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: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: E9AM52
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0019538 | protein metabolic process | 3 | 12 |
GO:0036211 | protein modification process | 4 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
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 | 3 |
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 | 3 |
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_NRD_NRD_1 | 121 | 123 | PF00675 | 0.230 |
CLV_NRD_NRD_1 | 128 | 130 | PF00675 | 0.230 |
CLV_NRD_NRD_1 | 188 | 190 | PF00675 | 0.268 |
CLV_NRD_NRD_1 | 233 | 235 | PF00675 | 0.323 |
CLV_NRD_NRD_1 | 255 | 257 | PF00675 | 0.243 |
CLV_NRD_NRD_1 | 276 | 278 | PF00675 | 0.617 |
CLV_NRD_NRD_1 | 413 | 415 | PF00675 | 0.350 |
CLV_NRD_NRD_1 | 432 | 434 | PF00675 | 0.260 |
CLV_NRD_NRD_1 | 549 | 551 | PF00675 | 0.462 |
CLV_NRD_NRD_1 | 592 | 594 | PF00675 | 0.527 |
CLV_PCSK_FUR_1 | 411 | 415 | PF00082 | 0.394 |
CLV_PCSK_KEX2_1 | 128 | 130 | PF00082 | 0.241 |
CLV_PCSK_KEX2_1 | 188 | 190 | PF00082 | 0.268 |
CLV_PCSK_KEX2_1 | 238 | 240 | PF00082 | 0.315 |
CLV_PCSK_KEX2_1 | 276 | 278 | PF00082 | 0.616 |
CLV_PCSK_KEX2_1 | 413 | 415 | PF00082 | 0.371 |
CLV_PCSK_KEX2_1 | 432 | 434 | PF00082 | 0.253 |
CLV_PCSK_KEX2_1 | 549 | 551 | PF00082 | 0.462 |
CLV_PCSK_KEX2_1 | 592 | 594 | PF00082 | 0.527 |
CLV_PCSK_PC1ET2_1 | 238 | 240 | PF00082 | 0.326 |
CLV_PCSK_PC7_1 | 234 | 240 | PF00082 | 0.326 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.232 |
CLV_PCSK_SKI1_1 | 189 | 193 | PF00082 | 0.349 |
CLV_PCSK_SKI1_1 | 202 | 206 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 249 | 253 | PF00082 | 0.326 |
CLV_PCSK_SKI1_1 | 343 | 347 | PF00082 | 0.329 |
CLV_PCSK_SKI1_1 | 549 | 553 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 80 | 84 | PF00082 | 0.551 |
CLV_Separin_Metazoa | 305 | 309 | PF03568 | 0.487 |
CLV_Separin_Metazoa | 429 | 433 | PF03568 | 0.452 |
DEG_APCC_DBOX_1 | 318 | 326 | PF00400 | 0.501 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.750 |
DOC_CKS1_1 | 81 | 86 | PF01111 | 0.487 |
DOC_CYCLIN_RxL_1 | 162 | 170 | PF00134 | 0.468 |
DOC_CYCLIN_yCln2_LP_2 | 169 | 175 | PF00134 | 0.514 |
DOC_CYCLIN_yCln2_LP_2 | 356 | 362 | PF00134 | 0.412 |
DOC_MAPK_DCC_7 | 462 | 471 | PF00069 | 0.526 |
DOC_MAPK_gen_1 | 234 | 245 | PF00069 | 0.502 |
DOC_MAPK_gen_1 | 256 | 264 | PF00069 | 0.440 |
DOC_MAPK_MEF2A_6 | 238 | 247 | PF00069 | 0.482 |
DOC_MAPK_MEF2A_6 | 256 | 264 | PF00069 | 0.346 |
DOC_MAPK_MEF2A_6 | 308 | 317 | PF00069 | 0.391 |
DOC_MAPK_NFAT4_5 | 257 | 265 | PF00069 | 0.514 |
DOC_PP1_RVXF_1 | 121 | 128 | PF00149 | 0.441 |
DOC_PP1_RVXF_1 | 200 | 207 | PF00149 | 0.514 |
DOC_PP1_RVXF_1 | 49 | 56 | PF00149 | 0.475 |
DOC_PP2B_LxvP_1 | 169 | 172 | PF13499 | 0.514 |
DOC_PP2B_LxvP_1 | 356 | 359 | PF13499 | 0.514 |
DOC_PP2B_LxvP_1 | 403 | 406 | PF13499 | 0.426 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.739 |
DOC_USP7_MATH_1 | 195 | 199 | PF00917 | 0.468 |
DOC_USP7_MATH_1 | 294 | 298 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 395 | 399 | PF00917 | 0.499 |
DOC_USP7_MATH_1 | 488 | 492 | PF00917 | 0.526 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.443 |
DOC_WW_Pin1_4 | 473 | 478 | PF00397 | 0.430 |
DOC_WW_Pin1_4 | 74 | 79 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 80 | 85 | PF00397 | 0.545 |
LIG_14-3-3_CanoR_1 | 220 | 225 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 276 | 281 | PF00244 | 0.720 |
LIG_14-3-3_CanoR_1 | 286 | 292 | PF00244 | 0.620 |
LIG_14-3-3_CanoR_1 | 411 | 417 | PF00244 | 0.383 |
LIG_14-3-3_CanoR_1 | 539 | 544 | PF00244 | 0.313 |
LIG_Actin_WH2_2 | 448 | 464 | PF00022 | 0.479 |
LIG_Actin_WH2_2 | 482 | 497 | PF00022 | 0.498 |
LIG_APCC_ABBA_1 | 1 | 6 | PF00400 | 0.548 |
LIG_APCC_ABBA_1 | 243 | 248 | PF00400 | 0.526 |
LIG_APCC_ABBA_1 | 315 | 320 | PF00400 | 0.430 |
LIG_Clathr_ClatBox_1 | 454 | 458 | PF01394 | 0.430 |
LIG_eIF4E_1 | 246 | 252 | PF01652 | 0.495 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.418 |
LIG_FHA_1 | 419 | 425 | PF00498 | 0.481 |
LIG_FHA_1 | 495 | 501 | PF00498 | 0.526 |
LIG_FHA_2 | 210 | 216 | PF00498 | 0.526 |
LIG_FHA_2 | 221 | 227 | PF00498 | 0.460 |
LIG_FHA_2 | 228 | 234 | PF00498 | 0.373 |
LIG_FHA_2 | 481 | 487 | PF00498 | 0.473 |
LIG_FHA_2 | 54 | 60 | PF00498 | 0.466 |
LIG_FHA_2 | 569 | 575 | PF00498 | 0.595 |
LIG_LIR_Gen_1 | 164 | 173 | PF02991 | 0.546 |
LIG_LIR_Gen_1 | 174 | 181 | PF02991 | 0.495 |
LIG_LIR_Gen_1 | 40 | 50 | PF02991 | 0.351 |
LIG_LIR_Gen_1 | 450 | 460 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 164 | 169 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 174 | 178 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 40 | 46 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 450 | 455 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 496 | 501 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 54 | 58 | PF02991 | 0.361 |
LIG_NRBOX | 261 | 267 | PF00104 | 0.514 |
LIG_REV1ctd_RIR_1 | 203 | 209 | PF16727 | 0.473 |
LIG_SH2_CRK | 108 | 112 | PF00017 | 0.526 |
LIG_SH2_CRK | 330 | 334 | PF00017 | 0.436 |
LIG_SH2_CRK | 43 | 47 | PF00017 | 0.313 |
LIG_SH2_NCK_1 | 330 | 334 | PF00017 | 0.430 |
LIG_SH2_PTP2 | 263 | 266 | PF00017 | 0.507 |
LIG_SH2_SRC | 357 | 360 | PF00017 | 0.514 |
LIG_SH2_STAP1 | 518 | 522 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 246 | 249 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 263 | 266 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 316 | 319 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 357 | 360 | PF00017 | 0.514 |
LIG_SH3_3 | 244 | 250 | PF00018 | 0.441 |
LIG_SH3_3 | 288 | 294 | PF00018 | 0.612 |
LIG_SH3_3 | 78 | 84 | PF00018 | 0.554 |
LIG_SUMO_SIM_anti_2 | 421 | 426 | PF11976 | 0.394 |
LIG_SUMO_SIM_par_1 | 263 | 269 | PF11976 | 0.535 |
LIG_SUMO_SIM_par_1 | 420 | 426 | PF11976 | 0.285 |
LIG_SUMO_SIM_par_1 | 586 | 591 | PF11976 | 0.477 |
LIG_TRAF2_1 | 224 | 227 | PF00917 | 0.451 |
LIG_TYR_ITSM | 39 | 46 | PF00017 | 0.366 |
LIG_WRC_WIRS_1 | 396 | 401 | PF05994 | 0.454 |
MOD_CDC14_SPxK_1 | 77 | 80 | PF00782 | 0.538 |
MOD_CDK_SPxK_1 | 74 | 80 | PF00069 | 0.509 |
MOD_CK1_1 | 138 | 144 | PF00069 | 0.515 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.434 |
MOD_CK1_1 | 275 | 281 | PF00069 | 0.703 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.660 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.597 |
MOD_CK1_1 | 301 | 307 | PF00069 | 0.547 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.310 |
MOD_CK2_1 | 158 | 164 | PF00069 | 0.560 |
MOD_CK2_1 | 209 | 215 | PF00069 | 0.556 |
MOD_CK2_1 | 220 | 226 | PF00069 | 0.479 |
MOD_CK2_1 | 227 | 233 | PF00069 | 0.393 |
MOD_CK2_1 | 395 | 401 | PF00069 | 0.474 |
MOD_CK2_1 | 412 | 418 | PF00069 | 0.379 |
MOD_CK2_1 | 423 | 429 | PF00069 | 0.309 |
MOD_CK2_1 | 447 | 453 | PF00069 | 0.514 |
MOD_CK2_1 | 57 | 63 | PF00069 | 0.462 |
MOD_Cter_Amidation | 254 | 257 | PF01082 | 0.295 |
MOD_DYRK1A_RPxSP_1 | 80 | 84 | PF00069 | 0.504 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.282 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.706 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.529 |
MOD_GlcNHglycan | 29 | 33 | PF01048 | 0.611 |
MOD_GlcNHglycan | 425 | 428 | PF01048 | 0.312 |
MOD_GlcNHglycan | 490 | 493 | PF01048 | 0.293 |
MOD_GlcNHglycan | 555 | 558 | PF01048 | 0.498 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.506 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.448 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.643 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.642 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.661 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.496 |
MOD_GSK3_1 | 385 | 392 | PF00069 | 0.553 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.438 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.443 |
MOD_GSK3_1 | 564 | 571 | PF00069 | 0.503 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.421 |
MOD_N-GLC_1 | 301 | 306 | PF02516 | 0.661 |
MOD_N-GLC_1 | 473 | 478 | PF02516 | 0.230 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.485 |
MOD_NEK2_1 | 167 | 172 | PF00069 | 0.516 |
MOD_NEK2_1 | 266 | 271 | PF00069 | 0.423 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.494 |
MOD_NEK2_1 | 480 | 485 | PF00069 | 0.455 |
MOD_NEK2_1 | 494 | 499 | PF00069 | 0.455 |
MOD_NEK2_1 | 500 | 505 | PF00069 | 0.321 |
MOD_PIKK_1 | 372 | 378 | PF00454 | 0.453 |
MOD_PK_1 | 539 | 545 | PF00069 | 0.311 |
MOD_PKA_1 | 276 | 282 | PF00069 | 0.721 |
MOD_PKA_2 | 219 | 225 | PF00069 | 0.526 |
MOD_PKA_2 | 275 | 281 | PF00069 | 0.708 |
MOD_PKA_2 | 38 | 44 | PF00069 | 0.468 |
MOD_PKA_2 | 412 | 418 | PF00069 | 0.371 |
MOD_PKA_2 | 494 | 500 | PF00069 | 0.514 |
MOD_Plk_1 | 159 | 165 | PF00069 | 0.468 |
MOD_Plk_1 | 53 | 59 | PF00069 | 0.501 |
MOD_Plk_1 | 93 | 99 | PF00069 | 0.357 |
MOD_Plk_2-3 | 227 | 233 | PF00069 | 0.489 |
MOD_Plk_2-3 | 59 | 65 | PF00069 | 0.558 |
MOD_Plk_4 | 352 | 358 | PF00069 | 0.514 |
MOD_Plk_4 | 395 | 401 | PF00069 | 0.469 |
MOD_Plk_4 | 420 | 426 | PF00069 | 0.311 |
MOD_Plk_4 | 475 | 481 | PF00069 | 0.430 |
MOD_Plk_4 | 93 | 99 | PF00069 | 0.357 |
MOD_ProDKin_1 | 221 | 227 | PF00069 | 0.443 |
MOD_ProDKin_1 | 473 | 479 | PF00069 | 0.430 |
MOD_ProDKin_1 | 74 | 80 | PF00069 | 0.509 |
MOD_SUMO_rev_2 | 519 | 528 | PF00179 | 0.533 |
TRG_DiLeu_BaLyEn_6 | 247 | 252 | PF01217 | 0.495 |
TRG_DiLeu_BaLyEn_6 | 496 | 501 | PF01217 | 0.455 |
TRG_DiLeu_BaLyEn_6 | 547 | 552 | PF01217 | 0.467 |
TRG_ENDOCYTIC_2 | 108 | 111 | PF00928 | 0.526 |
TRG_ENDOCYTIC_2 | 263 | 266 | PF00928 | 0.443 |
TRG_ENDOCYTIC_2 | 43 | 46 | PF00928 | 0.322 |
TRG_ER_diArg_1 | 127 | 129 | PF00400 | 0.479 |
TRG_ER_diArg_1 | 187 | 189 | PF00400 | 0.468 |
TRG_ER_diArg_1 | 410 | 413 | PF00400 | 0.404 |
TRG_ER_diArg_1 | 431 | 433 | PF00400 | 0.434 |
TRG_ER_diArg_1 | 548 | 550 | PF00400 | 0.460 |
TRG_ER_diArg_1 | 592 | 594 | PF00400 | 0.509 |
TRG_NES_CRM1_1 | 418 | 434 | PF08389 | 0.428 |
TRG_NES_CRM1_1 | 64 | 79 | PF08389 | 0.306 |
TRG_Pf-PMV_PEXEL_1 | 128 | 132 | PF00026 | 0.305 |
TRG_Pf-PMV_PEXEL_1 | 189 | 193 | PF00026 | 0.249 |
TRG_Pf-PMV_PEXEL_1 | 414 | 418 | PF00026 | 0.449 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IAP5 | Leptomonas seymouri | 25% | 80% |
A0A0N1IH77 | Leptomonas seymouri | 54% | 100% |
A0A0S4J7C9 | Bodo saltans | 25% | 90% |
A0A0S4JEF0 | Bodo saltans | 26% | 100% |
A0A0S4JH38 | Bodo saltans | 34% | 97% |
A0A0S4KQK8 | Bodo saltans | 28% | 91% |
A0A1X0NZP1 | Trypanosomatidae | 24% | 100% |
A0A1X0P0Y5 | Trypanosomatidae | 36% | 100% |
A0A1X0P6A0 | Trypanosomatidae | 25% | 89% |
A0A3Q8IDL7 | Leishmania donovani | 23% | 82% |
A0A3Q8III2 | Leishmania donovani | 27% | 82% |
A0A3S7X261 | Leishmania donovani | 90% | 96% |
A0A422N064 | Trypanosoma rangeli | 42% | 100% |
A0A422P136 | Trypanosoma rangeli | 25% | 91% |
A4HH59 | Leishmania braziliensis | 78% | 100% |
A4HNF6 | Leishmania braziliensis | 26% | 83% |
A4HYN9 | Leishmania infantum | 23% | 82% |
A4I479 | Leishmania infantum | 90% | 96% |
A4IC28 | Leishmania infantum | 27% | 82% |
A4Q9E8 | Mus musculus | 27% | 72% |
A4Q9F6 | Mus musculus | 25% | 74% |
A6NNM8 | Homo sapiens | 25% | 73% |
A8CVX7 | Danio rerio | 28% | 76% |
A8X9V4 | Caenorhabditis briggsae | 24% | 100% |
B6DTF7 | Bodo saltans | 23% | 100% |
C9ZI96 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 87% |
C9ZKP9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
C9ZPR8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
C9ZYH1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 91% |
D0A044 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 22% | 100% |
E9ADM8 | Leishmania major | 91% | 100% |
E9AFW7 | Leishmania major | 27% | 82% |
E9AID0 | Leishmania braziliensis | 24% | 100% |
E9AUL7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9AZF8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9B720 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 82% |
Q8N841 | Homo sapiens | 26% | 71% |
V5ARK1 | Trypanosoma cruzi | 26% | 100% |
V5B4U2 | Trypanosoma cruzi | 42% | 100% |