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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
Related structures:
AlphaFold database: E9AJK1
Term | Name | Level | Count |
---|---|---|---|
GO:0001510 | RNA methylation | 4 | 11 |
GO:0002128 | tRNA nucleoside ribose methylation | 6 | 11 |
GO:0002181 | cytoplasmic translation | 5 | 11 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
GO:0006396 | RNA processing | 6 | 11 |
GO:0006399 | tRNA metabolic process | 7 | 11 |
GO:0006400 | tRNA modification | 6 | 11 |
GO:0006412 | translation | 4 | 11 |
GO:0006518 | peptide metabolic process | 4 | 11 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008033 | tRNA processing | 8 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009058 | biosynthetic process | 2 | 11 |
GO:0009059 | macromolecule biosynthetic process | 4 | 11 |
GO:0009451 | RNA modification | 5 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016070 | RNA metabolic process | 5 | 11 |
GO:0019538 | protein metabolic process | 3 | 11 |
GO:0030488 | tRNA methylation | 5 | 11 |
GO:0032259 | methylation | 2 | 11 |
GO:0034470 | ncRNA processing | 7 | 11 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
GO:0034645 | obsolete cellular macromolecule biosynthetic process | 4 | 11 |
GO:0034660 | ncRNA metabolic process | 6 | 11 |
GO:0043043 | peptide biosynthetic process | 5 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0043412 | macromolecule modification | 4 | 11 |
GO:0043414 | macromolecule methylation | 3 | 11 |
GO:0043603 | amide metabolic process | 3 | 11 |
GO:0043604 | amide biosynthetic process | 4 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0044249 | cellular biosynthetic process | 3 | 11 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 11 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 11 |
GO:0046483 | heterocycle metabolic process | 3 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0090304 | nucleic acid metabolic process | 4 | 11 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 11 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 11 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 11 |
GO:1901576 | organic substance biosynthetic process | 3 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0008168 | methyltransferase activity | 4 | 11 |
GO:0008173 | RNA methyltransferase activity | 4 | 11 |
GO:0008175 | tRNA methyltransferase activity | 5 | 11 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 11 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 11 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 11 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 336 | 340 | PF00656 | 0.458 |
CLV_C14_Caspase3-7 | 423 | 427 | PF00656 | 0.751 |
CLV_NRD_NRD_1 | 14 | 16 | PF00675 | 0.389 |
CLV_NRD_NRD_1 | 159 | 161 | PF00675 | 0.276 |
CLV_PCSK_KEX2_1 | 14 | 16 | PF00082 | 0.389 |
CLV_PCSK_KEX2_1 | 431 | 433 | PF00082 | 0.509 |
CLV_PCSK_KEX2_1 | 8 | 10 | PF00082 | 0.453 |
CLV_PCSK_PC1ET2_1 | 431 | 433 | PF00082 | 0.509 |
CLV_PCSK_PC1ET2_1 | 8 | 10 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 14 | 18 | PF00082 | 0.387 |
CLV_PCSK_SKI1_1 | 230 | 234 | PF00082 | 0.292 |
DEG_APCC_DBOX_1 | 251 | 259 | PF00400 | 0.447 |
DEG_SPOP_SBC_1 | 126 | 130 | PF00917 | 0.396 |
DEG_SPOP_SBC_1 | 278 | 282 | PF00917 | 0.543 |
DOC_CYCLIN_yCln2_LP_2 | 399 | 405 | PF00134 | 0.577 |
DOC_MAPK_gen_1 | 160 | 166 | PF00069 | 0.460 |
DOC_PP2B_LxvP_1 | 124 | 127 | PF13499 | 0.526 |
DOC_PP2B_LxvP_1 | 399 | 402 | PF13499 | 0.545 |
DOC_PP4_FxxP_1 | 210 | 213 | PF00568 | 0.446 |
DOC_PP4_FxxP_1 | 251 | 254 | PF00568 | 0.383 |
DOC_USP7_MATH_1 | 141 | 145 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 234 | 238 | PF00917 | 0.443 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 279 | 283 | PF00917 | 0.515 |
DOC_USP7_MATH_1 | 305 | 309 | PF00917 | 0.733 |
DOC_USP7_MATH_1 | 409 | 413 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 425 | 429 | PF00917 | 0.678 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.548 |
DOC_WW_Pin1_4 | 315 | 320 | PF00397 | 0.567 |
DOC_WW_Pin1_4 | 37 | 42 | PF00397 | 0.413 |
DOC_WW_Pin1_4 | 434 | 439 | PF00397 | 0.683 |
DOC_WW_Pin1_4 | 84 | 89 | PF00397 | 0.505 |
LIG_14-3-3_CanoR_1 | 211 | 219 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 22 | 30 | PF00244 | 0.439 |
LIG_14-3-3_CanoR_1 | 238 | 243 | PF00244 | 0.446 |
LIG_Actin_WH2_2 | 185 | 202 | PF00022 | 0.460 |
LIG_Actin_WH2_2 | 300 | 315 | PF00022 | 0.456 |
LIG_BRCT_BRCA1_1 | 142 | 146 | PF00533 | 0.410 |
LIG_BRCT_BRCA1_1 | 221 | 225 | PF00533 | 0.460 |
LIG_eIF4E_1 | 182 | 188 | PF01652 | 0.446 |
LIG_FHA_1 | 110 | 116 | PF00498 | 0.549 |
LIG_FHA_1 | 193 | 199 | PF00498 | 0.446 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.440 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.448 |
LIG_FHA_1 | 85 | 91 | PF00498 | 0.532 |
LIG_FHA_2 | 114 | 120 | PF00498 | 0.434 |
LIG_FHA_2 | 131 | 137 | PF00498 | 0.528 |
LIG_FHA_2 | 295 | 301 | PF00498 | 0.542 |
LIG_FHA_2 | 343 | 349 | PF00498 | 0.703 |
LIG_FHA_2 | 357 | 363 | PF00498 | 0.685 |
LIG_FHA_2 | 421 | 427 | PF00498 | 0.722 |
LIG_FHA_2 | 446 | 452 | PF00498 | 0.701 |
LIG_LIR_Apic_2 | 207 | 213 | PF02991 | 0.446 |
LIG_LIR_Gen_1 | 223 | 234 | PF02991 | 0.480 |
LIG_LIR_Gen_1 | 34 | 44 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 57 | 66 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 223 | 229 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 25 | 30 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 34 | 39 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 57 | 61 | PF02991 | 0.446 |
LIG_LYPXL_SIV_4 | 402 | 410 | PF13949 | 0.333 |
LIG_MLH1_MIPbox_1 | 142 | 146 | PF16413 | 0.341 |
LIG_PCNA_PIPBox_1 | 176 | 185 | PF02747 | 0.460 |
LIG_PCNA_yPIPBox_3 | 233 | 246 | PF02747 | 0.446 |
LIG_SH2_CRK | 27 | 31 | PF00017 | 0.446 |
LIG_SH2_STAP1 | 326 | 330 | PF00017 | 0.670 |
LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.341 |
LIG_SH2_STAT5 | 182 | 185 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 257 | 260 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 324 | 327 | PF00017 | 0.666 |
LIG_SH2_STAT5 | 403 | 406 | PF00017 | 0.498 |
LIG_SH3_3 | 228 | 234 | PF00018 | 0.513 |
LIG_SH3_3 | 316 | 322 | PF00018 | 0.566 |
LIG_SH3_3 | 361 | 367 | PF00018 | 0.486 |
LIG_SH3_3 | 388 | 394 | PF00018 | 0.519 |
LIG_SH3_3 | 432 | 438 | PF00018 | 0.691 |
LIG_SUMO_SIM_anti_2 | 102 | 108 | PF11976 | 0.549 |
LIG_SUMO_SIM_par_1 | 89 | 94 | PF11976 | 0.446 |
LIG_TRAF2_1 | 16 | 19 | PF00917 | 0.382 |
LIG_TRAF2_1 | 297 | 300 | PF00917 | 0.483 |
LIG_WRC_WIRS_1 | 194 | 199 | PF05994 | 0.446 |
LIG_WRC_WIRS_1 | 242 | 247 | PF05994 | 0.526 |
MOD_CDK_SPK_2 | 84 | 89 | PF00069 | 0.549 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.460 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.509 |
MOD_CK1_1 | 241 | 247 | PF00069 | 0.524 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.687 |
MOD_CK1_1 | 315 | 321 | PF00069 | 0.632 |
MOD_CK1_1 | 333 | 339 | PF00069 | 0.707 |
MOD_CK2_1 | 113 | 119 | PF00069 | 0.434 |
MOD_CK2_1 | 132 | 138 | PF00069 | 0.534 |
MOD_CK2_1 | 284 | 290 | PF00069 | 0.740 |
MOD_CK2_1 | 294 | 300 | PF00069 | 0.503 |
MOD_CK2_1 | 37 | 43 | PF00069 | 0.413 |
MOD_CK2_1 | 445 | 451 | PF00069 | 0.704 |
MOD_DYRK1A_RPxSP_1 | 434 | 438 | PF00069 | 0.683 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.288 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.237 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.668 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.484 |
MOD_GlcNHglycan | 307 | 310 | PF01048 | 0.698 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.630 |
MOD_GlcNHglycan | 373 | 377 | PF01048 | 0.495 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.445 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.416 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.536 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.446 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.558 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.727 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.678 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.588 |
MOD_N-GLC_1 | 238 | 243 | PF02516 | 0.246 |
MOD_N-GLC_1 | 354 | 359 | PF02516 | 0.429 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.488 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.396 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.446 |
MOD_NEK2_1 | 312 | 317 | PF00069 | 0.711 |
MOD_PIKK_1 | 425 | 431 | PF00454 | 0.722 |
MOD_PIKK_1 | 56 | 62 | PF00454 | 0.446 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.516 |
MOD_PKA_2 | 312 | 318 | PF00069 | 0.674 |
MOD_PKA_2 | 420 | 426 | PF00069 | 0.735 |
MOD_PKA_2 | 443 | 449 | PF00069 | 0.703 |
MOD_Plk_1 | 238 | 244 | PF00069 | 0.446 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.494 |
MOD_Plk_4 | 141 | 147 | PF00069 | 0.427 |
MOD_Plk_4 | 193 | 199 | PF00069 | 0.446 |
MOD_Plk_4 | 241 | 247 | PF00069 | 0.519 |
MOD_Plk_4 | 79 | 85 | PF00069 | 0.341 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.548 |
MOD_ProDKin_1 | 315 | 321 | PF00069 | 0.570 |
MOD_ProDKin_1 | 37 | 43 | PF00069 | 0.413 |
MOD_ProDKin_1 | 434 | 440 | PF00069 | 0.684 |
MOD_ProDKin_1 | 84 | 90 | PF00069 | 0.505 |
MOD_SUMO_for_1 | 16 | 19 | PF00179 | 0.382 |
MOD_SUMO_for_1 | 220 | 223 | PF00179 | 0.384 |
TRG_DiLeu_BaEn_1 | 119 | 124 | PF01217 | 0.460 |
TRG_DiLeu_BaEn_1 | 79 | 84 | PF01217 | 0.341 |
TRG_DiLeu_BaEn_4 | 34 | 40 | PF01217 | 0.460 |
TRG_DiLeu_BaEn_4 | 387 | 393 | PF01217 | 0.450 |
TRG_DiLeu_LyEn_5 | 119 | 124 | PF01217 | 0.460 |
TRG_ENDOCYTIC_2 | 27 | 30 | PF00928 | 0.434 |
TRG_ER_diArg_1 | 13 | 15 | PF00400 | 0.414 |
TRG_ER_diArg_1 | 21 | 24 | PF00400 | 0.443 |
TRG_ER_diArg_1 | 432 | 435 | PF00400 | 0.505 |
TRG_NES_CRM1_1 | 96 | 110 | PF08389 | 0.446 |
TRG_NLS_MonoExtC_3 | 430 | 436 | PF00514 | 0.667 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HTF7 | Leptomonas seymouri | 62% | 100% |
A0A0S4JD71 | Bodo saltans | 45% | 100% |
A0A1X0NJR5 | Trypanosomatidae | 46% | 100% |
A0A3S7X469 | Leishmania donovani | 24% | 100% |
A0A451EJH4 | Leishmania donovani | 90% | 99% |
A4H3D4 | Leishmania braziliensis | 76% | 100% |
A4HRN5 | Leishmania infantum | 90% | 99% |
A4I6F9 | Leishmania infantum | 24% | 100% |
C9ZJ17 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
E9ACB3 | Leishmania major | 90% | 100% |
E9B1L6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 100% |
P38238 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 36% | 100% |
Q9BHC8 | Leishmania major | 24% | 100% |
V5BCX7 | Trypanosoma cruzi | 50% | 100% |