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. |
30 Blast
Analysis | Hit | Start | End | Strand | Length | Note | Hit Coverage | Hit Length | Hit Pident | E Val | Hit Description |
---|---|---|---|---|---|---|---|---|---|---|---|
blastp_kegg | lcl|mdm:103432207 | 1 | 71 | + | 71 | none | 22.61 | 314 | 71.83 | 2e-22 | beta-amylase 1 chloroplastic-like |
blastp_kegg | lcl|pmum:103323813 | 1 | 71 | + | 71 | none | 12.48 | 569 | 71.83 | 9e-22 | beta-amylase 1 chloroplastic |
blastp_kegg | lcl|mdm:103405347 | 1 | 71 | + | 71 | none | 12.43 | 571 | 71.83 | 1e-21 | beta-amylase 1 chloroplastic |
blastp_kegg | lcl|pper:PRUPE_ppa005431mg | 1 | 71 | + | 71 | none | 15.40 | 461 | 71.83 | 1e-21 | hypothetical protein |
blastp_kegg | lcl|csv:101221739 | 1 | 71 | + | 71 | none | 12.31 | 577 | 73.24 | 9e-21 | beta-amylase 1 chloroplastic-like |
blastp_kegg | lcl|fve:101312918 | 1 | 71 | + | 71 | none | 12.28 | 578 | 71.83 | 9e-21 | beta-amylase 1 chloroplastic-like |
blastp_kegg | lcl|pxb:103941625 | 1 | 71 | + | 71 | none | 12.43 | 571 | 70.42 | 1e-20 | beta-amylase 1 chloroplastic |
blastp_kegg | lcl|mdm:103453523 | 1 | 71 | + | 71 | none | 12.43 | 571 | 70.42 | 1e-20 | beta-amylase 1 chloroplastic-like |
blastp_kegg | lcl|cmo:103483532 | 1 | 71 | + | 71 | none | 12.31 | 577 | 73.24 | 1e-20 | beta-amylase 1 chloroplastic-like |
blastp_kegg | lcl|rcu:RCOM_1023980 | 1 | 71 | + | 71 | none | 12.37 | 574 | 71.83 | 8e-20 | Beta-amylase putative (EC:3.2.1.2) |
blastp_pdb | 1b1y_A | 1 | 71 | + | 71 | none | 14.20 | 500 | 38.03 | 5e-08 | mol:protein length:500 PROTEIN (BETA-AMYLASE) |
blastp_pdb | 2xgi_A | 1 | 71 | + | 71 | none | 13.27 | 535 | 38.03 | 9e-08 | mol:protein length:535 BETA-AMYLASE |
blastp_pdb | 2xgb_A | 1 | 71 | + | 71 | none | 13.27 | 535 | 38.03 | 9e-08 | mol:protein length:535 BETA-AMYLASE |
blastp_pdb | 2xg9_A | 1 | 71 | + | 71 | none | 13.27 | 535 | 38.03 | 9e-08 | mol:protein length:535 BETA-AMYLASE |
blastp_pdb | 2xfy_A | 1 | 71 | + | 71 | none | 13.27 | 535 | 38.03 | 9e-08 | mol:protein length:535 BETA-AMYLASE |
blastp_pdb | 2xfr_A | 1 | 71 | + | 71 | none | 13.27 | 535 | 38.03 | 9e-08 | mol:protein length:535 BETA-AMYLASE |
blastp_pdb | 2xff_A | 1 | 71 | + | 71 | none | 13.27 | 535 | 38.03 | 9e-08 | mol:protein length:535 BETA-AMYLASE |
blastp_pdb | 2dqx_A | 1 | 59 | + | 59 | none | 11.92 | 495 | 35.59 | 6e-06 | mol:protein length:495 Beta-amylase |
blastp_uniprot_sprot | sp|Q9LIR6|BAM1_ARATH | 1 | 71 | + | 71 | none | 12.35 | 575 | 67.61 | 7e-20 | Beta-amylase 1 chloroplastic OS Arabidopsis thaliana GN BAM1 PE 1 SV 1 |
blastp_uniprot_sprot | sp|O23553|BAM3_ARATH | 1 | 72 | + | 72 | none | 13.14 | 548 | 50.00 | 2e-12 | Beta-amylase 3 chloroplastic OS Arabidopsis thaliana GN BAM3 PE 1 SV 3 |
blastp_uniprot_sprot | sp|Q8VYW2|BAM9_ARATH | 2 | 94 | + | 93 | Gaps:1 | 17.54 | 536 | 39.36 | 5e-10 | Inactive beta-amylase 9 OS Arabidopsis thaliana GN BAM9 PE 2 SV 1 |
blastp_uniprot_sprot | sp|P16098|AMYB_HORVU | 1 | 71 | + | 71 | none | 13.27 | 535 | 38.03 | 3e-07 | Beta-amylase OS Hordeum vulgare GN BMY1 PE 1 SV 1 |
blastp_uniprot_sprot | sp|P82993|AMYB_HORVS | 1 | 71 | + | 71 | none | 13.27 | 535 | 38.03 | 3e-07 | Beta-amylase OS Hordeum vulgare subsp. spontaneum GN BMY1 PE 1 SV 1 |
blastp_uniprot_sprot | sp|P55005|AMYB_MAIZE | 1 | 59 | + | 59 | none | 12.09 | 488 | 40.68 | 4e-07 | Beta-amylase OS Zea mays GN BMY1 PE 2 SV 1 |
blastp_uniprot_sprot | sp|P93594|AMYB_WHEAT | 1 | 59 | + | 59 | none | 11.73 | 503 | 40.68 | 5e-07 | Beta-amylase OS Triticum aestivum GN BMY1 PE 2 SV 1 |
rpsblast_cdd | gnl|CDD|177789 | 1 | 71 | + | 71 | none | 12.39 | 573 | 69.01 | 3e-24 | PLN00197 PLN00197 beta-amylase Provisional. |
rpsblast_cdd | gnl|CDD|178400 | 1 | 72 | + | 72 | none | 13.14 | 548 | 50.00 | 2e-16 | PLN02803 PLN02803 beta-amylase. |
rpsblast_cdd | gnl|CDD|201755 | 13 | 96 | + | 84 | Gaps:9 | 18.80 | 399 | 38.67 | 5e-09 | pfam01373 Glyco_hydro_14 Glycosyl hydrolase family 14. This family are beta amylases. |
rpsblast_cdd | gnl|CDD|178398 | 1 | 59 | + | 59 | none | 11.41 | 517 | 38.98 | 3e-07 | PLN02801 PLN02801 beta-amylase. |
rpsblast_cdd | gnl|CDD|177820 | 1 | 56 | + | 56 | Gaps:4 | 11.30 | 531 | 40.00 | 7e-07 | PLN02161 PLN02161 beta-amylase. |
5 Domain Motifs
Analysis | Begin | End | Length | Domain Identifier | Cross Ref | Description | Inter Pro |
---|---|---|---|---|---|---|---|
Pfam | 2 | 58 | 57 | PF01373 | "KEGG:00500+3.2.1.2","MetaCyc:PWY-6724","MetaCyc:PWY-842" | Glycosyl hydrolase family 14 | IPR001554 |
PANTHER | 1 | 56 | 56 | PTHR31352 | none | none | none |
PANTHER | 1 | 56 | 56 | PTHR31352:SF1 | none | none | none |
Gene3D | 1 | 58 | 58 | G3DSA:3.20.20.80 | none | none | IPR013781 |
SUPERFAMILY | 4 | 65 | 62 | SSF51445 | none | none | IPR017853 |
18 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_nPriLBD*_3P | Qrob_Chr11 | 11 | v_12066_307 | s_1B15GJ_447 | 3,37 | 0,57 | 16,17 | lod | 3,4299 | 6,9 |
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 |
Bourran2_2014_nPriBD*_3P | Qrob_Chr06 | 6 | s_1B6WLL_980 | v_10064_133 | 11,49 | 0 | 31,52 | lod | 4,1208 | 9,1 |