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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005739 | mitochondrion | 5 | 2 |
GO:0005783 | endoplasmic reticulum | 5 | 2 |
GO:0016020 | membrane | 2 | 6 |
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:0071944 | cell periphery | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
Related structures:
AlphaFold database: Q4QIE9
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 2 |
GO:0006643 | membrane lipid metabolic process | 4 | 2 |
GO:0006644 | phospholipid metabolic process | 4 | 2 |
GO:0006665 | sphingolipid metabolic process | 4 | 2 |
GO:0006672 | ceramide metabolic process | 4 | 2 |
GO:0006684 | sphingomyelin metabolic process | 4 | 2 |
GO:0006685 | sphingomyelin catabolic process | 5 | 2 |
GO:0006793 | phosphorus metabolic process | 3 | 2 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0008610 | lipid biosynthetic process | 4 | 2 |
GO:0009056 | catabolic process | 2 | 2 |
GO:0009058 | biosynthetic process | 2 | 2 |
GO:0009268 | response to pH | 3 | 2 |
GO:0009395 | phospholipid catabolic process | 5 | 2 |
GO:0009628 | response to abiotic stimulus | 2 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0010447 | response to acidic pH | 4 | 2 |
GO:0016042 | lipid catabolic process | 4 | 2 |
GO:0019637 | organophosphate metabolic process | 3 | 2 |
GO:0030148 | sphingolipid biosynthetic process | 5 | 2 |
GO:0030149 | sphingolipid catabolic process | 5 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0043603 | amide metabolic process | 3 | 2 |
GO:0043604 | amide biosynthetic process | 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:0044249 | cellular biosynthetic process | 3 | 2 |
GO:0044255 | cellular lipid metabolic process | 3 | 2 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 2 |
GO:0046434 | organophosphate catabolic process | 4 | 2 |
GO:0046466 | membrane lipid catabolic process | 5 | 2 |
GO:0046467 | membrane lipid biosynthetic process | 4 | 2 |
GO:0046513 | ceramide biosynthetic process | 5 | 2 |
GO:0050896 | response to stimulus | 1 | 2 |
GO:0051716 | cellular response to stimulus | 2 | 2 |
GO:0071214 | cellular response to abiotic stimulus | 3 | 2 |
GO:0071467 | cellular response to pH | 4 | 2 |
GO:0071468 | cellular response to acidic pH | 5 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0104004 | cellular response to environmental stimulus | 3 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 2 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 2 |
GO:1901575 | organic substance catabolic process | 3 | 2 |
GO:1901576 | organic substance biosynthetic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004620 | phospholipase activity | 5 | 11 |
GO:0004767 | sphingomyelin phosphodiesterase activity | 6 | 11 |
GO:0008081 | phosphoric diester hydrolase activity | 5 | 11 |
GO:0016298 | lipase activity | 4 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 11 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 11 |
GO:0003676 | nucleic acid binding | 3 | 3 |
GO:0003743 | translation initiation factor activity | 4 | 3 |
GO:0005488 | binding | 1 | 3 |
GO:0008135 | translation factor activity, RNA binding | 3 | 3 |
GO:0045182 | translation regulator activity | 1 | 3 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 3 |
GO:0097159 | organic cyclic compound binding | 2 | 3 |
GO:1901363 | heterocyclic compound binding | 2 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 133 | 137 | PF00656 | 0.290 |
CLV_C14_Caspase3-7 | 300 | 304 | PF00656 | 0.391 |
CLV_C14_Caspase3-7 | 396 | 400 | PF00656 | 0.372 |
CLV_NRD_NRD_1 | 166 | 168 | PF00675 | 0.443 |
CLV_NRD_NRD_1 | 438 | 440 | PF00675 | 0.571 |
CLV_NRD_NRD_1 | 467 | 469 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 76 | 78 | PF00675 | 0.494 |
CLV_PCSK_KEX2_1 | 166 | 168 | PF00082 | 0.491 |
CLV_PCSK_KEX2_1 | 218 | 220 | PF00082 | 0.547 |
CLV_PCSK_KEX2_1 | 344 | 346 | PF00082 | 0.729 |
CLV_PCSK_KEX2_1 | 467 | 469 | PF00082 | 0.461 |
CLV_PCSK_KEX2_1 | 579 | 581 | PF00082 | 0.575 |
CLV_PCSK_KEX2_1 | 76 | 78 | PF00082 | 0.462 |
CLV_PCSK_PC1ET2_1 | 218 | 220 | PF00082 | 0.547 |
CLV_PCSK_PC1ET2_1 | 344 | 346 | PF00082 | 0.721 |
CLV_PCSK_PC1ET2_1 | 579 | 581 | PF00082 | 0.575 |
CLV_PCSK_SKI1_1 | 15 | 19 | PF00082 | 0.526 |
CLV_PCSK_SKI1_1 | 249 | 253 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 268 | 272 | PF00082 | 0.497 |
CLV_PCSK_SKI1_1 | 287 | 291 | PF00082 | 0.532 |
CLV_PCSK_SKI1_1 | 579 | 583 | PF00082 | 0.572 |
DEG_SPOP_SBC_1 | 363 | 367 | PF00917 | 0.396 |
DEG_SPOP_SBC_1 | 398 | 402 | PF00917 | 0.434 |
DEG_SPOP_SBC_1 | 570 | 574 | PF00917 | 0.676 |
DOC_CYCLIN_RxL_1 | 166 | 176 | PF00134 | 0.291 |
DOC_CYCLIN_RxL_1 | 263 | 275 | PF00134 | 0.344 |
DOC_MAPK_gen_1 | 166 | 173 | PF00069 | 0.320 |
DOC_MAPK_gen_1 | 28 | 36 | PF00069 | 0.313 |
DOC_MAPK_MEF2A_6 | 121 | 130 | PF00069 | 0.256 |
DOC_PP1_RVXF_1 | 13 | 20 | PF00149 | 0.359 |
DOC_PP2B_LxvP_1 | 228 | 231 | PF13499 | 0.348 |
DOC_PP4_FxxP_1 | 285 | 288 | PF00568 | 0.346 |
DOC_USP7_MATH_1 | 363 | 367 | PF00917 | 0.396 |
DOC_USP7_MATH_1 | 548 | 552 | PF00917 | 0.776 |
DOC_USP7_MATH_1 | 559 | 563 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 611 | 615 | PF00917 | 0.585 |
DOC_USP7_UBL2_3 | 358 | 362 | PF12436 | 0.566 |
DOC_WW_Pin1_4 | 417 | 422 | PF00397 | 0.428 |
DOC_WW_Pin1_4 | 534 | 539 | PF00397 | 0.710 |
DOC_WW_Pin1_4 | 544 | 549 | PF00397 | 0.697 |
DOC_WW_Pin1_4 | 581 | 586 | PF00397 | 0.731 |
DOC_WW_Pin1_4 | 63 | 68 | PF00397 | 0.318 |
LIG_14-3-3_CanoR_1 | 15 | 20 | PF00244 | 0.346 |
LIG_14-3-3_CanoR_1 | 174 | 181 | PF00244 | 0.256 |
LIG_14-3-3_CanoR_1 | 249 | 254 | PF00244 | 0.279 |
LIG_14-3-3_CanoR_1 | 256 | 260 | PF00244 | 0.279 |
LIG_14-3-3_CanoR_1 | 425 | 431 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 580 | 585 | PF00244 | 0.767 |
LIG_14-3-3_CanoR_1 | 71 | 76 | PF00244 | 0.358 |
LIG_14-3-3_CanoR_1 | 77 | 83 | PF00244 | 0.327 |
LIG_14-3-3_CanoR_1 | 92 | 100 | PF00244 | 0.273 |
LIG_Actin_WH2_2 | 220 | 237 | PF00022 | 0.365 |
LIG_APCC_ABBA_1 | 111 | 116 | PF00400 | 0.334 |
LIG_APCC_Cbox_1 | 168 | 174 | PF00515 | 0.334 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.501 |
LIG_BRCT_BRCA1_1 | 381 | 385 | PF00533 | 0.365 |
LIG_BRCT_BRCA1_1 | 613 | 617 | PF00533 | 0.454 |
LIG_BRCT_BRCA1_1 | 95 | 99 | PF00533 | 0.268 |
LIG_Clathr_ClatBox_1 | 269 | 273 | PF01394 | 0.346 |
LIG_EH1_1 | 384 | 392 | PF00400 | 0.369 |
LIG_FHA_1 | 100 | 106 | PF00498 | 0.240 |
LIG_FHA_1 | 147 | 153 | PF00498 | 0.267 |
LIG_FHA_1 | 16 | 22 | PF00498 | 0.243 |
LIG_FHA_1 | 190 | 196 | PF00498 | 0.270 |
LIG_FHA_1 | 351 | 357 | PF00498 | 0.541 |
LIG_FHA_1 | 400 | 406 | PF00498 | 0.531 |
LIG_FHA_1 | 412 | 418 | PF00498 | 0.346 |
LIG_FHA_1 | 493 | 499 | PF00498 | 0.746 |
LIG_FHA_1 | 524 | 530 | PF00498 | 0.658 |
LIG_FHA_1 | 618 | 624 | PF00498 | 0.403 |
LIG_FHA_2 | 131 | 137 | PF00498 | 0.291 |
LIG_FHA_2 | 250 | 256 | PF00498 | 0.245 |
LIG_FHA_2 | 318 | 324 | PF00498 | 0.408 |
LIG_FHA_2 | 37 | 43 | PF00498 | 0.343 |
LIG_FHA_2 | 418 | 424 | PF00498 | 0.342 |
LIG_FHA_2 | 512 | 518 | PF00498 | 0.584 |
LIG_FHA_2 | 581 | 587 | PF00498 | 0.695 |
LIG_LIR_Gen_1 | 180 | 186 | PF02991 | 0.294 |
LIG_LIR_Gen_1 | 258 | 267 | PF02991 | 0.323 |
LIG_LIR_Gen_1 | 335 | 341 | PF02991 | 0.491 |
LIG_LIR_Gen_1 | 42 | 49 | PF02991 | 0.306 |
LIG_LIR_Gen_1 | 447 | 458 | PF02991 | 0.354 |
LIG_LIR_Gen_1 | 56 | 65 | PF02991 | 0.201 |
LIG_LIR_Nem_3 | 168 | 173 | PF02991 | 0.242 |
LIG_LIR_Nem_3 | 180 | 184 | PF02991 | 0.244 |
LIG_LIR_Nem_3 | 264 | 270 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 303 | 308 | PF02991 | 0.311 |
LIG_LIR_Nem_3 | 330 | 336 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 42 | 47 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 447 | 453 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 56 | 61 | PF02991 | 0.201 |
LIG_LIR_Nem_3 | 594 | 598 | PF02991 | 0.607 |
LIG_LIR_Nem_3 | 72 | 78 | PF02991 | 0.259 |
LIG_LYPXL_yS_3 | 108 | 111 | PF13949 | 0.330 |
LIG_LYPXL_yS_3 | 305 | 308 | PF13949 | 0.301 |
LIG_Pex14_1 | 337 | 341 | PF04695 | 0.351 |
LIG_Pex14_2 | 58 | 62 | PF04695 | 0.383 |
LIG_Pex14_2 | 78 | 82 | PF04695 | 0.196 |
LIG_Pex14_2 | 99 | 103 | PF04695 | 0.334 |
LIG_REV1ctd_RIR_1 | 115 | 125 | PF16727 | 0.346 |
LIG_REV1ctd_RIR_1 | 282 | 287 | PF16727 | 0.291 |
LIG_SH2_CRK | 44 | 48 | PF00017 | 0.256 |
LIG_SH2_CRK | 450 | 454 | PF00017 | 0.408 |
LIG_SH2_NCK_1 | 156 | 160 | PF00017 | 0.291 |
LIG_SH2_NCK_1 | 485 | 489 | PF00017 | 0.601 |
LIG_SH2_STAP1 | 148 | 152 | PF00017 | 0.267 |
LIG_SH2_STAP1 | 44 | 48 | PF00017 | 0.256 |
LIG_SH2_STAP1 | 485 | 489 | PF00017 | 0.640 |
LIG_SH2_STAP1 | 608 | 612 | PF00017 | 0.655 |
LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 170 | 173 | PF00017 | 0.240 |
LIG_SH2_STAT5 | 266 | 269 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.367 |
LIG_SH2_STAT5 | 73 | 76 | PF00017 | 0.256 |
LIG_SH3_3 | 125 | 131 | PF00018 | 0.308 |
LIG_SH3_3 | 188 | 194 | PF00018 | 0.204 |
LIG_SH3_3 | 224 | 230 | PF00018 | 0.254 |
LIG_SH3_3 | 321 | 327 | PF00018 | 0.370 |
LIG_SH3_3 | 495 | 501 | PF00018 | 0.725 |
LIG_SH3_3 | 555 | 561 | PF00018 | 0.803 |
LIG_Sin3_3 | 289 | 296 | PF02671 | 0.248 |
LIG_SUMO_SIM_anti_2 | 45 | 51 | PF11976 | 0.259 |
LIG_SUMO_SIM_anti_2 | 455 | 461 | PF11976 | 0.427 |
LIG_SUMO_SIM_par_1 | 149 | 157 | PF11976 | 0.310 |
LIG_SUMO_SIM_par_1 | 45 | 51 | PF11976 | 0.256 |
LIG_SUMO_SIM_par_1 | 455 | 461 | PF11976 | 0.225 |
LIG_TRAF2_1 | 240 | 243 | PF00917 | 0.269 |
LIG_TRAF2_1 | 420 | 423 | PF00917 | 0.358 |
LIG_TRAF2_1 | 471 | 474 | PF00917 | 0.635 |
LIG_UBA3_1 | 212 | 218 | PF00899 | 0.313 |
LIG_UBA3_1 | 390 | 397 | PF00899 | 0.326 |
LIG_WRC_WIRS_1 | 16 | 21 | PF05994 | 0.265 |
LIG_WW_3 | 229 | 233 | PF00397 | 0.334 |
MOD_CK1_1 | 160 | 166 | PF00069 | 0.327 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.274 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.489 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.292 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.375 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.511 |
MOD_CK1_1 | 531 | 537 | PF00069 | 0.688 |
MOD_CK2_1 | 317 | 323 | PF00069 | 0.409 |
MOD_CK2_1 | 36 | 42 | PF00069 | 0.346 |
MOD_CK2_1 | 362 | 368 | PF00069 | 0.531 |
MOD_CK2_1 | 417 | 423 | PF00069 | 0.305 |
MOD_CK2_1 | 467 | 473 | PF00069 | 0.647 |
MOD_CK2_1 | 580 | 586 | PF00069 | 0.763 |
MOD_Cter_Amidation | 342 | 345 | PF01082 | 0.706 |
MOD_GlcNHglycan | 329 | 332 | PF01048 | 0.669 |
MOD_GlcNHglycan | 341 | 344 | PF01048 | 0.569 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.736 |
MOD_GlcNHglycan | 407 | 410 | PF01048 | 0.712 |
MOD_GlcNHglycan | 469 | 472 | PF01048 | 0.493 |
MOD_GlcNHglycan | 476 | 479 | PF01048 | 0.478 |
MOD_GlcNHglycan | 609 | 612 | PF01048 | 0.485 |
MOD_GlcNHglycan | 614 | 617 | PF01048 | 0.390 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.474 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.338 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.265 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.200 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.275 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.293 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.516 |
MOD_GSK3_1 | 404 | 411 | PF00069 | 0.529 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.405 |
MOD_GSK3_1 | 544 | 551 | PF00069 | 0.772 |
MOD_GSK3_1 | 565 | 572 | PF00069 | 0.787 |
MOD_GSK3_1 | 607 | 614 | PF00069 | 0.623 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.346 |
MOD_N-GLC_1 | 201 | 206 | PF02516 | 0.470 |
MOD_N-GLC_1 | 350 | 355 | PF02516 | 0.747 |
MOD_N-GLC_1 | 617 | 622 | PF02516 | 0.347 |
MOD_N-GLC_1 | 63 | 68 | PF02516 | 0.411 |
MOD_N-GLC_2 | 543 | 545 | PF02516 | 0.430 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.256 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.310 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.275 |
MOD_NEK2_1 | 201 | 206 | PF00069 | 0.198 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.310 |
MOD_NEK2_1 | 283 | 288 | PF00069 | 0.227 |
MOD_NEK2_1 | 404 | 409 | PF00069 | 0.504 |
MOD_NEK2_1 | 458 | 463 | PF00069 | 0.414 |
MOD_NEK2_1 | 607 | 612 | PF00069 | 0.641 |
MOD_NEK2_1 | 617 | 622 | PF00069 | 0.352 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.289 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.314 |
MOD_NEK2_2 | 504 | 509 | PF00069 | 0.703 |
MOD_NEK2_2 | 523 | 528 | PF00069 | 0.531 |
MOD_PIKK_1 | 157 | 163 | PF00454 | 0.311 |
MOD_PIKK_1 | 173 | 179 | PF00454 | 0.204 |
MOD_PIKK_1 | 201 | 207 | PF00454 | 0.270 |
MOD_PIKK_1 | 275 | 281 | PF00454 | 0.337 |
MOD_PIKK_1 | 440 | 446 | PF00454 | 0.403 |
MOD_PIKK_1 | 93 | 99 | PF00454 | 0.302 |
MOD_PKA_1 | 467 | 473 | PF00069 | 0.613 |
MOD_PKA_1 | 579 | 585 | PF00069 | 0.773 |
MOD_PKA_2 | 173 | 179 | PF00069 | 0.256 |
MOD_PKA_2 | 189 | 195 | PF00069 | 0.256 |
MOD_PKA_2 | 255 | 261 | PF00069 | 0.247 |
MOD_PKA_2 | 467 | 473 | PF00069 | 0.601 |
MOD_PKA_2 | 492 | 498 | PF00069 | 0.698 |
MOD_PKA_2 | 579 | 585 | PF00069 | 0.768 |
MOD_Plk_1 | 143 | 149 | PF00069 | 0.286 |
MOD_Plk_2-3 | 51 | 57 | PF00069 | 0.260 |
MOD_Plk_4 | 143 | 149 | PF00069 | 0.314 |
MOD_Plk_4 | 223 | 229 | PF00069 | 0.309 |
MOD_Plk_4 | 262 | 268 | PF00069 | 0.338 |
MOD_Plk_4 | 332 | 338 | PF00069 | 0.470 |
MOD_Plk_4 | 426 | 432 | PF00069 | 0.359 |
MOD_Plk_4 | 78 | 84 | PF00069 | 0.346 |
MOD_ProDKin_1 | 417 | 423 | PF00069 | 0.421 |
MOD_ProDKin_1 | 534 | 540 | PF00069 | 0.711 |
MOD_ProDKin_1 | 544 | 550 | PF00069 | 0.696 |
MOD_ProDKin_1 | 581 | 587 | PF00069 | 0.730 |
MOD_ProDKin_1 | 63 | 69 | PF00069 | 0.318 |
MOD_SUMO_for_1 | 270 | 273 | PF00179 | 0.334 |
MOD_SUMO_for_1 | 471 | 474 | PF00179 | 0.647 |
TRG_DiLeu_BaEn_1 | 56 | 61 | PF01217 | 0.346 |
TRG_ENDOCYTIC_2 | 108 | 111 | PF00928 | 0.330 |
TRG_ENDOCYTIC_2 | 156 | 159 | PF00928 | 0.315 |
TRG_ENDOCYTIC_2 | 170 | 173 | PF00928 | 0.200 |
TRG_ENDOCYTIC_2 | 266 | 269 | PF00928 | 0.325 |
TRG_ENDOCYTIC_2 | 305 | 308 | PF00928 | 0.301 |
TRG_ENDOCYTIC_2 | 333 | 336 | PF00928 | 0.384 |
TRG_ENDOCYTIC_2 | 378 | 381 | PF00928 | 0.396 |
TRG_ENDOCYTIC_2 | 44 | 47 | PF00928 | 0.256 |
TRG_ENDOCYTIC_2 | 450 | 453 | PF00928 | 0.372 |
TRG_ER_diArg_1 | 165 | 167 | PF00400 | 0.204 |
TRG_ER_diArg_1 | 466 | 468 | PF00400 | 0.609 |
TRG_ER_diArg_1 | 75 | 77 | PF00400 | 0.312 |
TRG_Pf-PMV_PEXEL_1 | 206 | 211 | PF00026 | 0.470 |
TRG_Pf-PMV_PEXEL_1 | 232 | 236 | PF00026 | 0.546 |
TRG_Pf-PMV_PEXEL_1 | 439 | 444 | PF00026 | 0.529 |
TRG_Pf-PMV_PEXEL_1 | 596 | 600 | PF00026 | 0.500 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P935 | Leptomonas seymouri | 57% | 100% |
A0A1X0NNY2 | Trypanosomatidae | 40% | 100% |
A0A3S5H634 | Leishmania donovani | 93% | 100% |
A0A422NTR5 | Trypanosoma rangeli | 37% | 100% |
A4H587 | Leishmania braziliensis | 70% | 99% |
A4HTH1 | Leishmania infantum | 94% | 100% |
C9ZPP9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9AM99 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
V5BLM5 | Trypanosoma cruzi | 37% | 100% |