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: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005942 | phosphatidylinositol 3-kinase complex | 3 | 11 |
GO:0032991 | protein-containing complex | 1 | 11 |
GO:0035032 | phosphatidylinositol 3-kinase complex, class III | 4 | 11 |
GO:0061695 | transferase complex, transferring phosphorus-containing groups | 4 | 11 |
GO:0070772 | PAS complex | 5 | 11 |
GO:0098796 | membrane protein complex | 2 | 11 |
GO:1902494 | catalytic complex | 2 | 11 |
GO:1990234 | transferase complex | 3 | 11 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0010008 | endosome membrane | 5 | 1 |
GO:0012506 | vesicle membrane | 4 | 1 |
GO:0016020 | membrane | 2 | 1 |
GO:0030659 | cytoplasmic vesicle membrane | 5 | 1 |
GO:0031090 | organelle membrane | 3 | 1 |
GO:0098588 | bounding membrane of organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9APZ3
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 11 |
GO:0006644 | phospholipid metabolic process | 4 | 11 |
GO:0006650 | glycerophospholipid metabolic process | 5 | 11 |
GO:0006661 | phosphatidylinositol biosynthetic process | 6 | 11 |
GO:0006793 | phosphorus metabolic process | 3 | 11 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0008610 | lipid biosynthetic process | 4 | 11 |
GO:0008654 | phospholipid biosynthetic process | 5 | 11 |
GO:0009058 | biosynthetic process | 2 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0019637 | organophosphate metabolic process | 3 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0044249 | cellular biosynthetic process | 3 | 11 |
GO:0044255 | cellular lipid metabolic process | 3 | 11 |
GO:0045017 | glycerolipid biosynthetic process | 4 | 11 |
GO:0046474 | glycerophospholipid biosynthetic process | 5 | 11 |
GO:0046486 | glycerolipid metabolic process | 4 | 11 |
GO:0046488 | phosphatidylinositol metabolic process | 6 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0090407 | organophosphate biosynthetic process | 4 | 11 |
GO:1901576 | organic substance biosynthetic process | 3 | 11 |
GO:0009893 | positive regulation of metabolic process | 4 | 1 |
GO:0010562 | positive regulation of phosphorus metabolic process | 6 | 1 |
GO:0019220 | regulation of phosphate metabolic process | 6 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031325 | positive regulation of cellular metabolic process | 5 | 1 |
GO:0033674 | positive regulation of kinase activity | 6 | 1 |
GO:0042325 | regulation of phosphorylation | 7 | 1 |
GO:0042327 | positive regulation of phosphorylation | 8 | 1 |
GO:0043085 | positive regulation of catalytic activity | 4 | 1 |
GO:0043549 | regulation of kinase activity | 5 | 1 |
GO:0044093 | positive regulation of molecular function | 3 | 1 |
GO:0045937 | positive regulation of phosphate metabolic process | 7 | 1 |
GO:0048518 | positive regulation of biological process | 3 | 1 |
GO:0048522 | positive regulation of cellular process | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050790 | regulation of catalytic activity | 3 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051174 | regulation of phosphorus metabolic process | 5 | 1 |
GO:0051338 | regulation of transferase activity | 4 | 1 |
GO:0051347 | positive regulation of transferase activity | 5 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065009 | regulation of molecular function | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 103 | 107 | PF00656 | 0.335 |
CLV_C14_Caspase3-7 | 327 | 331 | PF00656 | 0.531 |
CLV_C14_Caspase3-7 | 350 | 354 | PF00656 | 0.513 |
CLV_C14_Caspase3-7 | 369 | 373 | PF00656 | 0.278 |
CLV_NRD_NRD_1 | 10 | 12 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 459 | 461 | PF00675 | 0.428 |
CLV_NRD_NRD_1 | 466 | 468 | PF00675 | 0.385 |
CLV_NRD_NRD_1 | 526 | 528 | PF00675 | 0.422 |
CLV_NRD_NRD_1 | 566 | 568 | PF00675 | 0.334 |
CLV_NRD_NRD_1 | 636 | 638 | PF00675 | 0.285 |
CLV_NRD_NRD_1 | 69 | 71 | PF00675 | 0.304 |
CLV_PCSK_FUR_1 | 149 | 153 | PF00082 | 0.407 |
CLV_PCSK_KEX2_1 | 151 | 153 | PF00082 | 0.362 |
CLV_PCSK_KEX2_1 | 459 | 461 | PF00082 | 0.428 |
CLV_PCSK_KEX2_1 | 466 | 468 | PF00082 | 0.385 |
CLV_PCSK_KEX2_1 | 526 | 528 | PF00082 | 0.425 |
CLV_PCSK_KEX2_1 | 566 | 568 | PF00082 | 0.337 |
CLV_PCSK_KEX2_1 | 636 | 638 | PF00082 | 0.285 |
CLV_PCSK_KEX2_1 | 69 | 71 | PF00082 | 0.289 |
CLV_PCSK_PC1ET2_1 | 151 | 153 | PF00082 | 0.362 |
CLV_PCSK_PC7_1 | 522 | 528 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 11 | 15 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 151 | 155 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 216 | 220 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 235 | 239 | PF00082 | 0.345 |
CLV_PCSK_SKI1_1 | 365 | 369 | PF00082 | 0.455 |
CLV_PCSK_SKI1_1 | 503 | 507 | PF00082 | 0.314 |
CLV_PCSK_SKI1_1 | 522 | 526 | PF00082 | 0.148 |
CLV_PCSK_SKI1_1 | 527 | 531 | PF00082 | 0.318 |
CLV_Separin_Metazoa | 121 | 125 | PF03568 | 0.422 |
DEG_APCC_DBOX_1 | 364 | 372 | PF00400 | 0.451 |
DEG_APCC_DBOX_1 | 69 | 77 | PF00400 | 0.304 |
DEG_MDM2_SWIB_1 | 293 | 301 | PF02201 | 0.432 |
DOC_CYCLIN_RxL_1 | 232 | 241 | PF00134 | 0.351 |
DOC_CYCLIN_yCln2_LP_2 | 96 | 102 | PF00134 | 0.159 |
DOC_MAPK_gen_1 | 636 | 643 | PF00069 | 0.407 |
DOC_MAPK_gen_1 | 69 | 76 | PF00069 | 0.329 |
DOC_MAPK_HePTP_8 | 633 | 645 | PF00069 | 0.245 |
DOC_MAPK_MEF2A_6 | 408 | 415 | PF00069 | 0.401 |
DOC_MAPK_MEF2A_6 | 481 | 488 | PF00069 | 0.422 |
DOC_MAPK_MEF2A_6 | 499 | 508 | PF00069 | 0.329 |
DOC_MAPK_MEF2A_6 | 636 | 645 | PF00069 | 0.496 |
DOC_MAPK_NFAT4_5 | 408 | 416 | PF00069 | 0.401 |
DOC_MAPK_RevD_3 | 553 | 567 | PF00069 | 0.334 |
DOC_PP2B_LxvP_1 | 219 | 222 | PF13499 | 0.390 |
DOC_PP2B_LxvP_1 | 622 | 625 | PF13499 | 0.285 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.499 |
DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.499 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 347 | 351 | PF00917 | 0.461 |
DOC_USP7_MATH_1 | 395 | 399 | PF00917 | 0.520 |
DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.422 |
DOC_WW_Pin1_4 | 625 | 630 | PF00397 | 0.290 |
LIG_14-3-3_CanoR_1 | 132 | 142 | PF00244 | 0.381 |
LIG_14-3-3_CanoR_1 | 170 | 178 | PF00244 | 0.456 |
LIG_14-3-3_CanoR_1 | 32 | 40 | PF00244 | 0.453 |
LIG_14-3-3_CanoR_1 | 408 | 412 | PF00244 | 0.428 |
LIG_14-3-3_CanoR_1 | 466 | 472 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 490 | 498 | PF00244 | 0.422 |
LIG_14-3-3_CanoR_1 | 601 | 605 | PF00244 | 0.329 |
LIG_14-3-3_CanoR_1 | 62 | 68 | PF00244 | 0.418 |
LIG_Actin_WH2_1 | 408 | 425 | PF00022 | 0.299 |
LIG_Actin_WH2_2 | 200 | 218 | PF00022 | 0.479 |
LIG_Actin_WH2_2 | 458 | 474 | PF00022 | 0.352 |
LIG_Actin_WH2_2 | 46 | 64 | PF00022 | 0.443 |
LIG_Actin_WH2_2 | 485 | 501 | PF00022 | 0.407 |
LIG_Actin_WH2_2 | 585 | 603 | PF00022 | 0.407 |
LIG_AP2alpha_1 | 135 | 139 | PF02296 | 0.407 |
LIG_APCC_ABBA_1 | 304 | 309 | PF00400 | 0.460 |
LIG_BIR_III_2 | 106 | 110 | PF00653 | 0.407 |
LIG_BRCT_BRCA1_1 | 593 | 597 | PF00533 | 0.329 |
LIG_CaM_IQ_9 | 4 | 20 | PF13499 | 0.353 |
LIG_Clathr_ClatBox_1 | 644 | 648 | PF01394 | 0.469 |
LIG_deltaCOP1_diTrp_1 | 129 | 135 | PF00928 | 0.334 |
LIG_eIF4E_1 | 547 | 553 | PF01652 | 0.407 |
LIG_eIF4E_1 | 618 | 624 | PF01652 | 0.422 |
LIG_eIF4E_1 | 68 | 74 | PF01652 | 0.407 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.448 |
LIG_FHA_1 | 408 | 414 | PF00498 | 0.371 |
LIG_FHA_1 | 563 | 569 | PF00498 | 0.422 |
LIG_FHA_1 | 614 | 620 | PF00498 | 0.407 |
LIG_FHA_1 | 62 | 68 | PF00498 | 0.455 |
LIG_FHA_1 | 640 | 646 | PF00498 | 0.524 |
LIG_FHA_2 | 161 | 167 | PF00498 | 0.335 |
LIG_FHA_2 | 265 | 271 | PF00498 | 0.456 |
LIG_FHA_2 | 320 | 326 | PF00498 | 0.400 |
LIG_FHA_2 | 338 | 344 | PF00498 | 0.468 |
LIG_FHA_2 | 512 | 518 | PF00498 | 0.285 |
LIG_FHA_2 | 528 | 534 | PF00498 | 0.285 |
LIG_GBD_Chelix_1 | 504 | 512 | PF00786 | 0.422 |
LIG_GBD_Chelix_1 | 613 | 621 | PF00786 | 0.407 |
LIG_LIR_Gen_1 | 117 | 128 | PF02991 | 0.441 |
LIG_LIR_Gen_1 | 136 | 146 | PF02991 | 0.322 |
LIG_LIR_Gen_1 | 180 | 189 | PF02991 | 0.346 |
LIG_LIR_Gen_1 | 246 | 254 | PF02991 | 0.491 |
LIG_LIR_Gen_1 | 385 | 394 | PF02991 | 0.332 |
LIG_LIR_Gen_1 | 536 | 543 | PF02991 | 0.468 |
LIG_LIR_Gen_1 | 581 | 589 | PF02991 | 0.392 |
LIG_LIR_Gen_1 | 594 | 605 | PF02991 | 0.236 |
LIG_LIR_Gen_1 | 616 | 625 | PF02991 | 0.422 |
LIG_LIR_Gen_1 | 628 | 638 | PF02991 | 0.329 |
LIG_LIR_LC3C_4 | 196 | 201 | PF02991 | 0.624 |
LIG_LIR_Nem_3 | 117 | 123 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 136 | 142 | PF02991 | 0.302 |
LIG_LIR_Nem_3 | 180 | 184 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 246 | 252 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 34 | 40 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 361 | 367 | PF02991 | 0.248 |
LIG_LIR_Nem_3 | 385 | 389 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 514 | 518 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 536 | 541 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 581 | 585 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 594 | 600 | PF02991 | 0.220 |
LIG_LIR_Nem_3 | 616 | 621 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 628 | 634 | PF02991 | 0.292 |
LIG_NRBOX | 233 | 239 | PF00104 | 0.363 |
LIG_NRBOX | 383 | 389 | PF00104 | 0.435 |
LIG_NRBOX | 444 | 450 | PF00104 | 0.464 |
LIG_NRBOX | 616 | 622 | PF00104 | 0.407 |
LIG_NRBOX | 92 | 98 | PF00104 | 0.422 |
LIG_Pex14_1 | 131 | 135 | PF04695 | 0.352 |
LIG_Pex14_2 | 135 | 139 | PF04695 | 0.280 |
LIG_Pex14_2 | 293 | 297 | PF04695 | 0.429 |
LIG_SH2_CRK | 547 | 551 | PF00017 | 0.285 |
LIG_SH2_CRK | 631 | 635 | PF00017 | 0.314 |
LIG_SH2_NCK_1 | 547 | 551 | PF00017 | 0.285 |
LIG_SH2_PTP2 | 582 | 585 | PF00017 | 0.400 |
LIG_SH2_PTP2 | 618 | 621 | PF00017 | 0.422 |
LIG_SH2_STAP1 | 681 | 685 | PF00017 | 0.557 |
LIG_SH2_STAT3 | 453 | 456 | PF00017 | 0.292 |
LIG_SH2_STAT5 | 192 | 195 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 582 | 585 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 618 | 621 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 671 | 674 | PF00017 | 0.476 |
LIG_SH3_3 | 81 | 87 | PF00018 | 0.410 |
LIG_SUMO_SIM_anti_2 | 385 | 391 | PF11976 | 0.320 |
LIG_SUMO_SIM_anti_2 | 46 | 52 | PF11976 | 0.522 |
LIG_SUMO_SIM_par_1 | 193 | 202 | PF11976 | 0.595 |
LIG_SUMO_SIM_par_1 | 347 | 353 | PF11976 | 0.477 |
LIG_SUMO_SIM_par_1 | 410 | 418 | PF11976 | 0.279 |
LIG_SUMO_SIM_par_1 | 46 | 52 | PF11976 | 0.485 |
LIG_TRAF2_1 | 340 | 343 | PF00917 | 0.475 |
LIG_TRAF2_1 | 375 | 378 | PF00917 | 0.484 |
LIG_TRAF2_1 | 673 | 676 | PF00917 | 0.520 |
LIG_UBA3_1 | 4 | 12 | PF00899 | 0.278 |
LIG_WRC_WIRS_1 | 178 | 183 | PF05994 | 0.409 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.371 |
MOD_CK1_1 | 229 | 235 | PF00069 | 0.392 |
MOD_CK1_1 | 243 | 249 | PF00069 | 0.351 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.535 |
MOD_CK1_1 | 287 | 293 | PF00069 | 0.383 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.529 |
MOD_CK1_1 | 493 | 499 | PF00069 | 0.400 |
MOD_CK1_1 | 578 | 584 | PF00069 | 0.304 |
MOD_CK1_1 | 595 | 601 | PF00069 | 0.304 |
MOD_CK2_1 | 160 | 166 | PF00069 | 0.362 |
MOD_CK2_1 | 319 | 325 | PF00069 | 0.397 |
MOD_CK2_1 | 337 | 343 | PF00069 | 0.306 |
MOD_CK2_1 | 363 | 369 | PF00069 | 0.421 |
MOD_CK2_1 | 470 | 476 | PF00069 | 0.422 |
MOD_CK2_1 | 511 | 517 | PF00069 | 0.285 |
MOD_CK2_1 | 670 | 676 | PF00069 | 0.433 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.487 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.599 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.564 |
MOD_GlcNHglycan | 286 | 289 | PF01048 | 0.495 |
MOD_GlcNHglycan | 355 | 358 | PF01048 | 0.535 |
MOD_GlcNHglycan | 372 | 375 | PF01048 | 0.369 |
MOD_GlcNHglycan | 472 | 475 | PF01048 | 0.469 |
MOD_GlcNHglycan | 662 | 666 | PF01048 | 0.504 |
MOD_GlcNHglycan | 672 | 675 | PF01048 | 0.452 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.407 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.387 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.581 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.395 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.401 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.498 |
MOD_GSK3_1 | 527 | 534 | PF00069 | 0.159 |
MOD_GSK3_1 | 591 | 598 | PF00069 | 0.407 |
MOD_N-GLC_1 | 190 | 195 | PF02516 | 0.433 |
MOD_N-GLC_1 | 243 | 248 | PF02516 | 0.500 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.499 |
MOD_NEK2_1 | 226 | 231 | PF00069 | 0.470 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.280 |
MOD_NEK2_1 | 319 | 324 | PF00069 | 0.473 |
MOD_NEK2_1 | 363 | 368 | PF00069 | 0.428 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.486 |
MOD_NEK2_1 | 511 | 516 | PF00069 | 0.298 |
MOD_NEK2_1 | 537 | 542 | PF00069 | 0.370 |
MOD_NEK2_1 | 562 | 567 | PF00069 | 0.425 |
MOD_NEK2_1 | 592 | 597 | PF00069 | 0.413 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.378 |
MOD_NEK2_1 | 600 | 605 | PF00069 | 0.376 |
MOD_NEK2_1 | 613 | 618 | PF00069 | 0.285 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.455 |
MOD_PIKK_1 | 205 | 211 | PF00454 | 0.496 |
MOD_PIKK_1 | 257 | 263 | PF00454 | 0.526 |
MOD_PIKK_1 | 31 | 37 | PF00454 | 0.441 |
MOD_PKA_2 | 133 | 139 | PF00069 | 0.407 |
MOD_PKA_2 | 31 | 37 | PF00069 | 0.445 |
MOD_PKA_2 | 407 | 413 | PF00069 | 0.410 |
MOD_PKA_2 | 422 | 428 | PF00069 | 0.295 |
MOD_PKA_2 | 600 | 606 | PF00069 | 0.329 |
MOD_PKA_2 | 61 | 67 | PF00069 | 0.401 |
MOD_Plk_1 | 324 | 330 | PF00069 | 0.382 |
MOD_Plk_1 | 376 | 382 | PF00069 | 0.341 |
MOD_Plk_1 | 575 | 581 | PF00069 | 0.407 |
MOD_Plk_1 | 592 | 598 | PF00069 | 0.407 |
MOD_Plk_2-3 | 325 | 331 | PF00069 | 0.354 |
MOD_Plk_4 | 180 | 186 | PF00069 | 0.381 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.382 |
MOD_Plk_4 | 376 | 382 | PF00069 | 0.495 |
MOD_Plk_4 | 537 | 543 | PF00069 | 0.322 |
MOD_Plk_4 | 578 | 584 | PF00069 | 0.308 |
MOD_Plk_4 | 600 | 606 | PF00069 | 0.310 |
MOD_Plk_4 | 613 | 619 | PF00069 | 0.362 |
MOD_Plk_4 | 639 | 645 | PF00069 | 0.472 |
MOD_ProDKin_1 | 625 | 631 | PF00069 | 0.290 |
TRG_DiLeu_BaEn_4 | 46 | 52 | PF01217 | 0.398 |
TRG_DiLeu_BaLyEn_6 | 444 | 449 | PF01217 | 0.455 |
TRG_ENDOCYTIC_2 | 120 | 123 | PF00928 | 0.383 |
TRG_ENDOCYTIC_2 | 37 | 40 | PF00928 | 0.474 |
TRG_ENDOCYTIC_2 | 547 | 550 | PF00928 | 0.289 |
TRG_ENDOCYTIC_2 | 582 | 585 | PF00928 | 0.380 |
TRG_ENDOCYTIC_2 | 618 | 621 | PF00928 | 0.422 |
TRG_ENDOCYTIC_2 | 631 | 634 | PF00928 | 0.292 |
TRG_ER_diArg_1 | 131 | 134 | PF00400 | 0.159 |
TRG_ER_diArg_1 | 289 | 292 | PF00400 | 0.447 |
TRG_ER_diArg_1 | 458 | 460 | PF00400 | 0.428 |
TRG_ER_diArg_1 | 465 | 467 | PF00400 | 0.385 |
TRG_ER_diArg_1 | 525 | 527 | PF00400 | 0.422 |
TRG_ER_diArg_1 | 566 | 568 | PF00400 | 0.334 |
TRG_ER_diArg_1 | 636 | 638 | PF00400 | 0.288 |
TRG_ER_diArg_1 | 68 | 70 | PF00400 | 0.306 |
TRG_NES_CRM1_1 | 296 | 309 | PF08389 | 0.470 |
TRG_NES_CRM1_1 | 497 | 509 | PF08389 | 0.422 |
TRG_Pf-PMV_PEXEL_1 | 12 | 16 | PF00026 | 0.498 |
TRG_Pf-PMV_PEXEL_1 | 490 | 494 | PF00026 | 0.229 |
TRG_Pf-PMV_PEXEL_1 | 566 | 570 | PF00026 | 0.422 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PC70 | Leptomonas seymouri | 60% | 99% |
A0A1X0NNZ5 | Trypanosomatidae | 30% | 99% |
A0A3Q8IA32 | Leishmania donovani | 91% | 100% |
A0A422N3V6 | Trypanosoma rangeli | 30% | 99% |
A4H7W5 | Leishmania braziliensis | 84% | 100% |
A4HW92 | Leishmania infantum | 91% | 100% |
C9ZSR9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 99% |
P87145 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 84% |
Q4QFI8 | Leishmania major | 91% | 100% |
Q9ZU97 | Arabidopsis thaliana | 27% | 92% |
V5AVZ7 | Trypanosoma cruzi | 30% | 99% |