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: 3 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 12 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | yes | yes: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 6 |
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:0031974 | membrane-enclosed lumen | 2 | 2 |
GO:0031981 | nuclear lumen | 5 | 2 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 2 |
GO:0043233 | organelle lumen | 3 | 2 |
GO:0070013 | intracellular organelle lumen | 4 | 2 |
GO:0097014 | ciliary plasm | 5 | 2 |
GO:0099568 | cytoplasmic region | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: E9ADV2
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 4 |
GO:0010035 | response to inorganic substance | 3 | 2 |
GO:0010038 | response to metal ion | 4 | 2 |
GO:0010039 | response to iron ion | 5 | 2 |
GO:0010040 | response to iron(II) ion | 6 | 2 |
GO:0018158 | protein oxidation | 5 | 2 |
GO:0018171 | peptidyl-cysteine oxidation | 6 | 2 |
GO:0018193 | peptidyl-amino acid modification | 5 | 2 |
GO:0018198 | peptidyl-cysteine modification | 6 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0036211 | protein modification process | 4 | 2 |
GO:0042221 | response to chemical | 2 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043412 | macromolecule modification | 4 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0050896 | response to stimulus | 1 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
GO:0032259 | methylation | 2 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 2 |
GO:0005506 | iron ion binding | 6 | 2 |
GO:0008198 | ferrous iron binding | 7 | 2 |
GO:0043167 | ion binding | 2 | 2 |
GO:0043169 | cation binding | 3 | 2 |
GO:0046872 | metal ion binding | 4 | 2 |
GO:0046914 | transition metal ion binding | 5 | 2 |
GO:0003824 | catalytic activity | 1 | 2 |
GO:0008168 | methyltransferase activity | 4 | 2 |
GO:0016740 | transferase activity | 2 | 2 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 171 | 175 | PF00656 | 0.509 |
CLV_C14_Caspase3-7 | 692 | 696 | PF00656 | 0.711 |
CLV_NRD_NRD_1 | 143 | 145 | PF00675 | 0.431 |
CLV_NRD_NRD_1 | 476 | 478 | PF00675 | 0.356 |
CLV_NRD_NRD_1 | 536 | 538 | PF00675 | 0.484 |
CLV_NRD_NRD_1 | 579 | 581 | PF00675 | 0.484 |
CLV_NRD_NRD_1 | 754 | 756 | PF00675 | 0.454 |
CLV_PCSK_KEX2_1 | 143 | 145 | PF00082 | 0.431 |
CLV_PCSK_KEX2_1 | 361 | 363 | PF00082 | 0.368 |
CLV_PCSK_KEX2_1 | 476 | 478 | PF00082 | 0.356 |
CLV_PCSK_KEX2_1 | 536 | 538 | PF00082 | 0.468 |
CLV_PCSK_KEX2_1 | 579 | 581 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 622 | 624 | PF00082 | 0.556 |
CLV_PCSK_PC1ET2_1 | 361 | 363 | PF00082 | 0.368 |
CLV_PCSK_PC1ET2_1 | 622 | 624 | PF00082 | 0.553 |
CLV_PCSK_PC7_1 | 472 | 478 | PF00082 | 0.356 |
CLV_PCSK_SKI1_1 | 19 | 23 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 364 | 368 | PF00082 | 0.368 |
CLV_PCSK_SKI1_1 | 472 | 476 | PF00082 | 0.341 |
CLV_PCSK_SKI1_1 | 477 | 481 | PF00082 | 0.341 |
CLV_PCSK_SKI1_1 | 536 | 540 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 559 | 563 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 622 | 626 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 666 | 670 | PF00082 | 0.527 |
DEG_APCC_DBOX_1 | 189 | 197 | PF00400 | 0.300 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.603 |
DOC_CKS1_1 | 20 | 25 | PF01111 | 0.554 |
DOC_CYCLIN_yClb3_PxF_3 | 308 | 316 | PF00134 | 0.356 |
DOC_CYCLIN_yCln2_LP_2 | 161 | 167 | PF00134 | 0.409 |
DOC_CYCLIN_yCln2_LP_2 | 71 | 74 | PF00134 | 0.446 |
DOC_CYCLIN_yCln2_LP_2 | 78 | 84 | PF00134 | 0.337 |
DOC_MAPK_gen_1 | 147 | 155 | PF00069 | 0.368 |
DOC_MAPK_gen_1 | 666 | 675 | PF00069 | 0.434 |
DOC_MAPK_gen_1 | 77 | 84 | PF00069 | 0.382 |
DOC_MAPK_HePTP_8 | 155 | 167 | PF00069 | 0.466 |
DOC_MAPK_MEF2A_6 | 158 | 167 | PF00069 | 0.414 |
DOC_PP1_RVXF_1 | 299 | 306 | PF00149 | 0.400 |
DOC_PP1_RVXF_1 | 557 | 563 | PF00149 | 0.383 |
DOC_PP2B_LxvP_1 | 161 | 164 | PF13499 | 0.418 |
DOC_PP2B_LxvP_1 | 71 | 74 | PF13499 | 0.486 |
DOC_PP4_FxxP_1 | 443 | 446 | PF00568 | 0.324 |
DOC_PP4_FxxP_1 | 70 | 73 | PF00568 | 0.421 |
DOC_USP7_MATH_1 | 350 | 354 | PF00917 | 0.484 |
DOC_USP7_UBL2_3 | 158 | 162 | PF12436 | 0.440 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.487 |
LIG_14-3-3_CanoR_1 | 327 | 336 | PF00244 | 0.356 |
LIG_14-3-3_CanoR_1 | 364 | 373 | PF00244 | 0.370 |
LIG_14-3-3_CanoR_1 | 605 | 611 | PF00244 | 0.541 |
LIG_14-3-3_CanoR_1 | 623 | 627 | PF00244 | 0.328 |
LIG_AP2alpha_1 | 439 | 443 | PF02296 | 0.352 |
LIG_AP2alpha_1 | 517 | 521 | PF02296 | 0.553 |
LIG_BRCT_BRCA1_1 | 155 | 159 | PF00533 | 0.519 |
LIG_BRCT_BRCA1_1 | 611 | 615 | PF00533 | 0.502 |
LIG_deltaCOP1_diTrp_1 | 296 | 305 | PF00928 | 0.343 |
LIG_deltaCOP1_diTrp_1 | 309 | 314 | PF00928 | 0.347 |
LIG_deltaCOP1_diTrp_1 | 334 | 339 | PF00928 | 0.341 |
LIG_deltaCOP1_diTrp_1 | 368 | 375 | PF00928 | 0.356 |
LIG_eIF4E_1 | 576 | 582 | PF01652 | 0.543 |
LIG_eIF4E_1 | 66 | 72 | PF01652 | 0.467 |
LIG_eIF4E_1 | 698 | 704 | PF01652 | 0.592 |
LIG_FHA_1 | 101 | 107 | PF00498 | 0.541 |
LIG_FHA_1 | 193 | 199 | PF00498 | 0.376 |
LIG_FHA_1 | 328 | 334 | PF00498 | 0.356 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.352 |
LIG_FHA_1 | 698 | 704 | PF00498 | 0.627 |
LIG_FHA_1 | 741 | 747 | PF00498 | 0.575 |
LIG_FHA_2 | 136 | 142 | PF00498 | 0.403 |
LIG_FHA_2 | 169 | 175 | PF00498 | 0.492 |
LIG_FHA_2 | 365 | 371 | PF00498 | 0.341 |
LIG_LIR_Apic_2 | 128 | 134 | PF02991 | 0.444 |
LIG_LIR_Apic_2 | 334 | 340 | PF02991 | 0.341 |
LIG_LIR_Apic_2 | 441 | 446 | PF02991 | 0.441 |
LIG_LIR_Apic_2 | 592 | 598 | PF02991 | 0.579 |
LIG_LIR_Apic_2 | 67 | 73 | PF02991 | 0.414 |
LIG_LIR_Gen_1 | 120 | 131 | PF02991 | 0.470 |
LIG_LIR_Gen_1 | 279 | 289 | PF02991 | 0.341 |
LIG_LIR_Gen_1 | 368 | 379 | PF02991 | 0.341 |
LIG_LIR_Gen_1 | 412 | 420 | PF02991 | 0.435 |
LIG_LIR_Gen_1 | 55 | 65 | PF02991 | 0.384 |
LIG_LIR_Gen_1 | 565 | 576 | PF02991 | 0.396 |
LIG_LIR_Gen_1 | 678 | 688 | PF02991 | 0.595 |
LIG_LIR_Gen_1 | 712 | 723 | PF02991 | 0.412 |
LIG_LIR_LC3C_4 | 640 | 645 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 120 | 126 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 132 | 136 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 279 | 283 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 297 | 303 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 309 | 315 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 368 | 374 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 412 | 417 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 519 | 524 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 55 | 60 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 565 | 571 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 678 | 684 | PF02991 | 0.553 |
LIG_LIR_Nem_3 | 712 | 718 | PF02991 | 0.429 |
LIG_PCNA_yPIPBox_3 | 707 | 718 | PF02747 | 0.506 |
LIG_Pex14_1 | 252 | 256 | PF04695 | 0.341 |
LIG_Pex14_1 | 371 | 375 | PF04695 | 0.484 |
LIG_Pex14_2 | 439 | 443 | PF04695 | 0.334 |
LIG_Pex14_2 | 475 | 479 | PF04695 | 0.341 |
LIG_Pex14_2 | 517 | 521 | PF04695 | 0.469 |
LIG_Pex14_2 | 57 | 61 | PF04695 | 0.441 |
LIG_PTB_Apo_2 | 274 | 281 | PF02174 | 0.355 |
LIG_SH2_CRK | 414 | 418 | PF00017 | 0.435 |
LIG_SH2_CRK | 595 | 599 | PF00017 | 0.483 |
LIG_SH2_GRB2like | 256 | 259 | PF00017 | 0.435 |
LIG_SH2_GRB2like | 93 | 96 | PF00017 | 0.379 |
LIG_SH2_NCK_1 | 414 | 418 | PF00017 | 0.435 |
LIG_SH2_NCK_1 | 595 | 599 | PF00017 | 0.424 |
LIG_SH2_PTP2 | 482 | 485 | PF00017 | 0.375 |
LIG_SH2_SRC | 256 | 259 | PF00017 | 0.344 |
LIG_SH2_SRC | 487 | 490 | PF00017 | 0.377 |
LIG_SH2_SRC | 654 | 657 | PF00017 | 0.444 |
LIG_SH2_SRC | 66 | 69 | PF00017 | 0.582 |
LIG_SH2_STAP1 | 534 | 538 | PF00017 | 0.410 |
LIG_SH2_STAP1 | 66 | 70 | PF00017 | 0.450 |
LIG_SH2_STAT3 | 142 | 145 | PF00017 | 0.466 |
LIG_SH2_STAT3 | 289 | 292 | PF00017 | 0.341 |
LIG_SH2_STAT3 | 9 | 12 | PF00017 | 0.557 |
LIG_SH2_STAT5 | 207 | 210 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 378 | 381 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 482 | 485 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 487 | 490 | PF00017 | 0.368 |
LIG_SH2_STAT5 | 49 | 52 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 576 | 579 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 698 | 701 | PF00017 | 0.625 |
LIG_SH2_STAT5 | 93 | 96 | PF00017 | 0.379 |
LIG_SH3_3 | 305 | 311 | PF00018 | 0.341 |
LIG_SH3_3 | 485 | 491 | PF00018 | 0.484 |
LIG_SH3_3 | 728 | 734 | PF00018 | 0.440 |
LIG_SUMO_SIM_anti_2 | 639 | 645 | PF11976 | 0.373 |
LIG_SxIP_EBH_1 | 652 | 665 | PF03271 | 0.466 |
LIG_TRAF2_1 | 367 | 370 | PF00917 | 0.368 |
LIG_TRAF2_1 | 65 | 68 | PF00917 | 0.459 |
LIG_WRC_WIRS_1 | 280 | 285 | PF05994 | 0.416 |
LIG_WRC_WIRS_1 | 351 | 356 | PF05994 | 0.435 |
LIG_WRC_WIRS_1 | 445 | 450 | PF05994 | 0.341 |
LIG_WRC_WIRS_1 | 564 | 569 | PF05994 | 0.315 |
LIG_WRC_WIRS_1 | 703 | 708 | PF05994 | 0.465 |
MOD_CDK_SPK_2 | 19 | 24 | PF00069 | 0.536 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.512 |
MOD_CK1_1 | 353 | 359 | PF00069 | 0.409 |
MOD_CK1_1 | 444 | 450 | PF00069 | 0.341 |
MOD_CK1_1 | 498 | 504 | PF00069 | 0.405 |
MOD_CK1_1 | 629 | 635 | PF00069 | 0.555 |
MOD_CK1_1 | 639 | 645 | PF00069 | 0.410 |
MOD_CK2_1 | 135 | 141 | PF00069 | 0.429 |
MOD_CK2_1 | 273 | 279 | PF00069 | 0.341 |
MOD_CK2_1 | 364 | 370 | PF00069 | 0.341 |
MOD_CMANNOS | 302 | 305 | PF00535 | 0.341 |
MOD_Cter_Amidation | 359 | 362 | PF01082 | 0.400 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.452 |
MOD_GlcNHglycan | 321 | 324 | PF01048 | 0.417 |
MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.528 |
MOD_GlcNHglycan | 599 | 602 | PF01048 | 0.673 |
MOD_GlcNHglycan | 656 | 659 | PF01048 | 0.493 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.414 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.571 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.344 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.435 |
MOD_GSK3_1 | 593 | 600 | PF00069 | 0.487 |
MOD_GSK3_1 | 622 | 629 | PF00069 | 0.494 |
MOD_GSK3_1 | 650 | 657 | PF00069 | 0.431 |
MOD_N-GLC_1 | 168 | 173 | PF02516 | 0.454 |
MOD_N-GLC_2 | 112 | 114 | PF02516 | 0.466 |
MOD_N-GLC_2 | 258 | 260 | PF02516 | 0.368 |
MOD_N-GLC_2 | 526 | 528 | PF02516 | 0.379 |
MOD_NEK2_1 | 153 | 158 | PF00069 | 0.431 |
MOD_NEK2_1 | 268 | 273 | PF00069 | 0.341 |
MOD_NEK2_1 | 517 | 522 | PF00069 | 0.457 |
MOD_NEK2_1 | 562 | 567 | PF00069 | 0.386 |
MOD_NEK2_1 | 650 | 655 | PF00069 | 0.424 |
MOD_NEK2_2 | 350 | 355 | PF00069 | 0.435 |
MOD_NEK2_2 | 702 | 707 | PF00069 | 0.445 |
MOD_PIKK_1 | 327 | 333 | PF00454 | 0.344 |
MOD_PKA_1 | 622 | 628 | PF00069 | 0.549 |
MOD_PKA_2 | 319 | 325 | PF00069 | 0.417 |
MOD_PKA_2 | 517 | 523 | PF00069 | 0.437 |
MOD_PKA_2 | 622 | 628 | PF00069 | 0.460 |
MOD_PKB_1 | 362 | 370 | PF00069 | 0.368 |
MOD_Plk_1 | 119 | 125 | PF00069 | 0.463 |
MOD_Plk_1 | 441 | 447 | PF00069 | 0.341 |
MOD_Plk_1 | 562 | 568 | PF00069 | 0.311 |
MOD_Plk_1 | 639 | 645 | PF00069 | 0.378 |
MOD_Plk_1 | 650 | 656 | PF00069 | 0.390 |
MOD_Plk_1 | 66 | 72 | PF00069 | 0.467 |
MOD_Plk_1 | 694 | 700 | PF00069 | 0.628 |
MOD_Plk_2-3 | 119 | 125 | PF00069 | 0.463 |
MOD_Plk_4 | 207 | 213 | PF00069 | 0.516 |
MOD_Plk_4 | 563 | 569 | PF00069 | 0.345 |
MOD_Plk_4 | 622 | 628 | PF00069 | 0.483 |
MOD_Plk_4 | 639 | 645 | PF00069 | 0.429 |
MOD_Plk_4 | 66 | 72 | PF00069 | 0.473 |
MOD_Plk_4 | 694 | 700 | PF00069 | 0.655 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.487 |
MOD_SUMO_for_1 | 354 | 357 | PF00179 | 0.356 |
MOD_SUMO_for_1 | 41 | 44 | PF00179 | 0.575 |
MOD_SUMO_for_1 | 610 | 613 | PF00179 | 0.476 |
MOD_SUMO_for_1 | 738 | 741 | PF00179 | 0.457 |
TRG_DiLeu_BaEn_1 | 369 | 374 | PF01217 | 0.338 |
TRG_DiLeu_BaEn_1 | 67 | 72 | PF01217 | 0.466 |
TRG_DiLeu_BaEn_1 | 713 | 718 | PF01217 | 0.415 |
TRG_DiLeu_BaEn_2 | 278 | 284 | PF01217 | 0.341 |
TRG_DiLeu_BaEn_4 | 15 | 21 | PF01217 | 0.518 |
TRG_DiLeu_BaLyEn_6 | 699 | 704 | PF01217 | 0.453 |
TRG_ENDOCYTIC_2 | 414 | 417 | PF00928 | 0.429 |
TRG_ENDOCYTIC_2 | 440 | 443 | PF00928 | 0.354 |
TRG_ENDOCYTIC_2 | 482 | 485 | PF00928 | 0.375 |
TRG_ER_diArg_1 | 142 | 144 | PF00400 | 0.415 |
TRG_ER_diArg_1 | 362 | 365 | PF00400 | 0.368 |
TRG_ER_diArg_1 | 475 | 477 | PF00400 | 0.356 |
TRG_ER_diArg_1 | 536 | 538 | PF00400 | 0.514 |
TRG_ER_diArg_1 | 579 | 581 | PF00400 | 0.454 |
TRG_NES_CRM1_1 | 44 | 58 | PF08389 | 0.392 |
TRG_NES_CRM1_1 | 563 | 575 | PF08389 | 0.400 |
TRG_Pf-PMV_PEXEL_1 | 24 | 29 | PF00026 | 0.474 |
TRG_Pf-PMV_PEXEL_1 | 364 | 368 | PF00026 | 0.375 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMA1 | Leptomonas seymouri | 78% | 100% |
A0A0S4JIK4 | Bodo saltans | 57% | 100% |
A0A1X0NZP4 | Trypanosomatidae | 62% | 100% |
A0A3S7X2D6 | Leishmania donovani | 96% | 100% |
A0A422NF05 | Trypanosoma rangeli | 60% | 100% |
A4HHA6 | Leishmania braziliensis | 84% | 100% |
A4I4F2 | Leishmania infantum | 96% | 100% |
C9ZLK2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 60% | 100% |
E9ALX8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
V5BR85 | Trypanosoma cruzi | 61% | 100% |