardiomyopathy can present with negligible to extreme hypertrophy, minimal to extensive fibrosis and myocyte disarray, absent to severe left ventricular outflow tract obstruction, and distinct septal contours/morphologies with extremely varying clinical course.
- See alsoMIM:500015
Natural variants in MC5DM1
Variant ID | Position(s) | Change | Description | |
---|---|---|---|---|
VAR_000794 | 156 | L>P | in LS, MC5DM1 and APAO; dbSNP:rs199476133 |
Myopathy, lactic acidosis, and sideroblastic anemia 3 (MLASA3)
- Note
- DescriptionA rare mitochondrial disorder characterized by sideroblastic anemia, muscle weakness, and exercise intolerance associated with persistent lactic acidemia. Additional MLASA3 features are failure to thrive, hearing loss, epilepsy, stroke-like episodes, and severe developmental delay.
- See alsoMIM:500011
Natural variants in MLASA3
Variant ID | Position(s) | Change | Description | |
---|---|---|---|---|
VAR_073699 | 148 | S>N | in MLASA3; dbSNP:rs794726857 |
Ataxia and polyneuropathy, adult-onset (APAO)
- Note
- DescriptionA mitochondrial disease characterized by ataxia, axonal sensorimotor polyneuropathy, abnormal eye movements, and dysarthria.
- See alsoMIM:500010
Natural variants in APAO
Variant ID | Position(s) | Change | Description | |
---|---|---|---|---|
VAR_000794 | 156 | L>P | in LS, MC5DM1 and APAO; dbSNP:rs199476133 |
Cardiomyopathy, infantile hypertrophic (CMHI)
- Note
- DescriptionAn infantile form of hypertrophic cardiomyopathy, a heart disorder characterized by ventricular hypertrophy, which is usually asymmetric and often involves the interventricular septum. The symptoms include dyspnea, syncope, collapse, palpitations, and chest pain. They can be readily provoked by exercise. The disorder has inter- and intrafamilial variability ranging from benign to malignant forms with high risk of cardiac failure and sudden cardiac death.
- See alsoMIM:500006
Features
Showing features for natural variant.
Type | ID | Position(s) | Description | |||
---|---|---|---|---|---|---|
Natural variant | VAR_021178 | 7 | in dbSNP:rs1603221578 | |||
Sequence: A → T | ||||||
Natural variant | VAR_021179 | 11 | in dbSNP:rs386829040 | |||
Sequence: A → T | ||||||
Natural variant | VAR_021180 | 14 | in dbSNP:rs3020563 | |||
Sequence: I → V | ||||||
Natural variant | VAR_021181 | 16 | in dbSNP:rs28502681 | |||
Sequence: G → S | ||||||
Natural variant | VAR_008556 | 33 | in dbSNP:rs1603221645 | |||
Sequence: T → S | ||||||
Natural variant | VAR_021182 | 37 | in dbSNP:rs2124594840 | |||
Sequence: L → P | ||||||
Natural variant | VAR_021183 | 53 | in dbSNP:rs201336180 | |||
Sequence: T → I | ||||||
Natural variant | VAR_000792 | 59 | in dbSNP:rs2000975 | |||
Sequence: T → A | ||||||
Natural variant | VAR_021184 | 60 | in dbSNP:rs878959404 | |||
Sequence: M → T | ||||||
Natural variant | VAR_008557 | 61 | ||||
Sequence: H → Y | ||||||
Natural variant | VAR_021185 | 80 | in dbSNP:rs1556423534 | |||
Sequence: A → T | ||||||
Natural variant | VAR_008558 | 90 | in dbSNP:rs2298007 | |||
Sequence: H → Y | ||||||
Natural variant | VAR_008559 | 112 | in dbSNP:rs2001031 | |||
Sequence: T → A | ||||||
Natural variant | VAR_021186 | 117 | in dbSNP:rs201123510 | |||
Sequence: F → L | ||||||
Natural variant | VAR_021187 | 121 | in dbSNP:rs1556423565 | |||
Sequence: I → V | ||||||
Natural variant | VAR_021188 | 133 | in dbSNP:rs200329150 | |||
Sequence: T → A | ||||||
Natural variant | VAR_073699 | 148 | in MLASA3; dbSNP:rs794726857 | |||
Sequence: S → N | ||||||
Natural variant | VAR_008560 | 155 | in dbSNP:rs587776444 | |||
Sequence: A → T | ||||||
Natural variant | VAR_000794 | 156 | in LS, MC5DM1 and APAO; dbSNP:rs199476133 | |||
Sequence: L → P | ||||||
Natural variant | VAR_000793 | 156 | in NARP and LS; dbSNP:rs199476133 | |||
Sequence: L → R | ||||||
Natural variant | VAR_008561 | 177 | in dbSNP:rs193303045 | |||
Sequence: A → T | ||||||
Natural variant | VAR_021189 | 178 | in dbSNP:rs1556423599 | |||
Sequence: T → A | ||||||
Natural variant | VAR_021190 | 182 | in dbSNP:rs1603222032 | |||
Sequence: S → L | ||||||
Natural variant | VAR_000795 | 192 | in LHON; possible rate primary mutation; dbSNP:rs199476134 | |||
Sequence: I → T | ||||||
Natural variant | VAR_021191 | 192 | in dbSNP:rs1603222068 | |||
Sequence: I → V | ||||||
Natural variant | VAR_021192 | 193 | in dbSNP:rs1603222077 | |||
Sequence: F → L | ||||||
Natural variant | VAR_021193 | 204 | in dbSNP:rs1603222121 | |||
Sequence: I → T | ||||||
Natural variant | VAR_000796 | 213 | in dbSNP:rs2298010 | |||
Sequence: V → I | ||||||
Natural variant | VAR_000797 | 217 | in LS and MIBSN; dbSNP:rs199476135 | |||
Sequence: L → P | ||||||
Natural variant | VAR_008562 | 219 | in dbSNP:rs1556423628 | |||
Sequence: S → G | ||||||
Natural variant | VAR_073700 | 220 | in LS; dbSNP:rs199476138 | |||
Sequence: L → P |
Variants
We now provide the "Disease & Variants" viewer in its own tab.
The viewer provides 360 variants from UniProt as well as other sources including ClinVar and dbSNP.
Keywords
- Disease
Organism-specific databases
Miscellaneous
Chemistry
Genetic variation databases
PTM/Processing
Features
Showing features for chain.
Type | ID | Position(s) | Description | |||
---|---|---|---|---|---|---|
Chain | PRO_0000082128 | 1-226 | ATP synthase subunit a | |||
Sequence: MNENLFASFIAPTILGLPAAVLIILFPPLLIPTSKYLINNRLITTQQWLIKLTSKQMMTMHNTKGRTWSLMLVSLIIFIATTNLLGLLPHSFTPTTQLSMNLAMAIPLWAGTVIMGFRSKIKNALAHFLPQGTPTPLIPMLVIIETISLLIQPMALAVRLTANITAGHLLMHLIGSATLAMSTINLPSTLIIFTILILLTILEIAVALIQAYVFTLLVSLYLHDNT |
Proteomic databases
PTM databases
Expression
Interaction
Subunit
F-type ATPases have 2 components, CF1 - the catalytic core - and CF0 - the membrane proton channel. CF1 has five subunits: alpha3, beta3, gamma1, delta1, epsilon1. CF0 has three main subunits: a, b and c. Component of an ATP synthase complex composed of ATP5PB, ATP5MC1, ATP5F1E, ATP5PD, ATP5ME, ATP5PF, ATP5MF, MT-ATP6, MT-ATP8, ATP5F1A, ATP5F1B, ATP5F1D, ATP5F1C, ATP5PO, ATP5MG, ATP5MK and ATP5MJ (By similarity).
Interacts with DNAJC30; interaction is direct (PubMed:30318146).
Interacts with DNAJC30; interaction is direct (PubMed:30318146).
Protein-protein interaction databases
Miscellaneous
Structure
Sequence
- Sequence statusComplete
- Length226
- Mass (Da)24,817
- Last updated1986-07-21 v1
- Checksum7DB0F0BE86F55207
Keywords
- Technical term
Sequence databases
Nucleotide Sequence | Protein Sequence | Molecule Type | Status | |
---|---|---|---|---|
J01415 EMBL· GenBank· DDBJ | AAB58948.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
V00662 EMBL· GenBank· DDBJ | CAA24031.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
D38112 EMBL· GenBank· DDBJ | BAA07295.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AF346971 EMBL· GenBank· DDBJ | AAK17316.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AF347011 EMBL· GenBank· DDBJ | AAK17836.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AF381997 EMBL· GenBank· DDBJ | AAL54597.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AF382010 EMBL· GenBank· DDBJ | AAL54766.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AF465948 EMBL· GenBank· DDBJ | AAN14618.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AF465949 EMBL· GenBank· DDBJ | AAN14629.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AF465950 EMBL· GenBank· DDBJ | AAN14640.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AF465956 EMBL· GenBank· DDBJ | AAN14706.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AF465957 EMBL· GenBank· DDBJ | AAN14717.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AF465962 EMBL· GenBank· DDBJ | AAN14772.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AF465972 EMBL· GenBank· DDBJ | AAN14882.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AF465974 EMBL· GenBank· DDBJ | AAN14904.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AF465975 EMBL· GenBank· DDBJ | AAN14915.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AF465976 EMBL· GenBank· DDBJ | AAN14926.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY275529 EMBL· GenBank· DDBJ | AAQ19361.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY289076 EMBL· GenBank· DDBJ | AAP48210.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY289100 EMBL· GenBank· DDBJ | AAP48521.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY339407 EMBL· GenBank· DDBJ | AAP89106.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY339408 EMBL· GenBank· DDBJ | AAP89119.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY339510 EMBL· GenBank· DDBJ | AAP90445.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY339511 EMBL· GenBank· DDBJ | AAP90458.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY339512 EMBL· GenBank· DDBJ | AAP90471.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY339513 EMBL· GenBank· DDBJ | AAP90484.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY339530 EMBL· GenBank· DDBJ | AAP90705.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY339531 EMBL· GenBank· DDBJ | AAP90718.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY339532 EMBL· GenBank· DDBJ | AAP90731.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY339533 EMBL· GenBank· DDBJ | AAP90744.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY339534 EMBL· GenBank· DDBJ | AAP90757.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY339535 EMBL· GenBank· DDBJ | AAP90770.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY339536 EMBL· GenBank· DDBJ | AAP90783.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY339537 EMBL· GenBank· DDBJ | AAP90796.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY339538 EMBL· GenBank· DDBJ | AAP90809.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY339539 EMBL· GenBank· DDBJ | AAP90822.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY339540 EMBL· GenBank· DDBJ | AAP90835.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY339541 EMBL· GenBank· DDBJ | AAP90848.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY339543 EMBL· GenBank· DDBJ | AAP90874.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY339581 EMBL· GenBank· DDBJ | AAP91368.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY339582 EMBL· GenBank· DDBJ | AAP91381.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY339584 EMBL· GenBank· DDBJ | AAP91407.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY195749 EMBL· GenBank· DDBJ | AAO88337.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY195764 EMBL· GenBank· DDBJ | AAO88532.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY195773 EMBL· GenBank· DDBJ | AAO88649.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY195786 EMBL· GenBank· DDBJ | AAO88818.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY255144 EMBL· GenBank· DDBJ | AAO66766.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY255147 EMBL· GenBank· DDBJ | AAO66805.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY255180 EMBL· GenBank· DDBJ | AAO67233.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY738945 EMBL· GenBank· DDBJ | AAU13022.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY738967 EMBL· GenBank· DDBJ | AAU13308.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY713988 EMBL· GenBank· DDBJ | AAU02285.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY713999 EMBL· GenBank· DDBJ | AAU02428.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY714004 EMBL· GenBank· DDBJ | AAU02493.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY714013 EMBL· GenBank· DDBJ | AAU02610.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY714014 EMBL· GenBank· DDBJ | AAU02623.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY714028 EMBL· GenBank· DDBJ | AAU02805.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY714031 EMBL· GenBank· DDBJ | AAU02844.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY714035 EMBL· GenBank· DDBJ | AAU02896.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY714045 EMBL· GenBank· DDBJ | AAU03026.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY495147 EMBL· GenBank· DDBJ | AAR93242.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY495199 EMBL· GenBank· DDBJ | AAR93918.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY495231 EMBL· GenBank· DDBJ | AAR94334.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY495232 EMBL· GenBank· DDBJ | AAR94347.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY495233 EMBL· GenBank· DDBJ | AAR94360.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY495234 EMBL· GenBank· DDBJ | AAR94373.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY495235 EMBL· GenBank· DDBJ | AAR94386.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY495236 EMBL· GenBank· DDBJ | AAR94399.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY495237 EMBL· GenBank· DDBJ | AAR94412.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY495238 EMBL· GenBank· DDBJ | AAR94425.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY519488 EMBL· GenBank· DDBJ | AAR91263.1 EMBL· GenBank· DDBJ | Genomic DNA |