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:0016020 | membrane | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: E9B2Q8
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0019538 | protein metabolic process | 3 | 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:0070646 | protein modification by small protein removal | 5 | 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 | 12 |
GO:0008233 | peptidase activity | 3 | 12 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 283 | 287 | PF00656 | 0.257 |
CLV_C14_Caspase3-7 | 395 | 399 | PF00656 | 0.379 |
CLV_NRD_NRD_1 | 117 | 119 | PF00675 | 0.633 |
CLV_NRD_NRD_1 | 43 | 45 | PF00675 | 0.757 |
CLV_NRD_NRD_1 | 537 | 539 | PF00675 | 0.373 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.590 |
CLV_PCSK_KEX2_1 | 174 | 176 | PF00082 | 0.457 |
CLV_PCSK_KEX2_1 | 359 | 361 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 374 | 376 | PF00082 | 0.628 |
CLV_PCSK_KEX2_1 | 537 | 539 | PF00082 | 0.408 |
CLV_PCSK_KEX2_1 | 57 | 59 | PF00082 | 0.680 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.604 |
CLV_PCSK_PC1ET2_1 | 174 | 176 | PF00082 | 0.457 |
CLV_PCSK_PC1ET2_1 | 359 | 361 | PF00082 | 0.578 |
CLV_PCSK_PC1ET2_1 | 374 | 376 | PF00082 | 0.536 |
CLV_PCSK_PC1ET2_1 | 57 | 59 | PF00082 | 0.637 |
CLV_PCSK_SKI1_1 | 111 | 115 | PF00082 | 0.559 |
CLV_PCSK_SKI1_1 | 268 | 272 | PF00082 | 0.544 |
CLV_PCSK_SKI1_1 | 360 | 364 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 403 | 407 | PF00082 | 0.534 |
CLV_PCSK_SKI1_1 | 538 | 542 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 551 | 555 | PF00082 | 0.293 |
CLV_PCSK_SKI1_1 | 588 | 592 | PF00082 | 0.263 |
CLV_PCSK_SKI1_1 | 9 | 13 | PF00082 | 0.670 |
CLV_Separin_Metazoa | 471 | 475 | PF03568 | 0.171 |
DEG_APCC_DBOX_1 | 468 | 476 | PF00400 | 0.319 |
DEG_ODPH_VHL_1 | 400 | 411 | PF01847 | 0.247 |
DOC_ANK_TNKS_1 | 462 | 469 | PF00023 | 0.386 |
DOC_CYCLIN_RxL_1 | 115 | 123 | PF00134 | 0.351 |
DOC_CYCLIN_RxL_1 | 265 | 273 | PF00134 | 0.252 |
DOC_CYCLIN_RxL_1 | 356 | 366 | PF00134 | 0.358 |
DOC_CYCLIN_RxL_1 | 400 | 410 | PF00134 | 0.249 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 68 | 74 | PF00134 | 0.386 |
DOC_MAPK_gen_1 | 174 | 185 | PF00069 | 0.221 |
DOC_MAPK_gen_1 | 359 | 365 | PF00069 | 0.338 |
DOC_MAPK_gen_1 | 493 | 501 | PF00069 | 0.334 |
DOC_MAPK_JIP1_4 | 379 | 385 | PF00069 | 0.382 |
DOC_MAPK_MEF2A_6 | 178 | 185 | PF00069 | 0.162 |
DOC_MAPK_MEF2A_6 | 68 | 76 | PF00069 | 0.385 |
DOC_MAPK_RevD_3 | 524 | 538 | PF00069 | 0.371 |
DOC_PP1_RVXF_1 | 401 | 407 | PF00149 | 0.254 |
DOC_PP2B_LxvP_1 | 128 | 131 | PF13499 | 0.543 |
DOC_PP2B_LxvP_1 | 183 | 186 | PF13499 | 0.257 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 293 | 297 | PF00917 | 0.366 |
DOC_USP7_MATH_1 | 497 | 501 | PF00917 | 0.298 |
DOC_USP7_MATH_1 | 569 | 573 | PF00917 | 0.576 |
DOC_USP7_MATH_1 | 90 | 94 | PF00917 | 0.555 |
DOC_USP7_UBL2_3 | 174 | 178 | PF12436 | 0.234 |
DOC_USP7_UBL2_3 | 370 | 374 | PF12436 | 0.305 |
DOC_WW_Pin1_4 | 363 | 368 | PF00397 | 0.341 |
DOC_WW_Pin1_4 | 416 | 421 | PF00397 | 0.319 |
LIG_14-3-3_CanoR_1 | 317 | 322 | PF00244 | 0.354 |
LIG_14-3-3_CanoR_1 | 44 | 51 | PF00244 | 0.541 |
LIG_14-3-3_CanoR_1 | 551 | 556 | PF00244 | 0.584 |
LIG_14-3-3_CanoR_1 | 561 | 569 | PF00244 | 0.563 |
LIG_14-3-3_CanoR_1 | 75 | 82 | PF00244 | 0.560 |
LIG_Actin_WH2_2 | 458 | 476 | PF00022 | 0.320 |
LIG_Actin_WH2_2 | 536 | 553 | PF00022 | 0.469 |
LIG_APCC_ABBA_1 | 198 | 203 | PF00400 | 0.339 |
LIG_BRCT_BRCA1_1 | 232 | 236 | PF00533 | 0.257 |
LIG_BRCT_BRCA1_1 | 595 | 599 | PF00533 | 0.619 |
LIG_Clathr_ClatBox_1 | 180 | 184 | PF01394 | 0.339 |
LIG_eIF4E_1 | 356 | 362 | PF01652 | 0.201 |
LIG_FHA_1 | 2 | 8 | PF00498 | 0.484 |
LIG_FHA_1 | 220 | 226 | PF00498 | 0.281 |
LIG_FHA_1 | 343 | 349 | PF00498 | 0.361 |
LIG_FHA_1 | 395 | 401 | PF00498 | 0.388 |
LIG_FHA_1 | 411 | 417 | PF00498 | 0.318 |
LIG_FHA_1 | 529 | 535 | PF00498 | 0.390 |
LIG_FHA_1 | 552 | 558 | PF00498 | 0.481 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.558 |
LIG_FHA_2 | 153 | 159 | PF00498 | 0.354 |
LIG_FHA_2 | 587 | 593 | PF00498 | 0.436 |
LIG_FHA_2 | 622 | 628 | PF00498 | 0.569 |
LIG_FHA_2 | 75 | 81 | PF00498 | 0.593 |
LIG_GBD_Chelix_1 | 357 | 365 | PF00786 | 0.521 |
LIG_GBD_Chelix_1 | 552 | 560 | PF00786 | 0.323 |
LIG_LIR_Gen_1 | 496 | 506 | PF02991 | 0.290 |
LIG_LIR_Gen_1 | 570 | 581 | PF02991 | 0.561 |
LIG_LIR_Nem_3 | 222 | 227 | PF02991 | 0.289 |
LIG_LIR_Nem_3 | 233 | 239 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 251 | 255 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 423 | 427 | PF02991 | 0.314 |
LIG_LIR_Nem_3 | 460 | 464 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 496 | 501 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 570 | 576 | PF02991 | 0.609 |
LIG_MLH1_MIPbox_1 | 232 | 236 | PF16413 | 0.257 |
LIG_MYND_1 | 462 | 466 | PF01753 | 0.369 |
LIG_NRBOX | 551 | 557 | PF00104 | 0.510 |
LIG_NRBOX | 617 | 623 | PF00104 | 0.519 |
LIG_PCNA_yPIPBox_3 | 567 | 581 | PF02747 | 0.483 |
LIG_Pex14_1 | 424 | 428 | PF04695 | 0.356 |
LIG_PTB_Apo_2 | 276 | 283 | PF02174 | 0.162 |
LIG_PTB_Apo_2 | 440 | 447 | PF02174 | 0.310 |
LIG_REV1ctd_RIR_1 | 233 | 241 | PF16727 | 0.291 |
LIG_SH2_CRK | 252 | 256 | PF00017 | 0.304 |
LIG_SH2_STAP1 | 548 | 552 | PF00017 | 0.565 |
LIG_SH2_STAP1 | 603 | 607 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 172 | 175 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 224 | 227 | PF00017 | 0.283 |
LIG_SH2_STAT5 | 280 | 283 | PF00017 | 0.286 |
LIG_SH2_STAT5 | 356 | 359 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 368 | 371 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 408 | 411 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 515 | 518 | PF00017 | 0.289 |
LIG_SH2_STAT5 | 593 | 596 | PF00017 | 0.563 |
LIG_SH3_3 | 22 | 28 | PF00018 | 0.544 |
LIG_SH3_3 | 349 | 355 | PF00018 | 0.231 |
LIG_SH3_3 | 592 | 598 | PF00018 | 0.504 |
LIG_SH3_3 | 84 | 90 | PF00018 | 0.579 |
LIG_Sin3_3 | 382 | 389 | PF02671 | 0.252 |
LIG_SUMO_SIM_anti_2 | 452 | 457 | PF11976 | 0.272 |
LIG_SUMO_SIM_par_1 | 361 | 366 | PF11976 | 0.368 |
LIG_TRAF2_1 | 59 | 62 | PF00917 | 0.501 |
LIG_TYR_ITSM | 220 | 227 | PF00017 | 0.205 |
LIG_UBA3_1 | 575 | 582 | PF00899 | 0.376 |
MOD_CDK_SPxxK_3 | 363 | 370 | PF00069 | 0.360 |
MOD_CK1_1 | 332 | 338 | PF00069 | 0.372 |
MOD_CK1_1 | 46 | 52 | PF00069 | 0.541 |
MOD_CK1_1 | 509 | 515 | PF00069 | 0.205 |
MOD_CK1_1 | 586 | 592 | PF00069 | 0.556 |
MOD_CK1_1 | 612 | 618 | PF00069 | 0.591 |
MOD_CK2_1 | 293 | 299 | PF00069 | 0.335 |
MOD_CK2_1 | 586 | 592 | PF00069 | 0.490 |
MOD_CK2_1 | 74 | 80 | PF00069 | 0.594 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.454 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.540 |
MOD_GlcNHglycan | 481 | 484 | PF01048 | 0.431 |
MOD_GlcNHglycan | 563 | 566 | PF01048 | 0.393 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.530 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.263 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.374 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.362 |
MOD_GSK3_1 | 445 | 452 | PF00069 | 0.375 |
MOD_GSK3_1 | 509 | 516 | PF00069 | 0.205 |
MOD_GSK3_1 | 582 | 589 | PF00069 | 0.510 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.495 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.513 |
MOD_LATS_1 | 447 | 453 | PF00433 | 0.349 |
MOD_N-GLC_1 | 273 | 278 | PF02516 | 0.418 |
MOD_N-GLC_1 | 561 | 566 | PF02516 | 0.227 |
MOD_N-GLC_1 | 586 | 591 | PF02516 | 0.395 |
MOD_N-GLC_1 | 612 | 617 | PF02516 | 0.309 |
MOD_N-GLC_2 | 608 | 610 | PF02516 | 0.223 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.583 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.249 |
MOD_NEK2_1 | 301 | 306 | PF00069 | 0.420 |
MOD_NEK2_1 | 308 | 313 | PF00069 | 0.440 |
MOD_NEK2_1 | 329 | 334 | PF00069 | 0.379 |
MOD_NEK2_1 | 479 | 484 | PF00069 | 0.202 |
MOD_NEK2_1 | 506 | 511 | PF00069 | 0.354 |
MOD_NEK2_1 | 583 | 588 | PF00069 | 0.452 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.611 |
MOD_PIKK_1 | 538 | 544 | PF00454 | 0.557 |
MOD_PIKK_1 | 57 | 63 | PF00454 | 0.479 |
MOD_PK_1 | 323 | 329 | PF00069 | 0.408 |
MOD_PK_1 | 449 | 455 | PF00069 | 0.307 |
MOD_PK_1 | 94 | 100 | PF00069 | 0.467 |
MOD_PKA_1 | 57 | 63 | PF00069 | 0.383 |
MOD_PKA_2 | 43 | 49 | PF00069 | 0.572 |
MOD_PKA_2 | 57 | 63 | PF00069 | 0.539 |
MOD_PKA_2 | 74 | 80 | PF00069 | 0.413 |
MOD_PKB_1 | 213 | 221 | PF00069 | 0.214 |
MOD_Plk_1 | 132 | 138 | PF00069 | 0.432 |
MOD_Plk_1 | 273 | 279 | PF00069 | 0.218 |
MOD_Plk_1 | 538 | 544 | PF00069 | 0.608 |
MOD_Plk_1 | 586 | 592 | PF00069 | 0.607 |
MOD_Plk_4 | 143 | 149 | PF00069 | 0.343 |
MOD_Plk_4 | 28 | 34 | PF00069 | 0.573 |
MOD_Plk_4 | 412 | 418 | PF00069 | 0.294 |
MOD_Plk_4 | 449 | 455 | PF00069 | 0.333 |
MOD_Plk_4 | 497 | 503 | PF00069 | 0.283 |
MOD_Plk_4 | 509 | 515 | PF00069 | 0.254 |
MOD_Plk_4 | 551 | 557 | PF00069 | 0.475 |
MOD_ProDKin_1 | 363 | 369 | PF00069 | 0.338 |
MOD_ProDKin_1 | 416 | 422 | PF00069 | 0.322 |
MOD_SUMO_for_1 | 289 | 292 | PF00179 | 0.291 |
MOD_SUMO_rev_2 | 60 | 70 | PF00179 | 0.428 |
TRG_DiLeu_BaEn_1 | 614 | 619 | PF01217 | 0.502 |
TRG_DiLeu_BaEn_2 | 264 | 270 | PF01217 | 0.291 |
TRG_DiLeu_BaLyEn_6 | 108 | 113 | PF01217 | 0.375 |
TRG_DiLeu_BaLyEn_6 | 460 | 465 | PF01217 | 0.366 |
TRG_ENDOCYTIC_2 | 224 | 227 | PF00928 | 0.223 |
TRG_ENDOCYTIC_2 | 252 | 255 | PF00928 | 0.280 |
TRG_ENDOCYTIC_2 | 408 | 411 | PF00928 | 0.278 |
TRG_ENDOCYTIC_2 | 603 | 606 | PF00928 | 0.507 |
TRG_ER_diArg_1 | 213 | 216 | PF00400 | 0.280 |
TRG_ER_diArg_1 | 316 | 319 | PF00400 | 0.432 |
TRG_ER_diArg_1 | 536 | 538 | PF00400 | 0.569 |
TRG_ER_diArg_1 | 560 | 563 | PF00400 | 0.536 |
TRG_Pf-PMV_PEXEL_1 | 268 | 273 | PF00026 | 0.461 |
TRG_Pf-PMV_PEXEL_1 | 319 | 324 | PF00026 | 0.617 |
TRG_Pf-PMV_PEXEL_1 | 463 | 467 | PF00026 | 0.595 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ICK7 | Leptomonas seymouri | 63% | 100% |
A0A0S4J986 | Bodo saltans | 30% | 100% |
A0A1X0NUY4 | Trypanosomatidae | 40% | 100% |
A0A3Q8IFV8 | Leishmania donovani | 85% | 100% |
A0A3R7KQA7 | Trypanosoma rangeli | 33% | 100% |
A4HKC1 | Leishmania braziliensis | 74% | 100% |
A4I7V0 | Leishmania infantum | 85% | 100% |
D0AA08 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
Q4Q5E9 | Leishmania major | 86% | 100% |
V5BQT4 | Trypanosoma cruzi | 37% | 100% |