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. | yes | yes: 5 |
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: E9ANJ5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 245 | 249 | PF00656 | 0.663 |
CLV_C14_Caspase3-7 | 59 | 63 | PF00656 | 0.462 |
CLV_NRD_NRD_1 | 222 | 224 | PF00675 | 0.397 |
CLV_NRD_NRD_1 | 237 | 239 | PF00675 | 0.527 |
CLV_PCSK_FUR_1 | 220 | 224 | PF00082 | 0.448 |
CLV_PCSK_KEX2_1 | 222 | 224 | PF00082 | 0.380 |
CLV_PCSK_KEX2_1 | 237 | 239 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 366 | 368 | PF00082 | 0.628 |
CLV_PCSK_PC1ET2_1 | 366 | 368 | PF00082 | 0.628 |
CLV_PCSK_PC7_1 | 233 | 239 | PF00082 | 0.464 |
CLV_PCSK_SKI1_1 | 22 | 26 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 233 | 237 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 305 | 309 | PF00082 | 0.375 |
CLV_PCSK_SKI1_1 | 58 | 62 | PF00082 | 0.504 |
DEG_SPOP_SBC_1 | 271 | 275 | PF00917 | 0.640 |
DOC_CYCLIN_RxL_1 | 17 | 26 | PF00134 | 0.488 |
DOC_CYCLIN_RxL_1 | 305 | 316 | PF00134 | 0.472 |
DOC_PP1_RVXF_1 | 159 | 166 | PF00149 | 0.537 |
DOC_PP1_RVXF_1 | 199 | 206 | PF00149 | 0.265 |
DOC_PP1_SILK_1 | 233 | 238 | PF00149 | 0.414 |
DOC_USP7_MATH_1 | 209 | 213 | PF00917 | 0.401 |
DOC_USP7_MATH_1 | 231 | 235 | PF00917 | 0.519 |
DOC_USP7_MATH_1 | 250 | 254 | PF00917 | 0.768 |
DOC_USP7_MATH_1 | 271 | 275 | PF00917 | 0.689 |
DOC_USP7_UBL2_3 | 4 | 8 | PF12436 | 0.625 |
DOC_WW_Pin1_4 | 321 | 326 | PF00397 | 0.576 |
LIG_14-3-3_CanoR_1 | 112 | 117 | PF00244 | 0.271 |
LIG_14-3-3_CanoR_1 | 159 | 164 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 222 | 230 | PF00244 | 0.524 |
LIG_Actin_WH2_2 | 148 | 163 | PF00022 | 0.470 |
LIG_Actin_WH2_2 | 343 | 360 | PF00022 | 0.418 |
LIG_BRCT_BRCA1_1 | 161 | 165 | PF00533 | 0.426 |
LIG_BRCT_BRCA1_1 | 71 | 75 | PF00533 | 0.416 |
LIG_deltaCOP1_diTrp_1 | 110 | 116 | PF00928 | 0.399 |
LIG_FHA_1 | 128 | 134 | PF00498 | 0.428 |
LIG_FHA_1 | 333 | 339 | PF00498 | 0.442 |
LIG_FHA_2 | 116 | 122 | PF00498 | 0.530 |
LIG_FHA_2 | 282 | 288 | PF00498 | 0.528 |
LIG_FHA_2 | 57 | 63 | PF00498 | 0.530 |
LIG_HCF-1_HBM_1 | 140 | 143 | PF13415 | 0.398 |
LIG_LIR_Gen_1 | 115 | 123 | PF02991 | 0.375 |
LIG_LIR_Gen_1 | 180 | 189 | PF02991 | 0.283 |
LIG_LIR_Gen_1 | 314 | 325 | PF02991 | 0.468 |
LIG_LIR_Gen_1 | 383 | 393 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 115 | 119 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 215 | 221 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 314 | 320 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 383 | 388 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 72 | 78 | PF02991 | 0.444 |
LIG_PCNA_yPIPBox_3 | 339 | 352 | PF02747 | 0.444 |
LIG_PDZ_Class_1 | 402 | 407 | PF00595 | 0.499 |
LIG_SH2_CRK | 218 | 222 | PF00017 | 0.317 |
LIG_SH2_SRC | 122 | 125 | PF00017 | 0.453 |
LIG_SH2_SRC | 42 | 45 | PF00017 | 0.645 |
LIG_SH2_STAP1 | 95 | 99 | PF00017 | 0.334 |
LIG_SH2_STAT3 | 193 | 196 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 122 | 125 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 42 | 45 | PF00017 | 0.639 |
LIG_SUMO_SIM_par_1 | 130 | 136 | PF11976 | 0.542 |
LIG_TRAF2_1 | 285 | 288 | PF00917 | 0.443 |
LIG_WRC_WIRS_1 | 382 | 387 | PF05994 | 0.460 |
MOD_CK1_1 | 131 | 137 | PF00069 | 0.574 |
MOD_CK1_1 | 212 | 218 | PF00069 | 0.411 |
MOD_CK1_1 | 274 | 280 | PF00069 | 0.603 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.595 |
MOD_CK2_1 | 281 | 287 | PF00069 | 0.586 |
MOD_GlcNHglycan | 171 | 175 | PF01048 | 0.457 |
MOD_GlcNHglycan | 251 | 255 | PF01048 | 0.695 |
MOD_GlcNHglycan | 404 | 407 | PF01048 | 0.607 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.570 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.597 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.510 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.752 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.581 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.617 |
MOD_N-GLC_1 | 128 | 133 | PF02516 | 0.409 |
MOD_N-GLC_1 | 52 | 57 | PF02516 | 0.569 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.540 |
MOD_NEK2_1 | 402 | 407 | PF00069 | 0.543 |
MOD_PIKK_1 | 262 | 268 | PF00454 | 0.636 |
MOD_PK_1 | 159 | 165 | PF00069 | 0.535 |
MOD_Plk_1 | 127 | 133 | PF00069 | 0.385 |
MOD_Plk_1 | 231 | 237 | PF00069 | 0.447 |
MOD_Plk_1 | 332 | 338 | PF00069 | 0.410 |
MOD_Plk_1 | 68 | 74 | PF00069 | 0.537 |
MOD_Plk_2-3 | 242 | 248 | PF00069 | 0.635 |
MOD_Plk_4 | 128 | 134 | PF00069 | 0.459 |
MOD_Plk_4 | 332 | 338 | PF00069 | 0.532 |
MOD_Plk_4 | 384 | 390 | PF00069 | 0.502 |
MOD_ProDKin_1 | 321 | 327 | PF00069 | 0.572 |
MOD_SUMO_for_1 | 18 | 21 | PF00179 | 0.600 |
MOD_SUMO_rev_2 | 287 | 291 | PF00179 | 0.439 |
TRG_DiLeu_BaEn_4 | 354 | 360 | PF01217 | 0.514 |
TRG_ENDOCYTIC_2 | 183 | 186 | PF00928 | 0.454 |
TRG_ENDOCYTIC_2 | 218 | 221 | PF00928 | 0.430 |
TRG_ER_diArg_1 | 158 | 161 | PF00400 | 0.548 |
TRG_ER_diArg_1 | 220 | 223 | PF00400 | 0.390 |
TRG_ER_diArg_1 | 236 | 238 | PF00400 | 0.465 |
TRG_NES_CRM1_1 | 380 | 395 | PF08389 | 0.531 |
TRG_Pf-PMV_PEXEL_1 | 22 | 26 | PF00026 | 0.475 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P484 | Leptomonas seymouri | 60% | 99% |
A0A1X0NV58 | Trypanosomatidae | 44% | 100% |
A0A3R7R950 | Trypanosoma rangeli | 42% | 100% |
A0A3S7WRL3 | Leishmania donovani | 93% | 100% |
A4H6G7 | Leishmania braziliensis | 80% | 100% |
A4HUW8 | Leishmania infantum | 93% | 100% |
D0A7J3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
Q4QH31 | Leishmania major | 91% | 100% |
V5BRL9 | Trypanosoma cruzi | 41% | 100% |