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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: E9AQB8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 238 | 240 | PF00675 | 0.283 |
CLV_NRD_NRD_1 | 242 | 244 | PF00675 | 0.283 |
CLV_NRD_NRD_1 | 245 | 247 | PF00675 | 0.283 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.663 |
CLV_NRD_NRD_1 | 359 | 361 | PF00675 | 0.636 |
CLV_PCSK_FUR_1 | 239 | 243 | PF00082 | 0.332 |
CLV_PCSK_KEX2_1 | 238 | 240 | PF00082 | 0.285 |
CLV_PCSK_KEX2_1 | 241 | 243 | PF00082 | 0.281 |
CLV_PCSK_KEX2_1 | 245 | 247 | PF00082 | 0.279 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.661 |
CLV_PCSK_KEX2_1 | 359 | 361 | PF00082 | 0.534 |
CLV_PCSK_PC7_1 | 238 | 244 | PF00082 | 0.334 |
CLV_PCSK_SKI1_1 | 216 | 220 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 295 | 299 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 344 | 348 | PF00082 | 0.710 |
CLV_PCSK_SKI1_1 | 360 | 364 | PF00082 | 0.471 |
CLV_PCSK_SKI1_1 | 52 | 56 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 77 | 81 | PF00082 | 0.402 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.620 |
DEG_SCF_FBW7_1 | 125 | 132 | PF00400 | 0.285 |
DEG_SCF_FBW7_1 | 65 | 72 | PF00400 | 0.272 |
DOC_CYCLIN_RxL_1 | 47 | 59 | PF00134 | 0.469 |
DOC_MAPK_DCC_7 | 87 | 96 | PF00069 | 0.522 |
DOC_MAPK_gen_1 | 189 | 195 | PF00069 | 0.491 |
DOC_MAPK_HePTP_8 | 84 | 96 | PF00069 | 0.519 |
DOC_MAPK_MEF2A_6 | 87 | 96 | PF00069 | 0.522 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 384 | 388 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 394 | 398 | PF00917 | 0.659 |
DOC_WW_Pin1_4 | 125 | 130 | PF00397 | 0.502 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.508 |
DOC_WW_Pin1_4 | 385 | 390 | PF00397 | 0.793 |
DOC_WW_Pin1_4 | 59 | 64 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 65 | 70 | PF00397 | 0.502 |
LIG_14-3-3_CanoR_1 | 133 | 140 | PF00244 | 0.576 |
LIG_14-3-3_CanoR_1 | 181 | 185 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 313 | 320 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 348 | 355 | PF00244 | 0.598 |
LIG_14-3-3_CanoR_1 | 47 | 55 | PF00244 | 0.435 |
LIG_14-3-3_CanoR_1 | 77 | 82 | PF00244 | 0.421 |
LIG_14-3-3_CterR_2 | 401 | 403 | PF00244 | 0.508 |
LIG_Actin_WH2_2 | 233 | 250 | PF00022 | 0.502 |
LIG_Actin_WH2_2 | 280 | 297 | PF00022 | 0.554 |
LIG_APCC_ABBA_1 | 258 | 263 | PF00400 | 0.562 |
LIG_APCC_ABBA_1 | 36 | 41 | PF00400 | 0.449 |
LIG_BRCT_BRCA1_1 | 314 | 318 | PF00533 | 0.506 |
LIG_BRCT_BRCA1_1 | 7 | 11 | PF00533 | 0.664 |
LIG_BRCT_BRCA1_2 | 7 | 13 | PF00533 | 0.642 |
LIG_CaM_IQ_9 | 208 | 223 | PF13499 | 0.498 |
LIG_eIF4E_1 | 230 | 236 | PF01652 | 0.564 |
LIG_FHA_1 | 126 | 132 | PF00498 | 0.501 |
LIG_FHA_1 | 142 | 148 | PF00498 | 0.435 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.381 |
LIG_FHA_1 | 272 | 278 | PF00498 | 0.594 |
LIG_FHA_1 | 59 | 65 | PF00498 | 0.527 |
LIG_FHA_1 | 70 | 76 | PF00498 | 0.306 |
LIG_FHA_2 | 102 | 108 | PF00498 | 0.449 |
LIG_FHA_2 | 134 | 140 | PF00498 | 0.431 |
LIG_FHA_2 | 291 | 297 | PF00498 | 0.586 |
LIG_LIR_Gen_1 | 152 | 158 | PF02991 | 0.488 |
LIG_LIR_Gen_1 | 183 | 191 | PF02991 | 0.416 |
LIG_LIR_Gen_1 | 209 | 219 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 166 | 172 | PF02991 | 0.608 |
LIG_LIR_Nem_3 | 209 | 214 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 8 | 14 | PF02991 | 0.556 |
LIG_MLH1_MIPbox_1 | 7 | 11 | PF16413 | 0.384 |
LIG_Pex14_2 | 163 | 167 | PF04695 | 0.463 |
LIG_Pex14_2 | 318 | 322 | PF04695 | 0.398 |
LIG_PTB_Apo_2 | 200 | 207 | PF02174 | 0.511 |
LIG_SH2_CRK | 320 | 324 | PF00017 | 0.408 |
LIG_SH2_GRB2like | 230 | 233 | PF00017 | 0.449 |
LIG_SH2_STAP1 | 154 | 158 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 10 | 13 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 116 | 119 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 261 | 264 | PF00017 | 0.553 |
LIG_SH3_3 | 222 | 228 | PF00018 | 0.255 |
LIG_SH3_5 | 226 | 230 | PF00018 | 0.529 |
LIG_SUMO_SIM_anti_2 | 254 | 260 | PF11976 | 0.509 |
LIG_SUMO_SIM_anti_2 | 326 | 332 | PF11976 | 0.545 |
LIG_SUMO_SIM_par_1 | 326 | 332 | PF11976 | 0.545 |
LIG_SUMO_SIM_par_1 | 76 | 82 | PF11976 | 0.547 |
LIG_TRAF2_1 | 183 | 186 | PF00917 | 0.470 |
LIG_TRAF2_1 | 299 | 302 | PF00917 | 0.482 |
LIG_TYR_ITIM | 259 | 264 | PF00017 | 0.482 |
LIG_WW_1 | 227 | 230 | PF00397 | 0.379 |
MOD_CDK_SPxxK_3 | 149 | 156 | PF00069 | 0.507 |
MOD_CDK_SPxxK_3 | 385 | 392 | PF00069 | 0.728 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.584 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.530 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.442 |
MOD_CK2_1 | 101 | 107 | PF00069 | 0.280 |
MOD_CK2_1 | 133 | 139 | PF00069 | 0.585 |
MOD_CK2_1 | 180 | 186 | PF00069 | 0.436 |
MOD_CK2_1 | 326 | 332 | PF00069 | 0.541 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.366 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.509 |
MOD_GlcNHglycan | 381 | 384 | PF01048 | 0.688 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.306 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.462 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.554 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.443 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.356 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.201 |
MOD_N-GLC_1 | 141 | 146 | PF02516 | 0.288 |
MOD_N-GLC_1 | 265 | 270 | PF02516 | 0.335 |
MOD_N-GLC_1 | 271 | 276 | PF02516 | 0.335 |
MOD_N-GLC_1 | 82 | 87 | PF02516 | 0.268 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.361 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.434 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.603 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.539 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.392 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.536 |
MOD_NEK2_2 | 271 | 276 | PF00069 | 0.394 |
MOD_PIKK_1 | 46 | 52 | PF00454 | 0.472 |
MOD_PIKK_1 | 54 | 60 | PF00454 | 0.431 |
MOD_PKA_2 | 180 | 186 | PF00069 | 0.435 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.675 |
MOD_PKA_2 | 212 | 218 | PF00069 | 0.397 |
MOD_PKA_2 | 312 | 318 | PF00069 | 0.528 |
MOD_PKA_2 | 46 | 52 | PF00069 | 0.472 |
MOD_Plk_1 | 271 | 277 | PF00069 | 0.478 |
MOD_Plk_1 | 39 | 45 | PF00069 | 0.530 |
MOD_Plk_2-3 | 101 | 107 | PF00069 | 0.280 |
MOD_Plk_2-3 | 326 | 332 | PF00069 | 0.545 |
MOD_Plk_4 | 278 | 284 | PF00069 | 0.405 |
MOD_Plk_4 | 39 | 45 | PF00069 | 0.407 |
MOD_ProDKin_1 | 125 | 131 | PF00069 | 0.508 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.505 |
MOD_ProDKin_1 | 385 | 391 | PF00069 | 0.793 |
MOD_ProDKin_1 | 59 | 65 | PF00069 | 0.549 |
MOD_SUMO_for_1 | 206 | 209 | PF00179 | 0.523 |
MOD_SUMO_for_1 | 349 | 352 | PF00179 | 0.630 |
MOD_SUMO_rev_2 | 356 | 365 | PF00179 | 0.653 |
TRG_DiLeu_BaLyEn_6 | 74 | 79 | PF01217 | 0.390 |
TRG_ENDOCYTIC_2 | 116 | 119 | PF00928 | 0.346 |
TRG_ENDOCYTIC_2 | 154 | 157 | PF00928 | 0.489 |
TRG_ENDOCYTIC_2 | 184 | 187 | PF00928 | 0.443 |
TRG_ENDOCYTIC_2 | 261 | 264 | PF00928 | 0.434 |
TRG_ENDOCYTIC_2 | 320 | 323 | PF00928 | 0.403 |
TRG_ER_diArg_1 | 2 | 4 | PF00400 | 0.708 |
TRG_ER_diArg_1 | 237 | 239 | PF00400 | 0.340 |
TRG_ER_diArg_1 | 240 | 243 | PF00400 | 0.334 |
TRG_ER_diArg_1 | 244 | 246 | PF00400 | 0.329 |
TRG_Pf-PMV_PEXEL_1 | 156 | 160 | PF00026 | 0.406 |
TRG_Pf-PMV_PEXEL_1 | 248 | 252 | PF00026 | 0.363 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILL6 | Leptomonas seymouri | 68% | 99% |
A0A0S4JNX3 | Bodo saltans | 51% | 99% |
A0A1X0P9L0 | Trypanosomatidae | 59% | 100% |
A0A3S5H6V7 | Leishmania donovani | 91% | 99% |
A4H888 | Leishmania braziliensis | 86% | 100% |
A4HWL1 | Leishmania infantum | 91% | 99% |
C9ZMN5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 62% | 100% |
Q4QF56 | Leishmania major | 93% | 100% |
V5BKH7 | Trypanosoma cruzi | 63% | 100% |