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: 19 |
NetGPI | no | yes: 0, no: 19 |
Related structures:
AlphaFold database: A4HZY4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 145 | 147 | PF00675 | 0.489 |
CLV_NRD_NRD_1 | 348 | 350 | PF00675 | 0.435 |
CLV_NRD_NRD_1 | 44 | 46 | PF00675 | 0.350 |
CLV_NRD_NRD_1 | 5 | 7 | PF00675 | 0.553 |
CLV_PCSK_KEX2_1 | 145 | 147 | PF00082 | 0.504 |
CLV_PCSK_KEX2_1 | 348 | 350 | PF00082 | 0.451 |
CLV_PCSK_KEX2_1 | 44 | 46 | PF00082 | 0.352 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.553 |
CLV_PCSK_SKI1_1 | 403 | 407 | PF00082 | 0.476 |
DEG_APCC_DBOX_1 | 379 | 387 | PF00400 | 0.482 |
DEG_APCC_DBOX_1 | 5 | 13 | PF00400 | 0.336 |
DEG_ODPH_VHL_1 | 84 | 97 | PF01847 | 0.427 |
DEG_SPOP_SBC_1 | 123 | 127 | PF00917 | 0.213 |
DEG_SPOP_SBC_1 | 195 | 199 | PF00917 | 0.570 |
DOC_CDC14_PxL_1 | 150 | 158 | PF14671 | 0.354 |
DOC_MAPK_gen_1 | 216 | 225 | PF00069 | 0.497 |
DOC_MAPK_gen_1 | 376 | 385 | PF00069 | 0.516 |
DOC_MAPK_gen_1 | 44 | 52 | PF00069 | 0.350 |
DOC_MAPK_gen_1 | 5 | 11 | PF00069 | 0.487 |
DOC_MAPK_gen_1 | 74 | 83 | PF00069 | 0.309 |
DOC_MAPK_HePTP_8 | 375 | 387 | PF00069 | 0.377 |
DOC_MAPK_MEF2A_6 | 216 | 225 | PF00069 | 0.555 |
DOC_MAPK_MEF2A_6 | 313 | 321 | PF00069 | 0.311 |
DOC_MAPK_MEF2A_6 | 378 | 387 | PF00069 | 0.530 |
DOC_MAPK_MEF2A_6 | 44 | 52 | PF00069 | 0.394 |
DOC_PP1_RVXF_1 | 400 | 407 | PF00149 | 0.350 |
DOC_PP1_RVXF_1 | 6 | 12 | PF00149 | 0.325 |
DOC_PP2B_LxvP_1 | 151 | 154 | PF13499 | 0.333 |
DOC_USP7_MATH_1 | 123 | 127 | PF00917 | 0.223 |
DOC_USP7_MATH_1 | 182 | 186 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 195 | 199 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.608 |
DOC_USP7_MATH_1 | 272 | 276 | PF00917 | 0.468 |
DOC_USP7_MATH_1 | 301 | 305 | PF00917 | 0.493 |
DOC_USP7_MATH_1 | 328 | 332 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 388 | 392 | PF00917 | 0.471 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.443 |
DOC_WW_Pin1_4 | 160 | 165 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 226 | 231 | PF00397 | 0.548 |
LIG_14-3-3_CanoR_1 | 348 | 352 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 409 | 414 | PF00244 | 0.472 |
LIG_14-3-3_CanoR_1 | 45 | 51 | PF00244 | 0.412 |
LIG_14-3-3_CanoR_1 | 6 | 12 | PF00244 | 0.410 |
LIG_BRCT_BRCA1_1 | 303 | 307 | PF00533 | 0.486 |
LIG_BRCT_BRCA1_1 | 52 | 56 | PF00533 | 0.342 |
LIG_Clathr_ClatBox_1 | 311 | 315 | PF01394 | 0.386 |
LIG_eIF4E_1 | 91 | 97 | PF01652 | 0.380 |
LIG_FHA_1 | 348 | 354 | PF00498 | 0.299 |
LIG_FHA_1 | 367 | 373 | PF00498 | 0.462 |
LIG_FHA_2 | 204 | 210 | PF00498 | 0.437 |
LIG_IRF3_LxIS_1 | 48 | 53 | PF10401 | 0.426 |
LIG_LIR_Gen_1 | 64 | 70 | PF02991 | 0.352 |
LIG_LIR_Gen_1 | 78 | 87 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 246 | 252 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 64 | 68 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 78 | 83 | PF02991 | 0.328 |
LIG_Pex14_2 | 352 | 356 | PF04695 | 0.455 |
LIG_RPA_C_Fungi | 404 | 416 | PF08784 | 0.322 |
LIG_SH2_CRK | 250 | 254 | PF00017 | 0.373 |
LIG_SH2_CRK | 80 | 84 | PF00017 | 0.427 |
LIG_SH2_SRC | 91 | 94 | PF00017 | 0.380 |
LIG_SH2_STAT3 | 417 | 420 | PF00017 | 0.489 |
LIG_SH2_STAT5 | 260 | 263 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 293 | 296 | PF00017 | 0.347 |
LIG_SH2_STAT5 | 333 | 336 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 351 | 354 | PF00017 | 0.228 |
LIG_SH2_STAT5 | 91 | 94 | PF00017 | 0.393 |
LIG_SH3_2 | 39 | 44 | PF14604 | 0.462 |
LIG_SH3_3 | 221 | 227 | PF00018 | 0.467 |
LIG_SH3_3 | 36 | 42 | PF00018 | 0.499 |
LIG_SH3_3 | 382 | 388 | PF00018 | 0.397 |
LIG_SH3_3 | 80 | 86 | PF00018 | 0.380 |
LIG_SUMO_SIM_anti_2 | 315 | 320 | PF11976 | 0.285 |
LIG_SUMO_SIM_anti_2 | 381 | 387 | PF11976 | 0.365 |
LIG_SUMO_SIM_par_1 | 315 | 320 | PF11976 | 0.294 |
LIG_UBA3_1 | 210 | 217 | PF00899 | 0.499 |
LIG_WRC_WIRS_1 | 147 | 152 | PF05994 | 0.479 |
MOD_CK1_1 | 126 | 132 | PF00069 | 0.414 |
MOD_CK1_1 | 197 | 203 | PF00069 | 0.553 |
MOD_CK1_1 | 275 | 281 | PF00069 | 0.662 |
MOD_CK1_1 | 295 | 301 | PF00069 | 0.350 |
MOD_CK2_1 | 196 | 202 | PF00069 | 0.657 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.488 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.464 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.420 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.557 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.667 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.679 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.550 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.578 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.539 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.344 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.395 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.392 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.627 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.640 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.585 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.430 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.394 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.306 |
MOD_N-GLC_1 | 238 | 243 | PF02516 | 0.631 |
MOD_N-GLC_1 | 46 | 51 | PF02516 | 0.405 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.406 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.406 |
MOD_NEK2_1 | 95 | 100 | PF00069 | 0.430 |
MOD_NEK2_2 | 72 | 77 | PF00069 | 0.316 |
MOD_PIKK_1 | 165 | 171 | PF00454 | 0.342 |
MOD_PIKK_1 | 275 | 281 | PF00454 | 0.688 |
MOD_PKA_2 | 268 | 274 | PF00069 | 0.485 |
MOD_PKA_2 | 275 | 281 | PF00069 | 0.618 |
MOD_PKA_2 | 347 | 353 | PF00069 | 0.448 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.403 |
MOD_Plk_1 | 295 | 301 | PF00069 | 0.392 |
MOD_Plk_1 | 46 | 52 | PF00069 | 0.400 |
MOD_Plk_4 | 135 | 141 | PF00069 | 0.427 |
MOD_Plk_4 | 146 | 152 | PF00069 | 0.451 |
MOD_Plk_4 | 203 | 209 | PF00069 | 0.513 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.315 |
MOD_Plk_4 | 7 | 13 | PF00069 | 0.399 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.443 |
MOD_ProDKin_1 | 160 | 166 | PF00069 | 0.547 |
MOD_ProDKin_1 | 226 | 232 | PF00069 | 0.548 |
MOD_SUMO_rev_2 | 209 | 218 | PF00179 | 0.450 |
MOD_SUMO_rev_2 | 371 | 377 | PF00179 | 0.495 |
MOD_SUMO_rev_2 | 399 | 405 | PF00179 | 0.371 |
TRG_ENDOCYTIC_2 | 260 | 263 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 80 | 83 | PF00928 | 0.360 |
TRG_ER_diArg_1 | 144 | 146 | PF00400 | 0.511 |
TRG_ER_diArg_1 | 347 | 349 | PF00400 | 0.439 |
TRG_ER_diArg_1 | 4 | 6 | PF00400 | 0.533 |
TRG_NES_CRM1_1 | 202 | 215 | PF08389 | 0.390 |
TRG_NES_CRM1_1 | 309 | 320 | PF08389 | 0.381 |
TRG_NES_CRM1_1 | 366 | 381 | PF08389 | 0.291 |
TRG_Pf-PMV_PEXEL_1 | 370 | 374 | PF00026 | 0.531 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0M2 | Leptomonas seymouri | 39% | 94% |
A0A0N1PFX0 | Leptomonas seymouri | 58% | 94% |
A0A0S4J8Q0 | Bodo saltans | 35% | 100% |
A0A0S4JLW1 | Bodo saltans | 25% | 96% |
A0A1X0NTE2 | Trypanosomatidae | 41% | 100% |
A0A1X0NX03 | Trypanosomatidae | 24% | 100% |
A0A3Q8IFK3 | Leishmania donovani | 49% | 91% |
A0A3S7WXD8 | Leishmania donovani | 100% | 100% |
A0A422NHR8 | Trypanosoma rangeli | 41% | 100% |
A4HCF4 | Leishmania braziliensis | 46% | 100% |
A4HZY3 | Leishmania infantum | 44% | 100% |
C9ZSM3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
C9ZVB8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 100% |
E9AVU4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 47% | 91% |
E9AVU5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4QBN4 | Leishmania major | 93% | 99% |
Q4QBN5 | Leishmania major | 42% | 100% |
V5BVW3 | Trypanosoma cruzi | 41% | 100% |