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: 20 |
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: 7 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: E9ADT0
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004842 | ubiquitin-protein transferase activity | 4 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 12 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 278 | 282 | PF00656 | 0.424 |
CLV_C14_Caspase3-7 | 514 | 518 | PF00656 | 0.628 |
CLV_NRD_NRD_1 | 428 | 430 | PF00675 | 0.545 |
CLV_NRD_NRD_1 | 50 | 52 | PF00675 | 0.449 |
CLV_NRD_NRD_1 | 72 | 74 | PF00675 | 0.482 |
CLV_PCSK_KEX2_1 | 428 | 430 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 50 | 52 | PF00082 | 0.395 |
CLV_PCSK_KEX2_1 | 72 | 74 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 107 | 111 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 428 | 432 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 562 | 566 | PF00082 | 0.376 |
DOC_CDC14_PxL_1 | 477 | 485 | PF14671 | 0.628 |
DOC_CYCLIN_yClb1_LxF_4 | 368 | 374 | PF00134 | 0.462 |
DOC_MAPK_gen_1 | 107 | 117 | PF00069 | 0.534 |
DOC_MAPK_gen_1 | 484 | 493 | PF00069 | 0.567 |
DOC_MAPK_gen_1 | 50 | 57 | PF00069 | 0.482 |
DOC_MAPK_gen_1 | 72 | 81 | PF00069 | 0.349 |
DOC_MAPK_MEF2A_6 | 123 | 132 | PF00069 | 0.357 |
DOC_MAPK_MEF2A_6 | 209 | 218 | PF00069 | 0.337 |
DOC_PP1_RVXF_1 | 207 | 213 | PF00149 | 0.387 |
DOC_PP1_RVXF_1 | 89 | 96 | PF00149 | 0.429 |
DOC_PP4_FxxP_1 | 185 | 188 | PF00568 | 0.339 |
DOC_USP7_MATH_1 | 116 | 120 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 357 | 361 | PF00917 | 0.510 |
DOC_USP7_MATH_1 | 399 | 403 | PF00917 | 0.383 |
DOC_USP7_MATH_1 | 437 | 441 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 89 | 93 | PF00917 | 0.535 |
DOC_USP7_UBL2_3 | 205 | 209 | PF12436 | 0.453 |
DOC_USP7_UBL2_3 | 260 | 264 | PF12436 | 0.448 |
DOC_WW_Pin1_4 | 532 | 537 | PF00397 | 0.320 |
DOC_WW_Pin1_4 | 567 | 572 | PF00397 | 0.417 |
LIG_14-3-3_CanoR_1 | 123 | 131 | PF00244 | 0.370 |
LIG_14-3-3_CanoR_1 | 336 | 342 | PF00244 | 0.409 |
LIG_14-3-3_CanoR_1 | 401 | 405 | PF00244 | 0.508 |
LIG_14-3-3_CanoR_1 | 428 | 436 | PF00244 | 0.458 |
LIG_14-3-3_CanoR_1 | 475 | 483 | PF00244 | 0.726 |
LIG_14-3-3_CanoR_1 | 562 | 571 | PF00244 | 0.378 |
LIG_Actin_WH2_2 | 125 | 143 | PF00022 | 0.348 |
LIG_Actin_WH2_2 | 385 | 403 | PF00022 | 0.478 |
LIG_AP2alpha_1 | 342 | 346 | PF02296 | 0.477 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.398 |
LIG_BIR_III_4 | 378 | 382 | PF00653 | 0.405 |
LIG_BRCT_BRCA1_1 | 314 | 318 | PF00533 | 0.379 |
LIG_BRCT_BRCA1_1 | 439 | 443 | PF00533 | 0.458 |
LIG_BRCT_BRCA1_1 | 91 | 95 | PF00533 | 0.543 |
LIG_deltaCOP1_diTrp_1 | 421 | 427 | PF00928 | 0.507 |
LIG_EH1_1 | 154 | 162 | PF00400 | 0.345 |
LIG_EH1_1 | 385 | 393 | PF00400 | 0.641 |
LIG_eIF4E_1 | 386 | 392 | PF01652 | 0.567 |
LIG_EVH1_2 | 168 | 172 | PF00568 | 0.461 |
LIG_FHA_1 | 205 | 211 | PF00498 | 0.373 |
LIG_FHA_1 | 275 | 281 | PF00498 | 0.335 |
LIG_FHA_1 | 523 | 529 | PF00498 | 0.320 |
LIG_FHA_2 | 276 | 282 | PF00498 | 0.332 |
LIG_GBD_Chelix_1 | 291 | 299 | PF00786 | 0.447 |
LIG_GBD_Chelix_1 | 306 | 314 | PF00786 | 0.263 |
LIG_Integrin_RGD_1 | 39 | 41 | PF01839 | 0.359 |
LIG_LIR_Gen_1 | 23 | 31 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 340 | 350 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 440 | 451 | PF02991 | 0.356 |
LIG_LIR_Gen_1 | 75 | 84 | PF02991 | 0.418 |
LIG_LIR_Gen_1 | 92 | 101 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 317 | 323 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 340 | 345 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 421 | 427 | PF02991 | 0.562 |
LIG_LIR_Nem_3 | 440 | 446 | PF02991 | 0.237 |
LIG_LIR_Nem_3 | 75 | 80 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 92 | 98 | PF02991 | 0.303 |
LIG_MYND_1 | 481 | 485 | PF01753 | 0.693 |
LIG_NRBOX | 160 | 166 | PF00104 | 0.333 |
LIG_PDZ_Class_2 | 596 | 601 | PF00595 | 0.549 |
LIG_Pex14_1 | 423 | 427 | PF04695 | 0.450 |
LIG_Pex14_2 | 338 | 342 | PF04695 | 0.486 |
LIG_Pex14_2 | 419 | 423 | PF04695 | 0.417 |
LIG_SH2_GRB2like | 367 | 370 | PF00017 | 0.462 |
LIG_SH2_GRB2like | 60 | 63 | PF00017 | 0.347 |
LIG_SH2_PTP2 | 367 | 370 | PF00017 | 0.391 |
LIG_SH2_STAP1 | 170 | 174 | PF00017 | 0.405 |
LIG_SH2_STAP1 | 541 | 545 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 10 | 13 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 287 | 290 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 367 | 370 | PF00017 | 0.347 |
LIG_SH2_STAT5 | 60 | 63 | PF00017 | 0.362 |
LIG_SH3_2 | 482 | 487 | PF14604 | 0.586 |
LIG_SH3_3 | 381 | 387 | PF00018 | 0.546 |
LIG_SH3_3 | 461 | 467 | PF00018 | 0.574 |
LIG_SH3_3 | 479 | 485 | PF00018 | 0.714 |
LIG_SH3_3 | 530 | 536 | PF00018 | 0.305 |
LIG_SUMO_SIM_anti_2 | 125 | 132 | PF11976 | 0.330 |
LIG_SxIP_EBH_1 | 473 | 484 | PF03271 | 0.599 |
LIG_TRAF2_1 | 331 | 334 | PF00917 | 0.456 |
LIG_TYR_ITIM | 365 | 370 | PF00017 | 0.399 |
LIG_UBA3_1 | 132 | 141 | PF00899 | 0.452 |
LIG_UBA3_1 | 159 | 166 | PF00899 | 0.333 |
LIG_UBA3_1 | 255 | 260 | PF00899 | 0.499 |
LIG_WRC_WIRS_1 | 338 | 343 | PF05994 | 0.482 |
MOD_CK1_1 | 236 | 242 | PF00069 | 0.495 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.421 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.479 |
MOD_CK1_1 | 290 | 296 | PF00069 | 0.401 |
MOD_CK1_1 | 455 | 461 | PF00069 | 0.535 |
MOD_CK1_1 | 570 | 576 | PF00069 | 0.496 |
MOD_CK2_1 | 100 | 106 | PF00069 | 0.448 |
MOD_CK2_1 | 259 | 265 | PF00069 | 0.580 |
MOD_CK2_1 | 399 | 405 | PF00069 | 0.552 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.556 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.424 |
MOD_GlcNHglycan | 359 | 362 | PF01048 | 0.430 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.465 |
MOD_GlcNHglycan | 506 | 509 | PF01048 | 0.635 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.391 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.411 |
MOD_GSK3_1 | 570 | 577 | PF00069 | 0.483 |
MOD_N-GLC_1 | 248 | 253 | PF02516 | 0.536 |
MOD_N-GLC_1 | 552 | 557 | PF02516 | 0.340 |
MOD_N-GLC_1 | 82 | 87 | PF02516 | 0.509 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.405 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.373 |
MOD_NEK2_1 | 259 | 264 | PF00069 | 0.384 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.325 |
MOD_NEK2_1 | 280 | 285 | PF00069 | 0.358 |
MOD_NEK2_1 | 295 | 300 | PF00069 | 0.378 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.341 |
MOD_NEK2_1 | 346 | 351 | PF00069 | 0.380 |
MOD_NEK2_2 | 445 | 450 | PF00069 | 0.379 |
MOD_PIKK_1 | 150 | 156 | PF00454 | 0.408 |
MOD_PIKK_1 | 183 | 189 | PF00454 | 0.345 |
MOD_PIKK_1 | 264 | 270 | PF00454 | 0.373 |
MOD_PIKK_1 | 329 | 335 | PF00454 | 0.459 |
MOD_PIKK_1 | 452 | 458 | PF00454 | 0.585 |
MOD_PK_1 | 509 | 515 | PF00069 | 0.664 |
MOD_PKA_1 | 428 | 434 | PF00069 | 0.545 |
MOD_PKA_1 | 50 | 56 | PF00069 | 0.420 |
MOD_PKA_1 | 72 | 78 | PF00069 | 0.431 |
MOD_PKA_2 | 122 | 128 | PF00069 | 0.346 |
MOD_PKA_2 | 357 | 363 | PF00069 | 0.529 |
MOD_PKA_2 | 400 | 406 | PF00069 | 0.454 |
MOD_PKA_2 | 428 | 434 | PF00069 | 0.467 |
MOD_PKA_2 | 50 | 56 | PF00069 | 0.429 |
MOD_PKA_2 | 72 | 78 | PF00069 | 0.431 |
MOD_Plk_1 | 248 | 254 | PF00069 | 0.485 |
MOD_Plk_1 | 264 | 270 | PF00069 | 0.445 |
MOD_Plk_1 | 438 | 444 | PF00069 | 0.516 |
MOD_Plk_1 | 82 | 88 | PF00069 | 0.508 |
MOD_Plk_1 | 99 | 105 | PF00069 | 0.305 |
MOD_Plk_2-3 | 100 | 106 | PF00069 | 0.552 |
MOD_Plk_4 | 100 | 106 | PF00069 | 0.512 |
MOD_Plk_4 | 251 | 257 | PF00069 | 0.426 |
MOD_Plk_4 | 275 | 281 | PF00069 | 0.340 |
MOD_Plk_4 | 314 | 320 | PF00069 | 0.465 |
MOD_Plk_4 | 337 | 343 | PF00069 | 0.461 |
MOD_Plk_4 | 431 | 437 | PF00069 | 0.411 |
MOD_ProDKin_1 | 532 | 538 | PF00069 | 0.320 |
MOD_ProDKin_1 | 567 | 573 | PF00069 | 0.417 |
MOD_SUMO_for_1 | 109 | 112 | PF00179 | 0.467 |
MOD_SUMO_for_1 | 408 | 411 | PF00179 | 0.461 |
MOD_SUMO_rev_2 | 13 | 22 | PF00179 | 0.534 |
TRG_DiLeu_BaEn_2 | 207 | 213 | PF01217 | 0.412 |
TRG_DiLeu_BaLyEn_6 | 472 | 477 | PF01217 | 0.668 |
TRG_ENDOCYTIC_2 | 367 | 370 | PF00928 | 0.333 |
TRG_ENDOCYTIC_2 | 424 | 427 | PF00928 | 0.506 |
TRG_ER_diArg_1 | 427 | 429 | PF00400 | 0.523 |
TRG_ER_diArg_1 | 49 | 51 | PF00400 | 0.493 |
TRG_ER_diArg_1 | 71 | 73 | PF00400 | 0.489 |
TRG_NLS_MonoExtN_4 | 70 | 77 | PF00514 | 0.441 |
TRG_Pf-PMV_PEXEL_1 | 475 | 479 | PF00026 | 0.580 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMG8 | Leptomonas seymouri | 73% | 100% |
A0A0S4IVT7 | Bodo saltans | 48% | 98% |
A0A1X0NZM7 | Trypanosomatidae | 45% | 96% |
A0A3R7MLP4 | Trypanosoma rangeli | 45% | 99% |
A0A3S7X270 | Leishmania donovani | 97% | 100% |
A4HH85 | Leishmania braziliensis | 88% | 100% |
A4I4D1 | Leishmania infantum | 97% | 100% |
C9ZL32 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 96% |
E9AM00 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
V5DLG6 | Trypanosoma cruzi | 45% | 99% |