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: 19 |
NetGPI | no | yes: 0, no: 19 |
Related structures:
AlphaFold database: Q4QBN4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 149 | 151 | PF00675 | 0.379 |
CLV_NRD_NRD_1 | 348 | 350 | PF00675 | 0.410 |
CLV_NRD_NRD_1 | 44 | 46 | PF00675 | 0.323 |
CLV_NRD_NRD_1 | 5 | 7 | PF00675 | 0.539 |
CLV_PCSK_KEX2_1 | 149 | 151 | PF00082 | 0.393 |
CLV_PCSK_KEX2_1 | 348 | 350 | PF00082 | 0.452 |
CLV_PCSK_KEX2_1 | 44 | 46 | PF00082 | 0.324 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 403 | 407 | PF00082 | 0.472 |
DEG_APCC_DBOX_1 | 379 | 387 | PF00400 | 0.487 |
DEG_APCC_DBOX_1 | 5 | 13 | PF00400 | 0.298 |
DEG_ODPH_VHL_1 | 84 | 97 | PF01847 | 0.406 |
DEG_SPOP_SBC_1 | 199 | 203 | PF00917 | 0.247 |
DOC_CDC14_PxL_1 | 154 | 162 | PF14671 | 0.247 |
DOC_MAPK_gen_1 | 221 | 229 | PF00069 | 0.476 |
DOC_MAPK_gen_1 | 376 | 385 | PF00069 | 0.505 |
DOC_MAPK_gen_1 | 44 | 52 | PF00069 | 0.321 |
DOC_MAPK_gen_1 | 5 | 11 | PF00069 | 0.468 |
DOC_MAPK_gen_1 | 74 | 83 | PF00069 | 0.280 |
DOC_MAPK_HePTP_8 | 375 | 387 | PF00069 | 0.356 |
DOC_MAPK_MEF2A_6 | 221 | 229 | PF00069 | 0.528 |
DOC_MAPK_MEF2A_6 | 313 | 321 | PF00069 | 0.285 |
DOC_MAPK_MEF2A_6 | 378 | 387 | PF00069 | 0.539 |
DOC_MAPK_MEF2A_6 | 44 | 52 | PF00069 | 0.364 |
DOC_PP1_RVXF_1 | 400 | 407 | PF00149 | 0.329 |
DOC_PP1_RVXF_1 | 6 | 12 | PF00149 | 0.287 |
DOC_PP2B_LxvP_1 | 155 | 158 | PF13499 | 0.230 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.464 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.318 |
DOC_USP7_MATH_1 | 276 | 280 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 301 | 305 | PF00917 | 0.472 |
DOC_USP7_MATH_1 | 328 | 332 | PF00917 | 0.505 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 388 | 392 | PF00917 | 0.597 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.426 |
DOC_WW_Pin1_4 | 164 | 169 | PF00397 | 0.448 |
LIG_14-3-3_CanoR_1 | 121 | 127 | PF00244 | 0.302 |
LIG_14-3-3_CanoR_1 | 137 | 145 | PF00244 | 0.147 |
LIG_14-3-3_CanoR_1 | 200 | 208 | PF00244 | 0.381 |
LIG_14-3-3_CanoR_1 | 348 | 352 | PF00244 | 0.424 |
LIG_14-3-3_CanoR_1 | 409 | 414 | PF00244 | 0.451 |
LIG_14-3-3_CanoR_1 | 45 | 51 | PF00244 | 0.382 |
LIG_14-3-3_CanoR_1 | 6 | 12 | PF00244 | 0.385 |
LIG_Actin_WH2_2 | 136 | 151 | PF00022 | 0.189 |
LIG_BRCT_BRCA1_1 | 303 | 307 | PF00533 | 0.465 |
LIG_BRCT_BRCA1_1 | 52 | 56 | PF00533 | 0.311 |
LIG_Clathr_ClatBox_1 | 311 | 315 | PF01394 | 0.369 |
LIG_CtBP_PxDLS_1 | 231 | 235 | PF00389 | 0.405 |
LIG_eIF4E_1 | 91 | 97 | PF01652 | 0.353 |
LIG_FHA_1 | 348 | 354 | PF00498 | 0.326 |
LIG_FHA_2 | 208 | 214 | PF00498 | 0.319 |
LIG_FHA_2 | 394 | 400 | PF00498 | 0.362 |
LIG_IRF3_LxIS_1 | 48 | 53 | PF10401 | 0.397 |
LIG_LIR_Gen_1 | 64 | 70 | PF02991 | 0.325 |
LIG_LIR_Gen_1 | 78 | 87 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 250 | 256 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 64 | 68 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 78 | 83 | PF02991 | 0.332 |
LIG_Pex14_2 | 352 | 356 | PF04695 | 0.436 |
LIG_RPA_C_Fungi | 404 | 416 | PF08784 | 0.290 |
LIG_SH2_CRK | 254 | 258 | PF00017 | 0.339 |
LIG_SH2_CRK | 80 | 84 | PF00017 | 0.416 |
LIG_SH2_SRC | 91 | 94 | PF00017 | 0.353 |
LIG_SH2_STAP1 | 122 | 126 | PF00017 | 0.213 |
LIG_SH2_STAT3 | 417 | 420 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 264 | 267 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 293 | 296 | PF00017 | 0.316 |
LIG_SH2_STAT5 | 333 | 336 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 351 | 354 | PF00017 | 0.269 |
LIG_SH2_STAT5 | 91 | 94 | PF00017 | 0.385 |
LIG_SH3_2 | 39 | 44 | PF14604 | 0.438 |
LIG_SH3_3 | 225 | 231 | PF00018 | 0.442 |
LIG_SH3_3 | 36 | 42 | PF00018 | 0.475 |
LIG_SH3_3 | 382 | 388 | PF00018 | 0.450 |
LIG_SH3_3 | 80 | 86 | PF00018 | 0.353 |
LIG_SUMO_SIM_anti_2 | 315 | 320 | PF11976 | 0.261 |
LIG_SUMO_SIM_anti_2 | 381 | 387 | PF11976 | 0.373 |
LIG_SUMO_SIM_par_1 | 315 | 320 | PF11976 | 0.268 |
LIG_UBA3_1 | 214 | 221 | PF00899 | 0.400 |
LIG_WRC_WIRS_1 | 151 | 156 | PF05994 | 0.415 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.391 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.247 |
MOD_CK1_1 | 279 | 285 | PF00069 | 0.645 |
MOD_CK1_1 | 295 | 301 | PF00069 | 0.319 |
MOD_CK2_1 | 200 | 206 | PF00069 | 0.358 |
MOD_CK2_1 | 395 | 401 | PF00069 | 0.496 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.470 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.452 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.418 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.390 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.418 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.376 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.655 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.533 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.579 |
MOD_GlcNHglycan | 390 | 393 | PF01048 | 0.574 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.541 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.314 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.370 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.355 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.381 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.428 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.625 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.627 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.401 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.365 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.282 |
MOD_N-GLC_1 | 242 | 247 | PF02516 | 0.625 |
MOD_N-GLC_1 | 46 | 51 | PF02516 | 0.375 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.361 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.389 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.380 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.380 |
MOD_NEK2_1 | 95 | 100 | PF00069 | 0.410 |
MOD_NEK2_2 | 72 | 77 | PF00069 | 0.287 |
MOD_PIKK_1 | 169 | 175 | PF00454 | 0.222 |
MOD_PIKK_1 | 279 | 285 | PF00454 | 0.661 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.399 |
MOD_PKA_2 | 272 | 278 | PF00069 | 0.464 |
MOD_PKA_2 | 279 | 285 | PF00069 | 0.576 |
MOD_PKA_2 | 347 | 353 | PF00069 | 0.436 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.378 |
MOD_Plk_1 | 295 | 301 | PF00069 | 0.393 |
MOD_Plk_1 | 46 | 52 | PF00069 | 0.370 |
MOD_Plk_4 | 150 | 156 | PF00069 | 0.400 |
MOD_Plk_4 | 207 | 213 | PF00069 | 0.376 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.289 |
MOD_Plk_4 | 7 | 13 | PF00069 | 0.373 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.426 |
MOD_ProDKin_1 | 164 | 170 | PF00069 | 0.448 |
MOD_SUMO_rev_2 | 213 | 222 | PF00179 | 0.348 |
MOD_SUMO_rev_2 | 371 | 377 | PF00179 | 0.465 |
MOD_SUMO_rev_2 | 397 | 405 | PF00179 | 0.366 |
MOD_SUMO_rev_2 | 53 | 61 | PF00179 | 0.400 |
TRG_ENDOCYTIC_2 | 264 | 267 | PF00928 | 0.349 |
TRG_ENDOCYTIC_2 | 80 | 83 | PF00928 | 0.337 |
TRG_ER_diArg_1 | 148 | 150 | PF00400 | 0.393 |
TRG_ER_diArg_1 | 347 | 349 | PF00400 | 0.436 |
TRG_ER_diArg_1 | 4 | 6 | PF00400 | 0.518 |
TRG_NES_CRM1_1 | 206 | 219 | PF08389 | 0.338 |
TRG_NES_CRM1_1 | 309 | 320 | PF08389 | 0.357 |
TRG_Pf-PMV_PEXEL_1 | 370 | 374 | PF00026 | 0.506 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0M2 | Leptomonas seymouri | 37% | 94% |
A0A0N1PFX0 | Leptomonas seymouri | 57% | 94% |
A0A0S4J8Q0 | Bodo saltans | 35% | 100% |
A0A0S4JLW1 | Bodo saltans | 24% | 96% |
A0A1X0NTE2 | Trypanosomatidae | 41% | 100% |
A0A1X0NX03 | Trypanosomatidae | 23% | 100% |
A0A3Q8IFK3 | Leishmania donovani | 46% | 91% |
A0A3S7WXD8 | Leishmania donovani | 93% | 100% |
A0A422NHR8 | Trypanosoma rangeli | 41% | 100% |
A4HCF4 | Leishmania braziliensis | 45% | 91% |
A4HZY3 | Leishmania infantum | 46% | 91% |
A4HZY4 | Leishmania infantum | 93% | 100% |
C9ZSM3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
C9ZVB8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 100% |
E9AVU4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 91% |
E9AVU5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 99% |
Q4QBN5 | Leishmania major | 48% | 92% |
V5BVW3 | Trypanosoma cruzi | 40% | 100% |