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: 4 |
NetGPI | no | yes: 0, no: 4 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Term | Name | Level | Count |
---|---|---|---|
GO:0006996 | organelle organization | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 167 | 171 | PF00656 | 0.302 |
CLV_C14_Caspase3-7 | 259 | 263 | PF00656 | 0.363 |
CLV_C14_Caspase3-7 | 307 | 311 | PF00656 | 0.280 |
CLV_C14_Caspase3-7 | 508 | 512 | PF00656 | 0.319 |
CLV_C14_Caspase3-7 | 600 | 604 | PF00656 | 0.375 |
CLV_NRD_NRD_1 | 163 | 165 | PF00675 | 0.308 |
CLV_NRD_NRD_1 | 21 | 23 | PF00675 | 0.457 |
CLV_NRD_NRD_1 | 230 | 232 | PF00675 | 0.388 |
CLV_NRD_NRD_1 | 235 | 237 | PF00675 | 0.341 |
CLV_NRD_NRD_1 | 362 | 364 | PF00675 | 0.347 |
CLV_NRD_NRD_1 | 504 | 506 | PF00675 | 0.289 |
CLV_NRD_NRD_1 | 571 | 573 | PF00675 | 0.404 |
CLV_NRD_NRD_1 | 576 | 578 | PF00675 | 0.384 |
CLV_NRD_NRD_1 | 623 | 625 | PF00675 | 0.509 |
CLV_PCSK_FUR_1 | 161 | 165 | PF00082 | 0.304 |
CLV_PCSK_FUR_1 | 502 | 506 | PF00082 | 0.282 |
CLV_PCSK_KEX2_1 | 163 | 165 | PF00082 | 0.308 |
CLV_PCSK_KEX2_1 | 21 | 23 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 230 | 232 | PF00082 | 0.477 |
CLV_PCSK_KEX2_1 | 255 | 257 | PF00082 | 0.380 |
CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.351 |
CLV_PCSK_KEX2_1 | 504 | 506 | PF00082 | 0.288 |
CLV_PCSK_KEX2_1 | 571 | 573 | PF00082 | 0.404 |
CLV_PCSK_KEX2_1 | 596 | 598 | PF00082 | 0.324 |
CLV_PCSK_KEX2_1 | 622 | 624 | PF00082 | 0.351 |
CLV_PCSK_PC1ET2_1 | 255 | 257 | PF00082 | 0.380 |
CLV_PCSK_PC1ET2_1 | 596 | 598 | PF00082 | 0.322 |
CLV_PCSK_SKI1_1 | 200 | 204 | PF00082 | 0.615 |
CLV_PCSK_SKI1_1 | 541 | 545 | PF00082 | 0.353 |
DEG_APCC_DBOX_1 | 199 | 207 | PF00400 | 0.340 |
DEG_APCC_DBOX_1 | 540 | 548 | PF00400 | 0.333 |
DEG_APCC_KENBOX_2 | 437 | 441 | PF00400 | 0.343 |
DEG_APCC_KENBOX_2 | 96 | 100 | PF00400 | 0.343 |
DEG_ODPH_VHL_1 | 407 | 418 | PF01847 | 0.296 |
DEG_ODPH_VHL_1 | 66 | 77 | PF01847 | 0.304 |
DEG_SCF_FBW7_1 | 206 | 212 | PF00400 | 0.325 |
DEG_SCF_FBW7_1 | 547 | 553 | PF00400 | 0.320 |
DOC_CKS1_1 | 206 | 211 | PF01111 | 0.326 |
DOC_CKS1_1 | 547 | 552 | PF01111 | 0.320 |
DOC_CYCLIN_RxL_1 | 346 | 359 | PF00134 | 0.291 |
DOC_CYCLIN_RxL_1 | 5 | 18 | PF00134 | 0.311 |
DOC_MAPK_gen_1 | 101 | 109 | PF00069 | 0.342 |
DOC_MAPK_gen_1 | 185 | 193 | PF00069 | 0.333 |
DOC_MAPK_gen_1 | 195 | 203 | PF00069 | 0.318 |
DOC_MAPK_gen_1 | 442 | 450 | PF00069 | 0.365 |
DOC_MAPK_gen_1 | 526 | 534 | PF00069 | 0.330 |
DOC_MAPK_gen_1 | 536 | 544 | PF00069 | 0.300 |
DOC_USP7_MATH_1 | 102 | 106 | PF00917 | 0.346 |
DOC_USP7_MATH_1 | 209 | 213 | PF00917 | 0.319 |
DOC_USP7_MATH_1 | 443 | 447 | PF00917 | 0.346 |
DOC_USP7_MATH_1 | 550 | 554 | PF00917 | 0.314 |
DOC_USP7_UBL2_3 | 237 | 241 | PF12436 | 0.510 |
DOC_USP7_UBL2_3 | 339 | 343 | PF12436 | 0.266 |
DOC_USP7_UBL2_3 | 438 | 442 | PF12436 | 0.361 |
DOC_USP7_UBL2_3 | 578 | 582 | PF12436 | 0.318 |
DOC_USP7_UBL2_3 | 97 | 101 | PF12436 | 0.345 |
DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.332 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.435 |
DOC_WW_Pin1_4 | 371 | 376 | PF00397 | 0.380 |
DOC_WW_Pin1_4 | 546 | 551 | PF00397 | 0.466 |
LIG_Actin_WH2_2 | 150 | 165 | PF00022 | 0.314 |
LIG_Actin_WH2_2 | 491 | 506 | PF00022 | 0.291 |
LIG_Clathr_ClatBox_1 | 418 | 422 | PF01394 | 0.294 |
LIG_Clathr_ClatBox_1 | 77 | 81 | PF01394 | 0.487 |
LIG_CtBP_PxDLS_1 | 415 | 419 | PF00389 | 0.305 |
LIG_CtBP_PxDLS_1 | 74 | 78 | PF00389 | 0.313 |
LIG_FHA_1 | 141 | 147 | PF00498 | 0.317 |
LIG_FHA_1 | 482 | 488 | PF00498 | 0.294 |
LIG_FHA_2 | 165 | 171 | PF00498 | 0.304 |
LIG_FHA_2 | 318 | 324 | PF00498 | 0.290 |
LIG_FHA_2 | 506 | 512 | PF00498 | 0.403 |
LIG_LIR_Apic_2 | 403 | 409 | PF02991 | 0.292 |
LIG_LIR_Apic_2 | 62 | 68 | PF02991 | 0.486 |
LIG_LIR_Gen_1 | 151 | 162 | PF02991 | 0.330 |
LIG_LIR_Gen_1 | 297 | 304 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 492 | 503 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 137 | 141 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 17 | 23 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 358 | 364 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 478 | 482 | PF02991 | 0.324 |
LIG_NRBOX | 214 | 220 | PF00104 | 0.354 |
LIG_NRBOX | 555 | 561 | PF00104 | 0.350 |
LIG_SH2_STAT5 | 340 | 343 | PF00017 | 0.265 |
LIG_SH2_STAT5 | 406 | 409 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 65 | 68 | PF00017 | 0.479 |
LIG_TRAF2_1 | 248 | 251 | PF00917 | 0.502 |
LIG_TRAF2_1 | 589 | 592 | PF00917 | 0.386 |
MOD_CDK_SPxxK_3 | 30 | 37 | PF00069 | 0.393 |
MOD_CDK_SPxxK_3 | 371 | 378 | PF00069 | 0.374 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.330 |
MOD_CK1_1 | 546 | 552 | PF00069 | 0.324 |
MOD_CK2_1 | 317 | 323 | PF00069 | 0.506 |
MOD_GlcNHglycan | 103 | 107 | PF01048 | 0.345 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.480 |
MOD_GlcNHglycan | 444 | 448 | PF01048 | 0.341 |
MOD_GlcNHglycan | 552 | 555 | PF01048 | 0.336 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.320 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.296 |
MOD_GSK3_1 | 532 | 539 | PF00069 | 0.309 |
MOD_GSK3_1 | 546 | 553 | PF00069 | 0.301 |
MOD_NEK2_1 | 191 | 196 | PF00069 | 0.341 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.507 |
MOD_NEK2_1 | 532 | 537 | PF00069 | 0.312 |
MOD_PKA_1 | 195 | 201 | PF00069 | 0.317 |
MOD_PKA_1 | 536 | 542 | PF00069 | 0.308 |
MOD_PKA_2 | 109 | 115 | PF00069 | 0.389 |
MOD_PKA_2 | 450 | 456 | PF00069 | 0.305 |
MOD_PKA_2 | 609 | 615 | PF00069 | 0.422 |
MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.330 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.432 |
MOD_ProDKin_1 | 371 | 377 | PF00069 | 0.377 |
MOD_ProDKin_1 | 546 | 552 | PF00069 | 0.464 |
TRG_AP2beta_CARGO_1 | 17 | 27 | PF09066 | 0.543 |
TRG_AP2beta_CARGO_1 | 358 | 368 | PF09066 | 0.539 |
TRG_DiLeu_BaEn_1 | 129 | 134 | PF01217 | 0.308 |
TRG_DiLeu_BaEn_1 | 470 | 475 | PF01217 | 0.308 |
TRG_DiLeu_BaLyEn_6 | 313 | 318 | PF01217 | 0.318 |
TRG_ENDOCYTIC_2 | 138 | 141 | PF00928 | 0.453 |
TRG_ENDOCYTIC_2 | 300 | 303 | PF00928 | 0.453 |
TRG_ENDOCYTIC_2 | 479 | 482 | PF00928 | 0.309 |
TRG_ER_diArg_1 | 161 | 164 | PF00400 | 0.397 |
TRG_ER_diArg_1 | 184 | 187 | PF00400 | 0.326 |
TRG_ER_diArg_1 | 20 | 22 | PF00400 | 0.429 |
TRG_ER_diArg_1 | 230 | 233 | PF00400 | 0.435 |
TRG_ER_diArg_1 | 361 | 363 | PF00400 | 0.492 |
TRG_ER_diArg_1 | 397 | 400 | PF00400 | 0.291 |
TRG_ER_diArg_1 | 502 | 505 | PF00400 | 0.298 |
TRG_ER_diArg_1 | 525 | 528 | PF00400 | 0.453 |
TRG_ER_diArg_1 | 56 | 59 | PF00400 | 0.390 |
TRG_ER_diArg_1 | 571 | 574 | PF00400 | 0.408 |
TRG_ER_diArg_1 | 622 | 624 | PF00400 | 0.358 |
TRG_Pf-PMV_PEXEL_1 | 10 | 15 | PF00026 | 0.347 |
TRG_Pf-PMV_PEXEL_1 | 21 | 26 | PF00026 | 0.459 |
TRG_Pf-PMV_PEXEL_1 | 230 | 234 | PF00026 | 0.547 |
TRG_Pf-PMV_PEXEL_1 | 247 | 251 | PF00026 | 0.362 |
TRG_Pf-PMV_PEXEL_1 | 351 | 356 | PF00026 | 0.294 |
TRG_Pf-PMV_PEXEL_1 | 362 | 367 | PF00026 | 0.340 |
TRG_Pf-PMV_PEXEL_1 | 571 | 575 | PF00026 | 0.410 |
TRG_Pf-PMV_PEXEL_1 | 588 | 592 | PF00026 | 0.318 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0NYQ1 | Trypanosomatidae | 26% | 66% |
E8NHP1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 74% |
E8NHS4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |