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: E9AZ46
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 136 | 140 | PF00656 | 0.473 |
CLV_C14_Caspase3-7 | 15 | 19 | PF00656 | 0.440 |
CLV_NRD_NRD_1 | 289 | 291 | PF00675 | 0.513 |
CLV_NRD_NRD_1 | 69 | 71 | PF00675 | 0.456 |
CLV_PCSK_KEX2_1 | 289 | 291 | PF00082 | 0.416 |
CLV_PCSK_KEX2_1 | 69 | 71 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 204 | 208 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 223 | 227 | PF00082 | 0.274 |
CLV_PCSK_SKI1_1 | 275 | 279 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 289 | 293 | PF00082 | 0.327 |
CLV_PCSK_SKI1_1 | 349 | 353 | PF00082 | 0.426 |
DEG_APCC_DBOX_1 | 348 | 356 | PF00400 | 0.321 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.470 |
DEG_SPOP_SBC_1 | 134 | 138 | PF00917 | 0.551 |
DOC_CKS1_1 | 224 | 229 | PF01111 | 0.402 |
DOC_CYCLIN_RxL_1 | 284 | 293 | PF00134 | 0.326 |
DOC_CYCLIN_yCln2_LP_2 | 94 | 100 | PF00134 | 0.425 |
DOC_MAPK_MEF2A_6 | 342 | 350 | PF00069 | 0.340 |
DOC_MAPK_MEF2A_6 | 50 | 58 | PF00069 | 0.479 |
DOC_PP1_RVXF_1 | 175 | 182 | PF00149 | 0.288 |
DOC_PP2B_LxvP_1 | 299 | 302 | PF13499 | 0.467 |
DOC_PP4_FxxP_1 | 31 | 34 | PF00568 | 0.431 |
DOC_USP7_MATH_1 | 127 | 131 | PF00917 | 0.742 |
DOC_USP7_MATH_1 | 134 | 138 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 285 | 289 | PF00917 | 0.405 |
DOC_USP7_MATH_2 | 317 | 323 | PF00917 | 0.419 |
DOC_USP7_UBL2_3 | 12 | 16 | PF12436 | 0.322 |
DOC_WW_Pin1_4 | 120 | 125 | PF00397 | 0.701 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 223 | 228 | PF00397 | 0.425 |
DOC_WW_Pin1_4 | 236 | 241 | PF00397 | 0.305 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.463 |
LIG_14-3-3_CanoR_1 | 109 | 113 | PF00244 | 0.385 |
LIG_14-3-3_CanoR_1 | 141 | 147 | PF00244 | 0.432 |
LIG_14-3-3_CanoR_1 | 162 | 171 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 177 | 182 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 204 | 213 | PF00244 | 0.416 |
LIG_14-3-3_CanoR_1 | 342 | 346 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 50 | 54 | PF00244 | 0.502 |
LIG_APCC_ABBA_1 | 274 | 279 | PF00400 | 0.536 |
LIG_BRCT_BRCA1_1 | 23 | 27 | PF00533 | 0.482 |
LIG_FHA_1 | 191 | 197 | PF00498 | 0.419 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.380 |
LIG_FHA_1 | 269 | 275 | PF00498 | 0.418 |
LIG_FHA_1 | 304 | 310 | PF00498 | 0.331 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.629 |
LIG_FHA_1 | 60 | 66 | PF00498 | 0.498 |
LIG_FHA_2 | 153 | 159 | PF00498 | 0.394 |
LIG_FHA_2 | 88 | 94 | PF00498 | 0.323 |
LIG_LIR_Apic_2 | 29 | 34 | PF02991 | 0.427 |
LIG_LIR_Gen_1 | 111 | 120 | PF02991 | 0.603 |
LIG_LIR_Gen_1 | 183 | 192 | PF02991 | 0.375 |
LIG_LIR_Gen_1 | 256 | 267 | PF02991 | 0.218 |
LIG_LIR_Gen_1 | 310 | 317 | PF02991 | 0.406 |
LIG_LIR_Gen_1 | 43 | 51 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 111 | 116 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 183 | 188 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 256 | 262 | PF02991 | 0.284 |
LIG_LIR_Nem_3 | 310 | 316 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 43 | 47 | PF02991 | 0.349 |
LIG_NRP_CendR_1 | 374 | 375 | PF00754 | 0.584 |
LIG_Pex14_2 | 181 | 185 | PF04695 | 0.426 |
LIG_Pex14_2 | 188 | 192 | PF04695 | 0.472 |
LIG_Pex14_2 | 27 | 31 | PF04695 | 0.413 |
LIG_SH2_CRK | 144 | 148 | PF00017 | 0.423 |
LIG_SH2_CRK | 313 | 317 | PF00017 | 0.408 |
LIG_SH2_NCK_1 | 358 | 362 | PF00017 | 0.514 |
LIG_SH2_SRC | 358 | 361 | PF00017 | 0.511 |
LIG_SH2_STAT3 | 365 | 368 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 13 | 16 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 144 | 147 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 266 | 269 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 365 | 368 | PF00017 | 0.647 |
LIG_SH3_3 | 221 | 227 | PF00018 | 0.392 |
LIG_SUMO_SIM_par_1 | 114 | 119 | PF11976 | 0.454 |
LIG_SUMO_SIM_par_1 | 54 | 60 | PF11976 | 0.607 |
LIG_SUMO_SIM_par_1 | 89 | 96 | PF11976 | 0.484 |
LIG_TYR_ITIM | 257 | 262 | PF00017 | 0.385 |
LIG_WRC_WIRS_1 | 143 | 148 | PF05994 | 0.415 |
LIG_WRC_WIRS_1 | 178 | 183 | PF05994 | 0.448 |
MOD_CDK_SPxK_1 | 223 | 229 | PF00069 | 0.400 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.717 |
MOD_CK1_1 | 137 | 143 | PF00069 | 0.529 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.483 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.316 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.531 |
MOD_CK1_1 | 212 | 218 | PF00069 | 0.560 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.529 |
MOD_CK2_1 | 163 | 169 | PF00069 | 0.354 |
MOD_CK2_1 | 312 | 318 | PF00069 | 0.468 |
MOD_CK2_1 | 319 | 325 | PF00069 | 0.435 |
MOD_CK2_1 | 341 | 347 | PF00069 | 0.359 |
MOD_CK2_1 | 87 | 93 | PF00069 | 0.383 |
MOD_DYRK1A_RPxSP_1 | 223 | 227 | PF00069 | 0.396 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.458 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.417 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.620 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.591 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.603 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.661 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.595 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.369 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.566 |
MOD_N-GLC_1 | 370 | 375 | PF02516 | 0.577 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.553 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.413 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.288 |
MOD_NEK2_1 | 195 | 200 | PF00069 | 0.268 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.323 |
MOD_NEK2_1 | 312 | 317 | PF00069 | 0.596 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.491 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.344 |
MOD_NEK2_2 | 152 | 157 | PF00069 | 0.406 |
MOD_NEK2_2 | 64 | 69 | PF00069 | 0.271 |
MOD_PIKK_1 | 283 | 289 | PF00454 | 0.461 |
MOD_PIKK_1 | 49 | 55 | PF00454 | 0.397 |
MOD_PKA_2 | 108 | 114 | PF00069 | 0.384 |
MOD_PKA_2 | 171 | 177 | PF00069 | 0.490 |
MOD_PKA_2 | 341 | 347 | PF00069 | 0.453 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.592 |
MOD_Plk_1 | 17 | 23 | PF00069 | 0.601 |
MOD_Plk_1 | 42 | 48 | PF00069 | 0.370 |
MOD_Plk_2-3 | 319 | 325 | PF00069 | 0.407 |
MOD_Plk_4 | 108 | 114 | PF00069 | 0.419 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.568 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.375 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.278 |
MOD_Plk_4 | 319 | 325 | PF00069 | 0.407 |
MOD_Plk_4 | 87 | 93 | PF00069 | 0.381 |
MOD_ProDKin_1 | 120 | 126 | PF00069 | 0.703 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.628 |
MOD_ProDKin_1 | 223 | 229 | PF00069 | 0.433 |
MOD_ProDKin_1 | 236 | 242 | PF00069 | 0.313 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.461 |
MOD_SUMO_rev_2 | 80 | 88 | PF00179 | 0.477 |
TRG_DiLeu_BaEn_1 | 319 | 324 | PF01217 | 0.515 |
TRG_DiLeu_BaLyEn_6 | 287 | 292 | PF01217 | 0.383 |
TRG_ENDOCYTIC_2 | 144 | 147 | PF00928 | 0.418 |
TRG_ENDOCYTIC_2 | 259 | 262 | PF00928 | 0.364 |
TRG_ENDOCYTIC_2 | 313 | 316 | PF00928 | 0.545 |
TRG_ENDOCYTIC_2 | 358 | 361 | PF00928 | 0.456 |
TRG_ER_diArg_1 | 289 | 291 | PF00400 | 0.331 |
TRG_ER_diArg_1 | 302 | 305 | PF00400 | 0.372 |
TRG_ER_diArg_1 | 68 | 70 | PF00400 | 0.441 |
TRG_Pf-PMV_PEXEL_1 | 204 | 208 | PF00026 | 0.387 |
TRG_Pf-PMV_PEXEL_1 | 289 | 293 | PF00026 | 0.276 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5R9 | Leptomonas seymouri | 59% | 96% |
A0A0S4JR94 | Bodo saltans | 28% | 100% |
A0A3Q8IDF7 | Leishmania donovani | 93% | 100% |
A0A422NFS8 | Trypanosoma rangeli | 35% | 100% |
A4HFR8 | Leishmania braziliensis | 78% | 100% |
A4I2U3 | Leishmania infantum | 93% | 100% |
D0A609 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
E9ADC2 | Leishmania major | 93% | 100% |
V5B0Z1 | Trypanosoma cruzi | 36% | 100% |