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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: Q4QIT1
Term | Name | Level | Count |
---|---|---|---|
GO:0002097 | tRNA wobble base modification | 7 | 2 |
GO:0002098 | tRNA wobble uridine modification | 8 | 2 |
GO:0002143 | tRNA wobble position uridine thiolation | 8 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006396 | RNA processing | 6 | 2 |
GO:0006399 | tRNA metabolic process | 7 | 2 |
GO:0006400 | tRNA modification | 6 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008033 | tRNA processing | 8 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009451 | RNA modification | 5 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016070 | RNA metabolic process | 5 | 2 |
GO:0034227 | tRNA thio-modification | 7 | 2 |
GO:0034470 | ncRNA processing | 7 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0034660 | ncRNA metabolic process | 6 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043412 | macromolecule modification | 4 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 10 |
GO:0004808 | tRNA (5-methylaminomethyl-2-thiouridylate)-methyltransferase activity | 6 | 8 |
GO:0008168 | methyltransferase activity | 4 | 8 |
GO:0008173 | RNA methyltransferase activity | 4 | 8 |
GO:0008175 | tRNA methyltransferase activity | 5 | 8 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 8 |
GO:0016740 | transferase activity | 2 | 10 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 8 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 8 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 8 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 575 | 579 | PF00656 | 0.766 |
CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.359 |
CLV_NRD_NRD_1 | 221 | 223 | PF00675 | 0.334 |
CLV_NRD_NRD_1 | 300 | 302 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 415 | 417 | PF00675 | 0.547 |
CLV_NRD_NRD_1 | 536 | 538 | PF00675 | 0.304 |
CLV_PCSK_FUR_1 | 534 | 538 | PF00082 | 0.304 |
CLV_PCSK_KEX2_1 | 187 | 189 | PF00082 | 0.359 |
CLV_PCSK_KEX2_1 | 220 | 222 | PF00082 | 0.304 |
CLV_PCSK_KEX2_1 | 415 | 417 | PF00082 | 0.579 |
CLV_PCSK_KEX2_1 | 536 | 538 | PF00082 | 0.304 |
CLV_PCSK_PC1ET2_1 | 220 | 222 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 222 | 226 | PF00082 | 0.306 |
CLV_PCSK_SKI1_1 | 349 | 353 | PF00082 | 0.516 |
CLV_PCSK_SKI1_1 | 547 | 551 | PF00082 | 0.280 |
CLV_PCSK_SKI1_1 | 74 | 78 | PF00082 | 0.604 |
DOC_ANK_TNKS_1 | 414 | 421 | PF00023 | 0.549 |
DOC_CKS1_1 | 94 | 99 | PF01111 | 0.559 |
DOC_CYCLIN_RxL_1 | 125 | 136 | PF00134 | 0.508 |
DOC_CYCLIN_yCln2_LP_2 | 399 | 405 | PF00134 | 0.419 |
DOC_CYCLIN_yCln2_LP_2 | 481 | 487 | PF00134 | 0.524 |
DOC_MAPK_DCC_7 | 49 | 58 | PF00069 | 0.333 |
DOC_MAPK_gen_1 | 220 | 227 | PF00069 | 0.504 |
DOC_MAPK_gen_1 | 301 | 310 | PF00069 | 0.485 |
DOC_MAPK_gen_1 | 534 | 542 | PF00069 | 0.559 |
DOC_MAPK_MEF2A_6 | 220 | 227 | PF00069 | 0.504 |
DOC_MAPK_MEF2A_6 | 49 | 58 | PF00069 | 0.333 |
DOC_MAPK_MEF2A_6 | 7 | 16 | PF00069 | 0.534 |
DOC_PP1_RVXF_1 | 174 | 180 | PF00149 | 0.535 |
DOC_PP1_RVXF_1 | 537 | 543 | PF00149 | 0.559 |
DOC_PP2B_LxvP_1 | 337 | 340 | PF13499 | 0.591 |
DOC_PP2B_LxvP_1 | 361 | 364 | PF13499 | 0.579 |
DOC_PP2B_LxvP_1 | 481 | 484 | PF13499 | 0.533 |
DOC_PP4_FxxP_1 | 310 | 313 | PF00568 | 0.622 |
DOC_PP4_FxxP_1 | 45 | 48 | PF00568 | 0.592 |
DOC_PP4_FxxP_1 | 542 | 545 | PF00568 | 0.456 |
DOC_PP4_FxxP_1 | 600 | 603 | PF00568 | 0.386 |
DOC_USP7_MATH_1 | 272 | 276 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 372 | 376 | PF00917 | 0.515 |
DOC_USP7_UBL2_3 | 565 | 569 | PF12436 | 0.412 |
DOC_WW_Pin1_4 | 135 | 140 | PF00397 | 0.559 |
DOC_WW_Pin1_4 | 547 | 552 | PF00397 | 0.492 |
DOC_WW_Pin1_4 | 579 | 584 | PF00397 | 0.699 |
DOC_WW_Pin1_4 | 594 | 599 | PF00397 | 0.573 |
DOC_WW_Pin1_4 | 93 | 98 | PF00397 | 0.555 |
LIG_14-3-3_CanoR_1 | 228 | 236 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 273 | 277 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 301 | 311 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 31 | 39 | PF00244 | 0.424 |
LIG_14-3-3_CanoR_1 | 415 | 419 | PF00244 | 0.549 |
LIG_Actin_WH2_2 | 552 | 567 | PF00022 | 0.445 |
LIG_APCC_ABBAyCdc20_2 | 537 | 543 | PF00400 | 0.531 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.630 |
LIG_BIR_III_2 | 578 | 582 | PF00653 | 0.759 |
LIG_BIR_III_2 | 89 | 93 | PF00653 | 0.531 |
LIG_BRCT_BRCA1_1 | 325 | 329 | PF00533 | 0.635 |
LIG_BRCT_BRCA1_1 | 596 | 600 | PF00533 | 0.361 |
LIG_CSL_BTD_1 | 479 | 482 | PF09270 | 0.465 |
LIG_EVH1_1 | 337 | 341 | PF00568 | 0.558 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.511 |
LIG_FHA_1 | 164 | 170 | PF00498 | 0.469 |
LIG_FHA_1 | 181 | 187 | PF00498 | 0.456 |
LIG_FHA_1 | 204 | 210 | PF00498 | 0.486 |
LIG_FHA_1 | 23 | 29 | PF00498 | 0.442 |
LIG_FHA_1 | 238 | 244 | PF00498 | 0.438 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.733 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.431 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.480 |
LIG_FHA_2 | 33 | 39 | PF00498 | 0.425 |
LIG_FHA_2 | 355 | 361 | PF00498 | 0.492 |
LIG_FHA_2 | 75 | 81 | PF00498 | 0.580 |
LIG_LIR_Apic_2 | 206 | 210 | PF02991 | 0.504 |
LIG_LIR_Apic_2 | 335 | 339 | PF02991 | 0.514 |
LIG_LIR_Apic_2 | 476 | 482 | PF02991 | 0.473 |
LIG_LIR_Apic_2 | 597 | 603 | PF02991 | 0.446 |
LIG_LIR_Gen_1 | 151 | 162 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 326 | 332 | PF02991 | 0.593 |
LIG_LIR_Nem_3 | 395 | 399 | PF02991 | 0.575 |
LIG_LYPXL_SIV_4 | 426 | 434 | PF13949 | 0.435 |
LIG_LYPXL_yS_3 | 396 | 399 | PF13949 | 0.493 |
LIG_MYND_1 | 397 | 401 | PF01753 | 0.468 |
LIG_MYND_3 | 559 | 563 | PF01753 | 0.450 |
LIG_Pex14_2 | 99 | 103 | PF04695 | 0.456 |
LIG_REV1ctd_RIR_1 | 96 | 105 | PF16727 | 0.504 |
LIG_SH2_CRK | 384 | 388 | PF00017 | 0.476 |
LIG_SH2_CRK | 558 | 562 | PF00017 | 0.438 |
LIG_SH2_NCK_1 | 120 | 124 | PF00017 | 0.486 |
LIG_SH2_NCK_1 | 88 | 92 | PF00017 | 0.504 |
LIG_SH2_SRC | 120 | 123 | PF00017 | 0.535 |
LIG_SH2_SRC | 336 | 339 | PF00017 | 0.580 |
LIG_SH2_STAP1 | 203 | 207 | PF00017 | 0.456 |
LIG_SH2_STAP1 | 403 | 407 | PF00017 | 0.392 |
LIG_SH2_STAP1 | 468 | 472 | PF00017 | 0.497 |
LIG_SH2_STAT3 | 149 | 152 | PF00017 | 0.535 |
LIG_SH2_STAT3 | 468 | 471 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 149 | 152 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 336 | 339 | PF00017 | 0.542 |
LIG_SH2_STAT5 | 428 | 431 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 468 | 471 | PF00017 | 0.506 |
LIG_SH3_1 | 336 | 342 | PF00018 | 0.639 |
LIG_SH3_3 | 308 | 314 | PF00018 | 0.584 |
LIG_SH3_3 | 335 | 341 | PF00018 | 0.623 |
LIG_SH3_3 | 391 | 397 | PF00018 | 0.513 |
LIG_SH3_3 | 430 | 436 | PF00018 | 0.529 |
LIG_SH3_3 | 45 | 51 | PF00018 | 0.596 |
LIG_SH3_3 | 578 | 584 | PF00018 | 0.741 |
LIG_SH3_3 | 592 | 598 | PF00018 | 0.310 |
LIG_SUMO_SIM_anti_2 | 129 | 134 | PF11976 | 0.448 |
LIG_SUMO_SIM_par_1 | 560 | 566 | PF11976 | 0.521 |
LIG_TRAF2_1 | 357 | 360 | PF00917 | 0.568 |
LIG_TRAF2_1 | 523 | 526 | PF00917 | 0.559 |
LIG_TYR_ITIM | 394 | 399 | PF00017 | 0.367 |
LIG_TYR_ITIM | 556 | 561 | PF00017 | 0.350 |
LIG_UBA3_1 | 561 | 569 | PF00899 | 0.520 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.334 |
MOD_CK1_1 | 191 | 197 | PF00069 | 0.453 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.685 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.144 |
MOD_CK1_1 | 279 | 285 | PF00069 | 0.720 |
MOD_CK1_1 | 315 | 321 | PF00069 | 0.644 |
MOD_CK1_1 | 324 | 330 | PF00069 | 0.610 |
MOD_CK1_1 | 344 | 350 | PF00069 | 0.328 |
MOD_CK1_1 | 375 | 381 | PF00069 | 0.663 |
MOD_CK1_1 | 440 | 446 | PF00069 | 0.650 |
MOD_CK1_1 | 470 | 476 | PF00069 | 0.503 |
MOD_CK2_1 | 285 | 291 | PF00069 | 0.609 |
MOD_CK2_1 | 354 | 360 | PF00069 | 0.491 |
MOD_CK2_1 | 579 | 585 | PF00069 | 0.644 |
MOD_CK2_1 | 74 | 80 | PF00069 | 0.575 |
MOD_DYRK1A_RPxSP_1 | 547 | 551 | PF00069 | 0.373 |
MOD_GlcNHglycan | 105 | 109 | PF01048 | 0.429 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.350 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.315 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.306 |
MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.309 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.681 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.625 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.553 |
MOD_GlcNHglycan | 378 | 381 | PF01048 | 0.619 |
MOD_GlcNHglycan | 439 | 442 | PF01048 | 0.648 |
MOD_GlcNHglycan | 524 | 530 | PF01048 | 0.453 |
MOD_GlcNHglycan | 591 | 594 | PF01048 | 0.393 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.387 |
MOD_GSK3_1 | 237 | 244 | PF00069 | 0.328 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.328 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.532 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.439 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.699 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.617 |
MOD_GSK3_1 | 372 | 379 | PF00069 | 0.669 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.399 |
MOD_N-GLC_1 | 321 | 326 | PF02516 | 0.589 |
MOD_NEK2_1 | 172 | 177 | PF00069 | 0.418 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.243 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.329 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.599 |
MOD_NEK2_1 | 376 | 381 | PF00069 | 0.477 |
MOD_NEK2_1 | 466 | 471 | PF00069 | 0.414 |
MOD_OFUCOSY | 319 | 325 | PF10250 | 0.573 |
MOD_PIKK_1 | 467 | 473 | PF00454 | 0.512 |
MOD_PIKK_1 | 5 | 11 | PF00454 | 0.607 |
MOD_PK_1 | 188 | 194 | PF00069 | 0.452 |
MOD_PKA_1 | 301 | 307 | PF00069 | 0.475 |
MOD_PKA_2 | 186 | 192 | PF00069 | 0.453 |
MOD_PKA_2 | 272 | 278 | PF00069 | 0.513 |
MOD_PKA_2 | 414 | 420 | PF00069 | 0.552 |
MOD_Plk_1 | 237 | 243 | PF00069 | 0.309 |
MOD_Plk_4 | 188 | 194 | PF00069 | 0.375 |
MOD_Plk_4 | 237 | 243 | PF00069 | 0.317 |
MOD_ProDKin_1 | 135 | 141 | PF00069 | 0.453 |
MOD_ProDKin_1 | 547 | 553 | PF00069 | 0.360 |
MOD_ProDKin_1 | 579 | 585 | PF00069 | 0.685 |
MOD_ProDKin_1 | 594 | 600 | PF00069 | 0.575 |
MOD_ProDKin_1 | 93 | 99 | PF00069 | 0.449 |
MOD_SUMO_rev_2 | 440 | 448 | PF00179 | 0.646 |
TRG_DiLeu_BaLyEn_6 | 448 | 453 | PF01217 | 0.450 |
TRG_DiLeu_BaLyEn_6 | 51 | 56 | PF01217 | 0.330 |
TRG_DiLeu_BaLyEn_6 | 557 | 562 | PF01217 | 0.428 |
TRG_ENDOCYTIC_2 | 396 | 399 | PF00928 | 0.548 |
TRG_ENDOCYTIC_2 | 558 | 561 | PF00928 | 0.356 |
TRG_ER_diArg_1 | 186 | 188 | PF00400 | 0.453 |
TRG_ER_diArg_1 | 221 | 223 | PF00400 | 0.469 |
TRG_ER_diArg_1 | 410 | 413 | PF00400 | 0.504 |
TRG_ER_diArg_1 | 533 | 536 | PF00400 | 0.418 |
TRG_ER_diArg_1 | 537 | 540 | PF00400 | 0.423 |
TRG_Pf-PMV_PEXEL_1 | 234 | 238 | PF00026 | 0.421 |
TRG_Pf-PMV_PEXEL_1 | 451 | 455 | PF00026 | 0.489 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0V4 | Leptomonas seymouri | 48% | 100% |
A0A1X0NK59 | Trypanosomatidae | 36% | 100% |
A0A3S7WPQ8 | Leishmania donovani | 93% | 98% |
A0A422NTD5 | Trypanosoma rangeli | 40% | 100% |
A4H4V6 | Leishmania braziliensis | 79% | 100% |
A4HT56 | Leishmania infantum | 93% | 98% |
C9ZUV8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
E9AL23 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q1QBM4 | Psychrobacter cryohalolentis (strain ATCC BAA-1226 / DSM 17306 / VKM B-2378 / K5) | 27% | 100% |
Q4FSB4 | Psychrobacter arcticus (strain DSM 17307 / VKM B-2377 / 273-4) | 27% | 100% |
Q5ZKW0 | Gallus gallus | 26% | 100% |
V5BDF2 | Trypanosoma cruzi | 38% | 100% |