3 GO Terms
Identifier | Name | Description |
---|---|---|
GO:0006629 | lipid metabolic process | The chemical reactions and pathways involving lipids, compounds soluble in an organic solvent but not, or sparingly, in an aqueous solvent. Includes fatty acids; neutral fats, other fatty-acid esters, and soaps; long-chain (fatty) alcohols and waxes; sphingoids and other long-chain bases; glycolipids, phospholipids and sphingolipids; and carotenes, polyprenols, sterols, terpenes and other isoprenoids. |
GO:0006508 | proteolysis | The hydrolysis of proteins into smaller polypeptides and/or amino acids by cleavage of their peptide bonds. |
GO:0004190 | aspartic-type endopeptidase activity | Catalysis of the hydrolysis of internal, alpha-peptide bonds in a polypeptide chain by a mechanism in which a water molecule bound by the side chains of aspartic residues at the active center acts as a nucleophile. |
41 Blast
Analysis | Hit | Start | End | Strand | Length | Note | Hit Coverage | Hit Length | Hit Pident | E Val | Hit Description |
---|---|---|---|---|---|---|---|---|---|---|---|
blastp_kegg | lcl|pmum:103323394 | 7 | 476 | + | 470 | Gaps:42 | 98.43 | 510 | 63.15 | 0.0 | aspartic proteinase-like |
blastp_kegg | lcl|cit:102608561 | 1 | 477 | + | 477 | Gaps:51 | 100.00 | 504 | 61.31 | 0.0 | aspartic proteinase A2-like |
blastp_kegg | lcl|cit:102608269 | 1 | 477 | + | 477 | Gaps:51 | 100.00 | 504 | 61.31 | 0.0 | aspartic proteinase A2-like |
blastp_kegg | lcl|mdm:103452605 | 1 | 476 | + | 476 | Gaps:52 | 99.80 | 499 | 62.85 | 0.0 | aspartic proteinase-like |
blastp_kegg | lcl|cam:101503657 | 1 | 477 | + | 477 | Gaps:45 | 100.00 | 506 | 59.88 | 0.0 | aspartic proteinase oryzasin-1-like |
blastp_kegg | lcl|pxb:103944705 | 1 | 477 | + | 477 | Gaps:52 | 100.00 | 499 | 62.32 | 0.0 | aspartic proteinase oryzasin-1-like |
blastp_kegg | lcl|rcu:RCOM_1004030 | 1 | 477 | + | 477 | Gaps:53 | 98.80 | 500 | 61.54 | 0.0 | Aspartic proteinase oryzasin-1 precursor putative (EC:3.4.23.40) |
blastp_kegg | lcl|tcc:TCM_021510 | 1 | 477 | + | 477 | Gaps:52 | 99.80 | 500 | 62.12 | 0.0 | Aspartic proteinase oryzasin-1 isoform 1 |
blastp_kegg | lcl|fve:101304861 | 1 | 477 | + | 477 | Gaps:49 | 99.21 | 506 | 61.16 | 0.0 | aspartic proteinase A2-like |
blastp_kegg | lcl|pper:PRUPE_ppa004486mg | 7 | 476 | + | 470 | Gaps:41 | 98.42 | 507 | 61.92 | 0.0 | hypothetical protein |
blastp_pdb | 1qdm_C | 32 | 477 | + | 446 | Gaps:50 | 100.00 | 478 | 48.95 | 3e-157 | mol:protein length:478 PROPHYTEPSIN |
blastp_pdb | 1qdm_B | 32 | 477 | + | 446 | Gaps:50 | 100.00 | 478 | 48.95 | 3e-157 | mol:protein length:478 PROPHYTEPSIN |
blastp_pdb | 1qdm_A | 32 | 477 | + | 446 | Gaps:50 | 100.00 | 478 | 48.95 | 3e-157 | mol:protein length:478 PROPHYTEPSIN |
blastp_pdb | 1b5f_C | 77 | 280 | + | 204 | Gaps:39 | 98.33 | 239 | 50.21 | 9e-68 | mol:protein length:239 PROTEIN (CARDOSIN A) |
blastp_pdb | 1b5f_A | 77 | 280 | + | 204 | Gaps:39 | 98.33 | 239 | 50.21 | 9e-68 | mol:protein length:239 PROTEIN (CARDOSIN A) |
blastp_pdb | 2x0b_G | 32 | 476 | + | 445 | Gaps:89 | 95.04 | 383 | 42.03 | 4e-65 | mol:protein length:383 RENIN |
blastp_pdb | 2x0b_E | 32 | 476 | + | 445 | Gaps:89 | 95.04 | 383 | 42.03 | 4e-65 | mol:protein length:383 RENIN |
blastp_pdb | 2x0b_C | 32 | 476 | + | 445 | Gaps:89 | 95.04 | 383 | 42.03 | 4e-65 | mol:protein length:383 RENIN |
blastp_pdb | 2x0b_A | 32 | 476 | + | 445 | Gaps:89 | 95.04 | 383 | 42.03 | 4e-65 | mol:protein length:383 RENIN |
blastp_pdb | 3km4_B | 75 | 476 | + | 402 | Gaps:75 | 98.81 | 337 | 40.54 | 5e-63 | mol:protein length:337 Renin |
blastp_uniprot_sprot | sp|Q42456|ASPR1_ORYSJ | 26 | 477 | + | 452 | Gaps:45 | 95.68 | 509 | 50.10 | 4e-171 | Aspartic proteinase oryzasin-1 OS Oryza sativa subsp. japonica GN Os05g0567100 PE 2 SV 2 |
blastp_uniprot_sprot | sp|P42211|ASPRX_ORYSJ | 1 | 477 | + | 477 | Gaps:55 | 100.00 | 496 | 48.39 | 4e-170 | Aspartic proteinase OS Oryza sativa subsp. japonica GN RAP PE 2 SV 2 |
blastp_uniprot_sprot | sp|O65390|APA1_ARATH | 28 | 477 | + | 450 | Gaps:48 | 94.86 | 506 | 51.46 | 5e-169 | Aspartic proteinase A1 OS Arabidopsis thaliana GN APA1 PE 1 SV 1 |
blastp_uniprot_sprot | sp|Q8VYL3|APA2_ARATH | 28 | 476 | + | 449 | Gaps:43 | 94.74 | 513 | 50.00 | 8e-169 | Aspartic proteinase A2 OS Arabidopsis thaliana GN APA2 PE 2 SV 1 |
blastp_uniprot_sprot | sp|P42210|ASPR_HORVU | 26 | 477 | + | 452 | Gaps:50 | 95.28 | 508 | 48.97 | 1e-158 | Phytepsin OS Hordeum vulgare PE 1 SV 1 |
blastp_uniprot_sprot | sp|P40782|CYPR1_CYNCA | 36 | 477 | + | 442 | Gaps:43 | 100.00 | 473 | 48.41 | 2e-157 | Cyprosin (Fragment) OS Cynara cardunculus GN CYPRO1 PE 1 SV 2 |
blastp_uniprot_sprot | sp|Q9XEC4|APA3_ARATH | 29 | 477 | + | 449 | Gaps:46 | 94.29 | 508 | 46.14 | 5e-154 | Aspartic proteinase A3 OS Arabidopsis thaliana GN APA3 PE 1 SV 1 |
blastp_uniprot_sprot | sp|O04057|ASPR_CUCPE | 11 | 477 | + | 467 | Gaps:46 | 98.05 | 513 | 46.32 | 2e-152 | Aspartic proteinase OS Cucurbita pepo PE 2 SV 1 |
blastp_uniprot_sprot | sp|Q9XFX4|CARDB_CYNCA | 27 | 476 | + | 450 | Gaps:46 | 94.86 | 506 | 44.17 | 5e-143 | Procardosin-B OS Cynara cardunculus GN cardB PE 1 SV 1 |
blastp_uniprot_sprot | sp|Q9XFX3|CARDA_CYNCA | 3 | 477 | + | 475 | Gaps:53 | 99.21 | 504 | 45.40 | 4e-140 | Procardosin-A OS Cynara cardunculus GN cardA PE 1 SV 1 |
27 Domain Motifs
Analysis | Begin | End | Length | Domain Identifier | Cross Ref | Description | Inter Pro |
---|---|---|---|---|---|---|---|
Gene3D | 78 | 262 | 185 | G3DSA:2.40.70.10 | none | none | IPR021109 |
Phobius | 17 | 21 | 5 | SIGNAL_PEPTIDE_C_REGION | none | C-terminal region of a signal peptide. | none |
Phobius | 22 | 477 | 456 | NON_CYTOPLASMIC_DOMAIN | none | Region of a membrane-bound protein predicted to be outside the membrane, in the extracellular region. | none |
ProSiteProfiles | 283 | 323 | 41 | PS50015 | none | Saposin B type domain profile. | IPR008139 |
PANTHER | 380 | 476 | 97 | PTHR13683:SF253 | none | none | none |
PANTHER | 7 | 285 | 279 | PTHR13683:SF253 | none | none | none |
Phobius | 1 | 21 | 21 | SIGNAL_PEPTIDE | none | Signal peptide region | none |
ProSitePatterns | 103 | 114 | 12 | PS00141 | none | Eukaryotic and viral aspartyl proteases active site. | IPR001969 |
Phobius | 6 | 16 | 11 | SIGNAL_PEPTIDE_H_REGION | none | Hydrophobic region of a signal peptide. | none |
SUPERFAMILY | 285 | 386 | 102 | SSF47862 | none | none | IPR011001 |
PRINTS | 240 | 253 | 14 | PR00792 | none | Pepsin (A1) aspartic protease family signature | IPR001461 |
PRINTS | 94 | 114 | 21 | PR00792 | none | Pepsin (A1) aspartic protease family signature | IPR001461 |
PRINTS | 450 | 465 | 16 | PR00792 | none | Pepsin (A1) aspartic protease family signature | IPR001461 |
Phobius | 1 | 5 | 5 | SIGNAL_PEPTIDE_N_REGION | none | N-terminal region of a signal peptide. | none |
Gene3D | 280 | 320 | 41 | G3DSA:1.10.225.10 | none | none | IPR011001 |
Pfam | 287 | 319 | 33 | PF03489 | none | Saposin-like type B, region 2 | IPR008138 |
Pfam | 349 | 386 | 38 | PF05184 | none | Saposin-like type B, region 1 | IPR007856 |
SUPERFAMILY | 31 | 281 | 251 | SSF50630 | none | none | IPR021109 |
SUPERFAMILY | 386 | 476 | 91 | SSF50630 | none | none | IPR021109 |
ProSiteProfiles | 347 | 388 | 42 | PS50015 | none | Saposin B type domain profile. | IPR008139 |
PANTHER | 380 | 476 | 97 | PTHR13683 | none | none | IPR001461 |
PANTHER | 7 | 285 | 279 | PTHR13683 | none | none | IPR001461 |
Gene3D | 394 | 476 | 83 | G3DSA:2.40.70.10 | none | none | IPR021109 |
Gene3D | 263 | 279 | 17 | G3DSA:2.40.70.10 | none | none | IPR021109 |
Gene3D | 324 | 343 | 20 | G3DSA:2.40.70.10 | none | none | IPR021109 |
Pfam | 87 | 476 | 390 | PF00026 | none | Eukaryotic aspartyl protease | IPR001461 |
Gene3D | 348 | 391 | 44 | G3DSA:1.10.225.10 | none | none | IPR011001 |
3 Localization
Analysis | Start | End | Length |
---|---|---|---|
SignalP_GRAM_NEGATIVE | 1 | 21 | 20 |
SignalP_GRAM_POSITIVE | 1 | 21 | 20 |
SignalP_EUK | 1 | 21 | 20 |
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 |