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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: E9ATU1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 329 | 331 | PF00675 | 0.420 |
CLV_NRD_NRD_1 | 373 | 375 | PF00675 | 0.423 |
CLV_NRD_NRD_1 | 57 | 59 | PF00675 | 0.526 |
CLV_PCSK_FUR_1 | 55 | 59 | PF00082 | 0.554 |
CLV_PCSK_KEX2_1 | 160 | 162 | PF00082 | 0.429 |
CLV_PCSK_KEX2_1 | 329 | 331 | PF00082 | 0.484 |
CLV_PCSK_KEX2_1 | 373 | 375 | PF00082 | 0.491 |
CLV_PCSK_KEX2_1 | 57 | 59 | PF00082 | 0.516 |
CLV_PCSK_PC1ET2_1 | 160 | 162 | PF00082 | 0.442 |
CLV_PCSK_SKI1_1 | 10 | 14 | PF00082 | 0.736 |
CLV_PCSK_SKI1_1 | 160 | 164 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 373 | 377 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 379 | 383 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 46 | 50 | PF00082 | 0.556 |
DOC_CDC14_PxL_1 | 305 | 313 | PF14671 | 0.524 |
DOC_CKS1_1 | 318 | 323 | PF01111 | 0.417 |
DOC_MAPK_gen_1 | 248 | 257 | PF00069 | 0.563 |
DOC_MAPK_gen_1 | 329 | 340 | PF00069 | 0.457 |
DOC_MAPK_gen_1 | 34 | 42 | PF00069 | 0.584 |
DOC_MAPK_gen_1 | 373 | 382 | PF00069 | 0.424 |
DOC_MAPK_gen_1 | 97 | 105 | PF00069 | 0.575 |
DOC_MAPK_MEF2A_6 | 376 | 384 | PF00069 | 0.458 |
DOC_PP1_RVXF_1 | 208 | 215 | PF00149 | 0.437 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.486 |
DOC_WW_Pin1_4 | 198 | 203 | PF00397 | 0.511 |
DOC_WW_Pin1_4 | 250 | 255 | PF00397 | 0.545 |
DOC_WW_Pin1_4 | 317 | 322 | PF00397 | 0.382 |
LIG_14-3-3_CanoR_1 | 14 | 19 | PF00244 | 0.601 |
LIG_14-3-3_CanoR_1 | 165 | 170 | PF00244 | 0.474 |
LIG_14-3-3_CanoR_1 | 315 | 321 | PF00244 | 0.433 |
LIG_14-3-3_CanoR_1 | 358 | 367 | PF00244 | 0.322 |
LIG_14-3-3_CanoR_1 | 379 | 385 | PF00244 | 0.479 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.701 |
LIG_Clathr_ClatBox_1 | 368 | 372 | PF01394 | 0.489 |
LIG_CSL_BTD_1 | 154 | 157 | PF09270 | 0.458 |
LIG_FHA_1 | 317 | 323 | PF00498 | 0.419 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.584 |
LIG_FHA_1 | 87 | 93 | PF00498 | 0.416 |
LIG_FHA_2 | 107 | 113 | PF00498 | 0.582 |
LIG_FHA_2 | 251 | 257 | PF00498 | 0.554 |
LIG_LIR_Apic_2 | 168 | 174 | PF02991 | 0.349 |
LIG_LIR_Gen_1 | 116 | 125 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 166 | 176 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 73 | 79 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 116 | 120 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 166 | 172 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 73 | 78 | PF02991 | 0.372 |
LIG_PTB_Apo_2 | 299 | 306 | PF02174 | 0.472 |
LIG_PTB_Apo_2 | 340 | 347 | PF02174 | 0.524 |
LIG_SH2_CRK | 167 | 171 | PF00017 | 0.486 |
LIG_SH2_GRB2like | 233 | 236 | PF00017 | 0.444 |
LIG_SH2_SRC | 171 | 174 | PF00017 | 0.431 |
LIG_SH2_STAP1 | 167 | 171 | PF00017 | 0.442 |
LIG_SH2_STAP1 | 245 | 249 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 171 | 174 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 28 | 31 | PF00017 | 0.700 |
LIG_SH3_2 | 292 | 297 | PF14604 | 0.573 |
LIG_SH3_2 | 321 | 326 | PF14604 | 0.418 |
LIG_SH3_3 | 205 | 211 | PF00018 | 0.515 |
LIG_SH3_3 | 244 | 250 | PF00018 | 0.458 |
LIG_SH3_3 | 285 | 291 | PF00018 | 0.461 |
LIG_SH3_3 | 315 | 321 | PF00018 | 0.388 |
LIG_SUMO_SIM_anti_2 | 253 | 259 | PF11976 | 0.568 |
LIG_SUMO_SIM_anti_2 | 363 | 370 | PF11976 | 0.423 |
LIG_SUMO_SIM_par_1 | 380 | 386 | PF11976 | 0.491 |
LIG_TRAF2_1 | 179 | 182 | PF00917 | 0.574 |
LIG_WRC_WIRS_1 | 368 | 373 | PF05994 | 0.414 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.595 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.555 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.654 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.450 |
MOD_CK1_1 | 296 | 302 | PF00069 | 0.584 |
MOD_CK2_1 | 106 | 112 | PF00069 | 0.518 |
MOD_CK2_1 | 176 | 182 | PF00069 | 0.556 |
MOD_CK2_1 | 250 | 256 | PF00069 | 0.550 |
MOD_CK2_1 | 380 | 386 | PF00069 | 0.476 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.476 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.451 |
MOD_GlcNHglycan | 360 | 363 | PF01048 | 0.481 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.451 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.594 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.580 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.584 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.446 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.385 |
MOD_LATS_1 | 143 | 149 | PF00433 | 0.593 |
MOD_LATS_1 | 44 | 50 | PF00433 | 0.557 |
MOD_N-GLC_1 | 235 | 240 | PF02516 | 0.521 |
MOD_NEK2_1 | 134 | 139 | PF00069 | 0.716 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.449 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.391 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.418 |
MOD_NEK2_1 | 331 | 336 | PF00069 | 0.436 |
MOD_NEK2_1 | 348 | 353 | PF00069 | 0.344 |
MOD_NEK2_1 | 380 | 385 | PF00069 | 0.555 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.516 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.420 |
MOD_NEK2_1 | 92 | 97 | PF00069 | 0.402 |
MOD_PIKK_1 | 110 | 116 | PF00454 | 0.505 |
MOD_PIKK_1 | 86 | 92 | PF00454 | 0.441 |
MOD_PK_1 | 14 | 20 | PF00069 | 0.607 |
MOD_PKA_2 | 144 | 150 | PF00069 | 0.662 |
MOD_PKA_2 | 296 | 302 | PF00069 | 0.544 |
MOD_Plk_1 | 226 | 232 | PF00069 | 0.406 |
MOD_Plk_1 | 235 | 241 | PF00069 | 0.397 |
MOD_Plk_1 | 265 | 271 | PF00069 | 0.578 |
MOD_Plk_4 | 151 | 157 | PF00069 | 0.478 |
MOD_Plk_4 | 165 | 171 | PF00069 | 0.333 |
MOD_Plk_4 | 226 | 232 | PF00069 | 0.421 |
MOD_Plk_4 | 348 | 354 | PF00069 | 0.487 |
MOD_Plk_4 | 70 | 76 | PF00069 | 0.413 |
MOD_ProDKin_1 | 198 | 204 | PF00069 | 0.509 |
MOD_ProDKin_1 | 250 | 256 | PF00069 | 0.550 |
MOD_ProDKin_1 | 317 | 323 | PF00069 | 0.383 |
MOD_SUMO_rev_2 | 386 | 393 | PF00179 | 0.390 |
TRG_DiLeu_BaEn_1 | 313 | 318 | PF01217 | 0.498 |
TRG_DiLeu_BaEn_2 | 183 | 189 | PF01217 | 0.385 |
TRG_DiLeu_BaLyEn_6 | 199 | 204 | PF01217 | 0.573 |
TRG_DiLeu_BaLyEn_6 | 306 | 311 | PF01217 | 0.535 |
TRG_DiLeu_BaLyEn_6 | 312 | 317 | PF01217 | 0.401 |
TRG_DiLeu_BaLyEn_6 | 318 | 323 | PF01217 | 0.370 |
TRG_ENDOCYTIC_2 | 167 | 170 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 75 | 78 | PF00928 | 0.386 |
TRG_ER_diArg_1 | 269 | 272 | PF00400 | 0.495 |
TRG_ER_diArg_1 | 329 | 331 | PF00400 | 0.480 |
TRG_ER_diArg_1 | 373 | 375 | PF00400 | 0.491 |
TRG_ER_diArg_1 | 54 | 57 | PF00400 | 0.563 |
TRG_Pf-PMV_PEXEL_1 | 46 | 50 | PF00026 | 0.660 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HSQ0 | Leptomonas seymouri | 74% | 99% |
A0A0S4JP54 | Bodo saltans | 36% | 81% |
A0A1X0NDW4 | Trypanosomatidae | 50% | 93% |
A0A3Q8IHT7 | Leishmania donovani | 95% | 100% |
A0A3R7K3H2 | Trypanosoma rangeli | 55% | 95% |
A4HQ23 | Leishmania braziliensis | 88% | 100% |
A4IDT0 | Leishmania infantum | 95% | 100% |
D0A8U6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 53% | 94% |
Q4Q0Q5 | Leishmania major | 92% | 100% |
V5AZJ2 | Trypanosoma cruzi | 53% | 86% |