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: A4HFG8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 119 | 123 | PF00656 | 0.475 |
CLV_C14_Caspase3-7 | 191 | 195 | PF00656 | 0.338 |
CLV_C14_Caspase3-7 | 527 | 531 | PF00656 | 0.465 |
CLV_NRD_NRD_1 | 141 | 143 | PF00675 | 0.573 |
CLV_NRD_NRD_1 | 169 | 171 | PF00675 | 0.623 |
CLV_NRD_NRD_1 | 249 | 251 | PF00675 | 0.512 |
CLV_NRD_NRD_1 | 324 | 326 | PF00675 | 0.597 |
CLV_NRD_NRD_1 | 550 | 552 | PF00675 | 0.515 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.312 |
CLV_PCSK_FUR_1 | 169 | 173 | PF00082 | 0.438 |
CLV_PCSK_FUR_1 | 86 | 90 | PF00082 | 0.291 |
CLV_PCSK_KEX2_1 | 128 | 130 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 141 | 143 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 168 | 170 | PF00082 | 0.606 |
CLV_PCSK_KEX2_1 | 171 | 173 | PF00082 | 0.630 |
CLV_PCSK_KEX2_1 | 249 | 251 | PF00082 | 0.527 |
CLV_PCSK_KEX2_1 | 69 | 71 | PF00082 | 0.461 |
CLV_PCSK_KEX2_1 | 88 | 90 | PF00082 | 0.312 |
CLV_PCSK_PC1ET2_1 | 128 | 130 | PF00082 | 0.537 |
CLV_PCSK_PC1ET2_1 | 171 | 173 | PF00082 | 0.651 |
CLV_PCSK_PC1ET2_1 | 69 | 71 | PF00082 | 0.266 |
CLV_PCSK_SKI1_1 | 253 | 257 | PF00082 | 0.578 |
CLV_PCSK_SKI1_1 | 357 | 361 | PF00082 | 0.281 |
CLV_PCSK_SKI1_1 | 376 | 380 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 38 | 42 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 445 | 449 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 49 | 53 | PF00082 | 0.366 |
CLV_PCSK_SKI1_1 | 539 | 543 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 78 | 82 | PF00082 | 0.405 |
DEG_APCC_DBOX_1 | 312 | 320 | PF00400 | 0.392 |
DOC_CYCLIN_RxL_1 | 249 | 257 | PF00134 | 0.502 |
DOC_CYCLIN_RxL_1 | 370 | 381 | PF00134 | 0.461 |
DOC_MAPK_gen_1 | 313 | 320 | PF00069 | 0.308 |
DOC_MAPK_gen_1 | 33 | 43 | PF00069 | 0.433 |
DOC_MAPK_MEF2A_6 | 313 | 320 | PF00069 | 0.397 |
DOC_MAPK_NFAT4_5 | 313 | 321 | PF00069 | 0.279 |
DOC_PP1_RVXF_1 | 76 | 83 | PF00149 | 0.428 |
DOC_PP2B_LxvP_1 | 12 | 15 | PF13499 | 0.374 |
DOC_PP4_FxxP_1 | 379 | 382 | PF00568 | 0.313 |
DOC_USP7_MATH_1 | 101 | 105 | PF00917 | 0.468 |
DOC_USP7_MATH_1 | 134 | 138 | PF00917 | 0.322 |
DOC_USP7_MATH_1 | 192 | 196 | PF00917 | 0.478 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.606 |
DOC_USP7_MATH_1 | 232 | 236 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 243 | 247 | PF00917 | 0.461 |
DOC_USP7_MATH_1 | 293 | 297 | PF00917 | 0.442 |
DOC_USP7_MATH_1 | 343 | 347 | PF00917 | 0.548 |
DOC_USP7_UBL2_3 | 539 | 543 | PF12436 | 0.399 |
DOC_WW_Pin1_4 | 217 | 222 | PF00397 | 0.574 |
DOC_WW_Pin1_4 | 364 | 369 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 378 | 383 | PF00397 | 0.304 |
DOC_WW_Pin1_4 | 465 | 470 | PF00397 | 0.596 |
DOC_WW_Pin1_4 | 519 | 524 | PF00397 | 0.390 |
LIG_14-3-3_CanoR_1 | 357 | 362 | PF00244 | 0.329 |
LIG_14-3-3_CanoR_1 | 400 | 408 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 503 | 513 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 70 | 76 | PF00244 | 0.379 |
LIG_Actin_WH2_2 | 287 | 305 | PF00022 | 0.503 |
LIG_APCC_ABBA_1 | 41 | 46 | PF00400 | 0.412 |
LIG_BRCT_BRCA1_1 | 410 | 414 | PF00533 | 0.398 |
LIG_BRCT_BRCA1_1 | 425 | 429 | PF00533 | 0.538 |
LIG_Clathr_ClatBox_1 | 185 | 189 | PF01394 | 0.471 |
LIG_CtBP_PxDLS_1 | 15 | 19 | PF00389 | 0.435 |
LIG_deltaCOP1_diTrp_1 | 73 | 82 | PF00928 | 0.346 |
LIG_EH_1 | 414 | 418 | PF12763 | 0.367 |
LIG_FHA_1 | 122 | 128 | PF00498 | 0.401 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.484 |
LIG_FHA_2 | 133 | 139 | PF00498 | 0.258 |
LIG_FHA_2 | 160 | 166 | PF00498 | 0.426 |
LIG_FHA_2 | 206 | 212 | PF00498 | 0.419 |
LIG_FHA_2 | 392 | 398 | PF00498 | 0.494 |
LIG_LIR_Gen_1 | 264 | 272 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 264 | 268 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 411 | 417 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 434 | 439 | PF02991 | 0.290 |
LIG_MYND_1 | 11 | 15 | PF01753 | 0.436 |
LIG_MYND_1 | 147 | 151 | PF01753 | 0.517 |
LIG_MYND_1 | 96 | 100 | PF01753 | 0.241 |
LIG_NBox_RRM_1 | 501 | 511 | PF00076 | 0.402 |
LIG_NRBOX | 224 | 230 | PF00104 | 0.530 |
LIG_NRBOX | 315 | 321 | PF00104 | 0.436 |
LIG_SH2_CRK | 265 | 269 | PF00017 | 0.548 |
LIG_SH2_SRC | 93 | 96 | PF00017 | 0.428 |
LIG_SH2_STAP1 | 534 | 538 | PF00017 | 0.425 |
LIG_SH2_STAT3 | 164 | 167 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 207 | 210 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 317 | 320 | PF00017 | 0.261 |
LIG_SH3_3 | 356 | 362 | PF00018 | 0.519 |
LIG_SUMO_SIM_par_1 | 10 | 17 | PF11976 | 0.545 |
LIG_SUMO_SIM_par_1 | 223 | 230 | PF11976 | 0.584 |
LIG_TRAF2_1 | 45 | 48 | PF00917 | 0.417 |
MOD_CDK_SPxK_1 | 364 | 370 | PF00069 | 0.492 |
MOD_CDK_SPxxK_3 | 217 | 224 | PF00069 | 0.568 |
MOD_CDK_SPxxK_3 | 519 | 526 | PF00069 | 0.388 |
MOD_CK1_1 | 241 | 247 | PF00069 | 0.597 |
MOD_CK1_1 | 296 | 302 | PF00069 | 0.446 |
MOD_CK1_1 | 423 | 429 | PF00069 | 0.514 |
MOD_CK1_1 | 464 | 470 | PF00069 | 0.696 |
MOD_CK1_1 | 490 | 496 | PF00069 | 0.521 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.510 |
MOD_CK2_1 | 343 | 349 | PF00069 | 0.547 |
MOD_CK2_1 | 391 | 397 | PF00069 | 0.500 |
MOD_CK2_1 | 42 | 48 | PF00069 | 0.409 |
MOD_CK2_1 | 512 | 518 | PF00069 | 0.493 |
MOD_Cter_Amidation | 549 | 552 | PF01082 | 0.487 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.516 |
MOD_GlcNHglycan | 295 | 298 | PF01048 | 0.479 |
MOD_GlcNHglycan | 401 | 404 | PF01048 | 0.370 |
MOD_GlcNHglycan | 469 | 472 | PF01048 | 0.743 |
MOD_GlcNHglycan | 506 | 509 | PF01048 | 0.433 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.537 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.555 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.388 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.479 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.649 |
MOD_LATS_1 | 67 | 73 | PF00433 | 0.411 |
MOD_N-GLC_1 | 3 | 8 | PF02516 | 0.467 |
MOD_N-GLC_2 | 37 | 39 | PF02516 | 0.473 |
MOD_NEK2_1 | 152 | 157 | PF00069 | 0.494 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.576 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.319 |
MOD_NEK2_1 | 408 | 413 | PF00069 | 0.300 |
MOD_NEK2_2 | 159 | 164 | PF00069 | 0.332 |
MOD_NEK2_2 | 431 | 436 | PF00069 | 0.318 |
MOD_PIKK_1 | 227 | 233 | PF00454 | 0.485 |
MOD_PIKK_1 | 5 | 11 | PF00454 | 0.554 |
MOD_PK_1 | 326 | 332 | PF00069 | 0.384 |
MOD_PKA_1 | 170 | 176 | PF00069 | 0.700 |
MOD_PKA_1 | 69 | 75 | PF00069 | 0.265 |
MOD_PKA_2 | 152 | 158 | PF00069 | 0.479 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.659 |
MOD_PKA_2 | 399 | 405 | PF00069 | 0.418 |
MOD_PKA_2 | 423 | 429 | PF00069 | 0.481 |
MOD_PKA_2 | 464 | 470 | PF00069 | 0.718 |
MOD_PKA_2 | 490 | 496 | PF00069 | 0.500 |
MOD_PKA_2 | 69 | 75 | PF00069 | 0.340 |
MOD_PKB_1 | 168 | 176 | PF00069 | 0.659 |
MOD_PKB_1 | 443 | 451 | PF00069 | 0.486 |
MOD_Plk_1 | 121 | 127 | PF00069 | 0.539 |
MOD_Plk_1 | 153 | 159 | PF00069 | 0.391 |
MOD_Plk_1 | 431 | 437 | PF00069 | 0.375 |
MOD_Plk_4 | 159 | 165 | PF00069 | 0.432 |
MOD_Plk_4 | 180 | 186 | PF00069 | 0.514 |
MOD_Plk_4 | 264 | 270 | PF00069 | 0.519 |
MOD_Plk_4 | 306 | 312 | PF00069 | 0.383 |
MOD_Plk_4 | 477 | 483 | PF00069 | 0.488 |
MOD_ProDKin_1 | 217 | 223 | PF00069 | 0.573 |
MOD_ProDKin_1 | 364 | 370 | PF00069 | 0.541 |
MOD_ProDKin_1 | 378 | 384 | PF00069 | 0.303 |
MOD_ProDKin_1 | 465 | 471 | PF00069 | 0.594 |
MOD_ProDKin_1 | 519 | 525 | PF00069 | 0.385 |
MOD_SUMO_for_1 | 51 | 54 | PF00179 | 0.448 |
MOD_SUMO_rev_2 | 195 | 205 | PF00179 | 0.463 |
MOD_SUMO_rev_2 | 522 | 531 | PF00179 | 0.320 |
TRG_DiLeu_BaLyEn_6 | 8 | 13 | PF01217 | 0.479 |
TRG_ENDOCYTIC_2 | 265 | 268 | PF00928 | 0.475 |
TRG_ENDOCYTIC_2 | 317 | 320 | PF00928 | 0.261 |
TRG_ENDOCYTIC_2 | 534 | 537 | PF00928 | 0.433 |
TRG_ER_diArg_1 | 140 | 142 | PF00400 | 0.566 |
TRG_ER_diArg_1 | 168 | 170 | PF00400 | 0.639 |
TRG_ER_diArg_1 | 248 | 250 | PF00400 | 0.488 |
TRG_ER_diArg_1 | 86 | 89 | PF00400 | 0.285 |
TRG_NLS_MonoExtC_3 | 169 | 174 | PF00514 | 0.727 |
TRG_NLS_MonoExtN_4 | 168 | 174 | PF00514 | 0.691 |
TRG_Pf-PMV_PEXEL_1 | 253 | 257 | PF00026 | 0.492 |
TRG_Pf-PMV_PEXEL_1 | 437 | 442 | PF00026 | 0.388 |
TRG_Pf-PMV_PEXEL_1 | 69 | 73 | PF00026 | 0.387 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKI5 | Leptomonas seymouri | 52% | 99% |
A0A1X0P429 | Trypanosomatidae | 26% | 100% |
A0A3R7MVK8 | Trypanosoma rangeli | 27% | 100% |
A0A3S7X0E6 | Leishmania donovani | 79% | 100% |
A4I2N0 | Leishmania infantum | 79% | 100% |
D0A5P5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 98% |
E9AD21 | Leishmania major | 79% | 99% |
E9AYU6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
V5DP58 | Trypanosoma cruzi | 27% | 100% |