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: E9AL23
Term | Name | Level | Count |
---|---|---|---|
GO:0002097 | tRNA wobble base modification | 7 | 1 |
GO:0002098 | tRNA wobble uridine modification | 8 | 1 |
GO:0002143 | tRNA wobble position uridine thiolation | 8 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006399 | tRNA metabolic process | 7 | 1 |
GO:0006400 | tRNA modification | 6 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008033 | tRNA processing | 8 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009451 | RNA modification | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0034227 | tRNA thio-modification | 7 | 1 |
GO:0034470 | ncRNA processing | 7 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034660 | ncRNA metabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
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 | 0.769 |
CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.360 |
CLV_NRD_NRD_1 | 221 | 223 | PF00675 | 0.331 |
CLV_NRD_NRD_1 | 385 | 387 | PF00675 | 0.632 |
CLV_NRD_NRD_1 | 415 | 417 | PF00675 | 0.581 |
CLV_NRD_NRD_1 | 536 | 538 | PF00675 | 0.351 |
CLV_PCSK_FUR_1 | 534 | 538 | PF00082 | 0.305 |
CLV_PCSK_KEX2_1 | 187 | 189 | PF00082 | 0.360 |
CLV_PCSK_KEX2_1 | 220 | 222 | PF00082 | 0.329 |
CLV_PCSK_KEX2_1 | 384 | 386 | PF00082 | 0.653 |
CLV_PCSK_KEX2_1 | 415 | 417 | PF00082 | 0.581 |
CLV_PCSK_KEX2_1 | 536 | 538 | PF00082 | 0.351 |
CLV_PCSK_PC1ET2_1 | 220 | 222 | PF00082 | 0.305 |
CLV_PCSK_SKI1_1 | 190 | 194 | PF00082 | 0.221 |
CLV_PCSK_SKI1_1 | 222 | 226 | PF00082 | 0.307 |
CLV_PCSK_SKI1_1 | 253 | 257 | PF00082 | 0.170 |
CLV_PCSK_SKI1_1 | 349 | 353 | PF00082 | 0.474 |
CLV_PCSK_SKI1_1 | 547 | 551 | PF00082 | 0.281 |
CLV_PCSK_SKI1_1 | 74 | 78 | PF00082 | 0.631 |
DEG_APCC_DBOX_1 | 385 | 393 | PF00400 | 0.405 |
DEG_SPOP_SBC_1 | 344 | 348 | PF00917 | 0.392 |
DOC_CKS1_1 | 94 | 99 | PF01111 | 0.455 |
DOC_CYCLIN_RxL_1 | 125 | 136 | PF00134 | 0.509 |
DOC_CYCLIN_yCln2_LP_2 | 399 | 405 | PF00134 | 0.416 |
DOC_CYCLIN_yCln2_LP_2 | 481 | 487 | PF00134 | 0.535 |
DOC_MAPK_gen_1 | 220 | 227 | PF00069 | 0.505 |
DOC_MAPK_gen_1 | 302 | 310 | PF00069 | 0.468 |
DOC_MAPK_gen_1 | 534 | 542 | PF00069 | 0.560 |
DOC_MAPK_MEF2A_6 | 220 | 227 | PF00069 | 0.505 |
DOC_MAPK_MEF2A_6 | 7 | 16 | PF00069 | 0.541 |
DOC_PP1_RVXF_1 | 174 | 180 | PF00149 | 0.537 |
DOC_PP1_RVXF_1 | 537 | 543 | PF00149 | 0.552 |
DOC_PP2B_LxvP_1 | 337 | 340 | PF13499 | 0.596 |
DOC_PP2B_LxvP_1 | 361 | 364 | PF13499 | 0.576 |
DOC_PP2B_LxvP_1 | 481 | 484 | PF13499 | 0.546 |
DOC_PP4_FxxP_1 | 310 | 313 | PF00568 | 0.617 |
DOC_PP4_FxxP_1 | 45 | 48 | PF00568 | 0.592 |
DOC_PP4_FxxP_1 | 542 | 545 | PF00568 | 0.457 |
DOC_USP7_MATH_1 | 272 | 276 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 292 | 296 | PF00917 | 0.341 |
DOC_USP7_MATH_1 | 344 | 348 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 375 | 379 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 436 | 440 | PF00917 | 0.512 |
DOC_USP7_UBL2_3 | 70 | 74 | PF12436 | 0.288 |
DOC_WW_Pin1_4 | 135 | 140 | PF00397 | 0.550 |
DOC_WW_Pin1_4 | 547 | 552 | PF00397 | 0.494 |
DOC_WW_Pin1_4 | 579 | 584 | PF00397 | 0.707 |
DOC_WW_Pin1_4 | 594 | 599 | PF00397 | 0.595 |
DOC_WW_Pin1_4 | 93 | 98 | PF00397 | 0.450 |
LIG_14-3-3_CanoR_1 | 187 | 193 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 228 | 236 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 273 | 277 | PF00244 | 0.547 |
LIG_14-3-3_CanoR_1 | 31 | 39 | PF00244 | 0.429 |
LIG_14-3-3_CanoR_1 | 415 | 419 | PF00244 | 0.568 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.631 |
LIG_BIR_III_2 | 578 | 582 | PF00653 | 0.770 |
LIG_BRCT_BRCA1_1 | 325 | 329 | PF00533 | 0.644 |
LIG_Clathr_ClatBox_1 | 561 | 565 | PF01394 | 0.375 |
LIG_CSL_BTD_1 | 479 | 482 | PF09270 | 0.485 |
LIG_EVH1_1 | 337 | 341 | PF00568 | 0.563 |
LIG_FHA_1 | 164 | 170 | PF00498 | 0.470 |
LIG_FHA_1 | 181 | 187 | PF00498 | 0.457 |
LIG_FHA_1 | 204 | 210 | PF00498 | 0.488 |
LIG_FHA_1 | 23 | 29 | PF00498 | 0.398 |
LIG_FHA_1 | 238 | 244 | PF00498 | 0.452 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.688 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.296 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.454 |
LIG_FHA_1 | 445 | 451 | PF00498 | 0.359 |
LIG_FHA_2 | 33 | 39 | PF00498 | 0.419 |
LIG_FHA_2 | 355 | 361 | PF00498 | 0.484 |
LIG_Integrin_RGD_1 | 576 | 578 | PF01839 | 0.616 |
LIG_LIR_Apic_2 | 206 | 210 | PF02991 | 0.505 |
LIG_LIR_Apic_2 | 335 | 339 | PF02991 | 0.526 |
LIG_LIR_Apic_2 | 476 | 482 | PF02991 | 0.492 |
LIG_LIR_Gen_1 | 151 | 162 | PF02991 | 0.486 |
LIG_LIR_Gen_1 | 85 | 95 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 326 | 332 | PF02991 | 0.605 |
LIG_LIR_Nem_3 | 395 | 399 | PF02991 | 0.562 |
LIG_LIR_Nem_3 | 85 | 91 | PF02991 | 0.534 |
LIG_LYPXL_SIV_4 | 426 | 434 | PF13949 | 0.441 |
LIG_LYPXL_yS_3 | 396 | 399 | PF13949 | 0.525 |
LIG_MYND_1 | 397 | 401 | PF01753 | 0.481 |
LIG_MYND_3 | 559 | 563 | PF01753 | 0.461 |
LIG_Pex14_2 | 99 | 103 | PF04695 | 0.457 |
LIG_PROFILIN_1 | 338 | 344 | PF00235 | 0.493 |
LIG_REV1ctd_RIR_1 | 96 | 105 | PF16727 | 0.505 |
LIG_SH2_CRK | 558 | 562 | PF00017 | 0.450 |
LIG_SH2_CRK | 88 | 92 | PF00017 | 0.298 |
LIG_SH2_NCK_1 | 120 | 124 | PF00017 | 0.488 |
LIG_SH2_NCK_1 | 88 | 92 | PF00017 | 0.512 |
LIG_SH2_SRC | 120 | 123 | PF00017 | 0.537 |
LIG_SH2_SRC | 336 | 339 | PF00017 | 0.590 |
LIG_SH2_STAP1 | 203 | 207 | PF00017 | 0.457 |
LIG_SH2_STAP1 | 403 | 407 | PF00017 | 0.391 |
LIG_SH2_STAP1 | 468 | 472 | PF00017 | 0.503 |
LIG_SH2_STAT3 | 149 | 152 | PF00017 | 0.537 |
LIG_SH2_STAT3 | 468 | 471 | PF00017 | 0.532 |
LIG_SH2_STAT5 | 149 | 152 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 336 | 339 | PF00017 | 0.551 |
LIG_SH2_STAT5 | 428 | 431 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 468 | 471 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 95 | 98 | PF00017 | 0.449 |
LIG_SH3_1 | 336 | 342 | PF00018 | 0.645 |
LIG_SH3_3 | 308 | 314 | PF00018 | 0.576 |
LIG_SH3_3 | 335 | 341 | PF00018 | 0.607 |
LIG_SH3_3 | 430 | 436 | PF00018 | 0.540 |
LIG_SH3_3 | 45 | 51 | PF00018 | 0.606 |
LIG_SH3_3 | 578 | 584 | PF00018 | 0.750 |
LIG_SH3_3 | 595 | 601 | PF00018 | 0.348 |
LIG_SUMO_SIM_par_1 | 560 | 566 | PF11976 | 0.525 |
LIG_TRAF2_1 | 357 | 360 | PF00917 | 0.555 |
LIG_TRAF2_1 | 523 | 526 | PF00917 | 0.560 |
LIG_TYR_ITIM | 556 | 561 | PF00017 | 0.360 |
LIG_UBA3_1 | 561 | 569 | PF00899 | 0.508 |
LIG_WW_2 | 53 | 56 | PF00397 | 0.357 |
MOD_CK1_1 | 191 | 197 | PF00069 | 0.455 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.677 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.145 |
MOD_CK1_1 | 324 | 330 | PF00069 | 0.660 |
MOD_CK1_1 | 347 | 353 | PF00069 | 0.549 |
MOD_CK1_1 | 373 | 379 | PF00069 | 0.625 |
MOD_CK1_1 | 440 | 446 | PF00069 | 0.660 |
MOD_CK1_1 | 470 | 476 | PF00069 | 0.507 |
MOD_CK1_1 | 597 | 603 | PF00069 | 0.641 |
MOD_CK2_1 | 354 | 360 | PF00069 | 0.465 |
MOD_CK2_1 | 494 | 500 | PF00069 | 0.282 |
MOD_CK2_1 | 579 | 585 | PF00069 | 0.714 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.424 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.365 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.332 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.366 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.318 |
MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.287 |
MOD_GlcNHglycan | 279 | 282 | PF01048 | 0.695 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.622 |
MOD_GlcNHglycan | 372 | 375 | PF01048 | 0.632 |
MOD_GlcNHglycan | 439 | 442 | PF01048 | 0.542 |
MOD_GlcNHglycan | 524 | 530 | PF01048 | 0.431 |
MOD_GlcNHglycan | 591 | 594 | PF01048 | 0.410 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.392 |
MOD_GSK3_1 | 237 | 244 | PF00069 | 0.330 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.450 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.680 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.584 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.667 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.571 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.477 |
MOD_N-GLC_1 | 444 | 449 | PF02516 | 0.367 |
MOD_NEK2_1 | 172 | 177 | PF00069 | 0.383 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.227 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.306 |
MOD_NEK2_1 | 345 | 350 | PF00069 | 0.574 |
MOD_NEK2_1 | 466 | 471 | PF00069 | 0.407 |
MOD_PIKK_1 | 297 | 303 | PF00454 | 0.290 |
MOD_PIKK_1 | 373 | 379 | PF00454 | 0.688 |
MOD_PIKK_1 | 467 | 473 | PF00454 | 0.513 |
MOD_PIKK_1 | 5 | 11 | PF00454 | 0.535 |
MOD_PK_1 | 188 | 194 | PF00069 | 0.453 |
MOD_PKA_1 | 302 | 308 | PF00069 | 0.477 |
MOD_PKA_1 | 385 | 391 | PF00069 | 0.417 |
MOD_PKA_2 | 186 | 192 | PF00069 | 0.455 |
MOD_PKA_2 | 272 | 278 | PF00069 | 0.452 |
MOD_PKA_2 | 385 | 391 | PF00069 | 0.649 |
MOD_PKA_2 | 414 | 420 | PF00069 | 0.570 |
MOD_Plk_1 | 237 | 243 | PF00069 | 0.310 |
MOD_Plk_1 | 444 | 450 | PF00069 | 0.350 |
MOD_Plk_1 | 494 | 500 | PF00069 | 0.498 |
MOD_Plk_4 | 193 | 199 | PF00069 | 0.395 |
MOD_Plk_4 | 237 | 243 | PF00069 | 0.310 |
MOD_ProDKin_1 | 135 | 141 | PF00069 | 0.441 |
MOD_ProDKin_1 | 547 | 553 | PF00069 | 0.361 |
MOD_ProDKin_1 | 579 | 585 | PF00069 | 0.698 |
MOD_ProDKin_1 | 594 | 600 | PF00069 | 0.605 |
MOD_ProDKin_1 | 93 | 99 | PF00069 | 0.450 |
MOD_SUMO_rev_2 | 439 | 448 | PF00179 | 0.658 |
TRG_DiLeu_BaLyEn_6 | 448 | 453 | PF01217 | 0.458 |
TRG_DiLeu_BaLyEn_6 | 557 | 562 | PF01217 | 0.440 |
TRG_ENDOCYTIC_2 | 396 | 399 | PF00928 | 0.583 |
TRG_ENDOCYTIC_2 | 558 | 561 | PF00928 | 0.366 |
TRG_ENDOCYTIC_2 | 88 | 91 | PF00928 | 0.432 |
TRG_ENDOCYTIC_2 | 95 | 98 | PF00928 | 0.275 |
TRG_ER_diArg_1 | 186 | 188 | PF00400 | 0.443 |
TRG_ER_diArg_1 | 221 | 223 | PF00400 | 0.417 |
TRG_ER_diArg_1 | 383 | 386 | PF00400 | 0.646 |
TRG_ER_diArg_1 | 410 | 413 | PF00400 | 0.498 |
TRG_ER_diArg_1 | 533 | 536 | PF00400 | 0.420 |
TRG_ER_diArg_1 | 537 | 540 | PF00400 | 0.419 |
TRG_Pf-PMV_PEXEL_1 | 234 | 238 | PF00026 | 0.409 |
TRG_Pf-PMV_PEXEL_1 | 451 | 455 | PF00026 | 0.495 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0V4 | Leptomonas seymouri | 48% | 100% |
A0A0S4J0D7 | Bodo saltans | 27% | 100% |
A0A1X0NK59 | Trypanosomatidae | 36% | 100% |
A0A3S7WPQ8 | Leishmania donovani | 90% | 98% |
A0A422NTD5 | Trypanosoma rangeli | 40% | 100% |
A4H4V6 | Leishmania braziliensis | 78% | 99% |
A4HT56 | Leishmania infantum | 90% | 98% |
C9ZUV8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
O13947 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 100% |
Q1QBM4 | Psychrobacter cryohalolentis (strain ATCC BAA-1226 / DSM 17306 / VKM B-2378 / K5) | 28% | 100% |
Q4FSB4 | Psychrobacter arcticus (strain DSM 17307 / VKM B-2377 / 273-4) | 28% | 100% |
Q4QIT1 | Leishmania major | 88% | 100% |
Q503J2 | Danio rerio | 25% | 100% |
Q5ZKW0 | Gallus gallus | 25% | 100% |
V5BDF2 | Trypanosoma cruzi | 39% | 100% |