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: A4HMG9
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 | 246 | 250 | PF00656 | 0.398 |
CLV_C14_Caspase3-7 | 70 | 74 | PF00656 | 0.699 |
CLV_NRD_NRD_1 | 411 | 413 | PF00675 | 0.304 |
CLV_NRD_NRD_1 | 419 | 421 | PF00675 | 0.304 |
CLV_NRD_NRD_1 | 444 | 446 | PF00675 | 0.302 |
CLV_PCSK_KEX2_1 | 390 | 392 | PF00082 | 0.324 |
CLV_PCSK_KEX2_1 | 419 | 421 | PF00082 | 0.326 |
CLV_PCSK_PC1ET2_1 | 390 | 392 | PF00082 | 0.362 |
CLV_PCSK_SKI1_1 | 199 | 203 | PF00082 | 0.271 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.565 |
CLV_PCSK_SKI1_1 | 295 | 299 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 323 | 327 | PF00082 | 0.358 |
CLV_PCSK_SKI1_1 | 37 | 41 | PF00082 | 0.613 |
CLV_PCSK_SKI1_1 | 385 | 389 | PF00082 | 0.348 |
CLV_PCSK_SKI1_1 | 445 | 449 | PF00082 | 0.307 |
CLV_Separin_Metazoa | 26 | 30 | PF03568 | 0.599 |
DEG_APCC_DBOX_1 | 587 | 595 | PF00400 | 0.525 |
DEG_SCF_FBW7_1 | 432 | 437 | PF00400 | 0.501 |
DOC_AGCK_PIF_2 | 465 | 470 | PF00069 | 0.480 |
DOC_ANK_TNKS_1 | 492 | 499 | PF00023 | 0.643 |
DOC_CKS1_1 | 307 | 312 | PF01111 | 0.548 |
DOC_CKS1_1 | 45 | 50 | PF01111 | 0.716 |
DOC_CYCLIN_RxL_1 | 151 | 162 | PF00134 | 0.507 |
DOC_CYCLIN_RxL_1 | 352 | 362 | PF00134 | 0.539 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 81 | 87 | PF00134 | 0.345 |
DOC_CYCLIN_yCln2_LP_2 | 297 | 303 | PF00134 | 0.577 |
DOC_MAPK_gen_1 | 356 | 366 | PF00069 | 0.562 |
DOC_MAPK_gen_1 | 390 | 397 | PF00069 | 0.539 |
DOC_MAPK_JIP1_4 | 154 | 160 | PF00069 | 0.720 |
DOC_MAPK_MEF2A_6 | 390 | 397 | PF00069 | 0.520 |
DOC_MAPK_MEF2A_6 | 461 | 468 | PF00069 | 0.483 |
DOC_PP1_RVXF_1 | 459 | 466 | PF00149 | 0.562 |
DOC_USP7_MATH_1 | 252 | 256 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 434 | 438 | PF00917 | 0.519 |
DOC_USP7_MATH_1 | 629 | 633 | PF00917 | 0.530 |
DOC_USP7_UBL2_3 | 446 | 450 | PF12436 | 0.511 |
DOC_USP7_UBL2_3 | 515 | 519 | PF12436 | 0.542 |
DOC_USP7_UBL2_3 | 94 | 98 | PF12436 | 0.591 |
DOC_WW_Pin1_4 | 141 | 146 | PF00397 | 0.709 |
DOC_WW_Pin1_4 | 229 | 234 | PF00397 | 0.491 |
DOC_WW_Pin1_4 | 259 | 264 | PF00397 | 0.480 |
DOC_WW_Pin1_4 | 306 | 311 | PF00397 | 0.528 |
DOC_WW_Pin1_4 | 430 | 435 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 44 | 49 | PF00397 | 0.659 |
DOC_WW_Pin1_4 | 581 | 586 | PF00397 | 0.598 |
LIG_14-3-3_CanoR_1 | 154 | 159 | PF00244 | 0.703 |
LIG_14-3-3_CanoR_1 | 370 | 374 | PF00244 | 0.469 |
LIG_AP2alpha_2 | 626 | 628 | PF02296 | 0.371 |
LIG_APCC_ABBAyCdc20_2 | 461 | 467 | PF00400 | 0.504 |
LIG_BIR_III_4 | 73 | 77 | PF00653 | 0.459 |
LIG_BRCT_BRCA1_1 | 439 | 443 | PF00533 | 0.562 |
LIG_CtBP_PxDLS_1 | 48 | 52 | PF00389 | 0.747 |
LIG_deltaCOP1_diTrp_1 | 124 | 133 | PF00928 | 0.479 |
LIG_FHA_1 | 198 | 204 | PF00498 | 0.405 |
LIG_FHA_1 | 254 | 260 | PF00498 | 0.471 |
LIG_FHA_1 | 369 | 375 | PF00498 | 0.510 |
LIG_FHA_1 | 590 | 596 | PF00498 | 0.425 |
LIG_FHA_1 | 78 | 84 | PF00498 | 0.597 |
LIG_FHA_2 | 148 | 154 | PF00498 | 0.591 |
LIG_FHA_2 | 307 | 313 | PF00498 | 0.531 |
LIG_FHA_2 | 481 | 487 | PF00498 | 0.480 |
LIG_FHA_2 | 585 | 591 | PF00498 | 0.504 |
LIG_FXI_DFP_1 | 193 | 197 | PF00024 | 0.596 |
LIG_LIR_Apic_2 | 304 | 310 | PF02991 | 0.556 |
LIG_LIR_Gen_1 | 268 | 276 | PF02991 | 0.563 |
LIG_LIR_Gen_1 | 278 | 289 | PF02991 | 0.564 |
LIG_LIR_Gen_1 | 30 | 39 | PF02991 | 0.550 |
LIG_LIR_Gen_1 | 371 | 381 | PF02991 | 0.562 |
LIG_LIR_Gen_1 | 467 | 478 | PF02991 | 0.546 |
LIG_LIR_Gen_1 | 58 | 69 | PF02991 | 0.636 |
LIG_LIR_Gen_1 | 606 | 616 | PF02991 | 0.410 |
LIG_LIR_Gen_1 | 647 | 655 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 124 | 129 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 215 | 220 | PF02991 | 0.577 |
LIG_LIR_Nem_3 | 238 | 244 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 268 | 273 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 278 | 284 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 30 | 36 | PF02991 | 0.542 |
LIG_LIR_Nem_3 | 353 | 358 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 371 | 376 | PF02991 | 0.557 |
LIG_LIR_Nem_3 | 467 | 473 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 499 | 505 | PF02991 | 0.526 |
LIG_LIR_Nem_3 | 516 | 521 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 58 | 64 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 606 | 611 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 636 | 640 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 647 | 651 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 8 | 14 | PF02991 | 0.634 |
LIG_NRBOX | 383 | 389 | PF00104 | 0.562 |
LIG_PCNA_yPIPBox_3 | 642 | 652 | PF02747 | 0.483 |
LIG_Pex14_1 | 57 | 61 | PF04695 | 0.460 |
LIG_Pex14_2 | 443 | 447 | PF04695 | 0.562 |
LIG_Rb_pABgroove_1 | 127 | 135 | PF01858 | 0.476 |
LIG_SH2_CRK | 307 | 311 | PF00017 | 0.397 |
LIG_SH2_CRK | 507 | 511 | PF00017 | 0.561 |
LIG_SH2_CRK | 61 | 65 | PF00017 | 0.448 |
LIG_SH2_NCK_1 | 307 | 311 | PF00017 | 0.577 |
LIG_SH2_NCK_1 | 470 | 474 | PF00017 | 0.480 |
LIG_SH2_NCK_1 | 61 | 65 | PF00017 | 0.448 |
LIG_SH2_PTP2 | 648 | 651 | PF00017 | 0.406 |
LIG_SH2_SRC | 33 | 36 | PF00017 | 0.583 |
LIG_SH2_STAP1 | 281 | 285 | PF00017 | 0.562 |
LIG_SH2_STAT3 | 514 | 517 | PF00017 | 0.583 |
LIG_SH2_STAT5 | 313 | 316 | PF00017 | 0.562 |
LIG_SH2_STAT5 | 333 | 336 | PF00017 | 0.577 |
LIG_SH2_STAT5 | 35 | 38 | PF00017 | 0.588 |
LIG_SH2_STAT5 | 470 | 473 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 491 | 494 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 507 | 510 | PF00017 | 0.483 |
LIG_SH2_STAT5 | 533 | 536 | PF00017 | 0.543 |
LIG_SH2_STAT5 | 569 | 572 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 637 | 640 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 648 | 651 | PF00017 | 0.331 |
LIG_SH3_2 | 194 | 199 | PF14604 | 0.603 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.546 |
LIG_SH3_3 | 191 | 197 | PF00018 | 0.582 |
LIG_SH3_3 | 523 | 529 | PF00018 | 0.314 |
LIG_SUMO_SIM_anti_2 | 380 | 386 | PF11976 | 0.562 |
LIG_SUMO_SIM_par_1 | 46 | 56 | PF11976 | 0.746 |
LIG_SUMO_SIM_par_1 | 66 | 73 | PF11976 | 0.487 |
LIG_TRAF2_1 | 510 | 513 | PF00917 | 0.556 |
LIG_UBA3_1 | 171 | 179 | PF00899 | 0.598 |
LIG_UBA3_1 | 383 | 390 | PF00899 | 0.562 |
LIG_WRC_WIRS_1 | 236 | 241 | PF05994 | 0.480 |
LIG_WRC_WIRS_1 | 281 | 286 | PF05994 | 0.573 |
LIG_WRC_WIRS_1 | 373 | 378 | PF05994 | 0.558 |
LIG_WRC_WIRS_1 | 607 | 612 | PF05994 | 0.464 |
LIG_WW_3 | 26 | 30 | PF00397 | 0.599 |
MOD_CDK_SPxxK_3 | 581 | 588 | PF00069 | 0.609 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.562 |
MOD_CK1_1 | 368 | 374 | PF00069 | 0.536 |
MOD_CK1_1 | 375 | 381 | PF00069 | 0.530 |
MOD_CK1_1 | 437 | 443 | PF00069 | 0.552 |
MOD_CK1_1 | 50 | 56 | PF00069 | 0.590 |
MOD_CK1_1 | 601 | 607 | PF00069 | 0.454 |
MOD_CK2_1 | 118 | 124 | PF00069 | 0.422 |
MOD_CK2_1 | 147 | 153 | PF00069 | 0.588 |
MOD_CK2_1 | 306 | 312 | PF00069 | 0.505 |
MOD_CK2_1 | 345 | 351 | PF00069 | 0.480 |
MOD_CK2_1 | 480 | 486 | PF00069 | 0.480 |
MOD_CK2_1 | 584 | 590 | PF00069 | 0.541 |
MOD_CK2_1 | 60 | 66 | PF00069 | 0.607 |
MOD_CMANNOS | 605 | 608 | PF00535 | 0.341 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.521 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.521 |
MOD_GlcNHglycan | 317 | 320 | PF01048 | 0.257 |
MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.377 |
MOD_GlcNHglycan | 576 | 579 | PF01048 | 0.495 |
MOD_GlcNHglycan | 632 | 635 | PF01048 | 0.426 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.733 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.496 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.445 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.494 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.562 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.716 |
MOD_GSK3_1 | 430 | 437 | PF00069 | 0.509 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.653 |
MOD_LATS_1 | 116 | 122 | PF00433 | 0.671 |
MOD_N-GLC_1 | 118 | 123 | PF02516 | 0.625 |
MOD_N-GLC_1 | 208 | 213 | PF02516 | 0.197 |
MOD_N-GLC_1 | 327 | 332 | PF02516 | 0.287 |
MOD_N-GLC_1 | 335 | 340 | PF02516 | 0.349 |
MOD_NEK2_1 | 302 | 307 | PF00069 | 0.405 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.561 |
MOD_NEK2_1 | 350 | 355 | PF00069 | 0.416 |
MOD_NEK2_1 | 395 | 400 | PF00069 | 0.545 |
MOD_NEK2_1 | 480 | 485 | PF00069 | 0.476 |
MOD_NEK2_1 | 531 | 536 | PF00069 | 0.535 |
MOD_NEK2_1 | 595 | 600 | PF00069 | 0.361 |
MOD_NEK2_1 | 603 | 608 | PF00069 | 0.311 |
MOD_NEK2_1 | 87 | 92 | PF00069 | 0.468 |
MOD_NEK2_2 | 35 | 40 | PF00069 | 0.593 |
MOD_PIKK_1 | 165 | 171 | PF00454 | 0.499 |
MOD_PIKK_1 | 302 | 308 | PF00454 | 0.475 |
MOD_PIKK_1 | 335 | 341 | PF00454 | 0.571 |
MOD_PIKK_1 | 41 | 47 | PF00454 | 0.684 |
MOD_PKA_2 | 21 | 27 | PF00069 | 0.499 |
MOD_PKA_2 | 369 | 375 | PF00069 | 0.444 |
MOD_PKA_2 | 492 | 498 | PF00069 | 0.464 |
MOD_Plk_1 | 118 | 124 | PF00069 | 0.622 |
MOD_Plk_1 | 165 | 171 | PF00069 | 0.531 |
MOD_Plk_1 | 350 | 356 | PF00069 | 0.543 |
MOD_Plk_1 | 53 | 59 | PF00069 | 0.733 |
MOD_Plk_4 | 197 | 203 | PF00069 | 0.418 |
MOD_Plk_4 | 261 | 267 | PF00069 | 0.520 |
MOD_Plk_4 | 280 | 286 | PF00069 | 0.577 |
MOD_Plk_4 | 369 | 375 | PF00069 | 0.495 |
MOD_ProDKin_1 | 141 | 147 | PF00069 | 0.712 |
MOD_ProDKin_1 | 229 | 235 | PF00069 | 0.491 |
MOD_ProDKin_1 | 259 | 265 | PF00069 | 0.480 |
MOD_ProDKin_1 | 306 | 312 | PF00069 | 0.528 |
MOD_ProDKin_1 | 430 | 436 | PF00069 | 0.469 |
MOD_ProDKin_1 | 44 | 50 | PF00069 | 0.658 |
MOD_ProDKin_1 | 581 | 587 | PF00069 | 0.593 |
TRG_DiLeu_BaEn_1 | 166 | 171 | PF01217 | 0.598 |
TRG_DiLeu_BaEn_1 | 268 | 273 | PF01217 | 0.562 |
TRG_DiLeu_BaEn_1 | 79 | 84 | PF01217 | 0.492 |
TRG_DiLeu_BaLyEn_6 | 125 | 130 | PF01217 | 0.564 |
TRG_DiLeu_BaLyEn_6 | 356 | 361 | PF01217 | 0.415 |
TRG_ENDOCYTIC_2 | 281 | 284 | PF00928 | 0.516 |
TRG_ENDOCYTIC_2 | 33 | 36 | PF00928 | 0.583 |
TRG_ENDOCYTIC_2 | 470 | 473 | PF00928 | 0.491 |
TRG_ENDOCYTIC_2 | 475 | 478 | PF00928 | 0.483 |
TRG_ENDOCYTIC_2 | 61 | 64 | PF00928 | 0.701 |
TRG_ENDOCYTIC_2 | 648 | 651 | PF00928 | 0.359 |
TRG_ER_diArg_1 | 228 | 231 | PF00400 | 0.577 |
TRG_ER_diArg_1 | 418 | 420 | PF00400 | 0.558 |
TRG_NES_CRM1_1 | 212 | 225 | PF08389 | 0.577 |
TRG_Pf-PMV_PEXEL_1 | 455 | 459 | PF00026 | 0.291 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZI3 | Leptomonas seymouri | 68% | 99% |
A0A0S4JCZ4 | Bodo saltans | 23% | 100% |
A0A1X0NH78 | Trypanosomatidae | 44% | 100% |
A0A1X0NIW4 | Trypanosomatidae | 44% | 100% |
A0A3Q8IPA3 | Leishmania donovani | 88% | 99% |
A0A422N9U8 | Trypanosoma rangeli | 42% | 100% |
A4IB50 | Leishmania infantum | 88% | 99% |
C9ZNP3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
E9AEX0 | Leishmania major | 87% | 100% |
E9B626 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 99% |
V5BC85 | Trypanosoma cruzi | 46% | 100% |