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: 3 |
NetGPI | no | yes: 0, no: 3 |
Related structures:
AlphaFold database: E9AXB1
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0016567 | protein ubiquitination | 7 | 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: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 | 1 |
GO:0004842 | ubiquitin-protein transferase activity | 4 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 1 |
GO:0061630 | ubiquitin protein ligase activity | 5 | 1 |
GO:0061659 | ubiquitin-like protein ligase activity | 4 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 349 | 353 | PF00656 | 0.646 |
CLV_NRD_NRD_1 | 259 | 261 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 389 | 391 | PF00675 | 0.607 |
CLV_NRD_NRD_1 | 466 | 468 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 479 | 481 | PF00675 | 0.605 |
CLV_NRD_NRD_1 | 61 | 63 | PF00675 | 0.334 |
CLV_PCSK_KEX2_1 | 381 | 383 | PF00082 | 0.722 |
CLV_PCSK_KEX2_1 | 466 | 468 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 479 | 481 | PF00082 | 0.605 |
CLV_PCSK_KEX2_1 | 61 | 63 | PF00082 | 0.334 |
CLV_PCSK_PC1ET2_1 | 381 | 383 | PF00082 | 0.727 |
CLV_PCSK_PC7_1 | 462 | 468 | PF00082 | 0.349 |
CLV_PCSK_PC7_1 | 57 | 63 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 187 | 191 | PF00082 | 0.279 |
CLV_PCSK_SKI1_1 | 61 | 65 | PF00082 | 0.330 |
CLV_PCSK_SKI1_1 | 630 | 634 | PF00082 | 0.282 |
CLV_Separin_Metazoa | 54 | 58 | PF03568 | 0.340 |
DEG_APCC_DBOX_1 | 60 | 68 | PF00400 | 0.336 |
DEG_SPOP_SBC_1 | 490 | 494 | PF00917 | 0.521 |
DOC_ANK_TNKS_1 | 450 | 457 | PF00023 | 0.341 |
DOC_CDC14_PxL_1 | 148 | 156 | PF14671 | 0.549 |
DOC_CYCLIN_RxL_1 | 184 | 194 | PF00134 | 0.274 |
DOC_CYCLIN_yCln2_LP_2 | 202 | 208 | PF00134 | 0.345 |
DOC_MAPK_gen_1 | 466 | 473 | PF00069 | 0.574 |
DOC_MAPK_gen_1 | 61 | 67 | PF00069 | 0.332 |
DOC_MAPK_MEF2A_6 | 596 | 605 | PF00069 | 0.452 |
DOC_PP1_RVXF_1 | 185 | 192 | PF00149 | 0.269 |
DOC_PP1_RVXF_1 | 227 | 233 | PF00149 | 0.426 |
DOC_PP1_RVXF_1 | 425 | 432 | PF00149 | 0.346 |
DOC_PP2B_LxvP_1 | 116 | 119 | PF13499 | 0.305 |
DOC_PP2B_LxvP_1 | 206 | 209 | PF13499 | 0.341 |
DOC_USP7_MATH_1 | 212 | 216 | PF00917 | 0.313 |
DOC_USP7_MATH_1 | 338 | 342 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 436 | 440 | PF00917 | 0.329 |
DOC_USP7_MATH_1 | 495 | 499 | PF00917 | 0.681 |
DOC_USP7_MATH_1 | 586 | 590 | PF00917 | 0.477 |
DOC_USP7_UBL2_3 | 146 | 150 | PF12436 | 0.548 |
DOC_WW_Pin1_4 | 491 | 496 | PF00397 | 0.612 |
LIG_14-3-3_CanoR_1 | 105 | 113 | PF00244 | 0.353 |
LIG_14-3-3_CanoR_1 | 187 | 192 | PF00244 | 0.391 |
LIG_14-3-3_CanoR_1 | 19 | 27 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 260 | 264 | PF00244 | 0.499 |
LIG_14-3-3_CanoR_1 | 312 | 317 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 406 | 415 | PF00244 | 0.606 |
LIG_14-3-3_CanoR_1 | 466 | 473 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 479 | 486 | PF00244 | 0.757 |
LIG_14-3-3_CanoR_1 | 489 | 495 | PF00244 | 0.714 |
LIG_14-3-3_CanoR_1 | 57 | 65 | PF00244 | 0.310 |
LIG_14-3-3_CanoR_1 | 580 | 588 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 590 | 598 | PF00244 | 0.356 |
LIG_14-3-3_CanoR_1 | 78 | 84 | PF00244 | 0.437 |
LIG_BRCT_BRCA1_1 | 144 | 148 | PF00533 | 0.372 |
LIG_BRCT_BRCA1_1 | 261 | 265 | PF00533 | 0.507 |
LIG_BRCT_BRCA1_1 | 409 | 413 | PF00533 | 0.514 |
LIG_BRCT_BRCA1_2 | 144 | 150 | PF00533 | 0.380 |
LIG_Clathr_ClatBox_1 | 64 | 68 | PF01394 | 0.342 |
LIG_deltaCOP1_diTrp_1 | 75 | 83 | PF00928 | 0.361 |
LIG_FHA_1 | 113 | 119 | PF00498 | 0.445 |
LIG_FHA_1 | 220 | 226 | PF00498 | 0.339 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.387 |
LIG_FHA_1 | 403 | 409 | PF00498 | 0.535 |
LIG_FHA_1 | 416 | 422 | PF00498 | 0.326 |
LIG_FHA_1 | 491 | 497 | PF00498 | 0.598 |
LIG_FHA_1 | 530 | 536 | PF00498 | 0.579 |
LIG_FHA_1 | 580 | 586 | PF00498 | 0.452 |
LIG_FHA_1 | 79 | 85 | PF00498 | 0.339 |
LIG_FHA_2 | 569 | 575 | PF00498 | 0.346 |
LIG_FHA_2 | 604 | 610 | PF00498 | 0.476 |
LIG_LIR_Gen_1 | 320 | 330 | PF02991 | 0.654 |
LIG_LIR_Gen_1 | 355 | 361 | PF02991 | 0.493 |
LIG_LIR_Gen_1 | 50 | 60 | PF02991 | 0.349 |
LIG_LIR_Gen_1 | 79 | 88 | PF02991 | 0.375 |
LIG_LIR_Gen_1 | 98 | 107 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 145 | 151 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 320 | 326 | PF02991 | 0.702 |
LIG_LIR_Nem_3 | 355 | 359 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 50 | 55 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 609 | 615 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 75 | 80 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 98 | 102 | PF02991 | 0.360 |
LIG_MYND_1 | 152 | 156 | PF01753 | 0.381 |
LIG_MYND_1 | 515 | 519 | PF01753 | 0.653 |
LIG_MYND_3 | 151 | 155 | PF01753 | 0.507 |
LIG_MYND_3 | 157 | 161 | PF01753 | 0.440 |
LIG_Pex14_2 | 292 | 296 | PF04695 | 0.448 |
LIG_Pex14_2 | 413 | 417 | PF04695 | 0.423 |
LIG_REV1ctd_RIR_1 | 272 | 282 | PF16727 | 0.258 |
LIG_SH2_CRK | 356 | 360 | PF00017 | 0.493 |
LIG_SH2_GRB2like | 237 | 240 | PF00017 | 0.540 |
LIG_SH2_NCK_1 | 356 | 360 | PF00017 | 0.493 |
LIG_SH2_PTP2 | 52 | 55 | PF00017 | 0.345 |
LIG_SH2_SRC | 52 | 55 | PF00017 | 0.345 |
LIG_SH2_STAP1 | 162 | 166 | PF00017 | 0.328 |
LIG_SH2_STAP1 | 80 | 84 | PF00017 | 0.333 |
LIG_SH2_STAT3 | 276 | 279 | PF00017 | 0.331 |
LIG_SH2_STAT3 | 644 | 647 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 124 | 127 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 213 | 216 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 361 | 364 | PF00017 | 0.651 |
LIG_SH2_STAT5 | 52 | 55 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 58 | 61 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 80 | 83 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 99 | 102 | PF00017 | 0.353 |
LIG_SH3_1 | 381 | 387 | PF00018 | 0.667 |
LIG_SH3_1 | 509 | 515 | PF00018 | 0.654 |
LIG_SH3_3 | 381 | 387 | PF00018 | 0.548 |
LIG_SH3_3 | 397 | 403 | PF00018 | 0.596 |
LIG_SH3_3 | 509 | 515 | PF00018 | 0.654 |
LIG_SH3_3 | 645 | 651 | PF00018 | 0.381 |
LIG_SH3_4 | 146 | 153 | PF00018 | 0.546 |
LIG_SUMO_SIM_anti_2 | 177 | 183 | PF11976 | 0.277 |
LIG_SUMO_SIM_par_1 | 177 | 183 | PF11976 | 0.277 |
LIG_SUMO_SIM_par_1 | 526 | 534 | PF11976 | 0.592 |
LIG_TRAF2_1 | 606 | 609 | PF00917 | 0.462 |
LIG_TYR_ITIM | 354 | 359 | PF00017 | 0.493 |
LIG_WRC_WIRS_1 | 414 | 419 | PF05994 | 0.416 |
LIG_WRC_WIRS_1 | 80 | 85 | PF05994 | 0.419 |
MOD_CDK_SPxK_1 | 491 | 497 | PF00069 | 0.521 |
MOD_CK1_1 | 219 | 225 | PF00069 | 0.340 |
MOD_CK1_1 | 259 | 265 | PF00069 | 0.562 |
MOD_CK1_1 | 317 | 323 | PF00069 | 0.465 |
MOD_CK1_1 | 332 | 338 | PF00069 | 0.579 |
MOD_CK1_1 | 365 | 371 | PF00069 | 0.545 |
MOD_CK1_1 | 499 | 505 | PF00069 | 0.635 |
MOD_CK1_1 | 589 | 595 | PF00069 | 0.313 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.583 |
MOD_CK2_1 | 177 | 183 | PF00069 | 0.436 |
MOD_CK2_1 | 431 | 437 | PF00069 | 0.305 |
MOD_CK2_1 | 603 | 609 | PF00069 | 0.487 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.380 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.471 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.466 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.509 |
MOD_GlcNHglycan | 392 | 395 | PF01048 | 0.556 |
MOD_GlcNHglycan | 409 | 412 | PF01048 | 0.505 |
MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.705 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.658 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.562 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.359 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.417 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.564 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.550 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.613 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.634 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.567 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.643 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.422 |
MOD_GSK3_1 | 454 | 461 | PF00069 | 0.424 |
MOD_GSK3_1 | 491 | 498 | PF00069 | 0.674 |
MOD_GSK3_1 | 653 | 660 | PF00069 | 0.480 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.415 |
MOD_N-GLC_1 | 352 | 357 | PF02516 | 0.594 |
MOD_N-GLC_1 | 394 | 399 | PF02516 | 0.672 |
MOD_N-GLC_1 | 630 | 635 | PF02516 | 0.250 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.353 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.373 |
MOD_NEK2_1 | 191 | 196 | PF00069 | 0.562 |
MOD_NEK2_1 | 27 | 32 | PF00069 | 0.485 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.462 |
MOD_NEK2_1 | 326 | 331 | PF00069 | 0.662 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.412 |
MOD_NEK2_1 | 413 | 418 | PF00069 | 0.357 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.330 |
MOD_PIKK_1 | 130 | 136 | PF00454 | 0.470 |
MOD_PIKK_1 | 244 | 250 | PF00454 | 0.430 |
MOD_PIKK_1 | 332 | 338 | PF00454 | 0.590 |
MOD_PIKK_1 | 466 | 472 | PF00454 | 0.563 |
MOD_PIKK_1 | 653 | 659 | PF00454 | 0.603 |
MOD_PK_1 | 312 | 318 | PF00069 | 0.580 |
MOD_PKA_1 | 390 | 396 | PF00069 | 0.524 |
MOD_PKA_1 | 466 | 472 | PF00069 | 0.563 |
MOD_PKA_2 | 259 | 265 | PF00069 | 0.445 |
MOD_PKA_2 | 466 | 472 | PF00069 | 0.530 |
MOD_PKA_2 | 478 | 484 | PF00069 | 0.748 |
MOD_PKA_2 | 56 | 62 | PF00069 | 0.267 |
MOD_PKA_2 | 579 | 585 | PF00069 | 0.451 |
MOD_PKA_2 | 589 | 595 | PF00069 | 0.334 |
MOD_PKB_1 | 310 | 318 | PF00069 | 0.472 |
MOD_Plk_1 | 14 | 20 | PF00069 | 0.484 |
MOD_Plk_1 | 318 | 324 | PF00069 | 0.639 |
MOD_Plk_1 | 352 | 358 | PF00069 | 0.540 |
MOD_Plk_1 | 436 | 442 | PF00069 | 0.541 |
MOD_Plk_1 | 630 | 636 | PF00069 | 0.331 |
MOD_Plk_2-3 | 177 | 183 | PF00069 | 0.436 |
MOD_Plk_4 | 338 | 344 | PF00069 | 0.507 |
MOD_Plk_4 | 513 | 519 | PF00069 | 0.538 |
MOD_Plk_4 | 79 | 85 | PF00069 | 0.489 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.262 |
MOD_ProDKin_1 | 491 | 497 | PF00069 | 0.614 |
MOD_SUMO_for_1 | 65 | 68 | PF00179 | 0.347 |
TRG_DiLeu_BaLyEn_6 | 116 | 121 | PF01217 | 0.469 |
TRG_ENDOCYTIC_2 | 356 | 359 | PF00928 | 0.494 |
TRG_ENDOCYTIC_2 | 52 | 55 | PF00928 | 0.345 |
TRG_ENDOCYTIC_2 | 80 | 83 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 99 | 102 | PF00928 | 0.353 |
TRG_ER_diArg_1 | 309 | 312 | PF00400 | 0.408 |
TRG_ER_diArg_1 | 459 | 462 | PF00400 | 0.478 |
TRG_ER_diArg_1 | 465 | 467 | PF00400 | 0.444 |
TRG_ER_diArg_1 | 61 | 63 | PF00400 | 0.334 |
TRG_Pf-PMV_PEXEL_1 | 31 | 35 | PF00026 | 0.324 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0D4 | Leptomonas seymouri | 50% | 93% |
Q4QA61 | Leishmania major | 83% | 100% |