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. | yes | yes: 20 |
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: 8 |
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:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q1U2
Term | Name | Level | Count |
---|---|---|---|
GO:0006473 | protein acetylation | 6 | 2 |
GO:0006474 | N-terminal protein amino acid acetylation | 5 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0017196 | N-terminal peptidyl-methionine acetylation | 6 | 2 |
GO:0018193 | peptidyl-amino acid modification | 5 | 2 |
GO:0018206 | peptidyl-methionine modification | 6 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0031365 | N-terminal protein amino acid modification | 5 | 2 |
GO:0036211 | protein modification process | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043412 | macromolecule modification | 4 | 2 |
GO:0043543 | protein acylation | 5 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0051604 | protein maturation | 4 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 176 | 180 | PF00656 | 0.427 |
CLV_C14_Caspase3-7 | 254 | 258 | PF00656 | 0.551 |
CLV_C14_Caspase3-7 | 692 | 696 | PF00656 | 0.469 |
CLV_NRD_NRD_1 | 265 | 267 | PF00675 | 0.244 |
CLV_NRD_NRD_1 | 390 | 392 | PF00675 | 0.351 |
CLV_NRD_NRD_1 | 440 | 442 | PF00675 | 0.316 |
CLV_NRD_NRD_1 | 505 | 507 | PF00675 | 0.274 |
CLV_NRD_NRD_1 | 539 | 541 | PF00675 | 0.249 |
CLV_PCSK_KEX2_1 | 104 | 106 | PF00082 | 0.432 |
CLV_PCSK_KEX2_1 | 243 | 245 | PF00082 | 0.273 |
CLV_PCSK_KEX2_1 | 302 | 304 | PF00082 | 0.249 |
CLV_PCSK_KEX2_1 | 390 | 392 | PF00082 | 0.351 |
CLV_PCSK_KEX2_1 | 440 | 442 | PF00082 | 0.316 |
CLV_PCSK_KEX2_1 | 505 | 507 | PF00082 | 0.325 |
CLV_PCSK_KEX2_1 | 539 | 541 | PF00082 | 0.273 |
CLV_PCSK_KEX2_1 | 605 | 607 | PF00082 | 0.259 |
CLV_PCSK_PC1ET2_1 | 104 | 106 | PF00082 | 0.429 |
CLV_PCSK_PC1ET2_1 | 243 | 245 | PF00082 | 0.273 |
CLV_PCSK_PC1ET2_1 | 302 | 304 | PF00082 | 0.328 |
CLV_PCSK_PC1ET2_1 | 605 | 607 | PF00082 | 0.259 |
CLV_PCSK_SKI1_1 | 101 | 105 | PF00082 | 0.301 |
CLV_PCSK_SKI1_1 | 139 | 143 | PF00082 | 0.374 |
CLV_PCSK_SKI1_1 | 224 | 228 | PF00082 | 0.273 |
CLV_PCSK_SKI1_1 | 290 | 294 | PF00082 | 0.355 |
CLV_PCSK_SKI1_1 | 303 | 307 | PF00082 | 0.176 |
CLV_PCSK_SKI1_1 | 382 | 386 | PF00082 | 0.290 |
CLV_PCSK_SKI1_1 | 452 | 456 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 560 | 564 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 605 | 609 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 658 | 662 | PF00082 | 0.359 |
CLV_PCSK_SKI1_1 | 664 | 668 | PF00082 | 0.333 |
CLV_Separin_Metazoa | 115 | 119 | PF03568 | 0.492 |
DEG_APCC_DBOX_1 | 302 | 310 | PF00400 | 0.434 |
DEG_SCF_FBW7_2 | 406 | 413 | PF00400 | 0.459 |
DOC_CKS1_1 | 321 | 326 | PF01111 | 0.551 |
DOC_CYCLIN_RxL_1 | 101 | 110 | PF00134 | 0.429 |
DOC_CYCLIN_RxL_1 | 49 | 60 | PF00134 | 0.364 |
DOC_MAPK_gen_1 | 101 | 109 | PF00069 | 0.429 |
DOC_MAPK_gen_1 | 558 | 565 | PF00069 | 0.485 |
DOC_MAPK_gen_1 | 673 | 682 | PF00069 | 0.587 |
DOC_MAPK_MEF2A_6 | 676 | 684 | PF00069 | 0.450 |
DOC_PP1_RVXF_1 | 103 | 110 | PF00149 | 0.429 |
DOC_PP4_FxxP_1 | 321 | 324 | PF00568 | 0.551 |
DOC_PP4_FxxP_1 | 473 | 476 | PF00568 | 0.491 |
DOC_USP7_MATH_1 | 143 | 147 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 487 | 491 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 693 | 697 | PF00917 | 0.514 |
DOC_USP7_UBL2_3 | 560 | 564 | PF12436 | 0.473 |
DOC_USP7_UBL2_3 | 608 | 612 | PF12436 | 0.538 |
DOC_WW_Pin1_4 | 1 | 6 | PF00397 | 0.472 |
DOC_WW_Pin1_4 | 320 | 325 | PF00397 | 0.551 |
DOC_WW_Pin1_4 | 406 | 411 | PF00397 | 0.449 |
LIG_14-3-3_CanoR_1 | 105 | 110 | PF00244 | 0.436 |
LIG_14-3-3_CanoR_1 | 33 | 41 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 539 | 544 | PF00244 | 0.459 |
LIG_Actin_WH2_2 | 261 | 277 | PF00022 | 0.503 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.598 |
LIG_Clathr_ClatBox_1 | 414 | 418 | PF01394 | 0.551 |
LIG_Clathr_ClatBox_1 | 516 | 520 | PF01394 | 0.551 |
LIG_deltaCOP1_diTrp_1 | 129 | 133 | PF00928 | 0.331 |
LIG_FHA_1 | 112 | 118 | PF00498 | 0.450 |
LIG_FHA_1 | 221 | 227 | PF00498 | 0.528 |
LIG_FHA_1 | 321 | 327 | PF00498 | 0.497 |
LIG_FHA_1 | 407 | 413 | PF00498 | 0.453 |
LIG_FHA_1 | 467 | 473 | PF00498 | 0.526 |
LIG_FHA_1 | 5 | 11 | PF00498 | 0.449 |
LIG_FHA_1 | 643 | 649 | PF00498 | 0.489 |
LIG_FHA_1 | 675 | 681 | PF00498 | 0.421 |
LIG_FHA_2 | 484 | 490 | PF00498 | 0.474 |
LIG_FHA_2 | 652 | 658 | PF00498 | 0.455 |
LIG_FHA_2 | 690 | 696 | PF00498 | 0.553 |
LIG_Integrin_RGD_1 | 506 | 508 | PF01839 | 0.330 |
LIG_KLC1_Yacidic_2 | 413 | 418 | PF13176 | 0.551 |
LIG_LIR_Apic_2 | 271 | 276 | PF02991 | 0.551 |
LIG_LIR_Gen_1 | 242 | 253 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 281 | 292 | PF02991 | 0.494 |
LIG_LIR_Gen_1 | 332 | 342 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 352 | 361 | PF02991 | 0.551 |
LIG_LIR_Gen_1 | 365 | 373 | PF02991 | 0.392 |
LIG_LIR_Gen_1 | 572 | 578 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 593 | 604 | PF02991 | 0.503 |
LIG_LIR_Gen_1 | 63 | 74 | PF02991 | 0.535 |
LIG_LIR_Nem_3 | 129 | 133 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 242 | 248 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 281 | 287 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 332 | 337 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 365 | 369 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 531 | 536 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 572 | 576 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 593 | 599 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 629 | 634 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 63 | 69 | PF02991 | 0.479 |
LIG_NRBOX | 512 | 518 | PF00104 | 0.551 |
LIG_PALB2_WD40_1 | 542 | 550 | PF16756 | 0.473 |
LIG_PCNA_TLS_4 | 267 | 274 | PF02747 | 0.551 |
LIG_Pex14_1 | 380 | 384 | PF04695 | 0.449 |
LIG_Pex14_2 | 561 | 565 | PF04695 | 0.551 |
LIG_PTB_Apo_2 | 22 | 29 | PF02174 | 0.490 |
LIG_PTB_Apo_2 | 371 | 378 | PF02174 | 0.457 |
LIG_PTB_Apo_2 | 532 | 539 | PF02174 | 0.459 |
LIG_PTB_Phospho_1 | 22 | 28 | PF10480 | 0.490 |
LIG_PTB_Phospho_1 | 371 | 377 | PF10480 | 0.500 |
LIG_REV1ctd_RIR_1 | 559 | 566 | PF16727 | 0.459 |
LIG_SH2_CRK | 573 | 577 | PF00017 | 0.491 |
LIG_SH2_GRB2like | 23 | 26 | PF00017 | 0.560 |
LIG_SH2_GRB2like | 448 | 451 | PF00017 | 0.449 |
LIG_SH2_NCK_1 | 653 | 657 | PF00017 | 0.484 |
LIG_SH2_PTP2 | 245 | 248 | PF00017 | 0.468 |
LIG_SH2_SRC | 245 | 248 | PF00017 | 0.468 |
LIG_SH2_SRC | 341 | 344 | PF00017 | 0.551 |
LIG_SH2_SRC | 448 | 451 | PF00017 | 0.449 |
LIG_SH2_STAP1 | 28 | 32 | PF00017 | 0.399 |
LIG_SH2_STAP1 | 280 | 284 | PF00017 | 0.503 |
LIG_SH2_STAP1 | 495 | 499 | PF00017 | 0.449 |
LIG_SH2_STAP1 | 689 | 693 | PF00017 | 0.316 |
LIG_SH2_STAT5 | 245 | 248 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.551 |
LIG_SH2_STAT5 | 280 | 283 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 325 | 328 | PF00017 | 0.543 |
LIG_SH2_STAT5 | 341 | 344 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 377 | 380 | PF00017 | 0.485 |
LIG_SH2_STAT5 | 401 | 404 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 416 | 419 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 448 | 451 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 457 | 460 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 484 | 487 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 509 | 512 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 536 | 539 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 614 | 617 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 634 | 637 | PF00017 | 0.538 |
LIG_SH2_STAT5 | 653 | 656 | PF00017 | 0.284 |
LIG_SH2_STAT5 | 689 | 692 | PF00017 | 0.451 |
LIG_SH3_3 | 586 | 592 | PF00018 | 0.491 |
LIG_SH3_5 | 296 | 300 | PF00018 | 0.452 |
LIG_SUMO_SIM_anti_2 | 411 | 416 | PF11976 | 0.473 |
LIG_SUMO_SIM_par_1 | 182 | 189 | PF11976 | 0.481 |
LIG_SUMO_SIM_par_1 | 215 | 223 | PF11976 | 0.499 |
LIG_SUMO_SIM_par_1 | 6 | 11 | PF11976 | 0.375 |
LIG_SUMO_SIM_par_1 | 644 | 651 | PF11976 | 0.435 |
LIG_UBA3_1 | 329 | 338 | PF00899 | 0.326 |
LIG_UBA3_1 | 414 | 421 | PF00899 | 0.285 |
LIG_WRC_WIRS_1 | 381 | 386 | PF05994 | 0.369 |
LIG_WRC_WIRS_1 | 46 | 51 | PF05994 | 0.408 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.582 |
MOD_CK1_1 | 332 | 338 | PF00069 | 0.325 |
MOD_CK1_1 | 644 | 650 | PF00069 | 0.416 |
MOD_CK2_1 | 21 | 27 | PF00069 | 0.546 |
MOD_CK2_1 | 483 | 489 | PF00069 | 0.353 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.436 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.429 |
MOD_GlcNHglycan | 510 | 513 | PF01048 | 0.285 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.501 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.439 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.285 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.414 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.291 |
MOD_GSK3_1 | 638 | 645 | PF00069 | 0.456 |
MOD_GSK3_1 | 683 | 690 | PF00069 | 0.485 |
MOD_N-GLC_1 | 406 | 411 | PF02516 | 0.429 |
MOD_N-GLC_2 | 526 | 528 | PF02516 | 0.429 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.470 |
MOD_NEK2_1 | 384 | 389 | PF00069 | 0.327 |
MOD_NEK2_2 | 143 | 148 | PF00069 | 0.462 |
MOD_NEK2_2 | 65 | 70 | PF00069 | 0.499 |
MOD_PIKK_1 | 487 | 493 | PF00454 | 0.285 |
MOD_PIKK_1 | 638 | 644 | PF00454 | 0.364 |
MOD_PKA_1 | 539 | 545 | PF00069 | 0.301 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.506 |
MOD_PKA_2 | 389 | 395 | PF00069 | 0.361 |
MOD_PKA_2 | 539 | 545 | PF00069 | 0.331 |
MOD_PKA_2 | 638 | 644 | PF00069 | 0.388 |
MOD_PKA_2 | 672 | 678 | PF00069 | 0.506 |
MOD_Plk_1 | 364 | 370 | PF00069 | 0.329 |
MOD_Plk_1 | 466 | 472 | PF00069 | 0.368 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.426 |
MOD_Plk_4 | 329 | 335 | PF00069 | 0.338 |
MOD_Plk_4 | 336 | 342 | PF00069 | 0.346 |
MOD_Plk_4 | 474 | 480 | PF00069 | 0.347 |
MOD_Plk_4 | 76 | 82 | PF00069 | 0.474 |
MOD_ProDKin_1 | 1 | 7 | PF00069 | 0.466 |
MOD_ProDKin_1 | 320 | 326 | PF00069 | 0.429 |
MOD_ProDKin_1 | 406 | 412 | PF00069 | 0.285 |
MOD_SUMO_rev_2 | 216 | 226 | PF00179 | 0.348 |
MOD_SUMO_rev_2 | 358 | 366 | PF00179 | 0.429 |
MOD_SUMO_rev_2 | 597 | 607 | PF00179 | 0.304 |
TRG_DiLeu_BaEn_1 | 222 | 227 | PF01217 | 0.379 |
TRG_DiLeu_BaLyEn_6 | 656 | 661 | PF01217 | 0.381 |
TRG_ENDOCYTIC_2 | 245 | 248 | PF00928 | 0.285 |
TRG_ENDOCYTIC_2 | 284 | 287 | PF00928 | 0.301 |
TRG_ENDOCYTIC_2 | 573 | 576 | PF00928 | 0.285 |
TRG_ENDOCYTIC_2 | 66 | 69 | PF00928 | 0.472 |
TRG_ER_diArg_1 | 389 | 391 | PF00400 | 0.429 |
TRG_ER_diArg_1 | 440 | 442 | PF00400 | 0.379 |
TRG_ER_diArg_1 | 504 | 506 | PF00400 | 0.399 |
TRG_ER_diArg_1 | 538 | 540 | PF00400 | 0.285 |
TRG_NES_CRM1_1 | 508 | 520 | PF08389 | 0.429 |
TRG_Pf-PMV_PEXEL_1 | 105 | 110 | PF00026 | 0.429 |
TRG_Pf-PMV_PEXEL_1 | 440 | 445 | PF00026 | 0.285 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2R8 | Leptomonas seymouri | 78% | 100% |
A0A0S4IZ29 | Bodo saltans | 52% | 100% |
A0A1X0P802 | Trypanosomatidae | 56% | 100% |
A0A3S7XAS1 | Leishmania donovani | 96% | 100% |
A0A422N0I1 | Trypanosoma rangeli | 60% | 100% |
A4HNZ1 | Leishmania braziliensis | 90% | 100% |
A4ICK2 | Leishmania infantum | 96% | 100% |
D0A2V9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 100% |
E9ASQ3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
O74985 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 28% | 98% |
P12945 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 24% | 83% |
Q5R4J9 | Pongo abelii | 28% | 82% |
Q6N069 | Homo sapiens | 29% | 82% |
Q80UM3 | Mus musculus | 28% | 82% |
Q8VZM1 | Arabidopsis thaliana | 29% | 79% |
Q9BXJ9 | Homo sapiens | 28% | 82% |
Q9DBB4 | Mus musculus | 28% | 82% |
Q9Y7X2 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 22% | 100% |
V5DRE7 | Trypanosoma cruzi | 59% | 100% |