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: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
Related structures:
AlphaFold database: A4HB80
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 13 |
GO:0008152 | metabolic process | 1 | 13 |
GO:0044238 | primary metabolic process | 2 | 13 |
GO:0071704 | organic substance metabolic process | 2 | 13 |
GO:0009056 | catabolic process | 2 | 2 |
GO:0016042 | lipid catabolic process | 4 | 2 |
GO:1901575 | organic substance catabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 13 |
GO:0004806 | triglyceride lipase activity | 5 | 12 |
GO:0016298 | lipase activity | 4 | 12 |
GO:0016787 | hydrolase activity | 2 | 13 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 12 |
GO:0052689 | carboxylic ester hydrolase activity | 4 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 261 | 265 | PF00656 | 0.508 |
CLV_C14_Caspase3-7 | 74 | 78 | PF00656 | 0.508 |
CLV_MEL_PAP_1 | 156 | 162 | PF00089 | 0.327 |
CLV_NRD_NRD_1 | 133 | 135 | PF00675 | 0.350 |
CLV_NRD_NRD_1 | 168 | 170 | PF00675 | 0.368 |
CLV_NRD_NRD_1 | 322 | 324 | PF00675 | 0.349 |
CLV_PCSK_KEX2_1 | 133 | 135 | PF00082 | 0.336 |
CLV_PCSK_KEX2_1 | 168 | 170 | PF00082 | 0.358 |
CLV_PCSK_KEX2_1 | 322 | 324 | PF00082 | 0.322 |
CLV_PCSK_KEX2_1 | 564 | 566 | PF00082 | 0.404 |
CLV_PCSK_PC1ET2_1 | 564 | 566 | PF00082 | 0.404 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 375 | 379 | PF00082 | 0.390 |
CLV_PCSK_SKI1_1 | 419 | 423 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 462 | 466 | PF00082 | 0.273 |
CLV_PCSK_SKI1_1 | 497 | 501 | PF00082 | 0.410 |
DEG_APCC_DBOX_1 | 434 | 442 | PF00400 | 0.593 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.430 |
DEG_SPOP_SBC_1 | 358 | 362 | PF00917 | 0.492 |
DOC_CYCLIN_RxL_1 | 372 | 381 | PF00134 | 0.557 |
DOC_CYCLIN_yCln2_LP_2 | 214 | 220 | PF00134 | 0.332 |
DOC_CYCLIN_yCln2_LP_2 | 309 | 315 | PF00134 | 0.373 |
DOC_MAPK_DCC_7 | 307 | 316 | PF00069 | 0.397 |
DOC_MAPK_gen_1 | 322 | 331 | PF00069 | 0.497 |
DOC_MAPK_gen_1 | 417 | 426 | PF00069 | 0.587 |
DOC_MAPK_MEF2A_6 | 307 | 316 | PF00069 | 0.536 |
DOC_MAPK_MEF2A_6 | 322 | 331 | PF00069 | 0.438 |
DOC_MAPK_RevD_3 | 309 | 324 | PF00069 | 0.469 |
DOC_PP1_RVXF_1 | 476 | 483 | PF00149 | 0.627 |
DOC_PP2B_LxvP_1 | 309 | 312 | PF13499 | 0.536 |
DOC_PP2B_LxvP_1 | 41 | 44 | PF13499 | 0.650 |
DOC_SPAK_OSR1_1 | 425 | 429 | PF12202 | 0.565 |
DOC_USP7_MATH_1 | 315 | 319 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 358 | 362 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 512 | 516 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 68 | 72 | PF00917 | 0.537 |
DOC_WW_Pin1_4 | 334 | 339 | PF00397 | 0.522 |
DOC_WW_Pin1_4 | 349 | 354 | PF00397 | 0.475 |
DOC_WW_Pin1_4 | 489 | 494 | PF00397 | 0.666 |
DOC_WW_Pin1_4 | 522 | 527 | PF00397 | 0.573 |
LIG_14-3-3_CanoR_1 | 133 | 139 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 550 | 556 | PF00244 | 0.556 |
LIG_14-3-3_CterR_2 | 565 | 570 | PF00244 | 0.503 |
LIG_Actin_WH2_2 | 93 | 109 | PF00022 | 0.469 |
LIG_BRCT_BRCA1_1 | 199 | 203 | PF00533 | 0.421 |
LIG_BRCT_BRCA1_1 | 27 | 31 | PF00533 | 0.463 |
LIG_BRCT_BRCA1_1 | 87 | 91 | PF00533 | 0.536 |
LIG_deltaCOP1_diTrp_1 | 264 | 270 | PF00928 | 0.509 |
LIG_deltaCOP1_diTrp_1 | 459 | 465 | PF00928 | 0.594 |
LIG_eIF4E_1 | 185 | 191 | PF01652 | 0.469 |
LIG_FAT_LD_1 | 112 | 120 | PF03623 | 0.469 |
LIG_FHA_1 | 172 | 178 | PF00498 | 0.563 |
LIG_FHA_1 | 185 | 191 | PF00498 | 0.449 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.555 |
LIG_FHA_1 | 303 | 309 | PF00498 | 0.455 |
LIG_FHA_1 | 372 | 378 | PF00498 | 0.638 |
LIG_FHA_1 | 382 | 388 | PF00498 | 0.572 |
LIG_FHA_2 | 290 | 296 | PF00498 | 0.460 |
LIG_FHA_2 | 334 | 340 | PF00498 | 0.532 |
LIG_FHA_2 | 496 | 502 | PF00498 | 0.727 |
LIG_FHA_2 | 59 | 65 | PF00498 | 0.472 |
LIG_FHA_2 | 70 | 76 | PF00498 | 0.536 |
LIG_FHA_2 | 97 | 103 | PF00498 | 0.536 |
LIG_GBD_Chelix_1 | 22 | 30 | PF00786 | 0.392 |
LIG_GBD_Chelix_1 | 472 | 480 | PF00786 | 0.371 |
LIG_LIR_Gen_1 | 148 | 157 | PF02991 | 0.457 |
LIG_LIR_Gen_1 | 176 | 185 | PF02991 | 0.515 |
LIG_LIR_Gen_1 | 514 | 524 | PF02991 | 0.572 |
LIG_LIR_Nem_3 | 148 | 152 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 179 | 185 | PF02991 | 0.550 |
LIG_LIR_Nem_3 | 20 | 24 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 264 | 270 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 459 | 463 | PF02991 | 0.580 |
LIG_LIR_Nem_3 | 514 | 520 | PF02991 | 0.567 |
LIG_LIR_Nem_3 | 64 | 69 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 88 | 93 | PF02991 | 0.471 |
LIG_MLH1_MIPbox_1 | 87 | 91 | PF16413 | 0.536 |
LIG_NRBOX | 437 | 443 | PF00104 | 0.594 |
LIG_NRBOX | 475 | 481 | PF00104 | 0.478 |
LIG_Pex14_2 | 422 | 426 | PF04695 | 0.573 |
LIG_Pex14_2 | 465 | 469 | PF04695 | 0.511 |
LIG_PTB_Apo_2 | 307 | 314 | PF02174 | 0.465 |
LIG_SH2_CRK | 149 | 153 | PF00017 | 0.492 |
LIG_SH2_CRK | 27 | 31 | PF00017 | 0.392 |
LIG_SH2_CRK | 485 | 489 | PF00017 | 0.635 |
LIG_SH2_CRK | 50 | 54 | PF00017 | 0.536 |
LIG_SH2_NCK_1 | 485 | 489 | PF00017 | 0.635 |
LIG_SH2_SRC | 390 | 393 | PF00017 | 0.554 |
LIG_SH2_STAP1 | 27 | 31 | PF00017 | 0.392 |
LIG_SH2_STAP1 | 399 | 403 | PF00017 | 0.644 |
LIG_SH2_STAP1 | 63 | 67 | PF00017 | 0.477 |
LIG_SH2_STAT3 | 437 | 440 | PF00017 | 0.538 |
LIG_SH2_STAT5 | 21 | 24 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 334 | 337 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.628 |
LIG_SH2_STAT5 | 463 | 466 | PF00017 | 0.587 |
LIG_SH2_STAT5 | 468 | 471 | PF00017 | 0.567 |
LIG_SH2_STAT5 | 519 | 522 | PF00017 | 0.602 |
LIG_SH2_STAT5 | 90 | 93 | PF00017 | 0.508 |
LIG_SH3_3 | 276 | 282 | PF00018 | 0.532 |
LIG_SUMO_SIM_par_1 | 101 | 108 | PF11976 | 0.504 |
LIG_SUMO_SIM_par_1 | 281 | 287 | PF11976 | 0.492 |
LIG_SUMO_SIM_par_1 | 39 | 45 | PF11976 | 0.612 |
LIG_SUMO_SIM_par_1 | 532 | 537 | PF11976 | 0.522 |
LIG_TRAF2_1 | 62 | 65 | PF00917 | 0.508 |
LIG_TRAF2_1 | 99 | 102 | PF00917 | 0.524 |
LIG_TYR_ITIM | 25 | 30 | PF00017 | 0.392 |
LIG_TYR_ITIM | 483 | 488 | PF00017 | 0.357 |
LIG_UBA3_1 | 115 | 121 | PF00899 | 0.391 |
LIG_WRC_WIRS_1 | 496 | 501 | PF05994 | 0.622 |
LIG_WRC_WIRS_1 | 90 | 95 | PF05994 | 0.421 |
MOD_CK1_1 | 137 | 143 | PF00069 | 0.392 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.394 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.302 |
MOD_CK1_1 | 360 | 366 | PF00069 | 0.627 |
MOD_CK1_1 | 430 | 436 | PF00069 | 0.386 |
MOD_CK1_1 | 492 | 498 | PF00069 | 0.676 |
MOD_CK1_1 | 515 | 521 | PF00069 | 0.469 |
MOD_CK1_1 | 525 | 531 | PF00069 | 0.527 |
MOD_CK2_1 | 247 | 253 | PF00069 | 0.418 |
MOD_CK2_1 | 294 | 300 | PF00069 | 0.293 |
MOD_CK2_1 | 495 | 501 | PF00069 | 0.674 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.330 |
MOD_CK2_1 | 96 | 102 | PF00069 | 0.403 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.389 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.378 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.373 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.326 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.654 |
MOD_GlcNHglycan | 444 | 447 | PF01048 | 0.600 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.397 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.458 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.437 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.264 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.344 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.589 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.421 |
MOD_GSK3_1 | 491 | 498 | PF00069 | 0.657 |
MOD_GSK3_1 | 511 | 518 | PF00069 | 0.297 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.393 |
MOD_LATS_1 | 132 | 138 | PF00433 | 0.395 |
MOD_N-GLC_1 | 57 | 62 | PF02516 | 0.293 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.510 |
MOD_NEK2_1 | 197 | 202 | PF00069 | 0.400 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.379 |
MOD_NEK2_1 | 227 | 232 | PF00069 | 0.467 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.321 |
MOD_NEK2_1 | 258 | 263 | PF00069 | 0.311 |
MOD_NEK2_1 | 289 | 294 | PF00069 | 0.379 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.345 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.463 |
MOD_NEK2_1 | 442 | 447 | PF00069 | 0.618 |
MOD_NEK2_1 | 549 | 554 | PF00069 | 0.421 |
MOD_NEK2_1 | 559 | 564 | PF00069 | 0.416 |
MOD_PKA_2 | 381 | 387 | PF00069 | 0.523 |
MOD_PKA_2 | 549 | 555 | PF00069 | 0.435 |
MOD_Plk_1 | 1 | 7 | PF00069 | 0.506 |
MOD_Plk_1 | 236 | 242 | PF00069 | 0.335 |
MOD_Plk_1 | 294 | 300 | PF00069 | 0.306 |
MOD_Plk_1 | 430 | 436 | PF00069 | 0.395 |
MOD_Plk_1 | 85 | 91 | PF00069 | 0.423 |
MOD_Plk_4 | 141 | 147 | PF00069 | 0.337 |
MOD_Plk_4 | 148 | 154 | PF00069 | 0.282 |
MOD_Plk_4 | 17 | 23 | PF00069 | 0.357 |
MOD_Plk_4 | 227 | 233 | PF00069 | 0.399 |
MOD_Plk_4 | 237 | 243 | PF00069 | 0.404 |
MOD_Plk_4 | 247 | 253 | PF00069 | 0.409 |
MOD_Plk_4 | 315 | 321 | PF00069 | 0.300 |
MOD_Plk_4 | 352 | 358 | PF00069 | 0.395 |
MOD_Plk_4 | 383 | 389 | PF00069 | 0.516 |
MOD_Plk_4 | 512 | 518 | PF00069 | 0.464 |
MOD_Plk_4 | 86 | 92 | PF00069 | 0.423 |
MOD_ProDKin_1 | 334 | 340 | PF00069 | 0.401 |
MOD_ProDKin_1 | 349 | 355 | PF00069 | 0.335 |
MOD_ProDKin_1 | 489 | 495 | PF00069 | 0.598 |
MOD_ProDKin_1 | 522 | 528 | PF00069 | 0.474 |
TRG_DiLeu_BaEn_4 | 101 | 107 | PF01217 | 0.421 |
TRG_DiLeu_BaLyEn_6 | 269 | 274 | PF01217 | 0.380 |
TRG_DiLeu_BaLyEn_6 | 475 | 480 | PF01217 | 0.541 |
TRG_ENDOCYTIC_2 | 149 | 152 | PF00928 | 0.332 |
TRG_ENDOCYTIC_2 | 16 | 19 | PF00928 | 0.461 |
TRG_ENDOCYTIC_2 | 27 | 30 | PF00928 | 0.356 |
TRG_ENDOCYTIC_2 | 409 | 412 | PF00928 | 0.668 |
TRG_ENDOCYTIC_2 | 485 | 488 | PF00928 | 0.579 |
TRG_ENDOCYTIC_2 | 50 | 53 | PF00928 | 0.492 |
TRG_ENDOCYTIC_2 | 519 | 522 | PF00928 | 0.526 |
TRG_ENDOCYTIC_2 | 90 | 93 | PF00928 | 0.367 |
TRG_ER_diArg_1 | 133 | 135 | PF00400 | 0.440 |
TRG_ER_diArg_1 | 168 | 170 | PF00400 | 0.554 |
TRG_ER_diArg_1 | 172 | 175 | PF00400 | 0.492 |
TRG_ER_diArg_1 | 321 | 323 | PF00400 | 0.435 |
TRG_ER_diArg_1 | 380 | 383 | PF00400 | 0.508 |
TRG_NES_CRM1_1 | 416 | 431 | PF08389 | 0.395 |
TRG_Pf-PMV_PEXEL_1 | 291 | 295 | PF00026 | 0.444 |
TRG_Pf-PMV_PEXEL_1 | 98 | 102 | PF00026 | 0.377 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8P1 | Leptomonas seymouri | 27% | 69% |
A0A0N1P9M9 | Leptomonas seymouri | 57% | 99% |
A0A0S4JME6 | Bodo saltans | 28% | 100% |
A0A0S4JR20 | Bodo saltans | 28% | 100% |
A0A1X0P1R5 | Trypanosomatidae | 25% | 77% |
A0A1X0PA17 | Trypanosomatidae | 33% | 100% |
A0A3Q8INR2 | Leishmania donovani | 85% | 100% |
A0A3R7LQ57 | Trypanosoma rangeli | 26% | 82% |
A0A422N5R5 | Trypanosoma rangeli | 32% | 100% |
A1CRG6 | Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1 / QM 1276 / 107) | 24% | 80% |
A1D4C8 | Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / CBS 544.65 / FGSC A1164 / JCM 1740 / NRRL 181 / WB 181) | 24% | 80% |
A2Q8F7 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 24% | 76% |
A4HIE6 | Leishmania braziliensis | 29% | 75% |
A4IAC8 | Leishmania infantum | 85% | 100% |
A4R8V2 | Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) | 24% | 72% |
A5DIR3 | Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) | 26% | 79% |
A5DUA8 | Lodderomyces elongisporus (strain ATCC 11503 / CBS 2605 / JCM 1781 / NBRC 1676 / NRRL YB-4239) | 26% | 70% |
E9B0Y7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 75% |
E9B5F1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 92% |
O14115 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 26% | 90% |
P0CT18 | Magnaporthe oryzae (strain Y34) | 24% | 72% |
Q0CUP0 | Aspergillus terreus (strain NIH 2624 / FGSC A1156) | 24% | 80% |
Q12043 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 24% | 76% |
Q1DXR6 | Coccidioides immitis (strain RS) | 25% | 78% |
Q2HA54 | Chaetomium globosum (strain ATCC 6205 / CBS 148.51 / DSM 1962 / NBRC 6347 / NRRL 1970) | 26% | 67% |
Q2UKE6 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 28% | 79% |
Q4Q2I2 | Leishmania major | 83% | 100% |
Q4Q779 | Leishmania major | 27% | 70% |
Q4WJS4 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 24% | 80% |
Q5AM72 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 24% | 67% |
Q5BGC2 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 26% | 76% |
Q6BXC8 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 25% | 72% |
Q6C8W4 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 25% | 70% |
Q9LZA6 | Arabidopsis thaliana | 24% | 69% |
Q9M1I6 | Arabidopsis thaliana | 25% | 71% |
Q9Y7P3 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 26% | 100% |
V5BLA0 | Trypanosoma cruzi | 25% | 98% |
V5BW64 | Trypanosoma cruzi | 33% | 100% |