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|pper:PRUPE_ppa004116mg | 1 | 536 | + | 536 | Gaps:13 | 100.00 | 529 | 75.43 | 0.0 | hypothetical protein |
blastp_kegg | lcl|pmum:103322923 | 1 | 536 | + | 536 | Gaps:13 | 99.81 | 530 | 74.86 | 0.0 | inactive beta-amylase 9 |
blastp_kegg | lcl|fve:101294256 | 1 | 536 | + | 536 | Gaps:12 | 100.00 | 530 | 72.45 | 0.0 | inactive beta-amylase 9-like |
blastp_kegg | lcl|cit:102577946 | 1 | 536 | + | 536 | Gaps:17 | 100.00 | 543 | 72.93 | 0.0 | SD3 putative beta-amylase |
blastp_kegg | lcl|cic:CICLE_v10004689mg | 1 | 536 | + | 536 | Gaps:17 | 100.00 | 543 | 72.74 | 0.0 | hypothetical protein |
blastp_kegg | lcl|pxb:103958554 | 1 | 536 | + | 536 | Gaps:14 | 100.00 | 530 | 73.58 | 0.0 | inactive beta-amylase 9-like |
blastp_kegg | lcl|mdm:103414626 | 1 | 536 | + | 536 | Gaps:13 | 100.00 | 529 | 74.10 | 0.0 | inactive beta-amylase 9-like |
blastp_kegg | lcl|mdm:103452992 | 1 | 536 | + | 536 | Gaps:13 | 100.00 | 529 | 74.10 | 0.0 | inactive beta-amylase 9 |
blastp_kegg | lcl|vvi:100263193 | 1 | 536 | + | 536 | Gaps:15 | 100.00 | 541 | 70.43 | 0.0 | inactive beta-amylase 9-like |
blastp_kegg | lcl|mdm:103403788 | 1 | 536 | + | 536 | Gaps:14 | 100.00 | 530 | 73.02 | 0.0 | inactive beta-amylase 9-like |
blastp_pdb | 1b1y_A | 84 | 503 | + | 420 | Gaps:19 | 86.20 | 500 | 36.43 | 3e-88 | mol:protein length:500 PROTEIN (BETA-AMYLASE) |
blastp_pdb | 1fa2_A | 84 | 503 | + | 420 | Gaps:18 | 86.75 | 498 | 35.42 | 2e-87 | mol:protein length:498 BETA-AMYLASE |
blastp_pdb | 2xgi_A | 84 | 503 | + | 420 | Gaps:19 | 80.56 | 535 | 35.73 | 9e-86 | mol:protein length:535 BETA-AMYLASE |
blastp_pdb | 2xgb_A | 84 | 503 | + | 420 | Gaps:19 | 80.56 | 535 | 35.73 | 9e-86 | mol:protein length:535 BETA-AMYLASE |
blastp_pdb | 2xg9_A | 84 | 503 | + | 420 | Gaps:19 | 80.56 | 535 | 35.73 | 9e-86 | mol:protein length:535 BETA-AMYLASE |
blastp_pdb | 2xfy_A | 84 | 503 | + | 420 | Gaps:19 | 80.56 | 535 | 35.73 | 9e-86 | mol:protein length:535 BETA-AMYLASE |
blastp_pdb | 2xfr_A | 84 | 503 | + | 420 | Gaps:19 | 80.56 | 535 | 35.73 | 9e-86 | mol:protein length:535 BETA-AMYLASE |
blastp_pdb | 2xff_A | 84 | 503 | + | 420 | Gaps:19 | 80.56 | 535 | 35.73 | 9e-86 | mol:protein length:535 BETA-AMYLASE |
blastp_pdb | 1v3i_A | 84 | 530 | + | 447 | Gaps:20 | 92.32 | 495 | 33.92 | 2e-85 | mol:protein length:495 Beta-amylase |
blastp_pdb | 1q6d_A | 84 | 530 | + | 447 | Gaps:20 | 92.32 | 495 | 33.70 | 4e-85 | mol:protein length:495 beta-amylase |
blastp_uniprot_sprot | sp|Q8VYW2|BAM9_ARATH | 1 | 527 | + | 527 | Gaps:21 | 98.13 | 536 | 62.93 | 0.0 | Inactive beta-amylase 9 OS Arabidopsis thaliana GN BAM9 PE 2 SV 1 |
blastp_uniprot_sprot | sp|Q9LIR6|BAM1_ARATH | 84 | 504 | + | 421 | Gaps:14 | 75.65 | 575 | 41.61 | 2e-109 | Beta-amylase 1 chloroplastic OS Arabidopsis thaliana GN BAM1 PE 1 SV 1 |
blastp_uniprot_sprot | sp|O23553|BAM3_ARATH | 78 | 521 | + | 444 | Gaps:9 | 81.93 | 548 | 39.64 | 1e-107 | Beta-amylase 3 chloroplastic OS Arabidopsis thaliana GN BAM3 PE 1 SV 3 |
blastp_uniprot_sprot | sp|Q9FM68|BAM4_ARATH | 78 | 503 | + | 426 | Gaps:17 | 83.43 | 531 | 38.60 | 3e-103 | Inactive beta-amylase 4 chloroplastic OS Arabidopsis thaliana GN BAM4 PE 2 SV 1 |
blastp_uniprot_sprot | sp|O65258|BAM2_ARATH | 84 | 514 | + | 431 | Gaps:24 | 80.26 | 542 | 38.39 | 2e-90 | Beta-amylase 2 chloroplastic OS Arabidopsis thaliana GN BAM2 PE 1 SV 2 |
blastp_uniprot_sprot | sp|Q8L762|BAM6_ARATH | 24 | 525 | + | 502 | Gaps:31 | 91.33 | 577 | 33.59 | 3e-90 | Beta-amylase 6 OS Arabidopsis thaliana GN BAM6 PE 2 SV 1 |
blastp_uniprot_sprot | sp|O65015|AMYB_TRIRP | 84 | 530 | + | 447 | Gaps:20 | 92.14 | 496 | 35.89 | 9e-90 | Beta-amylase OS Trifolium repens GN BMY1 PE 2 SV 1 |
blastp_uniprot_sprot | sp|O64407|AMYB_VIGUN | 84 | 530 | + | 447 | Gaps:20 | 92.14 | 496 | 35.45 | 2e-89 | Beta-amylase OS Vigna unguiculata GN BMY1 PE 2 SV 1 |
blastp_uniprot_sprot | sp|P55005|AMYB_MAIZE | 84 | 503 | + | 420 | Gaps:25 | 88.32 | 488 | 36.66 | 1e-87 | Beta-amylase OS Zea mays GN BMY1 PE 2 SV 1 |
blastp_uniprot_sprot | sp|O22585|AMYB_MEDSA | 84 | 530 | + | 447 | Gaps:20 | 92.14 | 496 | 35.01 | 3e-87 | Beta-amylase OS Medicago sativa GN BMY1 PE 1 SV 1 |
13 Domain Motifs
Analysis | Begin | End | Length | Domain Identifier | Cross Ref | Description | Inter Pro |
---|---|---|---|---|---|---|---|
PRINTS | 139 | 157 | 19 | PR00750 | "KEGG:00500+3.2.1.2","MetaCyc:PWY-6724","MetaCyc:PWY-842" | Beta-amylase (glycosyl hydrolase family 14) signature | IPR001554 |
PRINTS | 248 | 270 | 23 | PR00750 | "KEGG:00500+3.2.1.2","MetaCyc:PWY-6724","MetaCyc:PWY-842" | Beta-amylase (glycosyl hydrolase family 14) signature | IPR001554 |
PRINTS | 360 | 376 | 17 | PR00750 | "KEGG:00500+3.2.1.2","MetaCyc:PWY-6724","MetaCyc:PWY-842" | Beta-amylase (glycosyl hydrolase family 14) signature | IPR001554 |
PRINTS | 324 | 343 | 20 | PR00750 | "KEGG:00500+3.2.1.2","MetaCyc:PWY-6724","MetaCyc:PWY-842" | Beta-amylase (glycosyl hydrolase family 14) signature | IPR001554 |
PRINTS | 118 | 132 | 15 | PR00750 | "KEGG:00500+3.2.1.2","MetaCyc:PWY-6724","MetaCyc:PWY-842" | Beta-amylase (glycosyl hydrolase family 14) signature | IPR001554 |
PRINTS | 377 | 388 | 12 | PR00750 | "KEGG:00500+3.2.1.2","MetaCyc:PWY-6724","MetaCyc:PWY-842" | Beta-amylase (glycosyl hydrolase family 14) signature | IPR001554 |
PRINTS | 395 | 418 | 24 | PR00750 | "KEGG:00500+3.2.1.2","MetaCyc:PWY-6724","MetaCyc:PWY-842" | Beta-amylase (glycosyl hydrolase family 14) signature | IPR001554 |
PRINTS | 432 | 454 | 23 | PR00750 | "KEGG:00500+3.2.1.2","MetaCyc:PWY-6724","MetaCyc:PWY-842" | Beta-amylase (glycosyl hydrolase family 14) signature | IPR001554 |
Pfam | 87 | 487 | 401 | PF01373 | "KEGG:00500+3.2.1.2","MetaCyc:PWY-6724","MetaCyc:PWY-842" | Glycosyl hydrolase family 14 | IPR001554 |
PANTHER | 1 | 511 | 511 | PTHR31352 | none | none | none |
SUPERFAMILY | 82 | 517 | 436 | SSF51445 | none | none | IPR017853 |
Gene3D | 79 | 528 | 450 | G3DSA:3.20.20.80 | none | none | IPR013781 |
PANTHER | 1 | 511 | 511 | PTHR31352:SF3 | none | none | none |
14 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_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_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 |
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 |