| 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: A4HUE3
| Leishmania | From | To | Domain/Motif | Score | 
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 108 | 112 | PF00656 | 0.693 | 
| CLV_C14_Caspase3-7 | 203 | 207 | PF00656 | 0.664 | 
| CLV_C14_Caspase3-7 | 263 | 267 | PF00656 | 0.646 | 
| CLV_NRD_NRD_1 | 252 | 254 | PF00675 | 0.461 | 
| CLV_NRD_NRD_1 | 384 | 386 | PF00675 | 0.509 | 
| CLV_PCSK_FUR_1 | 419 | 423 | PF00082 | 0.714 | 
| CLV_PCSK_KEX2_1 | 252 | 254 | PF00082 | 0.461 | 
| CLV_PCSK_KEX2_1 | 384 | 386 | PF00082 | 0.509 | 
| CLV_PCSK_KEX2_1 | 421 | 423 | PF00082 | 0.811 | 
| CLV_PCSK_PC1ET2_1 | 421 | 423 | PF00082 | 0.811 | 
| CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.727 | 
| CLV_PCSK_SKI1_1 | 167 | 171 | PF00082 | 0.609 | 
| CLV_PCSK_SKI1_1 | 22 | 26 | PF00082 | 0.612 | 
| CLV_Separin_Metazoa | 320 | 324 | PF03568 | 0.494 | 
| DEG_APCC_DBOX_1 | 73 | 81 | PF00400 | 0.597 | 
| DEG_SPOP_SBC_1 | 10 | 14 | PF00917 | 0.730 | 
| DEG_SPOP_SBC_1 | 239 | 243 | PF00917 | 0.579 | 
| DOC_MAPK_MEF2A_6 | 295 | 304 | PF00069 | 0.600 | 
| DOC_PP2B_LxvP_1 | 197 | 200 | PF13499 | 0.491 | 
| DOC_PP4_FxxP_1 | 32 | 35 | PF00568 | 0.469 | 
| DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.614 | 
| DOC_USP7_MATH_1 | 239 | 243 | PF00917 | 0.640 | 
| DOC_USP7_MATH_1 | 390 | 394 | PF00917 | 0.715 | 
| DOC_WW_Pin1_4 | 183 | 188 | PF00397 | 0.644 | 
| DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.569 | 
| DOC_WW_Pin1_4 | 394 | 399 | PF00397 | 0.626 | 
| LIG_14-3-3_CanoR_1 | 114 | 118 | PF00244 | 0.612 | 
| LIG_14-3-3_CanoR_1 | 147 | 153 | PF00244 | 0.538 | 
| LIG_14-3-3_CanoR_1 | 22 | 32 | PF00244 | 0.569 | 
| LIG_14-3-3_CanoR_1 | 252 | 260 | PF00244 | 0.546 | 
| LIG_14-3-3_CanoR_1 | 323 | 333 | PF00244 | 0.515 | 
| LIG_14-3-3_CanoR_1 | 369 | 374 | PF00244 | 0.478 | 
| LIG_14-3-3_CanoR_1 | 37 | 46 | PF00244 | 0.622 | 
| LIG_14-3-3_CanoR_1 | 384 | 391 | PF00244 | 0.404 | 
| LIG_Actin_WH2_2 | 131 | 149 | PF00022 | 0.567 | 
| LIG_Actin_WH2_2 | 315 | 332 | PF00022 | 0.625 | 
| LIG_BIR_III_2 | 206 | 210 | PF00653 | 0.599 | 
| LIG_CaM_IQ_9 | 361 | 377 | PF13499 | 0.435 | 
| LIG_DLG_GKlike_1 | 369 | 377 | PF00625 | 0.440 | 
| LIG_FHA_1 | 147 | 153 | PF00498 | 0.557 | 
| LIG_FHA_1 | 155 | 161 | PF00498 | 0.453 | 
| LIG_FHA_1 | 208 | 214 | PF00498 | 0.632 | 
| LIG_FHA_1 | 23 | 29 | PF00498 | 0.506 | 
| LIG_FHA_1 | 39 | 45 | PF00498 | 0.715 | 
| LIG_FHA_2 | 201 | 207 | PF00498 | 0.533 | 
| LIG_FHA_2 | 312 | 318 | PF00498 | 0.632 | 
| LIG_GBD_Chelix_1 | 290 | 298 | PF00786 | 0.590 | 
| LIG_LIR_Apic_2 | 31 | 35 | PF02991 | 0.473 | 
| LIG_LIR_Gen_1 | 157 | 165 | PF02991 | 0.412 | 
| LIG_LIR_Gen_1 | 219 | 230 | PF02991 | 0.625 | 
| LIG_LIR_Nem_3 | 157 | 162 | PF02991 | 0.414 | 
| LIG_LIR_Nem_3 | 219 | 225 | PF02991 | 0.509 | 
| LIG_PROFILIN_1 | 403 | 409 | PF00235 | 0.565 | 
| LIG_RPA_C_Fungi | 379 | 391 | PF08784 | 0.479 | 
| LIG_SH2_SRC | 198 | 201 | PF00017 | 0.499 | 
| LIG_SH2_STAP1 | 165 | 169 | PF00017 | 0.575 | 
| LIG_SH2_STAT5 | 198 | 201 | PF00017 | 0.563 | 
| LIG_SH2_STAT5 | 259 | 262 | PF00017 | 0.602 | 
| LIG_SH2_STAT5 | 90 | 93 | PF00017 | 0.441 | 
| LIG_SH3_3 | 178 | 184 | PF00018 | 0.694 | 
| LIG_SH3_3 | 331 | 337 | PF00018 | 0.625 | 
| LIG_SH3_3 | 338 | 344 | PF00018 | 0.627 | 
| LIG_SH3_3 | 400 | 406 | PF00018 | 0.742 | 
| LIG_SUMO_SIM_anti_2 | 317 | 324 | PF11976 | 0.621 | 
| LIG_SUMO_SIM_par_1 | 160 | 166 | PF11976 | 0.413 | 
| LIG_SUMO_SIM_par_1 | 357 | 363 | PF11976 | 0.480 | 
| LIG_TRAF2_1 | 209 | 212 | PF00917 | 0.672 | 
| LIG_TRAF2_1 | 286 | 289 | PF00917 | 0.612 | 
| LIG_TRAF2_1 | 351 | 354 | PF00917 | 0.611 | 
| MOD_CDK_SPK_2 | 394 | 399 | PF00069 | 0.739 | 
| MOD_CK1_1 | 113 | 119 | PF00069 | 0.486 | 
| MOD_CK1_1 | 154 | 160 | PF00069 | 0.512 | 
| MOD_CK1_1 | 238 | 244 | PF00069 | 0.611 | 
| MOD_CK1_1 | 272 | 278 | PF00069 | 0.582 | 
| MOD_CK1_1 | 307 | 313 | PF00069 | 0.696 | 
| MOD_CK1_1 | 335 | 341 | PF00069 | 0.636 | 
| MOD_CK1_1 | 383 | 389 | PF00069 | 0.592 | 
| MOD_CK1_1 | 96 | 102 | PF00069 | 0.689 | 
| MOD_CK2_1 | 412 | 418 | PF00069 | 0.706 | 
| MOD_GlcNHglycan | 104 | 107 | PF01048 | 0.675 | 
| MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.662 | 
| MOD_GlcNHglycan | 18 | 21 | PF01048 | 0.653 | 
| MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.754 | 
| MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.753 | 
| MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.409 | 
| MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.639 | 
| MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.566 | 
| MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.529 | 
| MOD_GlcNHglycan | 422 | 425 | PF01048 | 0.746 | 
| MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.546 | 
| MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.676 | 
| MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.579 | 
| MOD_GSK3_1 | 147 | 154 | PF00069 | 0.586 | 
| MOD_GSK3_1 | 207 | 214 | PF00069 | 0.636 | 
| MOD_GSK3_1 | 235 | 242 | PF00069 | 0.628 | 
| MOD_GSK3_1 | 24 | 31 | PF00069 | 0.542 | 
| MOD_GSK3_1 | 269 | 276 | PF00069 | 0.713 | 
| MOD_GSK3_1 | 305 | 312 | PF00069 | 0.626 | 
| MOD_GSK3_1 | 379 | 386 | PF00069 | 0.559 | 
| MOD_GSK3_1 | 390 | 397 | PF00069 | 0.618 | 
| MOD_GSK3_1 | 420 | 427 | PF00069 | 0.802 | 
| MOD_GSK3_1 | 93 | 100 | PF00069 | 0.527 | 
| MOD_N-GLC_1 | 147 | 152 | PF02516 | 0.399 | 
| MOD_N-GLC_1 | 226 | 231 | PF02516 | 0.569 | 
| MOD_NEK2_1 | 1 | 6 | PF00069 | 0.581 | 
| MOD_NEK2_1 | 146 | 151 | PF00069 | 0.537 | 
| MOD_NEK2_1 | 278 | 283 | PF00069 | 0.609 | 
| MOD_NEK2_1 | 290 | 295 | PF00069 | 0.431 | 
| MOD_NEK2_1 | 304 | 309 | PF00069 | 0.552 | 
| MOD_NEK2_1 | 321 | 326 | PF00069 | 0.553 | 
| MOD_NEK2_1 | 380 | 385 | PF00069 | 0.652 | 
| MOD_NMyristoyl | 1 | 7 | PF02799 | 0.555 | 
| MOD_PIKK_1 | 270 | 276 | PF00454 | 0.660 | 
| MOD_PIKK_1 | 278 | 284 | PF00454 | 0.459 | 
| MOD_PIKK_1 | 335 | 341 | PF00454 | 0.676 | 
| MOD_PK_1 | 147 | 153 | PF00069 | 0.506 | 
| MOD_PKA_2 | 113 | 119 | PF00069 | 0.486 | 
| MOD_PKA_2 | 146 | 152 | PF00069 | 0.536 | 
| MOD_PKA_2 | 335 | 341 | PF00069 | 0.578 | 
| MOD_PKA_2 | 383 | 389 | PF00069 | 0.481 | 
| MOD_PKA_2 | 96 | 102 | PF00069 | 0.673 | 
| MOD_PKB_1 | 369 | 377 | PF00069 | 0.485 | 
| MOD_Plk_1 | 147 | 153 | PF00069 | 0.395 | 
| MOD_Plk_1 | 211 | 217 | PF00069 | 0.623 | 
| MOD_Plk_1 | 226 | 232 | PF00069 | 0.507 | 
| MOD_Plk_4 | 147 | 153 | PF00069 | 0.506 | 
| MOD_Plk_4 | 226 | 232 | PF00069 | 0.574 | 
| MOD_ProDKin_1 | 183 | 189 | PF00069 | 0.640 | 
| MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.573 | 
| MOD_ProDKin_1 | 394 | 400 | PF00069 | 0.631 | 
| MOD_SUMO_for_1 | 124 | 127 | PF00179 | 0.713 | 
| TRG_DiLeu_BaLyEn_6 | 292 | 297 | PF01217 | 0.467 | 
| TRG_ER_diArg_1 | 251 | 253 | PF00400 | 0.483 | 
| TRG_ER_diArg_1 | 368 | 371 | PF00400 | 0.488 | 
| TRG_NES_CRM1_1 | 288 | 303 | PF08389 | 0.534 | 
| TRG_NES_CRM1_1 | 354 | 365 | PF08389 | 0.614 | 
| TRG_NLS_MonoExtC_3 | 121 | 127 | PF00514 | 0.606 | 
| TRG_Pf-PMV_PEXEL_1 | 299 | 303 | PF00026 | 0.543 | 
| Protein | Taxonomy | Sequence identity | Coverage | 
|---|---|---|---|
| A0A0N1HYC0 | Leptomonas seymouri | 36% | 80% | 
| A0A3Q8I7N0 | Leishmania donovani | 99% | 100% | 
| A4H616 | Leishmania braziliensis | 69% | 100% | 
| E9AN43 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% | 
| Q4QHI3 | Leishmania major | 91% | 100% |