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: E9AT32
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 174 | 176 | PF00675 | 0.645 |
CLV_NRD_NRD_1 | 218 | 220 | PF00675 | 0.598 |
CLV_NRD_NRD_1 | 258 | 260 | PF00675 | 0.590 |
CLV_NRD_NRD_1 | 311 | 313 | PF00675 | 0.489 |
CLV_NRD_NRD_1 | 322 | 324 | PF00675 | 0.558 |
CLV_NRD_NRD_1 | 348 | 350 | PF00675 | 0.605 |
CLV_NRD_NRD_1 | 42 | 44 | PF00675 | 0.566 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.657 |
CLV_PCSK_KEX2_1 | 174 | 176 | PF00082 | 0.645 |
CLV_PCSK_KEX2_1 | 258 | 260 | PF00082 | 0.590 |
CLV_PCSK_KEX2_1 | 311 | 313 | PF00082 | 0.489 |
CLV_PCSK_KEX2_1 | 321 | 323 | PF00082 | 0.553 |
CLV_PCSK_KEX2_1 | 348 | 350 | PF00082 | 0.635 |
CLV_PCSK_KEX2_1 | 42 | 44 | PF00082 | 0.552 |
CLV_PCSK_PC1ET2_1 | 321 | 323 | PF00082 | 0.562 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.573 |
CLV_PCSK_SKI1_1 | 259 | 263 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 312 | 316 | PF00082 | 0.547 |
DEG_APCC_DBOX_1 | 300 | 308 | PF00400 | 0.576 |
DEG_SPOP_SBC_1 | 35 | 39 | PF00917 | 0.545 |
DOC_CKS1_1 | 270 | 275 | PF01111 | 0.596 |
DOC_CYCLIN_RxL_1 | 257 | 266 | PF00134 | 0.545 |
DOC_MAPK_gen_1 | 112 | 120 | PF00069 | 0.552 |
DOC_MAPK_gen_1 | 308 | 317 | PF00069 | 0.589 |
DOC_MAPK_gen_1 | 40 | 49 | PF00069 | 0.556 |
DOC_MAPK_MEF2A_6 | 190 | 197 | PF00069 | 0.498 |
DOC_MAPK_MEF2A_6 | 40 | 49 | PF00069 | 0.667 |
DOC_PP1_RVXF_1 | 257 | 264 | PF00149 | 0.688 |
DOC_PP4_FxxP_1 | 146 | 149 | PF00568 | 0.680 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 283 | 287 | PF00917 | 0.634 |
DOC_USP7_MATH_1 | 324 | 328 | PF00917 | 0.610 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.548 |
DOC_WW_Pin1_4 | 145 | 150 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 269 | 274 | PF00397 | 0.596 |
DOC_WW_Pin1_4 | 279 | 284 | PF00397 | 0.501 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.605 |
LIG_14-3-3_CanoR_1 | 154 | 158 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 232 | 237 | PF00244 | 0.610 |
LIG_14-3-3_CanoR_1 | 284 | 288 | PF00244 | 0.684 |
LIG_14-3-3_CanoR_1 | 306 | 311 | PF00244 | 0.569 |
LIG_14-3-3_CanoR_1 | 80 | 86 | PF00244 | 0.614 |
LIG_Actin_WH2_2 | 300 | 318 | PF00022 | 0.450 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.661 |
LIG_BRCT_BRCA1_1 | 147 | 151 | PF00533 | 0.571 |
LIG_FHA_1 | 201 | 207 | PF00498 | 0.669 |
LIG_FHA_1 | 332 | 338 | PF00498 | 0.704 |
LIG_FHA_2 | 184 | 190 | PF00498 | 0.468 |
LIG_FHA_2 | 21 | 27 | PF00498 | 0.643 |
LIG_FHA_2 | 225 | 231 | PF00498 | 0.642 |
LIG_FHA_2 | 236 | 242 | PF00498 | 0.619 |
LIG_FHA_2 | 326 | 332 | PF00498 | 0.638 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.462 |
LIG_LIR_Apic_2 | 144 | 149 | PF02991 | 0.679 |
LIG_LIR_Gen_1 | 356 | 365 | PF02991 | 0.507 |
LIG_LIR_Gen_1 | 70 | 79 | PF02991 | 0.658 |
LIG_LIR_Nem_3 | 230 | 234 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 246 | 252 | PF02991 | 0.547 |
LIG_LIR_Nem_3 | 345 | 350 | PF02991 | 0.587 |
LIG_LIR_Nem_3 | 356 | 360 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 50 | 55 | PF02991 | 0.573 |
LIG_LIR_Nem_3 | 70 | 74 | PF02991 | 0.670 |
LIG_LYPXL_yS_3 | 52 | 55 | PF13949 | 0.626 |
LIG_PDZ_Class_3 | 368 | 373 | PF00595 | 0.617 |
LIG_SH2_CRK | 231 | 235 | PF00017 | 0.527 |
LIG_SH2_CRK | 347 | 351 | PF00017 | 0.684 |
LIG_SH2_PTP2 | 357 | 360 | PF00017 | 0.500 |
LIG_SH2_SRC | 247 | 250 | PF00017 | 0.654 |
LIG_SH2_STAP1 | 247 | 251 | PF00017 | 0.603 |
LIG_SH2_STAT5 | 161 | 164 | PF00017 | 0.548 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.620 |
LIG_SH2_STAT5 | 357 | 360 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 93 | 96 | PF00017 | 0.464 |
LIG_SH3_3 | 334 | 340 | PF00018 | 0.690 |
LIG_SH3_3 | 355 | 361 | PF00018 | 0.554 |
LIG_SUMO_SIM_par_1 | 97 | 106 | PF11976 | 0.609 |
LIG_TRAF2_1 | 300 | 303 | PF00917 | 0.536 |
LIG_TYR_ITSM | 343 | 350 | PF00017 | 0.447 |
MOD_CDK_SPK_2 | 279 | 284 | PF00069 | 0.553 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.560 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.638 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.550 |
MOD_CK1_1 | 250 | 256 | PF00069 | 0.448 |
MOD_CK2_1 | 147 | 153 | PF00069 | 0.693 |
MOD_CK2_1 | 183 | 189 | PF00069 | 0.478 |
MOD_CK2_1 | 20 | 26 | PF00069 | 0.652 |
MOD_CK2_1 | 235 | 241 | PF00069 | 0.649 |
MOD_CK2_1 | 272 | 278 | PF00069 | 0.705 |
MOD_CK2_1 | 283 | 289 | PF00069 | 0.562 |
MOD_CK2_1 | 89 | 95 | PF00069 | 0.705 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.575 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.678 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.635 |
MOD_GlcNHglycan | 317 | 320 | PF01048 | 0.382 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.658 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.536 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.519 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.543 |
MOD_N-GLC_1 | 353 | 358 | PF02516 | 0.588 |
MOD_N-GLC_2 | 107 | 109 | PF02516 | 0.529 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.598 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.593 |
MOD_NEK2_1 | 243 | 248 | PF00069 | 0.542 |
MOD_NEK2_1 | 263 | 268 | PF00069 | 0.387 |
MOD_NEK2_1 | 277 | 282 | PF00069 | 0.479 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.560 |
MOD_NEK2_1 | 315 | 320 | PF00069 | 0.554 |
MOD_NEK2_1 | 342 | 347 | PF00069 | 0.454 |
MOD_PIKK_1 | 224 | 230 | PF00454 | 0.589 |
MOD_PKA_2 | 111 | 117 | PF00069 | 0.641 |
MOD_PKA_2 | 153 | 159 | PF00069 | 0.534 |
MOD_PKA_2 | 283 | 289 | PF00069 | 0.553 |
MOD_PKA_2 | 315 | 321 | PF00069 | 0.494 |
MOD_Plk_1 | 152 | 158 | PF00069 | 0.647 |
MOD_Plk_1 | 263 | 269 | PF00069 | 0.593 |
MOD_Plk_1 | 277 | 283 | PF00069 | 0.476 |
MOD_Plk_1 | 69 | 75 | PF00069 | 0.723 |
MOD_Plk_2-3 | 183 | 189 | PF00069 | 0.584 |
MOD_Plk_2-3 | 70 | 76 | PF00069 | 0.663 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.549 |
MOD_Plk_4 | 272 | 278 | PF00069 | 0.636 |
MOD_Plk_4 | 283 | 289 | PF00069 | 0.580 |
MOD_Plk_4 | 333 | 339 | PF00069 | 0.588 |
MOD_Plk_4 | 353 | 359 | PF00069 | 0.431 |
MOD_ProDKin_1 | 145 | 151 | PF00069 | 0.574 |
MOD_ProDKin_1 | 269 | 275 | PF00069 | 0.597 |
MOD_ProDKin_1 | 279 | 285 | PF00069 | 0.501 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.605 |
MOD_SUMO_rev_2 | 183 | 191 | PF00179 | 0.577 |
MOD_SUMO_rev_2 | 326 | 334 | PF00179 | 0.678 |
TRG_DiLeu_BaEn_4 | 302 | 308 | PF01217 | 0.495 |
TRG_ENDOCYTIC_2 | 201 | 204 | PF00928 | 0.543 |
TRG_ENDOCYTIC_2 | 231 | 234 | PF00928 | 0.530 |
TRG_ENDOCYTIC_2 | 347 | 350 | PF00928 | 0.579 |
TRG_ENDOCYTIC_2 | 357 | 360 | PF00928 | 0.481 |
TRG_ENDOCYTIC_2 | 367 | 370 | PF00928 | 0.497 |
TRG_ENDOCYTIC_2 | 52 | 55 | PF00928 | 0.650 |
TRG_ER_diArg_1 | 173 | 175 | PF00400 | 0.542 |
TRG_ER_diArg_1 | 257 | 259 | PF00400 | 0.582 |
TRG_ER_diArg_1 | 310 | 312 | PF00400 | 0.488 |
TRG_ER_diArg_1 | 347 | 349 | PF00400 | 0.638 |
TRG_ER_diArg_1 | 42 | 44 | PF00400 | 0.552 |
TRG_NLS_Bipartite_1 | 311 | 325 | PF00514 | 0.390 |
TRG_NLS_MonoExtC_3 | 320 | 326 | PF00514 | 0.426 |
TRG_Pf-PMV_PEXEL_1 | 308 | 313 | PF00026 | 0.450 |
TRG_Pf-PMV_PEXEL_1 | 42 | 46 | PF00026 | 0.551 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYX6 | Leptomonas seymouri | 58% | 97% |
A0A1X0P7K9 | Trypanosomatidae | 39% | 100% |
A0A3Q8IKB1 | Leishmania donovani | 92% | 100% |
A0A3R7K7R7 | Trypanosoma rangeli | 41% | 100% |
A4HPC3 | Leishmania braziliensis | 79% | 100% |
A4ICG1 | Leishmania infantum | 92% | 100% |
D0A3D6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
Q4Q1G6 | Leishmania major | 93% | 100% |
V5BH32 | Trypanosoma cruzi | 38% | 100% |