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: 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: Q4Q3S1
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 6 |
GO:0008152 | metabolic process | 1 | 6 |
GO:0019538 | protein metabolic process | 3 | 6 |
GO:0032446 | protein modification by small protein conjugation | 6 | 6 |
GO:0036211 | protein modification process | 4 | 6 |
GO:0043170 | macromolecule metabolic process | 3 | 6 |
GO:0043412 | macromolecule modification | 4 | 6 |
GO:0044238 | primary metabolic process | 2 | 6 |
GO:0045116 | protein neddylation | 7 | 6 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 6 |
GO:0071704 | organic substance metabolic process | 2 | 6 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0008641 | ubiquitin-like modifier activating enzyme activity | 2 | 12 |
GO:0016874 | ligase activity | 2 | 12 |
GO:0016877 | ligase activity, forming carbon-sulfur bonds | 3 | 12 |
GO:0019781 | NEDD8 activating enzyme activity | 3 | 6 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 12 |
GO:0140657 | ATP-dependent activity | 1 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 301 | 305 | PF00656 | 0.539 |
CLV_NRD_NRD_1 | 145 | 147 | PF00675 | 0.480 |
CLV_NRD_NRD_1 | 323 | 325 | PF00675 | 0.465 |
CLV_NRD_NRD_1 | 365 | 367 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 460 | 462 | PF00675 | 0.515 |
CLV_NRD_NRD_1 | 558 | 560 | PF00675 | 0.566 |
CLV_NRD_NRD_1 | 642 | 644 | PF00675 | 0.495 |
CLV_PCSK_KEX2_1 | 145 | 147 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 323 | 325 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 334 | 336 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 365 | 367 | PF00082 | 0.470 |
CLV_PCSK_KEX2_1 | 558 | 560 | PF00082 | 0.467 |
CLV_PCSK_KEX2_1 | 642 | 644 | PF00082 | 0.495 |
CLV_PCSK_PC1ET2_1 | 334 | 336 | PF00082 | 0.474 |
CLV_PCSK_PC1ET2_1 | 558 | 560 | PF00082 | 0.467 |
CLV_PCSK_SKI1_1 | 168 | 172 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 21 | 25 | PF00082 | 0.556 |
CLV_PCSK_SKI1_1 | 411 | 415 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 582 | 586 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 67 | 71 | PF00082 | 0.456 |
CLV_Separin_Metazoa | 399 | 403 | PF03568 | 0.384 |
DEG_APCC_DBOX_1 | 572 | 580 | PF00400 | 0.300 |
DEG_MDM2_SWIB_1 | 322 | 329 | PF02201 | 0.512 |
DOC_CYCLIN_RxL_1 | 579 | 589 | PF00134 | 0.501 |
DOC_CYCLIN_yCln2_LP_2 | 344 | 350 | PF00134 | 0.356 |
DOC_MAPK_DCC_7 | 232 | 242 | PF00069 | 0.507 |
DOC_MAPK_gen_1 | 21 | 31 | PF00069 | 0.428 |
DOC_MAPK_gen_1 | 337 | 346 | PF00069 | 0.398 |
DOC_MAPK_MEF2A_6 | 232 | 241 | PF00069 | 0.475 |
DOC_MAPK_MEF2A_6 | 573 | 581 | PF00069 | 0.287 |
DOC_MAPK_MEF2A_6 | 762 | 769 | PF00069 | 0.495 |
DOC_PP1_RVXF_1 | 19 | 26 | PF00149 | 0.548 |
DOC_PP1_RVXF_1 | 598 | 605 | PF00149 | 0.503 |
DOC_PP1_RVXF_1 | 621 | 627 | PF00149 | 0.513 |
DOC_PP4_FxxP_1 | 4 | 7 | PF00568 | 0.535 |
DOC_PP4_FxxP_1 | 568 | 571 | PF00568 | 0.534 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 190 | 194 | PF00917 | 0.785 |
DOC_USP7_MATH_1 | 355 | 359 | PF00917 | 0.467 |
DOC_USP7_MATH_1 | 415 | 419 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 424 | 428 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.428 |
DOC_USP7_UBL2_3 | 380 | 384 | PF12436 | 0.572 |
DOC_USP7_UBL2_3 | 554 | 558 | PF12436 | 0.442 |
DOC_WW_Pin1_4 | 186 | 191 | PF00397 | 0.773 |
DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.598 |
DOC_WW_Pin1_4 | 203 | 208 | PF00397 | 0.507 |
DOC_WW_Pin1_4 | 418 | 423 | PF00397 | 0.534 |
DOC_WW_Pin1_4 | 440 | 445 | PF00397 | 0.450 |
DOC_WW_Pin1_4 | 92 | 97 | PF00397 | 0.425 |
LIG_14-3-3_CanoR_1 | 129 | 133 | PF00244 | 0.391 |
LIG_14-3-3_CanoR_1 | 146 | 156 | PF00244 | 0.611 |
LIG_14-3-3_CanoR_1 | 324 | 330 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 337 | 347 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 354 | 360 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 365 | 370 | PF00244 | 0.589 |
LIG_14-3-3_CanoR_1 | 573 | 577 | PF00244 | 0.432 |
LIG_14-3-3_CanoR_1 | 600 | 605 | PF00244 | 0.521 |
LIG_14-3-3_CanoR_1 | 629 | 634 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 67 | 72 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 75 | 82 | PF00244 | 0.416 |
LIG_Actin_WH2_2 | 386 | 404 | PF00022 | 0.518 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.804 |
LIG_BRCT_BRCA1_1 | 342 | 346 | PF00533 | 0.584 |
LIG_deltaCOP1_diTrp_1 | 594 | 604 | PF00928 | 0.469 |
LIG_FHA_1 | 11 | 17 | PF00498 | 0.690 |
LIG_FHA_1 | 161 | 167 | PF00498 | 0.593 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.527 |
LIG_FHA_1 | 458 | 464 | PF00498 | 0.554 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.429 |
LIG_FHA_1 | 512 | 518 | PF00498 | 0.526 |
LIG_FHA_1 | 587 | 593 | PF00498 | 0.336 |
LIG_FHA_1 | 626 | 632 | PF00498 | 0.494 |
LIG_FHA_1 | 66 | 72 | PF00498 | 0.435 |
LIG_FHA_1 | 750 | 756 | PF00498 | 0.410 |
LIG_FHA_1 | 779 | 785 | PF00498 | 0.559 |
LIG_FHA_1 | 88 | 94 | PF00498 | 0.431 |
LIG_FHA_2 | 326 | 332 | PF00498 | 0.486 |
LIG_FHA_2 | 68 | 74 | PF00498 | 0.377 |
LIG_LIR_Apic_2 | 2 | 7 | PF02991 | 0.535 |
LIG_LIR_Gen_1 | 218 | 226 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 171 | 176 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 213 | 219 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 278 | 283 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 352 | 356 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 516 | 522 | PF02991 | 0.371 |
LIG_LYPXL_yS_3 | 314 | 317 | PF13949 | 0.458 |
LIG_NRBOX | 396 | 402 | PF00104 | 0.448 |
LIG_PDZ_Class_2 | 782 | 787 | PF00595 | 0.516 |
LIG_Pex14_1 | 124 | 128 | PF04695 | 0.391 |
LIG_Pex14_1 | 136 | 140 | PF04695 | 0.422 |
LIG_Pex14_2 | 322 | 326 | PF04695 | 0.491 |
LIG_PTB_Apo_2 | 779 | 786 | PF02174 | 0.515 |
LIG_SH2_CRK | 173 | 177 | PF00017 | 0.475 |
LIG_SH2_CRK | 353 | 357 | PF00017 | 0.400 |
LIG_SH2_CRK | 501 | 505 | PF00017 | 0.494 |
LIG_SH2_GRB2like | 780 | 783 | PF00017 | 0.525 |
LIG_SH2_SRC | 140 | 143 | PF00017 | 0.615 |
LIG_SH2_STAP1 | 780 | 784 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 140 | 143 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 508 | 511 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 651 | 654 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 780 | 783 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 86 | 89 | PF00017 | 0.421 |
LIG_SH3_1 | 232 | 238 | PF00018 | 0.524 |
LIG_SH3_3 | 232 | 238 | PF00018 | 0.524 |
LIG_SH3_3 | 260 | 266 | PF00018 | 0.579 |
LIG_SH3_3 | 293 | 299 | PF00018 | 0.538 |
LIG_SH3_3 | 4 | 10 | PF00018 | 0.526 |
LIG_SH3_3 | 740 | 746 | PF00018 | 0.550 |
LIG_SUMO_SIM_anti_2 | 208 | 214 | PF11976 | 0.412 |
LIG_SUMO_SIM_anti_2 | 220 | 226 | PF11976 | 0.384 |
LIG_SUMO_SIM_anti_2 | 68 | 74 | PF11976 | 0.428 |
LIG_SUMO_SIM_par_1 | 208 | 214 | PF11976 | 0.358 |
LIG_SUMO_SIM_par_1 | 238 | 245 | PF11976 | 0.477 |
LIG_SUMO_SIM_par_1 | 50 | 56 | PF11976 | 0.428 |
LIG_SUMO_SIM_par_1 | 67 | 74 | PF11976 | 0.187 |
LIG_SUMO_SIM_par_1 | 95 | 100 | PF11976 | 0.228 |
LIG_TRAF2_1 | 116 | 119 | PF00917 | 0.428 |
LIG_TRAF2_1 | 330 | 333 | PF00917 | 0.587 |
LIG_TRAF2_1 | 369 | 372 | PF00917 | 0.440 |
LIG_TRAF2_1 | 396 | 399 | PF00917 | 0.320 |
LIG_TRAF2_1 | 478 | 481 | PF00917 | 0.579 |
LIG_TRAF2_1 | 685 | 688 | PF00917 | 0.509 |
LIG_TRAF2_1 | 725 | 728 | PF00917 | 0.489 |
LIG_TRAF2_1 | 756 | 759 | PF00917 | 0.348 |
LIG_TYR_ITIM | 312 | 317 | PF00017 | 0.363 |
LIG_TYR_ITIM | 517 | 522 | PF00017 | 0.498 |
LIG_UBA3_1 | 344 | 351 | PF00899 | 0.499 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.644 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.539 |
MOD_CK1_1 | 220 | 226 | PF00069 | 0.504 |
MOD_CK1_1 | 340 | 346 | PF00069 | 0.603 |
MOD_CK1_1 | 418 | 424 | PF00069 | 0.549 |
MOD_CK1_1 | 572 | 578 | PF00069 | 0.545 |
MOD_CK1_1 | 603 | 609 | PF00069 | 0.517 |
MOD_CK1_1 | 683 | 689 | PF00069 | 0.573 |
MOD_CK2_1 | 325 | 331 | PF00069 | 0.526 |
MOD_CK2_1 | 365 | 371 | PF00069 | 0.536 |
MOD_Cter_Amidation | 143 | 146 | PF01082 | 0.445 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.782 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.619 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.608 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.536 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.734 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.483 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.347 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.459 |
MOD_GlcNHglycan | 428 | 431 | PF01048 | 0.463 |
MOD_GlcNHglycan | 505 | 508 | PF01048 | 0.497 |
MOD_GlcNHglycan | 605 | 608 | PF01048 | 0.557 |
MOD_GlcNHglycan | 668 | 672 | PF01048 | 0.591 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.674 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.664 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.619 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.794 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.615 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.359 |
MOD_GSK3_1 | 625 | 632 | PF00069 | 0.542 |
MOD_GSK3_1 | 711 | 718 | PF00069 | 0.553 |
MOD_GSK3_1 | 744 | 751 | PF00069 | 0.521 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.423 |
MOD_N-GLC_1 | 180 | 185 | PF02516 | 0.602 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.746 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.462 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.482 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.483 |
MOD_NEK2_1 | 425 | 430 | PF00069 | 0.499 |
MOD_NEK2_1 | 457 | 462 | PF00069 | 0.396 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.321 |
MOD_NEK2_1 | 512 | 517 | PF00069 | 0.469 |
MOD_NEK2_1 | 586 | 591 | PF00069 | 0.433 |
MOD_NEK2_1 | 669 | 674 | PF00069 | 0.531 |
MOD_NEK2_1 | 705 | 710 | PF00069 | 0.704 |
MOD_NEK2_1 | 87 | 92 | PF00069 | 0.440 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.445 |
MOD_NEK2_2 | 12 | 17 | PF00069 | 0.516 |
MOD_PIKK_1 | 264 | 270 | PF00454 | 0.612 |
MOD_PIKK_1 | 680 | 686 | PF00454 | 0.546 |
MOD_PIKK_1 | 715 | 721 | PF00454 | 0.430 |
MOD_PKA_1 | 365 | 371 | PF00069 | 0.419 |
MOD_PKA_2 | 128 | 134 | PF00069 | 0.353 |
MOD_PKA_2 | 16 | 22 | PF00069 | 0.437 |
MOD_PKA_2 | 242 | 248 | PF00069 | 0.469 |
MOD_PKA_2 | 338 | 344 | PF00069 | 0.529 |
MOD_PKA_2 | 365 | 371 | PF00069 | 0.429 |
MOD_PKA_2 | 572 | 578 | PF00069 | 0.432 |
MOD_PKB_1 | 335 | 343 | PF00069 | 0.585 |
MOD_Plk_1 | 217 | 223 | PF00069 | 0.529 |
MOD_Plk_1 | 705 | 711 | PF00069 | 0.638 |
MOD_Plk_4 | 205 | 211 | PF00069 | 0.391 |
MOD_Plk_4 | 220 | 226 | PF00069 | 0.478 |
MOD_Plk_4 | 340 | 346 | PF00069 | 0.593 |
MOD_Plk_4 | 355 | 361 | PF00069 | 0.510 |
MOD_Plk_4 | 513 | 519 | PF00069 | 0.506 |
MOD_Plk_4 | 57 | 63 | PF00069 | 0.362 |
MOD_Plk_4 | 572 | 578 | PF00069 | 0.479 |
MOD_Plk_4 | 67 | 73 | PF00069 | 0.308 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.484 |
MOD_ProDKin_1 | 186 | 192 | PF00069 | 0.776 |
MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.595 |
MOD_ProDKin_1 | 203 | 209 | PF00069 | 0.497 |
MOD_ProDKin_1 | 418 | 424 | PF00069 | 0.529 |
MOD_ProDKin_1 | 440 | 446 | PF00069 | 0.445 |
MOD_ProDKin_1 | 92 | 98 | PF00069 | 0.425 |
MOD_SUMO_rev_2 | 331 | 336 | PF00179 | 0.579 |
TRG_DiLeu_BaEn_1 | 677 | 682 | PF01217 | 0.517 |
TRG_DiLeu_BaEn_1 | 759 | 764 | PF01217 | 0.343 |
TRG_DiLeu_BaLyEn_6 | 580 | 585 | PF01217 | 0.501 |
TRG_ENDOCYTIC_2 | 173 | 176 | PF00928 | 0.525 |
TRG_ENDOCYTIC_2 | 216 | 219 | PF00928 | 0.528 |
TRG_ENDOCYTIC_2 | 314 | 317 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 353 | 356 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 519 | 522 | PF00928 | 0.380 |
TRG_ER_diArg_1 | 145 | 147 | PF00400 | 0.495 |
TRG_ER_diArg_1 | 322 | 324 | PF00400 | 0.456 |
TRG_ER_diArg_1 | 364 | 366 | PF00400 | 0.436 |
TRG_ER_diArg_1 | 616 | 619 | PF00400 | 0.517 |
TRG_ER_diArg_1 | 765 | 768 | PF00400 | 0.353 |
TRG_Pf-PMV_PEXEL_1 | 520 | 524 | PF00026 | 0.443 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5J2 | Leptomonas seymouri | 50% | 100% |
A0A0S4JRQ2 | Bodo saltans | 24% | 96% |
A0A1X0NR91 | Trypanosomatidae | 26% | 100% |
A0A3R7MGL1 | Trypanosoma rangeli | 27% | 100% |
A0A3S7X724 | Leishmania donovani | 85% | 98% |
A4HLX6 | Leishmania braziliensis | 72% | 100% |
A4I9A5 | Leishmania infantum | 85% | 98% |
C9ZJC1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
E9B4A5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
V5AV29 | Trypanosoma cruzi | 27% | 100% |