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:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4IB50
Term | Name | Level | Count |
---|---|---|---|
GO:0006793 | phosphorus metabolic process | 3 | 13 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 13 |
GO:0008152 | metabolic process | 1 | 13 |
GO:0009987 | cellular process | 1 | 13 |
GO:0016310 | phosphorylation | 5 | 13 |
GO:0044237 | cellular metabolic process | 2 | 13 |
GO:0006629 | lipid metabolic process | 3 | 1 |
GO:0006644 | phospholipid metabolic process | 4 | 1 |
GO:0006646 | phosphatidylethanolamine biosynthetic process | 6 | 1 |
GO:0006650 | glycerophospholipid metabolic process | 5 | 1 |
GO:0008610 | lipid biosynthetic process | 4 | 1 |
GO:0008654 | phospholipid biosynthetic process | 5 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0019637 | organophosphate metabolic process | 3 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044255 | cellular lipid metabolic process | 3 | 1 |
GO:0045017 | glycerolipid biosynthetic process | 4 | 1 |
GO:0046337 | phosphatidylethanolamine metabolic process | 6 | 1 |
GO:0046474 | glycerophospholipid biosynthetic process | 5 | 1 |
GO:0046486 | glycerolipid metabolic process | 4 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090407 | organophosphate biosynthetic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 13 |
GO:0016301 | kinase activity | 4 | 13 |
GO:0016740 | transferase activity | 2 | 13 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 13 |
GO:0004305 | ethanolamine kinase activity | 5 | 3 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 3 |
GO:0004103 | choline kinase activity | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 585 | 589 | PF00656 | 0.543 |
CLV_C14_Caspase3-7 | 67 | 71 | PF00656 | 0.721 |
CLV_NRD_NRD_1 | 415 | 417 | PF00675 | 0.304 |
CLV_NRD_NRD_1 | 423 | 425 | PF00675 | 0.304 |
CLV_NRD_NRD_1 | 448 | 450 | PF00675 | 0.302 |
CLV_PCSK_KEX2_1 | 323 | 325 | PF00082 | 0.294 |
CLV_PCSK_KEX2_1 | 394 | 396 | PF00082 | 0.324 |
CLV_PCSK_KEX2_1 | 423 | 425 | PF00082 | 0.326 |
CLV_PCSK_PC1ET2_1 | 323 | 325 | PF00082 | 0.294 |
CLV_PCSK_PC1ET2_1 | 394 | 396 | PF00082 | 0.362 |
CLV_PCSK_SKI1_1 | 203 | 207 | PF00082 | 0.271 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.629 |
CLV_PCSK_SKI1_1 | 299 | 303 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 323 | 327 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 37 | 41 | PF00082 | 0.669 |
CLV_PCSK_SKI1_1 | 389 | 393 | PF00082 | 0.348 |
CLV_PCSK_SKI1_1 | 449 | 453 | PF00082 | 0.307 |
CLV_Separin_Metazoa | 26 | 30 | PF03568 | 0.653 |
DEG_APCC_DBOX_1 | 594 | 602 | PF00400 | 0.518 |
DOC_AGCK_PIF_2 | 469 | 474 | PF00069 | 0.480 |
DOC_ANK_TNKS_1 | 496 | 503 | PF00023 | 0.641 |
DOC_CKS1_1 | 311 | 316 | PF01111 | 0.548 |
DOC_CKS1_1 | 45 | 50 | PF01111 | 0.725 |
DOC_CYCLIN_RxL_1 | 356 | 366 | PF00134 | 0.539 |
DOC_CYCLIN_yCln2_LP_2 | 301 | 307 | PF00134 | 0.577 |
DOC_MAPK_gen_1 | 107 | 116 | PF00069 | 0.737 |
DOC_MAPK_gen_1 | 323 | 330 | PF00069 | 0.494 |
DOC_MAPK_gen_1 | 360 | 370 | PF00069 | 0.562 |
DOC_MAPK_gen_1 | 394 | 401 | PF00069 | 0.539 |
DOC_MAPK_JIP1_4 | 158 | 164 | PF00069 | 0.669 |
DOC_MAPK_MEF2A_6 | 110 | 118 | PF00069 | 0.558 |
DOC_MAPK_MEF2A_6 | 394 | 401 | PF00069 | 0.520 |
DOC_MAPK_MEF2A_6 | 465 | 472 | PF00069 | 0.483 |
DOC_PP1_RVXF_1 | 463 | 470 | PF00149 | 0.562 |
DOC_USP7_MATH_1 | 256 | 260 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 349 | 353 | PF00917 | 0.497 |
DOC_USP7_MATH_1 | 438 | 442 | PF00917 | 0.519 |
DOC_USP7_MATH_1 | 558 | 562 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 636 | 640 | PF00917 | 0.534 |
DOC_USP7_UBL2_3 | 323 | 327 | PF12436 | 0.494 |
DOC_USP7_UBL2_3 | 450 | 454 | PF12436 | 0.511 |
DOC_WW_Pin1_4 | 145 | 150 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 233 | 238 | PF00397 | 0.491 |
DOC_WW_Pin1_4 | 263 | 268 | PF00397 | 0.480 |
DOC_WW_Pin1_4 | 310 | 315 | PF00397 | 0.511 |
DOC_WW_Pin1_4 | 44 | 49 | PF00397 | 0.665 |
DOC_WW_Pin1_4 | 588 | 593 | PF00397 | 0.578 |
LIG_14-3-3_CanoR_1 | 110 | 115 | PF00244 | 0.700 |
LIG_14-3-3_CanoR_1 | 158 | 163 | PF00244 | 0.645 |
LIG_14-3-3_CanoR_1 | 363 | 370 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 374 | 378 | PF00244 | 0.469 |
LIG_APCC_ABBAyCdc20_2 | 465 | 471 | PF00400 | 0.504 |
LIG_BIR_III_2 | 348 | 352 | PF00653 | 0.522 |
LIG_BRCT_BRCA1_1 | 443 | 447 | PF00533 | 0.562 |
LIG_CtBP_PxDLS_1 | 48 | 52 | PF00389 | 0.743 |
LIG_deltaCOP1_diTrp_1 | 129 | 137 | PF00928 | 0.407 |
LIG_FHA_1 | 202 | 208 | PF00498 | 0.405 |
LIG_FHA_1 | 258 | 264 | PF00498 | 0.471 |
LIG_FHA_1 | 363 | 369 | PF00498 | 0.556 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.557 |
LIG_FHA_2 | 311 | 317 | PF00498 | 0.531 |
LIG_FHA_2 | 485 | 491 | PF00498 | 0.480 |
LIG_FHA_2 | 583 | 589 | PF00498 | 0.580 |
LIG_FHA_2 | 592 | 598 | PF00498 | 0.496 |
LIG_FXI_DFP_1 | 197 | 201 | PF00024 | 0.556 |
LIG_KLC1_Yacidic_2 | 335 | 339 | PF13176 | 0.522 |
LIG_LIR_Apic_2 | 310 | 314 | PF02991 | 0.561 |
LIG_LIR_Gen_1 | 272 | 280 | PF02991 | 0.563 |
LIG_LIR_Gen_1 | 282 | 293 | PF02991 | 0.564 |
LIG_LIR_Gen_1 | 30 | 39 | PF02991 | 0.621 |
LIG_LIR_Gen_1 | 315 | 325 | PF02991 | 0.522 |
LIG_LIR_Gen_1 | 376 | 385 | PF02991 | 0.561 |
LIG_LIR_Gen_1 | 471 | 482 | PF02991 | 0.562 |
LIG_LIR_Gen_1 | 613 | 623 | PF02991 | 0.402 |
LIG_LIR_Gen_1 | 63 | 72 | PF02991 | 0.724 |
LIG_LIR_Gen_1 | 654 | 662 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 129 | 133 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 141 | 145 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 219 | 224 | PF02991 | 0.583 |
LIG_LIR_Nem_3 | 242 | 248 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 272 | 277 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 282 | 288 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 30 | 36 | PF02991 | 0.618 |
LIG_LIR_Nem_3 | 315 | 320 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 357 | 362 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 376 | 380 | PF02991 | 0.555 |
LIG_LIR_Nem_3 | 471 | 477 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 503 | 509 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 613 | 618 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 643 | 647 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 654 | 658 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 8 | 14 | PF02991 | 0.628 |
LIG_NRBOX | 387 | 393 | PF00104 | 0.562 |
LIG_PCNA_yPIPBox_3 | 12 | 20 | PF02747 | 0.584 |
LIG_PCNA_yPIPBox_3 | 649 | 663 | PF02747 | 0.473 |
LIG_Pex14_2 | 447 | 451 | PF04695 | 0.562 |
LIG_Rb_pABgroove_1 | 131 | 139 | PF01858 | 0.394 |
LIG_SH2_CRK | 511 | 515 | PF00017 | 0.564 |
LIG_SH2_NCK_1 | 311 | 315 | PF00017 | 0.577 |
LIG_SH2_NCK_1 | 474 | 478 | PF00017 | 0.480 |
LIG_SH2_PTP2 | 655 | 658 | PF00017 | 0.386 |
LIG_SH2_SRC | 33 | 36 | PF00017 | 0.656 |
LIG_SH2_STAP1 | 285 | 289 | PF00017 | 0.562 |
LIG_SH2_STAT3 | 518 | 521 | PF00017 | 0.579 |
LIG_SH2_STAT5 | 317 | 320 | PF00017 | 0.540 |
LIG_SH2_STAT5 | 337 | 340 | PF00017 | 0.562 |
LIG_SH2_STAT5 | 35 | 38 | PF00017 | 0.667 |
LIG_SH2_STAT5 | 474 | 477 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 495 | 498 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 511 | 514 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 537 | 540 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 576 | 579 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 644 | 647 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 655 | 658 | PF00017 | 0.311 |
LIG_SH3_2 | 198 | 203 | PF14604 | 0.562 |
LIG_SH3_3 | 195 | 201 | PF00018 | 0.544 |
LIG_SH3_3 | 552 | 558 | PF00018 | 0.566 |
LIG_SUMO_SIM_anti_2 | 384 | 390 | PF11976 | 0.562 |
LIG_SUMO_SIM_par_1 | 46 | 56 | PF11976 | 0.718 |
LIG_TRAF2_1 | 313 | 316 | PF00917 | 0.536 |
LIG_TRAF2_1 | 514 | 517 | PF00917 | 0.551 |
LIG_UBA3_1 | 175 | 183 | PF00899 | 0.565 |
LIG_UBA3_1 | 387 | 394 | PF00899 | 0.562 |
LIG_WRC_WIRS_1 | 240 | 245 | PF05994 | 0.480 |
LIG_WRC_WIRS_1 | 285 | 290 | PF05994 | 0.577 |
LIG_WRC_WIRS_1 | 377 | 382 | PF05994 | 0.558 |
LIG_WW_3 | 26 | 30 | PF00397 | 0.653 |
MOD_CDK_SPxxK_3 | 588 | 595 | PF00069 | 0.593 |
MOD_CK1_1 | 212 | 218 | PF00069 | 0.562 |
MOD_CK1_1 | 376 | 382 | PF00069 | 0.531 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.657 |
MOD_CK1_1 | 441 | 447 | PF00069 | 0.553 |
MOD_CK1_1 | 50 | 56 | PF00069 | 0.553 |
MOD_CK1_1 | 608 | 614 | PF00069 | 0.453 |
MOD_CK2_1 | 310 | 316 | PF00069 | 0.496 |
MOD_CK2_1 | 349 | 355 | PF00069 | 0.480 |
MOD_CK2_1 | 484 | 490 | PF00069 | 0.480 |
MOD_CK2_1 | 591 | 597 | PF00069 | 0.532 |
MOD_CMANNOS | 612 | 615 | PF00535 | 0.340 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.517 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.354 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.569 |
MOD_GlcNHglycan | 381 | 384 | PF01048 | 0.377 |
MOD_GlcNHglycan | 639 | 642 | PF01048 | 0.410 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.699 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.483 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.494 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.562 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.725 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.515 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.642 |
MOD_LATS_1 | 120 | 126 | PF00433 | 0.683 |
MOD_N-GLC_1 | 122 | 127 | PF02516 | 0.632 |
MOD_N-GLC_1 | 339 | 344 | PF02516 | 0.349 |
MOD_N-GLC_1 | 70 | 75 | PF02516 | 0.654 |
MOD_NEK2_1 | 338 | 343 | PF00069 | 0.564 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.416 |
MOD_NEK2_1 | 362 | 367 | PF00069 | 0.486 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.545 |
MOD_NEK2_1 | 484 | 489 | PF00069 | 0.480 |
MOD_NEK2_1 | 535 | 540 | PF00069 | 0.524 |
MOD_NEK2_1 | 602 | 607 | PF00069 | 0.357 |
MOD_NEK2_1 | 610 | 615 | PF00069 | 0.310 |
MOD_NEK2_1 | 91 | 96 | PF00069 | 0.415 |
MOD_NEK2_2 | 35 | 40 | PF00069 | 0.667 |
MOD_PIKK_1 | 169 | 175 | PF00454 | 0.443 |
MOD_PIKK_1 | 339 | 345 | PF00454 | 0.571 |
MOD_PIKK_1 | 41 | 47 | PF00454 | 0.698 |
MOD_PK_1 | 110 | 116 | PF00069 | 0.702 |
MOD_PKA_2 | 362 | 368 | PF00069 | 0.495 |
MOD_PKA_2 | 373 | 379 | PF00069 | 0.444 |
MOD_PKA_2 | 496 | 502 | PF00069 | 0.464 |
MOD_Plk_1 | 122 | 128 | PF00069 | 0.630 |
MOD_Plk_1 | 169 | 175 | PF00069 | 0.475 |
MOD_Plk_1 | 354 | 360 | PF00069 | 0.543 |
MOD_Plk_1 | 53 | 59 | PF00069 | 0.717 |
MOD_Plk_4 | 138 | 144 | PF00069 | 0.506 |
MOD_Plk_4 | 201 | 207 | PF00069 | 0.418 |
MOD_Plk_4 | 265 | 271 | PF00069 | 0.520 |
MOD_Plk_4 | 284 | 290 | PF00069 | 0.577 |
MOD_Plk_4 | 373 | 379 | PF00069 | 0.495 |
MOD_ProDKin_1 | 145 | 151 | PF00069 | 0.681 |
MOD_ProDKin_1 | 233 | 239 | PF00069 | 0.491 |
MOD_ProDKin_1 | 263 | 269 | PF00069 | 0.480 |
MOD_ProDKin_1 | 310 | 316 | PF00069 | 0.511 |
MOD_ProDKin_1 | 44 | 50 | PF00069 | 0.662 |
MOD_ProDKin_1 | 588 | 594 | PF00069 | 0.576 |
MOD_SUMO_for_1 | 39 | 42 | PF00179 | 0.644 |
TRG_DiLeu_BaEn_1 | 170 | 175 | PF01217 | 0.546 |
TRG_DiLeu_BaEn_1 | 272 | 277 | PF01217 | 0.562 |
TRG_DiLeu_BaEn_1 | 83 | 88 | PF01217 | 0.453 |
TRG_DiLeu_BaLyEn_6 | 129 | 134 | PF01217 | 0.498 |
TRG_ENDOCYTIC_2 | 285 | 288 | PF00928 | 0.523 |
TRG_ENDOCYTIC_2 | 317 | 320 | PF00928 | 0.522 |
TRG_ENDOCYTIC_2 | 33 | 36 | PF00928 | 0.656 |
TRG_ENDOCYTIC_2 | 474 | 477 | PF00928 | 0.498 |
TRG_ENDOCYTIC_2 | 479 | 482 | PF00928 | 0.488 |
TRG_ENDOCYTIC_2 | 65 | 68 | PF00928 | 0.741 |
TRG_ENDOCYTIC_2 | 655 | 658 | PF00928 | 0.339 |
TRG_ER_diArg_1 | 232 | 235 | PF00400 | 0.573 |
TRG_ER_diArg_1 | 422 | 424 | PF00400 | 0.558 |
TRG_NES_CRM1_1 | 216 | 229 | PF08389 | 0.577 |
TRG_NLS_MonoExtC_3 | 322 | 327 | PF00514 | 0.494 |
TRG_Pf-PMV_PEXEL_1 | 459 | 463 | PF00026 | 0.291 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZI3 | Leptomonas seymouri | 69% | 100% |
A0A0S4JCZ4 | Bodo saltans | 23% | 100% |
A0A1X0NH78 | Trypanosomatidae | 41% | 100% |
A0A1X0NIW4 | Trypanosomatidae | 41% | 100% |
A0A3Q8IPA3 | Leishmania donovani | 100% | 100% |
A0A422N9U8 | Trypanosoma rangeli | 43% | 100% |
A4HMG9 | Leishmania braziliensis | 88% | 99% |
C9ZNP3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
E9AEX0 | Leishmania major | 96% | 100% |
E9B626 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
V5BC85 | Trypanosoma cruzi | 45% | 100% |