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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 10 |
GO:0042995 | cell projection | 2 | 10 |
GO:0043226 | organelle | 2 | 10 |
GO:0043227 | membrane-bounded organelle | 3 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 10 |
GO:0000151 | ubiquitin ligase complex | 3 | 1 |
GO:0019005 | SCF ubiquitin ligase complex | 5 | 1 |
GO:0031461 | cullin-RING ubiquitin ligase complex | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0140535 | intracellular protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1990234 | transferase complex | 3 | 1 |
Related structures:
AlphaFold database: A0A3Q8IAE2
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 1 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009057 | macromolecule catabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010498 | proteasomal protein catabolic process | 5 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 1 |
GO:0030163 | protein catabolic process | 4 | 1 |
GO:0031146 | SCF-dependent proteasomal ubiquitin-dependent protein catabolic process | 7 | 1 |
GO:0043161 | proteasome-mediated ubiquitin-dependent protein catabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 1 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
GO:0006950 | response to stress | 2 | 1 |
GO:0006952 | defense response | 3 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 4 |
GO:0016787 | hydrolase activity | 2 | 4 |
GO:0005488 | binding | 1 | 1 |
GO:0043167 | ion binding | 2 | 1 |
GO:0043169 | cation binding | 3 | 1 |
GO:0046872 | metal ion binding | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 307 | 311 | PF00656 | 0.511 |
CLV_C14_Caspase3-7 | 55 | 59 | PF00656 | 0.521 |
CLV_NRD_NRD_1 | 227 | 229 | PF00675 | 0.528 |
CLV_NRD_NRD_1 | 359 | 361 | PF00675 | 0.288 |
CLV_PCSK_KEX2_1 | 227 | 229 | PF00082 | 0.532 |
CLV_PCSK_KEX2_1 | 359 | 361 | PF00082 | 0.288 |
CLV_PCSK_SKI1_1 | 227 | 231 | PF00082 | 0.467 |
CLV_PCSK_SKI1_1 | 379 | 383 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 449 | 453 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 72 | 76 | PF00082 | 0.434 |
CLV_Separin_Metazoa | 546 | 550 | PF03568 | 0.291 |
DEG_APCC_DBOX_1 | 359 | 367 | PF00400 | 0.267 |
DEG_APCC_KENBOX_2 | 139 | 143 | PF00400 | 0.329 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.528 |
DEG_SCF_FBW7_1 | 20 | 26 | PF00400 | 0.485 |
DOC_ANK_TNKS_1 | 60 | 67 | PF00023 | 0.448 |
DOC_CDC14_PxL_1 | 516 | 524 | PF14671 | 0.483 |
DOC_CKS1_1 | 20 | 25 | PF01111 | 0.491 |
DOC_CYCLIN_RxL_1 | 275 | 284 | PF00134 | 0.339 |
DOC_CYCLIN_RxL_1 | 379 | 392 | PF00134 | 0.270 |
DOC_CYCLIN_RxL_1 | 520 | 531 | PF00134 | 0.415 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 406 | 415 | PF00134 | 0.270 |
DOC_MAPK_gen_1 | 138 | 146 | PF00069 | 0.378 |
DOC_MAPK_gen_1 | 227 | 237 | PF00069 | 0.343 |
DOC_MAPK_gen_1 | 356 | 366 | PF00069 | 0.296 |
DOC_MAPK_gen_1 | 379 | 389 | PF00069 | 0.427 |
DOC_MAPK_gen_1 | 446 | 456 | PF00069 | 0.314 |
DOC_MAPK_MEF2A_6 | 132 | 139 | PF00069 | 0.351 |
DOC_MAPK_MEF2A_6 | 169 | 176 | PF00069 | 0.381 |
DOC_MAPK_MEF2A_6 | 227 | 236 | PF00069 | 0.383 |
DOC_MAPK_MEF2A_6 | 540 | 547 | PF00069 | 0.380 |
DOC_MAPK_NFAT4_5 | 227 | 235 | PF00069 | 0.350 |
DOC_MIT_MIM_1 | 224 | 232 | PF04212 | 0.354 |
DOC_PP2B_LxvP_1 | 198 | 201 | PF13499 | 0.429 |
DOC_PP2B_LxvP_1 | 586 | 589 | PF13499 | 0.457 |
DOC_PP4_FxxP_1 | 322 | 325 | PF00568 | 0.347 |
DOC_USP7_MATH_1 | 153 | 157 | PF00917 | 0.464 |
DOC_USP7_MATH_1 | 315 | 319 | PF00917 | 0.366 |
DOC_USP7_MATH_1 | 377 | 381 | PF00917 | 0.336 |
DOC_USP7_MATH_1 | 521 | 525 | PF00917 | 0.397 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 622 | 626 | PF00917 | 0.521 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.506 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.515 |
DOC_WW_Pin1_4 | 333 | 338 | PF00397 | 0.360 |
DOC_WW_Pin1_4 | 39 | 44 | PF00397 | 0.481 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.479 |
DOC_WW_Pin1_4 | 508 | 513 | PF00397 | 0.420 |
DOC_WW_Pin1_4 | 579 | 584 | PF00397 | 0.485 |
LIG_14-3-3_CanoR_1 | 169 | 175 | PF00244 | 0.408 |
LIG_14-3-3_CanoR_1 | 257 | 261 | PF00244 | 0.361 |
LIG_14-3-3_CanoR_1 | 287 | 293 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 317 | 322 | PF00244 | 0.508 |
LIG_14-3-3_CanoR_1 | 348 | 353 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 416 | 421 | PF00244 | 0.386 |
LIG_14-3-3_CanoR_1 | 6 | 10 | PF00244 | 0.511 |
LIG_Actin_WH2_2 | 438 | 454 | PF00022 | 0.382 |
LIG_Actin_WH2_2 | 555 | 571 | PF00022 | 0.472 |
LIG_BIR_III_2 | 149 | 153 | PF00653 | 0.402 |
LIG_BIR_III_2 | 272 | 276 | PF00653 | 0.356 |
LIG_BIR_III_2 | 518 | 522 | PF00653 | 0.410 |
LIG_BRCT_BRCA1_1 | 23 | 27 | PF00533 | 0.526 |
LIG_DLG_GKlike_1 | 348 | 355 | PF00625 | 0.328 |
LIG_DLG_GKlike_1 | 416 | 423 | PF00625 | 0.270 |
LIG_FHA_1 | 109 | 115 | PF00498 | 0.447 |
LIG_FHA_1 | 171 | 177 | PF00498 | 0.494 |
LIG_FHA_1 | 266 | 272 | PF00498 | 0.444 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.498 |
LIG_FHA_1 | 594 | 600 | PF00498 | 0.398 |
LIG_FHA_1 | 608 | 614 | PF00498 | 0.498 |
LIG_FHA_2 | 219 | 225 | PF00498 | 0.511 |
LIG_FHA_2 | 31 | 37 | PF00498 | 0.530 |
LIG_FHA_2 | 402 | 408 | PF00498 | 0.354 |
LIG_FHA_2 | 435 | 441 | PF00498 | 0.402 |
LIG_FHA_2 | 473 | 479 | PF00498 | 0.369 |
LIG_FHA_2 | 480 | 486 | PF00498 | 0.318 |
LIG_Integrin_RGD_1 | 46 | 48 | PF01839 | 0.532 |
LIG_LIR_Apic_2 | 320 | 325 | PF02991 | 0.337 |
LIG_LIR_Apic_2 | 509 | 513 | PF02991 | 0.381 |
LIG_LIR_Gen_1 | 478 | 487 | PF02991 | 0.322 |
LIG_LIR_Gen_1 | 73 | 83 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 149 | 154 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 478 | 484 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 73 | 78 | PF02991 | 0.418 |
LIG_LYPXL_yS_3 | 151 | 154 | PF13949 | 0.406 |
LIG_RPA_C_Fungi | 343 | 355 | PF08784 | 0.291 |
LIG_SH2_CRK | 510 | 514 | PF00017 | 0.397 |
LIG_SH2_SRC | 18 | 21 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 182 | 185 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 386 | 389 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 77 | 80 | PF00017 | 0.486 |
LIG_SH3_3 | 17 | 23 | PF00018 | 0.482 |
LIG_SH3_3 | 212 | 218 | PF00018 | 0.356 |
LIG_SH3_3 | 47 | 53 | PF00018 | 0.495 |
LIG_Sin3_3 | 143 | 150 | PF02671 | 0.324 |
LIG_SUMO_SIM_anti_2 | 557 | 564 | PF11976 | 0.483 |
LIG_SUMO_SIM_par_1 | 233 | 239 | PF11976 | 0.353 |
LIG_SUMO_SIM_par_1 | 569 | 574 | PF11976 | 0.351 |
LIG_TRAF2_1 | 302 | 305 | PF00917 | 0.541 |
LIG_TRAF2_2 | 43 | 48 | PF00917 | 0.497 |
LIG_TYR_ITIM | 384 | 389 | PF00017 | 0.331 |
LIG_WW_3 | 541 | 545 | PF00397 | 0.351 |
MOD_CDC14_SPxK_1 | 582 | 585 | PF00782 | 0.403 |
MOD_CDK_SPxK_1 | 579 | 585 | PF00069 | 0.404 |
MOD_CDK_SPxxK_3 | 333 | 340 | PF00069 | 0.372 |
MOD_CDK_SPxxK_3 | 39 | 46 | PF00069 | 0.495 |
MOD_CK1_1 | 170 | 176 | PF00069 | 0.493 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.523 |
MOD_CK1_1 | 299 | 305 | PF00069 | 0.605 |
MOD_CK1_1 | 401 | 407 | PF00069 | 0.473 |
MOD_CK1_1 | 419 | 425 | PF00069 | 0.174 |
MOD_CK1_1 | 435 | 441 | PF00069 | 0.304 |
MOD_CK1_1 | 472 | 478 | PF00069 | 0.486 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.535 |
MOD_CK1_1 | 531 | 537 | PF00069 | 0.383 |
MOD_CK1_1 | 557 | 563 | PF00069 | 0.381 |
MOD_CK1_1 | 577 | 583 | PF00069 | 0.291 |
MOD_CK2_1 | 299 | 305 | PF00069 | 0.638 |
MOD_CK2_1 | 401 | 407 | PF00069 | 0.357 |
MOD_CK2_1 | 434 | 440 | PF00069 | 0.323 |
MOD_CK2_1 | 491 | 497 | PF00069 | 0.555 |
MOD_CK2_1 | 5 | 11 | PF00069 | 0.515 |
MOD_CK2_1 | 531 | 537 | PF00069 | 0.476 |
MOD_DYRK1A_RPxSP_1 | 579 | 583 | PF00069 | 0.405 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.487 |
MOD_GlcNHglycan | 305 | 309 | PF01048 | 0.632 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.527 |
MOD_GlcNHglycan | 379 | 382 | PF01048 | 0.403 |
MOD_GlcNHglycan | 455 | 459 | PF01048 | 0.290 |
MOD_GlcNHglycan | 493 | 496 | PF01048 | 0.332 |
MOD_GlcNHglycan | 563 | 566 | PF01048 | 0.553 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.483 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.508 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.481 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.589 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.398 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.540 |
MOD_GSK3_1 | 491 | 498 | PF00069 | 0.407 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.527 |
MOD_GSK3_1 | 521 | 528 | PF00069 | 0.350 |
MOD_GSK3_1 | 557 | 564 | PF00069 | 0.483 |
MOD_GSK3_1 | 573 | 580 | PF00069 | 0.331 |
MOD_GSK3_1 | 593 | 600 | PF00069 | 0.336 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.344 |
MOD_N-GLC_1 | 528 | 533 | PF02516 | 0.437 |
MOD_N-GLC_1 | 574 | 579 | PF02516 | 0.490 |
MOD_N-GLC_2 | 412 | 414 | PF02516 | 0.242 |
MOD_N-GLC_2 | 551 | 553 | PF02516 | 0.351 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.640 |
MOD_NEK2_1 | 167 | 172 | PF00069 | 0.485 |
MOD_NEK2_1 | 265 | 270 | PF00069 | 0.466 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.478 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.736 |
MOD_NEK2_1 | 387 | 392 | PF00069 | 0.440 |
MOD_NEK2_1 | 432 | 437 | PF00069 | 0.323 |
MOD_NEK2_1 | 479 | 484 | PF00069 | 0.424 |
MOD_NEK2_1 | 525 | 530 | PF00069 | 0.323 |
MOD_NEK2_1 | 573 | 578 | PF00069 | 0.446 |
MOD_NEK2_1 | 607 | 612 | PF00069 | 0.602 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.425 |
MOD_NEK2_2 | 209 | 214 | PF00069 | 0.359 |
MOD_NEK2_2 | 495 | 500 | PF00069 | 0.319 |
MOD_NEK2_2 | 66 | 71 | PF00069 | 0.388 |
MOD_OFUCOSY | 166 | 171 | PF10250 | 0.391 |
MOD_PIKK_1 | 291 | 297 | PF00454 | 0.461 |
MOD_PIKK_1 | 398 | 404 | PF00454 | 0.365 |
MOD_PIKK_1 | 469 | 475 | PF00454 | 0.349 |
MOD_PK_1 | 317 | 323 | PF00069 | 0.284 |
MOD_PKA_2 | 256 | 262 | PF00069 | 0.434 |
MOD_PKA_2 | 286 | 292 | PF00069 | 0.393 |
MOD_PKA_2 | 347 | 353 | PF00069 | 0.417 |
MOD_PKA_2 | 435 | 441 | PF00069 | 0.297 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.515 |
MOD_Plk_1 | 167 | 173 | PF00069 | 0.468 |
MOD_Plk_1 | 477 | 483 | PF00069 | 0.453 |
MOD_Plk_1 | 485 | 491 | PF00069 | 0.380 |
MOD_Plk_1 | 528 | 534 | PF00069 | 0.449 |
MOD_Plk_1 | 557 | 563 | PF00069 | 0.385 |
MOD_Plk_1 | 573 | 579 | PF00069 | 0.383 |
MOD_Plk_1 | 597 | 603 | PF00069 | 0.518 |
MOD_Plk_1 | 66 | 72 | PF00069 | 0.401 |
MOD_Plk_2-3 | 256 | 262 | PF00069 | 0.285 |
MOD_Plk_4 | 23 | 29 | PF00069 | 0.497 |
MOD_Plk_4 | 317 | 323 | PF00069 | 0.420 |
MOD_Plk_4 | 438 | 444 | PF00069 | 0.373 |
MOD_Plk_4 | 9 | 15 | PF00069 | 0.529 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.506 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.514 |
MOD_ProDKin_1 | 333 | 339 | PF00069 | 0.353 |
MOD_ProDKin_1 | 39 | 45 | PF00069 | 0.480 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.479 |
MOD_ProDKin_1 | 508 | 514 | PF00069 | 0.434 |
MOD_ProDKin_1 | 579 | 585 | PF00069 | 0.492 |
TRG_DiLeu_LyEn_5 | 250 | 255 | PF01217 | 0.352 |
TRG_ENDOCYTIC_2 | 151 | 154 | PF00928 | 0.466 |
TRG_ENDOCYTIC_2 | 386 | 389 | PF00928 | 0.331 |
TRG_ENDOCYTIC_2 | 493 | 496 | PF00928 | 0.347 |
TRG_ER_diArg_1 | 226 | 228 | PF00400 | 0.542 |
TRG_ER_diArg_1 | 359 | 361 | PF00400 | 0.358 |
TRG_ER_diArg_1 | 415 | 418 | PF00400 | 0.315 |
TRG_ER_diArg_1 | 499 | 502 | PF00400 | 0.321 |
TRG_ER_diArg_1 | 567 | 570 | PF00400 | 0.401 |
TRG_Pf-PMV_PEXEL_1 | 228 | 233 | PF00026 | 0.532 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1P921 | Leptomonas seymouri | 25% | 77% |
A4HCY0 | Leishmania braziliensis | 26% | 100% |
C9ZK22 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 77% |
C9ZZI9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 100% |
E9AEF0 | Leishmania major | 26% | 81% |
E9AGT5 | Leishmania infantum | 100% | 100% |
Q4QD45 | Leishmania major | 82% | 100% |
Q4QJ80 | Leishmania major | 81% | 100% |