| 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: 13 |
| NetGPI | no | yes: 0, no: 13 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0016020 | membrane | 2 | 14 |
| GO:0110165 | cellular anatomical entity | 1 | 14 |
Related structures:
AlphaFold database: A4HQ64
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0038023 | signaling receptor activity | 2 | 2 |
| GO:0060089 | molecular transducer activity | 1 | 2 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 109 | 113 | PF00656 | 0.725 |
| CLV_NRD_NRD_1 | 203 | 205 | PF00675 | 0.529 |
| CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.470 |
| CLV_PCSK_KEX2_1 | 202 | 204 | PF00082 | 0.598 |
| CLV_PCSK_PC1ET2_1 | 202 | 204 | PF00082 | 0.595 |
| CLV_PCSK_PC7_1 | 199 | 205 | PF00082 | 0.401 |
| CLV_PCSK_SKI1_1 | 266 | 270 | PF00082 | 0.316 |
| CLV_PCSK_SKI1_1 | 28 | 32 | PF00082 | 0.445 |
| CLV_PCSK_SKI1_1 | 302 | 306 | PF00082 | 0.492 |
| CLV_PCSK_SKI1_1 | 343 | 347 | PF00082 | 0.330 |
| DEG_ODPH_VHL_1 | 421 | 433 | PF01847 | 0.336 |
| DEG_SIAH_1 | 48 | 56 | PF03145 | 0.596 |
| DEG_SPOP_SBC_1 | 132 | 136 | PF00917 | 0.692 |
| DOC_CKS1_1 | 436 | 441 | PF01111 | 0.198 |
| DOC_MAPK_gen_1 | 199 | 207 | PF00069 | 0.610 |
| DOC_MAPK_gen_1 | 21 | 31 | PF00069 | 0.654 |
| DOC_MAPK_gen_1 | 227 | 235 | PF00069 | 0.507 |
| DOC_MAPK_MEF2A_6 | 350 | 358 | PF00069 | 0.467 |
| DOC_MAPK_MEF2A_6 | 409 | 418 | PF00069 | 0.405 |
| DOC_PP4_FxxP_1 | 364 | 367 | PF00568 | 0.343 |
| DOC_USP7_MATH_1 | 132 | 136 | PF00917 | 0.752 |
| DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.757 |
| DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.690 |
| DOC_USP7_MATH_1 | 424 | 428 | PF00917 | 0.440 |
| DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.647 |
| DOC_WW_Pin1_4 | 171 | 176 | PF00397 | 0.737 |
| DOC_WW_Pin1_4 | 177 | 182 | PF00397 | 0.745 |
| DOC_WW_Pin1_4 | 190 | 195 | PF00397 | 0.723 |
| DOC_WW_Pin1_4 | 435 | 440 | PF00397 | 0.198 |
| LIG_14-3-3_CanoR_1 | 203 | 208 | PF00244 | 0.687 |
| LIG_14-3-3_CanoR_1 | 256 | 265 | PF00244 | 0.529 |
| LIG_14-3-3_CanoR_1 | 343 | 351 | PF00244 | 0.530 |
| LIG_14-3-3_CanoR_1 | 409 | 413 | PF00244 | 0.471 |
| LIG_AP2alpha_2 | 137 | 139 | PF02296 | 0.593 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.693 |
| LIG_deltaCOP1_diTrp_1 | 404 | 413 | PF00928 | 0.398 |
| LIG_deltaCOP1_diTrp_1 | 472 | 481 | PF00928 | 0.538 |
| LIG_eIF4E_1 | 382 | 388 | PF01652 | 0.403 |
| LIG_FHA_1 | 148 | 154 | PF00498 | 0.751 |
| LIG_FHA_1 | 161 | 167 | PF00498 | 0.784 |
| LIG_FHA_1 | 230 | 236 | PF00498 | 0.634 |
| LIG_FHA_1 | 273 | 279 | PF00498 | 0.481 |
| LIG_FHA_1 | 290 | 296 | PF00498 | 0.346 |
| LIG_FHA_1 | 355 | 361 | PF00498 | 0.346 |
| LIG_FHA_1 | 378 | 384 | PF00498 | 0.333 |
| LIG_FHA_1 | 389 | 395 | PF00498 | 0.298 |
| LIG_FHA_1 | 88 | 94 | PF00498 | 0.655 |
| LIG_FHA_2 | 132 | 138 | PF00498 | 0.600 |
| LIG_FHA_2 | 7 | 13 | PF00498 | 0.787 |
| LIG_FHA_2 | 98 | 104 | PF00498 | 0.669 |
| LIG_GBD_Chelix_1 | 81 | 89 | PF00786 | 0.379 |
| LIG_HCF-1_HBM_1 | 195 | 198 | PF13415 | 0.617 |
| LIG_LIR_Apic_2 | 362 | 367 | PF02991 | 0.348 |
| LIG_LIR_Gen_1 | 136 | 147 | PF02991 | 0.678 |
| LIG_LIR_Gen_1 | 284 | 293 | PF02991 | 0.376 |
| LIG_LIR_Gen_1 | 400 | 410 | PF02991 | 0.484 |
| LIG_LIR_Nem_3 | 136 | 142 | PF02991 | 0.764 |
| LIG_LIR_Nem_3 | 253 | 258 | PF02991 | 0.569 |
| LIG_LIR_Nem_3 | 284 | 288 | PF02991 | 0.376 |
| LIG_LIR_Nem_3 | 330 | 336 | PF02991 | 0.422 |
| LIG_LIR_Nem_3 | 341 | 345 | PF02991 | 0.498 |
| LIG_LIR_Nem_3 | 352 | 356 | PF02991 | 0.344 |
| LIG_LIR_Nem_3 | 404 | 410 | PF02991 | 0.514 |
| LIG_LIR_Nem_3 | 411 | 416 | PF02991 | 0.323 |
| LIG_NRBOX | 441 | 447 | PF00104 | 0.206 |
| LIG_PCNA_PIPBox_1 | 487 | 496 | PF02747 | 0.206 |
| LIG_PCNA_yPIPBox_3 | 329 | 343 | PF02747 | 0.403 |
| LIG_Pex14_1 | 398 | 402 | PF04695 | 0.538 |
| LIG_Pex14_2 | 265 | 269 | PF04695 | 0.460 |
| LIG_SH2_CRK | 296 | 300 | PF00017 | 0.403 |
| LIG_SH2_CRK | 342 | 346 | PF00017 | 0.398 |
| LIG_SH2_GRB2like | 493 | 496 | PF00017 | 0.252 |
| LIG_SH2_PTP2 | 353 | 356 | PF00017 | 0.206 |
| LIG_SH2_STAP1 | 259 | 263 | PF00017 | 0.510 |
| LIG_SH2_STAP1 | 279 | 283 | PF00017 | 0.176 |
| LIG_SH2_STAP1 | 296 | 300 | PF00017 | 0.469 |
| LIG_SH2_STAP1 | 403 | 407 | PF00017 | 0.398 |
| LIG_SH2_STAT3 | 259 | 262 | PF00017 | 0.494 |
| LIG_SH2_STAT5 | 250 | 253 | PF00017 | 0.567 |
| LIG_SH2_STAT5 | 259 | 262 | PF00017 | 0.523 |
| LIG_SH2_STAT5 | 296 | 299 | PF00017 | 0.380 |
| LIG_SH2_STAT5 | 353 | 356 | PF00017 | 0.250 |
| LIG_SH2_STAT5 | 369 | 372 | PF00017 | 0.385 |
| LIG_SH2_STAT5 | 382 | 385 | PF00017 | 0.343 |
| LIG_SH2_STAT5 | 451 | 454 | PF00017 | 0.380 |
| LIG_SH2_STAT5 | 458 | 461 | PF00017 | 0.319 |
| LIG_SH2_STAT5 | 493 | 496 | PF00017 | 0.362 |
| LIG_SH3_3 | 433 | 439 | PF00018 | 0.263 |
| LIG_SH3_3 | 89 | 95 | PF00018 | 0.712 |
| LIG_SUMO_SIM_anti_2 | 357 | 363 | PF11976 | 0.354 |
| LIG_SUMO_SIM_anti_2 | 384 | 391 | PF11976 | 0.403 |
| LIG_SUMO_SIM_anti_2 | 427 | 432 | PF11976 | 0.484 |
| LIG_SUMO_SIM_par_1 | 356 | 363 | PF11976 | 0.356 |
| LIG_SUMO_SIM_par_1 | 384 | 391 | PF11976 | 0.403 |
| LIG_SxIP_EBH_1 | 45 | 54 | PF03271 | 0.603 |
| LIG_TYR_ITIM | 294 | 299 | PF00017 | 0.403 |
| LIG_TYR_ITIM | 351 | 356 | PF00017 | 0.363 |
| LIG_Vh1_VBS_1 | 377 | 395 | PF01044 | 0.276 |
| LIG_WRC_WIRS_1 | 282 | 287 | PF05994 | 0.403 |
| LIG_WRC_WIRS_1 | 361 | 366 | PF05994 | 0.346 |
| LIG_WW_1 | 366 | 369 | PF00397 | 0.343 |
| MOD_CDK_SPxxK_3 | 171 | 178 | PF00069 | 0.614 |
| MOD_CK1_1 | 116 | 122 | PF00069 | 0.688 |
| MOD_CK1_1 | 177 | 183 | PF00069 | 0.668 |
| MOD_CK1_1 | 33 | 39 | PF00069 | 0.737 |
| MOD_CK2_1 | 85 | 91 | PF00069 | 0.696 |
| MOD_CK2_1 | 97 | 103 | PF00069 | 0.749 |
| MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.524 |
| MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.499 |
| MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.568 |
| MOD_GlcNHglycan | 418 | 421 | PF01048 | 0.346 |
| MOD_GlcNHglycan | 452 | 455 | PF01048 | 0.389 |
| MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.463 |
| MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.493 |
| MOD_GSK3_1 | 113 | 120 | PF00069 | 0.689 |
| MOD_GSK3_1 | 153 | 160 | PF00069 | 0.690 |
| MOD_GSK3_1 | 161 | 168 | PF00069 | 0.763 |
| MOD_GSK3_1 | 20 | 27 | PF00069 | 0.657 |
| MOD_GSK3_1 | 203 | 210 | PF00069 | 0.610 |
| MOD_GSK3_1 | 246 | 253 | PF00069 | 0.547 |
| MOD_GSK3_1 | 277 | 284 | PF00069 | 0.395 |
| MOD_GSK3_1 | 294 | 301 | PF00069 | 0.309 |
| MOD_GSK3_1 | 305 | 312 | PF00069 | 0.288 |
| MOD_GSK3_1 | 377 | 384 | PF00069 | 0.414 |
| MOD_GSK3_1 | 43 | 50 | PF00069 | 0.609 |
| MOD_LATS_1 | 71 | 77 | PF00433 | 0.619 |
| MOD_N-GLC_1 | 272 | 277 | PF02516 | 0.298 |
| MOD_N-GLC_1 | 328 | 333 | PF02516 | 0.354 |
| MOD_N-GLC_1 | 36 | 41 | PF02516 | 0.461 |
| MOD_N-GLC_1 | 71 | 76 | PF02516 | 0.433 |
| MOD_N-GLC_2 | 113 | 115 | PF02516 | 0.396 |
| MOD_NEK2_1 | 106 | 111 | PF00069 | 0.615 |
| MOD_NEK2_1 | 207 | 212 | PF00069 | 0.582 |
| MOD_NEK2_1 | 289 | 294 | PF00069 | 0.360 |
| MOD_NEK2_1 | 295 | 300 | PF00069 | 0.335 |
| MOD_NEK2_1 | 309 | 314 | PF00069 | 0.176 |
| MOD_NEK2_1 | 327 | 332 | PF00069 | 0.345 |
| MOD_NEK2_1 | 359 | 364 | PF00069 | 0.333 |
| MOD_NEK2_1 | 416 | 421 | PF00069 | 0.371 |
| MOD_NEK2_1 | 450 | 455 | PF00069 | 0.418 |
| MOD_NEK2_1 | 457 | 462 | PF00069 | 0.371 |
| MOD_NEK2_1 | 483 | 488 | PF00069 | 0.378 |
| MOD_NEK2_1 | 85 | 90 | PF00069 | 0.602 |
| MOD_NEK2_2 | 264 | 269 | PF00069 | 0.443 |
| MOD_OFUCOSY | 57 | 62 | PF10250 | 0.417 |
| MOD_PIKK_1 | 118 | 124 | PF00454 | 0.669 |
| MOD_PIKK_1 | 157 | 163 | PF00454 | 0.647 |
| MOD_PIKK_1 | 30 | 36 | PF00454 | 0.698 |
| MOD_PKA_1 | 203 | 209 | PF00069 | 0.686 |
| MOD_PKA_2 | 203 | 209 | PF00069 | 0.686 |
| MOD_PKA_2 | 408 | 414 | PF00069 | 0.476 |
| MOD_PKB_1 | 227 | 235 | PF00069 | 0.507 |
| MOD_Plk_1 | 229 | 235 | PF00069 | 0.648 |
| MOD_Plk_1 | 24 | 30 | PF00069 | 0.671 |
| MOD_Plk_1 | 272 | 278 | PF00069 | 0.515 |
| MOD_Plk_1 | 328 | 334 | PF00069 | 0.354 |
| MOD_Plk_1 | 36 | 42 | PF00069 | 0.736 |
| MOD_Plk_1 | 6 | 12 | PF00069 | 0.655 |
| MOD_Plk_4 | 203 | 209 | PF00069 | 0.593 |
| MOD_Plk_4 | 246 | 252 | PF00069 | 0.560 |
| MOD_Plk_4 | 264 | 270 | PF00069 | 0.647 |
| MOD_Plk_4 | 281 | 287 | PF00069 | 0.262 |
| MOD_Plk_4 | 295 | 301 | PF00069 | 0.300 |
| MOD_Plk_4 | 320 | 326 | PF00069 | 0.381 |
| MOD_Plk_4 | 328 | 334 | PF00069 | 0.403 |
| MOD_Plk_4 | 360 | 366 | PF00069 | 0.346 |
| MOD_Plk_4 | 408 | 414 | PF00069 | 0.476 |
| MOD_Plk_4 | 426 | 432 | PF00069 | 0.352 |
| MOD_Plk_4 | 495 | 501 | PF00069 | 0.365 |
| MOD_ProDKin_1 | 171 | 177 | PF00069 | 0.737 |
| MOD_ProDKin_1 | 190 | 196 | PF00069 | 0.722 |
| MOD_ProDKin_1 | 435 | 441 | PF00069 | 0.198 |
| MOD_SUMO_rev_2 | 185 | 194 | PF00179 | 0.658 |
| MOD_SUMO_rev_2 | 38 | 47 | PF00179 | 0.613 |
| TRG_DiLeu_BaEn_2 | 102 | 108 | PF01217 | 0.700 |
| TRG_ENDOCYTIC_2 | 255 | 258 | PF00928 | 0.511 |
| TRG_ENDOCYTIC_2 | 279 | 282 | PF00928 | 0.331 |
| TRG_ENDOCYTIC_2 | 296 | 299 | PF00928 | 0.336 |
| TRG_ENDOCYTIC_2 | 316 | 319 | PF00928 | 0.391 |
| TRG_ENDOCYTIC_2 | 333 | 336 | PF00928 | 0.496 |
| TRG_ENDOCYTIC_2 | 342 | 345 | PF00928 | 0.538 |
| TRG_ENDOCYTIC_2 | 353 | 356 | PF00928 | 0.298 |
| TRG_ENDOCYTIC_2 | 369 | 372 | PF00928 | 0.368 |
| TRG_ENDOCYTIC_2 | 403 | 406 | PF00928 | 0.479 |
| TRG_ER_diArg_1 | 203 | 205 | PF00400 | 0.743 |
| TRG_NLS_MonoExtN_4 | 199 | 206 | PF00514 | 0.643 |
| TRG_Pf-PMV_PEXEL_1 | 79 | 83 | PF00026 | 0.385 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1I280 | Leptomonas seymouri | 35% | 100% |
| A0A0N1PEB9 | Leptomonas seymouri | 50% | 95% |
| A0A1X0P1Q2 | Trypanosomatidae | 37% | 100% |
| A0A3S7XBT4 | Leishmania donovani | 36% | 100% |
| A0A3S7XBU6 | Leishmania donovani | 67% | 100% |
| A4HQ67 | Leishmania braziliensis | 36% | 100% |
| A4IDW4 | Leishmania infantum | 36% | 100% |
| A4IDW5 | Leishmania infantum | 68% | 100% |
| E9ATY5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
| E9ATY6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 66% | 100% |
| Q4Q0L0 | Leishmania major | 68% | 98% |
| Q4Q0L1 | Leishmania major | 37% | 100% |