| 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: 6 |
| NetGPI | no | yes: 0, no: 6 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005737 | cytoplasm | 2 | 7 |
| GO:0110165 | cellular anatomical entity | 1 | 7 |
| GO:0005813 | centrosome | 3 | 1 |
| GO:0005815 | microtubule organizing center | 2 | 1 |
| GO:0036064 | ciliary basal body | 3 | 1 |
Related structures:
AlphaFold database: A4HHJ3
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0019220 | regulation of phosphate metabolic process | 6 | 7 |
| GO:0019222 | regulation of metabolic process | 3 | 7 |
| GO:0031323 | regulation of cellular metabolic process | 4 | 7 |
| GO:0035303 | regulation of dephosphorylation | 7 | 7 |
| GO:0050789 | regulation of biological process | 2 | 7 |
| GO:0050794 | regulation of cellular process | 3 | 7 |
| GO:0051174 | regulation of phosphorus metabolic process | 5 | 7 |
| GO:0065007 | biological regulation | 1 | 7 |
| GO:0000226 | microtubule cytoskeleton organization | 3 | 1 |
| GO:0006996 | organelle organization | 4 | 1 |
| GO:0007010 | cytoskeleton organization | 5 | 1 |
| GO:0007017 | microtubule-based process | 2 | 1 |
| GO:0009987 | cellular process | 1 | 1 |
| GO:0016043 | cellular component organization | 3 | 1 |
| GO:0030865 | cortical cytoskeleton organization | 6 | 1 |
| GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005488 | binding | 1 | 7 |
| GO:0043167 | ion binding | 2 | 7 |
| GO:0043169 | cation binding | 3 | 7 |
| GO:0046872 | metal ion binding | 4 | 7 |
| GO:0005509 | calcium ion binding | 5 | 5 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 342 | 346 | PF00656 | 0.436 |
| CLV_NRD_NRD_1 | 17 | 19 | PF00675 | 0.431 |
| CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.726 |
| CLV_NRD_NRD_1 | 384 | 386 | PF00675 | 0.334 |
| CLV_NRD_NRD_1 | 499 | 501 | PF00675 | 0.362 |
| CLV_NRD_NRD_1 | 60 | 62 | PF00675 | 0.665 |
| CLV_PCSK_KEX2_1 | 17 | 19 | PF00082 | 0.431 |
| CLV_PCSK_KEX2_1 | 171 | 173 | PF00082 | 0.725 |
| CLV_PCSK_KEX2_1 | 241 | 243 | PF00082 | 0.697 |
| CLV_PCSK_KEX2_1 | 384 | 386 | PF00082 | 0.372 |
| CLV_PCSK_KEX2_1 | 60 | 62 | PF00082 | 0.495 |
| CLV_PCSK_KEX2_1 | 607 | 609 | PF00082 | 0.347 |
| CLV_PCSK_PC1ET2_1 | 241 | 243 | PF00082 | 0.697 |
| CLV_PCSK_PC1ET2_1 | 607 | 609 | PF00082 | 0.347 |
| CLV_PCSK_SKI1_1 | 238 | 242 | PF00082 | 0.466 |
| CLV_PCSK_SKI1_1 | 30 | 34 | PF00082 | 0.451 |
| CLV_PCSK_SKI1_1 | 372 | 376 | PF00082 | 0.488 |
| CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.348 |
| CLV_PCSK_SKI1_1 | 395 | 399 | PF00082 | 0.396 |
| CLV_PCSK_SKI1_1 | 438 | 442 | PF00082 | 0.442 |
| CLV_Separin_Metazoa | 574 | 578 | PF03568 | 0.305 |
| DEG_SPOP_SBC_1 | 4 | 8 | PF00917 | 0.543 |
| DOC_CKS1_1 | 532 | 537 | PF01111 | 0.360 |
| DOC_CYCLIN_RxL_1 | 242 | 256 | PF00134 | 0.476 |
| DOC_CYCLIN_RxL_1 | 381 | 391 | PF00134 | 0.340 |
| DOC_MAPK_MEF2A_6 | 298 | 305 | PF00069 | 0.417 |
| DOC_MAPK_MEF2A_6 | 93 | 101 | PF00069 | 0.382 |
| DOC_PP1_RVXF_1 | 324 | 331 | PF00149 | 0.272 |
| DOC_PP1_RVXF_1 | 382 | 389 | PF00149 | 0.337 |
| DOC_PP1_RVXF_1 | 499 | 506 | PF00149 | 0.341 |
| DOC_PP2B_LxvP_1 | 150 | 153 | PF13499 | 0.565 |
| DOC_PP2B_LxvP_1 | 554 | 557 | PF13499 | 0.399 |
| DOC_USP7_MATH_1 | 209 | 213 | PF00917 | 0.749 |
| DOC_USP7_MATH_1 | 223 | 227 | PF00917 | 0.684 |
| DOC_USP7_MATH_1 | 261 | 265 | PF00917 | 0.574 |
| DOC_USP7_MATH_1 | 476 | 480 | PF00917 | 0.420 |
| DOC_USP7_MATH_1 | 513 | 517 | PF00917 | 0.385 |
| DOC_USP7_UBL2_3 | 102 | 106 | PF12436 | 0.427 |
| DOC_USP7_UBL2_3 | 177 | 181 | PF12436 | 0.551 |
| DOC_WW_Pin1_4 | 185 | 190 | PF00397 | 0.746 |
| DOC_WW_Pin1_4 | 196 | 201 | PF00397 | 0.602 |
| DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.751 |
| DOC_WW_Pin1_4 | 255 | 260 | PF00397 | 0.574 |
| DOC_WW_Pin1_4 | 472 | 477 | PF00397 | 0.387 |
| DOC_WW_Pin1_4 | 531 | 536 | PF00397 | 0.366 |
| DOC_WW_Pin1_4 | 583 | 588 | PF00397 | 0.376 |
| DOC_WW_Pin1_4 | 7 | 12 | PF00397 | 0.524 |
| LIG_14-3-3_CanoR_1 | 123 | 129 | PF00244 | 0.441 |
| LIG_14-3-3_CanoR_1 | 229 | 234 | PF00244 | 0.641 |
| LIG_14-3-3_CanoR_1 | 30 | 38 | PF00244 | 0.508 |
| LIG_14-3-3_CanoR_1 | 347 | 353 | PF00244 | 0.399 |
| LIG_14-3-3_CanoR_1 | 399 | 404 | PF00244 | 0.375 |
| LIG_14-3-3_CanoR_1 | 60 | 68 | PF00244 | 0.472 |
| LIG_Actin_RPEL_3 | 578 | 597 | PF02755 | 0.352 |
| LIG_Actin_WH2_2 | 562 | 579 | PF00022 | 0.288 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.787 |
| LIG_BIR_III_4 | 221 | 225 | PF00653 | 0.623 |
| LIG_BRCT_BRCA1_1 | 64 | 68 | PF00533 | 0.517 |
| LIG_deltaCOP1_diTrp_1 | 39 | 46 | PF00928 | 0.573 |
| LIG_eIF4E_1 | 436 | 442 | PF01652 | 0.447 |
| LIG_EVH1_1 | 150 | 154 | PF00568 | 0.537 |
| LIG_FHA_1 | 206 | 212 | PF00498 | 0.716 |
| LIG_FHA_1 | 430 | 436 | PF00498 | 0.358 |
| LIG_FHA_1 | 442 | 448 | PF00498 | 0.391 |
| LIG_FHA_1 | 48 | 54 | PF00498 | 0.484 |
| LIG_FHA_1 | 486 | 492 | PF00498 | 0.517 |
| LIG_FHA_1 | 528 | 534 | PF00498 | 0.378 |
| LIG_FHA_1 | 7 | 13 | PF00498 | 0.520 |
| LIG_FHA_1 | 82 | 88 | PF00498 | 0.492 |
| LIG_FHA_2 | 154 | 160 | PF00498 | 0.613 |
| LIG_FHA_2 | 417 | 423 | PF00498 | 0.490 |
| LIG_FHA_2 | 462 | 468 | PF00498 | 0.475 |
| LIG_FHA_2 | 491 | 497 | PF00498 | 0.445 |
| LIG_FHA_2 | 577 | 583 | PF00498 | 0.370 |
| LIG_LIR_Gen_1 | 129 | 138 | PF02991 | 0.414 |
| LIG_LIR_Gen_1 | 232 | 240 | PF02991 | 0.547 |
| LIG_LIR_Gen_1 | 268 | 276 | PF02991 | 0.462 |
| LIG_LIR_Gen_1 | 410 | 418 | PF02991 | 0.382 |
| LIG_LIR_Gen_1 | 565 | 575 | PF02991 | 0.381 |
| LIG_LIR_Nem_3 | 129 | 134 | PF02991 | 0.420 |
| LIG_LIR_Nem_3 | 232 | 236 | PF02991 | 0.564 |
| LIG_LIR_Nem_3 | 268 | 272 | PF02991 | 0.471 |
| LIG_LIR_Nem_3 | 410 | 415 | PF02991 | 0.373 |
| LIG_LIR_Nem_3 | 496 | 502 | PF02991 | 0.357 |
| LIG_LIR_Nem_3 | 565 | 570 | PF02991 | 0.358 |
| LIG_LIR_Nem_3 | 601 | 605 | PF02991 | 0.364 |
| LIG_LIR_Nem_3 | 67 | 72 | PF02991 | 0.437 |
| LIG_LIR_Nem_3 | 98 | 104 | PF02991 | 0.422 |
| LIG_NRBOX | 113 | 119 | PF00104 | 0.405 |
| LIG_NRP_CendR_1 | 608 | 611 | PF00754 | 0.476 |
| LIG_PALB2_WD40_1 | 422 | 430 | PF16756 | 0.459 |
| LIG_PCNA_yPIPBox_3 | 277 | 289 | PF02747 | 0.600 |
| LIG_PTB_Apo_2 | 284 | 291 | PF02174 | 0.583 |
| LIG_PTB_Apo_2 | 536 | 543 | PF02174 | 0.361 |
| LIG_PTB_Phospho_1 | 284 | 290 | PF10480 | 0.583 |
| LIG_REV1ctd_RIR_1 | 539 | 547 | PF16727 | 0.360 |
| LIG_SH2_STAP1 | 131 | 135 | PF00017 | 0.403 |
| LIG_SH2_STAT3 | 146 | 149 | PF00017 | 0.518 |
| LIG_SH2_STAT5 | 290 | 293 | PF00017 | 0.469 |
| LIG_SH2_STAT5 | 356 | 359 | PF00017 | 0.374 |
| LIG_SH2_STAT5 | 378 | 381 | PF00017 | 0.324 |
| LIG_SH2_STAT5 | 485 | 488 | PF00017 | 0.367 |
| LIG_SH2_STAT5 | 519 | 522 | PF00017 | 0.422 |
| LIG_SH3_3 | 148 | 154 | PF00018 | 0.534 |
| LIG_SH3_3 | 197 | 203 | PF00018 | 0.598 |
| LIG_SH3_3 | 291 | 297 | PF00018 | 0.445 |
| LIG_SH3_3 | 529 | 535 | PF00018 | 0.370 |
| LIG_SH3_3 | 581 | 587 | PF00018 | 0.377 |
| LIG_SUMO_SIM_par_1 | 504 | 510 | PF11976 | 0.335 |
| LIG_SUMO_SIM_par_1 | 523 | 528 | PF11976 | 0.363 |
| LIG_TRAF2_1 | 23 | 26 | PF00917 | 0.513 |
| LIG_TRAF2_1 | 37 | 40 | PF00917 | 0.480 |
| LIG_TRAF2_1 | 579 | 582 | PF00917 | 0.296 |
| LIG_TRAF2_1 | 80 | 83 | PF00917 | 0.403 |
| LIG_WRC_WIRS_1 | 321 | 326 | PF05994 | 0.373 |
| LIG_WW_3 | 295 | 299 | PF00397 | 0.409 |
| MOD_CK1_1 | 193 | 199 | PF00069 | 0.672 |
| MOD_CK1_1 | 2 | 8 | PF00069 | 0.627 |
| MOD_CK1_1 | 205 | 211 | PF00069 | 0.773 |
| MOD_CK1_1 | 212 | 218 | PF00069 | 0.629 |
| MOD_CK1_1 | 265 | 271 | PF00069 | 0.580 |
| MOD_CK1_1 | 601 | 607 | PF00069 | 0.372 |
| MOD_CK1_1 | 62 | 68 | PF00069 | 0.486 |
| MOD_CK2_1 | 158 | 164 | PF00069 | 0.633 |
| MOD_CK2_1 | 346 | 352 | PF00069 | 0.404 |
| MOD_CK2_1 | 490 | 496 | PF00069 | 0.452 |
| MOD_CK2_1 | 576 | 582 | PF00069 | 0.381 |
| MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.502 |
| MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.667 |
| MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.691 |
| MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.732 |
| MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.570 |
| MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.433 |
| MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.524 |
| MOD_GSK3_1 | 190 | 197 | PF00069 | 0.676 |
| MOD_GSK3_1 | 2 | 9 | PF00069 | 0.531 |
| MOD_GSK3_1 | 205 | 212 | PF00069 | 0.674 |
| MOD_GSK3_1 | 225 | 232 | PF00069 | 0.595 |
| MOD_GSK3_1 | 261 | 268 | PF00069 | 0.627 |
| MOD_GSK3_1 | 399 | 406 | PF00069 | 0.375 |
| MOD_GSK3_1 | 472 | 479 | PF00069 | 0.453 |
| MOD_GSK3_1 | 527 | 534 | PF00069 | 0.377 |
| MOD_N-GLC_1 | 262 | 267 | PF02516 | 0.514 |
| MOD_NEK2_1 | 190 | 195 | PF00069 | 0.566 |
| MOD_NEK2_1 | 3 | 8 | PF00069 | 0.611 |
| MOD_NEK2_1 | 303 | 308 | PF00069 | 0.447 |
| MOD_NEK2_1 | 32 | 37 | PF00069 | 0.523 |
| MOD_NEK2_1 | 339 | 344 | PF00069 | 0.414 |
| MOD_NEK2_1 | 403 | 408 | PF00069 | 0.365 |
| MOD_NEK2_1 | 441 | 446 | PF00069 | 0.465 |
| MOD_NEK2_1 | 542 | 547 | PF00069 | 0.407 |
| MOD_NEK2_1 | 558 | 563 | PF00069 | 0.378 |
| MOD_NEK2_1 | 88 | 93 | PF00069 | 0.442 |
| MOD_NEK2_2 | 262 | 267 | PF00069 | 0.503 |
| MOD_NEK2_2 | 476 | 481 | PF00069 | 0.417 |
| MOD_NEK2_2 | 64 | 69 | PF00069 | 0.433 |
| MOD_PIKK_1 | 40 | 46 | PF00454 | 0.546 |
| MOD_PIKK_1 | 429 | 435 | PF00454 | 0.346 |
| MOD_PIKK_1 | 59 | 65 | PF00454 | 0.376 |
| MOD_PKA_2 | 122 | 128 | PF00069 | 0.441 |
| MOD_PKA_2 | 346 | 352 | PF00069 | 0.404 |
| MOD_PKA_2 | 542 | 548 | PF00069 | 0.361 |
| MOD_PKA_2 | 558 | 564 | PF00069 | 0.380 |
| MOD_PKA_2 | 576 | 582 | PF00069 | 0.381 |
| MOD_PKA_2 | 59 | 65 | PF00069 | 0.487 |
| MOD_Plk_1 | 262 | 268 | PF00069 | 0.510 |
| MOD_Plk_1 | 82 | 88 | PF00069 | 0.488 |
| MOD_Plk_4 | 153 | 159 | PF00069 | 0.609 |
| MOD_Plk_4 | 326 | 332 | PF00069 | 0.361 |
| MOD_Plk_4 | 399 | 405 | PF00069 | 0.380 |
| MOD_Plk_4 | 461 | 467 | PF00069 | 0.550 |
| MOD_Plk_4 | 476 | 482 | PF00069 | 0.296 |
| MOD_Plk_4 | 487 | 493 | PF00069 | 0.383 |
| MOD_Plk_4 | 558 | 564 | PF00069 | 0.380 |
| MOD_Plk_4 | 598 | 604 | PF00069 | 0.354 |
| MOD_Plk_4 | 64 | 70 | PF00069 | 0.514 |
| MOD_ProDKin_1 | 185 | 191 | PF00069 | 0.746 |
| MOD_ProDKin_1 | 196 | 202 | PF00069 | 0.605 |
| MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.751 |
| MOD_ProDKin_1 | 255 | 261 | PF00069 | 0.574 |
| MOD_ProDKin_1 | 472 | 478 | PF00069 | 0.379 |
| MOD_ProDKin_1 | 531 | 537 | PF00069 | 0.362 |
| MOD_ProDKin_1 | 583 | 589 | PF00069 | 0.369 |
| MOD_ProDKin_1 | 7 | 13 | PF00069 | 0.520 |
| MOD_SUMO_for_1 | 331 | 334 | PF00179 | 0.353 |
| TRG_DiLeu_BaEn_1 | 245 | 250 | PF01217 | 0.460 |
| TRG_DiLeu_BaEn_1 | 487 | 492 | PF01217 | 0.429 |
| TRG_DiLeu_BaEn_1 | 565 | 570 | PF01217 | 0.358 |
| TRG_DiLeu_BaEn_1 | 83 | 88 | PF01217 | 0.487 |
| TRG_DiLeu_BaLyEn_6 | 186 | 191 | PF01217 | 0.538 |
| TRG_DiLeu_LyEn_5 | 245 | 250 | PF01217 | 0.460 |
| TRG_DiLeu_LyEn_5 | 83 | 88 | PF01217 | 0.487 |
| TRG_ENDOCYTIC_2 | 131 | 134 | PF00928 | 0.409 |
| TRG_ENDOCYTIC_2 | 269 | 272 | PF00928 | 0.470 |
| TRG_ENDOCYTIC_2 | 321 | 324 | PF00928 | 0.381 |
| TRG_ENDOCYTIC_2 | 436 | 439 | PF00928 | 0.361 |
| TRG_ENDOCYTIC_2 | 499 | 502 | PF00928 | 0.353 |
| TRG_ER_diArg_1 | 16 | 18 | PF00400 | 0.431 |
| TRG_ER_diArg_1 | 384 | 386 | PF00400 | 0.334 |
| TRG_ER_diArg_1 | 74 | 77 | PF00400 | 0.636 |
| TRG_NES_CRM1_1 | 359 | 373 | PF08389 | 0.307 |
| TRG_Pf-PMV_PEXEL_1 | 248 | 253 | PF00026 | 0.475 |
| TRG_Pf-PMV_PEXEL_1 | 384 | 389 | PF00026 | 0.342 |
| TRG_Pf-PMV_PEXEL_1 | 55 | 59 | PF00026 | 0.567 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1PC66 | Leptomonas seymouri | 69% | 97% |
| A0A3Q8IFG2 | Leishmania donovani | 86% | 100% |
| A4I4Q1 | Leishmania infantum | 86% | 100% |
| E9AE54 | Leishmania major | 87% | 100% |
| E9ALN1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |