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: A4HLP7
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_NRD_NRD_1 | 37 | 39 | PF00675 | 0.403 |
CLV_NRD_NRD_1 | 619 | 621 | PF00675 | 0.564 |
CLV_PCSK_KEX2_1 | 315 | 317 | PF00082 | 0.239 |
CLV_PCSK_KEX2_1 | 36 | 38 | PF00082 | 0.402 |
CLV_PCSK_PC1ET2_1 | 315 | 317 | PF00082 | 0.229 |
CLV_PCSK_SKI1_1 | 127 | 131 | PF00082 | 0.398 |
CLV_PCSK_SKI1_1 | 152 | 156 | PF00082 | 0.254 |
CLV_PCSK_SKI1_1 | 213 | 217 | PF00082 | 0.287 |
CLV_PCSK_SKI1_1 | 318 | 322 | PF00082 | 0.261 |
CLV_PCSK_SKI1_1 | 463 | 467 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 505 | 509 | PF00082 | 0.498 |
CLV_PCSK_SKI1_1 | 568 | 572 | PF00082 | 0.431 |
CLV_PCSK_SKI1_1 | 573 | 577 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 616 | 620 | PF00082 | 0.439 |
DEG_APCC_DBOX_1 | 103 | 111 | PF00400 | 0.348 |
DEG_APCC_DBOX_1 | 398 | 406 | PF00400 | 0.336 |
DEG_APCC_DBOX_1 | 567 | 575 | PF00400 | 0.260 |
DEG_APCC_DBOX_1 | 615 | 623 | PF00400 | 0.227 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 163 | 170 | PF00134 | 0.484 |
DOC_MAPK_gen_1 | 104 | 111 | PF00069 | 0.225 |
DOC_MAPK_gen_1 | 401 | 410 | PF00069 | 0.389 |
DOC_MAPK_gen_1 | 566 | 574 | PF00069 | 0.319 |
DOC_MAPK_gen_1 | 620 | 629 | PF00069 | 0.354 |
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 | 0.325 |
DOC_MAPK_MEF2A_6 | 74 | 83 | PF00069 | 0.448 |
DOC_MAPK_NFAT4_5 | 104 | 112 | PF00069 | 0.269 |
DOC_MAPK_RevD_3 | 25 | 38 | PF00069 | 0.378 |
DOC_PP1_RVXF_1 | 67 | 73 | PF00149 | 0.592 |
DOC_PP1_RVXF_1 | 9 | 16 | PF00149 | 0.341 |
DOC_PP2B_LxvP_1 | 140 | 143 | PF13499 | 0.397 |
DOC_PP2B_LxvP_1 | 367 | 370 | PF13499 | 0.273 |
DOC_SPAK_OSR1_1 | 120 | 124 | PF12202 | 0.159 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.470 |
DOC_USP7_MATH_1 | 435 | 439 | PF00917 | 0.427 |
DOC_USP7_MATH_1 | 535 | 539 | PF00917 | 0.301 |
DOC_USP7_UBL2_3 | 172 | 176 | PF12436 | 0.471 |
DOC_WW_Pin1_4 | 233 | 238 | PF00397 | 0.159 |
DOC_WW_Pin1_4 | 430 | 435 | PF00397 | 0.295 |
DOC_WW_Pin1_4 | 445 | 450 | PF00397 | 0.300 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.715 |
LIG_14-3-3_CanoR_1 | 104 | 110 | PF00244 | 0.266 |
LIG_14-3-3_CanoR_1 | 196 | 204 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 302 | 308 | PF00244 | 0.383 |
LIG_14-3-3_CanoR_1 | 451 | 455 | PF00244 | 0.275 |
LIG_14-3-3_CanoR_1 | 47 | 53 | PF00244 | 0.624 |
LIG_14-3-3_CanoR_1 | 480 | 484 | PF00244 | 0.159 |
LIG_14-3-3_CanoR_1 | 505 | 511 | PF00244 | 0.284 |
LIG_14-3-3_CanoR_1 | 624 | 630 | PF00244 | 0.412 |
LIG_14-3-3_CanoR_1 | 85 | 90 | PF00244 | 0.458 |
LIG_Actin_WH2_2 | 139 | 154 | PF00022 | 0.173 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.439 |
LIG_BRCT_BRCA1_1 | 117 | 121 | PF00533 | 0.238 |
LIG_BRCT_BRCA1_1 | 8 | 12 | PF00533 | 0.392 |
LIG_BRCT_BRCA1_1 | 87 | 91 | PF00533 | 0.465 |
LIG_Clathr_ClatBox_1 | 343 | 347 | PF01394 | 0.330 |
LIG_eIF4E_1 | 338 | 344 | PF01652 | 0.348 |
LIG_FHA_1 | 22 | 28 | PF00498 | 0.288 |
LIG_FHA_1 | 222 | 228 | PF00498 | 0.283 |
LIG_FHA_1 | 315 | 321 | PF00498 | 0.565 |
LIG_FHA_1 | 586 | 592 | PF00498 | 0.221 |
LIG_FHA_2 | 483 | 489 | PF00498 | 0.319 |
LIG_FHA_2 | 541 | 547 | PF00498 | 0.226 |
LIG_GBD_Chelix_1 | 335 | 343 | PF00786 | 0.397 |
LIG_LIR_Apic_2 | 497 | 501 | PF02991 | 0.249 |
LIG_LIR_Gen_1 | 108 | 115 | PF02991 | 0.288 |
LIG_LIR_Gen_1 | 243 | 252 | PF02991 | 0.315 |
LIG_LIR_Gen_1 | 488 | 498 | PF02991 | 0.159 |
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 | 0.275 |
LIG_LIR_Nem_3 | 325 | 331 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 488 | 493 | PF02991 | 0.159 |
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 | 0.335 |
LIG_LIR_Nem_3 | 88 | 94 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 9 | 15 | PF02991 | 0.326 |
LIG_LYPXL_yS_3 | 510 | 513 | PF13949 | 0.260 |
LIG_NRBOX | 74 | 80 | PF00104 | 0.502 |
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_PTB_Apo_2 | 413 | 420 | PF02174 | 0.266 |
LIG_PTB_Phospho_1 | 413 | 419 | PF10480 | 0.269 |
LIG_SH2_CRK | 600 | 604 | PF00017 | 0.273 |
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 | 0.337 |
LIG_SH2_STAT3 | 16 | 19 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 102 | 105 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 153 | 156 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 174 | 177 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 245 | 248 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 338 | 341 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 361 | 364 | PF00017 | 0.284 |
LIG_SH2_STAT5 | 368 | 371 | PF00017 | 0.239 |
LIG_SH2_STAT5 | 498 | 501 | PF00017 | 0.228 |
LIG_SH2_STAT5 | 512 | 515 | PF00017 | 0.228 |
LIG_SH2_STAT5 | 55 | 58 | PF00017 | 0.563 |
LIG_SH3_3 | 232 | 238 | PF00018 | 0.362 |
LIG_SH3_3 | 251 | 257 | PF00018 | 0.381 |
LIG_SH3_3 | 478 | 484 | PF00018 | 0.247 |
LIG_SH3_3 | 78 | 84 | PF00018 | 0.383 |
LIG_SUMO_SIM_anti_2 | 105 | 111 | PF11976 | 0.308 |
LIG_SUMO_SIM_anti_2 | 342 | 347 | PF11976 | 0.330 |
LIG_SUMO_SIM_anti_2 | 427 | 433 | PF11976 | 0.297 |
LIG_SUMO_SIM_anti_2 | 93 | 99 | PF11976 | 0.252 |
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 | 0.250 |
LIG_SUMO_SIM_par_1 | 625 | 630 | PF11976 | 0.273 |
LIG_SUMO_SIM_par_1 | 93 | 99 | PF11976 | 0.251 |
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 | 146 | 152 | PF00899 | 0.173 |
LIG_UBA3_1 | 378 | 383 | PF00899 | 0.290 |
LIG_ULM_U2AF65_1 | 315 | 320 | PF00076 | 0.442 |
MOD_CDK_SPxK_1 | 445 | 451 | PF00069 | 0.337 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.735 |
MOD_CK1_1 | 458 | 464 | PF00069 | 0.289 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.714 |
MOD_CK1_1 | 534 | 540 | PF00069 | 0.220 |
MOD_CK1_1 | 589 | 595 | PF00069 | 0.300 |
MOD_CK2_1 | 279 | 285 | PF00069 | 0.471 |
MOD_CK2_1 | 350 | 356 | PF00069 | 0.311 |
MOD_CK2_1 | 482 | 488 | PF00069 | 0.311 |
MOD_CK2_1 | 559 | 565 | PF00069 | 0.246 |
MOD_CK2_1 | 56 | 62 | PF00069 | 0.550 |
MOD_CK2_1 | 589 | 595 | PF00069 | 0.406 |
MOD_CK2_1 | 611 | 617 | PF00069 | 0.287 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.401 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.514 |
MOD_GlcNHglycan | 460 | 463 | PF01048 | 0.467 |
MOD_GlcNHglycan | 470 | 473 | PF01048 | 0.474 |
MOD_GlcNHglycan | 533 | 536 | PF01048 | 0.497 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.421 |
MOD_GlcNHglycan | 561 | 564 | PF01048 | 0.429 |
MOD_GlcNHglycan | 588 | 591 | PF01048 | 0.485 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.456 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.461 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.258 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.500 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.696 |
MOD_GSK3_1 | 482 | 489 | PF00069 | 0.322 |
MOD_GSK3_1 | 531 | 538 | PF00069 | 0.339 |
MOD_GSK3_1 | 585 | 592 | PF00069 | 0.217 |
MOD_N-GLC_1 | 186 | 191 | PF02516 | 0.241 |
MOD_N-GLC_1 | 443 | 448 | PF02516 | 0.445 |
MOD_N-GLC_1 | 458 | 463 | PF02516 | 0.456 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.473 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.485 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.401 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.208 |
MOD_NEK2_1 | 240 | 245 | PF00069 | 0.232 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.180 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.399 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.437 |
MOD_NEK2_1 | 339 | 344 | PF00069 | 0.397 |
MOD_NEK2_1 | 388 | 393 | PF00069 | 0.262 |
MOD_NEK2_1 | 443 | 448 | PF00069 | 0.230 |
MOD_NEK2_1 | 539 | 544 | PF00069 | 0.203 |
MOD_NEK2_1 | 598 | 603 | PF00069 | 0.257 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.427 |
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 | 0.290 |
MOD_PIKK_1 | 589 | 595 | PF00454 | 0.289 |
MOD_PKA_2 | 105 | 111 | PF00069 | 0.214 |
MOD_PKA_2 | 195 | 201 | PF00069 | 0.428 |
MOD_PKA_2 | 450 | 456 | PF00069 | 0.275 |
MOD_PKA_2 | 479 | 485 | PF00069 | 0.248 |
MOD_PKB_1 | 36 | 44 | PF00069 | 0.639 |
MOD_Plk_1 | 186 | 192 | PF00069 | 0.368 |
MOD_Plk_1 | 355 | 361 | PF00069 | 0.361 |
MOD_Plk_1 | 443 | 449 | PF00069 | 0.273 |
MOD_Plk_4 | 105 | 111 | PF00069 | 0.274 |
MOD_Plk_4 | 176 | 182 | PF00069 | 0.490 |
MOD_Plk_4 | 250 | 256 | PF00069 | 0.346 |
MOD_Plk_4 | 323 | 329 | PF00069 | 0.452 |
MOD_Plk_4 | 331 | 337 | PF00069 | 0.314 |
MOD_Plk_4 | 339 | 345 | PF00069 | 0.125 |
MOD_Plk_4 | 435 | 441 | PF00069 | 0.382 |
MOD_Plk_4 | 450 | 456 | PF00069 | 0.275 |
MOD_Plk_4 | 486 | 492 | PF00069 | 0.309 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.692 |
MOD_Plk_4 | 540 | 546 | PF00069 | 0.244 |
MOD_Plk_4 | 598 | 604 | PF00069 | 0.271 |
MOD_Plk_4 | 606 | 612 | PF00069 | 0.296 |
MOD_Plk_4 | 74 | 80 | PF00069 | 0.504 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.363 |
MOD_ProDKin_1 | 233 | 239 | PF00069 | 0.159 |
MOD_ProDKin_1 | 430 | 436 | PF00069 | 0.298 |
MOD_ProDKin_1 | 445 | 451 | PF00069 | 0.300 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.715 |
MOD_SUMO_rev_2 | 306 | 314 | PF00179 | 0.519 |
TRG_DiLeu_BaLyEn_6 | 299 | 304 | PF01217 | 0.442 |
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 | 0.258 |
TRG_ER_diArg_1 | 103 | 106 | PF00400 | 0.279 |
TRG_ER_diArg_1 | 36 | 38 | PF00400 | 0.602 |
TRG_ER_diArg_1 | 566 | 569 | PF00400 | 0.228 |
TRG_NES_CRM1_1 | 400 | 413 | PF08389 | 0.379 |
TRG_NES_CRM1_1 | 617 | 630 | PF08389 | 0.364 |
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 | 25% | 75% |
A0A0N1I7J3 | Leptomonas seymouri | 67% | 100% |
A0A0S4IIU4 | Bodo saltans | 34% | 100% |
A0A1X0NJ54 | Trypanosomatidae | 29% | 92% |
A0A1X0NRS8 | Trypanosomatidae | 24% | 87% |
A0A1X0P3R6 | Trypanosomatidae | 44% | 100% |
A0A1X0P474 | Trypanosomatidae | 21% | 95% |
A0A3Q8ICD7 | Leishmania donovani | 27% | 76% |
A0A3R7KWF0 | Trypanosoma rangeli | 27% | 95% |
A0A3R7NBD2 | Trypanosoma rangeli | 44% | 100% |
A0A3S7X621 | Leishmania donovani | 22% | 72% |
A0A3S7X6Y1 | Leishmania donovani | 85% | 100% |
A0A422NTH3 | Trypanosoma rangeli | 21% | 96% |
A4HFH3 | Leishmania braziliensis | 20% | 100% |
A4HJ32 | Leishmania braziliensis | 26% | 100% |
A4I6L1 | Leishmania infantum | 27% | 76% |
A4I8D3 | Leishmania infantum | 22% | 91% |
A4I948 | Leishmania infantum | 85% | 100% |
C9ZN63 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 94% |
D0A6C8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
D3ZHR2 | Rattus norvegicus | 30% | 87% |
E9AD24 | Leishmania major | 21% | 100% |
E9B1K4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 78% |
E9B392 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 22% | 91% |
E9B422 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
F1RBC8 | Danio rerio | 29% | 84% |
O14678 | Homo sapiens | 28% | 100% |
O89016 | Mus musculus | 28% | 100% |
P16970 | Rattus norvegicus | 31% | 97% |
P28288 | Homo sapiens | 32% | 97% |
P33897 | Homo sapiens | 31% | 86% |
P34230 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 75% |
P41909 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 24% | 74% |
P45221 | Haemophilus influenzae (strain ATCC 51907 / DSM 11121 / KW20 / Rd) | 25% | 100% |
P48410 | Mus musculus | 30% | 87% |
P55096 | Mus musculus | 32% | 97% |
P9WQI8 | Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) | 27% | 100% |
P9WQI9 | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | 27% | 100% |
Q0A4U4 | Alkalilimnicola ehrlichii (strain ATCC BAA-1101 / DSM 17681 / MLHE-1) | 22% | 100% |
Q2P3E7 | Xanthomonas oryzae pv. oryzae (strain MAFF 311018) | 22% | 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 | 84% | 100% |
Q4Q4W3 | Leishmania major | 22% | 100% |
Q4UV65 | Xanthomonas campestris pv. campestris (strain 8004) | 22% | 100% |
Q55774 | Synechocystis sp. (strain PCC 6803 / Kazusa) | 31% | 97% |
Q57335 | Haemophilus influenzae (strain ATCC 51907 / DSM 11121 / KW20 / Rd) | 25% | 100% |
Q5B1Q2 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 23% | 89% |
Q5H0H0 | Xanthomonas oryzae pv. oryzae (strain KACC10331 / KXO85) | 22% | 100% |
Q61285 | Mus musculus | 29% | 86% |
Q6NLC1 | Arabidopsis thaliana | 28% | 91% |
Q7JUN3 | Drosophila melanogaster | 29% | 88% |
Q7RX59 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 23% | 89% |
Q7VR44 | Blochmannia floridanus | 21% | 100% |
Q83LP0 | Shigella flexneri | 20% | 100% |
Q87EF0 | Xylella fastidiosa (strain Temecula1 / ATCC 700964) | 21% | 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% |
Q9BHG2 | Leishmania major | 27% | 100% |
Q9NRK6 | Homo sapiens | 23% | 87% |
Q9PEE7 | Xylella fastidiosa (strain 9a5c) | 21% | 100% |
Q9QY44 | Rattus norvegicus | 28% | 86% |
Q9UBJ2 | Homo sapiens | 28% | 86% |
V5AYI7 | Trypanosoma cruzi | 27% | 100% |
V5BPB7 | Trypanosoma cruzi | 44% | 100% |
V5BXE1 | Trypanosoma cruzi | 20% | 96% |