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: A4HUJ6
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 | 167 | 171 | PF00656 | 0.521 |
CLV_C14_Caspase3-7 | 410 | 414 | PF00656 | 0.526 |
CLV_C14_Caspase3-7 | 554 | 558 | PF00656 | 0.527 |
CLV_C14_Caspase3-7 | 609 | 613 | PF00656 | 0.596 |
CLV_NRD_NRD_1 | 173 | 175 | PF00675 | 0.477 |
CLV_NRD_NRD_1 | 177 | 179 | PF00675 | 0.497 |
CLV_NRD_NRD_1 | 275 | 277 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 342 | 344 | PF00675 | 0.568 |
CLV_NRD_NRD_1 | 372 | 374 | PF00675 | 0.429 |
CLV_NRD_NRD_1 | 405 | 407 | PF00675 | 0.488 |
CLV_NRD_NRD_1 | 505 | 507 | PF00675 | 0.636 |
CLV_NRD_NRD_1 | 536 | 538 | PF00675 | 0.430 |
CLV_NRD_NRD_1 | 95 | 97 | PF00675 | 0.586 |
CLV_PCSK_FUR_1 | 503 | 507 | PF00082 | 0.495 |
CLV_PCSK_KEX2_1 | 173 | 175 | PF00082 | 0.477 |
CLV_PCSK_KEX2_1 | 177 | 179 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 274 | 276 | PF00082 | 0.487 |
CLV_PCSK_KEX2_1 | 342 | 344 | PF00082 | 0.568 |
CLV_PCSK_KEX2_1 | 372 | 374 | PF00082 | 0.453 |
CLV_PCSK_KEX2_1 | 405 | 407 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 503 | 505 | PF00082 | 0.586 |
CLV_PCSK_KEX2_1 | 536 | 538 | PF00082 | 0.432 |
CLV_PCSK_KEX2_1 | 94 | 96 | PF00082 | 0.628 |
CLV_PCSK_PC1ET2_1 | 94 | 96 | PF00082 | 0.626 |
CLV_PCSK_PC7_1 | 169 | 175 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 135 | 139 | PF00082 | 0.358 |
CLV_PCSK_SKI1_1 | 276 | 280 | PF00082 | 0.430 |
CLV_PCSK_SKI1_1 | 284 | 288 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 293 | 297 | PF00082 | 0.290 |
CLV_PCSK_SKI1_1 | 300 | 304 | PF00082 | 0.390 |
CLV_PCSK_SKI1_1 | 513 | 517 | PF00082 | 0.398 |
CLV_PCSK_SKI1_1 | 574 | 578 | PF00082 | 0.353 |
CLV_PCSK_SKI1_1 | 583 | 587 | PF00082 | 0.345 |
DEG_APCC_DBOX_1 | 275 | 283 | PF00400 | 0.477 |
DEG_APCC_DBOX_1 | 631 | 639 | PF00400 | 0.339 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.634 |
DEG_SCF_FBW7_1 | 100 | 107 | PF00400 | 0.506 |
DEG_SCF_FBW7_1 | 417 | 424 | PF00400 | 0.319 |
DEG_SCF_FBW7_1 | 706 | 713 | PF00400 | 0.458 |
DEG_SPOP_SBC_1 | 361 | 365 | PF00917 | 0.507 |
DOC_CDC14_PxL_1 | 33 | 41 | PF14671 | 0.378 |
DOC_CYCLIN_RxL_1 | 289 | 297 | PF00134 | 0.398 |
DOC_CYCLIN_RxL_1 | 580 | 589 | PF00134 | 0.387 |
DOC_CYCLIN_yCln2_LP_2 | 641 | 647 | PF00134 | 0.431 |
DOC_MAPK_DCC_7 | 6 | 14 | PF00069 | 0.434 |
DOC_MAPK_gen_1 | 94 | 102 | PF00069 | 0.481 |
DOC_MAPK_HePTP_8 | 286 | 298 | PF00069 | 0.322 |
DOC_MAPK_MEF2A_6 | 289 | 298 | PF00069 | 0.318 |
DOC_MAPK_MEF2A_6 | 418 | 425 | PF00069 | 0.424 |
DOC_PP1_RVXF_1 | 36 | 42 | PF00149 | 0.344 |
DOC_PP2B_LxvP_1 | 262 | 265 | PF13499 | 0.412 |
DOC_PP2B_LxvP_1 | 441 | 444 | PF13499 | 0.443 |
DOC_PP2B_LxvP_1 | 641 | 644 | PF13499 | 0.335 |
DOC_PP2B_PxIxI_1 | 420 | 426 | PF00149 | 0.313 |
DOC_PP4_FxxP_1 | 452 | 455 | PF00568 | 0.487 |
DOC_PP4_FxxP_1 | 562 | 565 | PF00568 | 0.330 |
DOC_PP4_FxxP_1 | 639 | 642 | PF00568 | 0.294 |
DOC_USP7_MATH_1 | 104 | 108 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 217 | 221 | PF00917 | 0.404 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 359 | 363 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 553 | 557 | PF00917 | 0.603 |
DOC_USP7_MATH_1 | 659 | 663 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 710 | 714 | PF00917 | 0.515 |
DOC_WW_Pin1_4 | 100 | 105 | PF00397 | 0.663 |
DOC_WW_Pin1_4 | 115 | 120 | PF00397 | 0.489 |
DOC_WW_Pin1_4 | 349 | 354 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 357 | 362 | PF00397 | 0.561 |
DOC_WW_Pin1_4 | 417 | 422 | PF00397 | 0.429 |
DOC_WW_Pin1_4 | 614 | 619 | PF00397 | 0.499 |
DOC_WW_Pin1_4 | 695 | 700 | PF00397 | 0.479 |
DOC_WW_Pin1_4 | 706 | 711 | PF00397 | 0.375 |
LIG_14-3-3_CanoR_1 | 165 | 169 | PF00244 | 0.346 |
LIG_14-3-3_CanoR_1 | 173 | 177 | PF00244 | 0.400 |
LIG_14-3-3_CanoR_1 | 284 | 292 | PF00244 | 0.452 |
LIG_14-3-3_CanoR_1 | 293 | 299 | PF00244 | 0.374 |
LIG_14-3-3_CanoR_1 | 3 | 13 | PF00244 | 0.450 |
LIG_14-3-3_CanoR_1 | 300 | 308 | PF00244 | 0.390 |
LIG_14-3-3_CanoR_1 | 632 | 636 | PF00244 | 0.298 |
LIG_14-3-3_CanoR_1 | 690 | 696 | PF00244 | 0.368 |
LIG_Actin_WH2_2 | 157 | 175 | PF00022 | 0.355 |
LIG_deltaCOP1_diTrp_1 | 445 | 452 | PF00928 | 0.375 |
LIG_deltaCOP1_diTrp_1 | 681 | 688 | PF00928 | 0.484 |
LIG_deltaCOP1_diTrp_1 | 719 | 727 | PF00928 | 0.338 |
LIG_FHA_1 | 209 | 215 | PF00498 | 0.353 |
LIG_FHA_1 | 375 | 381 | PF00498 | 0.337 |
LIG_FHA_1 | 418 | 424 | PF00498 | 0.488 |
LIG_FHA_1 | 520 | 526 | PF00498 | 0.540 |
LIG_FHA_1 | 559 | 565 | PF00498 | 0.443 |
LIG_FHA_1 | 618 | 624 | PF00498 | 0.425 |
LIG_FHA_1 | 701 | 707 | PF00498 | 0.616 |
LIG_FHA_2 | 101 | 107 | PF00498 | 0.668 |
LIG_FHA_2 | 116 | 122 | PF00498 | 0.510 |
LIG_FHA_2 | 126 | 132 | PF00498 | 0.328 |
LIG_FHA_2 | 151 | 157 | PF00498 | 0.334 |
LIG_FHA_2 | 191 | 197 | PF00498 | 0.386 |
LIG_FHA_2 | 379 | 385 | PF00498 | 0.309 |
LIG_FHA_2 | 5 | 11 | PF00498 | 0.508 |
LIG_FHA_2 | 607 | 613 | PF00498 | 0.671 |
LIG_GBD_Chelix_1 | 160 | 168 | PF00786 | 0.457 |
LIG_LIR_Apic_2 | 560 | 565 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 128 | 137 | PF02991 | 0.341 |
LIG_LIR_Gen_1 | 687 | 696 | PF02991 | 0.482 |
LIG_LIR_Gen_1 | 719 | 727 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 128 | 133 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 255 | 261 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 280 | 286 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 445 | 450 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 514 | 519 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 684 | 688 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 719 | 723 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 724 | 730 | PF02991 | 0.399 |
LIG_NRBOX | 488 | 494 | PF00104 | 0.494 |
LIG_NRBOX | 56 | 62 | PF00104 | 0.416 |
LIG_Pex14_1 | 250 | 254 | PF04695 | 0.329 |
LIG_Pex14_2 | 626 | 630 | PF04695 | 0.392 |
LIG_PTB_Apo_2 | 136 | 143 | PF02174 | 0.298 |
LIG_PTB_Apo_2 | 563 | 570 | PF02174 | 0.312 |
LIG_SH2_CRK | 258 | 262 | PF00017 | 0.396 |
LIG_SH2_NCK_1 | 254 | 258 | PF00017 | 0.456 |
LIG_SH2_NCK_1 | 656 | 660 | PF00017 | 0.588 |
LIG_SH2_STAP1 | 254 | 258 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 125 | 128 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 190 | 193 | PF00017 | 0.326 |
LIG_SH2_STAT5 | 277 | 280 | PF00017 | 0.420 |
LIG_SH3_3 | 350 | 356 | PF00018 | 0.621 |
LIG_SH3_3 | 541 | 547 | PF00018 | 0.556 |
LIG_SUMO_SIM_anti_2 | 156 | 163 | PF11976 | 0.399 |
LIG_SUMO_SIM_par_1 | 10 | 16 | PF11976 | 0.487 |
LIG_SUMO_SIM_par_1 | 205 | 211 | PF11976 | 0.459 |
LIG_SUMO_SIM_par_1 | 98 | 103 | PF11976 | 0.503 |
LIG_TRAF2_1 | 154 | 157 | PF00917 | 0.339 |
LIG_TRAF2_1 | 181 | 184 | PF00917 | 0.606 |
MOD_CDK_SPxxK_3 | 115 | 122 | PF00069 | 0.474 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.455 |
MOD_CK1_1 | 352 | 358 | PF00069 | 0.679 |
MOD_CK1_1 | 362 | 368 | PF00069 | 0.494 |
MOD_CK1_1 | 568 | 574 | PF00069 | 0.321 |
MOD_CK1_1 | 657 | 663 | PF00069 | 0.634 |
MOD_CK1_1 | 713 | 719 | PF00069 | 0.445 |
MOD_CK2_1 | 115 | 121 | PF00069 | 0.570 |
MOD_CK2_1 | 150 | 156 | PF00069 | 0.307 |
MOD_CK2_1 | 190 | 196 | PF00069 | 0.391 |
MOD_CK2_1 | 4 | 10 | PF00069 | 0.549 |
MOD_CK2_1 | 495 | 501 | PF00069 | 0.590 |
MOD_CK2_1 | 695 | 701 | PF00069 | 0.559 |
MOD_CK2_1 | 713 | 719 | PF00069 | 0.260 |
MOD_CMANNOS | 682 | 685 | PF00535 | 0.484 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.613 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.308 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.477 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.530 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.802 |
MOD_GlcNHglycan | 384 | 388 | PF01048 | 0.326 |
MOD_GlcNHglycan | 413 | 417 | PF01048 | 0.554 |
MOD_GlcNHglycan | 457 | 461 | PF01048 | 0.474 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.437 |
MOD_GlcNHglycan | 513 | 516 | PF01048 | 0.515 |
MOD_GlcNHglycan | 546 | 550 | PF01048 | 0.716 |
MOD_GlcNHglycan | 609 | 612 | PF01048 | 0.607 |
MOD_GlcNHglycan | 706 | 709 | PF01048 | 0.489 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.712 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.694 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.364 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.460 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.692 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.648 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.239 |
MOD_GSK3_1 | 417 | 424 | PF00069 | 0.392 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.366 |
MOD_GSK3_1 | 471 | 478 | PF00069 | 0.368 |
MOD_GSK3_1 | 495 | 502 | PF00069 | 0.501 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.655 |
MOD_GSK3_1 | 553 | 560 | PF00069 | 0.579 |
MOD_GSK3_1 | 691 | 698 | PF00069 | 0.449 |
MOD_GSK3_1 | 700 | 707 | PF00069 | 0.583 |
MOD_N-GLC_1 | 284 | 289 | PF02516 | 0.523 |
MOD_N-GLC_1 | 347 | 352 | PF02516 | 0.725 |
MOD_N-GLC_1 | 45 | 50 | PF02516 | 0.309 |
MOD_N-GLC_1 | 539 | 544 | PF02516 | 0.503 |
MOD_N-GLC_1 | 565 | 570 | PF02516 | 0.308 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.320 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.278 |
MOD_NEK2_1 | 172 | 177 | PF00069 | 0.475 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.344 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.399 |
MOD_NEK2_1 | 383 | 388 | PF00069 | 0.367 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.539 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.316 |
MOD_NEK2_1 | 470 | 475 | PF00069 | 0.350 |
MOD_NEK2_1 | 495 | 500 | PF00069 | 0.530 |
MOD_NEK2_1 | 577 | 582 | PF00069 | 0.365 |
MOD_NEK2_1 | 586 | 591 | PF00069 | 0.360 |
MOD_NEK2_2 | 125 | 130 | PF00069 | 0.365 |
MOD_NEK2_2 | 421 | 426 | PF00069 | 0.498 |
MOD_NEK2_2 | 565 | 570 | PF00069 | 0.336 |
MOD_PIKK_1 | 229 | 235 | PF00454 | 0.466 |
MOD_PIKK_1 | 314 | 320 | PF00454 | 0.481 |
MOD_PIKK_1 | 586 | 592 | PF00454 | 0.466 |
MOD_PIKK_1 | 88 | 94 | PF00454 | 0.573 |
MOD_PKA_1 | 342 | 348 | PF00069 | 0.577 |
MOD_PKA_2 | 164 | 170 | PF00069 | 0.392 |
MOD_PKA_2 | 172 | 178 | PF00069 | 0.442 |
MOD_PKA_2 | 311 | 317 | PF00069 | 0.484 |
MOD_PKA_2 | 342 | 348 | PF00069 | 0.717 |
MOD_PKA_2 | 374 | 380 | PF00069 | 0.341 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.432 |
MOD_PKA_2 | 599 | 605 | PF00069 | 0.548 |
MOD_PKA_2 | 631 | 637 | PF00069 | 0.297 |
MOD_PKA_2 | 713 | 719 | PF00069 | 0.540 |
MOD_Plk_1 | 266 | 272 | PF00069 | 0.593 |
MOD_Plk_1 | 456 | 462 | PF00069 | 0.397 |
MOD_Plk_1 | 539 | 545 | PF00069 | 0.511 |
MOD_Plk_1 | 565 | 571 | PF00069 | 0.338 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.327 |
MOD_Plk_4 | 257 | 263 | PF00069 | 0.414 |
MOD_Plk_4 | 28 | 34 | PF00069 | 0.389 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.424 |
MOD_Plk_4 | 558 | 564 | PF00069 | 0.503 |
MOD_Plk_4 | 684 | 690 | PF00069 | 0.526 |
MOD_ProDKin_1 | 100 | 106 | PF00069 | 0.663 |
MOD_ProDKin_1 | 115 | 121 | PF00069 | 0.484 |
MOD_ProDKin_1 | 349 | 355 | PF00069 | 0.615 |
MOD_ProDKin_1 | 357 | 363 | PF00069 | 0.555 |
MOD_ProDKin_1 | 417 | 423 | PF00069 | 0.427 |
MOD_ProDKin_1 | 614 | 620 | PF00069 | 0.486 |
MOD_ProDKin_1 | 695 | 701 | PF00069 | 0.494 |
MOD_ProDKin_1 | 706 | 712 | PF00069 | 0.361 |
TRG_DiLeu_BaLyEn_6 | 290 | 295 | PF01217 | 0.350 |
TRG_DiLeu_BaLyEn_6 | 56 | 61 | PF01217 | 0.399 |
TRG_ENDOCYTIC_2 | 134 | 137 | PF00928 | 0.329 |
TRG_ENDOCYTIC_2 | 254 | 257 | PF00928 | 0.362 |
TRG_ENDOCYTIC_2 | 258 | 261 | PF00928 | 0.356 |
TRG_ENDOCYTIC_2 | 394 | 397 | PF00928 | 0.491 |
TRG_ER_diArg_1 | 172 | 174 | PF00400 | 0.468 |
TRG_ER_diArg_1 | 176 | 178 | PF00400 | 0.457 |
TRG_ER_diArg_1 | 274 | 276 | PF00400 | 0.428 |
TRG_ER_diArg_1 | 372 | 375 | PF00400 | 0.446 |
TRG_ER_diArg_1 | 503 | 506 | PF00400 | 0.512 |
TRG_ER_diArg_1 | 535 | 537 | PF00400 | 0.434 |
TRG_Pf-PMV_PEXEL_1 | 284 | 288 | PF00026 | 0.428 |
TRG_Pf-PMV_PEXEL_1 | 372 | 376 | PF00026 | 0.467 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6F9 | Leptomonas seymouri | 49% | 98% |
A0A1X0NRU3 | Trypanosomatidae | 32% | 100% |
A0A3S5IS54 | Trypanosoma rangeli | 36% | 100% |
A0A3S7WR98 | Leishmania donovani | 99% | 100% |
A4H672 | Leishmania braziliensis | 74% | 99% |
C9ZVM1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
E9AN94 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 98% |
Q4QHD0 | Leishmania major | 92% | 99% |
V5BTS5 | Trypanosoma cruzi | 36% | 100% |