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: 18 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 273 | 277 | PF00656 | 0.538 |
CLV_C14_Caspase3-7 | 97 | 101 | PF00656 | 0.421 |
CLV_MEL_PAP_1 | 425 | 431 | PF00089 | 0.400 |
CLV_NRD_NRD_1 | 184 | 186 | PF00675 | 0.414 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.629 |
CLV_NRD_NRD_1 | 427 | 429 | PF00675 | 0.414 |
CLV_PCSK_KEX2_1 | 184 | 186 | PF00082 | 0.416 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.571 |
CLV_PCSK_KEX2_1 | 427 | 429 | PF00082 | 0.414 |
CLV_PCSK_SKI1_1 | 152 | 156 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 241 | 245 | PF00082 | 0.542 |
CLV_PCSK_SKI1_1 | 387 | 391 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 99 | 103 | PF00082 | 0.381 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.553 |
DOC_CYCLIN_RxL_1 | 382 | 393 | PF00134 | 0.500 |
DOC_MAPK_MEF2A_6 | 140 | 148 | PF00069 | 0.303 |
DOC_MAPK_MEF2A_6 | 211 | 218 | PF00069 | 0.557 |
DOC_PP2B_LxvP_1 | 195 | 198 | PF13499 | 0.605 |
DOC_PP4_FxxP_1 | 131 | 134 | PF00568 | 0.492 |
DOC_PP4_FxxP_1 | 191 | 194 | PF00568 | 0.530 |
DOC_PP4_FxxP_1 | 37 | 40 | PF00568 | 0.371 |
DOC_PP4_FxxP_1 | 65 | 68 | PF00568 | 0.403 |
DOC_USP7_MATH_1 | 101 | 105 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 177 | 181 | PF00917 | 0.494 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 366 | 370 | PF00917 | 0.540 |
DOC_WW_Pin1_4 | 154 | 159 | PF00397 | 0.418 |
DOC_WW_Pin1_4 | 178 | 183 | PF00397 | 0.370 |
DOC_WW_Pin1_4 | 224 | 229 | PF00397 | 0.521 |
DOC_WW_Pin1_4 | 369 | 374 | PF00397 | 0.561 |
LIG_14-3-3_CanoR_1 | 185 | 195 | PF00244 | 0.462 |
LIG_14-3-3_CanoR_1 | 211 | 217 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 231 | 239 | PF00244 | 0.282 |
LIG_14-3-3_CanoR_1 | 241 | 247 | PF00244 | 0.477 |
LIG_Actin_WH2_2 | 84 | 101 | PF00022 | 0.485 |
LIG_APCC_ABBA_1 | 345 | 350 | PF00400 | 0.522 |
LIG_BRCT_BRCA1_1 | 265 | 269 | PF00533 | 0.459 |
LIG_deltaCOP1_diTrp_1 | 400 | 406 | PF00928 | 0.369 |
LIG_deltaCOP1_diTrp_1 | 84 | 90 | PF00928 | 0.403 |
LIG_FHA_1 | 100 | 106 | PF00498 | 0.482 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.385 |
LIG_FHA_1 | 374 | 380 | PF00498 | 0.679 |
LIG_FHA_1 | 384 | 390 | PF00498 | 0.392 |
LIG_FHA_2 | 230 | 236 | PF00498 | 0.398 |
LIG_FHA_2 | 243 | 249 | PF00498 | 0.324 |
LIG_FHA_2 | 57 | 63 | PF00498 | 0.348 |
LIG_IBAR_NPY_1 | 93 | 95 | PF08397 | 0.443 |
LIG_LIR_Apic_2 | 129 | 134 | PF02991 | 0.512 |
LIG_LIR_Apic_2 | 189 | 194 | PF02991 | 0.416 |
LIG_LIR_Apic_2 | 224 | 228 | PF02991 | 0.638 |
LIG_LIR_Apic_2 | 62 | 68 | PF02991 | 0.401 |
LIG_LIR_Gen_1 | 257 | 267 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 398 | 406 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 118 | 124 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 257 | 263 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 398 | 404 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 424 | 429 | PF02991 | 0.400 |
LIG_NRBOX | 238 | 244 | PF00104 | 0.363 |
LIG_PDZ_Class_3 | 440 | 445 | PF00595 | 0.470 |
LIG_Pex14_1 | 86 | 90 | PF04695 | 0.388 |
LIG_Pex14_2 | 397 | 401 | PF04695 | 0.376 |
LIG_PTB_Apo_2 | 405 | 412 | PF02174 | 0.385 |
LIG_PTB_Phospho_1 | 405 | 411 | PF10480 | 0.389 |
LIG_Rb_LxCxE_1 | 102 | 118 | PF01857 | 0.420 |
LIG_SH2_CRK | 225 | 229 | PF00017 | 0.526 |
LIG_SH2_NCK_1 | 225 | 229 | PF00017 | 0.526 |
LIG_SH2_NCK_1 | 256 | 260 | PF00017 | 0.336 |
LIG_SH2_STAP1 | 256 | 260 | PF00017 | 0.418 |
LIG_SH2_STAT3 | 74 | 77 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 321 | 324 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 33 | 36 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 46 | 49 | PF00017 | 0.344 |
LIG_SH3_3 | 141 | 147 | PF00018 | 0.479 |
LIG_SH3_3 | 37 | 43 | PF00018 | 0.371 |
LIG_SH3_3 | 88 | 94 | PF00018 | 0.433 |
LIG_SUMO_SIM_par_1 | 79 | 85 | PF11976 | 0.386 |
LIG_TRAF2_1 | 329 | 332 | PF00917 | 0.447 |
LIG_TRAF2_1 | 94 | 97 | PF00917 | 0.409 |
LIG_UBA3_1 | 288 | 294 | PF00899 | 0.427 |
LIG_WRC_WIRS_1 | 128 | 133 | PF05994 | 0.511 |
LIG_WRC_WIRS_1 | 243 | 248 | PF05994 | 0.403 |
MOD_CDC14_SPxK_1 | 372 | 375 | PF00782 | 0.382 |
MOD_CDK_SPxK_1 | 178 | 184 | PF00069 | 0.373 |
MOD_CDK_SPxK_1 | 369 | 375 | PF00069 | 0.372 |
MOD_CDK_SPxxK_3 | 154 | 161 | PF00069 | 0.468 |
MOD_CDK_SPxxK_3 | 178 | 185 | PF00069 | 0.374 |
MOD_CDK_SPxxK_3 | 224 | 231 | PF00069 | 0.390 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.550 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.643 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.525 |
MOD_CK1_1 | 258 | 264 | PF00069 | 0.455 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.372 |
MOD_CK1_1 | 313 | 319 | PF00069 | 0.568 |
MOD_CK1_1 | 369 | 375 | PF00069 | 0.609 |
MOD_CK1_1 | 393 | 399 | PF00069 | 0.465 |
MOD_CK2_1 | 230 | 236 | PF00069 | 0.502 |
MOD_CK2_1 | 242 | 248 | PF00069 | 0.346 |
MOD_CK2_1 | 353 | 359 | PF00069 | 0.455 |
MOD_CK2_1 | 415 | 421 | PF00069 | 0.420 |
MOD_CK2_1 | 56 | 62 | PF00069 | 0.337 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.557 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.424 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.379 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.429 |
MOD_GlcNHglycan | 283 | 286 | PF01048 | 0.433 |
MOD_GlcNHglycan | 289 | 292 | PF01048 | 0.466 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.483 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.377 |
MOD_GlcNHglycan | 369 | 372 | PF01048 | 0.599 |
MOD_GlcNHglycan | 392 | 395 | PF01048 | 0.452 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.457 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.513 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.462 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.403 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.403 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.497 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.440 |
MOD_LATS_1 | 22 | 28 | PF00433 | 0.417 |
MOD_N-GLC_1 | 171 | 176 | PF02516 | 0.455 |
MOD_N-GLC_1 | 267 | 272 | PF02516 | 0.384 |
MOD_N-GLC_1 | 281 | 286 | PF02516 | 0.432 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.391 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.321 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.202 |
MOD_NEK2_1 | 311 | 316 | PF00069 | 0.521 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.446 |
MOD_NEK2_1 | 390 | 395 | PF00069 | 0.448 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.370 |
MOD_PKA_2 | 12 | 18 | PF00069 | 0.478 |
MOD_PKA_2 | 230 | 236 | PF00069 | 0.336 |
MOD_PKA_2 | 335 | 341 | PF00069 | 0.387 |
MOD_Plk_1 | 171 | 177 | PF00069 | 0.464 |
MOD_Plk_2-3 | 353 | 359 | PF00069 | 0.399 |
MOD_Plk_4 | 101 | 107 | PF00069 | 0.382 |
MOD_Plk_4 | 28 | 34 | PF00069 | 0.385 |
MOD_Plk_4 | 421 | 427 | PF00069 | 0.407 |
MOD_ProDKin_1 | 154 | 160 | PF00069 | 0.414 |
MOD_ProDKin_1 | 178 | 184 | PF00069 | 0.373 |
MOD_ProDKin_1 | 224 | 230 | PF00069 | 0.519 |
MOD_ProDKin_1 | 369 | 375 | PF00069 | 0.562 |
MOD_SUMO_rev_2 | 233 | 240 | PF00179 | 0.398 |
MOD_SUMO_rev_2 | 350 | 357 | PF00179 | 0.458 |
MOD_SUMO_rev_2 | 96 | 101 | PF00179 | 0.464 |
TRG_DiLeu_BaLyEn_6 | 238 | 243 | PF01217 | 0.477 |
TRG_ENDOCYTIC_2 | 121 | 124 | PF00928 | 0.445 |
TRG_ENDOCYTIC_2 | 95 | 98 | PF00928 | 0.553 |
TRG_ER_diArg_1 | 184 | 186 | PF00400 | 0.402 |
TRG_ER_diArg_1 | 2 | 4 | PF00400 | 0.638 |
TRG_ER_diArg_1 | 374 | 377 | PF00400 | 0.395 |
TRG_ER_diArg_1 | 426 | 428 | PF00400 | 0.416 |
TRG_Pf-PMV_PEXEL_1 | 107 | 111 | PF00026 | 0.473 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IGW5 | Leptomonas seymouri | 70% | 100% |
A0A1X0NU50 | Trypanosomatidae | 51% | 99% |
A0A3R7M6E1 | Trypanosoma rangeli | 51% | 100% |
A0A3S7WXB0 | Leishmania donovani | 93% | 100% |
A4HCI5 | Leishmania braziliensis | 82% | 100% |
A4I006 | Leishmania infantum | 93% | 100% |
C9ZSQ8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 99% |
Q4QBK0 | Leishmania major | 94% | 100% |
V5B8Q9 | Trypanosoma cruzi | 49% | 98% |