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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: Q4QHD0
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006152 | purine nucleoside catabolic process | 6 | 2 |
GO:0006154 | adenosine catabolic process | 8 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009056 | catabolic process | 2 | 2 |
GO:0009058 | biosynthetic process | 2 | 2 |
GO:0009116 | nucleoside metabolic process | 4 | 2 |
GO:0009119 | ribonucleoside metabolic process | 5 | 2 |
GO:0009163 | nucleoside biosynthetic process | 5 | 2 |
GO:0009164 | nucleoside catabolic process | 5 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0018130 | heterocycle biosynthetic process | 4 | 2 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 2 |
GO:0019439 | aromatic compound catabolic process | 4 | 2 |
GO:0034404 | nucleobase-containing small molecule biosynthetic process | 4 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 2 |
GO:0034655 | nucleobase-containing compound catabolic process | 4 | 2 |
GO:0034656 | nucleobase-containing small molecule catabolic process | 4 | 2 |
GO:0042278 | purine nucleoside metabolic process | 5 | 2 |
GO:0042451 | purine nucleoside biosynthetic process | 6 | 2 |
GO:0042454 | ribonucleoside catabolic process | 6 | 2 |
GO:0042455 | ribonucleoside biosynthetic process | 6 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044248 | cellular catabolic process | 3 | 2 |
GO:0044249 | cellular biosynthetic process | 3 | 2 |
GO:0044270 | cellular nitrogen compound catabolic process | 4 | 2 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 2 |
GO:0044281 | small molecule metabolic process | 2 | 2 |
GO:0044282 | small molecule catabolic process | 3 | 2 |
GO:0044283 | small molecule biosynthetic process | 3 | 2 |
GO:0046085 | adenosine metabolic process | 7 | 2 |
GO:0046102 | inosine metabolic process | 7 | 2 |
GO:0046103 | inosine biosynthetic process | 8 | 2 |
GO:0046128 | purine ribonucleoside metabolic process | 6 | 2 |
GO:0046129 | purine ribonucleoside biosynthetic process | 7 | 2 |
GO:0046130 | purine ribonucleoside catabolic process | 7 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0046700 | heterocycle catabolic process | 4 | 2 |
GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0072521 | purine-containing compound metabolic process | 4 | 2 |
GO:0072522 | purine-containing compound biosynthetic process | 5 | 2 |
GO:0072523 | purine-containing compound catabolic process | 5 | 2 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 2 |
GO:1901136 | carbohydrate derivative catabolic process | 4 | 2 |
GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
GO:1901361 | organic cyclic compound catabolic process | 4 | 2 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 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 |
GO:1901657 | glycosyl compound metabolic process | 4 | 2 |
GO:1901658 | glycosyl compound catabolic process | 5 | 2 |
GO:1901659 | glycosyl compound biosynthetic process | 5 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004000 | adenosine deaminase activity | 4 | 2 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0016810 | hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds | 3 | 2 |
GO:0016814 | hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in cyclic amidines | 4 | 2 |
GO:0019239 | deaminase activity | 3 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 165 | 169 | PF00656 | 0.506 |
CLV_C14_Caspase3-7 | 406 | 410 | PF00656 | 0.524 |
CLV_C14_Caspase3-7 | 605 | 609 | PF00656 | 0.568 |
CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.458 |
CLV_NRD_NRD_1 | 175 | 177 | PF00675 | 0.487 |
CLV_NRD_NRD_1 | 273 | 275 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 340 | 342 | PF00675 | 0.562 |
CLV_NRD_NRD_1 | 368 | 370 | PF00675 | 0.386 |
CLV_NRD_NRD_1 | 401 | 403 | PF00675 | 0.445 |
CLV_NRD_NRD_1 | 501 | 503 | PF00675 | 0.646 |
CLV_NRD_NRD_1 | 532 | 534 | PF00675 | 0.427 |
CLV_NRD_NRD_1 | 95 | 97 | PF00675 | 0.500 |
CLV_PCSK_FUR_1 | 499 | 503 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 171 | 173 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 175 | 177 | PF00082 | 0.487 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.477 |
CLV_PCSK_KEX2_1 | 340 | 342 | PF00082 | 0.562 |
CLV_PCSK_KEX2_1 | 368 | 370 | PF00082 | 0.413 |
CLV_PCSK_KEX2_1 | 401 | 403 | PF00082 | 0.408 |
CLV_PCSK_KEX2_1 | 499 | 501 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 532 | 534 | PF00082 | 0.426 |
CLV_PCSK_KEX2_1 | 94 | 96 | PF00082 | 0.572 |
CLV_PCSK_PC1ET2_1 | 94 | 96 | PF00082 | 0.572 |
CLV_PCSK_PC7_1 | 167 | 173 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 133 | 137 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 274 | 278 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 282 | 286 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 291 | 295 | PF00082 | 0.273 |
CLV_PCSK_SKI1_1 | 298 | 302 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 570 | 574 | PF00082 | 0.355 |
CLV_PCSK_SKI1_1 | 579 | 583 | PF00082 | 0.335 |
DEG_APCC_DBOX_1 | 273 | 281 | PF00400 | 0.465 |
DEG_APCC_DBOX_1 | 627 | 635 | PF00400 | 0.334 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.623 |
DEG_SCF_FBW7_1 | 702 | 709 | PF00400 | 0.456 |
DOC_CDC14_PxL_1 | 33 | 41 | PF14671 | 0.365 |
DOC_CYCLIN_RxL_1 | 287 | 295 | PF00134 | 0.385 |
DOC_CYCLIN_RxL_1 | 576 | 585 | PF00134 | 0.371 |
DOC_CYCLIN_yCln2_LP_2 | 637 | 643 | PF00134 | 0.428 |
DOC_MAPK_DCC_7 | 6 | 14 | PF00069 | 0.579 |
DOC_MAPK_HePTP_8 | 284 | 296 | PF00069 | 0.310 |
DOC_MAPK_MEF2A_6 | 287 | 296 | PF00069 | 0.305 |
DOC_PP1_RVXF_1 | 36 | 42 | PF00149 | 0.322 |
DOC_PP2B_LxvP_1 | 260 | 263 | PF13499 | 0.395 |
DOC_PP2B_LxvP_1 | 437 | 440 | PF13499 | 0.420 |
DOC_PP2B_LxvP_1 | 637 | 640 | PF13499 | 0.331 |
DOC_PP4_FxxP_1 | 448 | 451 | PF00568 | 0.474 |
DOC_PP4_FxxP_1 | 635 | 638 | PF00568 | 0.289 |
DOC_USP7_MATH_1 | 104 | 108 | PF00917 | 0.685 |
DOC_USP7_MATH_1 | 215 | 219 | PF00917 | 0.402 |
DOC_USP7_MATH_1 | 263 | 267 | PF00917 | 0.472 |
DOC_USP7_MATH_1 | 357 | 361 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 541 | 545 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 604 | 608 | PF00917 | 0.451 |
DOC_USP7_MATH_1 | 655 | 659 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 661 | 665 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 706 | 710 | PF00917 | 0.518 |
DOC_WW_Pin1_4 | 113 | 118 | PF00397 | 0.470 |
DOC_WW_Pin1_4 | 347 | 352 | PF00397 | 0.606 |
DOC_WW_Pin1_4 | 355 | 360 | PF00397 | 0.536 |
DOC_WW_Pin1_4 | 691 | 696 | PF00397 | 0.465 |
DOC_WW_Pin1_4 | 702 | 707 | PF00397 | 0.386 |
LIG_14-3-3_CanoR_1 | 163 | 167 | PF00244 | 0.331 |
LIG_14-3-3_CanoR_1 | 171 | 175 | PF00244 | 0.393 |
LIG_14-3-3_CanoR_1 | 282 | 287 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 291 | 297 | PF00244 | 0.357 |
LIG_14-3-3_CanoR_1 | 298 | 306 | PF00244 | 0.370 |
LIG_14-3-3_CanoR_1 | 414 | 421 | PF00244 | 0.358 |
LIG_14-3-3_CanoR_1 | 6 | 10 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 628 | 638 | PF00244 | 0.290 |
LIG_14-3-3_CanoR_1 | 686 | 692 | PF00244 | 0.360 |
LIG_Actin_WH2_2 | 155 | 173 | PF00022 | 0.346 |
LIG_BIR_III_4 | 505 | 509 | PF00653 | 0.507 |
LIG_BIR_III_4 | 548 | 552 | PF00653 | 0.495 |
LIG_deltaCOP1_diTrp_1 | 441 | 448 | PF00928 | 0.358 |
LIG_deltaCOP1_diTrp_1 | 677 | 684 | PF00928 | 0.483 |
LIG_deltaCOP1_diTrp_1 | 715 | 723 | PF00928 | 0.334 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.343 |
LIG_FHA_1 | 371 | 377 | PF00498 | 0.326 |
LIG_FHA_1 | 414 | 420 | PF00498 | 0.450 |
LIG_FHA_1 | 516 | 522 | PF00498 | 0.539 |
LIG_FHA_1 | 555 | 561 | PF00498 | 0.490 |
LIG_FHA_1 | 614 | 620 | PF00498 | 0.361 |
LIG_FHA_1 | 697 | 703 | PF00498 | 0.625 |
LIG_FHA_2 | 114 | 120 | PF00498 | 0.475 |
LIG_FHA_2 | 124 | 130 | PF00498 | 0.324 |
LIG_FHA_2 | 149 | 155 | PF00498 | 0.320 |
LIG_FHA_2 | 189 | 195 | PF00498 | 0.377 |
LIG_FHA_2 | 375 | 381 | PF00498 | 0.299 |
LIG_FHA_2 | 5 | 11 | PF00498 | 0.468 |
LIG_FHA_2 | 603 | 609 | PF00498 | 0.655 |
LIG_GBD_Chelix_1 | 158 | 166 | PF00786 | 0.450 |
LIG_HCF-1_HBM_1 | 2 | 5 | PF13415 | 0.364 |
LIG_LIR_Apic_2 | 632 | 638 | PF02991 | 0.320 |
LIG_LIR_Gen_1 | 126 | 135 | PF02991 | 0.336 |
LIG_LIR_Gen_1 | 683 | 692 | PF02991 | 0.480 |
LIG_LIR_Gen_1 | 715 | 723 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 126 | 131 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 253 | 259 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 278 | 284 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 441 | 446 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 510 | 515 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 680 | 684 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 715 | 719 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 720 | 726 | PF02991 | 0.409 |
LIG_NRBOX | 484 | 490 | PF00104 | 0.490 |
LIG_NRBOX | 56 | 62 | PF00104 | 0.399 |
LIG_Pex14_1 | 248 | 252 | PF04695 | 0.322 |
LIG_PTB_Apo_2 | 134 | 141 | PF02174 | 0.290 |
LIG_PTB_Apo_2 | 559 | 566 | PF02174 | 0.324 |
LIG_SH2_CRK | 256 | 260 | PF00017 | 0.388 |
LIG_SH2_NCK_1 | 252 | 256 | PF00017 | 0.449 |
LIG_SH2_NCK_1 | 652 | 656 | PF00017 | 0.622 |
LIG_SH2_STAP1 | 252 | 256 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 123 | 126 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 188 | 191 | PF00017 | 0.316 |
LIG_SH2_STAT5 | 275 | 278 | PF00017 | 0.396 |
LIG_SH3_3 | 180 | 186 | PF00018 | 0.304 |
LIG_SH3_3 | 348 | 354 | PF00018 | 0.612 |
LIG_SH3_3 | 356 | 362 | PF00018 | 0.512 |
LIG_SH3_3 | 537 | 543 | PF00018 | 0.557 |
LIG_SUMO_SIM_anti_2 | 154 | 161 | PF11976 | 0.393 |
LIG_SUMO_SIM_par_1 | 10 | 16 | PF11976 | 0.467 |
LIG_SUMO_SIM_par_1 | 203 | 209 | PF11976 | 0.433 |
LIG_TRAF2_1 | 152 | 155 | PF00917 | 0.326 |
LIG_TRAF2_1 | 179 | 182 | PF00917 | 0.628 |
MOD_CDK_SPxxK_3 | 113 | 120 | PF00069 | 0.468 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.456 |
MOD_CK1_1 | 350 | 356 | PF00069 | 0.673 |
MOD_CK1_1 | 360 | 366 | PF00069 | 0.447 |
MOD_CK1_1 | 564 | 570 | PF00069 | 0.294 |
MOD_CK1_1 | 653 | 659 | PF00069 | 0.634 |
MOD_CK1_1 | 709 | 715 | PF00069 | 0.440 |
MOD_CK2_1 | 113 | 119 | PF00069 | 0.552 |
MOD_CK2_1 | 148 | 154 | PF00069 | 0.299 |
MOD_CK2_1 | 188 | 194 | PF00069 | 0.381 |
MOD_CK2_1 | 4 | 10 | PF00069 | 0.548 |
MOD_CK2_1 | 491 | 497 | PF00069 | 0.591 |
MOD_CK2_1 | 501 | 507 | PF00069 | 0.478 |
MOD_CK2_1 | 691 | 697 | PF00069 | 0.535 |
MOD_CK2_1 | 709 | 715 | PF00069 | 0.237 |
MOD_CMANNOS | 678 | 681 | PF00535 | 0.488 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.588 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.301 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.479 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.525 |
MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.630 |
MOD_GlcNHglycan | 380 | 384 | PF01048 | 0.309 |
MOD_GlcNHglycan | 454 | 457 | PF01048 | 0.465 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.445 |
MOD_GlcNHglycan | 509 | 512 | PF01048 | 0.523 |
MOD_GlcNHglycan | 542 | 546 | PF01048 | 0.746 |
MOD_GlcNHglycan | 657 | 660 | PF01048 | 0.507 |
MOD_GlcNHglycan | 663 | 666 | PF01048 | 0.436 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.671 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.370 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.422 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.690 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.552 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.233 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.369 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.363 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.367 |
MOD_GSK3_1 | 467 | 474 | PF00069 | 0.356 |
MOD_GSK3_1 | 491 | 498 | PF00069 | 0.518 |
MOD_GSK3_1 | 687 | 694 | PF00069 | 0.450 |
MOD_GSK3_1 | 696 | 703 | PF00069 | 0.584 |
MOD_N-GLC_1 | 282 | 287 | PF02516 | 0.525 |
MOD_N-GLC_1 | 345 | 350 | PF02516 | 0.726 |
MOD_N-GLC_1 | 45 | 50 | PF02516 | 0.281 |
MOD_N-GLC_1 | 452 | 457 | PF02516 | 0.378 |
MOD_N-GLC_1 | 535 | 540 | PF02516 | 0.507 |
MOD_N-GLC_1 | 561 | 566 | PF02516 | 0.316 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.308 |
MOD_NEK2_1 | 148 | 153 | PF00069 | 0.269 |
MOD_NEK2_1 | 170 | 175 | PF00069 | 0.426 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.327 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.389 |
MOD_NEK2_1 | 379 | 384 | PF00069 | 0.350 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.543 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.299 |
MOD_NEK2_1 | 466 | 471 | PF00069 | 0.338 |
MOD_NEK2_1 | 491 | 496 | PF00069 | 0.619 |
MOD_NEK2_1 | 573 | 578 | PF00069 | 0.330 |
MOD_NEK2_1 | 582 | 587 | PF00069 | 0.333 |
MOD_NEK2_1 | 629 | 634 | PF00069 | 0.351 |
MOD_NEK2_2 | 123 | 128 | PF00069 | 0.360 |
MOD_NEK2_2 | 417 | 422 | PF00069 | 0.483 |
MOD_NEK2_2 | 561 | 566 | PF00069 | 0.344 |
MOD_PIKK_1 | 227 | 233 | PF00454 | 0.452 |
MOD_PIKK_1 | 312 | 318 | PF00454 | 0.473 |
MOD_PIKK_1 | 582 | 588 | PF00454 | 0.464 |
MOD_PIKK_1 | 629 | 635 | PF00454 | 0.348 |
MOD_PIKK_1 | 88 | 94 | PF00454 | 0.573 |
MOD_PKA_1 | 340 | 346 | PF00069 | 0.568 |
MOD_PKA_1 | 501 | 507 | PF00069 | 0.521 |
MOD_PKA_2 | 162 | 168 | PF00069 | 0.339 |
MOD_PKA_2 | 170 | 176 | PF00069 | 0.396 |
MOD_PKA_2 | 309 | 315 | PF00069 | 0.475 |
MOD_PKA_2 | 340 | 346 | PF00069 | 0.718 |
MOD_PKA_2 | 370 | 376 | PF00069 | 0.330 |
MOD_PKA_2 | 413 | 419 | PF00069 | 0.361 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.581 |
MOD_PKA_2 | 501 | 507 | PF00069 | 0.703 |
MOD_PKA_2 | 595 | 601 | PF00069 | 0.548 |
MOD_PKA_2 | 627 | 633 | PF00069 | 0.293 |
MOD_PKA_2 | 709 | 715 | PF00069 | 0.542 |
MOD_PKB_1 | 499 | 507 | PF00069 | 0.530 |
MOD_Plk_1 | 264 | 270 | PF00069 | 0.587 |
MOD_Plk_1 | 282 | 288 | PF00069 | 0.260 |
MOD_Plk_1 | 452 | 458 | PF00069 | 0.385 |
MOD_Plk_1 | 535 | 541 | PF00069 | 0.511 |
MOD_Plk_1 | 561 | 567 | PF00069 | 0.326 |
MOD_Plk_4 | 188 | 194 | PF00069 | 0.317 |
MOD_Plk_4 | 255 | 261 | PF00069 | 0.371 |
MOD_Plk_4 | 28 | 34 | PF00069 | 0.371 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.428 |
MOD_Plk_4 | 680 | 686 | PF00069 | 0.523 |
MOD_ProDKin_1 | 113 | 119 | PF00069 | 0.466 |
MOD_ProDKin_1 | 347 | 353 | PF00069 | 0.608 |
MOD_ProDKin_1 | 355 | 361 | PF00069 | 0.526 |
MOD_ProDKin_1 | 691 | 697 | PF00069 | 0.479 |
MOD_ProDKin_1 | 702 | 708 | PF00069 | 0.370 |
MOD_SUMO_rev_2 | 544 | 554 | PF00179 | 0.493 |
TRG_DiLeu_BaEn_2 | 433 | 439 | PF01217 | 0.303 |
TRG_DiLeu_BaLyEn_6 | 288 | 293 | PF01217 | 0.335 |
TRG_DiLeu_BaLyEn_6 | 56 | 61 | PF01217 | 0.362 |
TRG_ENDOCYTIC_2 | 132 | 135 | PF00928 | 0.327 |
TRG_ENDOCYTIC_2 | 252 | 255 | PF00928 | 0.353 |
TRG_ENDOCYTIC_2 | 256 | 259 | PF00928 | 0.349 |
TRG_ENDOCYTIC_2 | 390 | 393 | PF00928 | 0.485 |
TRG_ER_diArg_1 | 170 | 172 | PF00400 | 0.446 |
TRG_ER_diArg_1 | 174 | 176 | PF00400 | 0.446 |
TRG_ER_diArg_1 | 272 | 274 | PF00400 | 0.406 |
TRG_ER_diArg_1 | 368 | 371 | PF00400 | 0.399 |
TRG_ER_diArg_1 | 499 | 502 | PF00400 | 0.528 |
TRG_ER_diArg_1 | 531 | 533 | PF00400 | 0.433 |
TRG_Pf-PMV_PEXEL_1 | 368 | 372 | PF00026 | 0.459 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6F9 | Leptomonas seymouri | 48% | 98% |
A0A1X0NRU3 | Trypanosomatidae | 33% | 99% |
A0A3S5IS54 | Trypanosoma rangeli | 36% | 100% |
A0A3S7WR98 | Leishmania donovani | 92% | 99% |
A4H672 | Leishmania braziliensis | 74% | 100% |
A4HUJ6 | Leishmania infantum | 92% | 99% |
C9ZVM1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
E9AN94 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
V5BTS5 | Trypanosoma cruzi | 37% | 100% |