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:0016020 | membrane | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0005777 | peroxisome | 6 | 1 |
GO:0005778 | peroxisomal membrane | 6 | 1 |
GO:0020015 | glycosome | 7 | 1 |
GO:0020022 | acidocalcisome | 5 | 1 |
GO:0031090 | organelle membrane | 3 | 1 |
GO:0031903 | microbody membrane | 5 | 1 |
GO:0042579 | microbody | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0098588 | bounding membrane of organelle | 4 | 1 |
Related structures:
AlphaFold database: A4HFH3
Term | Name | Level | Count |
---|---|---|---|
GO:0000038 | very long-chain fatty acid metabolic process | 5 | 1 |
GO:0006082 | organic acid metabolic process | 3 | 1 |
GO:0006629 | lipid metabolic process | 3 | 1 |
GO:0006631 | fatty acid metabolic process | 4 | 1 |
GO:0006635 | fatty acid beta-oxidation | 6 | 1 |
GO:0006810 | transport | 3 | 1 |
GO:0006869 | lipid transport | 5 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007031 | peroxisome organization | 5 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009062 | fatty acid catabolic process | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0015849 | organic acid transport | 5 | 1 |
GO:0015908 | fatty acid transport | 6 | 1 |
GO:0015909 | long-chain fatty acid transport | 7 | 1 |
GO:0015910 | long-chain fatty acid import into peroxisome | 5 | 1 |
GO:0015919 | peroxisomal membrane transport | 5 | 1 |
GO:0016042 | lipid catabolic process | 4 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0016054 | organic acid catabolic process | 4 | 1 |
GO:0019395 | fatty acid oxidation | 5 | 1 |
GO:0019752 | carboxylic acid metabolic process | 5 | 1 |
GO:0030258 | lipid modification | 4 | 1 |
GO:0032365 | intracellular lipid transport | 4 | 1 |
GO:0032787 | monocarboxylic acid metabolic process | 6 | 1 |
GO:0034440 | lipid oxidation | 5 | 1 |
GO:0042760 | very long-chain fatty acid catabolic process | 6 | 1 |
GO:0043436 | oxoacid metabolic process | 4 | 1 |
GO:0043574 | peroxisomal transport | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044242 | cellular lipid catabolic process | 4 | 1 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0044255 | cellular lipid metabolic process | 3 | 1 |
GO:0044281 | small molecule metabolic process | 2 | 1 |
GO:0044282 | small molecule catabolic process | 3 | 1 |
GO:0046395 | carboxylic acid catabolic process | 5 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0055085 | transmembrane transport | 2 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0072329 | monocarboxylic acid catabolic process | 6 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
GO:1902001 | fatty acid transmembrane transport | 5 | 1 |
GO:1903825 | organic acid transmembrane transport | 3 | 1 |
GO:1905039 | carboxylic acid transmembrane transport | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0005215 | transporter activity | 1 | 12 |
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:0005319 | lipid transporter activity | 2 | 1 |
GO:0005324 | long-chain fatty acid transporter activity | 3 | 1 |
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 | 0.239 |
CLV_NRD_NRD_1 | 174 | 176 | PF00675 | 0.441 |
CLV_NRD_NRD_1 | 25 | 27 | PF00675 | 0.237 |
CLV_NRD_NRD_1 | 635 | 637 | PF00675 | 0.488 |
CLV_PCSK_KEX2_1 | 174 | 176 | PF00082 | 0.439 |
CLV_PCSK_KEX2_1 | 25 | 27 | PF00082 | 0.159 |
CLV_PCSK_KEX2_1 | 300 | 302 | PF00082 | 0.188 |
CLV_PCSK_KEX2_1 | 635 | 637 | PF00082 | 0.511 |
CLV_PCSK_PC1ET2_1 | 300 | 302 | PF00082 | 0.213 |
CLV_PCSK_PC7_1 | 170 | 176 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 102 | 106 | PF00082 | 0.256 |
CLV_PCSK_SKI1_1 | 139 | 143 | PF00082 | 0.211 |
CLV_PCSK_SKI1_1 | 238 | 242 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 255 | 259 | PF00082 | 0.203 |
CLV_PCSK_SKI1_1 | 277 | 281 | PF00082 | 0.228 |
CLV_PCSK_SKI1_1 | 430 | 434 | PF00082 | 0.595 |
CLV_PCSK_SKI1_1 | 508 | 512 | PF00082 | 0.433 |
CLV_PCSK_SKI1_1 | 546 | 550 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 597 | 601 | PF00082 | 0.469 |
CLV_PCSK_SKI1_1 | 78 | 82 | PF00082 | 0.453 |
DOC_CDC14_PxL_1 | 216 | 224 | PF14671 | 0.284 |
DOC_MAPK_gen_1 | 128 | 138 | PF00069 | 0.414 |
DOC_MAPK_gen_1 | 607 | 615 | PF00069 | 0.259 |
DOC_MAPK_gen_1 | 670 | 677 | PF00069 | 0.378 |
DOC_MAPK_MEF2A_6 | 102 | 109 | PF00069 | 0.347 |
DOC_MAPK_MEF2A_6 | 131 | 140 | PF00069 | 0.448 |
DOC_MAPK_MEF2A_6 | 353 | 362 | PF00069 | 0.303 |
DOC_PP1_RVXF_1 | 595 | 601 | PF00149 | 0.319 |
DOC_PP2B_LxvP_1 | 493 | 496 | PF13499 | 0.255 |
DOC_PP4_FxxP_1 | 217 | 220 | PF00568 | 0.217 |
DOC_PP4_FxxP_1 | 510 | 513 | PF00568 | 0.193 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.434 |
DOC_USP7_MATH_1 | 513 | 517 | PF00917 | 0.256 |
DOC_USP7_MATH_1 | 89 | 93 | PF00917 | 0.334 |
DOC_WW_Pin1_4 | 255 | 260 | PF00397 | 0.388 |
DOC_WW_Pin1_4 | 419 | 424 | PF00397 | 0.374 |
DOC_WW_Pin1_4 | 450 | 455 | PF00397 | 0.294 |
DOC_WW_Pin1_4 | 608 | 613 | PF00397 | 0.275 |
LIG_14-3-3_CanoR_1 | 167 | 173 | PF00244 | 0.277 |
LIG_14-3-3_CanoR_1 | 263 | 270 | PF00244 | 0.421 |
LIG_14-3-3_CanoR_1 | 347 | 355 | PF00244 | 0.412 |
LIG_14-3-3_CanoR_1 | 640 | 645 | PF00244 | 0.224 |
LIG_14-3-3_CterR_2 | 685 | 688 | PF00244 | 0.370 |
LIG_Actin_WH2_2 | 222 | 240 | PF00022 | 0.313 |
LIG_Actin_WH2_2 | 385 | 402 | PF00022 | 0.313 |
LIG_BRCT_BRCA1_1 | 168 | 172 | PF00533 | 0.241 |
LIG_BRCT_BRCA1_1 | 505 | 509 | PF00533 | 0.284 |
LIG_BRCT_BRCA1_1 | 91 | 95 | PF00533 | 0.347 |
LIG_Clathr_ClatBox_1 | 443 | 447 | PF01394 | 0.334 |
LIG_CSL_BTD_1 | 493 | 496 | PF09270 | 0.241 |
LIG_EH1_1 | 35 | 43 | PF00400 | 0.283 |
LIG_eIF4E_1 | 359 | 365 | PF01652 | 0.375 |
LIG_FHA_1 | 224 | 230 | PF00498 | 0.157 |
LIG_FHA_1 | 246 | 252 | PF00498 | 0.451 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.519 |
LIG_FHA_1 | 278 | 284 | PF00498 | 0.441 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.407 |
LIG_FHA_1 | 438 | 444 | PF00498 | 0.370 |
LIG_FHA_1 | 482 | 488 | PF00498 | 0.227 |
LIG_FHA_1 | 536 | 542 | PF00498 | 0.321 |
LIG_FHA_1 | 64 | 70 | PF00498 | 0.418 |
LIG_FHA_1 | 653 | 659 | PF00498 | 0.260 |
LIG_FHA_2 | 184 | 190 | PF00498 | 0.222 |
LIG_FHA_2 | 521 | 527 | PF00498 | 0.217 |
LIG_FHA_2 | 57 | 63 | PF00498 | 0.394 |
LIG_FHA_2 | 624 | 630 | PF00498 | 0.348 |
LIG_FHA_2 | 643 | 649 | PF00498 | 0.186 |
LIG_GBD_Chelix_1 | 140 | 148 | PF00786 | 0.409 |
LIG_LIR_Apic_2 | 516 | 520 | PF02991 | 0.218 |
LIG_LIR_Gen_1 | 208 | 218 | PF02991 | 0.197 |
LIG_LIR_Gen_1 | 272 | 283 | PF02991 | 0.350 |
LIG_LIR_Gen_1 | 327 | 338 | PF02991 | 0.458 |
LIG_LIR_Gen_1 | 406 | 414 | PF02991 | 0.474 |
LIG_LIR_Gen_1 | 470 | 478 | PF02991 | 0.229 |
LIG_LIR_Gen_1 | 523 | 533 | PF02991 | 0.281 |
LIG_LIR_Gen_1 | 66 | 74 | PF02991 | 0.322 |
LIG_LIR_Gen_1 | 92 | 103 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 208 | 213 | PF02991 | 0.213 |
LIG_LIR_Nem_3 | 327 | 333 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 439 | 444 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 470 | 476 | PF02991 | 0.229 |
LIG_LIR_Nem_3 | 523 | 528 | PF02991 | 0.281 |
LIG_LIR_Nem_3 | 579 | 585 | PF02991 | 0.217 |
LIG_LIR_Nem_3 | 66 | 70 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 92 | 98 | PF02991 | 0.318 |
LIG_PCNA_yPIPBox_3 | 347 | 359 | PF02747 | 0.264 |
LIG_PCNA_yPIPBox_3 | 369 | 380 | PF02747 | 0.339 |
LIG_Pex14_2 | 172 | 176 | PF04695 | 0.241 |
LIG_Pex14_2 | 206 | 210 | PF04695 | 0.197 |
LIG_Pex14_2 | 375 | 379 | PF04695 | 0.305 |
LIG_Pex14_2 | 70 | 74 | PF04695 | 0.217 |
LIG_Pex14_2 | 95 | 99 | PF04695 | 0.253 |
LIG_PTB_Apo_2 | 410 | 417 | PF02174 | 0.312 |
LIG_PTB_Phospho_1 | 410 | 416 | PF10480 | 0.312 |
LIG_SH2_CRK | 517 | 521 | PF00017 | 0.241 |
LIG_SH2_PTP2 | 416 | 419 | PF00017 | 0.303 |
LIG_SH2_SRC | 359 | 362 | PF00017 | 0.348 |
LIG_SH2_STAP1 | 19 | 23 | PF00017 | 0.489 |
LIG_SH2_STAP1 | 564 | 568 | PF00017 | 0.271 |
LIG_SH2_STAT3 | 6 | 9 | PF00017 | 0.543 |
LIG_SH2_STAT5 | 202 | 205 | PF00017 | 0.224 |
LIG_SH2_STAT5 | 216 | 219 | PF00017 | 0.198 |
LIG_SH2_STAT5 | 282 | 285 | PF00017 | 0.501 |
LIG_SH2_STAT5 | 359 | 362 | PF00017 | 0.292 |
LIG_SH2_STAT5 | 416 | 419 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 426 | 429 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 46 | 49 | PF00017 | 0.362 |
LIG_SH3_3 | 414 | 420 | PF00018 | 0.397 |
LIG_SH3_3 | 531 | 537 | PF00018 | 0.240 |
LIG_SH3_3 | 668 | 674 | PF00018 | 0.367 |
LIG_SUMO_SIM_anti_2 | 226 | 233 | PF11976 | 0.199 |
LIG_SUMO_SIM_anti_2 | 248 | 255 | PF11976 | 0.179 |
LIG_SUMO_SIM_anti_2 | 37 | 42 | PF11976 | 0.172 |
LIG_SUMO_SIM_anti_2 | 556 | 562 | PF11976 | 0.168 |
LIG_SUMO_SIM_anti_2 | 610 | 618 | PF11976 | 0.256 |
LIG_SUMO_SIM_par_1 | 226 | 233 | PF11976 | 0.180 |
LIG_SUMO_SIM_par_1 | 537 | 543 | PF11976 | 0.159 |
LIG_SUMO_SIM_par_1 | 610 | 618 | PF11976 | 0.225 |
LIG_SUMO_SIM_par_1 | 640 | 645 | PF11976 | 0.273 |
LIG_TRFH_1 | 509 | 513 | PF08558 | 0.319 |
LIG_TYR_ITIM | 213 | 218 | PF00017 | 0.217 |
LIG_TYR_ITSM | 521 | 528 | PF00017 | 0.319 |
LIG_UBA3_1 | 364 | 373 | PF00899 | 0.403 |
LIG_UBA3_1 | 489 | 497 | PF00899 | 0.319 |
LIG_UBA3_1 | 657 | 665 | PF00899 | 0.344 |
LIG_UBA3_1 | 94 | 102 | PF00899 | 0.297 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.687 |
MOD_CK1_1 | 383 | 389 | PF00069 | 0.293 |
MOD_CK1_1 | 502 | 508 | PF00069 | 0.271 |
MOD_CK1_1 | 581 | 587 | PF00069 | 0.264 |
MOD_CK2_1 | 281 | 287 | PF00069 | 0.397 |
MOD_CK2_1 | 520 | 526 | PF00069 | 0.217 |
MOD_CK2_1 | 642 | 648 | PF00069 | 0.236 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.313 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.319 |
MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.292 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.508 |
MOD_GlcNHglycan | 460 | 463 | PF01048 | 0.539 |
MOD_GlcNHglycan | 497 | 500 | PF01048 | 0.489 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.553 |
MOD_GlcNHglycan | 565 | 568 | PF01048 | 0.555 |
MOD_GlcNHglycan | 585 | 588 | PF01048 | 0.435 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.234 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.381 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.478 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.355 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.284 |
MOD_GSK3_1 | 495 | 502 | PF00069 | 0.290 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.444 |
MOD_GSK3_1 | 576 | 583 | PF00069 | 0.250 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.690 |
MOD_N-GLC_1 | 351 | 356 | PF02516 | 0.575 |
MOD_N-GLC_1 | 368 | 373 | PF02516 | 0.508 |
MOD_N-GLC_1 | 430 | 435 | PF02516 | 0.539 |
MOD_N-GLC_2 | 479 | 481 | PF02516 | 0.441 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.319 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.391 |
MOD_NEK2_1 | 27 | 32 | PF00069 | 0.124 |
MOD_NEK2_1 | 302 | 307 | PF00069 | 0.527 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.158 |
MOD_NEK2_1 | 368 | 373 | PF00069 | 0.290 |
MOD_NEK2_1 | 395 | 400 | PF00069 | 0.284 |
MOD_NEK2_1 | 424 | 429 | PF00069 | 0.471 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.649 |
MOD_NEK2_2 | 520 | 525 | PF00069 | 0.284 |
MOD_PIKK_1 | 263 | 269 | PF00454 | 0.519 |
MOD_PIKK_1 | 424 | 430 | PF00454 | 0.388 |
MOD_PIKK_1 | 499 | 505 | PF00454 | 0.271 |
MOD_PIKK_1 | 60 | 66 | PF00454 | 0.459 |
MOD_PK_1 | 640 | 646 | PF00069 | 0.271 |
MOD_PKA_2 | 166 | 172 | PF00069 | 0.217 |
MOD_PKA_2 | 346 | 352 | PF00069 | 0.442 |
MOD_PKA_2 | 591 | 597 | PF00069 | 0.268 |
MOD_Plk_1 | 302 | 308 | PF00069 | 0.522 |
MOD_Plk_1 | 351 | 357 | PF00069 | 0.279 |
MOD_Plk_1 | 368 | 374 | PF00069 | 0.293 |
MOD_Plk_1 | 380 | 386 | PF00069 | 0.242 |
MOD_Plk_1 | 395 | 401 | PF00069 | 0.290 |
MOD_Plk_1 | 503 | 509 | PF00069 | 0.230 |
MOD_Plk_1 | 576 | 582 | PF00069 | 0.219 |
MOD_Plk_1 | 60 | 66 | PF00069 | 0.390 |
MOD_Plk_1 | 617 | 623 | PF00069 | 0.217 |
MOD_Plk_2-3 | 466 | 472 | PF00069 | 0.280 |
MOD_Plk_2-3 | 535 | 541 | PF00069 | 0.159 |
MOD_Plk_2-3 | 618 | 624 | PF00069 | 0.312 |
MOD_Plk_4 | 116 | 122 | PF00069 | 0.384 |
MOD_Plk_4 | 183 | 189 | PF00069 | 0.239 |
MOD_Plk_4 | 224 | 230 | PF00069 | 0.160 |
MOD_Plk_4 | 329 | 335 | PF00069 | 0.289 |
MOD_Plk_4 | 36 | 42 | PF00069 | 0.223 |
MOD_Plk_4 | 403 | 409 | PF00069 | 0.382 |
MOD_Plk_4 | 482 | 488 | PF00069 | 0.217 |
MOD_Plk_4 | 513 | 519 | PF00069 | 0.243 |
MOD_Plk_4 | 520 | 526 | PF00069 | 0.264 |
MOD_Plk_4 | 553 | 559 | PF00069 | 0.224 |
MOD_Plk_4 | 618 | 624 | PF00069 | 0.312 |
MOD_Plk_4 | 89 | 95 | PF00069 | 0.356 |
MOD_ProDKin_1 | 255 | 261 | PF00069 | 0.388 |
MOD_ProDKin_1 | 419 | 425 | PF00069 | 0.365 |
MOD_ProDKin_1 | 450 | 456 | PF00069 | 0.299 |
MOD_ProDKin_1 | 608 | 614 | PF00069 | 0.275 |
MOD_SUMO_for_1 | 444 | 447 | PF00179 | 0.307 |
TRG_DiLeu_BaEn_1 | 540 | 545 | PF01217 | 0.159 |
TRG_ENDOCYTIC_2 | 177 | 180 | PF00928 | 0.227 |
TRG_ENDOCYTIC_2 | 215 | 218 | PF00928 | 0.217 |
TRG_ENDOCYTIC_2 | 275 | 278 | PF00928 | 0.434 |
TRG_ENDOCYTIC_2 | 359 | 362 | PF00928 | 0.305 |
TRG_ENDOCYTIC_2 | 416 | 419 | PF00928 | 0.398 |
TRG_ENDOCYTIC_2 | 426 | 429 | PF00928 | 0.350 |
TRG_ENDOCYTIC_2 | 46 | 49 | PF00928 | 0.346 |
TRG_ENDOCYTIC_2 | 525 | 528 | PF00928 | 0.277 |
TRG_ER_diArg_1 | 174 | 176 | PF00400 | 0.236 |
TRG_ER_diArg_1 | 25 | 27 | PF00400 | 0.359 |
TRG_ER_diArg_1 | 634 | 636 | PF00400 | 0.321 |
TRG_ER_diArg_1 | 84 | 87 | PF00400 | 0.319 |
TRG_NES_CRM1_1 | 324 | 339 | PF08389 | 0.519 |
TRG_NES_CRM1_1 | 366 | 381 | PF08389 | 0.297 |
TRG_NES_CRM1_1 | 540 | 555 | PF08389 | 0.271 |
TRG_Pf-PMV_PEXEL_1 | 542 | 547 | PF00026 | 0.437 |
TRG_PTS1 | 685 | 688 | PF00515 | 0.370 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I6W7 | Leptomonas seymouri | 71% | 100% |
A0A0S4JRH8 | Bodo saltans | 37% | 91% |
A0A1X0P3R6 | Trypanosomatidae | 22% | 100% |
A0A1X0P474 | Trypanosomatidae | 53% | 100% |
A0A3Q8ICD7 | Leishmania donovani | 23% | 82% |
A0A3Q8ICJ2 | Leishmania donovani | 82% | 100% |
A0A3R7KWF0 | Trypanosoma rangeli | 23% | 100% |
A0A3S7X6Y1 | Leishmania donovani | 21% | 95% |
A0A422NTH3 | Trypanosoma rangeli | 50% | 100% |
A4HJ32 | Leishmania braziliensis | 23% | 82% |
A4HLP7 | Leishmania braziliensis | 20% | 100% |
A4I2N3 | Leishmania infantum | 83% | 100% |
A4I6L1 | Leishmania infantum | 23% | 82% |
C9ZN63 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 22% | 100% |
D0A5P9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
D3ZHR2 | Rattus norvegicus | 23% | 93% |
E9AD24 | Leishmania major | 81% | 100% |
E9AYU9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
E9B1K4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 84% |
E9B422 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 20% | 98% |
F1RBC8 | Danio rerio | 24% | 90% |
O14678 | Homo sapiens | 22% | 100% |
O89016 | Mus musculus | 21% | 100% |
P16970 | Rattus norvegicus | 24% | 100% |
P28288 | Homo sapiens | 24% | 100% |
P33897 | Homo sapiens | 24% | 92% |
P48410 | Mus musculus | 23% | 93% |
P55096 | Mus musculus | 25% | 100% |
Q4Q402 | Leishmania major | 21% | 98% |
Q55774 | Synechocystis sp. (strain PCC 6803 / Kazusa) | 23% | 100% |
Q61285 | Mus musculus | 22% | 93% |
Q6NLC1 | Arabidopsis thaliana | 23% | 97% |
Q7JUN3 | Drosophila melanogaster | 23% | 94% |
Q8T8P3 | Dictyostelium discoideum | 21% | 93% |
Q9BHG2 | Leishmania major | 23% | 100% |
Q9QY44 | Rattus norvegicus | 22% | 93% |
Q9UBJ2 | Homo sapiens | 23% | 93% |
V5AYI7 | Trypanosoma cruzi | 23% | 100% |
V5BXE1 | Trypanosoma cruzi | 50% | 100% |