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: 18 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0016020 | membrane | 2 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
Related structures:
AlphaFold database: E9ACF5
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 2 |
GO:0006644 | phospholipid metabolic process | 4 | 2 |
GO:0006793 | phosphorus metabolic process | 3 | 2 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0008610 | lipid biosynthetic process | 4 | 2 |
GO:0008654 | phospholipid biosynthetic process | 5 | 2 |
GO:0009058 | biosynthetic process | 2 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0019637 | organophosphate metabolic process | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044255 | cellular lipid metabolic process | 3 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0090407 | organophosphate biosynthetic process | 4 | 2 |
GO:1901576 | organic substance biosynthetic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004366 | glycerol-3-phosphate O-acyltransferase activity | 6 | 6 |
GO:0008374 | O-acyltransferase activity | 5 | 6 |
GO:0016287 | glycerone-phosphate O-acyltransferase activity | 7 | 3 |
GO:0016407 | acetyltransferase activity | 5 | 3 |
GO:0016413 | O-acetyltransferase activity | 6 | 3 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016746 | acyltransferase activity | 3 | 12 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 6 |
GO:0043772 | acyl-phosphate glycerol-3-phosphate acyltransferase activity | 5 | 2 |
GO:0102420 | sn-1-glycerol-3-phosphate C16:0-DCA-CoA acyl transferase activity | 5 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 18 | 20 | PF00675 | 0.448 |
CLV_NRD_NRD_1 | 325 | 327 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 380 | 382 | PF00675 | 0.479 |
CLV_NRD_NRD_1 | 389 | 391 | PF00675 | 0.528 |
CLV_NRD_NRD_1 | 44 | 46 | PF00675 | 0.470 |
CLV_NRD_NRD_1 | 440 | 442 | PF00675 | 0.498 |
CLV_NRD_NRD_1 | 571 | 573 | PF00675 | 0.314 |
CLV_NRD_NRD_1 | 622 | 624 | PF00675 | 0.408 |
CLV_PCSK_KEX2_1 | 18 | 20 | PF00082 | 0.435 |
CLV_PCSK_KEX2_1 | 325 | 327 | PF00082 | 0.523 |
CLV_PCSK_KEX2_1 | 380 | 382 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 423 | 425 | PF00082 | 0.598 |
CLV_PCSK_KEX2_1 | 440 | 442 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 475 | 477 | PF00082 | 0.376 |
CLV_PCSK_KEX2_1 | 571 | 573 | PF00082 | 0.312 |
CLV_PCSK_KEX2_1 | 621 | 623 | PF00082 | 0.405 |
CLV_PCSK_PC1ET2_1 | 325 | 327 | PF00082 | 0.534 |
CLV_PCSK_PC1ET2_1 | 423 | 425 | PF00082 | 0.481 |
CLV_PCSK_PC1ET2_1 | 475 | 477 | PF00082 | 0.401 |
CLV_PCSK_PC7_1 | 617 | 623 | PF00082 | 0.448 |
CLV_PCSK_SKI1_1 | 21 | 25 | PF00082 | 0.407 |
CLV_PCSK_SKI1_1 | 326 | 330 | PF00082 | 0.505 |
CLV_PCSK_SKI1_1 | 341 | 345 | PF00082 | 0.461 |
CLV_PCSK_SKI1_1 | 423 | 427 | PF00082 | 0.624 |
CLV_PCSK_SKI1_1 | 440 | 444 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 475 | 479 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 495 | 499 | PF00082 | 0.117 |
CLV_PCSK_SKI1_1 | 521 | 525 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 549 | 553 | PF00082 | 0.290 |
CLV_PCSK_SKI1_1 | 623 | 627 | PF00082 | 0.484 |
CLV_PCSK_SKI1_1 | 78 | 82 | PF00082 | 0.473 |
DEG_APCC_DBOX_1 | 40 | 48 | PF00400 | 0.617 |
DEG_APCC_DBOX_1 | 520 | 528 | PF00400 | 0.309 |
DEG_APCC_DBOX_1 | 548 | 556 | PF00400 | 0.597 |
DOC_CKS1_1 | 218 | 223 | PF01111 | 0.329 |
DOC_CYCLIN_RxL_1 | 420 | 429 | PF00134 | 0.431 |
DOC_CYCLIN_RxL_1 | 464 | 474 | PF00134 | 0.431 |
DOC_MAPK_gen_1 | 298 | 307 | PF00069 | 0.286 |
DOC_MAPK_gen_1 | 325 | 333 | PF00069 | 0.300 |
DOC_MAPK_gen_1 | 41 | 49 | PF00069 | 0.586 |
DOC_MAPK_gen_1 | 440 | 447 | PF00069 | 0.248 |
DOC_MAPK_MEF2A_6 | 521 | 528 | PF00069 | 0.259 |
DOC_MAPK_MEF2A_6 | 549 | 556 | PF00069 | 0.509 |
DOC_MAPK_NFAT4_5 | 549 | 557 | PF00069 | 0.508 |
DOC_PP1_RVXF_1 | 114 | 121 | PF00149 | 0.248 |
DOC_PP1_RVXF_1 | 349 | 356 | PF00149 | 0.378 |
DOC_PP1_RVXF_1 | 493 | 499 | PF00149 | 0.553 |
DOC_PP1_RVXF_1 | 71 | 78 | PF00149 | 0.475 |
DOC_PP4_FxxP_1 | 127 | 130 | PF00568 | 0.259 |
DOC_PP4_FxxP_1 | 311 | 314 | PF00568 | 0.301 |
DOC_PP4_FxxP_1 | 528 | 531 | PF00568 | 0.335 |
DOC_USP7_MATH_1 | 123 | 127 | PF00917 | 0.245 |
DOC_USP7_MATH_1 | 195 | 199 | PF00917 | 0.343 |
DOC_USP7_MATH_1 | 600 | 604 | PF00917 | 0.588 |
DOC_WW_Pin1_4 | 217 | 222 | PF00397 | 0.285 |
DOC_WW_Pin1_4 | 309 | 314 | PF00397 | 0.305 |
LIG_14-3-3_CanoR_1 | 12 | 22 | PF00244 | 0.666 |
LIG_14-3-3_CanoR_1 | 137 | 143 | PF00244 | 0.309 |
LIG_14-3-3_CanoR_1 | 199 | 208 | PF00244 | 0.309 |
LIG_14-3-3_CanoR_1 | 280 | 285 | PF00244 | 0.273 |
LIG_14-3-3_CanoR_1 | 390 | 398 | PF00244 | 0.358 |
LIG_14-3-3_CanoR_1 | 45 | 50 | PF00244 | 0.612 |
LIG_14-3-3_CanoR_1 | 476 | 485 | PF00244 | 0.588 |
LIG_14-3-3_CanoR_1 | 55 | 61 | PF00244 | 0.522 |
LIG_Actin_WH2_2 | 458 | 474 | PF00022 | 0.484 |
LIG_Actin_WH2_2 | 533 | 551 | PF00022 | 0.401 |
LIG_Actin_WH2_2 | 57 | 75 | PF00022 | 0.527 |
LIG_APCC_ABBA_1 | 249 | 254 | PF00400 | 0.247 |
LIG_APCC_ABBA_1 | 514 | 519 | PF00400 | 0.461 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.631 |
LIG_BRCT_BRCA1_1 | 391 | 395 | PF00533 | 0.403 |
LIG_BRCT_BRCA1_1 | 73 | 77 | PF00533 | 0.476 |
LIG_DLG_GKlike_1 | 609 | 616 | PF00625 | 0.607 |
LIG_EH1_1 | 445 | 453 | PF00400 | 0.316 |
LIG_FHA_1 | 2 | 8 | PF00498 | 0.573 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.277 |
LIG_FHA_1 | 259 | 265 | PF00498 | 0.243 |
LIG_FHA_1 | 342 | 348 | PF00498 | 0.287 |
LIG_FHA_1 | 509 | 515 | PF00498 | 0.391 |
LIG_FHA_1 | 520 | 526 | PF00498 | 0.264 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.243 |
LIG_FHA_2 | 199 | 205 | PF00498 | 0.316 |
LIG_LIR_Apic_2 | 124 | 130 | PF02991 | 0.259 |
LIG_LIR_Apic_2 | 184 | 188 | PF02991 | 0.270 |
LIG_LIR_Apic_2 | 309 | 314 | PF02991 | 0.304 |
LIG_LIR_Gen_1 | 172 | 182 | PF02991 | 0.317 |
LIG_LIR_Gen_1 | 233 | 243 | PF02991 | 0.248 |
LIG_LIR_Gen_1 | 301 | 311 | PF02991 | 0.343 |
LIG_LIR_Gen_1 | 374 | 382 | PF02991 | 0.297 |
LIG_LIR_Gen_1 | 392 | 402 | PF02991 | 0.193 |
LIG_LIR_Gen_1 | 403 | 413 | PF02991 | 0.310 |
LIG_LIR_Gen_1 | 511 | 517 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 172 | 177 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 233 | 239 | PF02991 | 0.248 |
LIG_LIR_Nem_3 | 301 | 307 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 349 | 353 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 358 | 362 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 374 | 378 | PF02991 | 0.207 |
LIG_LIR_Nem_3 | 392 | 398 | PF02991 | 0.195 |
LIG_LIR_Nem_3 | 403 | 408 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 491 | 497 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 511 | 515 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 74 | 80 | PF02991 | 0.382 |
LIG_MLH1_MIPbox_1 | 73 | 77 | PF16413 | 0.476 |
LIG_NRBOX | 421 | 427 | PF00104 | 0.429 |
LIG_Pex14_2 | 307 | 311 | PF04695 | 0.394 |
LIG_Pex14_2 | 355 | 359 | PF04695 | 0.275 |
LIG_Pex14_2 | 494 | 498 | PF04695 | 0.553 |
LIG_Rb_pABgroove_1 | 315 | 323 | PF01858 | 0.404 |
LIG_SH2_CRK | 236 | 240 | PF00017 | 0.241 |
LIG_SH2_CRK | 350 | 354 | PF00017 | 0.357 |
LIG_SH2_CRK | 363 | 367 | PF00017 | 0.294 |
LIG_SH2_NCK_1 | 236 | 240 | PF00017 | 0.248 |
LIG_SH2_PTP2 | 535 | 538 | PF00017 | 0.300 |
LIG_SH2_SRC | 293 | 296 | PF00017 | 0.385 |
LIG_SH2_SRC | 363 | 366 | PF00017 | 0.337 |
LIG_SH2_STAP1 | 226 | 230 | PF00017 | 0.313 |
LIG_SH2_STAP1 | 236 | 240 | PF00017 | 0.179 |
LIG_SH2_STAT3 | 586 | 589 | PF00017 | 0.595 |
LIG_SH2_STAT5 | 293 | 296 | PF00017 | 0.299 |
LIG_SH2_STAT5 | 304 | 307 | PF00017 | 0.270 |
LIG_SH2_STAT5 | 375 | 378 | PF00017 | 0.293 |
LIG_SH2_STAT5 | 446 | 449 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 468 | 471 | PF00017 | 0.552 |
LIG_SH2_STAT5 | 535 | 538 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 76 | 79 | PF00017 | 0.301 |
LIG_SH3_3 | 141 | 147 | PF00018 | 0.248 |
LIG_SH3_3 | 205 | 211 | PF00018 | 0.277 |
LIG_SH3_3 | 215 | 221 | PF00018 | 0.233 |
LIG_SH3_3 | 455 | 461 | PF00018 | 0.306 |
LIG_SUMO_SIM_anti_2 | 522 | 529 | PF11976 | 0.349 |
LIG_SUMO_SIM_anti_2 | 537 | 543 | PF11976 | 0.224 |
LIG_SUMO_SIM_anti_2 | 79 | 84 | PF11976 | 0.248 |
LIG_SUMO_SIM_par_1 | 522 | 529 | PF11976 | 0.372 |
LIG_SUMO_SIM_par_1 | 537 | 543 | PF11976 | 0.209 |
LIG_TRAF2_1 | 202 | 205 | PF00917 | 0.353 |
LIG_TRAF2_1 | 33 | 36 | PF00917 | 0.636 |
LIG_TYR_ITIM | 466 | 471 | PF00017 | 0.481 |
LIG_UBA3_1 | 263 | 267 | PF00899 | 0.300 |
LIG_UBA3_1 | 465 | 472 | PF00899 | 0.434 |
LIG_WRC_WIRS_1 | 356 | 361 | PF05994 | 0.467 |
LIG_WRC_WIRS_1 | 509 | 514 | PF05994 | 0.382 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.459 |
MOD_CK1_1 | 198 | 204 | PF00069 | 0.447 |
MOD_CK1_1 | 479 | 485 | PF00069 | 0.482 |
MOD_CK1_1 | 557 | 563 | PF00069 | 0.429 |
MOD_CK1_1 | 612 | 618 | PF00069 | 0.531 |
MOD_CK2_1 | 198 | 204 | PF00069 | 0.339 |
MOD_CK2_1 | 45 | 51 | PF00069 | 0.418 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.494 |
MOD_GlcNHglycan | 391 | 394 | PF01048 | 0.575 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.662 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.607 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.402 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.399 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.300 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.464 |
MOD_GSK3_1 | 414 | 421 | PF00069 | 0.405 |
MOD_GSK3_1 | 515 | 522 | PF00069 | 0.391 |
MOD_N-GLC_1 | 403 | 408 | PF02516 | 0.463 |
MOD_N-GLC_2 | 246 | 248 | PF02516 | 0.316 |
MOD_NEK2_1 | 109 | 114 | PF00069 | 0.421 |
MOD_NEK2_1 | 224 | 229 | PF00069 | 0.361 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.485 |
MOD_NEK2_1 | 471 | 476 | PF00069 | 0.404 |
MOD_NEK2_1 | 478 | 483 | PF00069 | 0.428 |
MOD_NEK2_1 | 508 | 513 | PF00069 | 0.348 |
MOD_NEK2_1 | 534 | 539 | PF00069 | 0.316 |
MOD_NEK2_1 | 554 | 559 | PF00069 | 0.215 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.366 |
MOD_PIKK_1 | 414 | 420 | PF00454 | 0.389 |
MOD_PIKK_1 | 557 | 563 | PF00454 | 0.576 |
MOD_PK_1 | 280 | 286 | PF00069 | 0.335 |
MOD_PKA_1 | 326 | 332 | PF00069 | 0.405 |
MOD_PKA_1 | 45 | 51 | PF00069 | 0.564 |
MOD_PKA_2 | 17 | 23 | PF00069 | 0.582 |
MOD_PKA_2 | 175 | 181 | PF00069 | 0.417 |
MOD_PKA_2 | 198 | 204 | PF00069 | 0.436 |
MOD_PKA_2 | 389 | 395 | PF00069 | 0.491 |
MOD_PKA_2 | 414 | 420 | PF00069 | 0.401 |
MOD_PKB_1 | 43 | 51 | PF00069 | 0.464 |
MOD_Plk_1 | 123 | 129 | PF00069 | 0.300 |
MOD_Plk_1 | 206 | 212 | PF00069 | 0.336 |
MOD_Plk_1 | 258 | 264 | PF00069 | 0.300 |
MOD_Plk_1 | 479 | 485 | PF00069 | 0.477 |
MOD_Plk_1 | 51 | 57 | PF00069 | 0.515 |
MOD_Plk_1 | 78 | 84 | PF00069 | 0.321 |
MOD_Plk_4 | 259 | 265 | PF00069 | 0.292 |
MOD_Plk_4 | 289 | 295 | PF00069 | 0.342 |
MOD_Plk_4 | 351 | 357 | PF00069 | 0.486 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.525 |
MOD_Plk_4 | 508 | 514 | PF00069 | 0.300 |
MOD_Plk_4 | 534 | 540 | PF00069 | 0.335 |
MOD_Plk_4 | 554 | 560 | PF00069 | 0.215 |
MOD_Plk_4 | 56 | 62 | PF00069 | 0.312 |
MOD_Plk_4 | 609 | 615 | PF00069 | 0.564 |
MOD_Plk_4 | 78 | 84 | PF00069 | 0.382 |
MOD_ProDKin_1 | 217 | 223 | PF00069 | 0.353 |
MOD_ProDKin_1 | 309 | 315 | PF00069 | 0.387 |
MOD_SUMO_rev_2 | 154 | 160 | PF00179 | 0.370 |
MOD_SUMO_rev_2 | 587 | 596 | PF00179 | 0.564 |
TRG_DiLeu_BaLyEn_6 | 374 | 379 | PF01217 | 0.469 |
TRG_DiLeu_BaLyEn_6 | 421 | 426 | PF01217 | 0.342 |
TRG_DiLeu_BaLyEn_6 | 550 | 555 | PF01217 | 0.528 |
TRG_DiLeu_BaLyEn_6 | 577 | 582 | PF01217 | 0.523 |
TRG_ENDOCYTIC_2 | 236 | 239 | PF00928 | 0.288 |
TRG_ENDOCYTIC_2 | 240 | 243 | PF00928 | 0.288 |
TRG_ENDOCYTIC_2 | 304 | 307 | PF00928 | 0.417 |
TRG_ENDOCYTIC_2 | 350 | 353 | PF00928 | 0.460 |
TRG_ENDOCYTIC_2 | 375 | 378 | PF00928 | 0.361 |
TRG_ENDOCYTIC_2 | 405 | 408 | PF00928 | 0.478 |
TRG_ENDOCYTIC_2 | 468 | 471 | PF00928 | 0.482 |
TRG_ENDOCYTIC_2 | 535 | 538 | PF00928 | 0.374 |
TRG_ER_diArg_1 | 299 | 302 | PF00400 | 0.368 |
TRG_ER_diArg_1 | 379 | 381 | PF00400 | 0.347 |
TRG_ER_diArg_1 | 439 | 441 | PF00400 | 0.375 |
TRG_ER_diArg_1 | 620 | 623 | PF00400 | 0.505 |
TRG_NES_CRM1_1 | 334 | 349 | PF08389 | 0.445 |
TRG_Pf-PMV_PEXEL_1 | 119 | 124 | PF00026 | 0.421 |
TRG_Pf-PMV_PEXEL_1 | 360 | 364 | PF00026 | 0.350 |
TRG_Pf-PMV_PEXEL_1 | 424 | 429 | PF00026 | 0.363 |
TRG_Pf-PMV_PEXEL_1 | 476 | 480 | PF00026 | 0.443 |
TRG_Pf-PMV_PEXEL_1 | 566 | 570 | PF00026 | 0.432 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I239 | Leptomonas seymouri | 80% | 87% |
A0A0S4JH62 | Bodo saltans | 55% | 86% |
A0A1X0P8Y7 | Trypanosomatidae | 61% | 89% |
A0A3R7K7V0 | Trypanosoma rangeli | 60% | 89% |
A0A3S5H521 | Leishmania donovani | 97% | 100% |
A4H3I0 | Leishmania braziliensis | 92% | 88% |
D0A214 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 58% | 90% |
E9AG27 | Leishmania infantum | 97% | 100% |
E9AJP3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
P32784 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 30% | 83% |
P36148 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 28% | 85% |
Q9P7P0 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 29% | 93% |
V5B455 | Trypanosoma cruzi | 62% | 90% |