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: A4H672
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006152 | purine nucleoside catabolic process | 6 | 1 |
GO:0006154 | adenosine catabolic process | 8 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009116 | nucleoside metabolic process | 4 | 1 |
GO:0009119 | ribonucleoside metabolic process | 5 | 1 |
GO:0009163 | nucleoside biosynthetic process | 5 | 1 |
GO:0009164 | nucleoside catabolic process | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0018130 | heterocycle biosynthetic process | 4 | 1 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 1 |
GO:0019439 | aromatic compound catabolic process | 4 | 1 |
GO:0034404 | nucleobase-containing small molecule biosynthetic process | 4 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 1 |
GO:0034655 | nucleobase-containing compound catabolic process | 4 | 1 |
GO:0034656 | nucleobase-containing small molecule catabolic process | 4 | 1 |
GO:0042278 | purine nucleoside metabolic process | 5 | 1 |
GO:0042451 | purine nucleoside biosynthetic process | 6 | 1 |
GO:0042454 | ribonucleoside catabolic process | 6 | 1 |
GO:0042455 | ribonucleoside biosynthetic process | 6 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044270 | cellular nitrogen compound catabolic process | 4 | 1 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 1 |
GO:0044281 | small molecule metabolic process | 2 | 1 |
GO:0044282 | small molecule catabolic process | 3 | 1 |
GO:0044283 | small molecule biosynthetic process | 3 | 1 |
GO:0046085 | adenosine metabolic process | 7 | 1 |
GO:0046102 | inosine metabolic process | 7 | 1 |
GO:0046103 | inosine biosynthetic process | 8 | 1 |
GO:0046128 | purine ribonucleoside metabolic process | 6 | 1 |
GO:0046129 | purine ribonucleoside biosynthetic process | 7 | 1 |
GO:0046130 | purine ribonucleoside catabolic process | 7 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0046700 | heterocycle catabolic process | 4 | 1 |
GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0072521 | purine-containing compound metabolic process | 4 | 1 |
GO:0072522 | purine-containing compound biosynthetic process | 5 | 1 |
GO:0072523 | purine-containing compound catabolic process | 5 | 1 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 1 |
GO:1901136 | carbohydrate derivative catabolic process | 4 | 1 |
GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1901361 | organic cyclic compound catabolic process | 4 | 1 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 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 |
GO:1901657 | glycosyl compound metabolic process | 4 | 1 |
GO:1901658 | glycosyl compound catabolic process | 5 | 1 |
GO:1901659 | glycosyl compound biosynthetic process | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0019239 | deaminase activity | 3 | 11 |
GO:0004000 | adenosine deaminase activity | 4 | 1 |
GO:0016810 | hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds | 3 | 1 |
GO:0016814 | hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in cyclic amidines | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 166 | 170 | PF00656 | 0.523 |
CLV_C14_Caspase3-7 | 354 | 358 | PF00656 | 0.628 |
CLV_C14_Caspase3-7 | 608 | 612 | PF00656 | 0.620 |
CLV_NRD_NRD_1 | 172 | 174 | PF00675 | 0.486 |
CLV_NRD_NRD_1 | 274 | 276 | PF00675 | 0.515 |
CLV_NRD_NRD_1 | 367 | 369 | PF00675 | 0.370 |
CLV_NRD_NRD_1 | 399 | 401 | PF00675 | 0.427 |
CLV_NRD_NRD_1 | 535 | 537 | PF00675 | 0.438 |
CLV_NRD_NRD_1 | 96 | 98 | PF00675 | 0.578 |
CLV_PCSK_KEX2_1 | 172 | 174 | PF00082 | 0.486 |
CLV_PCSK_KEX2_1 | 273 | 275 | PF00082 | 0.492 |
CLV_PCSK_KEX2_1 | 367 | 369 | PF00082 | 0.397 |
CLV_PCSK_KEX2_1 | 535 | 537 | PF00082 | 0.437 |
CLV_PCSK_KEX2_1 | 96 | 98 | PF00082 | 0.637 |
CLV_PCSK_PC1ET2_1 | 96 | 98 | PF00082 | 0.637 |
CLV_PCSK_PC7_1 | 168 | 174 | PF00082 | 0.483 |
CLV_PCSK_SKI1_1 | 124 | 128 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 275 | 279 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 292 | 296 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 299 | 303 | PF00082 | 0.373 |
CLV_PCSK_SKI1_1 | 573 | 577 | PF00082 | 0.388 |
DEG_APCC_DBOX_1 | 274 | 282 | PF00400 | 0.475 |
DEG_APCC_DBOX_1 | 630 | 638 | PF00400 | 0.337 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.622 |
DEG_SCF_FBW7_1 | 705 | 712 | PF00400 | 0.479 |
DEG_SCF_TRCP1_1 | 553 | 559 | PF00400 | 0.444 |
DOC_CYCLIN_RxL_1 | 288 | 296 | PF00134 | 0.411 |
DOC_CYCLIN_RxL_1 | 579 | 588 | PF00134 | 0.400 |
DOC_CYCLIN_yCln2_LP_2 | 640 | 646 | PF00134 | 0.441 |
DOC_MAPK_gen_1 | 535 | 543 | PF00069 | 0.532 |
DOC_MAPK_HePTP_8 | 285 | 297 | PF00069 | 0.316 |
DOC_MAPK_MEF2A_6 | 288 | 297 | PF00069 | 0.311 |
DOC_PP2B_LxvP_1 | 443 | 446 | PF13499 | 0.428 |
DOC_PP2B_LxvP_1 | 640 | 643 | PF13499 | 0.342 |
DOC_PP4_FxxP_1 | 561 | 564 | PF00568 | 0.332 |
DOC_PP4_FxxP_1 | 638 | 641 | PF00568 | 0.298 |
DOC_USP7_MATH_1 | 216 | 220 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 709 | 713 | PF00917 | 0.525 |
DOC_USP7_UBL2_3 | 227 | 231 | PF12436 | 0.307 |
DOC_WW_Pin1_4 | 102 | 107 | PF00397 | 0.661 |
DOC_WW_Pin1_4 | 114 | 119 | PF00397 | 0.493 |
DOC_WW_Pin1_4 | 613 | 618 | PF00397 | 0.489 |
DOC_WW_Pin1_4 | 694 | 699 | PF00397 | 0.496 |
DOC_WW_Pin1_4 | 705 | 710 | PF00397 | 0.394 |
LIG_14-3-3_CanoR_1 | 124 | 129 | PF00244 | 0.379 |
LIG_14-3-3_CanoR_1 | 164 | 168 | PF00244 | 0.348 |
LIG_14-3-3_CanoR_1 | 172 | 176 | PF00244 | 0.404 |
LIG_14-3-3_CanoR_1 | 299 | 307 | PF00244 | 0.374 |
LIG_14-3-3_CanoR_1 | 3 | 13 | PF00244 | 0.628 |
LIG_14-3-3_CanoR_1 | 347 | 353 | PF00244 | 0.692 |
LIG_14-3-3_CanoR_1 | 368 | 378 | PF00244 | 0.302 |
LIG_14-3-3_CanoR_1 | 420 | 427 | PF00244 | 0.364 |
LIG_14-3-3_CanoR_1 | 599 | 605 | PF00244 | 0.428 |
LIG_14-3-3_CanoR_1 | 631 | 635 | PF00244 | 0.295 |
LIG_BRCT_BRCA1_1 | 137 | 141 | PF00533 | 0.301 |
LIG_deltaCOP1_diTrp_1 | 447 | 454 | PF00928 | 0.362 |
LIG_deltaCOP1_diTrp_1 | 680 | 687 | PF00928 | 0.510 |
LIG_deltaCOP1_diTrp_1 | 718 | 726 | PF00928 | 0.340 |
LIG_FHA_1 | 192 | 198 | PF00498 | 0.336 |
LIG_FHA_1 | 208 | 214 | PF00498 | 0.346 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.309 |
LIG_FHA_1 | 370 | 376 | PF00498 | 0.327 |
LIG_FHA_1 | 386 | 392 | PF00498 | 0.322 |
LIG_FHA_1 | 420 | 426 | PF00498 | 0.477 |
LIG_FHA_1 | 473 | 479 | PF00498 | 0.343 |
LIG_FHA_1 | 519 | 525 | PF00498 | 0.530 |
LIG_FHA_1 | 558 | 564 | PF00498 | 0.464 |
LIG_FHA_1 | 599 | 605 | PF00498 | 0.527 |
LIG_FHA_2 | 115 | 121 | PF00498 | 0.494 |
LIG_FHA_2 | 125 | 131 | PF00498 | 0.331 |
LIG_FHA_2 | 233 | 239 | PF00498 | 0.559 |
LIG_FHA_2 | 338 | 344 | PF00498 | 0.554 |
LIG_FHA_2 | 374 | 380 | PF00498 | 0.304 |
LIG_FHA_2 | 5 | 11 | PF00498 | 0.492 |
LIG_FHA_2 | 540 | 546 | PF00498 | 0.655 |
LIG_FHA_2 | 606 | 612 | PF00498 | 0.682 |
LIG_GBD_Chelix_1 | 159 | 167 | PF00786 | 0.459 |
LIG_KLC1_Yacidic_2 | 187 | 191 | PF13176 | 0.268 |
LIG_LIR_Apic_2 | 559 | 564 | PF02991 | 0.474 |
LIG_LIR_Gen_1 | 127 | 136 | PF02991 | 0.342 |
LIG_LIR_Gen_1 | 138 | 149 | PF02991 | 0.300 |
LIG_LIR_Gen_1 | 254 | 263 | PF02991 | 0.322 |
LIG_LIR_Gen_1 | 326 | 332 | PF02991 | 0.401 |
LIG_LIR_Gen_1 | 388 | 397 | PF02991 | 0.360 |
LIG_LIR_Gen_1 | 653 | 663 | PF02991 | 0.484 |
LIG_LIR_Gen_1 | 683 | 690 | PF02991 | 0.483 |
LIG_LIR_Gen_1 | 718 | 726 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 127 | 132 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 138 | 144 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 254 | 260 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 326 | 330 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 359 | 364 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 388 | 392 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 447 | 452 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 512 | 518 | PF02991 | 0.566 |
LIG_LIR_Nem_3 | 653 | 658 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 683 | 687 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 718 | 722 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 723 | 729 | PF02991 | 0.404 |
LIG_NRBOX | 490 | 496 | PF00104 | 0.496 |
LIG_NRBOX | 56 | 62 | PF00104 | 0.446 |
LIG_Pex14_1 | 249 | 253 | PF04695 | 0.323 |
LIG_PTB_Apo_2 | 562 | 569 | PF02174 | 0.313 |
LIG_SH2_CRK | 257 | 261 | PF00017 | 0.428 |
LIG_SH2_CRK | 655 | 659 | PF00017 | 0.476 |
LIG_SH2_GRB2like | 253 | 256 | PF00017 | 0.247 |
LIG_SH2_NCK_1 | 253 | 257 | PF00017 | 0.456 |
LIG_SH2_NCK_1 | 655 | 659 | PF00017 | 0.635 |
LIG_SH2_SRC | 253 | 256 | PF00017 | 0.247 |
LIG_SH2_STAP1 | 253 | 257 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 133 | 136 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 189 | 192 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 257 | 260 | PF00017 | 0.355 |
LIG_SH2_STAT5 | 276 | 279 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 518 | 521 | PF00017 | 0.318 |
LIG_SH3_3 | 388 | 394 | PF00018 | 0.496 |
LIG_SH3_3 | 46 | 52 | PF00018 | 0.251 |
LIG_SH3_3 | 655 | 661 | PF00018 | 0.400 |
LIG_SUMO_SIM_anti_2 | 156 | 162 | PF11976 | 0.391 |
LIG_SUMO_SIM_par_1 | 10 | 16 | PF11976 | 0.519 |
LIG_SUMO_SIM_par_1 | 204 | 210 | PF11976 | 0.434 |
LIG_SUMO_SIM_par_1 | 539 | 549 | PF11976 | 0.460 |
LIG_TRAF2_1 | 180 | 183 | PF00917 | 0.632 |
LIG_TRAF2_1 | 240 | 243 | PF00917 | 0.505 |
LIG_WRC_WIRS_1 | 361 | 366 | PF05994 | 0.304 |
MOD_CDK_SPxxK_3 | 102 | 109 | PF00069 | 0.712 |
MOD_CK1_1 | 265 | 271 | PF00069 | 0.381 |
MOD_CK1_1 | 283 | 289 | PF00069 | 0.466 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.614 |
MOD_CK1_1 | 409 | 415 | PF00069 | 0.547 |
MOD_CK1_1 | 544 | 550 | PF00069 | 0.612 |
MOD_CK1_1 | 554 | 560 | PF00069 | 0.539 |
MOD_CK1_1 | 567 | 573 | PF00069 | 0.343 |
MOD_CK1_1 | 618 | 624 | PF00069 | 0.265 |
MOD_CK1_1 | 656 | 662 | PF00069 | 0.655 |
MOD_CK1_1 | 712 | 718 | PF00069 | 0.449 |
MOD_CK1_1 | 86 | 92 | PF00069 | 0.499 |
MOD_CK2_1 | 114 | 120 | PF00069 | 0.570 |
MOD_CK2_1 | 124 | 130 | PF00069 | 0.487 |
MOD_CK2_1 | 150 | 156 | PF00069 | 0.303 |
MOD_CK2_1 | 4 | 10 | PF00069 | 0.551 |
MOD_CK2_1 | 497 | 503 | PF00069 | 0.588 |
MOD_CK2_1 | 539 | 545 | PF00069 | 0.498 |
MOD_CK2_1 | 712 | 718 | PF00069 | 0.241 |
MOD_CMANNOS | 681 | 684 | PF00535 | 0.514 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.308 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.521 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.512 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.696 |
MOD_GlcNHglycan | 379 | 383 | PF01048 | 0.312 |
MOD_GlcNHglycan | 460 | 463 | PF01048 | 0.459 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.461 |
MOD_GlcNHglycan | 553 | 556 | PF01048 | 0.689 |
MOD_GlcNHglycan | 617 | 620 | PF01048 | 0.315 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.503 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.358 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.385 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.436 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.667 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.528 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.226 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.562 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.379 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.412 |
MOD_GSK3_1 | 473 | 480 | PF00069 | 0.358 |
MOD_GSK3_1 | 497 | 504 | PF00069 | 0.489 |
MOD_GSK3_1 | 539 | 546 | PF00069 | 0.553 |
MOD_GSK3_1 | 611 | 618 | PF00069 | 0.413 |
MOD_GSK3_1 | 690 | 697 | PF00069 | 0.466 |
MOD_GSK3_1 | 699 | 706 | PF00069 | 0.588 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.565 |
MOD_N-GLC_1 | 27 | 32 | PF02516 | 0.517 |
MOD_N-GLC_1 | 283 | 288 | PF02516 | 0.516 |
MOD_N-GLC_1 | 409 | 414 | PF02516 | 0.502 |
MOD_N-GLC_1 | 45 | 50 | PF02516 | 0.308 |
MOD_N-GLC_1 | 456 | 461 | PF02516 | 0.396 |
MOD_N-GLC_1 | 564 | 569 | PF02516 | 0.309 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.320 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.273 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.440 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.346 |
MOD_NEK2_1 | 369 | 374 | PF00069 | 0.398 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.400 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.546 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.327 |
MOD_NEK2_1 | 472 | 477 | PF00069 | 0.340 |
MOD_NEK2_1 | 497 | 502 | PF00069 | 0.519 |
MOD_NEK2_1 | 576 | 581 | PF00069 | 0.353 |
MOD_NEK2_1 | 600 | 605 | PF00069 | 0.515 |
MOD_NEK2_1 | 651 | 656 | PF00069 | 0.597 |
MOD_NEK2_2 | 226 | 231 | PF00069 | 0.295 |
MOD_NEK2_2 | 423 | 428 | PF00069 | 0.479 |
MOD_NEK2_2 | 564 | 569 | PF00069 | 0.338 |
MOD_PIKK_1 | 313 | 319 | PF00454 | 0.466 |
MOD_PIKK_1 | 585 | 591 | PF00454 | 0.480 |
MOD_PIKK_1 | 611 | 617 | PF00454 | 0.412 |
MOD_PIKK_1 | 90 | 96 | PF00454 | 0.615 |
MOD_PKA_2 | 163 | 169 | PF00069 | 0.356 |
MOD_PKA_2 | 171 | 177 | PF00069 | 0.409 |
MOD_PKA_2 | 310 | 316 | PF00069 | 0.476 |
MOD_PKA_2 | 346 | 352 | PF00069 | 0.755 |
MOD_PKA_2 | 369 | 375 | PF00069 | 0.328 |
MOD_PKA_2 | 419 | 425 | PF00069 | 0.368 |
MOD_PKA_2 | 598 | 604 | PF00069 | 0.530 |
MOD_PKA_2 | 630 | 636 | PF00069 | 0.294 |
MOD_PKA_2 | 712 | 718 | PF00069 | 0.541 |
MOD_Plk_1 | 356 | 362 | PF00069 | 0.513 |
MOD_Plk_1 | 455 | 461 | PF00069 | 0.484 |
MOD_Plk_1 | 564 | 570 | PF00069 | 0.322 |
MOD_Plk_2-3 | 238 | 244 | PF00069 | 0.510 |
MOD_Plk_4 | 131 | 137 | PF00069 | 0.246 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.409 |
MOD_Plk_4 | 356 | 362 | PF00069 | 0.386 |
MOD_Plk_4 | 385 | 391 | PF00069 | 0.436 |
MOD_Plk_4 | 557 | 563 | PF00069 | 0.548 |
MOD_Plk_4 | 683 | 689 | PF00069 | 0.537 |
MOD_Plk_4 | 86 | 92 | PF00069 | 0.479 |
MOD_ProDKin_1 | 102 | 108 | PF00069 | 0.663 |
MOD_ProDKin_1 | 114 | 120 | PF00069 | 0.487 |
MOD_ProDKin_1 | 613 | 619 | PF00069 | 0.474 |
MOD_ProDKin_1 | 694 | 700 | PF00069 | 0.507 |
MOD_ProDKin_1 | 705 | 711 | PF00069 | 0.379 |
MOD_SUMO_for_1 | 236 | 239 | PF00179 | 0.458 |
TRG_DiLeu_BaLyEn_6 | 289 | 294 | PF01217 | 0.342 |
TRG_DiLeu_BaLyEn_6 | 49 | 54 | PF01217 | 0.333 |
TRG_DiLeu_BaLyEn_6 | 56 | 61 | PF01217 | 0.392 |
TRG_ENDOCYTIC_2 | 133 | 136 | PF00928 | 0.330 |
TRG_ENDOCYTIC_2 | 253 | 256 | PF00928 | 0.384 |
TRG_ENDOCYTIC_2 | 257 | 260 | PF00928 | 0.345 |
TRG_ENDOCYTIC_2 | 389 | 392 | PF00928 | 0.475 |
TRG_ENDOCYTIC_2 | 655 | 658 | PF00928 | 0.468 |
TRG_ER_diArg_1 | 171 | 173 | PF00400 | 0.478 |
TRG_ER_diArg_1 | 273 | 275 | PF00400 | 0.438 |
TRG_ER_diArg_1 | 367 | 370 | PF00400 | 0.385 |
TRG_ER_diArg_1 | 534 | 536 | PF00400 | 0.444 |
TRG_Pf-PMV_PEXEL_1 | 319 | 323 | PF00026 | 0.394 |
TRG_Pf-PMV_PEXEL_1 | 367 | 371 | PF00026 | 0.445 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6F9 | Leptomonas seymouri | 48% | 98% |
A0A1X0NRU3 | Trypanosomatidae | 35% | 100% |
A0A3S5IS54 | Trypanosoma rangeli | 35% | 100% |
A0A3S7WR98 | Leishmania donovani | 74% | 100% |
A4HUJ6 | Leishmania infantum | 74% | 100% |
C9ZVM1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
E9AN94 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 100% |
Q4QHD0 | Leishmania major | 74% | 99% |
V5BTS5 | Trypanosoma cruzi | 36% | 100% |