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: 7 |
NetGPI | no | yes: 0, no: 7 |
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: A0A3S7X724
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0032446 | protein modification by small protein conjugation | 6 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0045116 | protein neddylation | 7 | 1 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 8 |
GO:0008641 | ubiquitin-like modifier activating enzyme activity | 2 | 8 |
GO:0016874 | ligase activity | 2 | 8 |
GO:0016877 | ligase activity, forming carbon-sulfur bonds | 3 | 8 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 8 |
GO:0140657 | ATP-dependent activity | 1 | 8 |
GO:0019781 | NEDD8 activating enzyme activity | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 130 | 134 | PF00656 | 0.336 |
CLV_NRD_NRD_1 | 323 | 325 | PF00675 | 0.450 |
CLV_NRD_NRD_1 | 365 | 367 | PF00675 | 0.460 |
CLV_NRD_NRD_1 | 571 | 573 | PF00675 | 0.543 |
CLV_NRD_NRD_1 | 655 | 657 | PF00675 | 0.423 |
CLV_NRD_NRD_1 | 672 | 674 | PF00675 | 0.489 |
CLV_NRD_NRD_1 | 730 | 732 | PF00675 | 0.387 |
CLV_PCSK_KEX2_1 | 323 | 325 | PF00082 | 0.450 |
CLV_PCSK_KEX2_1 | 334 | 336 | PF00082 | 0.428 |
CLV_PCSK_KEX2_1 | 365 | 367 | PF00082 | 0.460 |
CLV_PCSK_KEX2_1 | 655 | 657 | PF00082 | 0.423 |
CLV_PCSK_KEX2_1 | 672 | 674 | PF00082 | 0.489 |
CLV_PCSK_PC1ET2_1 | 334 | 336 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 168 | 172 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 21 | 25 | PF00082 | 0.471 |
CLV_PCSK_SKI1_1 | 595 | 599 | PF00082 | 0.443 |
CLV_PCSK_SKI1_1 | 67 | 71 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 731 | 735 | PF00082 | 0.422 |
DEG_MDM2_SWIB_1 | 322 | 329 | PF02201 | 0.444 |
DOC_CYCLIN_RxL_1 | 592 | 602 | PF00134 | 0.432 |
DOC_MAPK_DCC_7 | 232 | 242 | PF00069 | 0.424 |
DOC_MAPK_gen_1 | 21 | 31 | PF00069 | 0.349 |
DOC_MAPK_MEF2A_6 | 232 | 241 | PF00069 | 0.407 |
DOC_MAPK_MEF2A_6 | 774 | 781 | PF00069 | 0.425 |
DOC_PP1_RVXF_1 | 19 | 26 | PF00149 | 0.450 |
DOC_PP1_RVXF_1 | 611 | 618 | PF00149 | 0.424 |
DOC_PP1_RVXF_1 | 634 | 640 | PF00149 | 0.432 |
DOC_PP2B_LxvP_1 | 204 | 207 | PF13499 | 0.373 |
DOC_USP7_MATH_1 | 190 | 194 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 299 | 303 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 355 | 359 | PF00917 | 0.429 |
DOC_USP7_MATH_1 | 424 | 428 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.376 |
DOC_USP7_MATH_1 | 677 | 681 | PF00917 | 0.548 |
DOC_USP7_UBL2_3 | 380 | 384 | PF12436 | 0.482 |
DOC_USP7_UBL2_3 | 482 | 486 | PF12436 | 0.781 |
DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.642 |
DOC_WW_Pin1_4 | 217 | 222 | PF00397 | 0.426 |
DOC_WW_Pin1_4 | 418 | 423 | PF00397 | 0.500 |
DOC_WW_Pin1_4 | 426 | 431 | PF00397 | 0.445 |
DOC_WW_Pin1_4 | 440 | 445 | PF00397 | 0.311 |
DOC_WW_Pin1_4 | 92 | 97 | PF00397 | 0.353 |
LIG_14-3-3_CanoR_1 | 324 | 330 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 335 | 345 | PF00244 | 0.616 |
LIG_14-3-3_CanoR_1 | 354 | 360 | PF00244 | 0.448 |
LIG_14-3-3_CanoR_1 | 411 | 417 | PF00244 | 0.341 |
LIG_14-3-3_CanoR_1 | 586 | 590 | PF00244 | 0.441 |
LIG_14-3-3_CanoR_1 | 613 | 618 | PF00244 | 0.448 |
LIG_14-3-3_CanoR_1 | 642 | 647 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 67 | 72 | PF00244 | 0.402 |
LIG_Actin_WH2_2 | 386 | 404 | PF00022 | 0.460 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.678 |
LIG_BRCT_BRCA1_1 | 342 | 346 | PF00533 | 0.588 |
LIG_BRCT_BRCA1_1 | 83 | 87 | PF00533 | 0.273 |
LIG_FHA_1 | 161 | 167 | PF00498 | 0.672 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.421 |
LIG_FHA_1 | 458 | 464 | PF00498 | 0.466 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.350 |
LIG_FHA_1 | 525 | 531 | PF00498 | 0.495 |
LIG_FHA_1 | 585 | 591 | PF00498 | 0.445 |
LIG_FHA_1 | 600 | 606 | PF00498 | 0.485 |
LIG_FHA_1 | 639 | 645 | PF00498 | 0.519 |
LIG_FHA_1 | 66 | 72 | PF00498 | 0.360 |
LIG_FHA_1 | 762 | 768 | PF00498 | 0.419 |
LIG_FHA_1 | 791 | 797 | PF00498 | 0.469 |
LIG_FHA_2 | 197 | 203 | PF00498 | 0.550 |
LIG_FHA_2 | 326 | 332 | PF00498 | 0.455 |
LIG_FHA_2 | 68 | 74 | PF00498 | 0.360 |
LIG_LIR_Gen_1 | 171 | 179 | PF02991 | 0.551 |
LIG_LIR_Nem_3 | 171 | 176 | PF02991 | 0.584 |
LIG_LIR_Nem_3 | 213 | 219 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 278 | 283 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 310 | 314 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 352 | 356 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 529 | 535 | PF02991 | 0.377 |
LIG_LYPXL_yS_3 | 314 | 317 | PF13949 | 0.378 |
LIG_MLH1_MIPbox_1 | 83 | 87 | PF16413 | 0.273 |
LIG_NRBOX | 396 | 402 | PF00104 | 0.378 |
LIG_PDZ_Class_2 | 794 | 799 | PF00595 | 0.441 |
LIG_Pex14_1 | 124 | 128 | PF04695 | 0.425 |
LIG_Pex14_1 | 136 | 140 | PF04695 | 0.476 |
LIG_Pex14_2 | 322 | 326 | PF04695 | 0.463 |
LIG_PTB_Apo_2 | 791 | 798 | PF02174 | 0.440 |
LIG_SH2_CRK | 173 | 177 | PF00017 | 0.485 |
LIG_SH2_CRK | 353 | 357 | PF00017 | 0.425 |
LIG_SH2_CRK | 514 | 518 | PF00017 | 0.458 |
LIG_SH2_GRB2like | 792 | 795 | PF00017 | 0.450 |
LIG_SH2_NCK_1 | 173 | 177 | PF00017 | 0.400 |
LIG_SH2_SRC | 140 | 143 | PF00017 | 0.642 |
LIG_SH2_STAP1 | 173 | 177 | PF00017 | 0.400 |
LIG_SH2_STAP1 | 601 | 605 | PF00017 | 0.303 |
LIG_SH2_STAP1 | 792 | 796 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 140 | 143 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 311 | 314 | PF00017 | 0.355 |
LIG_SH2_STAT5 | 521 | 524 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 601 | 604 | PF00017 | 0.276 |
LIG_SH2_STAT5 | 664 | 667 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 792 | 795 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 86 | 89 | PF00017 | 0.376 |
LIG_SH3_1 | 153 | 159 | PF00018 | 0.558 |
LIG_SH3_1 | 232 | 238 | PF00018 | 0.440 |
LIG_SH3_3 | 153 | 159 | PF00018 | 0.599 |
LIG_SH3_3 | 232 | 238 | PF00018 | 0.475 |
LIG_SH3_3 | 260 | 266 | PF00018 | 0.557 |
LIG_SH3_3 | 293 | 299 | PF00018 | 0.446 |
LIG_SH3_3 | 486 | 492 | PF00018 | 0.549 |
LIG_SH3_3 | 752 | 758 | PF00018 | 0.460 |
LIG_SUMO_SIM_anti_2 | 175 | 180 | PF11976 | 0.433 |
LIG_SUMO_SIM_anti_2 | 208 | 214 | PF11976 | 0.353 |
LIG_SUMO_SIM_anti_2 | 68 | 74 | PF11976 | 0.376 |
LIG_SUMO_SIM_par_1 | 201 | 208 | PF11976 | 0.482 |
LIG_SUMO_SIM_par_1 | 238 | 245 | PF11976 | 0.396 |
LIG_SUMO_SIM_par_1 | 50 | 56 | PF11976 | 0.376 |
LIG_SUMO_SIM_par_1 | 67 | 74 | PF11976 | 0.201 |
LIG_TRAF2_1 | 116 | 119 | PF00917 | 0.376 |
LIG_TRAF2_1 | 199 | 202 | PF00917 | 0.516 |
LIG_TRAF2_1 | 330 | 333 | PF00917 | 0.516 |
LIG_TRAF2_1 | 488 | 491 | PF00917 | 0.575 |
LIG_TRAF2_1 | 698 | 701 | PF00917 | 0.505 |
LIG_TRAF2_1 | 737 | 740 | PF00917 | 0.397 |
LIG_TRAF2_1 | 768 | 771 | PF00917 | 0.347 |
LIG_TYR_ITIM | 312 | 317 | PF00017 | 0.331 |
LIG_TYR_ITIM | 530 | 535 | PF00017 | 0.430 |
LIG_TYR_ITSM | 169 | 176 | PF00017 | 0.401 |
MOD_CDK_SPxxK_3 | 426 | 433 | PF00069 | 0.388 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.637 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.504 |
MOD_CK1_1 | 220 | 226 | PF00069 | 0.437 |
MOD_CK1_1 | 336 | 342 | PF00069 | 0.590 |
MOD_CK1_1 | 418 | 424 | PF00069 | 0.592 |
MOD_CK1_1 | 585 | 591 | PF00069 | 0.610 |
MOD_CK1_1 | 616 | 622 | PF00069 | 0.449 |
MOD_CK1_1 | 680 | 686 | PF00069 | 0.494 |
MOD_CK1_1 | 696 | 702 | PF00069 | 0.583 |
MOD_CK2_1 | 196 | 202 | PF00069 | 0.532 |
MOD_CK2_1 | 325 | 331 | PF00069 | 0.445 |
MOD_CK2_1 | 696 | 702 | PF00069 | 0.518 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.736 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.584 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.532 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.570 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.414 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.457 |
MOD_GlcNHglycan | 518 | 521 | PF01048 | 0.426 |
MOD_GlcNHglycan | 618 | 621 | PF01048 | 0.481 |
MOD_GlcNHglycan | 681 | 685 | PF01048 | 0.542 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.304 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.636 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.540 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.603 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.646 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.571 |
MOD_GSK3_1 | 638 | 645 | PF00069 | 0.492 |
MOD_GSK3_1 | 723 | 730 | PF00069 | 0.618 |
MOD_GSK3_1 | 756 | 763 | PF00069 | 0.444 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.340 |
MOD_N-GLC_1 | 179 | 184 | PF02516 | 0.576 |
MOD_N-GLC_1 | 191 | 196 | PF02516 | 0.573 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.611 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.731 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.451 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.394 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.378 |
MOD_NEK2_1 | 425 | 430 | PF00069 | 0.476 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.320 |
MOD_NEK2_1 | 525 | 530 | PF00069 | 0.436 |
MOD_NEK2_1 | 599 | 604 | PF00069 | 0.375 |
MOD_NEK2_1 | 682 | 687 | PF00069 | 0.452 |
MOD_NEK2_1 | 717 | 722 | PF00069 | 0.673 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.359 |
MOD_PIKK_1 | 264 | 270 | PF00454 | 0.533 |
MOD_PIKK_1 | 693 | 699 | PF00454 | 0.498 |
MOD_PKA_2 | 242 | 248 | PF00069 | 0.470 |
MOD_PKA_2 | 336 | 342 | PF00069 | 0.559 |
MOD_PKA_2 | 585 | 591 | PF00069 | 0.439 |
MOD_PKB_1 | 335 | 343 | PF00069 | 0.540 |
MOD_Plk_1 | 40 | 46 | PF00069 | 0.243 |
MOD_Plk_1 | 717 | 723 | PF00069 | 0.676 |
MOD_Plk_4 | 205 | 211 | PF00069 | 0.388 |
MOD_Plk_4 | 220 | 226 | PF00069 | 0.462 |
MOD_Plk_4 | 307 | 313 | PF00069 | 0.371 |
MOD_Plk_4 | 341 | 347 | PF00069 | 0.560 |
MOD_Plk_4 | 355 | 361 | PF00069 | 0.420 |
MOD_Plk_4 | 526 | 532 | PF00069 | 0.463 |
MOD_Plk_4 | 57 | 63 | PF00069 | 0.360 |
MOD_Plk_4 | 585 | 591 | PF00069 | 0.576 |
MOD_Plk_4 | 67 | 73 | PF00069 | 0.360 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.470 |
MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.639 |
MOD_ProDKin_1 | 217 | 223 | PF00069 | 0.419 |
MOD_ProDKin_1 | 418 | 424 | PF00069 | 0.496 |
MOD_ProDKin_1 | 426 | 432 | PF00069 | 0.443 |
MOD_ProDKin_1 | 440 | 446 | PF00069 | 0.303 |
MOD_ProDKin_1 | 92 | 98 | PF00069 | 0.353 |
MOD_SUMO_rev_2 | 331 | 336 | PF00179 | 0.558 |
MOD_SUMO_rev_2 | 483 | 488 | PF00179 | 0.564 |
MOD_SUMO_rev_2 | 565 | 570 | PF00179 | 0.411 |
TRG_DiLeu_BaEn_1 | 690 | 695 | PF01217 | 0.461 |
TRG_DiLeu_BaEn_1 | 771 | 776 | PF01217 | 0.343 |
TRG_DiLeu_BaEn_4 | 201 | 207 | PF01217 | 0.419 |
TRG_DiLeu_BaEn_4 | 565 | 571 | PF01217 | 0.421 |
TRG_DiLeu_BaLyEn_6 | 593 | 598 | PF01217 | 0.431 |
TRG_ENDOCYTIC_2 | 173 | 176 | PF00928 | 0.521 |
TRG_ENDOCYTIC_2 | 216 | 219 | PF00928 | 0.440 |
TRG_ENDOCYTIC_2 | 314 | 317 | PF00928 | 0.330 |
TRG_ENDOCYTIC_2 | 353 | 356 | PF00928 | 0.368 |
TRG_ENDOCYTIC_2 | 532 | 535 | PF00928 | 0.430 |
TRG_ENDOCYTIC_2 | 601 | 604 | PF00928 | 0.276 |
TRG_ER_diArg_1 | 322 | 324 | PF00400 | 0.445 |
TRG_ER_diArg_1 | 364 | 366 | PF00400 | 0.426 |
TRG_ER_diArg_1 | 629 | 632 | PF00400 | 0.430 |
TRG_Pf-PMV_PEXEL_1 | 533 | 537 | PF00026 | 0.443 |
TRG_Pf-PMV_PEXEL_1 | 731 | 736 | PF00026 | 0.377 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5J2 | Leptomonas seymouri | 51% | 100% |
A0A0S4JRQ2 | Bodo saltans | 23% | 97% |
A4HLX6 | Leishmania braziliensis | 71% | 98% |
A4I9A5 | Leishmania infantum | 100% | 100% |
E9B4A5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 99% |
Q4Q3S1 | Leishmania major | 85% | 98% |