| 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: A4HYY0
| 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 | 176 | 180 | PF00656 | 0.534 |
| CLV_NRD_NRD_1 | 131 | 133 | PF00675 | 0.627 |
| CLV_NRD_NRD_1 | 19 | 21 | PF00675 | 0.567 |
| CLV_NRD_NRD_1 | 237 | 239 | PF00675 | 0.461 |
| CLV_NRD_NRD_1 | 246 | 248 | PF00675 | 0.393 |
| CLV_NRD_NRD_1 | 362 | 364 | PF00675 | 0.358 |
| CLV_NRD_NRD_1 | 532 | 534 | PF00675 | 0.638 |
| CLV_PCSK_KEX2_1 | 131 | 133 | PF00082 | 0.627 |
| CLV_PCSK_KEX2_1 | 19 | 21 | PF00082 | 0.497 |
| CLV_PCSK_KEX2_1 | 237 | 239 | PF00082 | 0.461 |
| CLV_PCSK_KEX2_1 | 246 | 248 | PF00082 | 0.393 |
| CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.358 |
| CLV_PCSK_KEX2_1 | 403 | 405 | PF00082 | 0.455 |
| CLV_PCSK_KEX2_1 | 429 | 431 | PF00082 | 0.525 |
| CLV_PCSK_KEX2_1 | 532 | 534 | PF00082 | 0.639 |
| CLV_PCSK_PC1ET2_1 | 403 | 405 | PF00082 | 0.455 |
| CLV_PCSK_PC1ET2_1 | 429 | 431 | PF00082 | 0.525 |
| CLV_PCSK_SKI1_1 | 163 | 167 | PF00082 | 0.419 |
| CLV_PCSK_SKI1_1 | 292 | 296 | PF00082 | 0.383 |
| CLV_PCSK_SKI1_1 | 362 | 366 | PF00082 | 0.383 |
| CLV_PCSK_SKI1_1 | 410 | 414 | PF00082 | 0.440 |
| CLV_PCSK_SKI1_1 | 456 | 460 | PF00082 | 0.537 |
| CLV_PCSK_SKI1_1 | 507 | 511 | PF00082 | 0.601 |
| CLV_Separin_Metazoa | 289 | 293 | PF03568 | 0.516 |
| CLV_Separin_Metazoa | 504 | 508 | PF03568 | 0.591 |
| DEG_APCC_DBOX_1 | 236 | 244 | PF00400 | 0.402 |
| DEG_APCC_DBOX_1 | 291 | 299 | PF00400 | 0.516 |
| DEG_APCC_DBOX_1 | 362 | 370 | PF00400 | 0.387 |
| DEG_APCC_DBOX_1 | 49 | 57 | PF00400 | 0.473 |
| DOC_CYCLIN_RxL_1 | 359 | 368 | PF00134 | 0.392 |
| DOC_MAPK_gen_1 | 188 | 196 | PF00069 | 0.470 |
| DOC_MAPK_MEF2A_6 | 188 | 196 | PF00069 | 0.470 |
| DOC_PP4_FxxP_1 | 45 | 48 | PF00568 | 0.575 |
| DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.648 |
| DOC_USP7_MATH_1 | 475 | 479 | PF00917 | 0.609 |
| DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.470 |
| DOC_USP7_MATH_1 | 512 | 516 | PF00917 | 0.596 |
| DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.650 |
| DOC_USP7_UBL2_3 | 421 | 425 | PF12436 | 0.441 |
| DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.423 |
| DOC_WW_Pin1_4 | 69 | 74 | PF00397 | 0.628 |
| LIG_14-3-3_CanoR_1 | 146 | 153 | PF00244 | 0.582 |
| LIG_14-3-3_CanoR_1 | 237 | 241 | PF00244 | 0.397 |
| LIG_14-3-3_CanoR_1 | 320 | 328 | PF00244 | 0.400 |
| LIG_14-3-3_CanoR_1 | 50 | 54 | PF00244 | 0.473 |
| LIG_14-3-3_CanoR_1 | 507 | 512 | PF00244 | 0.603 |
| LIG_14-3-3_CterR_2 | 541 | 546 | PF00244 | 0.625 |
| LIG_Actin_WH2_1 | 174 | 192 | PF00022 | 0.582 |
| LIG_Actin_WH2_1 | 362 | 379 | PF00022 | 0.560 |
| LIG_Actin_WH2_2 | 175 | 192 | PF00022 | 0.580 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.614 |
| LIG_CaM_IQ_9 | 413 | 429 | PF13499 | 0.560 |
| LIG_EH1_1 | 386 | 394 | PF00400 | 0.386 |
| LIG_FHA_1 | 128 | 134 | PF00498 | 0.502 |
| LIG_FHA_1 | 212 | 218 | PF00498 | 0.358 |
| LIG_FHA_1 | 330 | 336 | PF00498 | 0.511 |
| LIG_FHA_2 | 202 | 208 | PF00498 | 0.358 |
| LIG_LIR_Apic_2 | 44 | 48 | PF02991 | 0.576 |
| LIG_LIR_Gen_1 | 510 | 520 | PF02991 | 0.596 |
| LIG_LIR_Nem_3 | 304 | 309 | PF02991 | 0.358 |
| LIG_LIR_Nem_3 | 382 | 387 | PF02991 | 0.398 |
| LIG_LIR_Nem_3 | 401 | 405 | PF02991 | 0.287 |
| LIG_LIR_Nem_3 | 510 | 516 | PF02991 | 0.573 |
| LIG_SH2_SRC | 463 | 466 | PF00017 | 0.529 |
| LIG_SH2_SRC | 503 | 506 | PF00017 | 0.565 |
| LIG_SH2_STAT3 | 309 | 312 | PF00017 | 0.358 |
| LIG_SH2_STAT3 | 534 | 537 | PF00017 | 0.616 |
| LIG_SH2_STAT5 | 12 | 15 | PF00017 | 0.481 |
| LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.576 |
| LIG_SH2_STAT5 | 264 | 267 | PF00017 | 0.396 |
| LIG_SH2_STAT5 | 326 | 329 | PF00017 | 0.397 |
| LIG_SH3_1 | 499 | 505 | PF00018 | 0.577 |
| LIG_SH3_2 | 502 | 507 | PF14604 | 0.569 |
| LIG_SH3_3 | 120 | 126 | PF00018 | 0.587 |
| LIG_SH3_3 | 25 | 31 | PF00018 | 0.544 |
| LIG_SH3_3 | 367 | 373 | PF00018 | 0.566 |
| LIG_SH3_3 | 393 | 399 | PF00018 | 0.572 |
| LIG_SH3_3 | 428 | 434 | PF00018 | 0.681 |
| LIG_SH3_3 | 43 | 49 | PF00018 | 0.634 |
| LIG_SH3_3 | 499 | 505 | PF00018 | 0.599 |
| LIG_SH3_3 | 53 | 59 | PF00018 | 0.536 |
| LIG_SUMO_SIM_par_1 | 93 | 98 | PF11976 | 0.582 |
| LIG_UBA3_1 | 335 | 342 | PF00899 | 0.358 |
| LIG_WW_3 | 47 | 51 | PF00397 | 0.566 |
| LIG_WW_3 | 504 | 508 | PF00397 | 0.568 |
| MOD_CDK_SPxxK_3 | 156 | 163 | PF00069 | 0.419 |
| MOD_CK1_1 | 180 | 186 | PF00069 | 0.525 |
| MOD_CK1_1 | 233 | 239 | PF00069 | 0.418 |
| MOD_CK1_1 | 318 | 324 | PF00069 | 0.365 |
| MOD_CK1_1 | 482 | 488 | PF00069 | 0.603 |
| MOD_CK1_1 | 61 | 67 | PF00069 | 0.628 |
| MOD_CK2_1 | 201 | 207 | PF00069 | 0.358 |
| MOD_CK2_1 | 239 | 245 | PF00069 | 0.394 |
| MOD_CK2_1 | 482 | 488 | PF00069 | 0.718 |
| MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.547 |
| MOD_GlcNHglycan | 250 | 254 | PF01048 | 0.575 |
| MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.629 |
| MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.589 |
| MOD_GlcNHglycan | 477 | 480 | PF01048 | 0.547 |
| MOD_GlcNHglycan | 491 | 494 | PF01048 | 0.568 |
| MOD_GlcNHglycan | 518 | 521 | PF01048 | 0.622 |
| MOD_GlcNHglycan | 528 | 531 | PF01048 | 0.621 |
| MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.567 |
| MOD_GSK3_1 | 109 | 116 | PF00069 | 0.623 |
| MOD_GSK3_1 | 127 | 134 | PF00069 | 0.580 |
| MOD_GSK3_1 | 14 | 21 | PF00069 | 0.667 |
| MOD_GSK3_1 | 207 | 214 | PF00069 | 0.358 |
| MOD_GSK3_1 | 315 | 322 | PF00069 | 0.357 |
| MOD_GSK3_1 | 475 | 482 | PF00069 | 0.559 |
| MOD_GSK3_1 | 483 | 490 | PF00069 | 0.674 |
| MOD_GSK3_1 | 512 | 519 | PF00069 | 0.659 |
| MOD_N-GLC_2 | 228 | 230 | PF02516 | 0.385 |
| MOD_NEK2_1 | 221 | 226 | PF00069 | 0.430 |
| MOD_NEK2_1 | 265 | 270 | PF00069 | 0.410 |
| MOD_NEK2_1 | 336 | 341 | PF00069 | 0.516 |
| MOD_PIKK_1 | 169 | 175 | PF00454 | 0.603 |
| MOD_PIKK_1 | 230 | 236 | PF00454 | 0.419 |
| MOD_PIKK_1 | 265 | 271 | PF00454 | 0.404 |
| MOD_PKA_1 | 131 | 137 | PF00069 | 0.565 |
| MOD_PKA_2 | 131 | 137 | PF00069 | 0.582 |
| MOD_PKA_2 | 145 | 151 | PF00069 | 0.396 |
| MOD_PKA_2 | 18 | 24 | PF00069 | 0.589 |
| MOD_PKA_2 | 236 | 242 | PF00069 | 0.392 |
| MOD_PKA_2 | 319 | 325 | PF00069 | 0.414 |
| MOD_PKA_2 | 479 | 485 | PF00069 | 0.660 |
| MOD_PKA_2 | 49 | 55 | PF00069 | 0.473 |
| MOD_Plk_1 | 249 | 255 | PF00069 | 0.566 |
| MOD_Plk_4 | 177 | 183 | PF00069 | 0.493 |
| MOD_Plk_4 | 221 | 227 | PF00069 | 0.426 |
| MOD_Plk_4 | 239 | 245 | PF00069 | 0.268 |
| MOD_Plk_4 | 41 | 47 | PF00069 | 0.605 |
| MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.419 |
| MOD_ProDKin_1 | 69 | 75 | PF00069 | 0.630 |
| MOD_SUMO_for_1 | 420 | 423 | PF00179 | 0.437 |
| TRG_DiLeu_BaEn_2 | 503 | 509 | PF01217 | 0.607 |
| TRG_ENDOCYTIC_2 | 384 | 387 | PF00928 | 0.384 |
| TRG_ER_diArg_1 | 131 | 133 | PF00400 | 0.631 |
| TRG_ER_diArg_1 | 187 | 190 | PF00400 | 0.588 |
| TRG_ER_diArg_1 | 361 | 363 | PF00400 | 0.358 |
| TRG_ER_diArg_1 | 408 | 411 | PF00400 | 0.440 |
| TRG_ER_diArg_1 | 532 | 534 | PF00400 | 0.651 |
| TRG_NES_CRM1_1 | 184 | 195 | PF08389 | 0.412 |
| TRG_NES_CRM1_1 | 293 | 304 | PF08389 | 0.516 |
| TRG_Pf-PMV_PEXEL_1 | 203 | 207 | PF00026 | 0.358 |
| TRG_Pf-PMV_PEXEL_1 | 362 | 367 | PF00026 | 0.391 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1ILR0 | Leptomonas seymouri | 50% | 83% |
| A0A3Q8IA47 | Leishmania donovani | 96% | 93% |
| A0A3S7WW64 | Leishmania donovani | 99% | 100% |
| A4HYX9 | Leishmania infantum | 79% | 100% |
| E8NHJ3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
| E9AIJ1 | Leishmania braziliensis | 92% | 100% |
| E9AUS6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
| Q4QCQ8 | Leishmania major | 97% | 100% |
| Q4QCQ9 | Leishmania major | 75% | 100% |