3 GO Terms
Identifier | Name | Description |
---|---|---|
GO:0005975 | carbohydrate metabolic process | The chemical reactions and pathways involving carbohydrates, any of a group of organic compounds based of the general formula Cx(H2O)y. Includes the formation of carbohydrate derivatives by the addition of a carbohydrate residue to another molecule. |
GO:0000272 | polysaccharide catabolic process | The chemical reactions and pathways resulting in the breakdown of a polysaccharide, a polymer of many (typically more than 10) monosaccharide residues linked glycosidically. |
GO:0016161 | beta-amylase activity | Catalysis of the reaction: (1,4-alpha-D-glucosyl)(n+1) + H2O = (1,4-alpha-D-glucosyl)(n-1) + alpha-maltose. This reaction is the hydrolysis of 1,4-alpha-glucosidic linkages in polysaccharides so as to remove successive maltose units from the non-reducing ends of the chains. |
37 Blast
Analysis | Hit | Start | End | Strand | Length | Note | Hit Coverage | Hit Length | Hit Pident | E Val | Hit Description |
---|---|---|---|---|---|---|---|---|---|---|---|
blastp_kegg | lcl|mdm:103405347 | 1 | 580 | + | 580 | Gaps:9 | 100.00 | 571 | 81.44 | 0.0 | beta-amylase 1 chloroplastic |
blastp_kegg | lcl|cmo:103483532 | 1 | 579 | + | 579 | Gaps:3 | 99.83 | 577 | 81.60 | 0.0 | beta-amylase 1 chloroplastic-like |
blastp_kegg | lcl|csv:101221739 | 1 | 580 | + | 580 | Gaps:3 | 100.00 | 577 | 81.46 | 0.0 | beta-amylase 1 chloroplastic-like |
blastp_kegg | lcl|fve:101312918 | 1 | 580 | + | 580 | Gaps:4 | 100.00 | 578 | 80.45 | 0.0 | beta-amylase 1 chloroplastic-like |
blastp_kegg | lcl|mdm:103453523 | 1 | 580 | + | 580 | Gaps:9 | 100.00 | 571 | 81.26 | 0.0 | beta-amylase 1 chloroplastic-like |
blastp_kegg | lcl|pxb:103941625 | 1 | 579 | + | 579 | Gaps:19 | 99.82 | 571 | 81.05 | 0.0 | beta-amylase 1 chloroplastic |
blastp_kegg | lcl|pmum:103323813 | 1 | 580 | + | 580 | Gaps:11 | 100.00 | 569 | 82.43 | 0.0 | beta-amylase 1 chloroplastic |
blastp_kegg | lcl|rcu:RCOM_1023980 | 1 | 579 | + | 579 | Gaps:6 | 99.83 | 574 | 80.80 | 0.0 | Beta-amylase putative (EC:3.2.1.2) |
blastp_kegg | lcl|cam:101508440 | 1 | 574 | + | 574 | Gaps:6 | 99.13 | 573 | 80.63 | 0.0 | beta-amylase 1 chloroplastic-like |
blastp_kegg | lcl|pop:POPTR_0010s07340g | 1 | 579 | + | 579 | Gaps:12 | 99.83 | 586 | 77.61 | 0.0 | POPTRDRAFT_229995 hypothetical protein |
blastp_pdb | 1b1y_A | 109 | 543 | + | 435 | Gaps:7 | 86.80 | 500 | 53.00 | 7e-154 | mol:protein length:500 PROTEIN (BETA-AMYLASE) |
blastp_pdb | 2xgi_A | 109 | 543 | + | 435 | Gaps:7 | 81.12 | 535 | 52.30 | 2e-151 | mol:protein length:535 BETA-AMYLASE |
blastp_pdb | 2xgb_A | 109 | 543 | + | 435 | Gaps:7 | 81.12 | 535 | 52.30 | 2e-151 | mol:protein length:535 BETA-AMYLASE |
blastp_pdb | 2xg9_A | 109 | 543 | + | 435 | Gaps:7 | 81.12 | 535 | 52.30 | 2e-151 | mol:protein length:535 BETA-AMYLASE |
blastp_pdb | 2xfy_A | 109 | 543 | + | 435 | Gaps:7 | 81.12 | 535 | 52.30 | 2e-151 | mol:protein length:535 BETA-AMYLASE |
blastp_pdb | 2xfr_A | 109 | 543 | + | 435 | Gaps:7 | 81.12 | 535 | 52.30 | 2e-151 | mol:protein length:535 BETA-AMYLASE |
blastp_pdb | 2xff_A | 109 | 543 | + | 435 | Gaps:7 | 81.12 | 535 | 52.30 | 2e-151 | mol:protein length:535 BETA-AMYLASE |
blastp_pdb | 1wdp_A | 113 | 543 | + | 431 | Gaps:7 | 86.87 | 495 | 50.00 | 4e-149 | mol:protein length:495 Beta-amylase |
blastp_pdb | 1q6c_A | 113 | 543 | + | 431 | Gaps:7 | 86.87 | 495 | 50.00 | 4e-149 | mol:protein length:495 beta-amylase |
blastp_pdb | 1bfn_A | 113 | 543 | + | 431 | Gaps:7 | 86.87 | 495 | 50.00 | 4e-149 | mol:protein length:495 BETA-AMYLASE |
blastp_uniprot_sprot | sp|Q9LIR6|BAM1_ARATH | 1 | 578 | + | 578 | Gaps:17 | 99.65 | 575 | 77.14 | 0.0 | Beta-amylase 1 chloroplastic OS Arabidopsis thaliana GN BAM1 PE 1 SV 1 |
blastp_uniprot_sprot | sp|O23553|BAM3_ARATH | 106 | 546 | + | 441 | Gaps:6 | 79.38 | 548 | 65.06 | 0.0 | Beta-amylase 3 chloroplastic OS Arabidopsis thaliana GN BAM3 PE 1 SV 3 |
blastp_uniprot_sprot | sp|O22585|AMYB_MEDSA | 113 | 543 | + | 431 | Gaps:9 | 86.69 | 496 | 51.86 | 6e-153 | Beta-amylase OS Medicago sativa GN BMY1 PE 1 SV 1 |
blastp_uniprot_sprot | sp|P82993|AMYB_HORVS | 109 | 543 | + | 435 | Gaps:7 | 81.12 | 535 | 52.30 | 1e-150 | Beta-amylase OS Hordeum vulgare subsp. spontaneum GN BMY1 PE 1 SV 1 |
blastp_uniprot_sprot | sp|P16098|AMYB_HORVU | 109 | 543 | + | 435 | Gaps:7 | 81.12 | 535 | 52.30 | 5e-150 | Beta-amylase OS Hordeum vulgare GN BMY1 PE 1 SV 1 |
blastp_uniprot_sprot | sp|P10538|AMYB_SOYBN | 113 | 543 | + | 431 | Gaps:7 | 86.69 | 496 | 49.53 | 7e-147 | Beta-amylase OS Glycine max GN BMY1 PE 1 SV 3 |
blastp_uniprot_sprot | sp|P10537|AMYB_IPOBA | 110 | 543 | + | 434 | Gaps:10 | 86.97 | 499 | 50.69 | 1e-146 | Beta-amylase OS Ipomoea batatas GN BMY1 PE 1 SV 4 |
blastp_uniprot_sprot | sp|O65015|AMYB_TRIRP | 113 | 543 | + | 431 | Gaps:9 | 86.69 | 496 | 50.47 | 2e-146 | Beta-amylase OS Trifolium repens GN BMY1 PE 2 SV 1 |
blastp_uniprot_sprot | sp|O65258|BAM2_ARATH | 113 | 543 | + | 431 | Gaps:11 | 78.97 | 542 | 51.64 | 3e-146 | Beta-amylase 2 chloroplastic OS Arabidopsis thaliana GN BAM2 PE 1 SV 2 |
blastp_uniprot_sprot | sp|O64407|AMYB_VIGUN | 113 | 543 | + | 431 | Gaps:9 | 86.69 | 496 | 50.00 | 7e-146 | Beta-amylase OS Vigna unguiculata GN BMY1 PE 2 SV 1 |
21 Domain Motifs
16 Qtllist
Qtl Name | Chromosome Name | Linkage Group | Prox Marker | Dist Marker | Position QTL | Pos One | Pos Two | Test Type | Test Value | R 2 |
---|---|---|---|---|---|---|---|---|---|---|
Champenoux_2015_nPriLBD_3P | Qrob_Chr10 | 10 | v_15000_157 | v_15000_310 | 15,68 | 15,9 | 15,91 | lod | 2.4 | 5.5 |
Bourran2_2014_nSecLBD_3P | Qrob_Chr08 | 8 | s_1BN2OD_551 | s_1B5AYF_599 | 17,17 | 0 | 43,51 | lod | 1,9229 | 4,4 |
Bourran2_2014_nLBD*_3P | Qrob_Chr08 | 8 | v_5216_549 | v_11837_70 | 12,25 | 0 | 35,55 | lod | 2,5951 | 6 |
Bourran2_2014_nP*_3P | Qrob_Chr08 | 8 | v_5216_549 | v_11837_70 | 12,19 | 0 | 31,97 | lod | 2,8472 | 6 |
Bourran2_2002_QTL11_peak_Bud_burst_A4 | Qrob_Chr06 | 6 | s_1C41PA_791 | s_1AM1AV_1141 | 19,17 | 0 | 34,57 | lod | 2,3 | 2,9 |
Bourran2_2014_aSeqBC_3P | Qrob_Chr06 | 6 | v_506_189 | v_686_77 | 30,72 | 13,58 | 43,48 | lod | 2,2746 | 6,3 |
Bourran2_2014_aSeqBC*_A4 | Qrob_Chr06 | 6 | s_2F5MK3_712 | v_444_355 | 27,13 | 14,86 | 39,46 | lod | 3,7847 | 9,8 |
Bourran2_2014_nEpis*_3P | Qrob_Chr08 | 8 | s_1DA4QW_688 | s_1DNI7D_820 | 17,96 | 0 | 37,75 | lod | 2,9745 | 7,5 |
Bourran2_2014_nEpis*_A4 | Qrob_Chr07 | 7 | v_12400_446 | s_1BPEBU_1211 | 6,93 | 0 | 15,13 | lod | 4,7411 | 11 |
Bourran2_2014_nFork*_3P | Qrob_Chr06 | 6 | v_12930_125 | s_1AMZEI_909 | 34,28 | 7,43 | 41,48 | lod | 2,4044 | 5,5 |
Bourran2_2014_nLBD_A4 | Qrob_Chr06 | 6 | v_12930_125 | s_1AMZEI_909 | 37,41 | 9,8 | 50,1 | lod | 1,9524 | 4,1 |
Bourran2_2014_nPriBD_A4 | Qrob_Chr06 | 6 | v_12930_125 | s_1AMZEI_909 | 34,51 | 3,36 | 51,86 | lod | 1,6747 | 3,9 |
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_vEpiBC_A4 | Qrob_Chr06 | 6 | v_12930_125 | s_1AMZEI_909 | 37,55 | 14,41 | 50,01 | lod | 1,7882 | 4,8 |
Champenoux_2015_nEpis_3P | Qrob_Chr11 | 11 | s_1DG9PM_867 | s_1BZ083_1312 | 26,53 | 25,47 | 27,72 | lod | 4.4 | 8.9 |
Champenoux_2015_nP_3P | Qrob_Chr06 | 6 | s_1A386O_228 | s_1AYZFS_603 | 27,03 | 26,47 | 27,34 | lod | 2.8 | 7.2 |