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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
GO:0097014 | ciliary plasm | 5 | 1 |
GO:0099568 | cytoplasmic region | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9B4A5
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 5 |
GO:0008152 | metabolic process | 1 | 5 |
GO:0019538 | protein metabolic process | 3 | 5 |
GO:0032446 | protein modification by small protein conjugation | 6 | 5 |
GO:0036211 | protein modification process | 4 | 5 |
GO:0043170 | macromolecule metabolic process | 3 | 5 |
GO:0043412 | macromolecule modification | 4 | 5 |
GO:0044238 | primary metabolic process | 2 | 5 |
GO:0045116 | protein neddylation | 7 | 5 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 5 |
GO:0071704 | organic substance metabolic process | 2 | 5 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0008641 | ubiquitin-like modifier activating enzyme activity | 2 | 11 |
GO:0016874 | ligase activity | 2 | 11 |
GO:0016877 | ligase activity, forming carbon-sulfur bonds | 3 | 11 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 11 |
GO:0140657 | ATP-dependent activity | 1 | 11 |
GO:0019781 | NEDD8 activating enzyme activity | 3 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 301 | 305 | PF00656 | 0.481 |
CLV_MEL_PAP_1 | 416 | 422 | PF00089 | 0.264 |
CLV_NRD_NRD_1 | 145 | 147 | PF00675 | 0.440 |
CLV_NRD_NRD_1 | 323 | 325 | PF00675 | 0.478 |
CLV_NRD_NRD_1 | 365 | 367 | PF00675 | 0.470 |
CLV_NRD_NRD_1 | 644 | 646 | PF00675 | 0.478 |
CLV_NRD_NRD_1 | 720 | 722 | PF00675 | 0.478 |
CLV_PCSK_KEX2_1 | 145 | 147 | PF00082 | 0.440 |
CLV_PCSK_KEX2_1 | 323 | 325 | PF00082 | 0.478 |
CLV_PCSK_KEX2_1 | 365 | 367 | PF00082 | 0.459 |
CLV_PCSK_KEX2_1 | 644 | 646 | PF00082 | 0.478 |
CLV_PCSK_SKI1_1 | 411 | 415 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 584 | 588 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 67 | 71 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 721 | 725 | PF00082 | 0.392 |
DEG_MDM2_SWIB_1 | 322 | 329 | PF02201 | 0.494 |
DEG_SPOP_SBC_1 | 182 | 186 | PF00917 | 0.447 |
DEG_SPOP_SBC_1 | 88 | 92 | PF00917 | 0.173 |
DOC_CYCLIN_RxL_1 | 581 | 591 | PF00134 | 0.491 |
DOC_CYCLIN_yCln2_LP_2 | 467 | 473 | PF00134 | 0.461 |
DOC_MAPK_DCC_7 | 232 | 242 | PF00069 | 0.425 |
DOC_MAPK_gen_1 | 433 | 440 | PF00069 | 0.251 |
DOC_MAPK_MEF2A_6 | 232 | 241 | PF00069 | 0.449 |
DOC_MAPK_MEF2A_6 | 738 | 747 | PF00069 | 0.344 |
DOC_MAPK_MEF2A_6 | 764 | 771 | PF00069 | 0.470 |
DOC_PP1_RVXF_1 | 600 | 607 | PF00149 | 0.480 |
DOC_PP1_RVXF_1 | 623 | 629 | PF00149 | 0.483 |
DOC_PP1_RVXF_1 | 643 | 650 | PF00149 | 0.222 |
DOC_PP2B_LxvP_1 | 467 | 470 | PF13499 | 0.452 |
DOC_PP2B_LxvP_1 | 7 | 10 | PF13499 | 0.415 |
DOC_USP7_MATH_1 | 183 | 187 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 190 | 194 | PF00917 | 0.755 |
DOC_USP7_MATH_1 | 299 | 303 | PF00917 | 0.426 |
DOC_USP7_MATH_1 | 355 | 359 | PF00917 | 0.458 |
DOC_USP7_MATH_1 | 415 | 419 | PF00917 | 0.424 |
DOC_USP7_MATH_1 | 424 | 428 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.464 |
DOC_USP7_MATH_1 | 571 | 575 | PF00917 | 0.374 |
DOC_USP7_MATH_1 | 666 | 670 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 89 | 93 | PF00917 | 0.346 |
DOC_USP7_UBL2_3 | 380 | 384 | PF12436 | 0.539 |
DOC_USP7_UBL2_3 | 553 | 557 | PF12436 | 0.390 |
DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.685 |
DOC_WW_Pin1_4 | 202 | 207 | PF00397 | 0.391 |
DOC_WW_Pin1_4 | 217 | 222 | PF00397 | 0.388 |
DOC_WW_Pin1_4 | 418 | 423 | PF00397 | 0.449 |
DOC_WW_Pin1_4 | 440 | 445 | PF00397 | 0.407 |
DOC_WW_Pin1_4 | 92 | 97 | PF00397 | 0.417 |
LIG_14-3-3_CanoR_1 | 324 | 330 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 337 | 347 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 354 | 360 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 365 | 370 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 602 | 607 | PF00244 | 0.398 |
LIG_14-3-3_CanoR_1 | 631 | 636 | PF00244 | 0.489 |
LIG_14-3-3_CanoR_1 | 67 | 72 | PF00244 | 0.355 |
LIG_14-3-3_CanoR_1 | 75 | 82 | PF00244 | 0.199 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.609 |
LIG_BRCT_BRCA1_1 | 342 | 346 | PF00533 | 0.584 |
LIG_deltaCOP1_diTrp_1 | 596 | 606 | PF00928 | 0.439 |
LIG_FHA_1 | 220 | 226 | PF00498 | 0.352 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.541 |
LIG_FHA_1 | 458 | 464 | PF00498 | 0.540 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.428 |
LIG_FHA_1 | 514 | 520 | PF00498 | 0.509 |
LIG_FHA_1 | 589 | 595 | PF00498 | 0.376 |
LIG_FHA_1 | 628 | 634 | PF00498 | 0.410 |
LIG_FHA_1 | 66 | 72 | PF00498 | 0.458 |
LIG_FHA_1 | 752 | 758 | PF00498 | 0.408 |
LIG_FHA_1 | 781 | 787 | PF00498 | 0.432 |
LIG_FHA_1 | 88 | 94 | PF00498 | 0.404 |
LIG_FHA_2 | 326 | 332 | PF00498 | 0.433 |
LIG_FHA_2 | 347 | 353 | PF00498 | 0.375 |
LIG_FHA_2 | 560 | 566 | PF00498 | 0.533 |
LIG_FHA_2 | 591 | 597 | PF00498 | 0.447 |
LIG_FHA_2 | 68 | 74 | PF00498 | 0.340 |
LIG_LIR_Gen_1 | 2 | 12 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 2 | 7 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 213 | 219 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 278 | 283 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 310 | 314 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 350 | 356 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 518 | 524 | PF02991 | 0.350 |
LIG_LYPXL_yS_3 | 314 | 317 | PF13949 | 0.426 |
LIG_MYND_2 | 206 | 210 | PF01753 | 0.308 |
LIG_NRBOX | 396 | 402 | PF00104 | 0.435 |
LIG_PDZ_Class_2 | 784 | 789 | PF00595 | 0.494 |
LIG_Pex14_1 | 124 | 128 | PF04695 | 0.349 |
LIG_Pex14_2 | 322 | 326 | PF04695 | 0.475 |
LIG_PTB_Apo_2 | 781 | 788 | PF02174 | 0.491 |
LIG_SH2_CRK | 173 | 177 | PF00017 | 0.529 |
LIG_SH2_CRK | 353 | 357 | PF00017 | 0.392 |
LIG_SH2_CRK | 503 | 507 | PF00017 | 0.428 |
LIG_SH2_GRB2like | 782 | 785 | PF00017 | 0.498 |
LIG_SH2_SRC | 490 | 493 | PF00017 | 0.432 |
LIG_SH2_STAP1 | 782 | 786 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 311 | 314 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 510 | 513 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 653 | 656 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 782 | 785 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 86 | 89 | PF00017 | 0.402 |
LIG_SH3_1 | 153 | 159 | PF00018 | 0.533 |
LIG_SH3_1 | 232 | 238 | PF00018 | 0.490 |
LIG_SH3_3 | 153 | 159 | PF00018 | 0.574 |
LIG_SH3_3 | 200 | 206 | PF00018 | 0.416 |
LIG_SH3_3 | 232 | 238 | PF00018 | 0.500 |
LIG_SH3_3 | 260 | 266 | PF00018 | 0.561 |
LIG_SH3_3 | 293 | 299 | PF00018 | 0.423 |
LIG_SH3_3 | 742 | 748 | PF00018 | 0.517 |
LIG_SUMO_SIM_anti_2 | 208 | 214 | PF11976 | 0.381 |
LIG_SUMO_SIM_anti_2 | 68 | 74 | PF11976 | 0.355 |
LIG_SUMO_SIM_par_1 | 174 | 180 | PF11976 | 0.377 |
LIG_SUMO_SIM_par_1 | 208 | 214 | PF11976 | 0.328 |
LIG_SUMO_SIM_par_1 | 238 | 245 | PF11976 | 0.450 |
LIG_SUMO_SIM_par_1 | 50 | 56 | PF11976 | 0.398 |
LIG_SUMO_SIM_par_1 | 67 | 74 | PF11976 | 0.192 |
LIG_TRAF2_1 | 116 | 119 | PF00917 | 0.355 |
LIG_TRAF2_1 | 330 | 333 | PF00917 | 0.563 |
LIG_TRAF2_1 | 727 | 730 | PF00917 | 0.476 |
LIG_TRAF2_1 | 758 | 761 | PF00917 | 0.323 |
LIG_TYR_ITIM | 312 | 317 | PF00017 | 0.333 |
LIG_TYR_ITIM | 519 | 524 | PF00017 | 0.477 |
LIG_UBA3_1 | 345 | 351 | PF00899 | 0.472 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.523 |
MOD_CK1_1 | 220 | 226 | PF00069 | 0.348 |
MOD_CK1_1 | 340 | 346 | PF00069 | 0.595 |
MOD_CK1_1 | 418 | 424 | PF00069 | 0.445 |
MOD_CK1_1 | 574 | 580 | PF00069 | 0.558 |
MOD_CK1_1 | 605 | 611 | PF00069 | 0.564 |
MOD_CK1_1 | 669 | 675 | PF00069 | 0.543 |
MOD_CK1_1 | 685 | 691 | PF00069 | 0.491 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.341 |
MOD_CK2_1 | 325 | 331 | PF00069 | 0.500 |
MOD_CK2_1 | 365 | 371 | PF00069 | 0.496 |
MOD_CK2_1 | 559 | 565 | PF00069 | 0.718 |
MOD_CK2_1 | 590 | 596 | PF00069 | 0.447 |
MOD_CK2_1 | 685 | 691 | PF00069 | 0.589 |
MOD_Cter_Amidation | 143 | 146 | PF01082 | 0.421 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.722 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.498 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.578 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.510 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.432 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.372 |
MOD_GlcNHglycan | 507 | 510 | PF01048 | 0.497 |
MOD_GlcNHglycan | 607 | 610 | PF01048 | 0.541 |
MOD_GlcNHglycan | 667 | 671 | PF01048 | 0.610 |
MOD_GlcNHglycan | 673 | 676 | PF01048 | 0.535 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.524 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.633 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.691 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.624 |
MOD_GSK3_1 | 627 | 634 | PF00069 | 0.475 |
MOD_GSK3_1 | 713 | 720 | PF00069 | 0.523 |
MOD_GSK3_1 | 746 | 753 | PF00069 | 0.494 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.412 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.474 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.448 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.449 |
MOD_NEK2_1 | 307 | 312 | PF00069 | 0.347 |
MOD_NEK2_1 | 425 | 430 | PF00069 | 0.436 |
MOD_NEK2_1 | 457 | 462 | PF00069 | 0.351 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.306 |
MOD_NEK2_1 | 514 | 519 | PF00069 | 0.433 |
MOD_NEK2_1 | 588 | 593 | PF00069 | 0.399 |
MOD_NEK2_1 | 671 | 676 | PF00069 | 0.546 |
MOD_NEK2_1 | 87 | 92 | PF00069 | 0.282 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.304 |
MOD_PIKK_1 | 264 | 270 | PF00454 | 0.582 |
MOD_PIKK_1 | 682 | 688 | PF00454 | 0.589 |
MOD_PKA_1 | 365 | 371 | PF00069 | 0.393 |
MOD_PKA_2 | 242 | 248 | PF00069 | 0.405 |
MOD_PKA_2 | 338 | 344 | PF00069 | 0.482 |
MOD_PKA_2 | 365 | 371 | PF00069 | 0.393 |
MOD_PKA_2 | 732 | 738 | PF00069 | 0.359 |
MOD_PKB_1 | 337 | 345 | PF00069 | 0.488 |
MOD_Plk_1 | 707 | 713 | PF00069 | 0.666 |
MOD_Plk_4 | 205 | 211 | PF00069 | 0.353 |
MOD_Plk_4 | 220 | 226 | PF00069 | 0.374 |
MOD_Plk_4 | 307 | 313 | PF00069 | 0.477 |
MOD_Plk_4 | 341 | 347 | PF00069 | 0.560 |
MOD_Plk_4 | 355 | 361 | PF00069 | 0.511 |
MOD_Plk_4 | 515 | 521 | PF00069 | 0.481 |
MOD_Plk_4 | 57 | 63 | PF00069 | 0.362 |
MOD_Plk_4 | 574 | 580 | PF00069 | 0.435 |
MOD_Plk_4 | 590 | 596 | PF00069 | 0.400 |
MOD_Plk_4 | 67 | 73 | PF00069 | 0.298 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.355 |
MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.681 |
MOD_ProDKin_1 | 202 | 208 | PF00069 | 0.385 |
MOD_ProDKin_1 | 217 | 223 | PF00069 | 0.381 |
MOD_ProDKin_1 | 418 | 424 | PF00069 | 0.445 |
MOD_ProDKin_1 | 440 | 446 | PF00069 | 0.400 |
MOD_ProDKin_1 | 92 | 98 | PF00069 | 0.417 |
MOD_SUMO_rev_2 | 331 | 336 | PF00179 | 0.510 |
TRG_DiLeu_BaEn_1 | 679 | 684 | PF01217 | 0.433 |
TRG_DiLeu_BaEn_1 | 761 | 766 | PF01217 | 0.318 |
TRG_DiLeu_BaLyEn_6 | 582 | 587 | PF01217 | 0.488 |
TRG_ENDOCYTIC_2 | 173 | 176 | PF00928 | 0.559 |
TRG_ENDOCYTIC_2 | 216 | 219 | PF00928 | 0.478 |
TRG_ENDOCYTIC_2 | 314 | 317 | PF00928 | 0.313 |
TRG_ENDOCYTIC_2 | 353 | 356 | PF00928 | 0.349 |
TRG_ENDOCYTIC_2 | 521 | 524 | PF00928 | 0.345 |
TRG_ER_diArg_1 | 145 | 147 | PF00400 | 0.440 |
TRG_ER_diArg_1 | 322 | 324 | PF00400 | 0.439 |
TRG_ER_diArg_1 | 364 | 366 | PF00400 | 0.423 |
TRG_ER_diArg_1 | 618 | 621 | PF00400 | 0.487 |
TRG_ER_diArg_1 | 767 | 770 | PF00400 | 0.310 |
TRG_Pf-PMV_PEXEL_1 | 522 | 526 | PF00026 | 0.411 |
TRG_Pf-PMV_PEXEL_1 | 721 | 726 | PF00026 | 0.349 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5J2 | Leptomonas seymouri | 50% | 100% |
A0A1X0NR91 | Trypanosomatidae | 24% | 100% |
A0A3R7MGL1 | Trypanosoma rangeli | 27% | 100% |
A0A3S7X724 | Leishmania donovani | 83% | 99% |
A4HLX6 | Leishmania braziliensis | 73% | 99% |
A4I9A5 | Leishmania infantum | 83% | 99% |
C9ZJC1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 100% |
Q4Q3S1 | Leishmania major | 84% | 100% |
V5AV29 | Trypanosoma cruzi | 29% | 100% |