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: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0005794 | Golgi apparatus | 5 | 1 |
GO:0020016 | ciliary pocket | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: E9AXJ5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 465 | 467 | PF00675 | 0.417 |
CLV_PCSK_KEX2_1 | 465 | 467 | PF00082 | 0.416 |
CLV_PCSK_PC1ET2_1 | 465 | 467 | PF00082 | 0.465 |
CLV_PCSK_SKI1_1 | 304 | 308 | PF00082 | 0.371 |
CLV_PCSK_SKI1_1 | 374 | 378 | PF00082 | 0.271 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.400 |
DOC_ANK_TNKS_1 | 433 | 440 | PF00023 | 0.333 |
DOC_CYCLIN_yCln2_LP_2 | 56 | 62 | PF00134 | 0.292 |
DOC_MAPK_gen_1 | 264 | 272 | PF00069 | 0.566 |
DOC_MAPK_gen_1 | 434 | 442 | PF00069 | 0.231 |
DOC_MAPK_gen_1 | 465 | 476 | PF00069 | 0.659 |
DOC_MAPK_HePTP_8 | 240 | 252 | PF00069 | 0.498 |
DOC_MAPK_MEF2A_6 | 177 | 186 | PF00069 | 0.277 |
DOC_MAPK_MEF2A_6 | 232 | 241 | PF00069 | 0.522 |
DOC_MAPK_MEF2A_6 | 243 | 252 | PF00069 | 0.434 |
DOC_MAPK_MEF2A_6 | 41 | 50 | PF00069 | 0.331 |
DOC_MAPK_MEF2A_6 | 434 | 442 | PF00069 | 0.231 |
DOC_PP1_RVXF_1 | 372 | 379 | PF00149 | 0.471 |
DOC_PP2B_LxvP_1 | 56 | 59 | PF13499 | 0.292 |
DOC_USP7_MATH_1 | 164 | 168 | PF00917 | 0.291 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.451 |
DOC_USP7_UBL2_3 | 222 | 226 | PF12436 | 0.541 |
DOC_WW_Pin1_4 | 155 | 160 | PF00397 | 0.197 |
DOC_WW_Pin1_4 | 294 | 299 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.338 |
LIG_14-3-3_CanoR_1 | 177 | 183 | PF00244 | 0.188 |
LIG_Actin_WH2_2 | 420 | 438 | PF00022 | 0.284 |
LIG_AP2alpha_2 | 331 | 333 | PF02296 | 0.333 |
LIG_BIR_III_2 | 329 | 333 | PF00653 | 0.285 |
LIG_CaM_IQ_9 | 251 | 266 | PF13499 | 0.626 |
LIG_EH1_1 | 394 | 402 | PF00400 | 0.397 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.332 |
LIG_FHA_1 | 177 | 183 | PF00498 | 0.283 |
LIG_FHA_1 | 186 | 192 | PF00498 | 0.234 |
LIG_FHA_1 | 334 | 340 | PF00498 | 0.312 |
LIG_FHA_2 | 160 | 166 | PF00498 | 0.267 |
LIG_GBD_Chelix_1 | 7 | 15 | PF00786 | 0.411 |
LIG_LIR_Gen_1 | 21 | 28 | PF02991 | 0.394 |
LIG_LIR_Gen_1 | 33 | 44 | PF02991 | 0.556 |
LIG_LIR_Gen_1 | 361 | 370 | PF02991 | 0.408 |
LIG_LIR_Gen_1 | 403 | 412 | PF02991 | 0.371 |
LIG_LIR_Gen_1 | 417 | 424 | PF02991 | 0.299 |
LIG_LIR_Gen_1 | 446 | 455 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 149 | 155 | PF02991 | 0.295 |
LIG_LIR_Nem_3 | 21 | 26 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 297 | 302 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 33 | 39 | PF02991 | 0.556 |
LIG_LIR_Nem_3 | 361 | 365 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 403 | 408 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 414 | 418 | PF02991 | 0.219 |
LIG_LIR_Nem_3 | 446 | 450 | PF02991 | 0.283 |
LIG_NRBOX | 333 | 339 | PF00104 | 0.341 |
LIG_Pex14_1 | 199 | 203 | PF04695 | 0.302 |
LIG_Pex14_2 | 101 | 105 | PF04695 | 0.371 |
LIG_Pex14_2 | 197 | 201 | PF04695 | 0.451 |
LIG_Pex14_2 | 358 | 362 | PF04695 | 0.302 |
LIG_PTB_Apo_2 | 272 | 279 | PF02174 | 0.566 |
LIG_PTB_Phospho_1 | 272 | 278 | PF10480 | 0.566 |
LIG_SH2_CRK | 23 | 27 | PF00017 | 0.373 |
LIG_SH2_CRK | 302 | 306 | PF00017 | 0.478 |
LIG_SH2_CRK | 353 | 357 | PF00017 | 0.419 |
LIG_SH2_CRK | 405 | 409 | PF00017 | 0.397 |
LIG_SH2_NCK_1 | 291 | 295 | PF00017 | 0.575 |
LIG_SH2_NCK_1 | 405 | 409 | PF00017 | 0.429 |
LIG_SH2_NCK_1 | 60 | 64 | PF00017 | 0.285 |
LIG_SH2_STAP1 | 187 | 191 | PF00017 | 0.334 |
LIG_SH2_STAP1 | 23 | 27 | PF00017 | 0.373 |
LIG_SH2_STAP1 | 405 | 409 | PF00017 | 0.429 |
LIG_SH2_STAP1 | 74 | 78 | PF00017 | 0.211 |
LIG_SH2_STAT3 | 142 | 145 | PF00017 | 0.373 |
LIG_SH2_STAT5 | 171 | 174 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 187 | 190 | PF00017 | 0.260 |
LIG_SH2_STAT5 | 23 | 26 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 27 | 30 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 278 | 281 | PF00017 | 0.556 |
LIG_SH2_STAT5 | 291 | 294 | PF00017 | 0.534 |
LIG_SH2_STAT5 | 359 | 362 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 409 | 412 | PF00017 | 0.414 |
LIG_SH3_3 | 108 | 114 | PF00018 | 0.447 |
LIG_SH3_3 | 177 | 183 | PF00018 | 0.148 |
LIG_SH3_3 | 208 | 214 | PF00018 | 0.327 |
LIG_SH3_3 | 94 | 100 | PF00018 | 0.343 |
LIG_SUMO_SIM_anti_2 | 398 | 404 | PF11976 | 0.377 |
LIG_SUMO_SIM_anti_2 | 453 | 459 | PF11976 | 0.331 |
LIG_SUMO_SIM_anti_2 | 54 | 59 | PF11976 | 0.384 |
LIG_SUMO_SIM_par_1 | 134 | 139 | PF11976 | 0.256 |
LIG_SUMO_SIM_par_1 | 181 | 188 | PF11976 | 0.325 |
LIG_SUMO_SIM_par_1 | 398 | 404 | PF11976 | 0.349 |
LIG_TYR_ITIM | 300 | 305 | PF00017 | 0.484 |
LIG_TYR_ITIM | 407 | 412 | PF00017 | 0.448 |
LIG_TYR_ITSM | 19 | 26 | PF00017 | 0.429 |
LIG_TYR_ITSM | 401 | 408 | PF00017 | 0.429 |
LIG_UBA3_1 | 457 | 465 | PF00899 | 0.408 |
LIG_WRC_WIRS_1 | 22 | 27 | PF05994 | 0.276 |
LIG_WRC_WIRS_1 | 325 | 330 | PF05994 | 0.318 |
LIG_WRC_WIRS_1 | 412 | 417 | PF05994 | 0.329 |
MOD_CK1_1 | 115 | 121 | PF00069 | 0.501 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.296 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.214 |
MOD_CK1_1 | 185 | 191 | PF00069 | 0.242 |
MOD_CK1_1 | 258 | 264 | PF00069 | 0.618 |
MOD_CK1_1 | 453 | 459 | PF00069 | 0.380 |
MOD_CK2_1 | 159 | 165 | PF00069 | 0.223 |
MOD_GlcNHglycan | 165 | 169 | PF01048 | 0.452 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.213 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.288 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.277 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.238 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.581 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.556 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.657 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.325 |
MOD_N-GLC_1 | 155 | 160 | PF02516 | 0.463 |
MOD_N-GLC_1 | 395 | 400 | PF02516 | 0.371 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.245 |
MOD_NEK2_1 | 176 | 181 | PF00069 | 0.222 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.305 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.393 |
MOD_NEK2_1 | 395 | 400 | PF00069 | 0.366 |
MOD_NEK2_1 | 401 | 406 | PF00069 | 0.318 |
MOD_NEK2_1 | 450 | 455 | PF00069 | 0.371 |
MOD_PIKK_1 | 115 | 121 | PF00454 | 0.538 |
MOD_PIKK_1 | 77 | 83 | PF00454 | 0.333 |
MOD_PKA_1 | 465 | 471 | PF00069 | 0.656 |
MOD_PKA_2 | 176 | 182 | PF00069 | 0.260 |
MOD_PKA_2 | 258 | 264 | PF00069 | 0.601 |
MOD_PKA_2 | 465 | 471 | PF00069 | 0.656 |
MOD_Plk_1 | 164 | 170 | PF00069 | 0.283 |
MOD_Plk_1 | 395 | 401 | PF00069 | 0.366 |
MOD_Plk_4 | 124 | 130 | PF00069 | 0.341 |
MOD_Plk_4 | 18 | 24 | PF00069 | 0.380 |
MOD_Plk_4 | 182 | 188 | PF00069 | 0.251 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.371 |
MOD_Plk_4 | 333 | 339 | PF00069 | 0.299 |
MOD_Plk_4 | 385 | 391 | PF00069 | 0.458 |
MOD_Plk_4 | 395 | 401 | PF00069 | 0.284 |
MOD_Plk_4 | 450 | 456 | PF00069 | 0.331 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.424 |
MOD_ProDKin_1 | 155 | 161 | PF00069 | 0.197 |
MOD_ProDKin_1 | 294 | 300 | PF00069 | 0.553 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.338 |
TRG_DiLeu_BaEn_3 | 235 | 241 | PF01217 | 0.501 |
TRG_ENDOCYTIC_2 | 23 | 26 | PF00928 | 0.330 |
TRG_ENDOCYTIC_2 | 302 | 305 | PF00928 | 0.476 |
TRG_ENDOCYTIC_2 | 325 | 328 | PF00928 | 0.284 |
TRG_ENDOCYTIC_2 | 353 | 356 | PF00928 | 0.302 |
TRG_ENDOCYTIC_2 | 405 | 408 | PF00928 | 0.397 |
TRG_ENDOCYTIC_2 | 409 | 412 | PF00928 | 0.397 |
TRG_ENDOCYTIC_2 | 418 | 421 | PF00928 | 0.318 |
TRG_NLS_MonoExtC_3 | 464 | 469 | PF00514 | 0.685 |
TRG_NLS_MonoExtN_4 | 464 | 469 | PF00514 | 0.685 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HRR8 | Leptomonas seymouri | 73% | 100% |
A0A0N1I533 | Leptomonas seymouri | 23% | 100% |
A0A0S4IQ17 | Bodo saltans | 46% | 100% |
A0A0S4JTI8 | Bodo saltans | 34% | 94% |
A0A1X0NKT2 | Trypanosomatidae | 34% | 100% |
A0A1X0NM00 | Trypanosomatidae | 56% | 100% |
A0A3Q8IGK4 | Leishmania donovani | 94% | 100% |
A0A3S5H7Y2 | Leishmania donovani | 23% | 100% |
A0A422P212 | Trypanosoma rangeli | 55% | 100% |
A4HE60 | Leishmania braziliensis | 79% | 100% |
A4HM51 | Leishmania braziliensis | 24% | 97% |
A4I1F8 | Leishmania infantum | 94% | 100% |
A4IAR3 | Leishmania infantum | 23% | 100% |
A7RM45 | Nematostella vectensis | 21% | 88% |
C9ZK11 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 100% |
D0A2E9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
D8TFA8 | Selaginella moellendorffii | 27% | 100% |
E9AEI9 | Leishmania major | 24% | 96% |
E9B5Q0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
Q4Q9X7 | Leishmania major | 93% | 100% |
Q54BI3 | Dictyostelium discoideum | 31% | 95% |
Q54QP7 | Dictyostelium discoideum | 32% | 95% |
Q658I5 | Oryza sativa subsp. japonica | 29% | 94% |
Q9M028 | Arabidopsis thaliana | 30% | 94% |
Q9SR93 | Arabidopsis thaliana | 30% | 94% |