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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: Q4Q8W3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 111 | 113 | PF00675 | 0.593 |
CLV_NRD_NRD_1 | 114 | 116 | PF00675 | 0.586 |
CLV_NRD_NRD_1 | 135 | 137 | PF00675 | 0.475 |
CLV_NRD_NRD_1 | 17 | 19 | PF00675 | 0.715 |
CLV_NRD_NRD_1 | 339 | 341 | PF00675 | 0.467 |
CLV_NRD_NRD_1 | 83 | 85 | PF00675 | 0.571 |
CLV_PCSK_FUR_1 | 112 | 116 | PF00082 | 0.545 |
CLV_PCSK_KEX2_1 | 113 | 115 | PF00082 | 0.574 |
CLV_PCSK_KEX2_1 | 135 | 137 | PF00082 | 0.456 |
CLV_PCSK_KEX2_1 | 17 | 19 | PF00082 | 0.665 |
CLV_PCSK_KEX2_1 | 75 | 77 | PF00082 | 0.558 |
CLV_PCSK_PC1ET2_1 | 113 | 115 | PF00082 | 0.600 |
CLV_PCSK_PC1ET2_1 | 75 | 77 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 290 | 294 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 349 | 353 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 396 | 400 | PF00082 | 0.476 |
DEG_APCC_DBOX_1 | 357 | 365 | PF00400 | 0.438 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.567 |
DEG_SPOP_SBC_1 | 154 | 158 | PF00917 | 0.609 |
DOC_CDC14_PxL_1 | 332 | 340 | PF14671 | 0.389 |
DOC_CYCLIN_yCln2_LP_2 | 40 | 46 | PF00134 | 0.591 |
DOC_MAPK_gen_1 | 112 | 120 | PF00069 | 0.567 |
DOC_MAPK_gen_1 | 17 | 25 | PF00069 | 0.731 |
DOC_MAPK_gen_1 | 75 | 83 | PF00069 | 0.651 |
DOC_MAPK_MEF2A_6 | 247 | 254 | PF00069 | 0.564 |
DOC_PP1_RVXF_1 | 360 | 367 | PF00149 | 0.383 |
DOC_PP4_FxxP_1 | 223 | 226 | PF00568 | 0.356 |
DOC_WW_Pin1_4 | 102 | 107 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 178 | 183 | PF00397 | 0.485 |
DOC_WW_Pin1_4 | 238 | 243 | PF00397 | 0.354 |
DOC_WW_Pin1_4 | 308 | 313 | PF00397 | 0.475 |
LIG_14-3-3_CanoR_1 | 17 | 26 | PF00244 | 0.709 |
LIG_14-3-3_CanoR_1 | 396 | 405 | PF00244 | 0.655 |
LIG_Actin_WH2_2 | 144 | 162 | PF00022 | 0.576 |
LIG_Actin_WH2_2 | 347 | 364 | PF00022 | 0.438 |
LIG_deltaCOP1_diTrp_1 | 263 | 269 | PF00928 | 0.358 |
LIG_deltaCOP1_diTrp_1 | 343 | 350 | PF00928 | 0.413 |
LIG_deltaCOP1_diTrp_1 | 382 | 390 | PF00928 | 0.326 |
LIG_FHA_1 | 18 | 24 | PF00498 | 0.639 |
LIG_FHA_1 | 301 | 307 | PF00498 | 0.347 |
LIG_FHA_2 | 289 | 295 | PF00498 | 0.368 |
LIG_LIR_Gen_1 | 198 | 206 | PF02991 | 0.341 |
LIG_LIR_Gen_1 | 214 | 223 | PF02991 | 0.305 |
LIG_LIR_Gen_1 | 382 | 390 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 131 | 137 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 198 | 204 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 214 | 218 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 311 | 316 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 343 | 348 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 382 | 386 | PF02991 | 0.350 |
LIG_LYPXL_yS_3 | 199 | 202 | PF13949 | 0.357 |
LIG_PDZ_Class_2 | 400 | 405 | PF00595 | 0.649 |
LIG_Pex14_1 | 344 | 348 | PF04695 | 0.432 |
LIG_PTB_Apo_2 | 360 | 367 | PF02174 | 0.383 |
LIG_Rb_LxCxE_1 | 77 | 93 | PF01857 | 0.559 |
LIG_REV1ctd_RIR_1 | 220 | 225 | PF16727 | 0.344 |
LIG_SH2_CRK | 185 | 189 | PF00017 | 0.365 |
LIG_SH2_CRK | 201 | 205 | PF00017 | 0.272 |
LIG_SH2_CRK | 326 | 330 | PF00017 | 0.507 |
LIG_SH2_NCK_1 | 185 | 189 | PF00017 | 0.394 |
LIG_SH2_PTP2 | 141 | 144 | PF00017 | 0.564 |
LIG_SH2_PTP2 | 286 | 289 | PF00017 | 0.349 |
LIG_SH2_SRC | 141 | 144 | PF00017 | 0.484 |
LIG_SH2_SRC | 334 | 337 | PF00017 | 0.485 |
LIG_SH2_STAP1 | 185 | 189 | PF00017 | 0.463 |
LIG_SH2_STAP1 | 229 | 233 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 141 | 144 | PF00017 | 0.545 |
LIG_SH2_STAT5 | 286 | 289 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 334 | 337 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 389 | 392 | PF00017 | 0.375 |
LIG_SH3_3 | 115 | 121 | PF00018 | 0.538 |
LIG_SH3_3 | 148 | 154 | PF00018 | 0.610 |
LIG_SH3_3 | 194 | 200 | PF00018 | 0.393 |
LIG_SH3_3 | 28 | 34 | PF00018 | 0.778 |
LIG_SH3_3 | 309 | 315 | PF00018 | 0.474 |
LIG_SH3_3 | 330 | 336 | PF00018 | 0.335 |
LIG_SH3_3 | 354 | 360 | PF00018 | 0.538 |
LIG_SUMO_SIM_par_1 | 201 | 207 | PF11976 | 0.327 |
LIG_TYR_ITIM | 183 | 188 | PF00017 | 0.433 |
MOD_CDC14_SPxK_1 | 311 | 314 | PF00782 | 0.562 |
MOD_CDK_SPxK_1 | 308 | 314 | PF00069 | 0.474 |
MOD_CK1_1 | 19 | 25 | PF00069 | 0.746 |
MOD_CK2_1 | 288 | 294 | PF00069 | 0.359 |
MOD_CK2_1 | 51 | 57 | PF00069 | 0.660 |
MOD_DYRK1A_RPxSP_1 | 308 | 312 | PF00069 | 0.472 |
MOD_GlcNHglycan | 170 | 174 | PF01048 | 0.462 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.647 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.467 |
MOD_GlcNHglycan | 400 | 403 | PF01048 | 0.583 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.746 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.660 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.697 |
MOD_N-GLC_1 | 129 | 134 | PF02516 | 0.509 |
MOD_N-GLC_1 | 61 | 66 | PF02516 | 0.575 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.585 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.377 |
MOD_NEK2_1 | 306 | 311 | PF00069 | 0.414 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.623 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.641 |
MOD_PIKK_1 | 88 | 94 | PF00454 | 0.528 |
MOD_PIKK_1 | 96 | 102 | PF00454 | 0.582 |
MOD_PK_1 | 61 | 67 | PF00069 | 0.609 |
MOD_PKA_1 | 17 | 23 | PF00069 | 0.627 |
MOD_PKA_2 | 16 | 22 | PF00069 | 0.710 |
MOD_PKA_2 | 47 | 53 | PF00069 | 0.635 |
MOD_Plk_1 | 129 | 135 | PF00069 | 0.465 |
MOD_Plk_1 | 169 | 175 | PF00069 | 0.465 |
MOD_Plk_1 | 61 | 67 | PF00069 | 0.557 |
MOD_Plk_4 | 183 | 189 | PF00069 | 0.387 |
MOD_Plk_4 | 328 | 334 | PF00069 | 0.341 |
MOD_ProDKin_1 | 102 | 108 | PF00069 | 0.630 |
MOD_ProDKin_1 | 178 | 184 | PF00069 | 0.481 |
MOD_ProDKin_1 | 238 | 244 | PF00069 | 0.358 |
MOD_ProDKin_1 | 308 | 314 | PF00069 | 0.474 |
MOD_SUMO_rev_2 | 158 | 166 | PF00179 | 0.536 |
MOD_SUMO_rev_2 | 186 | 195 | PF00179 | 0.480 |
TRG_ENDOCYTIC_2 | 185 | 188 | PF00928 | 0.361 |
TRG_ENDOCYTIC_2 | 199 | 202 | PF00928 | 0.291 |
TRG_ENDOCYTIC_2 | 229 | 232 | PF00928 | 0.421 |
TRG_ENDOCYTIC_2 | 286 | 289 | PF00928 | 0.349 |
TRG_ENDOCYTIC_2 | 326 | 329 | PF00928 | 0.567 |
TRG_ENDOCYTIC_2 | 345 | 348 | PF00928 | 0.410 |
TRG_ENDOCYTIC_2 | 375 | 378 | PF00928 | 0.347 |
TRG_ER_diArg_1 | 111 | 114 | PF00400 | 0.565 |
TRG_ER_diArg_1 | 134 | 136 | PF00400 | 0.473 |
TRG_ER_diArg_1 | 356 | 359 | PF00400 | 0.465 |
TRG_NLS_MonoCore_2 | 111 | 116 | PF00514 | 0.594 |
TRG_NLS_MonoExtN_4 | 112 | 117 | PF00514 | 0.618 |
TRG_Pf-PMV_PEXEL_1 | 396 | 400 | PF00026 | 0.552 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2P2 | Leptomonas seymouri | 86% | 100% |
A0A0S4JRL5 | Bodo saltans | 61% | 100% |
A0A1X0P7G6 | Trypanosomatidae | 68% | 100% |
A0A3S7X061 | Leishmania donovani | 96% | 100% |
A4HF73 | Leishmania braziliensis | 87% | 100% |
A4I2F6 | Leishmania infantum | 96% | 100% |
C9ZX41 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 69% | 100% |
E9AYK9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
V5BI14 | Trypanosoma cruzi | 65% | 100% |