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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A4HHX0
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006396 | RNA processing | 6 | 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:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 3 |
GO:0008270 | zinc ion binding | 6 | 1 |
GO:0043167 | ion binding | 2 | 3 |
GO:0043169 | cation binding | 3 | 3 |
GO:0046872 | metal ion binding | 4 | 3 |
GO:0046914 | transition metal ion binding | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 128 | 132 | PF00656 | 0.428 |
CLV_C14_Caspase3-7 | 325 | 329 | PF00656 | 0.616 |
CLV_C14_Caspase3-7 | 586 | 590 | PF00656 | 0.533 |
CLV_NRD_NRD_1 | 221 | 223 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 408 | 410 | PF00675 | 0.462 |
CLV_NRD_NRD_1 | 624 | 626 | PF00675 | 0.615 |
CLV_NRD_NRD_1 | 629 | 631 | PF00675 | 0.612 |
CLV_PCSK_KEX2_1 | 221 | 223 | PF00082 | 0.581 |
CLV_PCSK_KEX2_1 | 408 | 410 | PF00082 | 0.527 |
CLV_PCSK_KEX2_1 | 513 | 515 | PF00082 | 0.214 |
CLV_PCSK_KEX2_1 | 629 | 631 | PF00082 | 0.566 |
CLV_PCSK_PC1ET2_1 | 513 | 515 | PF00082 | 0.214 |
CLV_PCSK_PC7_1 | 625 | 631 | PF00082 | 0.583 |
CLV_PCSK_SKI1_1 | 130 | 134 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 211 | 215 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 301 | 305 | PF00082 | 0.276 |
CLV_PCSK_SKI1_1 | 372 | 376 | PF00082 | 0.512 |
CLV_PCSK_SKI1_1 | 46 | 50 | PF00082 | 0.437 |
CLV_PCSK_SKI1_1 | 551 | 555 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 576 | 580 | PF00082 | 0.694 |
CLV_PCSK_SKI1_1 | 625 | 629 | PF00082 | 0.611 |
DEG_APCC_DBOX_1 | 102 | 110 | PF00400 | 0.455 |
DEG_APCC_DBOX_1 | 300 | 308 | PF00400 | 0.288 |
DEG_COP1_1 | 80 | 90 | PF00400 | 0.448 |
DEG_SCF_FBW7_1 | 579 | 584 | PF00400 | 0.431 |
DEG_SPOP_SBC_1 | 278 | 282 | PF00917 | 0.606 |
DOC_CDC14_PxL_1 | 465 | 473 | PF14671 | 0.417 |
DOC_CKS1_1 | 346 | 351 | PF01111 | 0.580 |
DOC_CKS1_1 | 578 | 583 | PF01111 | 0.572 |
DOC_CYCLIN_RxL_1 | 525 | 537 | PF00134 | 0.562 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 304 | 313 | PF00134 | 0.421 |
DOC_MAPK_gen_1 | 513 | 524 | PF00069 | 0.413 |
DOC_MAPK_MEF2A_6 | 139 | 146 | PF00069 | 0.548 |
DOC_MAPK_MEF2A_6 | 517 | 526 | PF00069 | 0.413 |
DOC_MAPK_RevD_3 | 616 | 631 | PF00069 | 0.626 |
DOC_PP1_RVXF_1 | 141 | 147 | PF00149 | 0.334 |
DOC_PP4_FxxP_1 | 387 | 390 | PF00568 | 0.424 |
DOC_PP4_FxxP_1 | 578 | 581 | PF00568 | 0.569 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 121 | 125 | PF00917 | 0.357 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.244 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 163 | 167 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 203 | 207 | PF00917 | 0.521 |
DOC_USP7_MATH_1 | 330 | 334 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 440 | 444 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 456 | 460 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 574 | 578 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 602 | 606 | PF00917 | 0.653 |
DOC_USP7_MATH_1 | 608 | 612 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 616 | 620 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 77 | 81 | PF00917 | 0.728 |
DOC_USP7_UBL2_3 | 139 | 143 | PF12436 | 0.466 |
DOC_WW_Pin1_4 | 187 | 192 | PF00397 | 0.467 |
DOC_WW_Pin1_4 | 215 | 220 | PF00397 | 0.440 |
DOC_WW_Pin1_4 | 328 | 333 | PF00397 | 0.468 |
DOC_WW_Pin1_4 | 339 | 344 | PF00397 | 0.717 |
DOC_WW_Pin1_4 | 345 | 350 | PF00397 | 0.737 |
DOC_WW_Pin1_4 | 577 | 582 | PF00397 | 0.561 |
DOC_WW_Pin1_4 | 611 | 616 | PF00397 | 0.631 |
DOC_WW_Pin1_4 | 64 | 69 | PF00397 | 0.593 |
LIG_14-3-3_CanoR_1 | 175 | 185 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 301 | 310 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 376 | 385 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 439 | 445 | PF00244 | 0.584 |
LIG_Actin_WH2_2 | 445 | 460 | PF00022 | 0.425 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.456 |
LIG_BIR_III_2 | 168 | 172 | PF00653 | 0.459 |
LIG_BIR_III_4 | 607 | 611 | PF00653 | 0.621 |
LIG_BIR_III_4 | 78 | 82 | PF00653 | 0.439 |
LIG_BRCT_BRCA1_1 | 123 | 127 | PF00533 | 0.456 |
LIG_BRCT_BRCA1_1 | 378 | 382 | PF00533 | 0.362 |
LIG_BRCT_BRCA1_1 | 461 | 465 | PF00533 | 0.414 |
LIG_FHA_1 | 13 | 19 | PF00498 | 0.565 |
LIG_FHA_1 | 230 | 236 | PF00498 | 0.597 |
LIG_FHA_1 | 59 | 65 | PF00498 | 0.606 |
LIG_FHA_2 | 106 | 112 | PF00498 | 0.563 |
LIG_FHA_2 | 175 | 181 | PF00498 | 0.505 |
LIG_FHA_2 | 226 | 232 | PF00498 | 0.595 |
LIG_FHA_2 | 28 | 34 | PF00498 | 0.448 |
LIG_FHA_2 | 584 | 590 | PF00498 | 0.695 |
LIG_FHA_2 | 632 | 638 | PF00498 | 0.527 |
LIG_IRF3_LxIS_1 | 522 | 527 | PF10401 | 0.350 |
LIG_LIR_Apic_2 | 577 | 581 | PF02991 | 0.659 |
LIG_LIR_Gen_1 | 116 | 127 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 145 | 154 | PF02991 | 0.568 |
LIG_LIR_Gen_1 | 379 | 390 | PF02991 | 0.398 |
LIG_LIR_Gen_1 | 462 | 473 | PF02991 | 0.667 |
LIG_LIR_Gen_1 | 97 | 107 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 116 | 122 | PF02991 | 0.578 |
LIG_LIR_Nem_3 | 145 | 149 | PF02991 | 0.564 |
LIG_LIR_Nem_3 | 297 | 303 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 379 | 385 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 462 | 468 | PF02991 | 0.680 |
LIG_LIR_Nem_3 | 515 | 519 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 97 | 102 | PF02991 | 0.515 |
LIG_RPA_C_Fungi | 202 | 214 | PF08784 | 0.441 |
LIG_SH2_CRK | 44 | 48 | PF00017 | 0.374 |
LIG_SH2_NCK_1 | 50 | 54 | PF00017 | 0.535 |
LIG_SH2_STAP1 | 115 | 119 | PF00017 | 0.490 |
LIG_SH2_STAP1 | 44 | 48 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 105 | 108 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 115 | 118 | PF00017 | 0.416 |
LIG_SH3_2 | 621 | 626 | PF14604 | 0.594 |
LIG_SH3_3 | 101 | 107 | PF00018 | 0.662 |
LIG_SH3_3 | 150 | 156 | PF00018 | 0.457 |
LIG_SH3_3 | 213 | 219 | PF00018 | 0.577 |
LIG_SH3_3 | 252 | 258 | PF00018 | 0.488 |
LIG_SH3_3 | 334 | 340 | PF00018 | 0.487 |
LIG_SH3_3 | 343 | 349 | PF00018 | 0.460 |
LIG_SH3_3 | 541 | 547 | PF00018 | 0.522 |
LIG_SH3_3 | 568 | 574 | PF00018 | 0.398 |
LIG_SH3_3 | 615 | 621 | PF00018 | 0.547 |
LIG_SUMO_SIM_anti_2 | 360 | 366 | PF11976 | 0.294 |
LIG_SUMO_SIM_par_1 | 212 | 218 | PF11976 | 0.437 |
LIG_TRAF2_1 | 228 | 231 | PF00917 | 0.453 |
LIG_TYR_ITIM | 42 | 47 | PF00017 | 0.263 |
LIG_UBA3_1 | 23 | 32 | PF00899 | 0.499 |
LIG_UBA3_1 | 309 | 316 | PF00899 | 0.519 |
LIG_WRC_WIRS_1 | 575 | 580 | PF05994 | 0.682 |
MOD_CDC14_SPxK_1 | 218 | 221 | PF00782 | 0.442 |
MOD_CDK_SPxK_1 | 215 | 221 | PF00069 | 0.549 |
MOD_CDK_SPxxK_3 | 215 | 222 | PF00069 | 0.552 |
MOD_CK1_1 | 276 | 282 | PF00069 | 0.665 |
MOD_CK1_1 | 342 | 348 | PF00069 | 0.647 |
MOD_CK1_1 | 355 | 361 | PF00069 | 0.640 |
MOD_CK1_1 | 441 | 447 | PF00069 | 0.547 |
MOD_CK1_1 | 459 | 465 | PF00069 | 0.634 |
MOD_CK1_1 | 487 | 493 | PF00069 | 0.359 |
MOD_CK1_1 | 577 | 583 | PF00069 | 0.589 |
MOD_CK1_1 | 609 | 615 | PF00069 | 0.623 |
MOD_CK2_1 | 105 | 111 | PF00069 | 0.485 |
MOD_CK2_1 | 174 | 180 | PF00069 | 0.471 |
MOD_CK2_1 | 225 | 231 | PF00069 | 0.582 |
MOD_CK2_1 | 27 | 33 | PF00069 | 0.497 |
MOD_CK2_1 | 354 | 360 | PF00069 | 0.562 |
MOD_CK2_1 | 517 | 523 | PF00069 | 0.159 |
MOD_CK2_1 | 555 | 561 | PF00069 | 0.492 |
MOD_CK2_1 | 77 | 83 | PF00069 | 0.437 |
MOD_Cter_Amidation | 370 | 373 | PF01082 | 0.329 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.363 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.381 |
MOD_GlcNHglycan | 170 | 174 | PF01048 | 0.581 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.596 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.440 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.643 |
MOD_GlcNHglycan | 354 | 357 | PF01048 | 0.707 |
MOD_GlcNHglycan | 378 | 381 | PF01048 | 0.345 |
MOD_GlcNHglycan | 445 | 448 | PF01048 | 0.690 |
MOD_GlcNHglycan | 458 | 461 | PF01048 | 0.698 |
MOD_GlcNHglycan | 465 | 468 | PF01048 | 0.396 |
MOD_GlcNHglycan | 489 | 492 | PF01048 | 0.438 |
MOD_GlcNHglycan | 607 | 611 | PF01048 | 0.753 |
MOD_GlcNHglycan | 618 | 621 | PF01048 | 0.641 |
MOD_GlcNHglycan | 78 | 82 | PF01048 | 0.499 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.592 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.389 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.437 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.500 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.689 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.665 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.633 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.568 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.695 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.440 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.706 |
MOD_GSK3_1 | 577 | 584 | PF00069 | 0.440 |
MOD_GSK3_1 | 602 | 609 | PF00069 | 0.661 |
MOD_GSK3_1 | 631 | 638 | PF00069 | 0.648 |
MOD_N-GLC_1 | 487 | 492 | PF02516 | 0.433 |
MOD_N-GLC_2 | 118 | 120 | PF02516 | 0.362 |
MOD_N-GLC_2 | 480 | 482 | PF02516 | 0.430 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.621 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.561 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.629 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.738 |
MOD_NEK2_1 | 375 | 380 | PF00069 | 0.471 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.338 |
MOD_NEK2_1 | 524 | 529 | PF00069 | 0.170 |
MOD_NEK2_1 | 91 | 96 | PF00069 | 0.555 |
MOD_NEK2_2 | 460 | 465 | PF00069 | 0.403 |
MOD_PKA_1 | 315 | 321 | PF00069 | 0.381 |
MOD_PKA_1 | 625 | 631 | PF00069 | 0.583 |
MOD_PKA_2 | 174 | 180 | PF00069 | 0.471 |
MOD_PKA_2 | 375 | 381 | PF00069 | 0.475 |
MOD_PKA_2 | 438 | 444 | PF00069 | 0.477 |
MOD_PKA_2 | 51 | 57 | PF00069 | 0.468 |
MOD_Plk_1 | 441 | 447 | PF00069 | 0.597 |
MOD_Plk_1 | 487 | 493 | PF00069 | 0.438 |
MOD_Plk_1 | 517 | 523 | PF00069 | 0.163 |
MOD_Plk_2-3 | 518 | 524 | PF00069 | 0.240 |
MOD_Plk_2-3 | 555 | 561 | PF00069 | 0.333 |
MOD_Plk_4 | 148 | 154 | PF00069 | 0.578 |
MOD_Plk_4 | 460 | 466 | PF00069 | 0.675 |
MOD_Plk_4 | 567 | 573 | PF00069 | 0.534 |
MOD_ProDKin_1 | 187 | 193 | PF00069 | 0.465 |
MOD_ProDKin_1 | 215 | 221 | PF00069 | 0.443 |
MOD_ProDKin_1 | 328 | 334 | PF00069 | 0.472 |
MOD_ProDKin_1 | 339 | 345 | PF00069 | 0.718 |
MOD_ProDKin_1 | 347 | 353 | PF00069 | 0.731 |
MOD_ProDKin_1 | 577 | 583 | PF00069 | 0.562 |
MOD_ProDKin_1 | 611 | 617 | PF00069 | 0.632 |
MOD_ProDKin_1 | 64 | 70 | PF00069 | 0.594 |
MOD_SUMO_for_1 | 237 | 240 | PF00179 | 0.579 |
MOD_SUMO_rev_2 | 366 | 374 | PF00179 | 0.449 |
TRG_ENDOCYTIC_2 | 300 | 303 | PF00928 | 0.570 |
TRG_ENDOCYTIC_2 | 44 | 47 | PF00928 | 0.425 |
TRG_ENDOCYTIC_2 | 50 | 53 | PF00928 | 0.432 |
TRG_ENDOCYTIC_2 | 99 | 102 | PF00928 | 0.383 |
TRG_ER_diArg_1 | 220 | 222 | PF00400 | 0.539 |
TRG_ER_diArg_1 | 408 | 410 | PF00400 | 0.369 |
TRG_ER_diArg_1 | 474 | 477 | PF00400 | 0.466 |
TRG_NLS_MonoExtN_4 | 629 | 634 | PF00514 | 0.494 |
TRG_Pf-PMV_PEXEL_1 | 400 | 404 | PF00026 | 0.535 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I7W2 | Leptomonas seymouri | 39% | 88% |
A0A0S4JVS9 | Bodo saltans | 27% | 95% |
A0A1X0P2C9 | Trypanosomatidae | 32% | 100% |
A0A3Q8IEK7 | Leishmania donovani | 72% | 100% |
A0A3R7MIW1 | Trypanosoma rangeli | 33% | 100% |
A4I520 | Leishmania infantum | 72% | 100% |
C9ZQH9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9B0F0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 71% | 100% |
O75467 | Homo sapiens | 26% | 100% |
Q4Q7T3 | Leishmania major | 71% | 100% |
Q585P3 | Trypanosoma brucei brucei (strain 927/4 GUTat10.1) | 33% | 100% |
V5DD36 | Trypanosoma cruzi | 33% | 100% |