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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000314 | organellar small ribosomal subunit | 5 | 1 |
GO:0005763 | mitochondrial small ribosomal subunit | 3 | 1 |
GO:0015935 | small ribosomal subunit | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 5 |
GO:0044391 | ribosomal subunit | 3 | 1 |
GO:0098798 | mitochondrial protein-containing complex | 2 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 5 |
GO:0005840 | ribosome | 5 | 4 |
GO:0043226 | organelle | 2 | 4 |
GO:0043228 | non-membrane-bounded organelle | 3 | 4 |
GO:0043229 | intracellular organelle | 3 | 4 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 4 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
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 | 40 | 44 | PF00656 | 0.551 |
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.602 |
CLV_NRD_NRD_1 | 163 | 165 | PF00675 | 0.400 |
CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.384 |
CLV_NRD_NRD_1 | 264 | 266 | PF00675 | 0.325 |
CLV_NRD_NRD_1 | 387 | 389 | PF00675 | 0.430 |
CLV_NRD_NRD_1 | 410 | 412 | PF00675 | 0.419 |
CLV_NRD_NRD_1 | 55 | 57 | PF00675 | 0.532 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.460 |
CLV_PCSK_KEX2_1 | 163 | 165 | PF00082 | 0.375 |
CLV_PCSK_KEX2_1 | 227 | 229 | PF00082 | 0.357 |
CLV_PCSK_KEX2_1 | 264 | 266 | PF00082 | 0.390 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.407 |
CLV_PCSK_KEX2_1 | 424 | 426 | PF00082 | 0.464 |
CLV_PCSK_KEX2_1 | 55 | 57 | PF00082 | 0.536 |
CLV_PCSK_PC1ET2_1 | 227 | 229 | PF00082 | 0.357 |
CLV_PCSK_PC1ET2_1 | 272 | 274 | PF00082 | 0.531 |
CLV_PCSK_PC1ET2_1 | 424 | 426 | PF00082 | 0.441 |
CLV_PCSK_PC7_1 | 420 | 426 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 186 | 190 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 227 | 231 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 249 | 253 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 35 | 39 | PF00082 | 0.535 |
CLV_PCSK_SKI1_1 | 366 | 370 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 411 | 415 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 94 | 98 | PF00082 | 0.392 |
DEG_MDM2_SWIB_1 | 271 | 278 | PF02201 | 0.343 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.512 |
DOC_CKS1_1 | 85 | 90 | PF01111 | 0.452 |
DOC_CYCLIN_RxL_1 | 408 | 416 | PF00134 | 0.412 |
DOC_MAPK_gen_1 | 227 | 234 | PF00069 | 0.461 |
DOC_MAPK_gen_1 | 264 | 271 | PF00069 | 0.367 |
DOC_MAPK_gen_1 | 385 | 395 | PF00069 | 0.465 |
DOC_MAPK_MEF2A_6 | 227 | 234 | PF00069 | 0.461 |
DOC_MAPK_MEF2A_6 | 388 | 397 | PF00069 | 0.450 |
DOC_PP1_RVXF_1 | 265 | 272 | PF00149 | 0.376 |
DOC_PP2B_LxvP_1 | 287 | 290 | PF13499 | 0.463 |
DOC_PP4_FxxP_1 | 171 | 174 | PF00568 | 0.371 |
DOC_SPAK_OSR1_1 | 170 | 174 | PF12202 | 0.372 |
DOC_USP7_UBL2_3 | 187 | 191 | PF12436 | 0.295 |
DOC_USP7_UBL2_3 | 227 | 231 | PF12436 | 0.356 |
DOC_USP7_UBL2_3 | 268 | 272 | PF12436 | 0.382 |
DOC_USP7_UBL2_3 | 396 | 400 | PF12436 | 0.452 |
DOC_WW_Pin1_4 | 105 | 110 | PF00397 | 0.393 |
DOC_WW_Pin1_4 | 15 | 20 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 217 | 222 | PF00397 | 0.356 |
DOC_WW_Pin1_4 | 84 | 89 | PF00397 | 0.440 |
LIG_14-3-3_CanoR_1 | 170 | 174 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 332 | 341 | PF00244 | 0.384 |
LIG_14-3-3_CanoR_1 | 420 | 428 | PF00244 | 0.498 |
LIG_14-3-3_CanoR_1 | 55 | 61 | PF00244 | 0.546 |
LIG_BRCT_BRCA1_1 | 390 | 394 | PF00533 | 0.404 |
LIG_BRCT_BRCA1_2 | 390 | 396 | PF00533 | 0.403 |
LIG_CtBP_PxDLS_1 | 289 | 293 | PF00389 | 0.477 |
LIG_FHA_1 | 344 | 350 | PF00498 | 0.424 |
LIG_FHA_2 | 193 | 199 | PF00498 | 0.508 |
LIG_LIR_Apic_2 | 168 | 174 | PF02991 | 0.371 |
LIG_LIR_Apic_2 | 344 | 348 | PF02991 | 0.413 |
LIG_LIR_Gen_1 | 23 | 31 | PF02991 | 0.680 |
LIG_LIR_Gen_1 | 391 | 399 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 5 | 12 | PF02991 | 0.564 |
LIG_LIR_Nem_3 | 23 | 28 | PF02991 | 0.689 |
LIG_LIR_Nem_3 | 270 | 274 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 299 | 303 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 391 | 397 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 408 | 413 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 5 | 11 | PF02991 | 0.562 |
LIG_LYPXL_SIV_4 | 88 | 96 | PF13949 | 0.360 |
LIG_Pex14_1 | 156 | 160 | PF04695 | 0.356 |
LIG_Pex14_2 | 271 | 275 | PF04695 | 0.359 |
LIG_Pex14_2 | 386 | 390 | PF04695 | 0.392 |
LIG_SH2_CRK | 345 | 349 | PF00017 | 0.404 |
LIG_SH2_CRK | 410 | 414 | PF00017 | 0.404 |
LIG_SH2_SRC | 211 | 214 | PF00017 | 0.389 |
LIG_SH2_STAP1 | 167 | 171 | PF00017 | 0.372 |
LIG_SH2_STAP1 | 181 | 185 | PF00017 | 0.395 |
LIG_SH2_STAP1 | 303 | 307 | PF00017 | 0.415 |
LIG_SH2_STAP1 | 364 | 368 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 345 | 348 | PF00017 | 0.410 |
LIG_SH3_1 | 80 | 86 | PF00018 | 0.394 |
LIG_SH3_3 | 119 | 125 | PF00018 | 0.448 |
LIG_SH3_3 | 283 | 289 | PF00018 | 0.429 |
LIG_SH3_3 | 315 | 321 | PF00018 | 0.409 |
LIG_SH3_3 | 401 | 407 | PF00018 | 0.391 |
LIG_SH3_3 | 80 | 86 | PF00018 | 0.416 |
LIG_TRAF2_1 | 195 | 198 | PF00917 | 0.407 |
LIG_TRAF2_1 | 348 | 351 | PF00917 | 0.486 |
LIG_TYR_ITIM | 362 | 367 | PF00017 | 0.400 |
LIG_UBA3_1 | 103 | 112 | PF00899 | 0.515 |
LIG_UBA3_1 | 138 | 144 | PF00899 | 0.411 |
LIG_UBA3_1 | 193 | 199 | PF00899 | 0.420 |
LIG_UBA3_1 | 393 | 400 | PF00899 | 0.455 |
MOD_CDK_SPxK_1 | 15 | 21 | PF00069 | 0.479 |
MOD_CDK_SPxxK_3 | 105 | 112 | PF00069 | 0.383 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.698 |
MOD_CK2_1 | 192 | 198 | PF00069 | 0.387 |
MOD_CK2_1 | 330 | 336 | PF00069 | 0.396 |
MOD_CMANNOS | 76 | 79 | PF00535 | 0.403 |
MOD_GlcNHglycan | 390 | 393 | PF01048 | 0.403 |
MOD_GlcNHglycan | 400 | 403 | PF01048 | 0.380 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.566 |
MOD_LATS_1 | 54 | 60 | PF00433 | 0.649 |
MOD_N-GLC_1 | 15 | 20 | PF02516 | 0.698 |
MOD_N-GLC_1 | 23 | 28 | PF02516 | 0.704 |
MOD_N-GLC_1 | 259 | 264 | PF02516 | 0.413 |
MOD_N-GLC_2 | 325 | 327 | PF02516 | 0.395 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.515 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.369 |
MOD_NEK2_1 | 259 | 264 | PF00069 | 0.413 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.368 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.402 |
MOD_NEK2_1 | 413 | 418 | PF00069 | 0.398 |
MOD_NEK2_2 | 181 | 186 | PF00069 | 0.444 |
MOD_PIKK_1 | 199 | 205 | PF00454 | 0.263 |
MOD_PIKK_1 | 310 | 316 | PF00454 | 0.511 |
MOD_PIKK_1 | 413 | 419 | PF00454 | 0.535 |
MOD_PKA_1 | 388 | 394 | PF00069 | 0.402 |
MOD_PKA_2 | 169 | 175 | PF00069 | 0.389 |
MOD_PKA_2 | 20 | 26 | PF00069 | 0.711 |
MOD_PKA_2 | 419 | 425 | PF00069 | 0.498 |
MOD_PKA_2 | 54 | 60 | PF00069 | 0.549 |
MOD_Plk_1 | 259 | 265 | PF00069 | 0.420 |
MOD_Plk_2-3 | 192 | 198 | PF00069 | 0.376 |
MOD_Plk_4 | 247 | 253 | PF00069 | 0.443 |
MOD_Plk_4 | 296 | 302 | PF00069 | 0.411 |
MOD_ProDKin_1 | 105 | 111 | PF00069 | 0.384 |
MOD_ProDKin_1 | 15 | 21 | PF00069 | 0.574 |
MOD_ProDKin_1 | 217 | 223 | PF00069 | 0.350 |
MOD_ProDKin_1 | 84 | 90 | PF00069 | 0.445 |
MOD_SUMO_for_1 | 37 | 40 | PF00179 | 0.662 |
MOD_SUMO_for_1 | 370 | 373 | PF00179 | 0.390 |
MOD_SUMO_rev_2 | 351 | 357 | PF00179 | 0.416 |
TRG_DiLeu_BaEn_2 | 381 | 387 | PF01217 | 0.400 |
TRG_DiLeu_BaLyEn_6 | 134 | 139 | PF01217 | 0.470 |
TRG_ENDOCYTIC_2 | 274 | 277 | PF00928 | 0.329 |
TRG_ENDOCYTIC_2 | 364 | 367 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 410 | 413 | PF00928 | 0.411 |
TRG_ER_diArg_1 | 263 | 265 | PF00400 | 0.422 |
TRG_ER_diArg_1 | 50 | 53 | PF00400 | 0.576 |
TRG_NLS_MonoExtC_3 | 34 | 40 | PF00514 | 0.524 |
TRG_NLS_MonoExtN_4 | 33 | 39 | PF00514 | 0.443 |
TRG_Pf-PMV_PEXEL_1 | 347 | 351 | PF00026 | 0.432 |
TRG_Pf-PMV_PEXEL_1 | 355 | 359 | PF00026 | 0.418 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDF7 | Leptomonas seymouri | 89% | 100% |
A0A0S4J4D7 | Bodo saltans | 64% | 100% |
A0A1X0NWF9 | Trypanosomatidae | 81% | 100% |
A0A3S7WVW4 | Leishmania donovani | 94% | 100% |
A0A422NCH8 | Trypanosoma rangeli | 80% | 100% |
A4HYR0 | Leishmania infantum | 94% | 100% |
C9ZI69 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 81% | 100% |
E9AUJ5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q4QCY9 | Leishmania major | 94% | 100% |