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: 13 |
NetGPI | no | yes: 0, no: 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 1 |
GO:0042995 | cell projection | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 1 |
Related structures:
AlphaFold database: A4HH59
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 14 |
GO:0008152 | metabolic process | 1 | 14 |
GO:0019538 | protein metabolic process | 3 | 14 |
GO:0036211 | protein modification process | 4 | 14 |
GO:0043170 | macromolecule metabolic process | 3 | 14 |
GO:0043412 | macromolecule modification | 4 | 14 |
GO:0044238 | primary metabolic process | 2 | 14 |
GO:0071704 | organic substance metabolic process | 2 | 14 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 14 |
GO:0000226 | microtubule cytoskeleton organization | 3 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007010 | cytoskeleton organization | 5 | 1 |
GO:0007017 | microtubule-based process | 2 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0018095 | protein polyglutamylation | 7 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018200 | peptidyl-glutamic acid modification | 6 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 5 |
GO:0005488 | binding | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0008092 | cytoskeletal protein binding | 3 | 1 |
GO:0015631 | tubulin binding | 4 | 1 |
GO:0016874 | ligase activity | 2 | 5 |
GO:0016879 | ligase activity, forming carbon-nitrogen bonds | 3 | 1 |
GO:0016881 | acid-amino acid ligase activity | 4 | 1 |
GO:0070739 | protein-glutamic acid ligase activity | 3 | 1 |
GO:0070740 | tubulin-glutamic acid ligase activity | 4 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 437 | 441 | PF00656 | 0.479 |
CLV_MEL_PAP_1 | 137 | 143 | PF00089 | 0.430 |
CLV_NRD_NRD_1 | 160 | 162 | PF00675 | 0.244 |
CLV_NRD_NRD_1 | 167 | 169 | PF00675 | 0.244 |
CLV_NRD_NRD_1 | 185 | 187 | PF00675 | 0.188 |
CLV_NRD_NRD_1 | 277 | 279 | PF00675 | 0.323 |
CLV_NRD_NRD_1 | 315 | 317 | PF00675 | 0.625 |
CLV_NRD_NRD_1 | 453 | 455 | PF00675 | 0.364 |
CLV_NRD_NRD_1 | 471 | 473 | PF00675 | 0.442 |
CLV_NRD_NRD_1 | 588 | 590 | PF00675 | 0.455 |
CLV_NRD_NRD_1 | 631 | 633 | PF00675 | 0.512 |
CLV_PCSK_KEX2_1 | 167 | 169 | PF00082 | 0.273 |
CLV_PCSK_KEX2_1 | 185 | 187 | PF00082 | 0.273 |
CLV_PCSK_KEX2_1 | 276 | 278 | PF00082 | 0.335 |
CLV_PCSK_KEX2_1 | 315 | 317 | PF00082 | 0.625 |
CLV_PCSK_KEX2_1 | 45 | 47 | PF00082 | 0.648 |
CLV_PCSK_KEX2_1 | 452 | 454 | PF00082 | 0.399 |
CLV_PCSK_KEX2_1 | 471 | 473 | PF00082 | 0.460 |
CLV_PCSK_KEX2_1 | 588 | 590 | PF00082 | 0.455 |
CLV_PCSK_KEX2_1 | 631 | 633 | PF00082 | 0.531 |
CLV_PCSK_PC1ET2_1 | 276 | 278 | PF00082 | 0.339 |
CLV_PCSK_PC1ET2_1 | 45 | 47 | PF00082 | 0.685 |
CLV_PCSK_PC7_1 | 273 | 279 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.260 |
CLV_PCSK_SKI1_1 | 204 | 208 | PF00082 | 0.171 |
CLV_PCSK_SKI1_1 | 228 | 232 | PF00082 | 0.340 |
CLV_PCSK_SKI1_1 | 241 | 245 | PF00082 | 0.310 |
CLV_PCSK_SKI1_1 | 288 | 292 | PF00082 | 0.318 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.464 |
CLV_PCSK_SKI1_1 | 332 | 336 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 382 | 386 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 588 | 592 | PF00082 | 0.440 |
CLV_Separin_Metazoa | 344 | 348 | PF03568 | 0.502 |
CLV_Separin_Metazoa | 468 | 472 | PF03568 | 0.507 |
DEG_APCC_DBOX_1 | 29 | 37 | PF00400 | 0.642 |
DEG_APCC_DBOX_1 | 338 | 346 | PF00400 | 0.627 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.613 |
DEG_SPOP_SBC_1 | 58 | 62 | PF00917 | 0.611 |
DOC_CYCLIN_yCln2_LP_2 | 208 | 214 | PF00134 | 0.552 |
DOC_MAPK_DCC_7 | 501 | 510 | PF00069 | 0.539 |
DOC_MAPK_gen_1 | 167 | 175 | PF00069 | 0.422 |
DOC_MAPK_gen_1 | 276 | 284 | PF00069 | 0.506 |
DOC_MAPK_gen_1 | 28 | 35 | PF00069 | 0.558 |
DOC_MAPK_gen_1 | 295 | 303 | PF00069 | 0.447 |
DOC_MAPK_gen_1 | 452 | 461 | PF00069 | 0.235 |
DOC_MAPK_HePTP_8 | 451 | 463 | PF00069 | 0.241 |
DOC_MAPK_MEF2A_6 | 277 | 286 | PF00069 | 0.493 |
DOC_MAPK_MEF2A_6 | 295 | 303 | PF00069 | 0.358 |
DOC_MAPK_MEF2A_6 | 347 | 356 | PF00069 | 0.446 |
DOC_MAPK_MEF2A_6 | 454 | 463 | PF00069 | 0.221 |
DOC_MAPK_NFAT4_5 | 296 | 304 | PF00069 | 0.552 |
DOC_PP1_RVXF_1 | 160 | 167 | PF00149 | 0.473 |
DOC_PP1_RVXF_1 | 239 | 246 | PF00149 | 0.552 |
DOC_PP1_RVXF_1 | 88 | 95 | PF00149 | 0.492 |
DOC_PP2B_LxvP_1 | 124 | 127 | PF13499 | 0.280 |
DOC_PP2B_LxvP_1 | 208 | 211 | PF13499 | 0.552 |
DOC_PP2B_LxvP_1 | 328 | 331 | PF13499 | 0.475 |
DOC_PP2B_LxvP_1 | 395 | 398 | PF13499 | 0.565 |
DOC_PP4_FxxP_1 | 326 | 329 | PF00568 | 0.480 |
DOC_USP7_MATH_1 | 16 | 20 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 322 | 326 | PF00917 | 0.685 |
DOC_USP7_MATH_1 | 434 | 438 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 527 | 531 | PF00917 | 0.518 |
DOC_USP7_MATH_1 | 58 | 62 | PF00917 | 0.755 |
DOC_USP7_MATH_1 | 596 | 600 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 7 | 11 | PF00917 | 0.647 |
DOC_WW_Pin1_4 | 197 | 202 | PF00397 | 0.501 |
DOC_WW_Pin1_4 | 318 | 323 | PF00397 | 0.722 |
DOC_WW_Pin1_4 | 512 | 517 | PF00397 | 0.447 |
LIG_14-3-3_CanoR_1 | 119 | 123 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 204 | 209 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 259 | 264 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 315 | 320 | PF00244 | 0.717 |
LIG_14-3-3_CanoR_1 | 339 | 349 | PF00244 | 0.414 |
LIG_14-3-3_CanoR_1 | 9 | 17 | PF00244 | 0.415 |
LIG_Actin_WH2_2 | 487 | 503 | PF00022 | 0.505 |
LIG_Actin_WH2_2 | 521 | 536 | PF00022 | 0.520 |
LIG_APCC_ABBA_1 | 282 | 287 | PF00400 | 0.539 |
LIG_APCC_ABBA_1 | 354 | 359 | PF00400 | 0.444 |
LIG_BRCT_BRCA1_1 | 4 | 8 | PF00533 | 0.414 |
LIG_Clathr_ClatBox_1 | 493 | 497 | PF01394 | 0.462 |
LIG_eIF4E_1 | 285 | 291 | PF01652 | 0.500 |
LIG_FHA_1 | 100 | 106 | PF00498 | 0.573 |
LIG_FHA_1 | 119 | 125 | PF00498 | 0.444 |
LIG_FHA_1 | 205 | 211 | PF00498 | 0.471 |
LIG_FHA_1 | 534 | 540 | PF00498 | 0.518 |
LIG_FHA_2 | 249 | 255 | PF00498 | 0.539 |
LIG_FHA_2 | 267 | 273 | PF00498 | 0.382 |
LIG_FHA_2 | 520 | 526 | PF00498 | 0.473 |
LIG_FHA_2 | 93 | 99 | PF00498 | 0.514 |
LIG_LIR_Apic_2 | 325 | 329 | PF02991 | 0.477 |
LIG_LIR_Apic_2 | 367 | 372 | PF02991 | 0.414 |
LIG_LIR_Gen_1 | 203 | 212 | PF02991 | 0.552 |
LIG_LIR_Gen_1 | 213 | 220 | PF02991 | 0.518 |
LIG_LIR_Gen_1 | 489 | 499 | PF02991 | 0.522 |
LIG_LIR_Gen_1 | 80 | 89 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 203 | 208 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 213 | 217 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 489 | 494 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 535 | 540 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 80 | 85 | PF02991 | 0.354 |
LIG_NRBOX | 168 | 174 | PF00104 | 0.371 |
LIG_NRBOX | 300 | 306 | PF00104 | 0.552 |
LIG_PCNA_PIPBox_1 | 199 | 208 | PF02747 | 0.371 |
LIG_REV1ctd_RIR_1 | 242 | 248 | PF16727 | 0.500 |
LIG_SH2_CRK | 147 | 151 | PF00017 | 0.518 |
LIG_SH2_CRK | 17 | 21 | PF00017 | 0.425 |
LIG_SH2_CRK | 369 | 373 | PF00017 | 0.462 |
LIG_SH2_CRK | 82 | 86 | PF00017 | 0.353 |
LIG_SH2_NCK_1 | 369 | 373 | PF00017 | 0.453 |
LIG_SH2_PTP2 | 302 | 305 | PF00017 | 0.526 |
LIG_SH2_SRC | 396 | 399 | PF00017 | 0.560 |
LIG_SH2_STAP1 | 557 | 561 | PF00017 | 0.547 |
LIG_SH2_STAT3 | 51 | 54 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 17 | 20 | PF00017 | 0.627 |
LIG_SH2_STAT5 | 285 | 288 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 302 | 305 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 396 | 399 | PF00017 | 0.560 |
LIG_SH3_1 | 412 | 418 | PF00018 | 0.432 |
LIG_SH3_3 | 107 | 113 | PF00018 | 0.311 |
LIG_SH3_3 | 117 | 123 | PF00018 | 0.639 |
LIG_SH3_3 | 283 | 289 | PF00018 | 0.444 |
LIG_SH3_3 | 316 | 322 | PF00018 | 0.557 |
LIG_SH3_3 | 327 | 333 | PF00018 | 0.641 |
LIG_SH3_3 | 412 | 418 | PF00018 | 0.675 |
LIG_SUMO_SIM_anti_2 | 465 | 471 | PF11976 | 0.342 |
LIG_SUMO_SIM_par_1 | 302 | 308 | PF11976 | 0.536 |
LIG_SUMO_SIM_par_1 | 506 | 511 | PF11976 | 0.371 |
LIG_SUMO_SIM_par_1 | 625 | 630 | PF11976 | 0.531 |
LIG_TRAF2_1 | 269 | 272 | PF00917 | 0.466 |
LIG_TYR_ITSM | 78 | 85 | PF00017 | 0.380 |
LIG_UBA3_1 | 169 | 178 | PF00899 | 0.482 |
LIG_WRC_WIRS_1 | 3 | 8 | PF05994 | 0.415 |
MOD_CDK_SPxxK_3 | 197 | 204 | PF00069 | 0.371 |
MOD_CK1_1 | 135 | 141 | PF00069 | 0.358 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.457 |
MOD_CK2_1 | 197 | 203 | PF00069 | 0.560 |
MOD_CK2_1 | 248 | 254 | PF00069 | 0.557 |
MOD_CK2_1 | 266 | 272 | PF00069 | 0.404 |
MOD_CK2_1 | 462 | 468 | PF00069 | 0.268 |
MOD_CK2_1 | 486 | 492 | PF00069 | 0.539 |
MOD_CK2_1 | 57 | 63 | PF00069 | 0.681 |
MOD_Cter_Amidation | 293 | 296 | PF01082 | 0.300 |
MOD_GlcNHglycan | 432 | 435 | PF01048 | 0.477 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.339 |
MOD_GlcNHglycan | 594 | 597 | PF01048 | 0.571 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.439 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.688 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.371 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.642 |
MOD_GSK3_1 | 430 | 437 | PF00069 | 0.495 |
MOD_GSK3_1 | 592 | 599 | PF00069 | 0.453 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.476 |
MOD_N-GLC_1 | 512 | 517 | PF02516 | 0.253 |
MOD_N-GLC_2 | 376 | 378 | PF02516 | 0.291 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.510 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.444 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.578 |
MOD_NEK2_1 | 438 | 443 | PF00069 | 0.515 |
MOD_NEK2_1 | 519 | 524 | PF00069 | 0.482 |
MOD_NEK2_1 | 533 | 538 | PF00069 | 0.450 |
MOD_NEK2_1 | 539 | 544 | PF00069 | 0.518 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.652 |
MOD_NEK2_2 | 447 | 452 | PF00069 | 0.255 |
MOD_OFUCOSY | 15 | 22 | PF10250 | 0.420 |
MOD_PKA_1 | 315 | 321 | PF00069 | 0.718 |
MOD_PKA_2 | 118 | 124 | PF00069 | 0.551 |
MOD_PKA_2 | 258 | 264 | PF00069 | 0.539 |
MOD_PKA_2 | 315 | 321 | PF00069 | 0.705 |
MOD_PKA_2 | 533 | 539 | PF00069 | 0.552 |
MOD_PKA_2 | 77 | 83 | PF00069 | 0.526 |
MOD_PKA_2 | 8 | 14 | PF00069 | 0.417 |
MOD_Plk_1 | 132 | 138 | PF00069 | 0.399 |
MOD_Plk_1 | 228 | 234 | PF00069 | 0.371 |
MOD_Plk_2-3 | 266 | 272 | PF00069 | 0.513 |
MOD_Plk_4 | 132 | 138 | PF00069 | 0.375 |
MOD_Plk_4 | 20 | 26 | PF00069 | 0.425 |
MOD_Plk_4 | 391 | 397 | PF00069 | 0.552 |
MOD_Plk_4 | 434 | 440 | PF00069 | 0.492 |
MOD_Plk_4 | 459 | 465 | PF00069 | 0.325 |
MOD_Plk_4 | 514 | 520 | PF00069 | 0.462 |
MOD_Plk_4 | 528 | 534 | PF00069 | 0.460 |
MOD_ProDKin_1 | 197 | 203 | PF00069 | 0.501 |
MOD_ProDKin_1 | 318 | 324 | PF00069 | 0.724 |
MOD_ProDKin_1 | 512 | 518 | PF00069 | 0.447 |
MOD_SUMO_rev_2 | 558 | 567 | PF00179 | 0.562 |
TRG_DiLeu_BaEn_1 | 572 | 577 | PF01217 | 0.455 |
TRG_DiLeu_BaEn_3 | 570 | 576 | PF01217 | 0.420 |
TRG_DiLeu_BaLyEn_6 | 286 | 291 | PF01217 | 0.500 |
TRG_DiLeu_BaLyEn_6 | 535 | 540 | PF01217 | 0.486 |
TRG_DiLeu_BaLyEn_6 | 586 | 591 | PF01217 | 0.484 |
TRG_ENDOCYTIC_2 | 147 | 150 | PF00928 | 0.518 |
TRG_ENDOCYTIC_2 | 153 | 156 | PF00928 | 0.518 |
TRG_ENDOCYTIC_2 | 17 | 20 | PF00928 | 0.426 |
TRG_ENDOCYTIC_2 | 302 | 305 | PF00928 | 0.444 |
TRG_ENDOCYTIC_2 | 82 | 85 | PF00928 | 0.341 |
TRG_ER_diArg_1 | 166 | 168 | PF00400 | 0.505 |
TRG_ER_diArg_1 | 315 | 317 | PF00400 | 0.527 |
TRG_ER_diArg_1 | 451 | 454 | PF00400 | 0.387 |
TRG_ER_diArg_1 | 470 | 472 | PF00400 | 0.438 |
TRG_ER_diArg_1 | 587 | 589 | PF00400 | 0.455 |
TRG_ER_diArg_1 | 631 | 633 | PF00400 | 0.542 |
TRG_NES_CRM1_1 | 457 | 473 | PF08389 | 0.480 |
TRG_Pf-PMV_PEXEL_1 | 167 | 171 | PF00026 | 0.325 |
TRG_Pf-PMV_PEXEL_1 | 453 | 457 | PF00026 | 0.461 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IH77 | Leptomonas seymouri | 55% | 100% |
A0A0S4IUG9 | Bodo saltans | 26% | 68% |
A0A0S4JH38 | Bodo saltans | 33% | 100% |
A0A1X0P0Y5 | Trypanosomatidae | 38% | 100% |
A0A3S7X261 | Leishmania donovani | 76% | 100% |
A0A422N064 | Trypanosoma rangeli | 44% | 100% |
A4H9E1 | Leishmania braziliensis | 22% | 100% |
A4HXR2 | Leishmania infantum | 22% | 100% |
A4I479 | Leishmania infantum | 75% | 100% |
A4Q9E4 | Mus musculus | 22% | 100% |
A4Q9F6 | Mus musculus | 26% | 79% |
B6DTF7 | Bodo saltans | 24% | 100% |
C9ZI96 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 93% |
C9ZKP9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
C9ZPR8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
C9ZYH1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 96% |
D0A044 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 100% |
E9ADM8 | Leishmania major | 76% | 100% |
E9AM52 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
E9ARH4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 22% | 100% |
Q4QE05 | Leishmania major | 22% | 100% |
Q8N841 | Homo sapiens | 26% | 75% |
V5ARK1 | Trypanosoma cruzi | 26% | 100% |
V5B4U2 | Trypanosoma cruzi | 42% | 100% |