| 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 |
Related structures:
AlphaFold database: E9B310
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 100 | 102 | PF00675 | 0.439 |
| CLV_NRD_NRD_1 | 152 | 154 | PF00675 | 0.614 |
| CLV_NRD_NRD_1 | 288 | 290 | PF00675 | 0.609 |
| CLV_NRD_NRD_1 | 332 | 334 | PF00675 | 0.492 |
| CLV_NRD_NRD_1 | 34 | 36 | PF00675 | 0.436 |
| CLV_NRD_NRD_1 | 377 | 379 | PF00675 | 0.573 |
| CLV_NRD_NRD_1 | 439 | 441 | PF00675 | 0.609 |
| CLV_NRD_NRD_1 | 71 | 73 | PF00675 | 0.452 |
| CLV_NRD_NRD_1 | 96 | 98 | PF00675 | 0.488 |
| CLV_PCSK_KEX2_1 | 152 | 154 | PF00082 | 0.614 |
| CLV_PCSK_KEX2_1 | 263 | 265 | PF00082 | 0.691 |
| CLV_PCSK_KEX2_1 | 34 | 36 | PF00082 | 0.436 |
| CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.564 |
| CLV_PCSK_KEX2_1 | 439 | 441 | PF00082 | 0.609 |
| CLV_PCSK_KEX2_1 | 71 | 73 | PF00082 | 0.574 |
| CLV_PCSK_KEX2_1 | 96 | 98 | PF00082 | 0.478 |
| CLV_PCSK_PC1ET2_1 | 263 | 265 | PF00082 | 0.646 |
| CLV_PCSK_PC1ET2_1 | 362 | 364 | PF00082 | 0.564 |
| CLV_PCSK_PC7_1 | 30 | 36 | PF00082 | 0.437 |
| CLV_PCSK_SKI1_1 | 153 | 157 | PF00082 | 0.710 |
| CLV_PCSK_SKI1_1 | 221 | 225 | PF00082 | 0.606 |
| CLV_PCSK_SKI1_1 | 242 | 246 | PF00082 | 0.634 |
| CLV_PCSK_SKI1_1 | 348 | 352 | PF00082 | 0.668 |
| CLV_PCSK_SKI1_1 | 96 | 100 | PF00082 | 0.473 |
| DOC_ANK_TNKS_1 | 249 | 256 | PF00023 | 0.517 |
| DOC_CYCLIN_yCln2_LP_2 | 157 | 163 | PF00134 | 0.523 |
| DOC_CYCLIN_yCln2_LP_2 | 415 | 421 | PF00134 | 0.633 |
| DOC_MAPK_DCC_7 | 412 | 421 | PF00069 | 0.629 |
| DOC_MAPK_gen_1 | 171 | 180 | PF00069 | 0.490 |
| DOC_MAPK_gen_1 | 260 | 267 | PF00069 | 0.613 |
| DOC_MAPK_gen_1 | 412 | 421 | PF00069 | 0.610 |
| DOC_PP1_RVXF_1 | 171 | 177 | PF00149 | 0.327 |
| DOC_PP1_RVXF_1 | 261 | 268 | PF00149 | 0.581 |
| DOC_PP2B_LxvP_1 | 415 | 418 | PF13499 | 0.626 |
| DOC_USP7_MATH_1 | 131 | 135 | PF00917 | 0.574 |
| DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.527 |
| DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.539 |
| DOC_USP7_MATH_1 | 361 | 365 | PF00917 | 0.562 |
| DOC_USP7_MATH_1 | 431 | 435 | PF00917 | 0.525 |
| DOC_USP7_MATH_1 | 82 | 86 | PF00917 | 0.435 |
| DOC_WW_Pin1_4 | 127 | 132 | PF00397 | 0.623 |
| DOC_WW_Pin1_4 | 255 | 260 | PF00397 | 0.798 |
| DOC_WW_Pin1_4 | 373 | 378 | PF00397 | 0.799 |
| DOC_WW_Pin1_4 | 420 | 425 | PF00397 | 0.734 |
| LIG_14-3-3_CanoR_1 | 126 | 131 | PF00244 | 0.500 |
| LIG_14-3-3_CanoR_1 | 171 | 177 | PF00244 | 0.326 |
| LIG_14-3-3_CanoR_1 | 348 | 353 | PF00244 | 0.535 |
| LIG_14-3-3_CanoR_1 | 439 | 443 | PF00244 | 0.622 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.451 |
| LIG_BRCT_BRCA1_1 | 337 | 341 | PF00533 | 0.588 |
| LIG_FHA_1 | 173 | 179 | PF00498 | 0.436 |
| LIG_FHA_1 | 34 | 40 | PF00498 | 0.498 |
| LIG_FHA_1 | 340 | 346 | PF00498 | 0.577 |
| LIG_FHA_2 | 23 | 29 | PF00498 | 0.434 |
| LIG_FHA_2 | 381 | 387 | PF00498 | 0.525 |
| LIG_LIR_Gen_1 | 9 | 18 | PF02991 | 0.353 |
| LIG_LIR_Nem_3 | 9 | 15 | PF02991 | 0.431 |
| LIG_NRBOX | 165 | 171 | PF00104 | 0.390 |
| LIG_SH2_GRB2like | 408 | 411 | PF00017 | 0.598 |
| LIG_SH2_STAT5 | 325 | 328 | PF00017 | 0.541 |
| LIG_SH2_STAT5 | 408 | 411 | PF00017 | 0.675 |
| LIG_SH2_STAT5 | 68 | 71 | PF00017 | 0.392 |
| LIG_SH3_3 | 182 | 188 | PF00018 | 0.662 |
| LIG_SH3_3 | 223 | 229 | PF00018 | 0.622 |
| LIG_SH3_3 | 233 | 239 | PF00018 | 0.566 |
| LIG_SH3_3 | 303 | 309 | PF00018 | 0.663 |
| LIG_SH3_3 | 400 | 406 | PF00018 | 0.529 |
| LIG_SUMO_SIM_par_1 | 105 | 111 | PF11976 | 0.383 |
| LIG_SUMO_SIM_par_1 | 166 | 172 | PF11976 | 0.391 |
| LIG_SUMO_SIM_par_1 | 417 | 423 | PF11976 | 0.635 |
| LIG_TRAF2_1 | 7 | 10 | PF00917 | 0.425 |
| LIG_TRAF2_1 | 88 | 91 | PF00917 | 0.486 |
| LIG_UBA3_1 | 166 | 173 | PF00899 | 0.424 |
| LIG_WW_1 | 405 | 408 | PF00397 | 0.561 |
| MOD_CDC14_SPxK_1 | 376 | 379 | PF00782 | 0.696 |
| MOD_CDK_SPK_2 | 255 | 260 | PF00069 | 0.570 |
| MOD_CDK_SPK_2 | 373 | 378 | PF00069 | 0.643 |
| MOD_CDK_SPK_2 | 420 | 425 | PF00069 | 0.644 |
| MOD_CDK_SPxK_1 | 373 | 379 | PF00069 | 0.690 |
| MOD_CDK_SPxxK_3 | 255 | 262 | PF00069 | 0.602 |
| MOD_CK1_1 | 127 | 133 | PF00069 | 0.744 |
| MOD_CK1_1 | 364 | 370 | PF00069 | 0.560 |
| MOD_CK1_1 | 390 | 396 | PF00069 | 0.638 |
| MOD_CK1_1 | 423 | 429 | PF00069 | 0.672 |
| MOD_CK1_1 | 434 | 440 | PF00069 | 0.618 |
| MOD_CK2_1 | 199 | 205 | PF00069 | 0.647 |
| MOD_CK2_1 | 255 | 261 | PF00069 | 0.603 |
| MOD_CK2_1 | 4 | 10 | PF00069 | 0.448 |
| MOD_Cter_Amidation | 437 | 440 | PF01082 | 0.565 |
| MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.614 |
| MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.640 |
| MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.690 |
| MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.471 |
| MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.530 |
| MOD_GlcNHglycan | 302 | 305 | PF01048 | 0.659 |
| MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.585 |
| MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.651 |
| MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.664 |
| MOD_GlcNHglycan | 425 | 428 | PF01048 | 0.677 |
| MOD_GlcNHglycan | 433 | 436 | PF01048 | 0.644 |
| MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.438 |
| MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.429 |
| MOD_GSK3_1 | 126 | 133 | PF00069 | 0.768 |
| MOD_GSK3_1 | 136 | 143 | PF00069 | 0.580 |
| MOD_GSK3_1 | 195 | 202 | PF00069 | 0.705 |
| MOD_GSK3_1 | 335 | 342 | PF00069 | 0.598 |
| MOD_GSK3_1 | 344 | 351 | PF00069 | 0.460 |
| MOD_GSK3_1 | 369 | 376 | PF00069 | 0.554 |
| MOD_GSK3_1 | 434 | 441 | PF00069 | 0.649 |
| MOD_GSK3_1 | 443 | 450 | PF00069 | 0.696 |
| MOD_N-GLC_1 | 127 | 132 | PF02516 | 0.556 |
| MOD_N-GLC_1 | 327 | 332 | PF02516 | 0.528 |
| MOD_N-GLC_1 | 370 | 375 | PF02516 | 0.594 |
| MOD_N-GLC_1 | 431 | 436 | PF02516 | 0.648 |
| MOD_NEK2_1 | 169 | 174 | PF00069 | 0.354 |
| MOD_NEK2_2 | 339 | 344 | PF00069 | 0.644 |
| MOD_PIKK_1 | 22 | 28 | PF00454 | 0.448 |
| MOD_PIKK_1 | 370 | 376 | PF00454 | 0.615 |
| MOD_PIKK_1 | 62 | 68 | PF00454 | 0.466 |
| MOD_PKA_2 | 117 | 123 | PF00069 | 0.553 |
| MOD_PKA_2 | 210 | 216 | PF00069 | 0.656 |
| MOD_PKA_2 | 274 | 280 | PF00069 | 0.724 |
| MOD_PKA_2 | 285 | 291 | PF00069 | 0.603 |
| MOD_PKA_2 | 300 | 306 | PF00069 | 0.509 |
| MOD_PKA_2 | 33 | 39 | PF00069 | 0.452 |
| MOD_PKA_2 | 364 | 370 | PF00069 | 0.726 |
| MOD_PKA_2 | 438 | 444 | PF00069 | 0.666 |
| MOD_PKA_2 | 446 | 452 | PF00069 | 0.743 |
| MOD_PKA_2 | 82 | 88 | PF00069 | 0.494 |
| MOD_Plk_1 | 153 | 159 | PF00069 | 0.612 |
| MOD_Plk_4 | 153 | 159 | PF00069 | 0.612 |
| MOD_Plk_4 | 222 | 228 | PF00069 | 0.627 |
| MOD_Plk_4 | 348 | 354 | PF00069 | 0.535 |
| MOD_ProDKin_1 | 127 | 133 | PF00069 | 0.623 |
| MOD_ProDKin_1 | 255 | 261 | PF00069 | 0.798 |
| MOD_ProDKin_1 | 373 | 379 | PF00069 | 0.802 |
| MOD_ProDKin_1 | 420 | 426 | PF00069 | 0.734 |
| MOD_SUMO_rev_2 | 257 | 265 | PF00179 | 0.645 |
| TRG_DiLeu_BaEn_1 | 10 | 15 | PF01217 | 0.429 |
| TRG_DiLeu_BaLyEn_6 | 226 | 231 | PF01217 | 0.484 |
| TRG_ENDOCYTIC_2 | 12 | 15 | PF00928 | 0.433 |
| TRG_ER_diArg_1 | 151 | 153 | PF00400 | 0.600 |
| TRG_ER_diArg_1 | 71 | 73 | PF00400 | 0.499 |
| TRG_Pf-PMV_PEXEL_1 | 71 | 75 | PF00026 | 0.452 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1HSL3 | Leptomonas seymouri | 30% | 95% |
| A0A3Q8ITE5 | Leishmania donovani | 77% | 100% |
| A4HKM1 | Leishmania braziliensis | 63% | 100% |
| A4I853 | Leishmania infantum | 77% | 100% |
| Q4Q545 | Leishmania major | 79% | 100% |