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:0005634 | nucleus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9B6E2
Term | Name | Level | Count |
---|---|---|---|
GO:0001522 | pseudouridine synthesis | 6 | 10 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 10 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009451 | RNA modification | 5 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0016070 | RNA metabolic process | 5 | 10 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 10 |
GO:0043170 | macromolecule metabolic process | 3 | 10 |
GO:0043412 | macromolecule modification | 4 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
GO:0046483 | heterocycle metabolic process | 3 | 10 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:0090304 | nucleic acid metabolic process | 4 | 10 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 10 |
GO:0003723 | RNA binding | 4 | 10 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0009982 | pseudouridine synthase activity | 4 | 10 |
GO:0016853 | isomerase activity | 2 | 10 |
GO:0016866 | intramolecular transferase activity | 3 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 462 | 466 | PF00656 | 0.475 |
CLV_C14_Caspase3-7 | 70 | 74 | PF00656 | 0.507 |
CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 232 | 234 | PF00675 | 0.565 |
CLV_NRD_NRD_1 | 244 | 246 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 271 | 273 | PF00675 | 0.482 |
CLV_NRD_NRD_1 | 313 | 315 | PF00675 | 0.580 |
CLV_NRD_NRD_1 | 42 | 44 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 428 | 430 | PF00675 | 0.548 |
CLV_NRD_NRD_1 | 543 | 545 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 560 | 562 | PF00675 | 0.400 |
CLV_NRD_NRD_1 | 568 | 570 | PF00675 | 0.401 |
CLV_PCSK_KEX2_1 | 232 | 234 | PF00082 | 0.565 |
CLV_PCSK_KEX2_1 | 244 | 246 | PF00082 | 0.376 |
CLV_PCSK_KEX2_1 | 271 | 273 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 313 | 315 | PF00082 | 0.580 |
CLV_PCSK_KEX2_1 | 42 | 44 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 428 | 430 | PF00082 | 0.491 |
CLV_PCSK_KEX2_1 | 509 | 511 | PF00082 | 0.490 |
CLV_PCSK_KEX2_1 | 543 | 545 | PF00082 | 0.446 |
CLV_PCSK_PC1ET2_1 | 509 | 511 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 225 | 229 | PF00082 | 0.379 |
CLV_PCSK_SKI1_1 | 244 | 248 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 374 | 378 | PF00082 | 0.534 |
CLV_PCSK_SKI1_1 | 388 | 392 | PF00082 | 0.549 |
CLV_PCSK_SKI1_1 | 429 | 433 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 488 | 492 | PF00082 | 0.448 |
CLV_PCSK_SKI1_1 | 49 | 53 | PF00082 | 0.371 |
CLV_PCSK_SKI1_1 | 561 | 565 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 592 | 596 | PF00082 | 0.348 |
DEG_ODPH_VHL_1 | 485 | 497 | PF01847 | 0.368 |
DEG_SPOP_SBC_1 | 67 | 71 | PF00917 | 0.457 |
DOC_CYCLIN_RxL_1 | 330 | 340 | PF00134 | 0.419 |
DOC_MAPK_DCC_7 | 330 | 338 | PF00069 | 0.365 |
DOC_MAPK_gen_1 | 357 | 367 | PF00069 | 0.518 |
DOC_MAPK_gen_1 | 75 | 84 | PF00069 | 0.424 |
DOC_MAPK_gen_1 | 99 | 108 | PF00069 | 0.418 |
DOC_MAPK_MEF2A_6 | 488 | 497 | PF00069 | 0.363 |
DOC_MAPK_MEF2A_6 | 75 | 84 | PF00069 | 0.412 |
DOC_MAPK_RevD_3 | 218 | 233 | PF00069 | 0.388 |
DOC_MAPK_RevD_3 | 495 | 510 | PF00069 | 0.356 |
DOC_PP1_SILK_1 | 532 | 537 | PF00149 | 0.326 |
DOC_PP4_FxxP_1 | 110 | 113 | PF00568 | 0.316 |
DOC_PP4_FxxP_1 | 564 | 567 | PF00568 | 0.396 |
DOC_PP4_FxxP_1 | 579 | 582 | PF00568 | 0.283 |
DOC_USP7_MATH_1 | 267 | 271 | PF00917 | 0.439 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.309 |
DOC_USP7_MATH_1 | 434 | 438 | PF00917 | 0.494 |
DOC_USP7_MATH_1 | 582 | 586 | PF00917 | 0.372 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.350 |
DOC_USP7_UBL2_3 | 562 | 566 | PF12436 | 0.494 |
DOC_WW_Pin1_4 | 109 | 114 | PF00397 | 0.372 |
DOC_WW_Pin1_4 | 154 | 159 | PF00397 | 0.392 |
DOC_WW_Pin1_4 | 263 | 268 | PF00397 | 0.434 |
DOC_WW_Pin1_4 | 536 | 541 | PF00397 | 0.333 |
DOC_WW_Pin1_4 | 598 | 603 | PF00397 | 0.441 |
LIG_14-3-3_CanoR_1 | 180 | 186 | PF00244 | 0.389 |
LIG_14-3-3_CanoR_1 | 244 | 253 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 522 | 528 | PF00244 | 0.515 |
LIG_14-3-3_CanoR_1 | 77 | 81 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 83 | 90 | PF00244 | 0.432 |
LIG_Actin_WH2_2 | 185 | 202 | PF00022 | 0.505 |
LIG_APCC_ABBAyCdc20_2 | 524 | 530 | PF00400 | 0.349 |
LIG_BIR_III_2 | 73 | 77 | PF00653 | 0.442 |
LIG_BRCT_BRCA1_1 | 137 | 141 | PF00533 | 0.438 |
LIG_BRCT_BRCA1_1 | 602 | 606 | PF00533 | 0.448 |
LIG_BRCT_BRCA1_1 | 62 | 66 | PF00533 | 0.517 |
LIG_CtBP_PxDLS_1 | 498 | 502 | PF00389 | 0.358 |
LIG_deltaCOP1_diTrp_1 | 409 | 413 | PF00928 | 0.420 |
LIG_eIF4E_1 | 224 | 230 | PF01652 | 0.441 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.411 |
LIG_FHA_1 | 248 | 254 | PF00498 | 0.439 |
LIG_FHA_1 | 362 | 368 | PF00498 | 0.396 |
LIG_FHA_1 | 440 | 446 | PF00498 | 0.475 |
LIG_FHA_1 | 586 | 592 | PF00498 | 0.436 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.448 |
LIG_FHA_2 | 375 | 381 | PF00498 | 0.707 |
LIG_FHA_2 | 430 | 436 | PF00498 | 0.474 |
LIG_FHA_2 | 68 | 74 | PF00498 | 0.545 |
LIG_FHA_2 | 90 | 96 | PF00498 | 0.452 |
LIG_Integrin_RGD_1 | 556 | 558 | PF01839 | 0.433 |
LIG_LIR_Apic_2 | 153 | 158 | PF02991 | 0.454 |
LIG_LIR_Gen_1 | 121 | 131 | PF02991 | 0.392 |
LIG_LIR_Gen_1 | 273 | 281 | PF02991 | 0.474 |
LIG_LIR_Gen_1 | 347 | 356 | PF02991 | 0.317 |
LIG_LIR_Gen_1 | 409 | 418 | PF02991 | 0.472 |
LIG_LIR_Gen_1 | 465 | 475 | PF02991 | 0.344 |
LIG_LIR_LC3C_4 | 78 | 82 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 121 | 126 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 234 | 238 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 273 | 277 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 347 | 353 | PF02991 | 0.321 |
LIG_LIR_Nem_3 | 409 | 413 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 465 | 471 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 502 | 506 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 603 | 609 | PF02991 | 0.466 |
LIG_MYND_1 | 173 | 177 | PF01753 | 0.400 |
LIG_PCNA_yPIPBox_3 | 186 | 196 | PF02747 | 0.477 |
LIG_PCNA_yPIPBox_3 | 433 | 445 | PF02747 | 0.387 |
LIG_REV1ctd_RIR_1 | 561 | 566 | PF16727 | 0.475 |
LIG_SH2_CRK | 427 | 431 | PF00017 | 0.405 |
LIG_SH2_NCK_1 | 210 | 214 | PF00017 | 0.299 |
LIG_SH2_NCK_1 | 32 | 36 | PF00017 | 0.481 |
LIG_SH2_PTP2 | 123 | 126 | PF00017 | 0.414 |
LIG_SH2_PTP2 | 155 | 158 | PF00017 | 0.375 |
LIG_SH2_SRC | 32 | 35 | PF00017 | 0.453 |
LIG_SH2_STAP1 | 181 | 185 | PF00017 | 0.348 |
LIG_SH2_STAP1 | 210 | 214 | PF00017 | 0.334 |
LIG_SH2_STAT3 | 528 | 531 | PF00017 | 0.381 |
LIG_SH2_STAT5 | 123 | 126 | PF00017 | 0.332 |
LIG_SH2_STAT5 | 155 | 158 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 221 | 224 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 439 | 442 | PF00017 | 0.307 |
LIG_SH2_STAT5 | 504 | 507 | PF00017 | 0.330 |
LIG_SH2_STAT5 | 55 | 58 | PF00017 | 0.346 |
LIG_SH3_3 | 297 | 303 | PF00018 | 0.368 |
LIG_SH3_3 | 441 | 447 | PF00018 | 0.343 |
LIG_SH3_3 | 492 | 498 | PF00018 | 0.390 |
LIG_SH3_4 | 566 | 573 | PF00018 | 0.431 |
LIG_SUMO_SIM_par_1 | 334 | 340 | PF11976 | 0.471 |
LIG_SUMO_SIM_par_1 | 363 | 369 | PF11976 | 0.505 |
LIG_TRAF2_1 | 158 | 161 | PF00917 | 0.516 |
LIG_TRAF2_1 | 414 | 417 | PF00917 | 0.339 |
LIG_TRFH_1 | 563 | 567 | PF08558 | 0.465 |
LIG_TYR_ITIM | 425 | 430 | PF00017 | 0.345 |
LIG_WRC_WIRS_1 | 446 | 451 | PF05994 | 0.437 |
MOD_CDK_SPK_2 | 263 | 268 | PF00069 | 0.514 |
MOD_CDK_SPxxK_3 | 536 | 543 | PF00069 | 0.445 |
MOD_CK1_1 | 118 | 124 | PF00069 | 0.509 |
MOD_CK1_1 | 266 | 272 | PF00069 | 0.471 |
MOD_CK1_1 | 361 | 367 | PF00069 | 0.260 |
MOD_CK1_1 | 411 | 417 | PF00069 | 0.536 |
MOD_CK1_1 | 460 | 466 | PF00069 | 0.658 |
MOD_CK1_1 | 539 | 545 | PF00069 | 0.480 |
MOD_CK1_1 | 585 | 591 | PF00069 | 0.417 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.503 |
MOD_CK2_1 | 273 | 279 | PF00069 | 0.494 |
MOD_CK2_1 | 411 | 417 | PF00069 | 0.416 |
MOD_CK2_1 | 429 | 435 | PF00069 | 0.335 |
MOD_CK2_1 | 89 | 95 | PF00069 | 0.390 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.367 |
MOD_GlcNHglycan | 360 | 363 | PF01048 | 0.508 |
MOD_GlcNHglycan | 380 | 383 | PF01048 | 0.690 |
MOD_GlcNHglycan | 404 | 407 | PF01048 | 0.449 |
MOD_GlcNHglycan | 409 | 413 | PF01048 | 0.488 |
MOD_GlcNHglycan | 588 | 591 | PF01048 | 0.388 |
MOD_GlcNHglycan | 602 | 605 | PF01048 | 0.379 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.533 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.392 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.451 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.301 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.483 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.536 |
MOD_GSK3_1 | 582 | 589 | PF00069 | 0.332 |
MOD_GSK3_1 | 596 | 603 | PF00069 | 0.295 |
MOD_N-GLC_1 | 208 | 213 | PF02516 | 0.309 |
MOD_N-GLC_1 | 499 | 504 | PF02516 | 0.313 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.543 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.302 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.351 |
MOD_NEK2_1 | 402 | 407 | PF00069 | 0.504 |
MOD_NEK2_1 | 499 | 504 | PF00069 | 0.293 |
MOD_NEK2_1 | 571 | 576 | PF00069 | 0.428 |
MOD_NEK2_1 | 577 | 582 | PF00069 | 0.377 |
MOD_NEK2_1 | 596 | 601 | PF00069 | 0.327 |
MOD_NEK2_1 | 66 | 71 | PF00069 | 0.508 |
MOD_NEK2_2 | 181 | 186 | PF00069 | 0.409 |
MOD_NEK2_2 | 352 | 357 | PF00069 | 0.319 |
MOD_PIKK_1 | 248 | 254 | PF00454 | 0.290 |
MOD_PIKK_1 | 434 | 440 | PF00454 | 0.385 |
MOD_PKA_1 | 244 | 250 | PF00069 | 0.414 |
MOD_PKA_2 | 179 | 185 | PF00069 | 0.342 |
MOD_PKA_2 | 244 | 250 | PF00069 | 0.493 |
MOD_PKA_2 | 267 | 273 | PF00069 | 0.511 |
MOD_PKA_2 | 295 | 301 | PF00069 | 0.495 |
MOD_PKA_2 | 542 | 548 | PF00069 | 0.579 |
MOD_PKA_2 | 76 | 82 | PF00069 | 0.441 |
MOD_PKA_2 | 8 | 14 | PF00069 | 0.463 |
MOD_PKB_1 | 372 | 380 | PF00069 | 0.521 |
MOD_Plk_1 | 21 | 27 | PF00069 | 0.486 |
MOD_Plk_1 | 408 | 414 | PF00069 | 0.545 |
MOD_Plk_1 | 434 | 440 | PF00069 | 0.385 |
MOD_Plk_1 | 499 | 505 | PF00069 | 0.409 |
MOD_Plk_2-3 | 273 | 279 | PF00069 | 0.482 |
MOD_Plk_4 | 273 | 279 | PF00069 | 0.563 |
MOD_Plk_4 | 499 | 505 | PF00069 | 0.435 |
MOD_Plk_4 | 523 | 529 | PF00069 | 0.467 |
MOD_Plk_4 | 76 | 82 | PF00069 | 0.504 |
MOD_Plk_4 | 89 | 95 | PF00069 | 0.390 |
MOD_ProDKin_1 | 109 | 115 | PF00069 | 0.371 |
MOD_ProDKin_1 | 154 | 160 | PF00069 | 0.400 |
MOD_ProDKin_1 | 263 | 269 | PF00069 | 0.427 |
MOD_ProDKin_1 | 536 | 542 | PF00069 | 0.331 |
MOD_ProDKin_1 | 598 | 604 | PF00069 | 0.439 |
MOD_SUMO_rev_2 | 68 | 76 | PF00179 | 0.528 |
TRG_AP2beta_CARGO_1 | 347 | 357 | PF09066 | 0.342 |
TRG_DiLeu_BaEn_2 | 233 | 239 | PF01217 | 0.433 |
TRG_DiLeu_BaLyEn_6 | 454 | 459 | PF01217 | 0.424 |
TRG_DiLeu_BaLyEn_6 | 604 | 609 | PF01217 | 0.347 |
TRG_DiLeu_BaLyEn_6 | 80 | 85 | PF01217 | 0.460 |
TRG_ENDOCYTIC_2 | 123 | 126 | PF00928 | 0.414 |
TRG_ENDOCYTIC_2 | 235 | 238 | PF00928 | 0.349 |
TRG_ENDOCYTIC_2 | 427 | 430 | PF00928 | 0.541 |
TRG_ER_diArg_1 | 231 | 233 | PF00400 | 0.399 |
TRG_ER_diArg_1 | 243 | 245 | PF00400 | 0.308 |
TRG_ER_diArg_1 | 312 | 314 | PF00400 | 0.558 |
TRG_ER_diArg_1 | 371 | 374 | PF00400 | 0.516 |
TRG_ER_diArg_1 | 42 | 44 | PF00400 | 0.370 |
TRG_ER_diArg_1 | 427 | 429 | PF00400 | 0.482 |
TRG_NES_CRM1_1 | 465 | 478 | PF08389 | 0.397 |
TRG_Pf-PMV_PEXEL_1 | 244 | 248 | PF00026 | 0.415 |
TRG_Pf-PMV_PEXEL_1 | 334 | 339 | PF00026 | 0.364 |
TRG_Pf-PMV_PEXEL_1 | 492 | 496 | PF00026 | 0.426 |
TRG_Pf-PMV_PEXEL_1 | 83 | 87 | PF00026 | 0.459 |
TRG_Pf-PMV_PEXEL_1 | 96 | 100 | PF00026 | 0.504 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I8H8 | Leptomonas seymouri | 63% | 98% |
A0A0S4JFS5 | Bodo saltans | 31% | 92% |
A0A1X0P5I6 | Trypanosomatidae | 41% | 100% |
A0A3Q8IJH4 | Leishmania donovani | 95% | 100% |
A0A3S5ISL3 | Trypanosoma rangeli | 44% | 100% |
A4IBD1 | Leishmania infantum | 94% | 100% |
C9ZZ88 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9AF87 | Leishmania major | 95% | 100% |