Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005811 | lipid droplet | 5 | 12 |
GO:0016020 | membrane | 2 | 11 |
GO:0043226 | organelle | 2 | 12 |
GO:0043228 | non-membrane-bounded organelle | 3 | 12 |
GO:0043229 | intracellular organelle | 3 | 12 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0005737 | cytoplasm | 2 | 1 |
Related structures:
AlphaFold database: A4H4N0
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 12 |
GO:0006720 | isoprenoid metabolic process | 4 | 12 |
GO:0006721 | terpenoid metabolic process | 5 | 12 |
GO:0006722 | triterpenoid metabolic process | 6 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0008299 | isoprenoid biosynthetic process | 4 | 12 |
GO:0008610 | lipid biosynthetic process | 4 | 12 |
GO:0009058 | biosynthetic process | 2 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016104 | triterpenoid biosynthetic process | 6 | 12 |
GO:0016114 | terpenoid biosynthetic process | 5 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044249 | cellular biosynthetic process | 3 | 12 |
GO:0044255 | cellular lipid metabolic process | 3 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:1901576 | organic substance biosynthetic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0016853 | isomerase activity | 2 | 12 |
GO:0016866 | intramolecular transferase activity | 3 | 12 |
GO:0016871 | cycloartenol synthase activity | 5 | 6 |
GO:0031559 | oxidosqualene cyclase activity | 4 | 7 |
GO:0000250 | lanosterol synthase activity | 5 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 902 | 906 | PF00656 | 0.486 |
CLV_NRD_NRD_1 | 141 | 143 | PF00675 | 0.495 |
CLV_NRD_NRD_1 | 264 | 266 | PF00675 | 0.419 |
CLV_NRD_NRD_1 | 336 | 338 | PF00675 | 0.490 |
CLV_NRD_NRD_1 | 526 | 528 | PF00675 | 0.521 |
CLV_NRD_NRD_1 | 579 | 581 | PF00675 | 0.435 |
CLV_NRD_NRD_1 | 667 | 669 | PF00675 | 0.512 |
CLV_NRD_NRD_1 | 740 | 742 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 816 | 818 | PF00675 | 0.446 |
CLV_NRD_NRD_1 | 941 | 943 | PF00675 | 0.210 |
CLV_PCSK_KEX2_1 | 141 | 143 | PF00082 | 0.495 |
CLV_PCSK_KEX2_1 | 264 | 266 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 336 | 338 | PF00082 | 0.601 |
CLV_PCSK_KEX2_1 | 579 | 581 | PF00082 | 0.429 |
CLV_PCSK_KEX2_1 | 667 | 669 | PF00082 | 0.512 |
CLV_PCSK_KEX2_1 | 740 | 742 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 815 | 817 | PF00082 | 0.446 |
CLV_PCSK_KEX2_1 | 941 | 943 | PF00082 | 0.210 |
CLV_PCSK_KEX2_1 | 997 | 999 | PF00082 | 0.332 |
CLV_PCSK_PC1ET2_1 | 997 | 999 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 265 | 269 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 296 | 300 | PF00082 | 0.431 |
CLV_PCSK_SKI1_1 | 336 | 340 | PF00082 | 0.430 |
CLV_PCSK_SKI1_1 | 580 | 584 | PF00082 | 0.437 |
CLV_PCSK_SKI1_1 | 727 | 731 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 740 | 744 | PF00082 | 0.504 |
CLV_Separin_Metazoa | 190 | 194 | PF03568 | 0.395 |
CLV_Separin_Metazoa | 217 | 221 | PF03568 | 0.274 |
DEG_APCC_DBOX_1 | 460 | 468 | PF00400 | 0.312 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.592 |
DEG_SPOP_SBC_1 | 351 | 355 | PF00917 | 0.366 |
DOC_MAPK_gen_1 | 108 | 117 | PF00069 | 0.499 |
DOC_MAPK_gen_1 | 579 | 585 | PF00069 | 0.159 |
DOC_MAPK_RevD_3 | 127 | 142 | PF00069 | 0.444 |
DOC_PP1_RVXF_1 | 874 | 881 | PF00149 | 0.427 |
DOC_PP2B_LxvP_1 | 371 | 374 | PF13499 | 0.488 |
DOC_PP2B_LxvP_1 | 431 | 434 | PF13499 | 0.312 |
DOC_PP2B_LxvP_1 | 483 | 486 | PF13499 | 0.157 |
DOC_PP2B_LxvP_1 | 730 | 733 | PF13499 | 0.312 |
DOC_PP4_FxxP_1 | 121 | 124 | PF00568 | 0.282 |
DOC_PP4_FxxP_1 | 188 | 191 | PF00568 | 0.356 |
DOC_PP4_MxPP_1 | 338 | 341 | PF00568 | 0.277 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.283 |
DOC_USP7_MATH_1 | 351 | 355 | PF00917 | 0.353 |
DOC_USP7_MATH_1 | 539 | 543 | PF00917 | 0.298 |
DOC_USP7_MATH_1 | 907 | 911 | PF00917 | 0.419 |
DOC_WW_Pin1_4 | 276 | 281 | PF00397 | 0.375 |
DOC_WW_Pin1_4 | 453 | 458 | PF00397 | 0.312 |
DOC_WW_Pin1_4 | 476 | 481 | PF00397 | 0.310 |
DOC_WW_Pin1_4 | 551 | 556 | PF00397 | 0.210 |
DOC_WW_Pin1_4 | 903 | 908 | PF00397 | 0.512 |
LIG_14-3-3_CanoR_1 | 108 | 118 | PF00244 | 0.464 |
LIG_14-3-3_CanoR_1 | 146 | 152 | PF00244 | 0.213 |
LIG_14-3-3_CanoR_1 | 237 | 247 | PF00244 | 0.358 |
LIG_14-3-3_CanoR_1 | 284 | 291 | PF00244 | 0.325 |
LIG_14-3-3_CanoR_1 | 360 | 367 | PF00244 | 0.413 |
LIG_14-3-3_CanoR_1 | 37 | 46 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 514 | 518 | PF00244 | 0.266 |
LIG_14-3-3_CanoR_1 | 631 | 638 | PF00244 | 0.254 |
LIG_14-3-3_CanoR_1 | 821 | 830 | PF00244 | 0.284 |
LIG_14-3-3_CanoR_1 | 900 | 904 | PF00244 | 0.467 |
LIG_Actin_WH2_2 | 269 | 286 | PF00022 | 0.227 |
LIG_Actin_WH2_2 | 498 | 516 | PF00022 | 0.312 |
LIG_Actin_WH2_2 | 602 | 619 | PF00022 | 0.238 |
LIG_Actin_WH2_2 | 739 | 755 | PF00022 | 0.253 |
LIG_AP2alpha_2 | 303 | 305 | PF02296 | 0.312 |
LIG_APCC_ABBA_1 | 339 | 344 | PF00400 | 0.345 |
LIG_APCC_ABBA_1 | 804 | 809 | PF00400 | 0.235 |
LIG_APCC_ABBAyCdc20_2 | 527 | 533 | PF00400 | 0.235 |
LIG_BRCT_BRCA1_1 | 166 | 170 | PF00533 | 0.295 |
LIG_BRCT_BRCA1_1 | 31 | 35 | PF00533 | 0.560 |
LIG_BRCT_BRCA1_1 | 556 | 560 | PF00533 | 0.181 |
LIG_BRCT_BRCA1_1 | 621 | 625 | PF00533 | 0.316 |
LIG_BRCT_BRCA1_1 | 632 | 636 | PF00533 | 0.247 |
LIG_BRCT_BRCA1_1 | 780 | 784 | PF00533 | 0.191 |
LIG_BRCT_BRCA1_1 | 966 | 970 | PF00533 | 0.410 |
LIG_deltaCOP1_diTrp_1 | 487 | 491 | PF00928 | 0.253 |
LIG_eIF4E_1 | 425 | 431 | PF01652 | 0.235 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.315 |
LIG_FHA_1 | 242 | 248 | PF00498 | 0.383 |
LIG_FHA_1 | 324 | 330 | PF00498 | 0.259 |
LIG_FHA_1 | 521 | 527 | PF00498 | 0.267 |
LIG_FHA_1 | 554 | 560 | PF00498 | 0.281 |
LIG_FHA_1 | 595 | 601 | PF00498 | 0.230 |
LIG_FHA_1 | 801 | 807 | PF00498 | 0.217 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.579 |
LIG_FHA_2 | 209 | 215 | PF00498 | 0.383 |
LIG_FHA_2 | 283 | 289 | PF00498 | 0.411 |
LIG_FHA_2 | 29 | 35 | PF00498 | 0.635 |
LIG_FHA_2 | 43 | 49 | PF00498 | 0.492 |
LIG_FHA_2 | 54 | 60 | PF00498 | 0.418 |
LIG_FHA_2 | 900 | 906 | PF00498 | 0.467 |
LIG_FHA_2 | 95 | 101 | PF00498 | 0.565 |
LIG_LIR_Apic_2 | 529 | 534 | PF02991 | 0.222 |
LIG_LIR_Gen_1 | 112 | 121 | PF02991 | 0.202 |
LIG_LIR_Gen_1 | 214 | 223 | PF02991 | 0.439 |
LIG_LIR_Gen_1 | 532 | 543 | PF02991 | 0.235 |
LIG_LIR_Gen_1 | 597 | 605 | PF02991 | 0.261 |
LIG_LIR_Gen_1 | 790 | 795 | PF02991 | 0.356 |
LIG_LIR_Gen_1 | 915 | 925 | PF02991 | 0.410 |
LIG_LIR_Gen_1 | 999 | 1004 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 112 | 117 | PF02991 | 0.233 |
LIG_LIR_Nem_3 | 214 | 218 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 456 | 462 | PF02991 | 0.215 |
LIG_LIR_Nem_3 | 471 | 475 | PF02991 | 0.194 |
LIG_LIR_Nem_3 | 487 | 491 | PF02991 | 0.182 |
LIG_LIR_Nem_3 | 508 | 513 | PF02991 | 0.235 |
LIG_LIR_Nem_3 | 532 | 538 | PF02991 | 0.221 |
LIG_LIR_Nem_3 | 542 | 546 | PF02991 | 0.220 |
LIG_LIR_Nem_3 | 597 | 602 | PF02991 | 0.235 |
LIG_LIR_Nem_3 | 760 | 766 | PF02991 | 0.287 |
LIG_LIR_Nem_3 | 781 | 787 | PF02991 | 0.218 |
LIG_LIR_Nem_3 | 790 | 794 | PF02991 | 0.227 |
LIG_LIR_Nem_3 | 809 | 814 | PF02991 | 0.126 |
LIG_LIR_Nem_3 | 999 | 1003 | PF02991 | 0.444 |
LIG_MLH1_MIPbox_1 | 632 | 636 | PF16413 | 0.255 |
LIG_NRBOX | 128 | 134 | PF00104 | 0.417 |
LIG_NRBOX | 725 | 731 | PF00104 | 0.277 |
LIG_PCNA_yPIPBox_3 | 962 | 970 | PF02747 | 0.351 |
LIG_Pex14_1 | 309 | 313 | PF04695 | 0.210 |
LIG_Pex14_1 | 654 | 658 | PF04695 | 0.210 |
LIG_Pex14_1 | 844 | 848 | PF04695 | 0.248 |
LIG_Pex14_1 | 996 | 1000 | PF04695 | 0.479 |
LIG_Pex14_2 | 114 | 118 | PF04695 | 0.349 |
LIG_Pex14_2 | 119 | 123 | PF04695 | 0.334 |
LIG_Pex14_2 | 305 | 309 | PF04695 | 0.312 |
LIG_Pex14_2 | 840 | 844 | PF04695 | 0.221 |
LIG_Rb_LxCxE_1 | 776 | 795 | PF01857 | 0.277 |
LIG_SH2_CRK | 1000 | 1004 | PF00017 | 0.482 |
LIG_SH2_CRK | 535 | 539 | PF00017 | 0.212 |
LIG_SH2_CRK | 735 | 739 | PF00017 | 0.231 |
LIG_SH2_NCK_1 | 1000 | 1004 | PF00017 | 0.542 |
LIG_SH2_NCK_1 | 531 | 535 | PF00017 | 0.226 |
LIG_SH2_PTP2 | 425 | 428 | PF00017 | 0.253 |
LIG_SH2_PTP2 | 682 | 685 | PF00017 | 0.210 |
LIG_SH2_SRC | 61 | 64 | PF00017 | 0.462 |
LIG_SH2_SRC | 682 | 685 | PF00017 | 0.210 |
LIG_SH2_SRC | 766 | 769 | PF00017 | 0.214 |
LIG_SH2_STAP1 | 1000 | 1004 | PF00017 | 0.462 |
LIG_SH2_STAP1 | 581 | 585 | PF00017 | 0.171 |
LIG_SH2_STAP1 | 61 | 65 | PF00017 | 0.559 |
LIG_SH2_STAP1 | 848 | 852 | PF00017 | 0.291 |
LIG_SH2_STAT5 | 101 | 104 | PF00017 | 0.581 |
LIG_SH2_STAT5 | 187 | 190 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 328 | 331 | PF00017 | 0.275 |
LIG_SH2_STAT5 | 397 | 400 | PF00017 | 0.210 |
LIG_SH2_STAT5 | 425 | 428 | PF00017 | 0.221 |
LIG_SH2_STAT5 | 509 | 512 | PF00017 | 0.224 |
LIG_SH2_STAT5 | 531 | 534 | PF00017 | 0.216 |
LIG_SH2_STAT5 | 635 | 638 | PF00017 | 0.239 |
LIG_SH2_STAT5 | 682 | 685 | PF00017 | 0.212 |
LIG_SH2_STAT5 | 697 | 700 | PF00017 | 0.253 |
LIG_SH2_STAT5 | 774 | 777 | PF00017 | 0.221 |
LIG_SH2_STAT5 | 793 | 796 | PF00017 | 0.221 |
LIG_SH2_STAT5 | 829 | 832 | PF00017 | 0.267 |
LIG_SH2_STAT5 | 848 | 851 | PF00017 | 0.390 |
LIG_SH3_2 | 277 | 282 | PF14604 | 0.344 |
LIG_SH3_3 | 160 | 166 | PF00018 | 0.322 |
LIG_SH3_3 | 274 | 280 | PF00018 | 0.415 |
LIG_SH3_3 | 474 | 480 | PF00018 | 0.244 |
LIG_SH3_3 | 515 | 521 | PF00018 | 0.284 |
LIG_SH3_3 | 549 | 555 | PF00018 | 0.265 |
LIG_SH3_3 | 88 | 94 | PF00018 | 0.501 |
LIG_SH3_3 | 901 | 907 | PF00018 | 0.421 |
LIG_SUMO_SIM_par_1 | 565 | 571 | PF11976 | 0.231 |
LIG_TRAF2_1 | 379 | 382 | PF00917 | 0.477 |
LIG_TYR_ITIM | 423 | 428 | PF00017 | 0.253 |
LIG_TYR_ITIM | 789 | 794 | PF00017 | 0.267 |
LIG_UBA3_1 | 254 | 261 | PF00899 | 0.248 |
MOD_CDC14_SPxK_1 | 279 | 282 | PF00782 | 0.263 |
MOD_CDK_SPxK_1 | 276 | 282 | PF00069 | 0.268 |
MOD_CDK_SPxxK_3 | 554 | 561 | PF00069 | 0.277 |
MOD_CK1_1 | 236 | 242 | PF00069 | 0.462 |
MOD_CK1_1 | 352 | 358 | PF00069 | 0.463 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.511 |
MOD_CK1_1 | 554 | 560 | PF00069 | 0.339 |
MOD_CK1_1 | 710 | 716 | PF00069 | 0.206 |
MOD_CK1_1 | 719 | 725 | PF00069 | 0.213 |
MOD_CK2_1 | 28 | 34 | PF00069 | 0.560 |
MOD_CK2_1 | 282 | 288 | PF00069 | 0.263 |
MOD_CK2_1 | 789 | 795 | PF00069 | 0.277 |
MOD_CMANNOS | 123 | 126 | PF00535 | 0.390 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.464 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.423 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.605 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.414 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.467 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.363 |
MOD_GlcNHglycan | 515 | 518 | PF01048 | 0.512 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.406 |
MOD_GlcNHglycan | 620 | 624 | PF01048 | 0.466 |
MOD_GlcNHglycan | 645 | 648 | PF01048 | 0.460 |
MOD_GlcNHglycan | 754 | 757 | PF01048 | 0.516 |
MOD_GlcNHglycan | 893 | 898 | PF01048 | 0.279 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.411 |
MOD_GlcNHglycan | 923 | 926 | PF01048 | 0.199 |
MOD_GlcNHglycan | 957 | 960 | PF01048 | 0.255 |
MOD_GlcNHglycan | 966 | 969 | PF01048 | 0.212 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.696 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.345 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.363 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.478 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.556 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.230 |
MOD_GSK3_1 | 438 | 445 | PF00069 | 0.227 |
MOD_GSK3_1 | 748 | 755 | PF00069 | 0.281 |
MOD_GSK3_1 | 762 | 769 | PF00069 | 0.180 |
MOD_GSK3_1 | 796 | 803 | PF00069 | 0.227 |
MOD_GSK3_1 | 889 | 896 | PF00069 | 0.535 |
MOD_GSK3_1 | 899 | 906 | PF00069 | 0.472 |
MOD_GSK3_1 | 928 | 935 | PF00069 | 0.465 |
MOD_LATS_1 | 347 | 353 | PF00433 | 0.448 |
MOD_N-GLC_1 | 648 | 653 | PF02516 | 0.432 |
MOD_N-GLC_1 | 707 | 712 | PF02516 | 0.410 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.322 |
MOD_NEK2_1 | 323 | 328 | PF00069 | 0.285 |
MOD_NEK2_1 | 350 | 355 | PF00069 | 0.412 |
MOD_NEK2_1 | 418 | 423 | PF00069 | 0.210 |
MOD_NEK2_1 | 513 | 518 | PF00069 | 0.301 |
MOD_NEK2_1 | 583 | 588 | PF00069 | 0.162 |
MOD_NEK2_1 | 611 | 616 | PF00069 | 0.240 |
MOD_NEK2_1 | 638 | 643 | PF00069 | 0.266 |
MOD_NEK2_1 | 653 | 658 | PF00069 | 0.167 |
MOD_NEK2_1 | 752 | 757 | PF00069 | 0.323 |
MOD_NEK2_1 | 840 | 845 | PF00069 | 0.263 |
MOD_NEK2_1 | 880 | 885 | PF00069 | 0.464 |
MOD_NEK2_1 | 950 | 955 | PF00069 | 0.421 |
MOD_NEK2_2 | 539 | 544 | PF00069 | 0.304 |
MOD_PIKK_1 | 648 | 654 | PF00454 | 0.210 |
MOD_PIKK_1 | 65 | 71 | PF00454 | 0.470 |
MOD_PIKK_1 | 710 | 716 | PF00454 | 0.191 |
MOD_PIKK_1 | 907 | 913 | PF00454 | 0.410 |
MOD_PKA_2 | 236 | 242 | PF00069 | 0.462 |
MOD_PKA_2 | 283 | 289 | PF00069 | 0.318 |
MOD_PKA_2 | 359 | 365 | PF00069 | 0.540 |
MOD_PKA_2 | 36 | 42 | PF00069 | 0.547 |
MOD_PKA_2 | 513 | 519 | PF00069 | 0.277 |
MOD_PKA_2 | 630 | 636 | PF00069 | 0.272 |
MOD_PKA_2 | 752 | 758 | PF00069 | 0.320 |
MOD_PKA_2 | 899 | 905 | PF00069 | 0.524 |
MOD_PKA_2 | 964 | 970 | PF00069 | 0.410 |
MOD_PKB_1 | 220 | 228 | PF00069 | 0.404 |
MOD_PKB_1 | 235 | 243 | PF00069 | 0.363 |
MOD_Plk_1 | 583 | 589 | PF00069 | 0.262 |
MOD_Plk_1 | 594 | 600 | PF00069 | 0.255 |
MOD_Plk_1 | 654 | 660 | PF00069 | 0.213 |
MOD_Plk_1 | 789 | 795 | PF00069 | 0.253 |
MOD_Plk_4 | 414 | 420 | PF00069 | 0.210 |
MOD_Plk_4 | 462 | 468 | PF00069 | 0.293 |
MOD_Plk_4 | 611 | 617 | PF00069 | 0.299 |
MOD_Plk_4 | 789 | 795 | PF00069 | 0.326 |
MOD_Plk_4 | 802 | 808 | PF00069 | 0.213 |
MOD_Plk_4 | 899 | 905 | PF00069 | 0.467 |
MOD_ProDKin_1 | 276 | 282 | PF00069 | 0.376 |
MOD_ProDKin_1 | 453 | 459 | PF00069 | 0.312 |
MOD_ProDKin_1 | 476 | 482 | PF00069 | 0.310 |
MOD_ProDKin_1 | 551 | 557 | PF00069 | 0.210 |
MOD_ProDKin_1 | 903 | 909 | PF00069 | 0.512 |
TRG_DiLeu_BaEn_2 | 594 | 600 | PF01217 | 0.241 |
TRG_DiLeu_BaEn_2 | 73 | 79 | PF01217 | 0.587 |
TRG_DiLeu_BaLyEn_6 | 250 | 255 | PF01217 | 0.300 |
TRG_DiLeu_BaLyEn_6 | 426 | 431 | PF01217 | 0.277 |
TRG_DiLeu_BaLyEn_6 | 873 | 878 | PF01217 | 0.391 |
TRG_ENDOCYTIC_2 | 1000 | 1003 | PF00928 | 0.543 |
TRG_ENDOCYTIC_2 | 215 | 218 | PF00928 | 0.419 |
TRG_ENDOCYTIC_2 | 425 | 428 | PF00928 | 0.221 |
TRG_ENDOCYTIC_2 | 535 | 538 | PF00928 | 0.218 |
TRG_ENDOCYTIC_2 | 635 | 638 | PF00928 | 0.226 |
TRG_ENDOCYTIC_2 | 682 | 685 | PF00928 | 0.211 |
TRG_ENDOCYTIC_2 | 774 | 777 | PF00928 | 0.237 |
TRG_ENDOCYTIC_2 | 791 | 794 | PF00928 | 0.236 |
TRG_ER_diArg_1 | 141 | 144 | PF00400 | 0.285 |
TRG_ER_diArg_1 | 183 | 186 | PF00400 | 0.246 |
TRG_ER_diArg_1 | 219 | 222 | PF00400 | 0.399 |
TRG_ER_diArg_1 | 234 | 237 | PF00400 | 0.364 |
TRG_ER_diArg_1 | 336 | 338 | PF00400 | 0.225 |
TRG_ER_diArg_1 | 578 | 580 | PF00400 | 0.235 |
TRG_ER_diArg_1 | 699 | 702 | PF00400 | 0.229 |
TRG_ER_diArg_1 | 739 | 741 | PF00400 | 0.284 |
TRG_ER_diArg_1 | 814 | 817 | PF00400 | 0.237 |
TRG_ER_diArg_1 | 940 | 942 | PF00400 | 0.466 |
TRG_Pf-PMV_PEXEL_1 | 740 | 744 | PF00026 | 0.512 |
TRG_Pf-PMV_PEXEL_1 | 821 | 825 | PF00026 | 0.453 |
TRG_Pf-PMV_PEXEL_1 | 863 | 867 | PF00026 | 0.191 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0E0SP71 | Gibberella zeae (strain ATCC MYA-4620 / CBS 123657 / FGSC 9075 / NRRL 31084 / PH-1) | 35% | 100% |
A0A0N0P5W0 | Leptomonas seymouri | 75% | 100% |
A0A0S4JCG8 | Bodo saltans | 52% | 100% |
A0A0U2U4F3 | Barbarea vulgaris | 35% | 100% |
A0A125SXN1 | Lycopodium clavatum | 33% | 100% |
A0A125SXN2 | Lycopodium clavatum | 31% | 100% |
A0A125SXN3 | Lycopodium clavatum | 38% | 100% |
A0A1X0NL88 | Trypanosomatidae | 55% | 100% |
A0A3R7KVQ6 | Trypanosoma rangeli | 57% | 100% |
A0A3S5H5R6 | Leishmania donovani | 82% | 100% |
A0A455LRW3 | Nectria sp. | 32% | 100% |
A1CVK0 | Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / CBS 544.65 / FGSC A1164 / JCM 1740 / NRRL 181 / WB 181) | 37% | 100% |
A4HSV6 | Leishmania infantum | 82% | 100% |
B0Y5B4 | Neosartorya fumigata (strain CEA10 / CBS 144.89 / FGSC A1163) | 37% | 100% |
B6EXY6 | Arabidopsis thaliana | 36% | 100% |
B9X0J1 | Stevia rebaudiana | 34% | 100% |
C9ZTG7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 100% |
D7NJ68 | Ganoderma lucidum | 39% | 100% |
E2IUA6 | Kalanchoe daigremontiana | 35% | 100% |
E2IUA8 | Kalanchoe daigremontiana | 37% | 100% |
E2IUB0 | Kalanchoe daigremontiana | 39% | 100% |
E4V6I8 | Arthroderma gypseum (strain ATCC MYA-4604 / CBS 118893) | 33% | 100% |
E7DN63 | Solanum lycopersicum | 36% | 100% |
E7DN64 | Solanum lycopersicum | 35% | 100% |
E9AKU4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
H2KWF1 | Oryza sativa subsp. japonica | 36% | 100% |
K7NBZ9 | Siraitia grosvenorii | 39% | 100% |
O23390 | Arabidopsis thaliana | 30% | 100% |
O82139 | Panax ginseng | 39% | 100% |
P0C8Y0 | Arabidopsis thaliana | 35% | 100% |
P38604 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 35% | 100% |
P38605 | Arabidopsis thaliana | 39% | 100% |
Q08IT1 | Panax ginseng | 31% | 100% |
Q10231 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 34% | 100% |
Q2XPU6 | Ricinus communis | 40% | 100% |
Q4QJ13 | Leishmania major | 83% | 100% |
Q4WES9 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 36% | 100% |
Q4WR16 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 37% | 100% |
Q6BE23 | Cucurbita pepo | 38% | 100% |
Q6BE25 | Cucurbita pepo | 40% | 100% |
Q6Z2X6 | Oryza sativa subsp. japonica | 40% | 100% |
Q8W3Z1 | Betula platyphylla | 36% | 100% |
Q8W3Z2 | Betula platyphylla | 35% | 100% |
Q8W3Z3 | Betula platyphylla | 40% | 100% |
Q8W3Z4 | Betula platyphylla | 40% | 100% |
Q948R6 | Luffa aegyptiaca | 34% | 100% |
Q96WJ0 | Pneumocystis carinii | 37% | 100% |
Q9C5M3 | Arabidopsis thaliana | 36% | 100% |
Q9FI37 | Arabidopsis thaliana | 33% | 100% |
Q9FJV8 | Arabidopsis thaliana | 29% | 100% |
Q9FR95 | Arabidopsis thaliana | 32% | 100% |
Q9FZI2 | Arabidopsis thaliana | 34% | 100% |
Q9LRH8 | Pisum sativum | 36% | 100% |
Q9LS68 | Arabidopsis thaliana | 31% | 100% |
Q9LVY2 | Arabidopsis thaliana | 31% | 100% |
Q9SLP9 | Luffa aegyptiaca | 40% | 100% |
Q9SXV6 | Glycyrrhiza glabra | 40% | 100% |
Q9SYN1 | Arabidopsis thaliana | 33% | 100% |
V5DPI3 | Trypanosoma cruzi | 58% | 100% |