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: 18 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005840 | ribosome | 5 | 5 |
GO:0032991 | protein-containing complex | 1 | 5 |
GO:0043226 | organelle | 2 | 5 |
GO:0043228 | non-membrane-bounded organelle | 3 | 5 |
GO:0043229 | intracellular organelle | 3 | 5 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
GO:1990904 | ribonucleoprotein complex | 2 | 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0006412 | translation | 4 | 5 |
GO:0006518 | peptide metabolic process | 4 | 5 |
GO:0006807 | nitrogen compound metabolic process | 2 | 5 |
GO:0008152 | metabolic process | 1 | 5 |
GO:0009058 | biosynthetic process | 2 | 5 |
GO:0009059 | macromolecule biosynthetic process | 4 | 5 |
GO:0009987 | cellular process | 1 | 5 |
GO:0019538 | protein metabolic process | 3 | 5 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 5 |
GO:0034645 | obsolete cellular macromolecule biosynthetic process | 4 | 5 |
GO:0043043 | peptide biosynthetic process | 5 | 5 |
GO:0043170 | macromolecule metabolic process | 3 | 5 |
GO:0043603 | amide metabolic process | 3 | 5 |
GO:0043604 | amide biosynthetic process | 4 | 5 |
GO:0044237 | cellular metabolic process | 2 | 5 |
GO:0044238 | primary metabolic process | 2 | 5 |
GO:0044249 | cellular biosynthetic process | 3 | 5 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 5 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 5 |
GO:0071704 | organic substance metabolic process | 2 | 5 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 5 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 5 |
GO:1901576 | organic substance biosynthetic process | 3 | 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003735 | structural constituent of ribosome | 2 | 5 |
GO:0005198 | structural molecule activity | 1 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 260 | 264 | PF00656 | 0.438 |
CLV_C14_Caspase3-7 | 66 | 70 | PF00656 | 0.612 |
CLV_NRD_NRD_1 | 162 | 164 | PF00675 | 0.550 |
CLV_NRD_NRD_1 | 234 | 236 | PF00675 | 0.431 |
CLV_NRD_NRD_1 | 276 | 278 | PF00675 | 0.421 |
CLV_NRD_NRD_1 | 419 | 421 | PF00675 | 0.472 |
CLV_NRD_NRD_1 | 435 | 437 | PF00675 | 0.398 |
CLV_PCSK_KEX2_1 | 234 | 236 | PF00082 | 0.431 |
CLV_PCSK_KEX2_1 | 418 | 420 | PF00082 | 0.474 |
CLV_PCSK_KEX2_1 | 435 | 437 | PF00082 | 0.472 |
CLV_PCSK_KEX2_1 | 44 | 46 | PF00082 | 0.350 |
CLV_PCSK_PC1ET2_1 | 435 | 437 | PF00082 | 0.488 |
CLV_PCSK_PC1ET2_1 | 44 | 46 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 191 | 195 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 2 | 6 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 221 | 225 | PF00082 | 0.408 |
CLV_PCSK_SKI1_1 | 243 | 247 | PF00082 | 0.423 |
CLV_PCSK_SKI1_1 | 314 | 318 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 437 | 441 | PF00082 | 0.519 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.570 |
DOC_MAPK_gen_1 | 234 | 246 | PF00069 | 0.421 |
DOC_MAPK_gen_1 | 409 | 416 | PF00069 | 0.435 |
DOC_MAPK_gen_1 | 44 | 51 | PF00069 | 0.362 |
DOC_MAPK_gen_1 | 59 | 67 | PF00069 | 0.454 |
DOC_MAPK_MEF2A_6 | 239 | 246 | PF00069 | 0.431 |
DOC_MAPK_MEF2A_6 | 285 | 292 | PF00069 | 0.499 |
DOC_MAPK_MEF2A_6 | 59 | 67 | PF00069 | 0.418 |
DOC_PP1_RVXF_1 | 241 | 247 | PF00149 | 0.426 |
DOC_PP1_RVXF_1 | 33 | 39 | PF00149 | 0.349 |
DOC_PP1_RVXF_1 | 358 | 364 | PF00149 | 0.545 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 376 | 380 | PF00917 | 0.439 |
DOC_USP7_UBL2_3 | 433 | 437 | PF12436 | 0.551 |
DOC_WW_Pin1_4 | 181 | 186 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.404 |
LIG_14-3-3_CanoR_1 | 17 | 23 | PF00244 | 0.342 |
LIG_14-3-3_CanoR_1 | 191 | 200 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 216 | 223 | PF00244 | 0.410 |
LIG_14-3-3_CanoR_1 | 35 | 39 | PF00244 | 0.333 |
LIG_Actin_WH2_2 | 108 | 123 | PF00022 | 0.337 |
LIG_Actin_WH2_2 | 393 | 411 | PF00022 | 0.441 |
LIG_APCC_ABBA_1 | 353 | 358 | PF00400 | 0.378 |
LIG_BIR_III_4 | 196 | 200 | PF00653 | 0.524 |
LIG_BRCT_BRCA1_1 | 338 | 342 | PF00533 | 0.501 |
LIG_Clathr_ClatBox_1 | 353 | 357 | PF01394 | 0.390 |
LIG_Clathr_ClatBox_1 | 413 | 417 | PF01394 | 0.437 |
LIG_eIF4E_1 | 165 | 171 | PF01652 | 0.424 |
LIG_eIF4E_1 | 315 | 321 | PF01652 | 0.385 |
LIG_FHA_1 | 170 | 176 | PF00498 | 0.496 |
LIG_FHA_1 | 206 | 212 | PF00498 | 0.433 |
LIG_FHA_1 | 316 | 322 | PF00498 | 0.409 |
LIG_FHA_1 | 396 | 402 | PF00498 | 0.438 |
LIG_FXI_DFP_1 | 363 | 367 | PF00024 | 0.406 |
LIG_GBD_Chelix_1 | 393 | 401 | PF00786 | 0.374 |
LIG_LIR_Gen_1 | 122 | 132 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 137 | 146 | PF02991 | 0.432 |
LIG_LIR_Gen_1 | 247 | 257 | PF02991 | 0.491 |
LIG_LIR_Gen_1 | 262 | 272 | PF02991 | 0.321 |
LIG_LIR_Gen_1 | 362 | 371 | PF02991 | 0.321 |
LIG_LIR_Nem_3 | 122 | 127 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 137 | 143 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 262 | 268 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 362 | 366 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 88 | 92 | PF02991 | 0.357 |
LIG_MAD2 | 173 | 181 | PF02301 | 0.514 |
LIG_NRP_CendR_1 | 440 | 441 | PF00754 | 0.536 |
LIG_PCNA_yPIPBox_3 | 163 | 175 | PF02747 | 0.536 |
LIG_SH2_CRK | 269 | 273 | PF00017 | 0.402 |
LIG_SH2_GRB2like | 207 | 210 | PF00017 | 0.437 |
LIG_SH2_NCK_1 | 140 | 144 | PF00017 | 0.435 |
LIG_SH2_SRC | 96 | 99 | PF00017 | 0.470 |
LIG_SH2_STAP1 | 165 | 169 | PF00017 | 0.426 |
LIG_SH2_STAP1 | 207 | 211 | PF00017 | 0.437 |
LIG_SH2_STAP1 | 265 | 269 | PF00017 | 0.412 |
LIG_SH2_STAT3 | 165 | 168 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 132 | 135 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 207 | 210 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 269 | 272 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 96 | 99 | PF00017 | 0.478 |
LIG_SH3_1 | 87 | 93 | PF00018 | 0.365 |
LIG_SH3_3 | 349 | 355 | PF00018 | 0.412 |
LIG_SH3_3 | 87 | 93 | PF00018 | 0.365 |
LIG_SUMO_SIM_anti_2 | 330 | 335 | PF11976 | 0.504 |
LIG_SUMO_SIM_anti_2 | 367 | 373 | PF11976 | 0.423 |
LIG_SUMO_SIM_par_1 | 411 | 417 | PF11976 | 0.430 |
LIG_SUMO_SIM_par_1 | 63 | 69 | PF11976 | 0.466 |
LIG_UBA3_1 | 158 | 164 | PF00899 | 0.566 |
MOD_CDC14_SPxK_1 | 184 | 187 | PF00782 | 0.555 |
MOD_CDK_SPK_2 | 3 | 8 | PF00069 | 0.404 |
MOD_CDK_SPxK_1 | 181 | 187 | PF00069 | 0.556 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.599 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.359 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.462 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.428 |
MOD_CK1_1 | 369 | 375 | PF00069 | 0.437 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.364 |
MOD_CK2_1 | 116 | 122 | PF00069 | 0.428 |
MOD_CK2_1 | 28 | 34 | PF00069 | 0.362 |
MOD_CK2_1 | 49 | 55 | PF00069 | 0.369 |
MOD_Cter_Amidation | 430 | 433 | PF01082 | 0.472 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.435 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.520 |
MOD_GlcNHglycan | 410 | 413 | PF01048 | 0.311 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.498 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.442 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.341 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.306 |
MOD_N-GLC_1 | 327 | 332 | PF02516 | 0.472 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.475 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.320 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.461 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.420 |
MOD_NEK2_1 | 230 | 235 | PF00069 | 0.402 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.314 |
MOD_NEK2_1 | 366 | 371 | PF00069 | 0.410 |
MOD_NEK2_1 | 408 | 413 | PF00069 | 0.334 |
MOD_NEK2_1 | 49 | 54 | PF00069 | 0.362 |
MOD_PIKK_1 | 164 | 170 | PF00454 | 0.308 |
MOD_PIKK_1 | 21 | 27 | PF00454 | 0.487 |
MOD_PIKK_1 | 43 | 49 | PF00454 | 0.430 |
MOD_PK_1 | 336 | 342 | PF00069 | 0.514 |
MOD_PKA_2 | 125 | 131 | PF00069 | 0.417 |
MOD_PKA_2 | 215 | 221 | PF00069 | 0.422 |
MOD_PKA_2 | 34 | 40 | PF00069 | 0.339 |
MOD_Plk_1 | 343 | 349 | PF00069 | 0.484 |
MOD_Plk_1 | 366 | 372 | PF00069 | 0.412 |
MOD_Plk_4 | 267 | 273 | PF00069 | 0.392 |
MOD_Plk_4 | 34 | 40 | PF00069 | 0.474 |
MOD_Plk_4 | 343 | 349 | PF00069 | 0.405 |
MOD_Plk_4 | 366 | 372 | PF00069 | 0.412 |
MOD_ProDKin_1 | 181 | 187 | PF00069 | 0.562 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.398 |
MOD_SUMO_for_1 | 107 | 110 | PF00179 | 0.372 |
MOD_SUMO_for_1 | 223 | 226 | PF00179 | 0.410 |
MOD_SUMO_rev_2 | 337 | 346 | PF00179 | 0.456 |
MOD_SUMO_rev_2 | 367 | 377 | PF00179 | 0.481 |
TRG_DiLeu_BaEn_1 | 166 | 171 | PF01217 | 0.401 |
TRG_DiLeu_BaEn_1 | 247 | 252 | PF01217 | 0.421 |
TRG_ENDOCYTIC_2 | 140 | 143 | PF00928 | 0.425 |
TRG_ENDOCYTIC_2 | 207 | 210 | PF00928 | 0.427 |
TRG_ENDOCYTIC_2 | 249 | 252 | PF00928 | 0.426 |
TRG_ENDOCYTIC_2 | 265 | 268 | PF00928 | 0.399 |
TRG_ENDOCYTIC_2 | 269 | 272 | PF00928 | 0.199 |
TRG_ER_diArg_1 | 418 | 420 | PF00400 | 0.488 |
TRG_NLS_Bipartite_1 | 418 | 439 | PF00514 | 0.477 |
TRG_NLS_MonoExtC_3 | 431 | 436 | PF00514 | 0.449 |
TRG_NLS_MonoExtN_4 | 432 | 439 | PF00514 | 0.481 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HRD2 | Leptomonas seymouri | 89% | 100% |
A0A0S4IXC2 | Bodo saltans | 73% | 100% |
A0A1X0NX23 | Trypanosomatidae | 77% | 99% |
A0A3Q8IBU6 | Leishmania donovani | 96% | 100% |
A0A422N7Q3 | Trypanosoma rangeli | 75% | 98% |
A4I0H3 | Leishmania infantum | 96% | 100% |
C9ZV98 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 78% | 100% |
E9AWD5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
Q4QB37 | Leishmania major | 96% | 100% |
V5AZ95 | Trypanosoma cruzi | 76% | 99% |