12 GO Terms
Identifier | Name | Description |
---|---|---|
GO:0005524 | ATP binding | Interacting selectively and non-covalently with ATP, adenosine 5'-triphosphate, a universally important coenzyme and enzyme regulator. |
GO:0015991 | ATP hydrolysis coupled proton transport | The transport of protons against an electrochemical gradient, using energy from ATP hydrolysis. |
GO:0016820 | hydrolase activity, acting on acid anhydrides, catalyzing transmembrane movement of substances | Catalysis of the hydrolysis of an acid anhydride to directly drive the transport of a substance across a membrane. |
GO:0046961 | proton-transporting ATPase activity, rotational mechanism | Catalysis of the transfer of protons from one side of a membrane to the other according to the reaction: ATP + H2O + H+(in) = ADP + phosphate + H+(out), by a rotational mechanism. |
GO:0015078 | hydrogen ion transmembrane transporter activity | Enables the transfer of hydrogen ions from one side of a membrane to the other. |
GO:0015986 | ATP synthesis coupled proton transport | The transport of protons across a membrane to generate an electrochemical gradient (proton-motive force) that powers ATP synthesis. |
GO:0045261 | proton-transporting ATP synthase complex, catalytic core F(1) | The sector of a hydrogen-transporting ATP synthase complex in which the catalytic activity resides; it comprises the catalytic core and central stalk, and is peripherally associated with a membrane, such as the plasma membrane or the mitochondrial inner membrane, when the entire ATP synthase is assembled. |
GO:0046933 | proton-transporting ATP synthase activity, rotational mechanism | Catalysis of the transfer of protons from one side of a membrane to the other according to the reaction: ADP + H2O + phosphate + H+(in) = ATP + H+(out), by a rotational mechanism. |
GO:0015992 | proton transport | The directed movement of protons (hydrogen ions) into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore. |
GO:0046034 | ATP metabolic process | The chemical reactions and pathways involving ATP, adenosine triphosphate, a universally important coenzyme and enzyme regulator. |
GO:0033178 | proton-transporting two-sector ATPase complex, catalytic domain | A protein complex that forms part of a proton-transporting two-sector ATPase complex and catalyzes ATP hydrolysis or synthesis. The catalytic domain (F1, V1, or A1) comprises a hexameric catalytic core and a central stalk, and is peripherally associated with the membrane when the two-sector ATPase is assembled. |
GO:0045263 | proton-transporting ATP synthase complex, coupling factor F(o) | All non-F1 subunits of a hydrogen-transporting ATP synthase, including integral and peripheral membrane proteins. |
44 Blast
27 Domain Motifs
Analysis | Begin | End | Length | Domain Identifier | Cross Ref | Description | Inter Pro |
---|---|---|---|---|---|---|---|
Gene3D | 181 | 264 | 84 | G3DSA:2.40.30.20 | "KEGG:00190+3.6.3.14","KEGG:00195+3.6.3.14","MetaCyc:PWY-7219" | none | IPR023366 |
Phobius | 1 | 21 | 21 | SIGNAL_PEPTIDE | none | Signal peptide region | none |
Pfam | 198 | 263 | 66 | PF02874 | "KEGG:00190+3.6.3.14","KEGG:00195+3.6.3.14","MetaCyc:PWY-7219" | ATP synthase alpha/beta family, beta-barrel domain | IPR004100 |
Phobius | 4 | 14 | 11 | SIGNAL_PEPTIDE_H_REGION | none | Hydrophobic region of a signal peptide. | none |
Phobius | 1 | 3 | 3 | SIGNAL_PEPTIDE_N_REGION | none | N-terminal region of a signal peptide. | none |
Pfam | 26 | 149 | 124 | PF00430 | none | ATP synthase B/B' CF(0) | IPR002146 |
Coils | 59 | 94 | 36 | Coil | none | none | none |
SUPERFAMILY | 181 | 265 | 85 | SSF50615 | "KEGG:00190+3.6.3.14","KEGG:00195+3.6.3.14","MetaCyc:PWY-7219" | none | IPR004100 |
SUPERFAMILY | 560 | 688 | 129 | SSF47917 | "KEGG:00190+3.6.3.14","KEGG:00195+3.6.3.14","MetaCyc:PWY-7219" | none | IPR000793 |
PANTHER | 135 | 479 | 345 | PTHR15184 | none | none | none |
PANTHER | 498 | 693 | 196 | PTHR15184 | none | none | none |
PANTHER | 135 | 479 | 345 | PTHR15184:SF37 | none | none | none |
PANTHER | 498 | 693 | 196 | PTHR15184:SF37 | none | none | none |
SUPERFAMILY | 475 | 558 | 84 | SSF52540 | none | none | IPR027417 |
Phobius | 31 | 49 | 19 | TRANSMEMBRANE | none | Region of a membrane-bound protein predicted to be embedded in the membrane. | none |
Hamap | 172 | 689 | 518 | MF_01346 | "KEGG:00190+3.6.3.14","KEGG:00195+3.6.3.14","MetaCyc:PWY-7219" | ATP synthase subunit alpha [atpA]. | IPR005294 |
SUPERFAMILY | 267 | 477 | 211 | SSF52540 | none | none | IPR027417 |
Pfam | 319 | 552 | 234 | PF00006 | "KEGG:00190+3.6.3.14","KEGG:00195+3.6.3.14","MetaCyc:PWY-7219" | ATP synthase alpha/beta family, nucleotide-binding domain | IPR000194 |
Gene3D | 476 | 559 | 84 | G3DSA:3.40.50.300 | none | none | IPR027417 |
Gene3D | 266 | 475 | 210 | G3DSA:3.40.50.300 | none | none | IPR027417 |
Phobius | 15 | 21 | 7 | SIGNAL_PEPTIDE_C_REGION | none | C-terminal region of a signal peptide. | none |
Gene3D | 560 | 688 | 129 | G3DSA:1.20.150.20 | none | none | none |
Phobius | 22 | 30 | 9 | NON_CYTOPLASMIC_DOMAIN | none | Region of a membrane-bound protein predicted to be outside the membrane, in the extracellular region. | none |
TIGRFAM | 181 | 474 | 294 | TIGR00962 | "KEGG:00190+3.6.3.14","KEGG:00195+3.6.3.14","MetaCyc:PWY-7219" | atpA: ATP synthase F1, alpha subunit | IPR005294 |
ProSitePatterns | 543 | 552 | 10 | PS00152 | "KEGG:00190+3.6.3.14","KEGG:00195+3.6.3.14","MetaCyc:PWY-7219" | ATP synthase alpha and beta subunits signature. | IPR020003 |
Phobius | 50 | 694 | 645 | CYTOPLASMIC_DOMAIN | none | Region of a membrane-bound protein predicted to be outside the membrane, in the cytoplasm. | none |
Pfam | 564 | 651 | 88 | PF00306 | "KEGG:00190+3.6.3.14","KEGG:00195+3.6.3.14","MetaCyc:PWY-7219" | ATP synthase alpha/beta chain, C terminal domain | IPR000793 |
12 Qtllist
Qtl Name | Chromosome Name | Linkage Group | Prox Marker | Dist Marker | Position QTL | Pos One | Pos Two | Test Type | Test Value | R 2 |
---|---|---|---|---|---|---|---|---|---|---|
Bourran2_2014_nLBD*_A4 | Qrob_Chr08 | 8 | v_12498_318 | v_12364_308 | 34,91 | 16,12 | 53,62 | lod | 2,4961 | 5,2 |
Bourran2_2014_nPriLBD_3P | Qrob_Chr08 | 8 | v_5216_549 | v_11837_70 | 12,36 | 0 | 30,43 | lod | 2,5806 | 5,1 |
Bourran2_2014_nSecLBD_A4 | Qrob_Chr07 | 7 | v_8327_222 | s_1A4WGY_363 | 16,04 | 0 | 44,69 | lod | 2,6373 | 6,5 |
Bourran2_2014_nP_A4 | Qrob_Chr11 | 11 | s_1B58GB_1413 | s_1A5BYY_1671 | 11,15 | 0 | 42,38 | lod | 1,8913 | 4,5 |
Bourran2_2015_nSeqBC_3P | Qrob_Chr11 | 11 | s_1DG9PM_867 | s_1BZ083_1312 | 26,06 | 25,47 | 27,72 | lod | 3.6 | 7.1 |
Bourran2_2014_nP_3P | Qrob_Chr11 | 11 | v_11486_194 | s_1AT3E_2335 | 7,9 | 0,09 | 30,09 | lod | 2,3636 | 5 |
Bourran2_2015_nEpis_A4 | Qrob_Chr09 | 9 | v_15847_485 | v_8329_369 | 34,94 | 34,88 | 37,45 | lod | 3.1 | 7 |
Bourran2_2015_nEpiBC_A4 | Qrob_Chr07 | 7 | s_1DP9TW_798 | v_8128_173 | 22,61 | 22,14 | 22,73 | lod | 3.1 | 8.5 |
Bourran2_2014_nEpiBC_A4 | Qrob_Chr07 | 7 | s_2FI9D9_500 | s_1AXDMJ_325 | 12,26 | 0 | 34,9 | lod | 2,2306 | 6,1 |
Bourran2_2014_nPriBD_3P | Qrob_Chr11 | 11 | v_11486_194 | s_1AT3E_2335 | 5,54 | 0,4 | 20,6 | lod | 2,6345 | 5,9 |
Bourran2_2002_QTL10_peak_Bud_burst_3P | Qrob_Chr07 | 7 | s_1CAWP_311 | s_1BEZ9M_461 | 7,5 | 0 | 21,5 | lod | 3,7 | 6,3 |
Bourran2_2014_nPriBD*_A4 | Qrob_Chr07 | 7 | s_1A7UI0_596 | s_1A3H6S_352 | 8,02 | 0 | 20,53 | lod | 4,1062 | 10,8 |