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 | 1 |
GO:0005783 | endoplasmic reticulum | 5 | 1 |
GO:0016020 | membrane | 2 | 5 |
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:0071944 | cell periphery | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
Related structures:
AlphaFold database: A4H587
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 1 |
GO:0006643 | membrane lipid metabolic process | 4 | 1 |
GO:0006644 | phospholipid metabolic process | 4 | 1 |
GO:0006665 | sphingolipid metabolic process | 4 | 1 |
GO:0006672 | ceramide metabolic process | 4 | 1 |
GO:0006684 | sphingomyelin metabolic process | 4 | 1 |
GO:0006685 | sphingomyelin catabolic process | 5 | 1 |
GO:0006793 | phosphorus metabolic process | 3 | 1 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0008610 | lipid biosynthetic process | 4 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009268 | response to pH | 3 | 1 |
GO:0009395 | phospholipid catabolic process | 5 | 1 |
GO:0009628 | response to abiotic stimulus | 2 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010447 | response to acidic pH | 4 | 1 |
GO:0016042 | lipid catabolic process | 4 | 1 |
GO:0019637 | organophosphate metabolic process | 3 | 1 |
GO:0030148 | sphingolipid biosynthetic process | 5 | 1 |
GO:0030149 | sphingolipid catabolic process | 5 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043603 | amide metabolic process | 3 | 1 |
GO:0043604 | amide biosynthetic process | 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:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044255 | cellular lipid metabolic process | 3 | 1 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 1 |
GO:0046434 | organophosphate catabolic process | 4 | 1 |
GO:0046466 | membrane lipid catabolic process | 5 | 1 |
GO:0046467 | membrane lipid biosynthetic process | 4 | 1 |
GO:0046513 | ceramide biosynthetic process | 5 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
GO:0071214 | cellular response to abiotic stimulus | 3 | 1 |
GO:0071467 | cellular response to pH | 4 | 1 |
GO:0071468 | cellular response to acidic pH | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0104004 | cellular response to environmental stimulus | 3 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 1 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
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 | 373 | 377 | PF00656 | 0.368 |
CLV_C14_Caspase3-7 | 405 | 409 | PF00656 | 0.452 |
CLV_NRD_NRD_1 | 164 | 166 | PF00675 | 0.467 |
CLV_NRD_NRD_1 | 469 | 471 | PF00675 | 0.472 |
CLV_NRD_NRD_1 | 76 | 78 | PF00675 | 0.519 |
CLV_PCSK_KEX2_1 | 218 | 220 | PF00082 | 0.554 |
CLV_PCSK_KEX2_1 | 346 | 348 | PF00082 | 0.725 |
CLV_PCSK_KEX2_1 | 469 | 471 | PF00082 | 0.472 |
CLV_PCSK_KEX2_1 | 511 | 513 | PF00082 | 0.401 |
CLV_PCSK_KEX2_1 | 581 | 583 | PF00082 | 0.631 |
CLV_PCSK_KEX2_1 | 76 | 78 | PF00082 | 0.489 |
CLV_PCSK_PC1ET2_1 | 218 | 220 | PF00082 | 0.554 |
CLV_PCSK_PC1ET2_1 | 346 | 348 | PF00082 | 0.725 |
CLV_PCSK_PC1ET2_1 | 511 | 513 | PF00082 | 0.354 |
CLV_PCSK_PC1ET2_1 | 581 | 583 | PF00082 | 0.631 |
CLV_PCSK_SKI1_1 | 225 | 229 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 258 | 262 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 340 | 344 | PF00082 | 0.648 |
CLV_PCSK_SKI1_1 | 581 | 585 | PF00082 | 0.624 |
DEG_SCF_FBW7_1 | 571 | 577 | PF00400 | 0.638 |
DEG_SPOP_SBC_1 | 490 | 494 | PF00917 | 0.611 |
DEG_SPOP_SBC_1 | 574 | 578 | PF00917 | 0.705 |
DOC_CKS1_1 | 287 | 292 | PF01111 | 0.205 |
DOC_CKS1_1 | 571 | 576 | PF01111 | 0.636 |
DOC_CYCLIN_RxL_1 | 267 | 277 | PF00134 | 0.339 |
DOC_CYCLIN_RxL_1 | 337 | 344 | PF00134 | 0.344 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 269 | 278 | PF00134 | 0.205 |
DOC_MAPK_gen_1 | 165 | 173 | PF00069 | 0.337 |
DOC_MAPK_gen_1 | 28 | 36 | PF00069 | 0.358 |
DOC_MAPK_MEF2A_6 | 121 | 130 | PF00069 | 0.282 |
DOC_PP1_RVXF_1 | 13 | 20 | PF00149 | 0.374 |
DOC_PP4_FxxP_1 | 287 | 290 | PF00568 | 0.335 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.292 |
DOC_USP7_MATH_1 | 260 | 264 | PF00917 | 0.358 |
DOC_USP7_MATH_1 | 310 | 314 | PF00917 | 0.307 |
DOC_USP7_MATH_1 | 329 | 333 | PF00917 | 0.333 |
DOC_USP7_MATH_1 | 454 | 458 | PF00917 | 0.349 |
DOC_USP7_MATH_1 | 561 | 565 | PF00917 | 0.794 |
DOC_WW_Pin1_4 | 227 | 232 | PF00397 | 0.205 |
DOC_WW_Pin1_4 | 236 | 241 | PF00397 | 0.180 |
DOC_WW_Pin1_4 | 286 | 291 | PF00397 | 0.269 |
DOC_WW_Pin1_4 | 419 | 424 | PF00397 | 0.436 |
DOC_WW_Pin1_4 | 546 | 551 | PF00397 | 0.717 |
DOC_WW_Pin1_4 | 570 | 575 | PF00397 | 0.697 |
DOC_WW_Pin1_4 | 582 | 587 | PF00397 | 0.778 |
LIG_14-3-3_CanoR_1 | 15 | 20 | PF00244 | 0.362 |
LIG_14-3-3_CanoR_1 | 174 | 181 | PF00244 | 0.282 |
LIG_14-3-3_CanoR_1 | 427 | 433 | PF00244 | 0.422 |
LIG_14-3-3_CanoR_1 | 495 | 503 | PF00244 | 0.702 |
LIG_14-3-3_CanoR_1 | 582 | 586 | PF00244 | 0.823 |
LIG_14-3-3_CanoR_1 | 77 | 83 | PF00244 | 0.344 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.500 |
LIG_BRCT_BRCA1_1 | 383 | 387 | PF00533 | 0.413 |
LIG_BRCT_BRCA1_1 | 617 | 621 | PF00533 | 0.461 |
LIG_BRCT_BRCA1_1 | 629 | 633 | PF00533 | 0.484 |
LIG_Clathr_ClatBox_1 | 271 | 275 | PF01394 | 0.362 |
LIG_EH1_1 | 386 | 394 | PF00400 | 0.378 |
LIG_FHA_1 | 147 | 153 | PF00498 | 0.285 |
LIG_FHA_1 | 190 | 196 | PF00498 | 0.296 |
LIG_FHA_1 | 477 | 483 | PF00498 | 0.540 |
LIG_FHA_1 | 589 | 595 | PF00498 | 0.744 |
LIG_FHA_1 | 622 | 628 | PF00498 | 0.430 |
LIG_FHA_2 | 320 | 326 | PF00498 | 0.392 |
LIG_FHA_2 | 37 | 43 | PF00498 | 0.386 |
LIG_FHA_2 | 420 | 426 | PF00498 | 0.365 |
LIG_FHA_2 | 429 | 435 | PF00498 | 0.308 |
LIG_FHA_2 | 503 | 509 | PF00498 | 0.633 |
LIG_GBD_Chelix_1 | 521 | 529 | PF00786 | 0.367 |
LIG_LIR_Gen_1 | 42 | 49 | PF02991 | 0.329 |
LIG_LIR_Gen_1 | 449 | 460 | PF02991 | 0.365 |
LIG_LIR_Gen_1 | 505 | 514 | PF02991 | 0.666 |
LIG_LIR_Gen_1 | 56 | 65 | PF02991 | 0.221 |
LIG_LIR_LC3C_4 | 316 | 320 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 265 | 271 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 337 | 342 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 42 | 47 | PF02991 | 0.329 |
LIG_LIR_Nem_3 | 449 | 455 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 505 | 510 | PF02991 | 0.669 |
LIG_LIR_Nem_3 | 551 | 556 | PF02991 | 0.608 |
LIG_LIR_Nem_3 | 56 | 61 | PF02991 | 0.221 |
LIG_LIR_Nem_3 | 598 | 602 | PF02991 | 0.601 |
LIG_LIR_Nem_3 | 72 | 78 | PF02991 | 0.255 |
LIG_LIR_Nem_3 | 91 | 96 | PF02991 | 0.181 |
LIG_LYPXL_yS_3 | 108 | 111 | PF13949 | 0.350 |
LIG_LYPXL_yS_3 | 93 | 96 | PF13949 | 0.374 |
LIG_MYND_1 | 419 | 423 | PF01753 | 0.291 |
LIG_NRBOX | 337 | 343 | PF00104 | 0.346 |
LIG_Pex14_2 | 113 | 117 | PF04695 | 0.220 |
LIG_Pex14_2 | 78 | 82 | PF04695 | 0.214 |
LIG_Pex14_2 | 99 | 103 | PF04695 | 0.386 |
LIG_REV1ctd_RIR_1 | 115 | 125 | PF16727 | 0.362 |
LIG_SH2_CRK | 156 | 160 | PF00017 | 0.249 |
LIG_SH2_CRK | 44 | 48 | PF00017 | 0.282 |
LIG_SH2_CRK | 452 | 456 | PF00017 | 0.480 |
LIG_SH2_STAP1 | 148 | 152 | PF00017 | 0.292 |
LIG_SH2_STAP1 | 44 | 48 | PF00017 | 0.282 |
LIG_SH2_STAP1 | 487 | 491 | PF00017 | 0.684 |
LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 268 | 271 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 439 | 442 | PF00017 | 0.375 |
LIG_SH3_3 | 125 | 131 | PF00018 | 0.325 |
LIG_SH3_3 | 323 | 329 | PF00018 | 0.390 |
LIG_SH3_3 | 560 | 566 | PF00018 | 0.785 |
LIG_SH3_3 | 591 | 597 | PF00018 | 0.580 |
LIG_SUMO_SIM_anti_2 | 45 | 51 | PF11976 | 0.282 |
LIG_SUMO_SIM_anti_2 | 456 | 462 | PF11976 | 0.445 |
LIG_SUMO_SIM_anti_2 | 624 | 630 | PF11976 | 0.404 |
LIG_SUMO_SIM_par_1 | 141 | 150 | PF11976 | 0.313 |
LIG_SUMO_SIM_par_1 | 45 | 51 | PF11976 | 0.282 |
LIG_TRAF2_1 | 473 | 476 | PF00917 | 0.685 |
LIG_TYR_ITSM | 448 | 455 | PF00017 | 0.385 |
LIG_UBA3_1 | 212 | 218 | PF00899 | 0.335 |
LIG_WRC_WIRS_1 | 16 | 21 | PF05994 | 0.292 |
MOD_CDK_SPK_2 | 227 | 232 | PF00069 | 0.205 |
MOD_CDK_SPxK_1 | 582 | 588 | PF00069 | 0.639 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.301 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.521 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.317 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.383 |
MOD_CK1_1 | 313 | 319 | PF00069 | 0.264 |
MOD_CK1_1 | 402 | 408 | PF00069 | 0.497 |
MOD_CK1_1 | 533 | 539 | PF00069 | 0.730 |
MOD_CK1_1 | 544 | 550 | PF00069 | 0.761 |
MOD_CK1_1 | 619 | 625 | PF00069 | 0.289 |
MOD_CK2_1 | 319 | 325 | PF00069 | 0.425 |
MOD_CK2_1 | 36 | 42 | PF00069 | 0.357 |
MOD_CK2_1 | 406 | 412 | PF00069 | 0.523 |
MOD_CK2_1 | 419 | 425 | PF00069 | 0.318 |
MOD_CK2_1 | 469 | 475 | PF00069 | 0.661 |
MOD_CK2_1 | 502 | 508 | PF00069 | 0.727 |
MOD_Cter_Amidation | 344 | 347 | PF01082 | 0.716 |
MOD_DYRK1A_RPxSP_1 | 582 | 586 | PF00069 | 0.643 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.636 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.728 |
MOD_GlcNHglycan | 372 | 375 | PF01048 | 0.736 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.640 |
MOD_GlcNHglycan | 408 | 412 | PF01048 | 0.738 |
MOD_GlcNHglycan | 471 | 474 | PF01048 | 0.481 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.550 |
MOD_GlcNHglycan | 541 | 544 | PF01048 | 0.541 |
MOD_GlcNHglycan | 563 | 566 | PF01048 | 0.500 |
MOD_GlcNHglycan | 618 | 621 | PF01048 | 0.426 |
MOD_GlcNHglycan | 629 | 632 | PF01048 | 0.318 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.489 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.343 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.257 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.207 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.296 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.205 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.332 |
MOD_GSK3_1 | 402 | 409 | PF00069 | 0.510 |
MOD_GSK3_1 | 442 | 449 | PF00069 | 0.419 |
MOD_GSK3_1 | 490 | 497 | PF00069 | 0.651 |
MOD_GSK3_1 | 502 | 509 | PF00069 | 0.691 |
MOD_GSK3_1 | 570 | 577 | PF00069 | 0.790 |
MOD_GSK3_1 | 611 | 618 | PF00069 | 0.642 |
MOD_GSK3_1 | 619 | 626 | PF00069 | 0.351 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.356 |
MOD_N-GLC_1 | 201 | 206 | PF02516 | 0.496 |
MOD_N-GLC_1 | 561 | 566 | PF02516 | 0.405 |
MOD_N-GLC_1 | 589 | 594 | PF02516 | 0.413 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.283 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.333 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.298 |
MOD_NEK2_1 | 201 | 206 | PF00069 | 0.201 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.337 |
MOD_NEK2_1 | 264 | 269 | PF00069 | 0.332 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.414 |
MOD_NEK2_1 | 406 | 411 | PF00069 | 0.550 |
MOD_NEK2_1 | 453 | 458 | PF00069 | 0.328 |
MOD_NEK2_1 | 489 | 494 | PF00069 | 0.616 |
MOD_NEK2_1 | 525 | 530 | PF00069 | 0.627 |
MOD_NEK2_1 | 556 | 561 | PF00069 | 0.606 |
MOD_NEK2_1 | 621 | 626 | PF00069 | 0.394 |
MOD_NEK2_1 | 627 | 632 | PF00069 | 0.383 |
MOD_NEK2_1 | 82 | 87 | PF00069 | 0.275 |
MOD_PIKK_1 | 157 | 163 | PF00454 | 0.321 |
MOD_PIKK_1 | 173 | 179 | PF00454 | 0.212 |
MOD_PIKK_1 | 201 | 207 | PF00454 | 0.296 |
MOD_PIKK_1 | 356 | 362 | PF00454 | 0.406 |
MOD_PIKK_1 | 442 | 448 | PF00454 | 0.417 |
MOD_PKA_1 | 346 | 352 | PF00069 | 0.526 |
MOD_PKA_1 | 469 | 475 | PF00069 | 0.657 |
MOD_PKA_1 | 581 | 587 | PF00069 | 0.823 |
MOD_PKA_2 | 173 | 179 | PF00069 | 0.282 |
MOD_PKA_2 | 189 | 195 | PF00069 | 0.282 |
MOD_PKA_2 | 346 | 352 | PF00069 | 0.475 |
MOD_PKA_2 | 447 | 453 | PF00069 | 0.297 |
MOD_PKA_2 | 469 | 475 | PF00069 | 0.623 |
MOD_PKA_2 | 494 | 500 | PF00069 | 0.708 |
MOD_PKA_2 | 581 | 587 | PF00069 | 0.823 |
MOD_Plk_1 | 264 | 270 | PF00069 | 0.205 |
MOD_Plk_1 | 589 | 595 | PF00069 | 0.607 |
MOD_Plk_4 | 143 | 149 | PF00069 | 0.323 |
MOD_Plk_4 | 264 | 270 | PF00069 | 0.356 |
MOD_Plk_4 | 334 | 340 | PF00069 | 0.487 |
MOD_Plk_4 | 362 | 368 | PF00069 | 0.559 |
MOD_Plk_4 | 428 | 434 | PF00069 | 0.376 |
MOD_Plk_4 | 454 | 460 | PF00069 | 0.331 |
MOD_Plk_4 | 612 | 618 | PF00069 | 0.560 |
MOD_Plk_4 | 623 | 629 | PF00069 | 0.235 |
MOD_Plk_4 | 78 | 84 | PF00069 | 0.335 |
MOD_ProDKin_1 | 227 | 233 | PF00069 | 0.205 |
MOD_ProDKin_1 | 236 | 242 | PF00069 | 0.180 |
MOD_ProDKin_1 | 286 | 292 | PF00069 | 0.269 |
MOD_ProDKin_1 | 419 | 425 | PF00069 | 0.431 |
MOD_ProDKin_1 | 546 | 552 | PF00069 | 0.716 |
MOD_ProDKin_1 | 570 | 576 | PF00069 | 0.698 |
MOD_ProDKin_1 | 582 | 588 | PF00069 | 0.777 |
MOD_SUMO_for_1 | 473 | 476 | PF00179 | 0.661 |
TRG_DiLeu_BaEn_1 | 56 | 61 | PF01217 | 0.362 |
TRG_DiLeu_BaLyEn_6 | 337 | 342 | PF01217 | 0.346 |
TRG_ENDOCYTIC_2 | 108 | 111 | PF00928 | 0.350 |
TRG_ENDOCYTIC_2 | 156 | 159 | PF00928 | 0.329 |
TRG_ENDOCYTIC_2 | 268 | 271 | PF00928 | 0.328 |
TRG_ENDOCYTIC_2 | 380 | 383 | PF00928 | 0.434 |
TRG_ENDOCYTIC_2 | 44 | 47 | PF00928 | 0.282 |
TRG_ENDOCYTIC_2 | 452 | 455 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 93 | 96 | PF00928 | 0.337 |
TRG_ER_diArg_1 | 468 | 470 | PF00400 | 0.648 |
TRG_ER_diArg_1 | 75 | 77 | PF00400 | 0.334 |
TRG_Pf-PMV_PEXEL_1 | 206 | 211 | PF00026 | 0.496 |
TRG_Pf-PMV_PEXEL_1 | 232 | 236 | PF00026 | 0.562 |
TRG_Pf-PMV_PEXEL_1 | 600 | 604 | PF00026 | 0.482 |
TRG_Pf-PMV_PEXEL_1 | 645 | 649 | PF00026 | 0.554 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P935 | Leptomonas seymouri | 55% | 100% |
A0A1X0NNY2 | Trypanosomatidae | 39% | 100% |
A0A3S5H634 | Leishmania donovani | 73% | 100% |
A0A422NTR5 | Trypanosoma rangeli | 36% | 100% |
A4HTH1 | Leishmania infantum | 73% | 100% |
C9ZPP9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9AM99 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 71% | 100% |
Q4QIE9 | Leishmania major | 70% | 99% |
V5BLM5 | Trypanosoma cruzi | 43% | 100% |