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: A4H4V6
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 | 559 | 563 | PF00656 | 0.635 |
CLV_NRD_NRD_1 | 183 | 185 | PF00675 | 0.296 |
CLV_NRD_NRD_1 | 399 | 401 | PF00675 | 0.612 |
CLV_PCSK_KEX2_1 | 183 | 185 | PF00082 | 0.296 |
CLV_PCSK_KEX2_1 | 399 | 401 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 76 | 78 | PF00082 | 0.476 |
CLV_PCSK_PC1ET2_1 | 76 | 78 | PF00082 | 0.429 |
CLV_PCSK_SKI1_1 | 473 | 477 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 531 | 535 | PF00082 | 0.266 |
CLV_PCSK_SKI1_1 | 70 | 74 | PF00082 | 0.663 |
DEG_APCC_DBOX_1 | 60 | 68 | PF00400 | 0.278 |
DOC_ANK_TNKS_1 | 398 | 405 | PF00023 | 0.581 |
DOC_CKS1_1 | 71 | 76 | PF01111 | 0.537 |
DOC_CKS1_1 | 90 | 95 | PF01111 | 0.496 |
DOC_CYCLIN_RxL_1 | 121 | 132 | PF00134 | 0.518 |
DOC_CYCLIN_yCln2_LP_2 | 465 | 471 | PF00134 | 0.435 |
DOC_MAPK_gen_1 | 286 | 294 | PF00069 | 0.454 |
DOC_MAPK_gen_1 | 518 | 526 | PF00069 | 0.536 |
DOC_MAPK_MEF2A_6 | 3 | 12 | PF00069 | 0.435 |
DOC_MAPK_MEF2A_6 | 462 | 469 | PF00069 | 0.406 |
DOC_MAPK_NFAT4_5 | 462 | 470 | PF00069 | 0.264 |
DOC_PP1_RVXF_1 | 170 | 176 | PF00149 | 0.536 |
DOC_PP1_RVXF_1 | 521 | 527 | PF00149 | 0.496 |
DOC_PP2B_LxvP_1 | 321 | 324 | PF13499 | 0.534 |
DOC_PP2B_LxvP_1 | 345 | 348 | PF13499 | 0.495 |
DOC_PP2B_LxvP_1 | 465 | 468 | PF13499 | 0.564 |
DOC_PP4_FxxP_1 | 294 | 297 | PF00568 | 0.496 |
DOC_PP4_FxxP_1 | 41 | 44 | PF00568 | 0.496 |
DOC_PP4_FxxP_1 | 526 | 529 | PF00568 | 0.442 |
DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.384 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.384 |
DOC_USP7_MATH_1 | 267 | 271 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 541 | 545 | PF00917 | 0.451 |
DOC_USP7_MATH_1 | 585 | 589 | PF00917 | 0.482 |
DOC_WW_Pin1_4 | 1 | 6 | PF00397 | 0.364 |
DOC_WW_Pin1_4 | 131 | 136 | PF00397 | 0.512 |
DOC_WW_Pin1_4 | 367 | 372 | PF00397 | 0.451 |
DOC_WW_Pin1_4 | 531 | 536 | PF00397 | 0.480 |
DOC_WW_Pin1_4 | 581 | 586 | PF00397 | 0.394 |
DOC_WW_Pin1_4 | 70 | 75 | PF00397 | 0.505 |
DOC_WW_Pin1_4 | 84 | 89 | PF00397 | 0.568 |
LIG_14-3-3_CanoR_1 | 223 | 231 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 27 | 35 | PF00244 | 0.435 |
LIG_14-3-3_CanoR_1 | 303 | 313 | PF00244 | 0.402 |
LIG_14-3-3_CanoR_1 | 366 | 373 | PF00244 | 0.453 |
LIG_14-3-3_CanoR_1 | 473 | 482 | PF00244 | 0.442 |
LIG_APCC_ABBAyCdc20_2 | 521 | 527 | PF00400 | 0.479 |
LIG_BIR_III_2 | 357 | 361 | PF00653 | 0.483 |
LIG_BIR_III_2 | 562 | 566 | PF00653 | 0.568 |
LIG_BIR_III_2 | 85 | 89 | PF00653 | 0.440 |
LIG_BRCT_BRCA1_1 | 137 | 141 | PF00533 | 0.388 |
LIG_BRCT_BRCA1_1 | 247 | 251 | PF00533 | 0.384 |
LIG_BRCT_BRCA1_1 | 309 | 313 | PF00533 | 0.513 |
LIG_BRCT_BRCA1_1 | 369 | 373 | PF00533 | 0.454 |
LIG_CSL_BTD_1 | 463 | 466 | PF09270 | 0.460 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.511 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.442 |
LIG_FHA_1 | 177 | 183 | PF00498 | 0.543 |
LIG_FHA_1 | 200 | 206 | PF00498 | 0.485 |
LIG_FHA_1 | 354 | 360 | PF00498 | 0.668 |
LIG_FHA_1 | 541 | 547 | PF00498 | 0.512 |
LIG_FHA_1 | 568 | 574 | PF00498 | 0.281 |
LIG_FHA_2 | 29 | 35 | PF00498 | 0.404 |
LIG_FHA_2 | 339 | 345 | PF00498 | 0.507 |
LIG_Integrin_RGD_1 | 207 | 209 | PF01839 | 0.315 |
LIG_LIR_Apic_2 | 319 | 323 | PF02991 | 0.449 |
LIG_LIR_Apic_2 | 460 | 466 | PF02991 | 0.474 |
LIG_LIR_Apic_2 | 576 | 581 | PF02991 | 0.436 |
LIG_LIR_Gen_1 | 147 | 158 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 310 | 316 | PF02991 | 0.575 |
LIG_LIR_Nem_3 | 370 | 376 | PF02991 | 0.555 |
LIG_Pex14_2 | 95 | 99 | PF04695 | 0.442 |
LIG_SH2_CRK | 542 | 546 | PF00017 | 0.537 |
LIG_SH2_NCK_1 | 116 | 120 | PF00017 | 0.473 |
LIG_SH2_SRC | 116 | 119 | PF00017 | 0.536 |
LIG_SH2_SRC | 320 | 323 | PF00017 | 0.534 |
LIG_SH2_STAP1 | 199 | 203 | PF00017 | 0.456 |
LIG_SH2_STAP1 | 387 | 391 | PF00017 | 0.367 |
LIG_SH2_STAP1 | 452 | 456 | PF00017 | 0.463 |
LIG_SH2_STAP1 | 542 | 546 | PF00017 | 0.422 |
LIG_SH2_STAT3 | 145 | 148 | PF00017 | 0.536 |
LIG_SH2_STAT3 | 452 | 455 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 320 | 323 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 412 | 415 | PF00017 | 0.355 |
LIG_SH2_STAT5 | 452 | 455 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 542 | 545 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 91 | 94 | PF00017 | 0.435 |
LIG_SH3_1 | 320 | 326 | PF00018 | 0.496 |
LIG_SH3_3 | 292 | 298 | PF00018 | 0.536 |
LIG_SH3_3 | 320 | 326 | PF00018 | 0.548 |
LIG_SH3_3 | 41 | 47 | PF00018 | 0.616 |
LIG_SH3_3 | 414 | 420 | PF00018 | 0.502 |
LIG_SH3_3 | 562 | 568 | PF00018 | 0.617 |
LIG_SH3_3 | 584 | 590 | PF00018 | 0.458 |
LIG_SUMO_SIM_anti_2 | 125 | 130 | PF11976 | 0.427 |
LIG_SUMO_SIM_par_1 | 543 | 550 | PF11976 | 0.509 |
LIG_TRAF2_1 | 341 | 344 | PF00917 | 0.593 |
LIG_TRAF2_1 | 507 | 510 | PF00917 | 0.505 |
LIG_TRAF2_1 | 547 | 550 | PF00917 | 0.320 |
LIG_TYR_ITIM | 540 | 545 | PF00017 | 0.318 |
LIG_UBA3_1 | 67 | 76 | PF00899 | 0.389 |
LIG_WRC_WIRS_1 | 313 | 318 | PF05994 | 0.322 |
LIG_WW_2 | 49 | 52 | PF00397 | 0.337 |
LIG_WW_3 | 322 | 326 | PF00397 | 0.356 |
MOD_CDC14_SPxK_1 | 4 | 7 | PF00782 | 0.300 |
MOD_CDK_SPxK_1 | 1 | 7 | PF00069 | 0.351 |
MOD_CDK_SPxK_1 | 70 | 76 | PF00069 | 0.426 |
MOD_CDK_SPxxK_3 | 70 | 77 | PF00069 | 0.431 |
MOD_CK1_1 | 187 | 193 | PF00069 | 0.361 |
MOD_CK1_1 | 299 | 305 | PF00069 | 0.684 |
MOD_CK1_1 | 308 | 314 | PF00069 | 0.647 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.481 |
MOD_CK1_1 | 424 | 430 | PF00069 | 0.663 |
MOD_CK1_1 | 454 | 460 | PF00069 | 0.487 |
MOD_CK2_1 | 338 | 344 | PF00069 | 0.504 |
MOD_Cter_Amidation | 74 | 77 | PF01082 | 0.453 |
MOD_DYRK1A_RPxSP_1 | 531 | 535 | PF00069 | 0.347 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.439 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.362 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.352 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.356 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.297 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.297 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.419 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.353 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.650 |
MOD_GlcNHglycan | 423 | 426 | PF01048 | 0.642 |
MOD_GlcNHglycan | 508 | 514 | PF01048 | 0.379 |
MOD_GlcNHglycan | 575 | 578 | PF01048 | 0.384 |
MOD_GlcNHglycan | 587 | 590 | PF01048 | 0.503 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.358 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.389 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.297 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.328 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.337 |
MOD_GSK3_1 | 267 | 274 | PF00069 | 0.355 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.612 |
MOD_GSK3_1 | 450 | 457 | PF00069 | 0.429 |
MOD_GSK3_1 | 581 | 588 | PF00069 | 0.415 |
MOD_LATS_1 | 471 | 477 | PF00433 | 0.302 |
MOD_N-GLC_1 | 203 | 208 | PF02516 | 0.197 |
MOD_N-GLC_1 | 305 | 310 | PF02516 | 0.613 |
MOD_N-GLC_1 | 556 | 561 | PF02516 | 0.481 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.431 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.261 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.330 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.405 |
MOD_NEK2_1 | 328 | 333 | PF00069 | 0.562 |
MOD_NEK2_1 | 450 | 455 | PF00069 | 0.375 |
MOD_PIKK_1 | 451 | 457 | PF00454 | 0.412 |
MOD_PKA_1 | 286 | 292 | PF00069 | 0.282 |
MOD_PKA_1 | 76 | 82 | PF00069 | 0.430 |
MOD_PKA_2 | 182 | 188 | PF00069 | 0.355 |
MOD_PKA_2 | 365 | 371 | PF00069 | 0.474 |
MOD_PKA_2 | 398 | 404 | PF00069 | 0.608 |
MOD_PKA_2 | 517 | 523 | PF00069 | 0.244 |
MOD_PKA_2 | 76 | 82 | PF00069 | 0.529 |
MOD_Plk_1 | 232 | 238 | PF00069 | 0.279 |
MOD_Plk_4 | 189 | 195 | PF00069 | 0.388 |
MOD_Plk_4 | 232 | 238 | PF00069 | 0.321 |
MOD_Plk_4 | 312 | 318 | PF00069 | 0.395 |
MOD_Plk_4 | 359 | 365 | PF00069 | 0.483 |
MOD_Plk_4 | 541 | 547 | PF00069 | 0.376 |
MOD_ProDKin_1 | 1 | 7 | PF00069 | 0.351 |
MOD_ProDKin_1 | 131 | 137 | PF00069 | 0.376 |
MOD_ProDKin_1 | 367 | 373 | PF00069 | 0.454 |
MOD_ProDKin_1 | 531 | 537 | PF00069 | 0.331 |
MOD_ProDKin_1 | 581 | 587 | PF00069 | 0.404 |
MOD_ProDKin_1 | 70 | 76 | PF00069 | 0.506 |
MOD_ProDKin_1 | 84 | 90 | PF00069 | 0.564 |
MOD_SUMO_rev_2 | 424 | 432 | PF00179 | 0.545 |
TRG_DiLeu_BaLyEn_6 | 324 | 329 | PF01217 | 0.489 |
TRG_ENDOCYTIC_2 | 542 | 545 | PF00928 | 0.364 |
TRG_ENDOCYTIC_2 | 91 | 94 | PF00928 | 0.248 |
TRG_ER_diArg_1 | 182 | 184 | PF00400 | 0.355 |
TRG_ER_diArg_1 | 394 | 397 | PF00400 | 0.534 |
TRG_ER_diArg_1 | 483 | 486 | PF00400 | 0.355 |
TRG_ER_diArg_1 | 521 | 524 | PF00400 | 0.414 |
TRG_Pf-PMV_PEXEL_1 | 229 | 233 | PF00026 | 0.410 |
TRG_Pf-PMV_PEXEL_1 | 435 | 439 | PF00026 | 0.538 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0V4 | Leptomonas seymouri | 49% | 100% |
A0A1X0NK59 | Trypanosomatidae | 38% | 100% |
A0A3S7WPQ8 | Leishmania donovani | 79% | 97% |
A0A422NTD5 | Trypanosoma rangeli | 41% | 100% |
A4HT56 | Leishmania infantum | 79% | 97% |
C9ZUV8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
E9AL23 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 98% |
Q4QIT1 | Leishmania major | 79% | 100% |
V5BDF2 | Trypanosoma cruzi | 39% | 100% |