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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
Related structures:
AlphaFold database: E9B5D1
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 4 |
GO:0004416 | hydroxyacylglutathione hydrolase activity | 5 | 3 |
GO:0016787 | hydrolase activity | 2 | 4 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 3 |
GO:0016790 | thiolester hydrolase activity | 4 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 421 | 425 | PF00656 | 0.624 |
CLV_NRD_NRD_1 | 511 | 513 | PF00675 | 0.401 |
CLV_PCSK_KEX2_1 | 510 | 512 | PF00082 | 0.368 |
CLV_PCSK_SKI1_1 | 158 | 162 | PF00082 | 0.199 |
CLV_PCSK_SKI1_1 | 427 | 431 | PF00082 | 0.375 |
DOC_CKS1_1 | 127 | 132 | PF01111 | 0.334 |
DOC_CYCLIN_yClb3_PxF_3 | 63 | 71 | PF00134 | 0.598 |
DOC_CYCLIN_yCln2_LP_2 | 206 | 212 | PF00134 | 0.535 |
DOC_MAPK_DCC_7 | 158 | 167 | PF00069 | 0.500 |
DOC_MAPK_MEF2A_6 | 158 | 167 | PF00069 | 0.483 |
DOC_MAPK_MEF2A_6 | 203 | 212 | PF00069 | 0.535 |
DOC_MAPK_MEF2A_6 | 471 | 479 | PF00069 | 0.459 |
DOC_PP1_RVXF_1 | 259 | 265 | PF00149 | 0.446 |
DOC_PP2B_LxvP_1 | 206 | 209 | PF13499 | 0.535 |
DOC_PP4_FxxP_1 | 456 | 459 | PF00568 | 0.621 |
DOC_USP7_MATH_1 | 457 | 461 | PF00917 | 0.541 |
DOC_USP7_MATH_2 | 343 | 349 | PF00917 | 0.604 |
DOC_USP7_UBL2_3 | 488 | 492 | PF12436 | 0.549 |
DOC_WW_Pin1_4 | 115 | 120 | PF00397 | 0.412 |
DOC_WW_Pin1_4 | 126 | 131 | PF00397 | 0.426 |
DOC_WW_Pin1_4 | 280 | 285 | PF00397 | 0.535 |
DOC_WW_Pin1_4 | 339 | 344 | PF00397 | 0.426 |
DOC_WW_Pin1_4 | 406 | 411 | PF00397 | 0.612 |
DOC_WW_Pin1_4 | 491 | 496 | PF00397 | 0.472 |
LIG_14-3-3_CanoR_1 | 158 | 163 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 356 | 360 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 364 | 369 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 402 | 410 | PF00244 | 0.692 |
LIG_14-3-3_CanoR_1 | 451 | 459 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 512 | 518 | PF00244 | 0.667 |
LIG_Actin_WH2_2 | 107 | 125 | PF00022 | 0.422 |
LIG_Actin_WH2_2 | 425 | 442 | PF00022 | 0.635 |
LIG_Actin_WH2_2 | 472 | 490 | PF00022 | 0.508 |
LIG_APCC_ABBA_1 | 165 | 170 | PF00400 | 0.564 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.622 |
LIG_BIR_III_2 | 281 | 285 | PF00653 | 0.478 |
LIG_BRCT_BRCA1_1 | 1 | 5 | PF00533 | 0.697 |
LIG_BRCT_BRCA1_1 | 282 | 286 | PF00533 | 0.535 |
LIG_BRCT_BRCA1_1 | 306 | 310 | PF00533 | 0.431 |
LIG_BRCT_BRCA1_1 | 66 | 70 | PF00533 | 0.625 |
LIG_BRCT_BRCA1_1 | 71 | 75 | PF00533 | 0.608 |
LIG_Clathr_ClatBox_1 | 476 | 480 | PF01394 | 0.571 |
LIG_EH_1 | 61 | 65 | PF12763 | 0.572 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.626 |
LIG_FHA_1 | 179 | 185 | PF00498 | 0.501 |
LIG_FHA_1 | 211 | 217 | PF00498 | 0.453 |
LIG_FHA_1 | 344 | 350 | PF00498 | 0.551 |
LIG_FHA_1 | 387 | 393 | PF00498 | 0.506 |
LIG_FHA_2 | 356 | 362 | PF00498 | 0.518 |
LIG_FHA_2 | 369 | 375 | PF00498 | 0.635 |
LIG_FHA_2 | 407 | 413 | PF00498 | 0.709 |
LIG_FHA_2 | 476 | 482 | PF00498 | 0.567 |
LIG_LIR_Apic_2 | 35 | 40 | PF02991 | 0.472 |
LIG_LIR_Apic_2 | 454 | 459 | PF02991 | 0.497 |
LIG_LIR_Apic_2 | 6 | 10 | PF02991 | 0.478 |
LIG_LIR_Gen_1 | 170 | 179 | PF02991 | 0.432 |
LIG_LIR_Gen_1 | 2 | 13 | PF02991 | 0.599 |
LIG_LIR_Gen_1 | 283 | 293 | PF02991 | 0.478 |
LIG_LIR_Gen_1 | 342 | 352 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 170 | 175 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 342 | 347 | PF02991 | 0.544 |
LIG_LIR_Nem_3 | 43 | 49 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 72 | 78 | PF02991 | 0.472 |
LIG_MYND_1 | 256 | 260 | PF01753 | 0.478 |
LIG_Pex14_2 | 135 | 139 | PF04695 | 0.406 |
LIG_Pex14_2 | 64 | 68 | PF04695 | 0.583 |
LIG_SH2_CRK | 172 | 176 | PF00017 | 0.498 |
LIG_SH2_CRK | 37 | 41 | PF00017 | 0.495 |
LIG_SH2_CRK | 46 | 50 | PF00017 | 0.417 |
LIG_SH2_CRK | 89 | 93 | PF00017 | 0.406 |
LIG_SH2_NCK_1 | 140 | 144 | PF00017 | 0.331 |
LIG_SH2_SRC | 174 | 177 | PF00017 | 0.535 |
LIG_SH2_SRC | 19 | 22 | PF00017 | 0.331 |
LIG_SH2_SRC | 85 | 88 | PF00017 | 0.210 |
LIG_SH2_STAP1 | 172 | 176 | PF00017 | 0.431 |
LIG_SH2_STAP1 | 19 | 23 | PF00017 | 0.355 |
LIG_SH2_STAP1 | 388 | 392 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 174 | 177 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 383 | 386 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 388 | 391 | PF00017 | 0.485 |
LIG_SH2_STAT5 | 418 | 421 | PF00017 | 0.552 |
LIG_SH2_STAT5 | 46 | 49 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 506 | 509 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 82 | 85 | PF00017 | 0.321 |
LIG_SH3_1 | 121 | 127 | PF00018 | 0.465 |
LIG_SH3_1 | 237 | 243 | PF00018 | 0.542 |
LIG_SH3_3 | 121 | 127 | PF00018 | 0.384 |
LIG_SH3_3 | 160 | 166 | PF00018 | 0.494 |
LIG_SH3_3 | 186 | 192 | PF00018 | 0.436 |
LIG_SH3_3 | 236 | 242 | PF00018 | 0.520 |
LIG_SH3_3 | 250 | 256 | PF00018 | 0.424 |
LIG_SH3_3 | 407 | 413 | PF00018 | 0.630 |
LIG_SH3_3 | 57 | 63 | PF00018 | 0.576 |
LIG_SH3_3 | 88 | 94 | PF00018 | 0.550 |
LIG_SH3_3 | 97 | 103 | PF00018 | 0.362 |
LIG_SH3_5 | 103 | 107 | PF00018 | 0.258 |
LIG_SUMO_SIM_anti_2 | 395 | 401 | PF11976 | 0.589 |
LIG_SUMO_SIM_par_1 | 395 | 401 | PF11976 | 0.589 |
LIG_SUMO_SIM_par_1 | 475 | 482 | PF11976 | 0.521 |
LIG_TRAF2_1 | 243 | 246 | PF00917 | 0.446 |
LIG_TRAF2_1 | 314 | 317 | PF00917 | 0.478 |
LIG_TRAF2_1 | 371 | 374 | PF00917 | 0.594 |
LIG_TYR_ITIM | 44 | 49 | PF00017 | 0.331 |
LIG_TYR_ITIM | 87 | 92 | PF00017 | 0.399 |
LIG_UBA3_1 | 175 | 183 | PF00899 | 0.535 |
LIG_UBA3_1 | 74 | 80 | PF00899 | 0.411 |
LIG_WRC_WIRS_1 | 231 | 236 | PF05994 | 0.360 |
LIG_WRC_WIRS_1 | 65 | 70 | PF05994 | 0.587 |
LIG_WW_3 | 241 | 245 | PF00397 | 0.401 |
MOD_CDC14_SPxK_1 | 118 | 121 | PF00782 | 0.461 |
MOD_CDK_SPxK_1 | 115 | 121 | PF00069 | 0.446 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.431 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.537 |
MOD_CK1_1 | 334 | 340 | PF00069 | 0.421 |
MOD_CK2_1 | 232 | 238 | PF00069 | 0.485 |
MOD_CK2_1 | 311 | 317 | PF00069 | 0.478 |
MOD_CK2_1 | 339 | 345 | PF00069 | 0.458 |
MOD_CK2_1 | 355 | 361 | PF00069 | 0.509 |
MOD_CK2_1 | 368 | 374 | PF00069 | 0.652 |
MOD_DYRK1A_RPxSP_1 | 406 | 410 | PF00069 | 0.621 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.650 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.309 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.698 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.241 |
MOD_GlcNHglycan | 435 | 438 | PF01048 | 0.296 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.325 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.433 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.455 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.559 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.634 |
MOD_GSK3_1 | 459 | 466 | PF00069 | 0.505 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.442 |
MOD_NEK2_1 | 230 | 235 | PF00069 | 0.447 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.571 |
MOD_NEK2_1 | 81 | 86 | PF00069 | 0.266 |
MOD_NEK2_2 | 40 | 45 | PF00069 | 0.331 |
MOD_PIKK_1 | 364 | 370 | PF00454 | 0.665 |
MOD_PIKK_1 | 404 | 410 | PF00454 | 0.581 |
MOD_PIKK_1 | 451 | 457 | PF00454 | 0.540 |
MOD_PKA_2 | 355 | 361 | PF00069 | 0.588 |
MOD_PKA_2 | 401 | 407 | PF00069 | 0.645 |
MOD_PKB_1 | 510 | 518 | PF00069 | 0.485 |
MOD_Plk_4 | 13 | 19 | PF00069 | 0.260 |
MOD_Plk_4 | 152 | 158 | PF00069 | 0.550 |
MOD_Plk_4 | 304 | 310 | PF00069 | 0.437 |
MOD_Plk_4 | 331 | 337 | PF00069 | 0.535 |
MOD_Plk_4 | 355 | 361 | PF00069 | 0.588 |
MOD_Plk_4 | 395 | 401 | PF00069 | 0.545 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.648 |
MOD_ProDKin_1 | 115 | 121 | PF00069 | 0.419 |
MOD_ProDKin_1 | 126 | 132 | PF00069 | 0.418 |
MOD_ProDKin_1 | 280 | 286 | PF00069 | 0.535 |
MOD_ProDKin_1 | 339 | 345 | PF00069 | 0.427 |
MOD_ProDKin_1 | 406 | 412 | PF00069 | 0.603 |
MOD_ProDKin_1 | 491 | 497 | PF00069 | 0.471 |
TRG_DiLeu_BaEn_1 | 377 | 382 | PF01217 | 0.554 |
TRG_DiLeu_BaEn_1 | 395 | 400 | PF01217 | 0.644 |
TRG_DiLeu_BaEn_4 | 268 | 274 | PF01217 | 0.439 |
TRG_DiLeu_BaEn_4 | 377 | 383 | PF01217 | 0.543 |
TRG_DiLeu_BaLyEn_6 | 253 | 258 | PF01217 | 0.478 |
TRG_DiLeu_BaLyEn_6 | 388 | 393 | PF01217 | 0.536 |
TRG_DiLeu_BaLyEn_6 | 472 | 477 | PF01217 | 0.482 |
TRG_DiLeu_BaLyEn_6 | 73 | 78 | PF01217 | 0.535 |
TRG_ENDOCYTIC_2 | 172 | 175 | PF00928 | 0.498 |
TRG_ENDOCYTIC_2 | 46 | 49 | PF00928 | 0.430 |
TRG_ENDOCYTIC_2 | 89 | 92 | PF00928 | 0.429 |
TRG_ER_diArg_1 | 363 | 366 | PF00400 | 0.560 |
TRG_ER_diArg_1 | 510 | 512 | PF00400 | 0.516 |
TRG_Pf-PMV_PEXEL_1 | 391 | 395 | PF00026 | 0.346 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PD83 | Leptomonas seymouri | 66% | 99% |
A0A0S4IM37 | Bodo saltans | 33% | 100% |
A0A1X0PA00 | Trypanosomatidae | 37% | 100% |
A0A3R7K9K9 | Trypanosoma rangeli | 39% | 100% |
A0A3S7X8A7 | Leishmania donovani | 90% | 100% |
A4HB60 | Leishmania braziliensis | 82% | 100% |
A4IAA8 | Leishmania infantum | 91% | 100% |
C9ZLY8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
Q4Q2K2 | Leishmania major | 91% | 100% |
V5B5D7 | Trypanosoma cruzi | 40% | 100% |