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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: A4HGU8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 290 | 294 | PF00656 | 0.518 |
CLV_C14_Caspase3-7 | 380 | 384 | PF00656 | 0.560 |
CLV_NRD_NRD_1 | 161 | 163 | PF00675 | 0.393 |
CLV_NRD_NRD_1 | 54 | 56 | PF00675 | 0.388 |
CLV_PCSK_FUR_1 | 158 | 162 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 160 | 162 | PF00082 | 0.362 |
CLV_PCSK_KEX2_1 | 188 | 190 | PF00082 | 0.569 |
CLV_PCSK_KEX2_1 | 54 | 56 | PF00082 | 0.388 |
CLV_PCSK_PC1ET2_1 | 160 | 162 | PF00082 | 0.347 |
CLV_PCSK_PC1ET2_1 | 188 | 190 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 118 | 122 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.362 |
CLV_PCSK_SKI1_1 | 371 | 375 | PF00082 | 0.712 |
CLV_PCSK_SKI1_1 | 72 | 76 | PF00082 | 0.337 |
DEG_APCC_DBOX_1 | 160 | 168 | PF00400 | 0.473 |
DEG_APCC_DBOX_1 | 282 | 290 | PF00400 | 0.360 |
DEG_APCC_DBOX_1 | 71 | 79 | PF00400 | 0.337 |
DEG_COP1_1 | 356 | 364 | PF00400 | 0.429 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.418 |
DEG_SCF_FBW7_1 | 350 | 357 | PF00400 | 0.393 |
DOC_CKS1_1 | 103 | 108 | PF01111 | 0.393 |
DOC_CKS1_1 | 351 | 356 | PF01111 | 0.401 |
DOC_CKS1_1 | 361 | 366 | PF01111 | 0.342 |
DOC_CYCLIN_RxL_1 | 158 | 166 | PF00134 | 0.301 |
DOC_CYCLIN_RxL_1 | 52 | 60 | PF00134 | 0.257 |
DOC_MAPK_FxFP_2 | 333 | 336 | PF00069 | 0.498 |
DOC_MAPK_gen_1 | 158 | 167 | PF00069 | 0.437 |
DOC_MAPK_MEF2A_6 | 158 | 167 | PF00069 | 0.319 |
DOC_MAPK_MEF2A_6 | 270 | 279 | PF00069 | 0.413 |
DOC_MAPK_MEF2A_6 | 312 | 319 | PF00069 | 0.337 |
DOC_MAPK_MEF2A_6 | 72 | 79 | PF00069 | 0.362 |
DOC_MAPK_NFAT4_5 | 312 | 320 | PF00069 | 0.335 |
DOC_MAPK_NFAT4_5 | 72 | 80 | PF00069 | 0.362 |
DOC_PP1_RVXF_1 | 53 | 60 | PF00149 | 0.462 |
DOC_PP2B_LxvP_1 | 252 | 255 | PF13499 | 0.391 |
DOC_PP4_FxxP_1 | 180 | 183 | PF00568 | 0.399 |
DOC_PP4_FxxP_1 | 333 | 336 | PF00568 | 0.498 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.356 |
DOC_USP7_MATH_1 | 217 | 221 | PF00917 | 0.349 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 373 | 377 | PF00917 | 0.643 |
DOC_WW_Pin1_4 | 102 | 107 | PF00397 | 0.390 |
DOC_WW_Pin1_4 | 246 | 251 | PF00397 | 0.574 |
DOC_WW_Pin1_4 | 350 | 355 | PF00397 | 0.370 |
DOC_WW_Pin1_4 | 360 | 365 | PF00397 | 0.419 |
DOC_WW_Pin1_4 | 375 | 380 | PF00397 | 0.524 |
DOC_WW_Pin1_4 | 393 | 398 | PF00397 | 0.429 |
LIG_14-3-3_CanoR_1 | 162 | 168 | PF00244 | 0.257 |
LIG_14-3-3_CanoR_1 | 321 | 331 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 371 | 381 | PF00244 | 0.538 |
LIG_Actin_WH2_2 | 59 | 74 | PF00022 | 0.437 |
LIG_APCC_ABBA_1 | 93 | 98 | PF00400 | 0.257 |
LIG_BRCT_BRCA1_1 | 176 | 180 | PF00533 | 0.369 |
LIG_BRCT_BRCA1_1 | 89 | 93 | PF00533 | 0.257 |
LIG_CSL_BTD_1 | 252 | 255 | PF09270 | 0.391 |
LIG_EH1_1 | 63 | 71 | PF00400 | 0.337 |
LIG_eIF4E_1 | 345 | 351 | PF01652 | 0.485 |
LIG_FHA_1 | 103 | 109 | PF00498 | 0.492 |
LIG_FHA_1 | 23 | 29 | PF00498 | 0.472 |
LIG_FHA_2 | 288 | 294 | PF00498 | 0.466 |
LIG_FHA_2 | 361 | 367 | PF00498 | 0.588 |
LIG_FHA_2 | 378 | 384 | PF00498 | 0.496 |
LIG_FHA_2 | 83 | 89 | PF00498 | 0.257 |
LIG_LIR_Apic_2 | 177 | 183 | PF02991 | 0.397 |
LIG_LIR_Gen_1 | 56 | 66 | PF02991 | 0.301 |
LIG_LIR_Gen_1 | 98 | 108 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 334 | 338 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 56 | 62 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 98 | 103 | PF02991 | 0.294 |
LIG_LYPXL_yS_3 | 335 | 338 | PF13949 | 0.542 |
LIG_MYND_1 | 250 | 254 | PF01753 | 0.563 |
LIG_Pex14_1 | 331 | 335 | PF04695 | 0.337 |
LIG_Pex14_2 | 93 | 97 | PF04695 | 0.257 |
LIG_SH2_STAT3 | 86 | 89 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 128 | 131 | PF00017 | 0.286 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 345 | 348 | PF00017 | 0.479 |
LIG_SH3_3 | 356 | 362 | PF00018 | 0.592 |
LIG_SUMO_SIM_par_1 | 75 | 80 | PF11976 | 0.257 |
LIG_TRAF2_1 | 234 | 237 | PF00917 | 0.430 |
LIG_TRAF2_1 | 363 | 366 | PF00917 | 0.596 |
LIG_Vh1_VBS_1 | 5 | 23 | PF01044 | 0.318 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.316 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.256 |
MOD_CK1_1 | 334 | 340 | PF00069 | 0.318 |
MOD_CK1_1 | 372 | 378 | PF00069 | 0.644 |
MOD_CK2_1 | 230 | 236 | PF00069 | 0.417 |
MOD_CK2_1 | 360 | 366 | PF00069 | 0.596 |
MOD_CK2_1 | 387 | 393 | PF00069 | 0.596 |
MOD_CK2_1 | 82 | 88 | PF00069 | 0.257 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.385 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.442 |
MOD_GlcNHglycan | 218 | 222 | PF01048 | 0.346 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.388 |
MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.393 |
MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.692 |
MOD_GlcNHglycan | 371 | 374 | PF01048 | 0.688 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.741 |
MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.720 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.685 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.386 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.288 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.351 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.558 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.629 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.604 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.589 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.615 |
MOD_NEK2_1 | 114 | 119 | PF00069 | 0.268 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.325 |
MOD_NEK2_1 | 174 | 179 | PF00069 | 0.356 |
MOD_NEK2_1 | 230 | 235 | PF00069 | 0.403 |
MOD_NEK2_1 | 322 | 327 | PF00069 | 0.457 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.641 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.437 |
MOD_PK_1 | 26 | 32 | PF00069 | 0.410 |
MOD_PKA_2 | 149 | 155 | PF00069 | 0.330 |
MOD_PKA_2 | 287 | 293 | PF00069 | 0.619 |
MOD_PKA_2 | 320 | 326 | PF00069 | 0.404 |
MOD_Plk_1 | 169 | 175 | PF00069 | 0.473 |
MOD_Plk_1 | 217 | 223 | PF00069 | 0.521 |
MOD_Plk_1 | 26 | 32 | PF00069 | 0.561 |
MOD_Plk_1 | 87 | 93 | PF00069 | 0.257 |
MOD_Plk_4 | 138 | 144 | PF00069 | 0.393 |
MOD_Plk_4 | 163 | 169 | PF00069 | 0.443 |
MOD_Plk_4 | 176 | 182 | PF00069 | 0.454 |
MOD_Plk_4 | 334 | 340 | PF00069 | 0.517 |
MOD_ProDKin_1 | 102 | 108 | PF00069 | 0.390 |
MOD_ProDKin_1 | 246 | 252 | PF00069 | 0.568 |
MOD_ProDKin_1 | 350 | 356 | PF00069 | 0.385 |
MOD_ProDKin_1 | 360 | 366 | PF00069 | 0.493 |
MOD_ProDKin_1 | 375 | 381 | PF00069 | 0.566 |
MOD_ProDKin_1 | 393 | 399 | PF00069 | 0.429 |
TRG_DiLeu_BaLyEn_6 | 73 | 78 | PF01217 | 0.257 |
TRG_ENDOCYTIC_2 | 335 | 338 | PF00928 | 0.506 |
TRG_ER_diArg_1 | 161 | 163 | PF00400 | 0.393 |
TRG_ER_diArg_1 | 282 | 285 | PF00400 | 0.544 |
TRG_NES_CRM1_1 | 349 | 365 | PF08389 | 0.403 |
TRG_NLS_MonoExtN_4 | 158 | 164 | PF00514 | 0.427 |
TRG_Pf-PMV_PEXEL_1 | 26 | 31 | PF00026 | 0.542 |
TRG_Pf-PMV_PEXEL_1 | 262 | 266 | PF00026 | 0.435 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3P6 | Leptomonas seymouri | 44% | 86% |
A0A1X0NR47 | Trypanosomatidae | 31% | 100% |
A0A3Q8IQU6 | Leishmania donovani | 55% | 82% |
A0A3R7K6Z5 | Trypanosoma rangeli | 30% | 100% |
A4I3X6 | Leishmania infantum | 56% | 82% |
D0A944 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9B066 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 51% | 81% |