| 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: 8 | 
| NetGPI | no | yes: 0, no: 8 | 
Related structures:
AlphaFold database: A4IBA4
| Leishmania | From | To | Domain/Motif | Score | 
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 111 | 115 | PF00656 | 0.721 | 
| CLV_C14_Caspase3-7 | 400 | 404 | PF00656 | 0.686 | 
| CLV_C14_Caspase3-7 | 438 | 442 | PF00656 | 0.740 | 
| CLV_NRD_NRD_1 | 237 | 239 | PF00675 | 0.739 | 
| CLV_NRD_NRD_1 | 302 | 304 | PF00675 | 0.341 | 
| CLV_NRD_NRD_1 | 316 | 318 | PF00675 | 0.344 | 
| CLV_NRD_NRD_1 | 447 | 449 | PF00675 | 0.737 | 
| CLV_NRD_NRD_1 | 451 | 453 | PF00675 | 0.750 | 
| CLV_NRD_NRD_1 | 5 | 7 | PF00675 | 0.822 | 
| CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.761 | 
| CLV_PCSK_FUR_1 | 314 | 318 | PF00082 | 0.333 | 
| CLV_PCSK_FUR_1 | 6 | 10 | PF00082 | 0.715 | 
| CLV_PCSK_KEX2_1 | 302 | 304 | PF00082 | 0.357 | 
| CLV_PCSK_KEX2_1 | 316 | 318 | PF00082 | 0.357 | 
| CLV_PCSK_KEX2_1 | 446 | 448 | PF00082 | 0.785 | 
| CLV_PCSK_KEX2_1 | 451 | 453 | PF00082 | 0.742 | 
| CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.771 | 
| CLV_PCSK_KEX2_1 | 8 | 10 | PF00082 | 0.760 | 
| CLV_PCSK_PC7_1 | 447 | 453 | PF00082 | 0.729 | 
| CLV_PCSK_SKI1_1 | 140 | 144 | PF00082 | 0.446 | 
| CLV_PCSK_SKI1_1 | 317 | 321 | PF00082 | 0.357 | 
| CLV_PCSK_SKI1_1 | 425 | 429 | PF00082 | 0.770 | 
| DOC_CKS1_1 | 392 | 397 | PF01111 | 0.691 | 
| DOC_CKS1_1 | 99 | 104 | PF01111 | 0.593 | 
| DOC_CYCLIN_yClb5_NLxxxL_5 | 425 | 431 | PF00134 | 0.654 | 
| DOC_PP4_FxxP_1 | 222 | 225 | PF00568 | 0.719 | 
| DOC_USP7_MATH_1 | 115 | 119 | PF00917 | 0.747 | 
| DOC_USP7_MATH_1 | 125 | 129 | PF00917 | 0.655 | 
| DOC_USP7_MATH_1 | 460 | 464 | PF00917 | 0.664 | 
| DOC_USP7_MATH_2 | 395 | 401 | PF00917 | 0.701 | 
| DOC_WW_Pin1_4 | 121 | 126 | PF00397 | 0.695 | 
| DOC_WW_Pin1_4 | 128 | 133 | PF00397 | 0.616 | 
| DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.391 | 
| DOC_WW_Pin1_4 | 391 | 396 | PF00397 | 0.675 | 
| DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.570 | 
| LIG_14-3-3_CanoR_1 | 153 | 159 | PF00244 | 0.664 | 
| LIG_14-3-3_CanoR_1 | 193 | 198 | PF00244 | 0.357 | 
| LIG_14-3-3_CanoR_1 | 238 | 244 | PF00244 | 0.539 | 
| LIG_14-3-3_CanoR_1 | 340 | 345 | PF00244 | 0.584 | 
| LIG_14-3-3_CanoR_1 | 429 | 434 | PF00244 | 0.705 | 
| LIG_14-3-3_CanoR_1 | 461 | 465 | PF00244 | 0.672 | 
| LIG_BRCT_BRCA1_1 | 218 | 222 | PF00533 | 0.707 | 
| LIG_BRCT_BRCA1_1 | 346 | 350 | PF00533 | 0.589 | 
| LIG_FHA_1 | 107 | 113 | PF00498 | 0.744 | 
| LIG_FHA_1 | 137 | 143 | PF00498 | 0.553 | 
| LIG_FHA_1 | 266 | 272 | PF00498 | 0.508 | 
| LIG_FHA_1 | 426 | 432 | PF00498 | 0.715 | 
| LIG_FHA_2 | 378 | 384 | PF00498 | 0.567 | 
| LIG_FHA_2 | 392 | 398 | PF00498 | 0.606 | 
| LIG_FHA_2 | 436 | 442 | PF00498 | 0.769 | 
| LIG_FHA_2 | 464 | 470 | PF00498 | 0.708 | 
| LIG_LIR_Apic_2 | 219 | 225 | PF02991 | 0.707 | 
| LIG_LIR_Apic_2 | 322 | 327 | PF02991 | 0.531 | 
| LIG_LIR_Gen_1 | 383 | 392 | PF02991 | 0.537 | 
| LIG_LIR_Gen_1 | 66 | 75 | PF02991 | 0.438 | 
| LIG_LIR_Nem_3 | 383 | 388 | PF02991 | 0.535 | 
| LIG_LIR_Nem_3 | 66 | 70 | PF02991 | 0.399 | 
| LIG_LIR_Nem_3 | 92 | 98 | PF02991 | 0.357 | 
| LIG_Pex14_2 | 266 | 270 | PF04695 | 0.567 | 
| LIG_SH2_CRK | 324 | 328 | PF00017 | 0.533 | 
| LIG_SH2_NCK_1 | 324 | 328 | PF00017 | 0.533 | 
| LIG_SH2_STAP1 | 171 | 175 | PF00017 | 0.391 | 
| LIG_SH2_STAP1 | 345 | 349 | PF00017 | 0.629 | 
| LIG_SH2_STAP1 | 351 | 355 | PF00017 | 0.507 | 
| LIG_SH2_STAT3 | 161 | 164 | PF00017 | 0.623 | 
| LIG_SH2_STAT3 | 171 | 174 | PF00017 | 0.438 | 
| LIG_SH2_STAT5 | 324 | 327 | PF00017 | 0.581 | 
| LIG_SH2_STAT5 | 374 | 377 | PF00017 | 0.561 | 
| LIG_SH2_STAT5 | 98 | 101 | PF00017 | 0.556 | 
| LIG_SH3_3 | 430 | 436 | PF00018 | 0.547 | 
| LIG_SH3_3 | 96 | 102 | PF00018 | 0.493 | 
| LIG_TYR_ITIM | 65 | 70 | PF00017 | 0.438 | 
| MOD_CK1_1 | 119 | 125 | PF00069 | 0.741 | 
| MOD_CK1_1 | 128 | 134 | PF00069 | 0.673 | 
| MOD_CK1_1 | 322 | 328 | PF00069 | 0.531 | 
| MOD_CK1_1 | 396 | 402 | PF00069 | 0.741 | 
| MOD_CK1_1 | 4 | 10 | PF00069 | 0.614 | 
| MOD_CK1_1 | 455 | 461 | PF00069 | 0.775 | 
| MOD_CK1_1 | 463 | 469 | PF00069 | 0.593 | 
| MOD_CK2_1 | 110 | 116 | PF00069 | 0.639 | 
| MOD_CK2_1 | 391 | 397 | PF00069 | 0.758 | 
| MOD_CK2_1 | 412 | 418 | PF00069 | 0.681 | 
| MOD_Cter_Amidation | 314 | 317 | PF01082 | 0.369 | 
| MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.733 | 
| MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.696 | 
| MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.383 | 
| MOD_GlcNHglycan | 230 | 234 | PF01048 | 0.751 | 
| MOD_GlcNHglycan | 452 | 455 | PF01048 | 0.789 | 
| MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.361 | 
| MOD_GSK3_1 | 106 | 113 | PF00069 | 0.671 | 
| MOD_GSK3_1 | 115 | 122 | PF00069 | 0.658 | 
| MOD_GSK3_1 | 12 | 19 | PF00069 | 0.783 | 
| MOD_GSK3_1 | 265 | 272 | PF00069 | 0.518 | 
| MOD_GSK3_1 | 340 | 347 | PF00069 | 0.579 | 
| MOD_GSK3_1 | 349 | 356 | PF00069 | 0.510 | 
| MOD_GSK3_1 | 393 | 400 | PF00069 | 0.734 | 
| MOD_GSK3_1 | 421 | 428 | PF00069 | 0.683 | 
| MOD_GSK3_1 | 51 | 58 | PF00069 | 0.623 | 
| MOD_GSK3_1 | 83 | 90 | PF00069 | 0.379 | 
| MOD_N-GLC_1 | 278 | 283 | PF02516 | 0.456 | 
| MOD_N-GLC_1 | 322 | 327 | PF02516 | 0.504 | 
| MOD_N-GLC_1 | 425 | 430 | PF02516 | 0.730 | 
| MOD_N-GLC_1 | 83 | 88 | PF02516 | 0.438 | 
| MOD_NEK2_1 | 1 | 6 | PF00069 | 0.722 | 
| MOD_NEK2_1 | 147 | 152 | PF00069 | 0.505 | 
| MOD_NEK2_1 | 154 | 159 | PF00069 | 0.589 | 
| MOD_NEK2_1 | 18 | 23 | PF00069 | 0.591 | 
| MOD_NEK2_1 | 231 | 236 | PF00069 | 0.532 | 
| MOD_NEK2_1 | 349 | 354 | PF00069 | 0.584 | 
| MOD_NEK2_1 | 412 | 417 | PF00069 | 0.755 | 
| MOD_NEK2_2 | 309 | 314 | PF00069 | 0.391 | 
| MOD_NEK2_2 | 345 | 350 | PF00069 | 0.503 | 
| MOD_PIKK_1 | 237 | 243 | PF00454 | 0.533 | 
| MOD_PK_1 | 429 | 435 | PF00069 | 0.550 | 
| MOD_PKA_2 | 136 | 142 | PF00069 | 0.683 | 
| MOD_PKA_2 | 192 | 198 | PF00069 | 0.357 | 
| MOD_PKA_2 | 237 | 243 | PF00069 | 0.738 | 
| MOD_PKA_2 | 4 | 10 | PF00069 | 0.720 | 
| MOD_PKA_2 | 412 | 418 | PF00069 | 0.794 | 
| MOD_PKA_2 | 450 | 456 | PF00069 | 0.815 | 
| MOD_PKA_2 | 460 | 466 | PF00069 | 0.731 | 
| MOD_Plk_1 | 179 | 185 | PF00069 | 0.438 | 
| MOD_Plk_1 | 278 | 284 | PF00069 | 0.415 | 
| MOD_Plk_1 | 322 | 328 | PF00069 | 0.505 | 
| MOD_Plk_1 | 396 | 402 | PF00069 | 0.688 | 
| MOD_Plk_1 | 404 | 410 | PF00069 | 0.753 | 
| MOD_Plk_1 | 73 | 79 | PF00069 | 0.389 | 
| MOD_Plk_2-3 | 397 | 403 | PF00069 | 0.727 | 
| MOD_Plk_4 | 125 | 131 | PF00069 | 0.712 | 
| MOD_Plk_4 | 179 | 185 | PF00069 | 0.427 | 
| MOD_Plk_4 | 345 | 351 | PF00069 | 0.624 | 
| MOD_Plk_4 | 429 | 435 | PF00069 | 0.679 | 
| MOD_Plk_4 | 460 | 466 | PF00069 | 0.674 | 
| MOD_ProDKin_1 | 121 | 127 | PF00069 | 0.696 | 
| MOD_ProDKin_1 | 128 | 134 | PF00069 | 0.614 | 
| MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.391 | 
| MOD_ProDKin_1 | 391 | 397 | PF00069 | 0.681 | 
| MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.583 | 
| MOD_SUMO_rev_2 | 50 | 58 | PF00179 | 0.677 | 
| TRG_ENDOCYTIC_2 | 67 | 70 | PF00928 | 0.438 | 
| TRG_ER_diArg_1 | 302 | 304 | PF00400 | 0.358 | 
| TRG_ER_diArg_1 | 313 | 316 | PF00400 | 0.360 | 
| TRG_ER_diArg_1 | 446 | 448 | PF00400 | 0.783 | 
| TRG_ER_diArg_1 | 5 | 8 | PF00400 | 0.808 | 
| Protein | Taxonomy | Sequence identity | Coverage | 
|---|---|---|---|
| A0A0N1HZT1 | Leptomonas seymouri | 53% | 100% | 
| A0A0S4JH24 | Bodo saltans | 38% | 100% | 
| A0A3Q8IJ10 | Leishmania donovani | 99% | 100% | 
| A0A422NNS8 | Trypanosoma rangeli | 44% | 100% | 
| A4HMM6 | Leishmania braziliensis | 73% | 99% | 
| E9AF28 | Leishmania major | 91% | 100% | 
| E9B684 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |