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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005829 | cytosol | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S7WSX9
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 8 |
GO:0006396 | RNA processing | 6 | 8 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 8 |
GO:0006807 | nitrogen compound metabolic process | 2 | 8 |
GO:0008152 | metabolic process | 1 | 8 |
GO:0009987 | cellular process | 1 | 8 |
GO:0016070 | RNA metabolic process | 5 | 8 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 8 |
GO:0043170 | macromolecule metabolic process | 3 | 8 |
GO:0044237 | cellular metabolic process | 2 | 8 |
GO:0044238 | primary metabolic process | 2 | 8 |
GO:0046483 | heterocycle metabolic process | 3 | 8 |
GO:0071704 | organic substance metabolic process | 2 | 8 |
GO:0090304 | nucleic acid metabolic process | 4 | 8 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 8 |
GO:0001510 | RNA methylation | 4 | 1 |
GO:0002128 | tRNA nucleoside ribose methylation | 6 | 1 |
GO:0006399 | tRNA metabolic process | 7 | 1 |
GO:0006400 | tRNA modification | 6 | 1 |
GO:0008033 | tRNA processing | 8 | 1 |
GO:0009451 | RNA modification | 5 | 1 |
GO:0030488 | tRNA methylation | 5 | 1 |
GO:0032259 | methylation | 2 | 1 |
GO:0034470 | ncRNA processing | 7 | 1 |
GO:0034660 | ncRNA metabolic process | 6 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0043414 | macromolecule methylation | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 8 |
GO:0008168 | methyltransferase activity | 4 | 8 |
GO:0008173 | RNA methyltransferase activity | 4 | 8 |
GO:0016740 | transferase activity | 2 | 8 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 8 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 8 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 8 |
GO:0008171 | O-methyltransferase activity | 5 | 1 |
GO:0008175 | tRNA methyltransferase activity | 5 | 1 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 1 |
GO:0016300 | tRNA (uracil) methyltransferase activity | 6 | 1 |
GO:0016427 | tRNA (cytosine) methyltransferase activity | 6 | 1 |
GO:0052665 | tRNA (uracil-2'-O-)-methyltransferase activity | 7 | 1 |
GO:0052666 | tRNA (cytosine-2'-O-)-methyltransferase activity | 7 | 1 |
GO:0062105 | RNA 2'-O-methyltransferase activity | 5 | 1 |
GO:0106050 | tRNA 2'-O-methyltransferase activity | 6 | 1 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 1 |
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 256 | 260 | PF00656 | 0.536 |
CLV_MEL_PAP_1 | 283 | 289 | PF00089 | 0.464 |
CLV_NRD_NRD_1 | 191 | 193 | PF00675 | 0.473 |
CLV_NRD_NRD_1 | 61 | 63 | PF00675 | 0.693 |
CLV_NRD_NRD_1 | 76 | 78 | PF00675 | 0.695 |
CLV_PCSK_FUR_1 | 74 | 78 | PF00082 | 0.572 |
CLV_PCSK_KEX2_1 | 145 | 147 | PF00082 | 0.716 |
CLV_PCSK_KEX2_1 | 191 | 193 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 76 | 78 | PF00082 | 0.596 |
CLV_PCSK_PC1ET2_1 | 145 | 147 | PF00082 | 0.716 |
CLV_PCSK_PC7_1 | 72 | 78 | PF00082 | 0.555 |
CLV_PCSK_SKI1_1 | 113 | 117 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 191 | 195 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 390 | 394 | PF00082 | 0.620 |
CLV_PCSK_SKI1_1 | 470 | 474 | PF00082 | 0.508 |
DEG_SPOP_SBC_1 | 20 | 24 | PF00917 | 0.648 |
DEG_SPOP_SBC_1 | 47 | 51 | PF00917 | 0.665 |
DOC_CKS1_1 | 222 | 227 | PF01111 | 0.402 |
DOC_CYCLIN_yCln2_LP_2 | 240 | 246 | PF00134 | 0.514 |
DOC_CYCLIN_yCln2_LP_2 | 82 | 88 | PF00134 | 0.552 |
DOC_MAPK_gen_1 | 74 | 82 | PF00069 | 0.576 |
DOC_MAPK_MEF2A_6 | 319 | 326 | PF00069 | 0.450 |
DOC_PP1_SILK_1 | 229 | 234 | PF00149 | 0.382 |
DOC_PP2B_LxvP_1 | 324 | 327 | PF13499 | 0.425 |
DOC_PP2B_LxvP_1 | 82 | 85 | PF13499 | 0.473 |
DOC_PP4_FxxP_1 | 376 | 379 | PF00568 | 0.507 |
DOC_USP7_MATH_1 | 141 | 145 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.764 |
DOC_USP7_MATH_1 | 279 | 283 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 350 | 354 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.661 |
DOC_WW_Pin1_4 | 207 | 212 | PF00397 | 0.606 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.361 |
DOC_WW_Pin1_4 | 23 | 28 | PF00397 | 0.682 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.596 |
DOC_WW_Pin1_4 | 346 | 351 | PF00397 | 0.719 |
DOC_WW_Pin1_4 | 43 | 48 | PF00397 | 0.671 |
DOC_WW_Pin1_4 | 484 | 489 | PF00397 | 0.536 |
LIG_14-3-3_CanoR_1 | 157 | 167 | PF00244 | 0.782 |
LIG_FHA_1 | 109 | 115 | PF00498 | 0.472 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.660 |
LIG_FHA_1 | 305 | 311 | PF00498 | 0.522 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.690 |
LIG_FHA_1 | 391 | 397 | PF00498 | 0.668 |
LIG_FHA_1 | 437 | 443 | PF00498 | 0.419 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.651 |
LIG_FHA_1 | 98 | 104 | PF00498 | 0.578 |
LIG_FHA_2 | 159 | 165 | PF00498 | 0.699 |
LIG_FHA_2 | 183 | 189 | PF00498 | 0.444 |
LIG_FHA_2 | 268 | 274 | PF00498 | 0.753 |
LIG_LIR_Apic_2 | 373 | 379 | PF02991 | 0.407 |
LIG_LIR_Gen_1 | 125 | 132 | PF02991 | 0.577 |
LIG_LIR_Gen_1 | 330 | 340 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 125 | 131 | PF02991 | 0.573 |
LIG_LIR_Nem_3 | 330 | 336 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 467 | 472 | PF02991 | 0.479 |
LIG_Pex14_1 | 469 | 473 | PF04695 | 0.495 |
LIG_Rb_pABgroove_1 | 327 | 335 | PF01858 | 0.377 |
LIG_SH2_CRK | 445 | 449 | PF00017 | 0.426 |
LIG_SH2_NCK_1 | 372 | 376 | PF00017 | 0.468 |
LIG_SH2_SRC | 372 | 375 | PF00017 | 0.462 |
LIG_SH2_STAP1 | 128 | 132 | PF00017 | 0.569 |
LIG_SH2_STAP1 | 306 | 310 | PF00017 | 0.545 |
LIG_SH2_STAT3 | 340 | 343 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 306 | 309 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 404 | 407 | PF00017 | 0.334 |
LIG_SH3_3 | 216 | 222 | PF00018 | 0.405 |
LIG_SH3_3 | 344 | 350 | PF00018 | 0.598 |
LIG_SH3_3 | 423 | 429 | PF00018 | 0.372 |
LIG_SH3_3 | 78 | 84 | PF00018 | 0.562 |
LIG_SUMO_SIM_par_1 | 356 | 361 | PF11976 | 0.349 |
LIG_TRAF2_1 | 160 | 163 | PF00917 | 0.634 |
LIG_TRAF2_1 | 253 | 256 | PF00917 | 0.626 |
LIG_TYR_ITIM | 443 | 448 | PF00017 | 0.411 |
LIG_WRC_WIRS_1 | 287 | 292 | PF05994 | 0.430 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.564 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.716 |
MOD_CK1_1 | 260 | 266 | PF00069 | 0.649 |
MOD_CK1_1 | 267 | 273 | PF00069 | 0.642 |
MOD_CK1_1 | 304 | 310 | PF00069 | 0.523 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.522 |
MOD_CK1_1 | 377 | 383 | PF00069 | 0.559 |
MOD_CK1_1 | 46 | 52 | PF00069 | 0.806 |
MOD_CK1_1 | 464 | 470 | PF00069 | 0.492 |
MOD_CK2_1 | 182 | 188 | PF00069 | 0.455 |
MOD_CK2_1 | 250 | 256 | PF00069 | 0.707 |
MOD_CK2_1 | 267 | 273 | PF00069 | 0.751 |
MOD_DYRK1A_RPxSP_1 | 348 | 352 | PF00069 | 0.540 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.567 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.611 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.590 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.631 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.642 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.315 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.433 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.565 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.720 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.637 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.632 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.648 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.751 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.397 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.579 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.611 |
MOD_N-GLC_1 | 207 | 212 | PF02516 | 0.663 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.626 |
MOD_NEK2_1 | 290 | 295 | PF00069 | 0.369 |
MOD_NEK2_1 | 436 | 441 | PF00069 | 0.418 |
MOD_NEK2_1 | 482 | 487 | PF00069 | 0.500 |
MOD_NEK2_2 | 122 | 127 | PF00069 | 0.555 |
MOD_NEK2_2 | 279 | 284 | PF00069 | 0.524 |
MOD_PIKK_1 | 170 | 176 | PF00454 | 0.618 |
MOD_PIKK_1 | 377 | 383 | PF00454 | 0.608 |
MOD_PKA_2 | 158 | 164 | PF00069 | 0.744 |
MOD_PKA_2 | 170 | 176 | PF00069 | 0.611 |
MOD_PKA_2 | 446 | 452 | PF00069 | 0.360 |
MOD_PKA_2 | 482 | 488 | PF00069 | 0.561 |
MOD_PKB_1 | 284 | 292 | PF00069 | 0.454 |
MOD_Plk_1 | 162 | 168 | PF00069 | 0.637 |
MOD_Plk_4 | 162 | 168 | PF00069 | 0.709 |
MOD_Plk_4 | 286 | 292 | PF00069 | 0.541 |
MOD_ProDKin_1 | 207 | 213 | PF00069 | 0.589 |
MOD_ProDKin_1 | 221 | 227 | PF00069 | 0.357 |
MOD_ProDKin_1 | 23 | 29 | PF00069 | 0.682 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.598 |
MOD_ProDKin_1 | 346 | 352 | PF00069 | 0.714 |
MOD_ProDKin_1 | 43 | 49 | PF00069 | 0.672 |
TRG_DiLeu_BaLyEn_6 | 189 | 194 | PF01217 | 0.460 |
TRG_DiLeu_BaLyEn_6 | 210 | 215 | PF01217 | 0.487 |
TRG_ENDOCYTIC_2 | 128 | 131 | PF00928 | 0.588 |
TRG_ENDOCYTIC_2 | 445 | 448 | PF00928 | 0.422 |
TRG_ENDOCYTIC_2 | 95 | 98 | PF00928 | 0.545 |
TRG_ER_diArg_1 | 190 | 192 | PF00400 | 0.469 |
TRG_ER_diArg_1 | 283 | 286 | PF00400 | 0.515 |
TRG_ER_diArg_1 | 481 | 484 | PF00400 | 0.486 |
TRG_ER_diArg_1 | 73 | 76 | PF00400 | 0.654 |
TRG_Pf-PMV_PEXEL_1 | 130 | 134 | PF00026 | 0.592 |
TRG_Pf-PMV_PEXEL_1 | 191 | 196 | PF00026 | 0.415 |
TRG_Pf-PMV_PEXEL_1 | 319 | 323 | PF00026 | 0.472 |