| 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 | 
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0016020 | membrane | 2 | 7 | 
| GO:0110165 | cellular anatomical entity | 1 | 7 | 
Related structures:
AlphaFold database: A0A3S7WPX9
| Leishmania | From | To | Domain/Motif | Score | 
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 118 | 122 | PF00656 | 0.753 | 
| CLV_C14_Caspase3-7 | 215 | 219 | PF00656 | 0.637 | 
| CLV_C14_Caspase3-7 | 394 | 398 | PF00656 | 0.621 | 
| CLV_C14_Caspase3-7 | 42 | 46 | PF00656 | 0.688 | 
| CLV_NRD_NRD_1 | 410 | 412 | PF00675 | 0.474 | 
| CLV_NRD_NRD_1 | 64 | 66 | PF00675 | 0.600 | 
| CLV_PCSK_KEX2_1 | 409 | 411 | PF00082 | 0.478 | 
| CLV_PCSK_KEX2_1 | 64 | 66 | PF00082 | 0.503 | 
| CLV_PCSK_PC1ET2_1 | 409 | 411 | PF00082 | 0.478 | 
| CLV_PCSK_SKI1_1 | 367 | 371 | PF00082 | 0.313 | 
| DEG_COP1_1 | 138 | 148 | PF00400 | 0.673 | 
| DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.674 | 
| DEG_SCF_FBW7_1 | 53 | 59 | PF00400 | 0.681 | 
| DEG_SPOP_SBC_1 | 120 | 124 | PF00917 | 0.774 | 
| DEG_SPOP_SBC_1 | 44 | 48 | PF00917 | 0.792 | 
| DOC_CKS1_1 | 53 | 58 | PF01111 | 0.683 | 
| DOC_CYCLIN_RxL_1 | 153 | 164 | PF00134 | 0.546 | 
| DOC_MAPK_MEF2A_6 | 367 | 376 | PF00069 | 0.313 | 
| DOC_PP2B_LxvP_1 | 320 | 323 | PF13499 | 0.522 | 
| DOC_PP2B_LxvP_1 | 347 | 350 | PF13499 | 0.526 | 
| DOC_USP7_MATH_1 | 105 | 109 | PF00917 | 0.756 | 
| DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.723 | 
| DOC_USP7_MATH_1 | 144 | 148 | PF00917 | 0.645 | 
| DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.733 | 
| DOC_USP7_MATH_1 | 31 | 35 | PF00917 | 0.782 | 
| DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.480 | 
| DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.699 | 
| DOC_USP7_MATH_1 | 56 | 60 | PF00917 | 0.784 | 
| DOC_USP7_MATH_1 | 81 | 85 | PF00917 | 0.755 | 
| DOC_USP7_MATH_1 | 97 | 101 | PF00917 | 0.696 | 
| DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.740 | 
| DOC_WW_Pin1_4 | 21 | 26 | PF00397 | 0.659 | 
| DOC_WW_Pin1_4 | 278 | 283 | PF00397 | 0.474 | 
| DOC_WW_Pin1_4 | 52 | 57 | PF00397 | 0.767 | 
| DOC_WW_Pin1_4 | 83 | 88 | PF00397 | 0.753 | 
| LIG_14-3-3_CanoR_1 | 247 | 253 | PF00244 | 0.725 | 
| LIG_14-3-3_CanoR_1 | 319 | 323 | PF00244 | 0.574 | 
| LIG_14-3-3_CanoR_1 | 324 | 330 | PF00244 | 0.509 | 
| LIG_Actin_WH2_2 | 209 | 227 | PF00022 | 0.517 | 
| LIG_CSL_BTD_1 | 347 | 350 | PF09270 | 0.526 | 
| LIG_EH1_1 | 354 | 362 | PF00400 | 0.458 | 
| LIG_FHA_1 | 13 | 19 | PF00498 | 0.792 | 
| LIG_FHA_1 | 140 | 146 | PF00498 | 0.715 | 
| LIG_FHA_1 | 155 | 161 | PF00498 | 0.506 | 
| LIG_FHA_1 | 278 | 284 | PF00498 | 0.554 | 
| LIG_FHA_1 | 288 | 294 | PF00498 | 0.475 | 
| LIG_FHA_1 | 380 | 386 | PF00498 | 0.335 | 
| LIG_FHA_1 | 84 | 90 | PF00498 | 0.709 | 
| LIG_FHA_2 | 129 | 135 | PF00498 | 0.761 | 
| LIG_FHA_2 | 202 | 208 | PF00498 | 0.609 | 
| LIG_FHA_2 | 224 | 230 | PF00498 | 0.558 | 
| LIG_FHA_2 | 247 | 253 | PF00498 | 0.709 | 
| LIG_FHA_2 | 40 | 46 | PF00498 | 0.688 | 
| LIG_GBD_Chelix_1 | 372 | 380 | PF00786 | 0.453 | 
| LIG_LIR_Apic_2 | 345 | 351 | PF02991 | 0.527 | 
| LIG_LIR_Gen_1 | 147 | 155 | PF02991 | 0.537 | 
| LIG_LIR_Gen_1 | 15 | 25 | PF02991 | 0.655 | 
| LIG_LIR_Gen_1 | 204 | 214 | PF02991 | 0.643 | 
| LIG_LIR_Gen_1 | 354 | 361 | PF02991 | 0.503 | 
| LIG_LIR_Nem_3 | 147 | 151 | PF02991 | 0.545 | 
| LIG_LIR_Nem_3 | 15 | 20 | PF02991 | 0.660 | 
| LIG_LIR_Nem_3 | 204 | 209 | PF02991 | 0.638 | 
| LIG_LIR_Nem_3 | 266 | 271 | PF02991 | 0.321 | 
| LIG_LIR_Nem_3 | 354 | 358 | PF02991 | 0.457 | 
| LIG_Pex14_1 | 274 | 278 | PF04695 | 0.471 | 
| LIG_SH2_CRK | 180 | 184 | PF00017 | 0.563 | 
| LIG_SH2_CRK | 206 | 210 | PF00017 | 0.555 | 
| LIG_SH2_CRK | 337 | 341 | PF00017 | 0.452 | 
| LIG_SH2_NCK_1 | 67 | 71 | PF00017 | 0.736 | 
| LIG_SH2_STAP1 | 206 | 210 | PF00017 | 0.639 | 
| LIG_SH2_STAP1 | 368 | 372 | PF00017 | 0.453 | 
| LIG_SH2_STAP1 | 67 | 71 | PF00017 | 0.736 | 
| LIG_SH3_3 | 50 | 56 | PF00018 | 0.749 | 
| LIG_TRAF2_1 | 131 | 134 | PF00917 | 0.799 | 
| LIG_TYR_ITIM | 335 | 340 | PF00017 | 0.453 | 
| LIG_WRC_WIRS_1 | 145 | 150 | PF05994 | 0.602 | 
| MOD_CK1_1 | 122 | 128 | PF00069 | 0.764 | 
| MOD_CK1_1 | 246 | 252 | PF00069 | 0.718 | 
| MOD_CK1_1 | 296 | 302 | PF00069 | 0.473 | 
| MOD_CK1_1 | 34 | 40 | PF00069 | 0.745 | 
| MOD_CK1_1 | 43 | 49 | PF00069 | 0.704 | 
| MOD_CK1_1 | 59 | 65 | PF00069 | 0.822 | 
| MOD_CK1_1 | 69 | 75 | PF00069 | 0.725 | 
| MOD_CK2_1 | 122 | 128 | PF00069 | 0.770 | 
| MOD_CK2_1 | 144 | 150 | PF00069 | 0.631 | 
| MOD_CK2_1 | 223 | 229 | PF00069 | 0.554 | 
| MOD_CK2_1 | 246 | 252 | PF00069 | 0.714 | 
| MOD_Cter_Amidation | 407 | 410 | PF01082 | 0.478 | 
| MOD_GlcNHglycan | 116 | 120 | PF01048 | 0.465 | 
| MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.482 | 
| MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.464 | 
| MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.448 | 
| MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.453 | 
| MOD_GlcNHglycan | 295 | 298 | PF01048 | 0.761 | 
| MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.678 | 
| MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.494 | 
| MOD_GlcNHglycan | 393 | 396 | PF01048 | 0.446 | 
| MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.612 | 
| MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.516 | 
| MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.628 | 
| MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.460 | 
| MOD_GSK3_1 | 115 | 122 | PF00069 | 0.757 | 
| MOD_GSK3_1 | 19 | 26 | PF00069 | 0.749 | 
| MOD_GSK3_1 | 243 | 250 | PF00069 | 0.684 | 
| MOD_GSK3_1 | 283 | 290 | PF00069 | 0.485 | 
| MOD_GSK3_1 | 338 | 345 | PF00069 | 0.463 | 
| MOD_GSK3_1 | 36 | 43 | PF00069 | 0.628 | 
| MOD_GSK3_1 | 52 | 59 | PF00069 | 0.827 | 
| MOD_GSK3_1 | 65 | 72 | PF00069 | 0.699 | 
| MOD_GSK3_1 | 77 | 84 | PF00069 | 0.710 | 
| MOD_N-GLC_1 | 202 | 207 | PF02516 | 0.441 | 
| MOD_NEK2_1 | 19 | 24 | PF00069 | 0.771 | 
| MOD_NEK2_1 | 243 | 248 | PF00069 | 0.732 | 
| MOD_NEK2_1 | 277 | 282 | PF00069 | 0.518 | 
| MOD_NEK2_1 | 360 | 365 | PF00069 | 0.475 | 
| MOD_NEK2_2 | 56 | 61 | PF00069 | 0.677 | 
| MOD_PIKK_1 | 299 | 305 | PF00454 | 0.427 | 
| MOD_PIKK_1 | 7 | 13 | PF00454 | 0.731 | 
| MOD_PKA_2 | 128 | 134 | PF00069 | 0.695 | 
| MOD_PKA_2 | 246 | 252 | PF00069 | 0.734 | 
| MOD_PKA_2 | 318 | 324 | PF00069 | 0.578 | 
| MOD_PKA_2 | 402 | 408 | PF00069 | 0.673 | 
| MOD_Plk_1 | 202 | 208 | PF00069 | 0.641 | 
| MOD_Plk_2-3 | 128 | 134 | PF00069 | 0.713 | 
| MOD_Plk_4 | 31 | 37 | PF00069 | 0.678 | 
| MOD_Plk_4 | 379 | 385 | PF00069 | 0.335 | 
| MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.740 | 
| MOD_ProDKin_1 | 21 | 27 | PF00069 | 0.660 | 
| MOD_ProDKin_1 | 278 | 284 | PF00069 | 0.477 | 
| MOD_ProDKin_1 | 52 | 58 | PF00069 | 0.766 | 
| MOD_ProDKin_1 | 83 | 89 | PF00069 | 0.753 | 
| MOD_SUMO_rev_2 | 128 | 136 | PF00179 | 0.795 | 
| TRG_DiLeu_BaEn_1 | 252 | 257 | PF01217 | 0.655 | 
| TRG_ENDOCYTIC_2 | 152 | 155 | PF00928 | 0.529 | 
| TRG_ENDOCYTIC_2 | 180 | 183 | PF00928 | 0.565 | 
| TRG_ENDOCYTIC_2 | 206 | 209 | PF00928 | 0.552 | 
| TRG_ENDOCYTIC_2 | 337 | 340 | PF00928 | 0.452 | 
| TRG_NES_CRM1_1 | 150 | 164 | PF08389 | 0.639 | 
| TRG_Pf-PMV_PEXEL_1 | 181 | 186 | PF00026 | 0.377 | 
| Protein | Taxonomy | Sequence identity | Coverage | 
|---|---|---|---|
| A0A0N1ILA2 | Leptomonas seymouri | 48% | 90% | 
| A4H529 | Leishmania braziliensis | 72% | 100% | 
| A4HTA3 | Leishmania infantum | 100% | 100% | 
| E9AL92 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% | 
| Q4QIL2 | Leishmania major | 90% | 100% |