| 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 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005737 | cytoplasm | 2 | 2 |
| GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: A4HYX9
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0010468 | regulation of gene expression | 5 | 2 |
| GO:0010608 | post-transcriptional regulation of gene expression | 6 | 2 |
| GO:0019222 | regulation of metabolic process | 3 | 2 |
| GO:0050789 | regulation of biological process | 2 | 2 |
| GO:0060255 | regulation of macromolecule metabolic process | 4 | 2 |
| GO:0065007 | biological regulation | 1 | 2 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003676 | nucleic acid binding | 3 | 11 |
| GO:0003723 | RNA binding | 4 | 11 |
| GO:0005488 | binding | 1 | 11 |
| GO:0097159 | organic cyclic compound binding | 2 | 11 |
| GO:1901363 | heterocyclic compound binding | 2 | 11 |
| GO:0003729 | mRNA binding | 5 | 2 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 175 | 179 | PF00656 | 0.534 |
| CLV_C14_Caspase3-7 | 554 | 558 | PF00656 | 0.613 |
| CLV_NRD_NRD_1 | 130 | 132 | PF00675 | 0.626 |
| CLV_NRD_NRD_1 | 23 | 25 | PF00675 | 0.698 |
| CLV_NRD_NRD_1 | 236 | 238 | PF00675 | 0.516 |
| CLV_NRD_NRD_1 | 245 | 247 | PF00675 | 0.474 |
| CLV_NRD_NRD_1 | 361 | 363 | PF00675 | 0.417 |
| CLV_NRD_NRD_1 | 569 | 571 | PF00675 | 0.650 |
| CLV_PCSK_KEX2_1 | 130 | 132 | PF00082 | 0.626 |
| CLV_PCSK_KEX2_1 | 236 | 238 | PF00082 | 0.516 |
| CLV_PCSK_KEX2_1 | 245 | 247 | PF00082 | 0.474 |
| CLV_PCSK_KEX2_1 | 361 | 363 | PF00082 | 0.417 |
| CLV_PCSK_KEX2_1 | 402 | 404 | PF00082 | 0.514 |
| CLV_PCSK_KEX2_1 | 428 | 430 | PF00082 | 0.581 |
| CLV_PCSK_KEX2_1 | 569 | 571 | PF00082 | 0.652 |
| CLV_PCSK_PC1ET2_1 | 402 | 404 | PF00082 | 0.514 |
| CLV_PCSK_PC1ET2_1 | 428 | 430 | PF00082 | 0.581 |
| CLV_PCSK_SKI1_1 | 162 | 166 | PF00082 | 0.477 |
| CLV_PCSK_SKI1_1 | 291 | 295 | PF00082 | 0.439 |
| CLV_PCSK_SKI1_1 | 361 | 365 | PF00082 | 0.450 |
| CLV_PCSK_SKI1_1 | 409 | 413 | PF00082 | 0.500 |
| CLV_Separin_Metazoa | 288 | 292 | PF03568 | 0.516 |
| DEG_APCC_DBOX_1 | 235 | 243 | PF00400 | 0.463 |
| DEG_APCC_DBOX_1 | 290 | 298 | PF00400 | 0.516 |
| DEG_APCC_DBOX_1 | 361 | 369 | PF00400 | 0.450 |
| DEG_APCC_DBOX_1 | 500 | 508 | PF00400 | 0.560 |
| DOC_CYCLIN_RxL_1 | 358 | 367 | PF00134 | 0.424 |
| DOC_MAPK_FxFP_2 | 533 | 536 | PF00069 | 0.636 |
| DOC_MAPK_gen_1 | 187 | 195 | PF00069 | 0.470 |
| DOC_MAPK_MEF2A_6 | 187 | 195 | PF00069 | 0.470 |
| DOC_PP2B_LxvP_1 | 453 | 456 | PF13499 | 0.611 |
| DOC_PP4_FxxP_1 | 44 | 47 | PF00568 | 0.653 |
| DOC_PP4_FxxP_1 | 533 | 536 | PF00568 | 0.636 |
| DOC_PP4_FxxP_1 | 580 | 583 | PF00568 | 0.587 |
| DOC_USP7_MATH_1 | 35 | 39 | PF00917 | 0.657 |
| DOC_USP7_MATH_1 | 480 | 484 | PF00917 | 0.702 |
| DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.683 |
| DOC_USP7_UBL2_3 | 420 | 424 | PF12436 | 0.501 |
| DOC_WW_Pin1_4 | 155 | 160 | PF00397 | 0.486 |
| DOC_WW_Pin1_4 | 48 | 53 | PF00397 | 0.558 |
| DOC_WW_Pin1_4 | 562 | 567 | PF00397 | 0.636 |
| DOC_WW_Pin1_4 | 68 | 73 | PF00397 | 0.640 |
| LIG_14-3-3_CanoR_1 | 12 | 22 | PF00244 | 0.635 |
| LIG_14-3-3_CanoR_1 | 145 | 152 | PF00244 | 0.583 |
| LIG_14-3-3_CanoR_1 | 236 | 240 | PF00244 | 0.460 |
| LIG_14-3-3_CanoR_1 | 319 | 327 | PF00244 | 0.472 |
| LIG_14-3-3_CanoR_1 | 451 | 456 | PF00244 | 0.609 |
| LIG_Actin_WH2_1 | 173 | 191 | PF00022 | 0.581 |
| LIG_Actin_WH2_1 | 361 | 378 | PF00022 | 0.561 |
| LIG_Actin_WH2_2 | 174 | 191 | PF00022 | 0.579 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.640 |
| LIG_CaM_IQ_9 | 412 | 428 | PF13499 | 0.560 |
| LIG_EH1_1 | 385 | 393 | PF00400 | 0.446 |
| LIG_FHA_1 | 127 | 133 | PF00498 | 0.501 |
| LIG_FHA_1 | 211 | 217 | PF00498 | 0.417 |
| LIG_FHA_1 | 329 | 335 | PF00498 | 0.517 |
| LIG_FHA_1 | 471 | 477 | PF00498 | 0.694 |
| LIG_FHA_2 | 201 | 207 | PF00498 | 0.417 |
| LIG_FHA_2 | 456 | 462 | PF00498 | 0.628 |
| LIG_HCF-1_HBM_1 | 525 | 528 | PF13415 | 0.534 |
| LIG_LIR_Apic_2 | 43 | 47 | PF02991 | 0.653 |
| LIG_LIR_Apic_2 | 531 | 536 | PF02991 | 0.638 |
| LIG_LIR_Nem_3 | 303 | 308 | PF02991 | 0.417 |
| LIG_LIR_Nem_3 | 381 | 386 | PF02991 | 0.464 |
| LIG_LIR_Nem_3 | 400 | 404 | PF02991 | 0.286 |
| LIG_PDZ_Class_2 | 583 | 588 | PF00595 | 0.597 |
| LIG_Pex14_2 | 580 | 584 | PF04695 | 0.589 |
| LIG_SH2_STAT3 | 308 | 311 | PF00017 | 0.417 |
| LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.579 |
| LIG_SH2_STAT5 | 263 | 266 | PF00017 | 0.444 |
| LIG_SH2_STAT5 | 325 | 328 | PF00017 | 0.471 |
| LIG_SH2_STAT5 | 494 | 497 | PF00017 | 0.806 |
| LIG_SH3_3 | 119 | 125 | PF00018 | 0.650 |
| LIG_SH3_3 | 366 | 372 | PF00018 | 0.565 |
| LIG_SH3_3 | 392 | 398 | PF00018 | 0.588 |
| LIG_SH3_3 | 42 | 48 | PF00018 | 0.653 |
| LIG_SH3_3 | 427 | 433 | PF00018 | 0.704 |
| LIG_SH3_3 | 462 | 468 | PF00018 | 0.623 |
| LIG_SH3_3 | 52 | 58 | PF00018 | 0.487 |
| LIG_SH3_3 | 558 | 564 | PF00018 | 0.591 |
| LIG_SUMO_SIM_par_1 | 92 | 97 | PF11976 | 0.638 |
| LIG_UBA3_1 | 334 | 341 | PF00899 | 0.417 |
| LIG_WW_3 | 46 | 50 | PF00397 | 0.646 |
| MOD_CDK_SPxxK_3 | 155 | 162 | PF00069 | 0.481 |
| MOD_CDK_SPxxK_3 | 562 | 569 | PF00069 | 0.623 |
| MOD_CK1_1 | 179 | 185 | PF00069 | 0.525 |
| MOD_CK1_1 | 232 | 238 | PF00069 | 0.479 |
| MOD_CK1_1 | 317 | 323 | PF00069 | 0.431 |
| MOD_CK1_1 | 60 | 66 | PF00069 | 0.655 |
| MOD_CK2_1 | 200 | 206 | PF00069 | 0.417 |
| MOD_CK2_1 | 238 | 244 | PF00069 | 0.454 |
| MOD_CK2_1 | 480 | 486 | PF00069 | 0.737 |
| MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.505 |
| MOD_GlcNHglycan | 249 | 253 | PF01048 | 0.576 |
| MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.659 |
| MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.624 |
| MOD_GlcNHglycan | 482 | 485 | PF01048 | 0.606 |
| MOD_GlcNHglycan | 557 | 560 | PF01048 | 0.644 |
| MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.593 |
| MOD_GSK3_1 | 108 | 115 | PF00069 | 0.649 |
| MOD_GSK3_1 | 126 | 133 | PF00069 | 0.628 |
| MOD_GSK3_1 | 206 | 213 | PF00069 | 0.417 |
| MOD_GSK3_1 | 314 | 321 | PF00069 | 0.416 |
| MOD_GSK3_1 | 451 | 458 | PF00069 | 0.600 |
| MOD_GSK3_1 | 466 | 473 | PF00069 | 0.670 |
| MOD_GSK3_1 | 539 | 546 | PF00069 | 0.655 |
| MOD_N-GLC_1 | 12 | 17 | PF02516 | 0.611 |
| MOD_N-GLC_2 | 227 | 229 | PF02516 | 0.448 |
| MOD_NEK2_1 | 1 | 6 | PF00069 | 0.543 |
| MOD_NEK2_1 | 220 | 225 | PF00069 | 0.484 |
| MOD_NEK2_1 | 264 | 269 | PF00069 | 0.457 |
| MOD_NEK2_1 | 335 | 340 | PF00069 | 0.516 |
| MOD_PIKK_1 | 168 | 174 | PF00454 | 0.602 |
| MOD_PIKK_1 | 229 | 235 | PF00454 | 0.479 |
| MOD_PIKK_1 | 264 | 270 | PF00454 | 0.452 |
| MOD_PIKK_1 | 474 | 480 | PF00454 | 0.591 |
| MOD_PIKK_1 | 488 | 494 | PF00454 | 0.665 |
| MOD_PK_1 | 451 | 457 | PF00069 | 0.578 |
| MOD_PKA_1 | 130 | 136 | PF00069 | 0.565 |
| MOD_PKA_2 | 130 | 136 | PF00069 | 0.582 |
| MOD_PKA_2 | 144 | 150 | PF00069 | 0.396 |
| MOD_PKA_2 | 235 | 241 | PF00069 | 0.454 |
| MOD_PKA_2 | 318 | 324 | PF00069 | 0.481 |
| MOD_PKA_2 | 470 | 476 | PF00069 | 0.715 |
| MOD_Plk_1 | 248 | 254 | PF00069 | 0.566 |
| MOD_Plk_4 | 176 | 182 | PF00069 | 0.493 |
| MOD_Plk_4 | 220 | 226 | PF00069 | 0.482 |
| MOD_Plk_4 | 238 | 244 | PF00069 | 0.294 |
| MOD_Plk_4 | 40 | 46 | PF00069 | 0.658 |
| MOD_ProDKin_1 | 155 | 161 | PF00069 | 0.481 |
| MOD_ProDKin_1 | 48 | 54 | PF00069 | 0.558 |
| MOD_ProDKin_1 | 562 | 568 | PF00069 | 0.632 |
| MOD_ProDKin_1 | 68 | 74 | PF00069 | 0.641 |
| MOD_SUMO_for_1 | 419 | 422 | PF00179 | 0.498 |
| TRG_ENDOCYTIC_2 | 383 | 386 | PF00928 | 0.452 |
| TRG_ER_diArg_1 | 130 | 132 | PF00400 | 0.655 |
| TRG_ER_diArg_1 | 186 | 189 | PF00400 | 0.588 |
| TRG_ER_diArg_1 | 360 | 362 | PF00400 | 0.417 |
| TRG_ER_diArg_1 | 407 | 410 | PF00400 | 0.499 |
| TRG_NES_CRM1_1 | 183 | 194 | PF08389 | 0.473 |
| TRG_NES_CRM1_1 | 292 | 303 | PF08389 | 0.516 |
| TRG_Pf-PMV_PEXEL_1 | 202 | 206 | PF00026 | 0.417 |
| TRG_Pf-PMV_PEXEL_1 | 361 | 366 | PF00026 | 0.457 |
| TRG_Pf-PMV_PEXEL_1 | 570 | 574 | PF00026 | 0.573 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1ILR0 | Leptomonas seymouri | 51% | 89% |
| A0A3Q8IA47 | Leishmania donovani | 100% | 100% |
| A0A3S7WW64 | Leishmania donovani | 79% | 100% |
| A4HYY0 | Leishmania infantum | 79% | 100% |
| E8NHJ3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
| E9AIJ1 | Leishmania braziliensis | 85% | 100% |
| E9AUS6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
| Q4QCQ8 | Leishmania major | 86% | 100% |
| Q4QCQ9 | Leishmania major | 95% | 100% |