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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0005778 | peroxisomal membrane | 6 | 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:0046860 | glycosome membrane | 7 | 1 |
GO:0098588 | bounding membrane of organelle | 4 | 1 |
Related structures:
AlphaFold database: A0A3S7X6Y1
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 | 516 | 520 | PF00656 | 0.220 |
CLV_NRD_NRD_1 | 37 | 39 | PF00675 | 0.404 |
CLV_NRD_NRD_1 | 49 | 51 | PF00675 | 0.404 |
CLV_NRD_NRD_1 | 619 | 621 | PF00675 | 0.570 |
CLV_PCSK_FUR_1 | 47 | 51 | PF00082 | 0.529 |
CLV_PCSK_KEX2_1 | 315 | 317 | PF00082 | 0.227 |
CLV_PCSK_KEX2_1 | 36 | 38 | PF00082 | 0.405 |
CLV_PCSK_KEX2_1 | 49 | 51 | PF00082 | 0.399 |
CLV_PCSK_PC1ET2_1 | 315 | 317 | PF00082 | 0.228 |
CLV_PCSK_SKI1_1 | 155 | 159 | PF00082 | 0.293 |
CLV_PCSK_SKI1_1 | 213 | 217 | PF00082 | 0.287 |
CLV_PCSK_SKI1_1 | 318 | 322 | PF00082 | 0.245 |
CLV_PCSK_SKI1_1 | 377 | 381 | PF00082 | 0.561 |
CLV_PCSK_SKI1_1 | 463 | 467 | PF00082 | 0.497 |
CLV_PCSK_SKI1_1 | 505 | 509 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 568 | 572 | PF00082 | 0.443 |
CLV_PCSK_SKI1_1 | 573 | 577 | PF00082 | 0.426 |
DEG_APCC_DBOX_1 | 103 | 111 | PF00400 | 0.348 |
DEG_APCC_DBOX_1 | 398 | 406 | PF00400 | 0.338 |
DEG_APCC_DBOX_1 | 567 | 575 | PF00400 | 0.272 |
DEG_ODPH_VHL_1 | 235 | 248 | PF01847 | 0.282 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 163 | 170 | PF00134 | 0.484 |
DOC_CYCLIN_yCln2_LP_2 | 235 | 241 | PF00134 | 0.257 |
DOC_CYCLIN_yCln2_LP_2 | 367 | 373 | PF00134 | 0.285 |
DOC_MAPK_gen_1 | 401 | 410 | PF00069 | 0.394 |
DOC_MAPK_gen_1 | 566 | 574 | PF00069 | 0.319 |
DOC_MAPK_gen_1 | 620 | 629 | PF00069 | 0.355 |
DOC_MAPK_MEF2A_6 | 104 | 111 | PF00069 | 0.267 |
DOC_MAPK_MEF2A_6 | 213 | 222 | PF00069 | 0.430 |
DOC_MAPK_MEF2A_6 | 568 | 576 | PF00069 | 0.284 |
DOC_MAPK_MEF2A_6 | 620 | 629 | PF00069 | 0.327 |
DOC_MAPK_MEF2A_6 | 74 | 83 | PF00069 | 0.448 |
DOC_MAPK_NFAT4_5 | 104 | 112 | PF00069 | 0.269 |
DOC_PP1_RVXF_1 | 67 | 73 | PF00149 | 0.596 |
DOC_PP1_RVXF_1 | 9 | 16 | PF00149 | 0.341 |
DOC_PP2B_LxvP_1 | 140 | 143 | PF13499 | 0.397 |
DOC_PP2B_LxvP_1 | 235 | 238 | PF13499 | 0.257 |
DOC_PP2B_LxvP_1 | 367 | 370 | PF13499 | 0.274 |
DOC_PP2B_LxvP_1 | 81 | 84 | PF13499 | 0.437 |
DOC_USP7_MATH_1 | 184 | 188 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 435 | 439 | PF00917 | 0.434 |
DOC_USP7_MATH_1 | 477 | 481 | PF00917 | 0.250 |
DOC_USP7_MATH_1 | 525 | 529 | PF00917 | 0.371 |
DOC_USP7_MATH_1 | 535 | 539 | PF00917 | 0.269 |
DOC_USP7_UBL2_3 | 172 | 176 | PF12436 | 0.501 |
DOC_WW_Pin1_4 | 430 | 435 | PF00397 | 0.305 |
DOC_WW_Pin1_4 | 445 | 450 | PF00397 | 0.330 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.716 |
LIG_14-3-3_CanoR_1 | 104 | 110 | PF00244 | 0.265 |
LIG_14-3-3_CanoR_1 | 196 | 204 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 505 | 511 | PF00244 | 0.284 |
LIG_14-3-3_CanoR_1 | 624 | 630 | PF00244 | 0.417 |
LIG_14-3-3_CanoR_1 | 74 | 79 | PF00244 | 0.532 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.436 |
LIG_BRCT_BRCA1_1 | 47 | 51 | PF00533 | 0.656 |
LIG_BRCT_BRCA1_1 | 8 | 12 | PF00533 | 0.396 |
LIG_Clathr_ClatBox_1 | 343 | 347 | PF01394 | 0.330 |
LIG_DLG_GKlike_1 | 74 | 81 | PF00625 | 0.478 |
LIG_EH1_1 | 337 | 345 | PF00400 | 0.325 |
LIG_eIF4E_1 | 338 | 344 | PF01652 | 0.348 |
LIG_FHA_1 | 315 | 321 | PF00498 | 0.565 |
LIG_FHA_1 | 586 | 592 | PF00498 | 0.244 |
LIG_FHA_2 | 351 | 357 | PF00498 | 0.299 |
LIG_FHA_2 | 483 | 489 | PF00498 | 0.319 |
LIG_GBD_Chelix_1 | 335 | 343 | PF00786 | 0.397 |
LIG_Integrin_isoDGR_2 | 118 | 120 | PF01839 | 0.507 |
LIG_LIR_Apic_2 | 497 | 501 | PF02991 | 0.256 |
LIG_LIR_Gen_1 | 108 | 115 | PF02991 | 0.288 |
LIG_LIR_Gen_1 | 243 | 252 | PF02991 | 0.349 |
LIG_LIR_Gen_1 | 347 | 357 | PF02991 | 0.306 |
LIG_LIR_Gen_1 | 554 | 561 | PF02991 | 0.243 |
LIG_LIR_LC3C_4 | 342 | 345 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 108 | 114 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 243 | 248 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 325 | 331 | PF02991 | 0.568 |
LIG_LIR_Nem_3 | 509 | 513 | PF02991 | 0.271 |
LIG_LIR_Nem_3 | 554 | 560 | PF02991 | 0.218 |
LIG_LIR_Nem_3 | 596 | 602 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 9 | 15 | PF02991 | 0.326 |
LIG_LYPXL_yS_3 | 510 | 513 | PF13949 | 0.260 |
LIG_NRBOX | 503 | 509 | PF00104 | 0.307 |
LIG_NRBOX | 74 | 80 | PF00104 | 0.501 |
LIG_PCNA_PIPBox_1 | 467 | 476 | PF02747 | 0.271 |
LIG_Pex14_2 | 212 | 216 | PF04695 | 0.519 |
LIG_PTAP_UEV_1 | 483 | 488 | PF05743 | 0.271 |
LIG_REV1ctd_RIR_1 | 596 | 605 | PF16727 | 0.282 |
LIG_SH2_CRK | 600 | 604 | PF00017 | 0.303 |
LIG_SH2_GRB2like | 419 | 422 | PF00017 | 0.278 |
LIG_SH2_PTP2 | 153 | 156 | PF00017 | 0.471 |
LIG_SH2_SRC | 498 | 501 | PF00017 | 0.228 |
LIG_SH2_STAP1 | 16 | 20 | PF00017 | 0.356 |
LIG_SH2_STAP1 | 419 | 423 | PF00017 | 0.339 |
LIG_SH2_STAT3 | 16 | 19 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 102 | 105 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 121 | 124 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 153 | 156 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 174 | 177 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 245 | 248 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 338 | 341 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 361 | 364 | PF00017 | 0.299 |
LIG_SH2_STAT5 | 368 | 371 | PF00017 | 0.223 |
LIG_SH2_STAT5 | 498 | 501 | PF00017 | 0.228 |
LIG_SH3_3 | 251 | 257 | PF00018 | 0.397 |
LIG_SH3_3 | 478 | 484 | PF00018 | 0.269 |
LIG_SUMO_SIM_anti_2 | 105 | 111 | PF11976 | 0.308 |
LIG_SUMO_SIM_anti_2 | 221 | 228 | PF11976 | 0.347 |
LIG_SUMO_SIM_anti_2 | 342 | 347 | PF11976 | 0.330 |
LIG_SUMO_SIM_anti_2 | 428 | 433 | PF11976 | 0.299 |
LIG_SUMO_SIM_par_1 | 218 | 224 | PF11976 | 0.348 |
LIG_SUMO_SIM_par_1 | 342 | 347 | PF11976 | 0.330 |
LIG_SUMO_SIM_par_1 | 609 | 614 | PF11976 | 0.282 |
LIG_SUMO_SIM_par_1 | 625 | 630 | PF11976 | 0.306 |
LIG_SUMO_SIM_par_1 | 93 | 99 | PF11976 | 0.251 |
LIG_TRFH_1 | 539 | 543 | PF08558 | 0.237 |
LIG_TYR_ITIM | 151 | 156 | PF00017 | 0.471 |
LIG_TYR_ITIM | 242 | 247 | PF00017 | 0.352 |
LIG_TYR_ITIM | 508 | 513 | PF00017 | 0.260 |
LIG_UBA3_1 | 378 | 383 | PF00899 | 0.292 |
LIG_ULM_U2AF65_1 | 315 | 320 | PF00076 | 0.442 |
MOD_CDC14_SPxK_1 | 52 | 55 | PF00782 | 0.679 |
MOD_CDK_SPxK_1 | 445 | 451 | PF00069 | 0.319 |
MOD_CDK_SPxK_1 | 49 | 55 | PF00069 | 0.683 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.731 |
MOD_CK1_1 | 458 | 464 | PF00069 | 0.311 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.462 |
MOD_CK1_1 | 589 | 595 | PF00069 | 0.300 |
MOD_CK1_1 | 88 | 94 | PF00069 | 0.403 |
MOD_CK2_1 | 279 | 285 | PF00069 | 0.471 |
MOD_CK2_1 | 482 | 488 | PF00069 | 0.300 |
MOD_CK2_1 | 559 | 565 | PF00069 | 0.228 |
MOD_CK2_1 | 589 | 595 | PF00069 | 0.344 |
MOD_CK2_1 | 611 | 617 | PF00069 | 0.288 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.282 |
MOD_GlcNHglycan | 371 | 374 | PF01048 | 0.562 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.508 |
MOD_GlcNHglycan | 460 | 463 | PF01048 | 0.480 |
MOD_GlcNHglycan | 470 | 473 | PF01048 | 0.444 |
MOD_GlcNHglycan | 533 | 536 | PF01048 | 0.514 |
MOD_GlcNHglycan | 561 | 564 | PF01048 | 0.417 |
MOD_GlcNHglycan | 588 | 591 | PF01048 | 0.506 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.211 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.457 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.500 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.692 |
MOD_GSK3_1 | 482 | 489 | PF00069 | 0.295 |
MOD_GSK3_1 | 531 | 538 | PF00069 | 0.328 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.664 |
MOD_GSK3_1 | 585 | 592 | PF00069 | 0.218 |
MOD_GSK3_1 | 611 | 618 | PF00069 | 0.277 |
MOD_N-GLC_1 | 443 | 448 | PF02516 | 0.445 |
MOD_N-GLC_1 | 458 | 463 | PF02516 | 0.404 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.384 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.485 |
MOD_NEK2_1 | 227 | 232 | PF00069 | 0.397 |
MOD_NEK2_1 | 240 | 245 | PF00069 | 0.248 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.180 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.467 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.437 |
MOD_NEK2_1 | 339 | 344 | PF00069 | 0.375 |
MOD_NEK2_1 | 388 | 393 | PF00069 | 0.286 |
MOD_NEK2_1 | 443 | 448 | PF00069 | 0.230 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.429 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.274 |
MOD_NEK2_2 | 323 | 328 | PF00069 | 0.454 |
MOD_PIKK_1 | 155 | 161 | PF00454 | 0.471 |
MOD_PIKK_1 | 182 | 188 | PF00454 | 0.505 |
MOD_PIKK_1 | 195 | 201 | PF00454 | 0.540 |
MOD_PIKK_1 | 263 | 269 | PF00454 | 0.479 |
MOD_PIKK_1 | 355 | 361 | PF00454 | 0.292 |
MOD_PIKK_1 | 589 | 595 | PF00454 | 0.289 |
MOD_PKA_2 | 124 | 130 | PF00069 | 0.339 |
MOD_PKA_2 | 195 | 201 | PF00069 | 0.428 |
MOD_PKB_1 | 36 | 44 | PF00069 | 0.637 |
MOD_Plk_1 | 355 | 361 | PF00069 | 0.360 |
MOD_Plk_1 | 443 | 449 | PF00069 | 0.284 |
MOD_Plk_1 | 61 | 67 | PF00069 | 0.590 |
MOD_Plk_4 | 105 | 111 | PF00069 | 0.274 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.340 |
MOD_Plk_4 | 176 | 182 | PF00069 | 0.490 |
MOD_Plk_4 | 221 | 227 | PF00069 | 0.387 |
MOD_Plk_4 | 250 | 256 | PF00069 | 0.346 |
MOD_Plk_4 | 303 | 309 | PF00069 | 0.435 |
MOD_Plk_4 | 323 | 329 | PF00069 | 0.403 |
MOD_Plk_4 | 331 | 337 | PF00069 | 0.275 |
MOD_Plk_4 | 339 | 345 | PF00069 | 0.254 |
MOD_Plk_4 | 435 | 441 | PF00069 | 0.398 |
MOD_Plk_4 | 450 | 456 | PF00069 | 0.219 |
MOD_Plk_4 | 486 | 492 | PF00069 | 0.290 |
MOD_Plk_4 | 606 | 612 | PF00069 | 0.267 |
MOD_Plk_4 | 74 | 80 | PF00069 | 0.503 |
MOD_Plk_4 | 96 | 102 | PF00069 | 0.283 |
MOD_ProDKin_1 | 430 | 436 | PF00069 | 0.309 |
MOD_ProDKin_1 | 445 | 451 | PF00069 | 0.330 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.717 |
MOD_SUMO_rev_2 | 306 | 314 | PF00179 | 0.519 |
MOD_SUMO_rev_2 | 515 | 522 | PF00179 | 0.328 |
TRG_DiLeu_BaLyEn_6 | 299 | 304 | PF01217 | 0.442 |
TRG_DiLeu_BaLyEn_6 | 598 | 603 | PF01217 | 0.359 |
TRG_DiLeu_BaLyEn_6 | 71 | 76 | PF01217 | 0.533 |
TRG_ENDOCYTIC_2 | 153 | 156 | PF00928 | 0.519 |
TRG_ENDOCYTIC_2 | 244 | 247 | PF00928 | 0.255 |
TRG_ENDOCYTIC_2 | 368 | 371 | PF00928 | 0.260 |
TRG_ENDOCYTIC_2 | 510 | 513 | PF00928 | 0.260 |
TRG_ENDOCYTIC_2 | 600 | 603 | PF00928 | 0.294 |
TRG_ER_diArg_1 | 35 | 38 | PF00400 | 0.605 |
TRG_ER_diArg_1 | 47 | 50 | PF00400 | 0.602 |
TRG_ER_diArg_1 | 566 | 569 | PF00400 | 0.240 |
TRG_NES_CRM1_1 | 400 | 413 | PF08389 | 0.389 |
TRG_NES_CRM1_1 | 617 | 630 | PF08389 | 0.365 |
TRG_NLS_MonoExtN_4 | 313 | 319 | PF00514 | 0.443 |
TRG_Pf-PMV_PEXEL_1 | 120 | 124 | PF00026 | 0.484 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1V4 | Leptomonas seymouri | 26% | 75% |
A0A0N1I6W7 | Leptomonas seymouri | 20% | 93% |
A0A0N1I7J3 | Leptomonas seymouri | 69% | 100% |
A0A0S4IIU4 | Bodo saltans | 34% | 100% |
A0A1X0NJ54 | Trypanosomatidae | 28% | 92% |
A0A1X0P3R6 | Trypanosomatidae | 46% | 100% |
A0A1X0P474 | Trypanosomatidae | 22% | 95% |
A0A3Q8ICD7 | Leishmania donovani | 28% | 100% |
A0A3Q8ICJ2 | Leishmania donovani | 22% | 100% |
A0A3R7KWF0 | Trypanosoma rangeli | 28% | 95% |
A0A3R7NBD2 | Trypanosoma rangeli | 45% | 100% |
A0A3S7X621 | Leishmania donovani | 23% | 72% |
A0A422NTH3 | Trypanosoma rangeli | 22% | 96% |
A4HFH3 | Leishmania braziliensis | 21% | 93% |
A4HJ32 | Leishmania braziliensis | 26% | 100% |
A4HLP7 | Leishmania braziliensis | 85% | 100% |
A4I2N3 | Leishmania infantum | 21% | 100% |
A4I6L1 | Leishmania infantum | 28% | 100% |
A4I8D3 | Leishmania infantum | 23% | 91% |
A4I948 | Leishmania infantum | 99% | 100% |
C9ZN63 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 94% |
D0A5P9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 22% | 94% |
D0A6C8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
D3ZHR2 | Rattus norvegicus | 29% | 87% |
E9AD24 | Leishmania major | 21% | 100% |
E9AYU9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 21% | 100% |
E9B1K4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9B392 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 22% | 91% |
E9B422 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
F1RBC8 | Danio rerio | 28% | 84% |
O14678 | Homo sapiens | 28% | 100% |
O89016 | Mus musculus | 28% | 100% |
P16970 | Rattus norvegicus | 31% | 97% |
P21958 | Mus musculus | 22% | 88% |
P28288 | Homo sapiens | 31% | 97% |
P33897 | Homo sapiens | 30% | 86% |
P34230 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 75% |
P36370 | Rattus norvegicus | 23% | 88% |
P41909 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 24% | 74% |
P45221 | Haemophilus influenzae (strain ATCC 51907 / DSM 11121 / KW20 / Rd) | 24% | 100% |
P48410 | Mus musculus | 29% | 87% |
P55096 | Mus musculus | 31% | 97% |
P60752 | Escherichia coli (strain K12) | 20% | 100% |
P60753 | Escherichia coli O157:H7 | 20% | 100% |
P63359 | Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) | 20% | 100% |
P63360 | Salmonella typhi | 20% | 100% |
P9WQI8 | Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) | 26% | 100% |
P9WQI9 | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | 26% | 100% |
Q080T2 | Shewanella frigidimarina (strain NCIMB 400) | 21% | 100% |
Q0A4U4 | Alkalilimnicola ehrlichii (strain ATCC BAA-1101 / DSM 17681 / MLHE-1) | 23% | 100% |
Q0TJD9 | Escherichia coli O6:K15:H31 (strain 536 / UPEC) | 20% | 100% |
Q12M46 | Shewanella denitrificans (strain OS217 / ATCC BAA-1090 / DSM 15013) | 20% | 100% |
Q1GZI0 | Methylobacillus flagellatus (strain KT / ATCC 51484 / DSM 6875) | 23% | 100% |
Q1RDU4 | Escherichia coli (strain UTI89 / UPEC) | 20% | 100% |
Q2NUA5 | Sodalis glossinidius (strain morsitans) | 20% | 100% |
Q31YT6 | Shigella boydii serotype 4 (strain Sb227) | 20% | 100% |
Q32E34 | Shigella dysenteriae serotype 1 (strain Sd197) | 20% | 100% |
Q3BTC8 | Xanthomonas campestris pv. vesicatoria (strain 85-10) | 22% | 100% |
Q3Z3K7 | Shigella sonnei (strain Ss046) | 20% | 100% |
Q492S9 | Blochmannia pennsylvanicus (strain BPEN) | 21% | 100% |
Q4Q402 | Leishmania major | 96% | 100% |
Q4UV65 | Xanthomonas campestris pv. campestris (strain 8004) | 22% | 100% |
Q55774 | Synechocystis sp. (strain PCC 6803 / Kazusa) | 32% | 97% |
Q57335 | Haemophilus influenzae (strain ATCC 51907 / DSM 11121 / KW20 / Rd) | 25% | 100% |
Q57R14 | Salmonella choleraesuis (strain SC-B67) | 20% | 100% |
Q5B1Q2 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 23% | 89% |
Q5PGH0 | Salmonella paratyphi A (strain ATCC 9150 / SARB42) | 20% | 100% |
Q61285 | Mus musculus | 28% | 86% |
Q6BXD7 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 20% | 92% |
Q6NLC1 | Arabidopsis thaliana | 29% | 91% |
Q7JUN3 | Drosophila melanogaster | 29% | 88% |
Q7RX59 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 22% | 89% |
Q7VR44 | Blochmannia floridanus | 21% | 100% |
Q83LP0 | Shigella flexneri | 20% | 100% |
Q87EF0 | Xylella fastidiosa (strain Temecula1 / ATCC 700964) | 20% | 100% |
Q87R16 | Vibrio parahaemolyticus serotype O3:K6 (strain RIMD 2210633) | 24% | 100% |
Q8D2U8 | Wigglesworthia glossinidia brevipalpis | 20% | 100% |
Q8FJB1 | Escherichia coli O6:H1 (strain CFT073 / ATCC 700928 / UPEC) | 20% | 100% |
Q8P8W4 | Xanthomonas campestris pv. campestris (strain ATCC 33913 / DSM 3586 / NCPPB 528 / LMG 568 / P 25) | 22% | 100% |
Q8PKS5 | Xanthomonas axonopodis pv. citri (strain 306) | 22% | 100% |
Q8T8P3 | Dictyostelium discoideum | 32% | 86% |
Q9BHG2 | Leishmania major | 28% | 100% |
Q9PEE7 | Xylella fastidiosa (strain 9a5c) | 21% | 100% |
Q9QY44 | Rattus norvegicus | 29% | 86% |
Q9UBJ2 | Homo sapiens | 28% | 86% |
V5AYI7 | Trypanosoma cruzi | 27% | 100% |
V5BPB7 | Trypanosoma cruzi | 44% | 100% |
V5BXE1 | Trypanosoma cruzi | 21% | 96% |