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:0005777 | peroxisome | 6 | 2 |
GO:0005778 | peroxisomal membrane | 6 | 2 |
GO:0016020 | membrane | 2 | 12 |
GO:0020015 | glycosome | 7 | 2 |
GO:0020022 | acidocalcisome | 5 | 2 |
GO:0031090 | organelle membrane | 3 | 2 |
GO:0031903 | microbody membrane | 5 | 2 |
GO:0042579 | microbody | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0098588 | bounding membrane of organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: E9AD24
Term | Name | Level | Count |
---|---|---|---|
GO:0000038 | very long-chain fatty acid metabolic process | 5 | 2 |
GO:0006082 | organic acid metabolic process | 3 | 2 |
GO:0006629 | lipid metabolic process | 3 | 2 |
GO:0006631 | fatty acid metabolic process | 4 | 2 |
GO:0006635 | fatty acid beta-oxidation | 6 | 2 |
GO:0006810 | transport | 3 | 2 |
GO:0006869 | lipid transport | 5 | 2 |
GO:0006996 | organelle organization | 4 | 2 |
GO:0007031 | peroxisome organization | 5 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009056 | catabolic process | 2 | 2 |
GO:0009062 | fatty acid catabolic process | 5 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0015849 | organic acid transport | 5 | 2 |
GO:0015908 | fatty acid transport | 6 | 2 |
GO:0015909 | long-chain fatty acid transport | 7 | 2 |
GO:0015910 | long-chain fatty acid import into peroxisome | 5 | 2 |
GO:0015919 | peroxisomal membrane transport | 5 | 2 |
GO:0016042 | lipid catabolic process | 4 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0016054 | organic acid catabolic process | 4 | 2 |
GO:0019395 | fatty acid oxidation | 5 | 2 |
GO:0019752 | carboxylic acid metabolic process | 5 | 2 |
GO:0030258 | lipid modification | 4 | 2 |
GO:0032365 | intracellular lipid transport | 4 | 2 |
GO:0032787 | monocarboxylic acid metabolic process | 6 | 2 |
GO:0034440 | lipid oxidation | 5 | 2 |
GO:0042760 | very long-chain fatty acid catabolic process | 6 | 2 |
GO:0043436 | oxoacid metabolic process | 4 | 2 |
GO:0043574 | peroxisomal transport | 4 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044242 | cellular lipid catabolic process | 4 | 2 |
GO:0044248 | cellular catabolic process | 3 | 2 |
GO:0044255 | cellular lipid metabolic process | 3 | 2 |
GO:0044281 | small molecule metabolic process | 2 | 2 |
GO:0044282 | small molecule catabolic process | 3 | 2 |
GO:0046395 | carboxylic acid catabolic process | 5 | 2 |
GO:0046907 | intracellular transport | 3 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0051641 | cellular localization | 2 | 2 |
GO:0051649 | establishment of localization in cell | 3 | 2 |
GO:0055085 | transmembrane transport | 2 | 2 |
GO:0071702 | organic substance transport | 4 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0072329 | monocarboxylic acid catabolic process | 6 | 2 |
GO:1901575 | organic substance catabolic process | 3 | 2 |
GO:1902001 | fatty acid transmembrane transport | 5 | 2 |
GO:1903825 | organic acid transmembrane transport | 3 | 2 |
GO:1905039 | carboxylic acid transmembrane transport | 4 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0005215 | transporter activity | 1 | 12 |
GO:0005319 | lipid transporter activity | 2 | 2 |
GO:0005324 | long-chain fatty acid transporter activity | 3 | 2 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0015399 | primary active transmembrane transporter activity | 4 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0022804 | active transmembrane transporter activity | 3 | 12 |
GO:0022857 | transmembrane transporter activity | 2 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0042626 | ATPase-coupled transmembrane transporter activity | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140359 | ABC-type transporter activity | 3 | 12 |
GO:0140657 | ATP-dependent activity | 1 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 186 | 190 | PF00656 | 0.277 |
CLV_NRD_NRD_1 | 174 | 176 | PF00675 | 0.479 |
CLV_NRD_NRD_1 | 255 | 257 | PF00675 | 0.276 |
CLV_NRD_NRD_1 | 276 | 278 | PF00675 | 0.242 |
CLV_NRD_NRD_1 | 347 | 349 | PF00675 | 0.623 |
CLV_NRD_NRD_1 | 48 | 50 | PF00675 | 0.601 |
CLV_NRD_NRD_1 | 635 | 637 | PF00675 | 0.516 |
CLV_PCSK_KEX2_1 | 174 | 176 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 255 | 257 | PF00082 | 0.276 |
CLV_PCSK_KEX2_1 | 276 | 278 | PF00082 | 0.242 |
CLV_PCSK_KEX2_1 | 347 | 349 | PF00082 | 0.623 |
CLV_PCSK_KEX2_1 | 48 | 50 | PF00082 | 0.601 |
CLV_PCSK_KEX2_1 | 635 | 637 | PF00082 | 0.548 |
CLV_PCSK_PC7_1 | 44 | 50 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 102 | 106 | PF00082 | 0.332 |
CLV_PCSK_SKI1_1 | 238 | 242 | PF00082 | 0.421 |
CLV_PCSK_SKI1_1 | 276 | 280 | PF00082 | 0.265 |
CLV_PCSK_SKI1_1 | 296 | 300 | PF00082 | 0.126 |
CLV_PCSK_SKI1_1 | 508 | 512 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 597 | 601 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 78 | 82 | PF00082 | 0.467 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.726 |
DEG_SCF_FBW7_1 | 518 | 523 | PF00400 | 0.193 |
DOC_CDC14_PxL_1 | 216 | 224 | PF14671 | 0.315 |
DOC_CKS1_1 | 517 | 522 | PF01111 | 0.301 |
DOC_MAPK_gen_1 | 607 | 615 | PF00069 | 0.295 |
DOC_MAPK_gen_1 | 670 | 677 | PF00069 | 0.472 |
DOC_MAPK_MEF2A_6 | 102 | 109 | PF00069 | 0.358 |
DOC_MAPK_MEF2A_6 | 135 | 144 | PF00069 | 0.549 |
DOC_MAPK_MEF2A_6 | 353 | 362 | PF00069 | 0.341 |
DOC_MAPK_MEF2A_6 | 439 | 446 | PF00069 | 0.358 |
DOC_PP1_RVXF_1 | 595 | 601 | PF00149 | 0.341 |
DOC_PP2B_LxvP_1 | 493 | 496 | PF13499 | 0.275 |
DOC_PP4_FxxP_1 | 217 | 220 | PF00568 | 0.255 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.460 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 433 | 437 | PF00917 | 0.441 |
DOC_USP7_MATH_1 | 513 | 517 | PF00917 | 0.279 |
DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.671 |
DOC_WW_Pin1_4 | 419 | 424 | PF00397 | 0.417 |
DOC_WW_Pin1_4 | 450 | 455 | PF00397 | 0.331 |
DOC_WW_Pin1_4 | 509 | 514 | PF00397 | 0.338 |
DOC_WW_Pin1_4 | 516 | 521 | PF00397 | 0.325 |
DOC_WW_Pin1_4 | 535 | 540 | PF00397 | 0.370 |
DOC_WW_Pin1_4 | 608 | 613 | PF00397 | 0.295 |
LIG_14-3-3_CanoR_1 | 167 | 173 | PF00244 | 0.310 |
LIG_14-3-3_CanoR_1 | 3 | 11 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 347 | 355 | PF00244 | 0.436 |
LIG_14-3-3_CanoR_1 | 592 | 596 | PF00244 | 0.263 |
LIG_Actin_WH2_2 | 224 | 240 | PF00022 | 0.333 |
LIG_Actin_WH2_2 | 295 | 312 | PF00022 | 0.562 |
LIG_Actin_WH2_2 | 385 | 402 | PF00022 | 0.349 |
LIG_BRCT_BRCA1_1 | 168 | 172 | PF00533 | 0.279 |
LIG_BRCT_BRCA1_1 | 32 | 36 | PF00533 | 0.404 |
LIG_BRCT_BRCA1_1 | 505 | 509 | PF00533 | 0.297 |
LIG_BRCT_BRCA1_1 | 91 | 95 | PF00533 | 0.392 |
LIG_Clathr_ClatBox_1 | 443 | 447 | PF01394 | 0.356 |
LIG_CSL_BTD_1 | 493 | 496 | PF09270 | 0.279 |
LIG_eIF4E_1 | 359 | 365 | PF01652 | 0.395 |
LIG_FHA_1 | 246 | 252 | PF00498 | 0.461 |
LIG_FHA_1 | 278 | 284 | PF00498 | 0.479 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.406 |
LIG_FHA_1 | 482 | 488 | PF00498 | 0.266 |
LIG_FHA_1 | 536 | 542 | PF00498 | 0.341 |
LIG_FHA_1 | 64 | 70 | PF00498 | 0.446 |
LIG_FHA_1 | 653 | 659 | PF00498 | 0.296 |
LIG_FHA_2 | 184 | 190 | PF00498 | 0.261 |
LIG_FHA_2 | 408 | 414 | PF00498 | 0.472 |
LIG_FHA_2 | 521 | 527 | PF00498 | 0.255 |
LIG_FHA_2 | 57 | 63 | PF00498 | 0.423 |
LIG_FHA_2 | 624 | 630 | PF00498 | 0.381 |
LIG_FHA_2 | 643 | 649 | PF00498 | 0.181 |
LIG_GBD_Chelix_1 | 140 | 148 | PF00786 | 0.436 |
LIG_IRF3_LxIS_1 | 298 | 305 | PF10401 | 0.504 |
LIG_LIR_Apic_2 | 516 | 520 | PF02991 | 0.246 |
LIG_LIR_Gen_1 | 322 | 330 | PF02991 | 0.491 |
LIG_LIR_Gen_1 | 33 | 41 | PF02991 | 0.298 |
LIG_LIR_Gen_1 | 331 | 341 | PF02991 | 0.352 |
LIG_LIR_Gen_1 | 413 | 424 | PF02991 | 0.508 |
LIG_LIR_Gen_1 | 470 | 478 | PF02991 | 0.261 |
LIG_LIR_Gen_1 | 523 | 533 | PF02991 | 0.311 |
LIG_LIR_Gen_1 | 68 | 77 | PF02991 | 0.333 |
LIG_LIR_Gen_1 | 92 | 103 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 212 | 218 | PF02991 | 0.251 |
LIG_LIR_Nem_3 | 327 | 333 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 33 | 39 | PF02991 | 0.286 |
LIG_LIR_Nem_3 | 413 | 419 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 470 | 476 | PF02991 | 0.261 |
LIG_LIR_Nem_3 | 523 | 528 | PF02991 | 0.311 |
LIG_LIR_Nem_3 | 579 | 585 | PF02991 | 0.255 |
LIG_LIR_Nem_3 | 66 | 70 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 9 | 14 | PF02991 | 0.681 |
LIG_LIR_Nem_3 | 92 | 98 | PF02991 | 0.310 |
LIG_PCNA_yPIPBox_3 | 369 | 380 | PF02747 | 0.362 |
LIG_Pex14_2 | 172 | 176 | PF04695 | 0.279 |
LIG_Pex14_2 | 375 | 379 | PF04695 | 0.348 |
LIG_Pex14_2 | 95 | 99 | PF04695 | 0.307 |
LIG_SH2_CRK | 177 | 181 | PF00017 | 0.294 |
LIG_SH2_CRK | 19 | 23 | PF00017 | 0.670 |
LIG_SH2_CRK | 416 | 420 | PF00017 | 0.465 |
LIG_SH2_CRK | 517 | 521 | PF00017 | 0.279 |
LIG_SH2_CRK | 70 | 74 | PF00017 | 0.255 |
LIG_SH2_GRB2like | 282 | 285 | PF00017 | 0.536 |
LIG_SH2_SRC | 359 | 362 | PF00017 | 0.378 |
LIG_SH2_STAP1 | 564 | 568 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 202 | 205 | PF00017 | 0.261 |
LIG_SH2_STAT5 | 216 | 219 | PF00017 | 0.234 |
LIG_SH2_STAT5 | 282 | 285 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 297 | 300 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 359 | 362 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 426 | 429 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 46 | 49 | PF00017 | 0.413 |
LIG_SH3_3 | 417 | 423 | PF00018 | 0.474 |
LIG_SH3_3 | 531 | 537 | PF00018 | 0.278 |
LIG_SH3_3 | 668 | 674 | PF00018 | 0.459 |
LIG_SUMO_SIM_anti_2 | 610 | 618 | PF11976 | 0.293 |
LIG_SUMO_SIM_par_1 | 37 | 42 | PF11976 | 0.414 |
LIG_SUMO_SIM_par_1 | 610 | 618 | PF11976 | 0.263 |
LIG_SUMO_SIM_par_1 | 640 | 645 | PF11976 | 0.307 |
LIG_TRFH_1 | 509 | 513 | PF08558 | 0.341 |
LIG_TYR_ITIM | 213 | 218 | PF00017 | 0.255 |
LIG_TYR_ITSM | 521 | 528 | PF00017 | 0.341 |
LIG_UBA3_1 | 364 | 373 | PF00899 | 0.392 |
LIG_UBA3_1 | 489 | 497 | PF00899 | 0.341 |
LIG_UBA3_1 | 657 | 665 | PF00899 | 0.426 |
LIG_UBA3_1 | 94 | 102 | PF00899 | 0.350 |
LIG_WRC_WIRS_1 | 330 | 335 | PF05994 | 0.374 |
MOD_CDK_SPxxK_3 | 535 | 542 | PF00069 | 0.304 |
MOD_CK1_1 | 245 | 251 | PF00069 | 0.376 |
MOD_CK1_1 | 328 | 334 | PF00069 | 0.369 |
MOD_CK1_1 | 383 | 389 | PF00069 | 0.310 |
MOD_CK1_1 | 502 | 508 | PF00069 | 0.360 |
MOD_CK1_1 | 516 | 522 | PF00069 | 0.367 |
MOD_CK1_1 | 583 | 589 | PF00069 | 0.269 |
MOD_CK1_1 | 89 | 95 | PF00069 | 0.376 |
MOD_CK2_1 | 3 | 9 | PF00069 | 0.562 |
MOD_CK2_1 | 520 | 526 | PF00069 | 0.255 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.364 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.323 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.283 |
MOD_GlcNHglycan | 497 | 500 | PF01048 | 0.513 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.620 |
MOD_GlcNHglycan | 565 | 568 | PF01048 | 0.550 |
MOD_GlcNHglycan | 585 | 588 | PF01048 | 0.451 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.536 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.330 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.249 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.407 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.498 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.509 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.310 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.384 |
MOD_GSK3_1 | 411 | 418 | PF00069 | 0.484 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.474 |
MOD_GSK3_1 | 495 | 502 | PF00069 | 0.318 |
MOD_GSK3_1 | 509 | 516 | PF00069 | 0.266 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.469 |
MOD_GSK3_1 | 576 | 583 | PF00069 | 0.271 |
MOD_LATS_1 | 409 | 415 | PF00433 | 0.466 |
MOD_N-GLC_1 | 368 | 373 | PF02516 | 0.527 |
MOD_N-GLC_2 | 479 | 481 | PF02516 | 0.479 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.332 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.423 |
MOD_NEK2_1 | 302 | 307 | PF00069 | 0.541 |
MOD_NEK2_1 | 325 | 330 | PF00069 | 0.444 |
MOD_NEK2_1 | 368 | 373 | PF00069 | 0.326 |
MOD_NEK2_1 | 395 | 400 | PF00069 | 0.322 |
MOD_NEK2_1 | 407 | 412 | PF00069 | 0.411 |
MOD_NEK2_1 | 424 | 429 | PF00069 | 0.476 |
MOD_NEK2_1 | 571 | 576 | PF00069 | 0.326 |
MOD_NEK2_2 | 520 | 525 | PF00069 | 0.315 |
MOD_PIKK_1 | 263 | 269 | PF00454 | 0.541 |
MOD_PIKK_1 | 39 | 45 | PF00454 | 0.521 |
MOD_PIKK_1 | 424 | 430 | PF00454 | 0.479 |
MOD_PIKK_1 | 499 | 505 | PF00454 | 0.360 |
MOD_PIKK_1 | 60 | 66 | PF00454 | 0.486 |
MOD_PK_1 | 10 | 16 | PF00069 | 0.662 |
MOD_PK_1 | 640 | 646 | PF00069 | 0.305 |
MOD_PKA_2 | 166 | 172 | PF00069 | 0.255 |
MOD_PKA_2 | 346 | 352 | PF00069 | 0.468 |
MOD_PKA_2 | 591 | 597 | PF00069 | 0.279 |
MOD_PKA_2 | 86 | 92 | PF00069 | 0.371 |
MOD_PKB_1 | 165 | 173 | PF00069 | 0.304 |
MOD_Plk_1 | 302 | 308 | PF00069 | 0.541 |
MOD_Plk_1 | 368 | 374 | PF00069 | 0.313 |
MOD_Plk_1 | 380 | 386 | PF00069 | 0.276 |
MOD_Plk_1 | 395 | 401 | PF00069 | 0.315 |
MOD_Plk_1 | 503 | 509 | PF00069 | 0.268 |
MOD_Plk_1 | 576 | 582 | PF00069 | 0.266 |
MOD_Plk_1 | 60 | 66 | PF00069 | 0.433 |
MOD_Plk_1 | 617 | 623 | PF00069 | 0.255 |
MOD_Plk_2-3 | 466 | 472 | PF00069 | 0.313 |
MOD_Plk_2-3 | 618 | 624 | PF00069 | 0.350 |
MOD_Plk_4 | 183 | 189 | PF00069 | 0.277 |
MOD_Plk_4 | 329 | 335 | PF00069 | 0.326 |
MOD_Plk_4 | 403 | 409 | PF00069 | 0.397 |
MOD_Plk_4 | 482 | 488 | PF00069 | 0.255 |
MOD_Plk_4 | 513 | 519 | PF00069 | 0.250 |
MOD_Plk_4 | 520 | 526 | PF00069 | 0.252 |
MOD_Plk_4 | 553 | 559 | PF00069 | 0.263 |
MOD_Plk_4 | 618 | 624 | PF00069 | 0.350 |
MOD_Plk_4 | 89 | 95 | PF00069 | 0.371 |
MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.670 |
MOD_ProDKin_1 | 419 | 425 | PF00069 | 0.408 |
MOD_ProDKin_1 | 450 | 456 | PF00069 | 0.335 |
MOD_ProDKin_1 | 509 | 515 | PF00069 | 0.338 |
MOD_ProDKin_1 | 516 | 522 | PF00069 | 0.325 |
MOD_ProDKin_1 | 535 | 541 | PF00069 | 0.370 |
MOD_ProDKin_1 | 608 | 614 | PF00069 | 0.295 |
MOD_SUMO_for_1 | 444 | 447 | PF00179 | 0.376 |
MOD_SUMO_rev_2 | 431 | 441 | PF00179 | 0.367 |
TRG_ENDOCYTIC_2 | 177 | 180 | PF00928 | 0.262 |
TRG_ENDOCYTIC_2 | 215 | 218 | PF00928 | 0.255 |
TRG_ENDOCYTIC_2 | 275 | 278 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 359 | 362 | PF00928 | 0.338 |
TRG_ENDOCYTIC_2 | 416 | 419 | PF00928 | 0.522 |
TRG_ENDOCYTIC_2 | 426 | 429 | PF00928 | 0.392 |
TRG_ENDOCYTIC_2 | 525 | 528 | PF00928 | 0.310 |
TRG_ENDOCYTIC_2 | 70 | 73 | PF00928 | 0.279 |
TRG_ER_diArg_1 | 174 | 176 | PF00400 | 0.272 |
TRG_ER_diArg_1 | 254 | 256 | PF00400 | 0.476 |
TRG_ER_diArg_1 | 275 | 277 | PF00400 | 0.442 |
TRG_ER_diArg_1 | 47 | 49 | PF00400 | 0.402 |
TRG_ER_diArg_1 | 634 | 636 | PF00400 | 0.341 |
TRG_ER_diArg_1 | 84 | 87 | PF00400 | 0.341 |
TRG_ER_FFAT_2 | 512 | 523 | PF00635 | 0.193 |
TRG_NES_CRM1_1 | 324 | 339 | PF08389 | 0.541 |
TRG_NES_CRM1_1 | 366 | 381 | PF08389 | 0.328 |
TRG_NES_CRM1_1 | 540 | 555 | PF08389 | 0.360 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I6W7 | Leptomonas seymouri | 72% | 100% |
A0A0S4JRH8 | Bodo saltans | 38% | 91% |
A0A1X0P3R6 | Trypanosomatidae | 22% | 100% |
A0A1X0P474 | Trypanosomatidae | 52% | 100% |
A0A3Q8ICD7 | Leishmania donovani | 23% | 82% |
A0A3Q8ICJ2 | Leishmania donovani | 93% | 100% |
A0A3R7KWF0 | Trypanosoma rangeli | 22% | 100% |
A0A3S7X6Y1 | Leishmania donovani | 21% | 100% |
A0A422NTH3 | Trypanosoma rangeli | 51% | 100% |
A4HFH3 | Leishmania braziliensis | 81% | 100% |
A4HJ32 | Leishmania braziliensis | 22% | 82% |
A4HLP7 | Leishmania braziliensis | 21% | 100% |
A4I2N3 | Leishmania infantum | 93% | 100% |
A4I6L1 | Leishmania infantum | 23% | 82% |
A4I948 | Leishmania infantum | 21% | 100% |
C9ZN63 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 21% | 100% |
D0A5P9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
D0A6C8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 100% |
D3ZHR2 | Rattus norvegicus | 24% | 93% |
E9AYU9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
E9B1K4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 84% |
E9B2Y6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 94% |
F1RBC8 | Danio rerio | 22% | 90% |
O14678 | Homo sapiens | 23% | 100% |
O89016 | Mus musculus | 21% | 100% |
P16970 | Rattus norvegicus | 25% | 100% |
P28288 | Homo sapiens | 25% | 100% |
P33897 | Homo sapiens | 24% | 92% |
P34230 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 22% | 81% |
P41909 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 22% | 79% |
P48410 | Mus musculus | 24% | 93% |
P55096 | Mus musculus | 26% | 100% |
Q4Q402 | Leishmania major | 21% | 100% |
Q55774 | Synechocystis sp. (strain PCC 6803 / Kazusa) | 23% | 100% |
Q61285 | Mus musculus | 23% | 93% |
Q6NLC1 | Arabidopsis thaliana | 24% | 97% |
Q7JUN3 | Drosophila melanogaster | 24% | 94% |
Q8T8P3 | Dictyostelium discoideum | 22% | 93% |
Q9BHG2 | Leishmania major | 23% | 82% |
Q9QY44 | Rattus norvegicus | 24% | 93% |
Q9UBJ2 | Homo sapiens | 24% | 93% |
V5BXE1 | Trypanosoma cruzi | 49% | 100% |