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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: Q4QHA4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 227 | 229 | PF00675 | 0.361 |
CLV_NRD_NRD_1 | 29 | 31 | PF00675 | 0.385 |
CLV_NRD_NRD_1 | 313 | 315 | PF00675 | 0.488 |
CLV_NRD_NRD_1 | 392 | 394 | PF00675 | 0.544 |
CLV_NRD_NRD_1 | 48 | 50 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 5 | 7 | PF00675 | 0.615 |
CLV_NRD_NRD_1 | 52 | 54 | PF00675 | 0.497 |
CLV_NRD_NRD_1 | 83 | 85 | PF00675 | 0.475 |
CLV_PCSK_FUR_1 | 98 | 102 | PF00082 | 0.446 |
CLV_PCSK_KEX2_1 | 100 | 102 | PF00082 | 0.609 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 227 | 229 | PF00082 | 0.361 |
CLV_PCSK_KEX2_1 | 29 | 31 | PF00082 | 0.394 |
CLV_PCSK_KEX2_1 | 392 | 394 | PF00082 | 0.544 |
CLV_PCSK_KEX2_1 | 48 | 50 | PF00082 | 0.500 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.615 |
CLV_PCSK_KEX2_1 | 52 | 54 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 83 | 85 | PF00082 | 0.440 |
CLV_PCSK_PC1ET2_1 | 100 | 102 | PF00082 | 0.649 |
CLV_PCSK_PC1ET2_1 | 192 | 194 | PF00082 | 0.480 |
CLV_PCSK_PC7_1 | 188 | 194 | PF00082 | 0.472 |
CLV_PCSK_PC7_1 | 48 | 54 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 193 | 197 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 245 | 249 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 332 | 336 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 349 | 353 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 380 | 384 | PF00082 | 0.467 |
CLV_PCSK_SKI1_1 | 6 | 10 | PF00082 | 0.595 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.481 |
DEG_APCC_DBOX_1 | 165 | 173 | PF00400 | 0.465 |
DEG_APCC_DBOX_1 | 227 | 235 | PF00400 | 0.379 |
DEG_APCC_DBOX_1 | 4 | 12 | PF00400 | 0.595 |
DOC_CDC14_PxL_1 | 277 | 285 | PF14671 | 0.382 |
DOC_CYCLIN_yCln2_LP_2 | 172 | 178 | PF00134 | 0.501 |
DOC_MAPK_DCC_7 | 112 | 120 | PF00069 | 0.574 |
DOC_MAPK_gen_1 | 12 | 20 | PF00069 | 0.503 |
DOC_MAPK_gen_1 | 227 | 233 | PF00069 | 0.380 |
DOC_MAPK_gen_1 | 59 | 69 | PF00069 | 0.484 |
DOC_MAPK_gen_1 | 83 | 93 | PF00069 | 0.485 |
DOC_MAPK_MEF2A_6 | 112 | 120 | PF00069 | 0.574 |
DOC_MAPK_MEF2A_6 | 14 | 22 | PF00069 | 0.529 |
DOC_MAPK_MEF2A_6 | 343 | 352 | PF00069 | 0.488 |
DOC_PP2B_LxvP_1 | 172 | 175 | PF13499 | 0.463 |
DOC_PP2B_LxvP_1 | 195 | 198 | PF13499 | 0.471 |
DOC_PP2B_LxvP_1 | 406 | 409 | PF13499 | 0.669 |
DOC_USP7_MATH_1 | 250 | 254 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 417 | 421 | PF00917 | 0.575 |
DOC_USP7_MATH_2 | 230 | 236 | PF00917 | 0.457 |
DOC_WW_Pin1_4 | 246 | 251 | PF00397 | 0.473 |
DOC_WW_Pin1_4 | 341 | 346 | PF00397 | 0.588 |
DOC_WW_Pin1_4 | 404 | 409 | PF00397 | 0.646 |
LIG_14-3-3_CanoR_1 | 133 | 142 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 179 | 187 | PF00244 | 0.499 |
LIG_14-3-3_CanoR_1 | 255 | 261 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 98 | 104 | PF00244 | 0.474 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.578 |
LIG_eIF4E_1 | 333 | 339 | PF01652 | 0.544 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.573 |
LIG_FHA_1 | 17 | 23 | PF00498 | 0.525 |
LIG_FHA_1 | 333 | 339 | PF00498 | 0.587 |
LIG_FHA_1 | 58 | 64 | PF00498 | 0.471 |
LIG_FHA_1 | 77 | 83 | PF00498 | 0.632 |
LIG_FHA_2 | 342 | 348 | PF00498 | 0.501 |
LIG_FHA_2 | 373 | 379 | PF00498 | 0.461 |
LIG_LIR_Gen_1 | 373 | 383 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 287 | 292 | PF02991 | 0.466 |
LIG_LYPXL_yS_3 | 274 | 277 | PF13949 | 0.409 |
LIG_LYPXL_yS_3 | 292 | 295 | PF13949 | 0.433 |
LIG_NRBOX | 261 | 267 | PF00104 | 0.388 |
LIG_Pex14_1 | 225 | 229 | PF04695 | 0.368 |
LIG_PROFILIN_1 | 408 | 414 | PF00235 | 0.556 |
LIG_PTB_Apo_2 | 55 | 62 | PF02174 | 0.528 |
LIG_Rb_LxCxE_1 | 72 | 92 | PF01857 | 0.478 |
LIG_RPA_C_Fungi | 25 | 37 | PF08784 | 0.373 |
LIG_RPA_C_Fungi | 309 | 321 | PF08784 | 0.564 |
LIG_SH2_SRC | 241 | 244 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 333 | 336 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 7 | 10 | PF00017 | 0.548 |
LIG_SH3_3 | 113 | 119 | PF00018 | 0.595 |
LIG_SH3_3 | 290 | 296 | PF00018 | 0.439 |
LIG_SH3_3 | 342 | 348 | PF00018 | 0.586 |
LIG_SH3_3 | 405 | 411 | PF00018 | 0.648 |
LIG_SUMO_SIM_par_1 | 18 | 24 | PF11976 | 0.477 |
LIG_SUMO_SIM_par_1 | 229 | 235 | PF11976 | 0.448 |
LIG_TRAF2_1 | 203 | 206 | PF00917 | 0.515 |
LIG_TRAF2_1 | 43 | 46 | PF00917 | 0.411 |
LIG_TRAF2_1 | 72 | 75 | PF00917 | 0.459 |
LIG_TYR_ITIM | 272 | 277 | PF00017 | 0.484 |
LIG_WRC_WIRS_1 | 237 | 242 | PF05994 | 0.455 |
LIG_WRC_WIRS_1 | 352 | 357 | PF05994 | 0.534 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.565 |
MOD_CK1_1 | 249 | 255 | PF00069 | 0.703 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.533 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.453 |
MOD_CK2_1 | 372 | 378 | PF00069 | 0.430 |
MOD_CK2_1 | 40 | 46 | PF00069 | 0.482 |
MOD_CK2_1 | 69 | 75 | PF00069 | 0.512 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.606 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.533 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.443 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.462 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.580 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.477 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.511 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.536 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.543 |
MOD_GSK3_1 | 417 | 424 | PF00069 | 0.598 |
MOD_N-GLC_1 | 57 | 62 | PF02516 | 0.523 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.560 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.356 |
MOD_NEK2_1 | 339 | 344 | PF00069 | 0.606 |
MOD_NEK2_1 | 351 | 356 | PF00069 | 0.415 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.487 |
MOD_NEK2_2 | 236 | 241 | PF00069 | 0.453 |
MOD_PIKK_1 | 370 | 376 | PF00454 | 0.521 |
MOD_PKA_2 | 132 | 138 | PF00069 | 0.544 |
MOD_PKA_2 | 211 | 217 | PF00069 | 0.413 |
MOD_PKA_2 | 254 | 260 | PF00069 | 0.490 |
MOD_PKA_2 | 321 | 327 | PF00069 | 0.678 |
MOD_PKA_2 | 339 | 345 | PF00069 | 0.446 |
MOD_Plk_1 | 57 | 63 | PF00069 | 0.451 |
MOD_Plk_4 | 155 | 161 | PF00069 | 0.537 |
MOD_Plk_4 | 236 | 242 | PF00069 | 0.418 |
MOD_Plk_4 | 261 | 267 | PF00069 | 0.492 |
MOD_ProDKin_1 | 246 | 252 | PF00069 | 0.480 |
MOD_ProDKin_1 | 341 | 347 | PF00069 | 0.585 |
MOD_ProDKin_1 | 404 | 410 | PF00069 | 0.643 |
MOD_SUMO_rev_2 | 239 | 247 | PF00179 | 0.420 |
MOD_SUMO_rev_2 | 324 | 334 | PF00179 | 0.510 |
MOD_SUMO_rev_2 | 88 | 96 | PF00179 | 0.436 |
TRG_DiLeu_BaEn_1 | 299 | 304 | PF01217 | 0.415 |
TRG_DiLeu_BaEn_4 | 267 | 273 | PF01217 | 0.474 |
TRG_DiLeu_BaLyEn_6 | 176 | 181 | PF01217 | 0.464 |
TRG_DiLeu_BaLyEn_6 | 346 | 351 | PF01217 | 0.492 |
TRG_ENDOCYTIC_2 | 274 | 277 | PF00928 | 0.409 |
TRG_ENDOCYTIC_2 | 292 | 295 | PF00928 | 0.433 |
TRG_ENDOCYTIC_2 | 376 | 379 | PF00928 | 0.456 |
TRG_ER_diArg_1 | 227 | 229 | PF00400 | 0.361 |
TRG_ER_diArg_1 | 391 | 393 | PF00400 | 0.562 |
TRG_ER_diArg_1 | 47 | 49 | PF00400 | 0.497 |
TRG_ER_diArg_1 | 5 | 7 | PF00400 | 0.615 |
TRG_ER_diArg_1 | 51 | 53 | PF00400 | 0.488 |
TRG_ER_diArg_1 | 61 | 64 | PF00400 | 0.368 |
TRG_ER_diArg_1 | 82 | 84 | PF00400 | 0.467 |
TRG_NES_CRM1_1 | 213 | 226 | PF08389 | 0.407 |
TRG_Pf-PMV_PEXEL_1 | 179 | 183 | PF00026 | 0.499 |
TRG_Pf-PMV_PEXEL_1 | 392 | 397 | PF00026 | 0.530 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDA4 | Leptomonas seymouri | 46% | 100% |
A0A3Q8IHA3 | Leishmania donovani | 89% | 100% |
A4H698 | Leishmania braziliensis | 67% | 80% |
A4HUM2 | Leishmania infantum | 90% | 100% |
E9ANC0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |