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: E9AN94
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 | 164 | 168 | PF00656 | 0.517 |
CLV_C14_Caspase3-7 | 402 | 406 | PF00656 | 0.530 |
CLV_C14_Caspase3-7 | 601 | 605 | PF00656 | 0.618 |
CLV_C14_Caspase3-7 | 69 | 73 | PF00656 | 0.739 |
CLV_NRD_NRD_1 | 170 | 172 | PF00675 | 0.482 |
CLV_NRD_NRD_1 | 174 | 176 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 272 | 274 | PF00675 | 0.526 |
CLV_NRD_NRD_1 | 339 | 341 | PF00675 | 0.575 |
CLV_NRD_NRD_1 | 364 | 366 | PF00675 | 0.389 |
CLV_NRD_NRD_1 | 397 | 399 | PF00675 | 0.453 |
CLV_NRD_NRD_1 | 496 | 498 | PF00675 | 0.561 |
CLV_NRD_NRD_1 | 528 | 530 | PF00675 | 0.419 |
CLV_NRD_NRD_1 | 95 | 97 | PF00675 | 0.548 |
CLV_PCSK_KEX2_1 | 170 | 172 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 174 | 176 | PF00082 | 0.502 |
CLV_PCSK_KEX2_1 | 271 | 273 | PF00082 | 0.495 |
CLV_PCSK_KEX2_1 | 339 | 341 | PF00082 | 0.575 |
CLV_PCSK_KEX2_1 | 364 | 366 | PF00082 | 0.417 |
CLV_PCSK_KEX2_1 | 397 | 399 | PF00082 | 0.459 |
CLV_PCSK_KEX2_1 | 495 | 497 | PF00082 | 0.558 |
CLV_PCSK_KEX2_1 | 528 | 530 | PF00082 | 0.418 |
CLV_PCSK_KEX2_1 | 94 | 96 | PF00082 | 0.599 |
CLV_PCSK_PC1ET2_1 | 94 | 96 | PF00082 | 0.599 |
CLV_PCSK_PC7_1 | 166 | 172 | PF00082 | 0.479 |
CLV_PCSK_PC7_1 | 267 | 273 | PF00082 | 0.278 |
CLV_PCSK_SKI1_1 | 132 | 136 | PF00082 | 0.362 |
CLV_PCSK_SKI1_1 | 273 | 277 | PF00082 | 0.474 |
CLV_PCSK_SKI1_1 | 281 | 285 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 290 | 294 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 297 | 301 | PF00082 | 0.379 |
CLV_PCSK_SKI1_1 | 566 | 570 | PF00082 | 0.399 |
CLV_PCSK_SKI1_1 | 575 | 579 | PF00082 | 0.442 |
DEG_APCC_DBOX_1 | 272 | 280 | PF00400 | 0.484 |
DEG_APCC_DBOX_1 | 623 | 631 | PF00400 | 0.337 |
DEG_Kelch_Keap1_1 | 205 | 210 | PF01344 | 0.237 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.691 |
DEG_SCF_FBW7_1 | 100 | 107 | PF00400 | 0.509 |
DEG_SPOP_SBC_1 | 356 | 360 | PF00917 | 0.436 |
DOC_CDC14_PxL_1 | 33 | 41 | PF14671 | 0.386 |
DOC_CYCLIN_RxL_1 | 286 | 294 | PF00134 | 0.420 |
DOC_CYCLIN_yCln2_LP_2 | 633 | 639 | PF00134 | 0.438 |
DOC_MAPK_DCC_7 | 6 | 14 | PF00069 | 0.659 |
DOC_MAPK_gen_1 | 94 | 102 | PF00069 | 0.462 |
DOC_MAPK_HePTP_8 | 283 | 295 | PF00069 | 0.324 |
DOC_MAPK_MEF2A_6 | 286 | 295 | PF00069 | 0.320 |
DOC_PP1_RVXF_1 | 36 | 42 | PF00149 | 0.345 |
DOC_PP2B_LxvP_1 | 259 | 262 | PF13499 | 0.426 |
DOC_PP2B_LxvP_1 | 433 | 436 | PF13499 | 0.446 |
DOC_PP2B_LxvP_1 | 633 | 636 | PF13499 | 0.341 |
DOC_PP4_FxxP_1 | 444 | 447 | PF00568 | 0.476 |
DOC_PP4_FxxP_1 | 631 | 634 | PF00568 | 0.296 |
DOC_USP7_MATH_1 | 104 | 108 | PF00917 | 0.723 |
DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.524 |
DOC_USP7_MATH_1 | 262 | 266 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 356 | 360 | PF00917 | 0.506 |
DOC_USP7_MATH_1 | 545 | 549 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 651 | 655 | PF00917 | 0.674 |
DOC_WW_Pin1_4 | 100 | 105 | PF00397 | 0.641 |
DOC_WW_Pin1_4 | 112 | 117 | PF00397 | 0.493 |
DOC_WW_Pin1_4 | 344 | 349 | PF00397 | 0.607 |
DOC_WW_Pin1_4 | 606 | 611 | PF00397 | 0.497 |
DOC_WW_Pin1_4 | 687 | 692 | PF00397 | 0.493 |
DOC_WW_Pin1_4 | 694 | 699 | PF00397 | 0.429 |
LIG_14-3-3_CanoR_1 | 162 | 166 | PF00244 | 0.342 |
LIG_14-3-3_CanoR_1 | 170 | 174 | PF00244 | 0.401 |
LIG_14-3-3_CanoR_1 | 253 | 259 | PF00244 | 0.320 |
LIG_14-3-3_CanoR_1 | 281 | 289 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 290 | 296 | PF00244 | 0.373 |
LIG_14-3-3_CanoR_1 | 297 | 305 | PF00244 | 0.383 |
LIG_14-3-3_CanoR_1 | 3 | 13 | PF00244 | 0.699 |
LIG_14-3-3_CanoR_1 | 365 | 375 | PF00244 | 0.309 |
LIG_14-3-3_CanoR_1 | 410 | 417 | PF00244 | 0.369 |
LIG_14-3-3_CanoR_1 | 592 | 600 | PF00244 | 0.460 |
LIG_14-3-3_CanoR_1 | 624 | 634 | PF00244 | 0.295 |
LIG_14-3-3_CanoR_1 | 682 | 688 | PF00244 | 0.380 |
LIG_Actin_WH2_2 | 154 | 172 | PF00022 | 0.358 |
LIG_APCC_ABBA_1 | 559 | 564 | PF00400 | 0.211 |
LIG_BIR_III_4 | 501 | 505 | PF00653 | 0.480 |
LIG_deltaCOP1_diTrp_1 | 437 | 444 | PF00928 | 0.368 |
LIG_deltaCOP1_diTrp_1 | 673 | 680 | PF00928 | 0.497 |
LIG_deltaCOP1_diTrp_1 | 707 | 715 | PF00928 | 0.343 |
LIG_FHA_1 | 206 | 212 | PF00498 | 0.353 |
LIG_FHA_1 | 367 | 373 | PF00498 | 0.334 |
LIG_FHA_1 | 406 | 412 | PF00498 | 0.511 |
LIG_FHA_1 | 512 | 518 | PF00498 | 0.528 |
LIG_FHA_1 | 532 | 538 | PF00498 | 0.406 |
LIG_FHA_1 | 551 | 557 | PF00498 | 0.476 |
LIG_FHA_1 | 610 | 616 | PF00498 | 0.391 |
LIG_FHA_2 | 101 | 107 | PF00498 | 0.637 |
LIG_FHA_2 | 113 | 119 | PF00498 | 0.495 |
LIG_FHA_2 | 123 | 129 | PF00498 | 0.334 |
LIG_FHA_2 | 148 | 154 | PF00498 | 0.340 |
LIG_FHA_2 | 188 | 194 | PF00498 | 0.390 |
LIG_FHA_2 | 371 | 377 | PF00498 | 0.305 |
LIG_FHA_2 | 5 | 11 | PF00498 | 0.565 |
LIG_FHA_2 | 599 | 605 | PF00498 | 0.684 |
LIG_GBD_Chelix_1 | 157 | 165 | PF00786 | 0.459 |
LIG_LIR_Apic_2 | 552 | 557 | PF02991 | 0.486 |
LIG_LIR_Apic_2 | 628 | 634 | PF02991 | 0.328 |
LIG_LIR_Gen_1 | 125 | 134 | PF02991 | 0.346 |
LIG_LIR_Gen_1 | 252 | 263 | PF02991 | 0.322 |
LIG_LIR_Gen_1 | 679 | 688 | PF02991 | 0.489 |
LIG_LIR_Gen_1 | 707 | 715 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 125 | 130 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 252 | 258 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 277 | 283 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 437 | 442 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 676 | 680 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 707 | 711 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 712 | 718 | PF02991 | 0.413 |
LIG_NRBOX | 480 | 486 | PF00104 | 0.497 |
LIG_NRBOX | 56 | 62 | PF00104 | 0.429 |
LIG_Pex14_1 | 247 | 251 | PF04695 | 0.321 |
LIG_Pex14_2 | 618 | 622 | PF04695 | 0.386 |
LIG_PTB_Apo_2 | 133 | 140 | PF02174 | 0.301 |
LIG_SH2_CRK | 255 | 259 | PF00017 | 0.425 |
LIG_SH2_NCK_1 | 251 | 255 | PF00017 | 0.455 |
LIG_SH2_NCK_1 | 648 | 652 | PF00017 | 0.632 |
LIG_SH2_PTP2 | 554 | 557 | PF00017 | 0.309 |
LIG_SH2_STAP1 | 251 | 255 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 122 | 125 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 187 | 190 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 255 | 258 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 274 | 277 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 554 | 557 | PF00017 | 0.309 |
LIG_SH3_3 | 347 | 353 | PF00018 | 0.628 |
LIG_SH3_3 | 533 | 539 | PF00018 | 0.554 |
LIG_SUMO_SIM_anti_2 | 153 | 160 | PF11976 | 0.404 |
LIG_SUMO_SIM_par_1 | 10 | 16 | PF11976 | 0.570 |
LIG_SUMO_SIM_par_1 | 98 | 103 | PF11976 | 0.485 |
LIG_TRAF2_1 | 151 | 154 | PF00917 | 0.346 |
LIG_TRAF2_1 | 178 | 181 | PF00917 | 0.627 |
LIG_TRAF2_1 | 238 | 241 | PF00917 | 0.493 |
MOD_CDK_SPxxK_3 | 112 | 119 | PF00069 | 0.488 |
MOD_CK1_1 | 324 | 330 | PF00069 | 0.450 |
MOD_CK1_1 | 349 | 355 | PF00069 | 0.671 |
MOD_CK1_1 | 540 | 546 | PF00069 | 0.609 |
MOD_CK1_1 | 547 | 553 | PF00069 | 0.537 |
MOD_CK1_1 | 560 | 566 | PF00069 | 0.343 |
MOD_CK1_1 | 591 | 597 | PF00069 | 0.394 |
MOD_CK1_1 | 649 | 655 | PF00069 | 0.652 |
MOD_CK2_1 | 112 | 118 | PF00069 | 0.572 |
MOD_CK2_1 | 147 | 153 | PF00069 | 0.310 |
MOD_CK2_1 | 187 | 193 | PF00069 | 0.393 |
MOD_CK2_1 | 204 | 210 | PF00069 | 0.440 |
MOD_CK2_1 | 4 | 10 | PF00069 | 0.626 |
MOD_CK2_1 | 487 | 493 | PF00069 | 0.591 |
MOD_CK2_1 | 497 | 503 | PF00069 | 0.458 |
MOD_CK2_1 | 687 | 693 | PF00069 | 0.543 |
MOD_CK2_1 | 701 | 707 | PF00069 | 0.242 |
MOD_CMANNOS | 674 | 677 | PF00535 | 0.500 |
MOD_GlcNHglycan | 150 | 153 | PF01048 | 0.311 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.451 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.516 |
MOD_GlcNHglycan | 376 | 380 | PF01048 | 0.316 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.467 |
MOD_GlcNHglycan | 505 | 508 | PF01048 | 0.587 |
MOD_GlcNHglycan | 538 | 542 | PF01048 | 0.724 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.474 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.694 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.696 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.383 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.436 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.665 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.233 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.451 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.383 |
MOD_GSK3_1 | 463 | 470 | PF00069 | 0.375 |
MOD_GSK3_1 | 487 | 494 | PF00069 | 0.505 |
MOD_GSK3_1 | 540 | 547 | PF00069 | 0.639 |
MOD_GSK3_1 | 604 | 611 | PF00069 | 0.420 |
MOD_GSK3_1 | 683 | 690 | PF00069 | 0.462 |
MOD_N-GLC_1 | 281 | 286 | PF02516 | 0.527 |
MOD_N-GLC_1 | 344 | 349 | PF02516 | 0.736 |
MOD_N-GLC_1 | 448 | 453 | PF02516 | 0.381 |
MOD_N-GLC_1 | 45 | 50 | PF02516 | 0.294 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.320 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.280 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.436 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.354 |
MOD_NEK2_1 | 366 | 371 | PF00069 | 0.407 |
MOD_NEK2_1 | 375 | 380 | PF00069 | 0.404 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.621 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.313 |
MOD_NEK2_1 | 462 | 467 | PF00069 | 0.353 |
MOD_NEK2_1 | 487 | 492 | PF00069 | 0.515 |
MOD_NEK2_1 | 569 | 574 | PF00069 | 0.353 |
MOD_NEK2_1 | 625 | 630 | PF00069 | 0.357 |
MOD_NEK2_2 | 122 | 127 | PF00069 | 0.369 |
MOD_NEK2_2 | 413 | 418 | PF00069 | 0.484 |
MOD_NEK2_2 | 557 | 562 | PF00069 | 0.342 |
MOD_PIKK_1 | 226 | 232 | PF00454 | 0.480 |
MOD_PIKK_1 | 311 | 317 | PF00454 | 0.479 |
MOD_PIKK_1 | 625 | 631 | PF00454 | 0.355 |
MOD_PIKK_1 | 88 | 94 | PF00454 | 0.589 |
MOD_PKA_1 | 339 | 345 | PF00069 | 0.586 |
MOD_PKA_2 | 161 | 167 | PF00069 | 0.351 |
MOD_PKA_2 | 169 | 175 | PF00069 | 0.404 |
MOD_PKA_2 | 339 | 345 | PF00069 | 0.721 |
MOD_PKA_2 | 366 | 372 | PF00069 | 0.337 |
MOD_PKA_2 | 409 | 415 | PF00069 | 0.373 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.656 |
MOD_PKA_2 | 591 | 597 | PF00069 | 0.539 |
MOD_PKA_2 | 623 | 629 | PF00069 | 0.295 |
MOD_PKA_2 | 701 | 707 | PF00069 | 0.542 |
MOD_PKB_1 | 495 | 503 | PF00069 | 0.500 |
MOD_Plk_1 | 224 | 230 | PF00069 | 0.296 |
MOD_Plk_1 | 263 | 269 | PF00069 | 0.591 |
MOD_Plk_1 | 404 | 410 | PF00069 | 0.335 |
MOD_Plk_1 | 448 | 454 | PF00069 | 0.386 |
MOD_Plk_4 | 187 | 193 | PF00069 | 0.329 |
MOD_Plk_4 | 254 | 260 | PF00069 | 0.404 |
MOD_Plk_4 | 28 | 34 | PF00069 | 0.403 |
MOD_Plk_4 | 448 | 454 | PF00069 | 0.239 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.451 |
MOD_Plk_4 | 550 | 556 | PF00069 | 0.557 |
MOD_Plk_4 | 676 | 682 | PF00069 | 0.526 |
MOD_ProDKin_1 | 100 | 106 | PF00069 | 0.647 |
MOD_ProDKin_1 | 112 | 118 | PF00069 | 0.488 |
MOD_ProDKin_1 | 344 | 350 | PF00069 | 0.608 |
MOD_ProDKin_1 | 606 | 612 | PF00069 | 0.480 |
MOD_ProDKin_1 | 687 | 693 | PF00069 | 0.503 |
MOD_ProDKin_1 | 694 | 700 | PF00069 | 0.414 |
TRG_DiLeu_BaLyEn_6 | 287 | 292 | PF01217 | 0.351 |
TRG_DiLeu_BaLyEn_6 | 56 | 61 | PF01217 | 0.378 |
TRG_ENDOCYTIC_2 | 131 | 134 | PF00928 | 0.333 |
TRG_ENDOCYTIC_2 | 251 | 254 | PF00928 | 0.381 |
TRG_ENDOCYTIC_2 | 255 | 258 | PF00928 | 0.353 |
TRG_ENDOCYTIC_2 | 386 | 389 | PF00928 | 0.490 |
TRG_ER_diArg_1 | 169 | 171 | PF00400 | 0.473 |
TRG_ER_diArg_1 | 173 | 175 | PF00400 | 0.462 |
TRG_ER_diArg_1 | 271 | 273 | PF00400 | 0.441 |
TRG_ER_diArg_1 | 364 | 367 | PF00400 | 0.404 |
TRG_ER_diArg_1 | 495 | 497 | PF00400 | 0.476 |
TRG_ER_diArg_1 | 527 | 529 | PF00400 | 0.422 |
TRG_Pf-PMV_PEXEL_1 | 317 | 321 | PF00026 | 0.411 |
TRG_Pf-PMV_PEXEL_1 | 364 | 368 | PF00026 | 0.463 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6F9 | Leptomonas seymouri | 50% | 97% |
A0A1X0NRU3 | Trypanosomatidae | 32% | 98% |
A0A3S5IS54 | Trypanosoma rangeli | 37% | 100% |
A0A3S7WR98 | Leishmania donovani | 90% | 98% |
A4H672 | Leishmania braziliensis | 74% | 100% |
A4HUJ6 | Leishmania infantum | 90% | 98% |
C9ZVM1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
Q4QHD0 | Leishmania major | 88% | 100% |
V5BTS5 | Trypanosoma cruzi | 36% | 100% |