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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
Related structures:
AlphaFold database: E9AJW6
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 8 |
GO:0006644 | phospholipid metabolic process | 4 | 8 |
GO:0006793 | phosphorus metabolic process | 3 | 8 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 8 |
GO:0008152 | metabolic process | 1 | 8 |
GO:0008610 | lipid biosynthetic process | 4 | 8 |
GO:0008654 | phospholipid biosynthetic process | 5 | 8 |
GO:0009058 | biosynthetic process | 2 | 8 |
GO:0009987 | cellular process | 1 | 8 |
GO:0019637 | organophosphate metabolic process | 3 | 8 |
GO:0044237 | cellular metabolic process | 2 | 8 |
GO:0044238 | primary metabolic process | 2 | 8 |
GO:0044255 | cellular lipid metabolic process | 3 | 8 |
GO:0071704 | organic substance metabolic process | 2 | 8 |
GO:0090407 | organophosphate biosynthetic process | 4 | 8 |
GO:1901576 | organic substance biosynthetic process | 3 | 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 8 |
GO:0016740 | transferase activity | 2 | 8 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 8 |
GO:0016780 | phosphotransferase activity, for other substituted phosphate groups | 4 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 118 | 122 | PF00656 | 0.407 |
CLV_C14_Caspase3-7 | 265 | 269 | PF00656 | 0.661 |
CLV_NRD_NRD_1 | 126 | 128 | PF00675 | 0.260 |
CLV_NRD_NRD_1 | 305 | 307 | PF00675 | 0.344 |
CLV_NRD_NRD_1 | 368 | 370 | PF00675 | 0.547 |
CLV_NRD_NRD_1 | 381 | 383 | PF00675 | 0.505 |
CLV_NRD_NRD_1 | 419 | 421 | PF00675 | 0.325 |
CLV_NRD_NRD_1 | 454 | 456 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 595 | 597 | PF00675 | 0.392 |
CLV_PCSK_KEX2_1 | 126 | 128 | PF00082 | 0.251 |
CLV_PCSK_KEX2_1 | 305 | 307 | PF00082 | 0.344 |
CLV_PCSK_KEX2_1 | 368 | 370 | PF00082 | 0.556 |
CLV_PCSK_KEX2_1 | 381 | 383 | PF00082 | 0.583 |
CLV_PCSK_KEX2_1 | 419 | 421 | PF00082 | 0.325 |
CLV_PCSK_KEX2_1 | 454 | 456 | PF00082 | 0.508 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.305 |
CLV_PCSK_SKI1_1 | 187 | 191 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 294 | 298 | PF00082 | 0.362 |
CLV_PCSK_SKI1_1 | 580 | 584 | PF00082 | 0.441 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.608 |
DEG_ODPH_VHL_1 | 457 | 469 | PF01847 | 0.259 |
DEG_ODPH_VHL_1 | 46 | 58 | PF01847 | 0.282 |
DEG_SCF_FBW7_2 | 367 | 374 | PF00400 | 0.361 |
DOC_CYCLIN_RxL_1 | 291 | 300 | PF00134 | 0.493 |
DOC_MAPK_gen_1 | 10 | 17 | PF00069 | 0.491 |
DOC_MAPK_gen_1 | 381 | 387 | PF00069 | 0.306 |
DOC_MAPK_MEF2A_6 | 10 | 17 | PF00069 | 0.491 |
DOC_MAPK_MEF2A_6 | 187 | 194 | PF00069 | 0.284 |
DOC_MAPK_MEF2A_6 | 339 | 347 | PF00069 | 0.419 |
DOC_MAPK_MEF2A_6 | 395 | 404 | PF00069 | 0.230 |
DOC_MAPK_MEF2A_6 | 435 | 442 | PF00069 | 0.230 |
DOC_MAPK_MEF2A_6 | 454 | 463 | PF00069 | 0.205 |
DOC_MAPK_NFAT4_5 | 10 | 18 | PF00069 | 0.492 |
DOC_MAPK_NFAT4_5 | 187 | 195 | PF00069 | 0.288 |
DOC_MAPK_NFAT4_5 | 435 | 443 | PF00069 | 0.230 |
DOC_MAPK_RevD_3 | 440 | 455 | PF00069 | 0.319 |
DOC_PP2B_LxvP_1 | 190 | 193 | PF13499 | 0.240 |
DOC_PP2B_LxvP_1 | 557 | 560 | PF13499 | 0.485 |
DOC_PP4_FxxP_1 | 562 | 565 | PF00568 | 0.476 |
DOC_SPAK_OSR1_1 | 382 | 386 | PF12202 | 0.303 |
DOC_USP7_MATH_1 | 156 | 160 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 267 | 271 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 334 | 338 | PF00917 | 0.435 |
DOC_USP7_MATH_1 | 353 | 357 | PF00917 | 0.259 |
DOC_USP7_MATH_1 | 590 | 594 | PF00917 | 0.521 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.429 |
DOC_WW_Pin1_4 | 367 | 372 | PF00397 | 0.397 |
DOC_WW_Pin1_4 | 86 | 91 | PF00397 | 0.510 |
LIG_14-3-3_CanoR_1 | 127 | 133 | PF00244 | 0.478 |
LIG_14-3-3_CanoR_1 | 327 | 336 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 339 | 344 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 454 | 458 | PF00244 | 0.257 |
LIG_14-3-3_CanoR_1 | 580 | 588 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 83 | 93 | PF00244 | 0.388 |
LIG_14-3-3_CterR_2 | 596 | 599 | PF00244 | 0.547 |
LIG_Actin_WH2_2 | 557 | 575 | PF00022 | 0.494 |
LIG_BRCT_BRCA1_1 | 383 | 387 | PF00533 | 0.358 |
LIG_BRCT_BRCA1_1 | 446 | 450 | PF00533 | 0.323 |
LIG_Clathr_ClatBox_1 | 276 | 280 | PF01394 | 0.476 |
LIG_eIF4E_1 | 185 | 191 | PF01652 | 0.205 |
LIG_EVH1_2 | 273 | 277 | PF00568 | 0.493 |
LIG_EVH1_2 | 98 | 102 | PF00568 | 0.247 |
LIG_FHA_1 | 164 | 170 | PF00498 | 0.416 |
LIG_FHA_1 | 210 | 216 | PF00498 | 0.317 |
LIG_FHA_1 | 291 | 297 | PF00498 | 0.568 |
LIG_FHA_1 | 340 | 346 | PF00498 | 0.405 |
LIG_FHA_1 | 426 | 432 | PF00498 | 0.230 |
LIG_FHA_1 | 541 | 547 | PF00498 | 0.442 |
LIG_FHA_1 | 551 | 557 | PF00498 | 0.560 |
LIG_FHA_1 | 583 | 589 | PF00498 | 0.543 |
LIG_FHA_1 | 60 | 66 | PF00498 | 0.307 |
LIG_FHA_1 | 86 | 92 | PF00498 | 0.520 |
LIG_FHA_2 | 179 | 185 | PF00498 | 0.310 |
LIG_FHA_2 | 259 | 265 | PF00498 | 0.667 |
LIG_GBD_Chelix_1 | 109 | 117 | PF00786 | 0.259 |
LIG_LIR_Gen_1 | 166 | 175 | PF02991 | 0.230 |
LIG_LIR_Gen_1 | 24 | 34 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 337 | 348 | PF02991 | 0.479 |
LIG_LIR_Gen_1 | 499 | 507 | PF02991 | 0.683 |
LIG_LIR_Gen_1 | 541 | 550 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 166 | 170 | PF02991 | 0.232 |
LIG_LIR_Nem_3 | 181 | 185 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 337 | 343 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 384 | 390 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 40 | 44 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 447 | 453 | PF02991 | 0.278 |
LIG_LIR_Nem_3 | 499 | 503 | PF02991 | 0.683 |
LIG_LIR_Nem_3 | 541 | 545 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 57 | 61 | PF02991 | 0.267 |
LIG_NRBOX | 112 | 118 | PF00104 | 0.342 |
LIG_PCNA_PIPBox_1 | 322 | 331 | PF02747 | 0.553 |
LIG_PCNA_yPIPBox_3 | 322 | 333 | PF02747 | 0.507 |
LIG_Pex14_1 | 182 | 186 | PF04695 | 0.205 |
LIG_Pex14_2 | 178 | 182 | PF04695 | 0.250 |
LIG_Pex14_2 | 383 | 387 | PF04695 | 0.295 |
LIG_SH2_CRK | 186 | 190 | PF00017 | 0.226 |
LIG_SH2_CRK | 340 | 344 | PF00017 | 0.419 |
LIG_SH2_CRK | 364 | 368 | PF00017 | 0.255 |
LIG_SH2_CRK | 433 | 437 | PF00017 | 0.282 |
LIG_SH2_GRB2like | 222 | 225 | PF00017 | 0.482 |
LIG_SH2_SRC | 222 | 225 | PF00017 | 0.482 |
LIG_SH2_SRC | 4 | 7 | PF00017 | 0.541 |
LIG_SH2_SRC | 41 | 44 | PF00017 | 0.481 |
LIG_SH2_STAP1 | 433 | 437 | PF00017 | 0.342 |
LIG_SH2_STAP1 | 518 | 522 | PF00017 | 0.653 |
LIG_SH2_STAP1 | 532 | 536 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 16 | 19 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 209 | 212 | PF00017 | 0.261 |
LIG_SH2_STAT5 | 25 | 28 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 259 | 262 | PF00017 | 0.561 |
LIG_SH2_STAT5 | 4 | 7 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 41 | 44 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 433 | 436 | PF00017 | 0.250 |
LIG_SH2_STAT5 | 471 | 474 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 505 | 508 | PF00017 | 0.620 |
LIG_SH3_1 | 286 | 292 | PF00018 | 0.504 |
LIG_SH3_2 | 289 | 294 | PF14604 | 0.566 |
LIG_SH3_3 | 212 | 218 | PF00018 | 0.328 |
LIG_SH3_3 | 223 | 229 | PF00018 | 0.507 |
LIG_SH3_3 | 286 | 292 | PF00018 | 0.530 |
LIG_SH3_3 | 91 | 97 | PF00018 | 0.454 |
LIG_SUMO_SIM_anti_2 | 166 | 173 | PF11976 | 0.259 |
LIG_SUMO_SIM_par_1 | 166 | 173 | PF11976 | 0.282 |
LIG_SUMO_SIM_par_1 | 397 | 403 | PF11976 | 0.284 |
LIG_TRAF2_1 | 181 | 184 | PF00917 | 0.250 |
LIG_TRAF2_1 | 261 | 264 | PF00917 | 0.511 |
LIG_TYR_ITIM | 112 | 117 | PF00017 | 0.181 |
LIG_TYR_ITIM | 338 | 343 | PF00017 | 0.468 |
LIG_TYR_ITIM | 39 | 44 | PF00017 | 0.553 |
LIG_TYR_ITIM | 431 | 436 | PF00017 | 0.282 |
LIG_UBA3_1 | 1 | 10 | PF00899 | 0.500 |
LIG_WRC_WIRS_1 | 174 | 179 | PF05994 | 0.259 |
LIG_WRC_WIRS_1 | 401 | 406 | PF05994 | 0.259 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.551 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.496 |
MOD_CK1_1 | 510 | 516 | PF00069 | 0.573 |
MOD_CK1_1 | 538 | 544 | PF00069 | 0.512 |
MOD_CK2_1 | 178 | 184 | PF00069 | 0.310 |
MOD_CK2_1 | 258 | 264 | PF00069 | 0.653 |
MOD_CMANNOS | 164 | 167 | PF00535 | 0.219 |
MOD_CMANNOS | 211 | 214 | PF00535 | 0.342 |
MOD_Cter_Amidation | 379 | 382 | PF01082 | 0.520 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.306 |
MOD_GlcNHglycan | 268 | 272 | PF01048 | 0.483 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.320 |
MOD_GlcNHglycan | 322 | 325 | PF01048 | 0.419 |
MOD_GlcNHglycan | 355 | 358 | PF01048 | 0.342 |
MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.267 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.572 |
MOD_GlcNHglycan | 485 | 488 | PF01048 | 0.488 |
MOD_GlcNHglycan | 518 | 521 | PF01048 | 0.510 |
MOD_GlcNHglycan | 537 | 540 | PF01048 | 0.211 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.602 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.440 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.460 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.484 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.484 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.373 |
MOD_GSK3_1 | 503 | 510 | PF00069 | 0.619 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.571 |
MOD_N-GLC_1 | 473 | 478 | PF02516 | 0.335 |
MOD_N-GLC_1 | 83 | 88 | PF02516 | 0.630 |
MOD_NEK2_1 | 279 | 284 | PF00069 | 0.615 |
MOD_NEK2_1 | 404 | 409 | PF00069 | 0.295 |
MOD_NEK2_1 | 410 | 415 | PF00069 | 0.386 |
MOD_NEK2_1 | 425 | 430 | PF00069 | 0.230 |
MOD_NEK2_1 | 431 | 436 | PF00069 | 0.230 |
MOD_NEK2_1 | 453 | 458 | PF00069 | 0.309 |
MOD_NEK2_1 | 535 | 540 | PF00069 | 0.517 |
MOD_NEK2_1 | 545 | 550 | PF00069 | 0.516 |
MOD_NEK2_2 | 334 | 339 | PF00069 | 0.491 |
MOD_PK_1 | 381 | 387 | PF00069 | 0.306 |
MOD_PKA_1 | 381 | 387 | PF00069 | 0.306 |
MOD_PKA_2 | 125 | 131 | PF00069 | 0.460 |
MOD_PKA_2 | 381 | 387 | PF00069 | 0.374 |
MOD_PKA_2 | 453 | 459 | PF00069 | 0.257 |
MOD_PKA_2 | 513 | 519 | PF00069 | 0.560 |
MOD_PKA_2 | 550 | 556 | PF00069 | 0.491 |
MOD_Plk_1 | 21 | 27 | PF00069 | 0.446 |
MOD_Plk_1 | 473 | 479 | PF00069 | 0.647 |
MOD_Plk_4 | 163 | 169 | PF00069 | 0.452 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.314 |
MOD_Plk_4 | 316 | 322 | PF00069 | 0.520 |
MOD_Plk_4 | 467 | 473 | PF00069 | 0.282 |
MOD_Plk_4 | 54 | 60 | PF00069 | 0.181 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.429 |
MOD_ProDKin_1 | 367 | 373 | PF00069 | 0.401 |
MOD_ProDKin_1 | 86 | 92 | PF00069 | 0.509 |
TRG_DiLeu_BaEn_1 | 552 | 557 | PF01217 | 0.463 |
TRG_DiLeu_BaLyEn_6 | 271 | 276 | PF01217 | 0.542 |
TRG_ENDOCYTIC_2 | 114 | 117 | PF00928 | 0.230 |
TRG_ENDOCYTIC_2 | 186 | 189 | PF00928 | 0.285 |
TRG_ENDOCYTIC_2 | 27 | 30 | PF00928 | 0.452 |
TRG_ENDOCYTIC_2 | 340 | 343 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 364 | 367 | PF00928 | 0.248 |
TRG_ENDOCYTIC_2 | 41 | 44 | PF00928 | 0.481 |
TRG_ENDOCYTIC_2 | 433 | 436 | PF00928 | 0.282 |
TRG_ENDOCYTIC_2 | 532 | 535 | PF00928 | 0.532 |
TRG_ER_diArg_1 | 367 | 369 | PF00400 | 0.348 |
TRG_ER_diArg_1 | 381 | 383 | PF00400 | 0.383 |
TRG_ER_diArg_1 | 418 | 420 | PF00400 | 0.513 |
TRG_ER_diArg_1 | 453 | 455 | PF00400 | 0.314 |
TRG_Pf-PMV_PEXEL_1 | 231 | 235 | PF00026 | 0.362 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2Y1 | Leptomonas seymouri | 63% | 100% |
A0A0S4J7L0 | Bodo saltans | 46% | 100% |
A0A1X0P8W0 | Trypanosomatidae | 45% | 100% |
A0A3S5H562 | Leishmania donovani | 84% | 97% |
E8NHC2 | Leishmania infantum | 84% | 97% |
V5BXC7 | Trypanosoma cruzi | 44% | 100% |