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: E9APQ4
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_MEL_PAP_1 | 302 | 308 | PF00089 | 0.460 |
CLV_NRD_NRD_1 | 210 | 212 | PF00675 | 0.489 |
CLV_NRD_NRD_1 | 314 | 316 | PF00675 | 0.337 |
CLV_NRD_NRD_1 | 80 | 82 | PF00675 | 0.585 |
CLV_NRD_NRD_1 | 95 | 97 | PF00675 | 0.475 |
CLV_PCSK_FUR_1 | 93 | 97 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 164 | 166 | PF00082 | 0.697 |
CLV_PCSK_KEX2_1 | 210 | 212 | PF00082 | 0.489 |
CLV_PCSK_KEX2_1 | 314 | 316 | PF00082 | 0.337 |
CLV_PCSK_KEX2_1 | 95 | 97 | PF00082 | 0.475 |
CLV_PCSK_PC1ET2_1 | 164 | 166 | PF00082 | 0.697 |
CLV_PCSK_PC7_1 | 206 | 212 | PF00082 | 0.352 |
CLV_PCSK_PC7_1 | 91 | 97 | PF00082 | 0.464 |
CLV_PCSK_SKI1_1 | 206 | 210 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 409 | 413 | PF00082 | 0.575 |
CLV_PCSK_SKI1_1 | 489 | 493 | PF00082 | 0.511 |
DEG_APCC_DBOX_1 | 205 | 213 | PF00400 | 0.300 |
DEG_SPOP_SBC_1 | 369 | 373 | PF00917 | 0.366 |
DEG_SPOP_SBC_1 | 66 | 70 | PF00917 | 0.644 |
DOC_CKS1_1 | 241 | 246 | PF01111 | 0.398 |
DOC_CYCLIN_yCln2_LP_2 | 101 | 107 | PF00134 | 0.500 |
DOC_CYCLIN_yCln2_LP_2 | 259 | 265 | PF00134 | 0.516 |
DOC_MAPK_gen_1 | 93 | 101 | PF00069 | 0.452 |
DOC_MAPK_MEF2A_6 | 338 | 345 | PF00069 | 0.446 |
DOC_PP1_SILK_1 | 248 | 253 | PF00149 | 0.381 |
DOC_PP2B_LxvP_1 | 101 | 104 | PF13499 | 0.415 |
DOC_PP2B_LxvP_1 | 343 | 346 | PF13499 | 0.455 |
DOC_PP4_FxxP_1 | 395 | 398 | PF00568 | 0.474 |
DOC_USP7_MATH_1 | 189 | 193 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 281 | 285 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.519 |
DOC_USP7_MATH_1 | 369 | 373 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.807 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.660 |
DOC_WW_Pin1_4 | 226 | 231 | PF00397 | 0.603 |
DOC_WW_Pin1_4 | 240 | 245 | PF00397 | 0.328 |
DOC_WW_Pin1_4 | 365 | 370 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.604 |
DOC_WW_Pin1_4 | 503 | 508 | PF00397 | 0.524 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.667 |
LIG_14-3-3_CanoR_1 | 176 | 186 | PF00244 | 0.739 |
LIG_14-3-3_CanoR_1 | 367 | 377 | PF00244 | 0.341 |
LIG_BRCT_BRCA1_1 | 13 | 17 | PF00533 | 0.355 |
LIG_Clathr_ClatBox_1 | 404 | 408 | PF01394 | 0.399 |
LIG_FHA_1 | 117 | 123 | PF00498 | 0.527 |
LIG_FHA_1 | 128 | 134 | PF00498 | 0.523 |
LIG_FHA_1 | 271 | 277 | PF00498 | 0.763 |
LIG_FHA_1 | 410 | 416 | PF00498 | 0.632 |
LIG_FHA_1 | 456 | 462 | PF00498 | 0.416 |
LIG_FHA_1 | 57 | 63 | PF00498 | 0.614 |
LIG_FHA_1 | 7 | 13 | PF00498 | 0.356 |
LIG_FHA_2 | 178 | 184 | PF00498 | 0.705 |
LIG_FHA_2 | 202 | 208 | PF00498 | 0.489 |
LIG_FHA_2 | 287 | 293 | PF00498 | 0.760 |
LIG_LIR_Apic_2 | 156 | 162 | PF02991 | 0.523 |
LIG_LIR_Apic_2 | 392 | 398 | PF02991 | 0.382 |
LIG_LIR_Gen_1 | 144 | 154 | PF02991 | 0.575 |
LIG_LIR_Gen_1 | 16 | 25 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 349 | 359 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 144 | 150 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 16 | 21 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 349 | 355 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 486 | 491 | PF02991 | 0.482 |
LIG_NRBOX | 208 | 214 | PF00104 | 0.430 |
LIG_Pex14_1 | 13 | 17 | PF04695 | 0.339 |
LIG_Pex14_1 | 488 | 492 | PF04695 | 0.500 |
LIG_Rb_pABgroove_1 | 346 | 354 | PF01858 | 0.371 |
LIG_SH2_CRK | 159 | 163 | PF00017 | 0.525 |
LIG_SH2_CRK | 464 | 468 | PF00017 | 0.428 |
LIG_SH2_NCK_1 | 147 | 151 | PF00017 | 0.523 |
LIG_SH2_NCK_1 | 159 | 163 | PF00017 | 0.509 |
LIG_SH2_NCK_1 | 391 | 395 | PF00017 | 0.453 |
LIG_SH2_SRC | 325 | 328 | PF00017 | 0.458 |
LIG_SH2_SRC | 391 | 394 | PF00017 | 0.452 |
LIG_SH2_STAP1 | 325 | 329 | PF00017 | 0.516 |
LIG_SH2_STAT3 | 359 | 362 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 423 | 426 | PF00017 | 0.329 |
LIG_SH3_3 | 235 | 241 | PF00018 | 0.400 |
LIG_SH3_3 | 442 | 448 | PF00018 | 0.364 |
LIG_SH3_3 | 97 | 103 | PF00018 | 0.428 |
LIG_SUMO_SIM_par_1 | 375 | 380 | PF11976 | 0.338 |
LIG_TRAF2_1 | 179 | 182 | PF00917 | 0.634 |
LIG_TYR_ITIM | 462 | 467 | PF00017 | 0.414 |
LIG_WRC_WIRS_1 | 306 | 311 | PF05994 | 0.427 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.527 |
MOD_CK1_1 | 160 | 166 | PF00069 | 0.642 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.583 |
MOD_CK1_1 | 279 | 285 | PF00069 | 0.696 |
MOD_CK1_1 | 286 | 292 | PF00069 | 0.662 |
MOD_CK1_1 | 368 | 374 | PF00069 | 0.537 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.496 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.705 |
MOD_CK1_1 | 481 | 487 | PF00069 | 0.516 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.714 |
MOD_CK2_1 | 148 | 154 | PF00069 | 0.719 |
MOD_CK2_1 | 177 | 183 | PF00069 | 0.653 |
MOD_CK2_1 | 201 | 207 | PF00069 | 0.497 |
MOD_CK2_1 | 286 | 292 | PF00069 | 0.787 |
MOD_CK2_1 | 74 | 80 | PF00069 | 0.451 |
MOD_Cter_Amidation | 312 | 315 | PF01082 | 0.279 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.517 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.536 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.667 |
MOD_GlcNHglycan | 296 | 299 | PF01048 | 0.646 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.316 |
MOD_GlcNHglycan | 432 | 435 | PF01048 | 0.435 |
MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.424 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.508 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.665 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.717 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.571 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.661 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.703 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.731 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.461 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.561 |
MOD_GSK3_1 | 396 | 403 | PF00069 | 0.460 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.621 |
MOD_N-GLC_1 | 224 | 229 | PF02516 | 0.659 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.598 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.368 |
MOD_NEK2_1 | 455 | 460 | PF00069 | 0.414 |
MOD_NEK2_1 | 501 | 506 | PF00069 | 0.513 |
MOD_NEK2_2 | 13 | 18 | PF00069 | 0.370 |
MOD_NEK2_2 | 141 | 146 | PF00069 | 0.607 |
MOD_NEK2_2 | 283 | 288 | PF00069 | 0.524 |
MOD_NEK2_2 | 298 | 303 | PF00069 | 0.522 |
MOD_PIKK_1 | 157 | 163 | PF00454 | 0.652 |
MOD_PIKK_1 | 189 | 195 | PF00454 | 0.619 |
MOD_PIKK_1 | 396 | 402 | PF00454 | 0.545 |
MOD_PKA_2 | 177 | 183 | PF00069 | 0.699 |
MOD_PKA_2 | 189 | 195 | PF00069 | 0.544 |
MOD_PKA_2 | 279 | 285 | PF00069 | 0.528 |
MOD_PKA_2 | 465 | 471 | PF00069 | 0.413 |
MOD_PKA_2 | 501 | 507 | PF00069 | 0.585 |
MOD_PKB_1 | 303 | 311 | PF00069 | 0.451 |
MOD_Plk_1 | 153 | 159 | PF00069 | 0.573 |
MOD_Plk_1 | 181 | 187 | PF00069 | 0.630 |
MOD_Plk_4 | 181 | 187 | PF00069 | 0.805 |
MOD_Plk_4 | 305 | 311 | PF00069 | 0.429 |
MOD_Plk_4 | 400 | 406 | PF00069 | 0.390 |
MOD_Plk_4 | 8 | 14 | PF00069 | 0.427 |
MOD_ProDKin_1 | 226 | 232 | PF00069 | 0.586 |
MOD_ProDKin_1 | 240 | 246 | PF00069 | 0.324 |
MOD_ProDKin_1 | 365 | 371 | PF00069 | 0.697 |
MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.681 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.604 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.667 |
MOD_SUMO_rev_2 | 77 | 83 | PF00179 | 0.427 |
TRG_DiLeu_BaLyEn_6 | 208 | 213 | PF01217 | 0.478 |
TRG_DiLeu_BaLyEn_6 | 229 | 234 | PF01217 | 0.479 |
TRG_ENDOCYTIC_2 | 114 | 117 | PF00928 | 0.481 |
TRG_ENDOCYTIC_2 | 147 | 150 | PF00928 | 0.605 |
TRG_ENDOCYTIC_2 | 464 | 467 | PF00928 | 0.425 |
TRG_ER_diArg_1 | 209 | 211 | PF00400 | 0.484 |
TRG_ER_diArg_1 | 302 | 305 | PF00400 | 0.499 |
TRG_ER_diArg_1 | 314 | 316 | PF00400 | 0.440 |
TRG_ER_diArg_1 | 500 | 503 | PF00400 | 0.477 |
TRG_ER_diArg_1 | 92 | 95 | PF00400 | 0.464 |
TRG_Pf-PMV_PEXEL_1 | 210 | 215 | PF00026 | 0.434 |
TRG_Pf-PMV_PEXEL_1 | 338 | 342 | PF00026 | 0.465 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IIC5 | Leptomonas seymouri | 45% | 98% |
A0A3S7WSX9 | Leishmania donovani | 89% | 100% |
A4H7L7 | Leishmania braziliensis | 70% | 100% |
A4HW02 | Leishmania infantum | 89% | 100% |
Q4QFS5 | Leishmania major | 89% | 100% |
V5BIX5 | Trypanosoma cruzi | 30% | 100% |