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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005840 | ribosome | 5 | 11 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0043226 | organelle | 2 | 11 |
GO:0043228 | non-membrane-bounded organelle | 3 | 11 |
GO:0043229 | intracellular organelle | 3 | 11 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:1990904 | ribonucleoprotein complex | 2 | 12 |
GO:0000315 | organellar large ribosomal subunit | 5 | 1 |
GO:0005762 | mitochondrial large ribosomal subunit | 3 | 1 |
GO:0015934 | large ribosomal subunit | 4 | 1 |
GO:0044391 | ribosomal subunit | 3 | 1 |
GO:0098798 | mitochondrial protein-containing complex | 2 | 1 |
GO:0016020 | membrane | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0006412 | translation | 4 | 12 |
GO:0006518 | peptide metabolic process | 4 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009058 | biosynthetic process | 2 | 12 |
GO:0009059 | macromolecule biosynthetic process | 4 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0019538 | protein metabolic process | 3 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0034645 | obsolete cellular macromolecule biosynthetic process | 4 | 12 |
GO:0043043 | peptide biosynthetic process | 5 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043603 | amide metabolic process | 3 | 12 |
GO:0043604 | amide biosynthetic process | 4 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044249 | cellular biosynthetic process | 3 | 12 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 12 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 12 |
GO:1901576 | organic substance biosynthetic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003735 | structural constituent of ribosome | 2 | 12 |
GO:0005198 | structural molecule activity | 1 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 320 | 324 | PF00656 | 0.373 |
CLV_NRD_NRD_1 | 17 | 19 | PF00675 | 0.616 |
CLV_NRD_NRD_1 | 271 | 273 | PF00675 | 0.276 |
CLV_NRD_NRD_1 | 28 | 30 | PF00675 | 0.417 |
CLV_NRD_NRD_1 | 424 | 426 | PF00675 | 0.453 |
CLV_NRD_NRD_1 | 428 | 430 | PF00675 | 0.474 |
CLV_NRD_NRD_1 | 435 | 437 | PF00675 | 0.488 |
CLV_NRD_NRD_1 | 455 | 457 | PF00675 | 0.302 |
CLV_PCSK_KEX2_1 | 17 | 19 | PF00082 | 0.617 |
CLV_PCSK_KEX2_1 | 271 | 273 | PF00082 | 0.276 |
CLV_PCSK_KEX2_1 | 28 | 30 | PF00082 | 0.402 |
CLV_PCSK_KEX2_1 | 282 | 284 | PF00082 | 0.276 |
CLV_PCSK_KEX2_1 | 455 | 457 | PF00082 | 0.491 |
CLV_PCSK_KEX2_1 | 463 | 465 | PF00082 | 0.491 |
CLV_PCSK_PC1ET2_1 | 282 | 284 | PF00082 | 0.276 |
CLV_PCSK_PC1ET2_1 | 463 | 465 | PF00082 | 0.516 |
CLV_PCSK_SKI1_1 | 137 | 141 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 229 | 233 | PF00082 | 0.276 |
CLV_PCSK_SKI1_1 | 366 | 370 | PF00082 | 0.542 |
CLV_PCSK_SKI1_1 | 402 | 406 | PF00082 | 0.552 |
CLV_PCSK_SKI1_1 | 455 | 459 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 463 | 467 | PF00082 | 0.514 |
DEG_APCC_DBOX_1 | 129 | 137 | PF00400 | 0.314 |
DOC_CDC14_PxL_1 | 315 | 323 | PF14671 | 0.364 |
DOC_CDC14_PxL_1 | 35 | 43 | PF14671 | 0.491 |
DOC_CKS1_1 | 213 | 218 | PF01111 | 0.517 |
DOC_MAPK_FxFP_2 | 156 | 159 | PF00069 | 0.367 |
DOC_MAPK_gen_1 | 229 | 239 | PF00069 | 0.476 |
DOC_MAPK_gen_1 | 434 | 443 | PF00069 | 0.479 |
DOC_MAPK_gen_1 | 90 | 100 | PF00069 | 0.377 |
DOC_MAPK_MEF2A_6 | 232 | 241 | PF00069 | 0.476 |
DOC_PP4_FxxP_1 | 156 | 159 | PF00568 | 0.367 |
DOC_PP4_FxxP_1 | 189 | 192 | PF00568 | 0.328 |
DOC_USP7_UBL2_3 | 426 | 430 | PF12436 | 0.594 |
DOC_WW_Pin1_4 | 212 | 217 | PF00397 | 0.476 |
DOC_WW_Pin1_4 | 347 | 352 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 373 | 378 | PF00397 | 0.427 |
LIG_14-3-3_CanoR_1 | 28 | 38 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 429 | 433 | PF00244 | 0.536 |
LIG_14-3-3_CterR_2 | 464 | 467 | PF00244 | 0.640 |
LIG_ActinCP_TwfCPI_2 | 189 | 199 | PF01115 | 0.363 |
LIG_AP2alpha_1 | 383 | 387 | PF02296 | 0.440 |
LIG_BRCT_BRCA1_1 | 127 | 131 | PF00533 | 0.381 |
LIG_BRCT_BRCA1_1 | 208 | 212 | PF00533 | 0.562 |
LIG_CSL_BTD_1 | 156 | 159 | PF09270 | 0.367 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.417 |
LIG_FHA_2 | 138 | 144 | PF00498 | 0.396 |
LIG_FHA_2 | 222 | 228 | PF00498 | 0.471 |
LIG_FHA_2 | 318 | 324 | PF00498 | 0.369 |
LIG_FHA_2 | 392 | 398 | PF00498 | 0.575 |
LIG_FHA_2 | 82 | 88 | PF00498 | 0.427 |
LIG_LIR_Apic_2 | 111 | 117 | PF02991 | 0.419 |
LIG_LIR_Apic_2 | 154 | 159 | PF02991 | 0.360 |
LIG_LIR_Apic_2 | 188 | 192 | PF02991 | 0.328 |
LIG_LIR_Gen_1 | 122 | 131 | PF02991 | 0.400 |
LIG_LIR_Gen_1 | 143 | 151 | PF02991 | 0.389 |
LIG_LIR_Gen_1 | 258 | 266 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 328 | 336 | PF02991 | 0.384 |
LIG_LIR_Gen_1 | 84 | 94 | PF02991 | 0.417 |
LIG_LIR_Gen_1 | 95 | 105 | PF02991 | 0.292 |
LIG_LIR_Nem_3 | 102 | 107 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 122 | 126 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 128 | 134 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 143 | 147 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 217 | 222 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 245 | 251 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 258 | 264 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 299 | 304 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 32 | 38 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 328 | 332 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 350 | 356 | PF02991 | 0.542 |
LIG_LIR_Nem_3 | 48 | 53 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 65 | 70 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 84 | 89 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 91 | 97 | PF02991 | 0.365 |
LIG_LYPXL_S_1 | 66 | 70 | PF13949 | 0.406 |
LIG_LYPXL_SIV_4 | 218 | 226 | PF13949 | 0.476 |
LIG_LYPXL_yS_3 | 38 | 41 | PF13949 | 0.442 |
LIG_LYPXL_yS_3 | 54 | 57 | PF13949 | 0.381 |
LIG_LYPXL_yS_3 | 67 | 70 | PF13949 | 0.415 |
LIG_Pex14_1 | 307 | 311 | PF04695 | 0.476 |
LIG_Pex14_1 | 34 | 38 | PF04695 | 0.442 |
LIG_Pex14_2 | 253 | 257 | PF04695 | 0.476 |
LIG_Pex14_2 | 383 | 387 | PF04695 | 0.427 |
LIG_PTB_Apo_2 | 240 | 247 | PF02174 | 0.473 |
LIG_PTB_Phospho_1 | 240 | 246 | PF10480 | 0.476 |
LIG_SH2_CRK | 219 | 223 | PF00017 | 0.486 |
LIG_SH2_CRK | 248 | 252 | PF00017 | 0.550 |
LIG_SH2_CRK | 301 | 305 | PF00017 | 0.476 |
LIG_SH2_CRK | 462 | 466 | PF00017 | 0.535 |
LIG_SH2_CRK | 86 | 90 | PF00017 | 0.416 |
LIG_SH2_NCK_1 | 219 | 223 | PF00017 | 0.487 |
LIG_SH2_PTP2 | 261 | 264 | PF00017 | 0.487 |
LIG_SH2_SRC | 219 | 222 | PF00017 | 0.476 |
LIG_SH2_STAP1 | 127 | 131 | PF00017 | 0.365 |
LIG_SH2_STAP1 | 94 | 98 | PF00017 | 0.366 |
LIG_SH2_STAT3 | 246 | 249 | PF00017 | 0.562 |
LIG_SH2_STAT5 | 179 | 182 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 261 | 264 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 317 | 320 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 329 | 332 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 341 | 344 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 382 | 385 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 421 | 424 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 56 | 59 | PF00017 | 0.385 |
LIG_SH3_1 | 348 | 354 | PF00018 | 0.425 |
LIG_SH3_3 | 210 | 216 | PF00018 | 0.504 |
LIG_SH3_3 | 348 | 354 | PF00018 | 0.425 |
LIG_SH3_3 | 65 | 71 | PF00018 | 0.405 |
LIG_SxIP_EBH_1 | 350 | 360 | PF03271 | 0.298 |
LIG_TRAF2_1 | 233 | 236 | PF00917 | 0.476 |
LIG_TRAF2_1 | 359 | 362 | PF00917 | 0.461 |
LIG_TYR_ITIM | 460 | 465 | PF00017 | 0.529 |
LIG_TYR_ITSM | 82 | 89 | PF00017 | 0.431 |
LIG_WRC_WIRS_1 | 353 | 358 | PF05994 | 0.440 |
LIG_WW_1 | 377 | 380 | PF00397 | 0.436 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.491 |
MOD_CK2_1 | 356 | 362 | PF00069 | 0.489 |
MOD_CK2_1 | 37 | 43 | PF00069 | 0.467 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.511 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.338 |
MOD_GlcNHglycan | 296 | 299 | PF01048 | 0.305 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.613 |
MOD_GSK3_1 | 237 | 244 | PF00069 | 0.476 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.435 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.383 |
MOD_GSK3_1 | 362 | 369 | PF00069 | 0.424 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.386 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.354 |
MOD_NEK2_1 | 264 | 269 | PF00069 | 0.476 |
MOD_NEK2_1 | 332 | 337 | PF00069 | 0.393 |
MOD_PIKK_1 | 391 | 397 | PF00454 | 0.471 |
MOD_PKA_1 | 419 | 425 | PF00069 | 0.597 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.458 |
MOD_PKA_2 | 332 | 338 | PF00069 | 0.521 |
MOD_PKA_2 | 428 | 434 | PF00069 | 0.486 |
MOD_Plk_1 | 151 | 157 | PF00069 | 0.362 |
MOD_Plk_1 | 235 | 241 | PF00069 | 0.477 |
MOD_Plk_4 | 311 | 317 | PF00069 | 0.377 |
MOD_Plk_4 | 325 | 331 | PF00069 | 0.371 |
MOD_Plk_4 | 339 | 345 | PF00069 | 0.430 |
MOD_Plk_4 | 352 | 358 | PF00069 | 0.437 |
MOD_Plk_4 | 37 | 43 | PF00069 | 0.447 |
MOD_Plk_4 | 62 | 68 | PF00069 | 0.409 |
MOD_ProDKin_1 | 212 | 218 | PF00069 | 0.476 |
MOD_ProDKin_1 | 347 | 353 | PF00069 | 0.552 |
MOD_ProDKin_1 | 373 | 379 | PF00069 | 0.426 |
MOD_SUMO_rev_2 | 397 | 404 | PF00179 | 0.509 |
TRG_ENDOCYTIC_2 | 144 | 147 | PF00928 | 0.402 |
TRG_ENDOCYTIC_2 | 219 | 222 | PF00928 | 0.475 |
TRG_ENDOCYTIC_2 | 248 | 251 | PF00928 | 0.519 |
TRG_ENDOCYTIC_2 | 261 | 264 | PF00928 | 0.432 |
TRG_ENDOCYTIC_2 | 301 | 304 | PF00928 | 0.476 |
TRG_ENDOCYTIC_2 | 329 | 332 | PF00928 | 0.375 |
TRG_ENDOCYTIC_2 | 38 | 41 | PF00928 | 0.442 |
TRG_ENDOCYTIC_2 | 380 | 383 | PF00928 | 0.415 |
TRG_ENDOCYTIC_2 | 438 | 441 | PF00928 | 0.538 |
TRG_ENDOCYTIC_2 | 462 | 465 | PF00928 | 0.513 |
TRG_ENDOCYTIC_2 | 54 | 57 | PF00928 | 0.381 |
TRG_ENDOCYTIC_2 | 67 | 70 | PF00928 | 0.415 |
TRG_ENDOCYTIC_2 | 86 | 89 | PF00928 | 0.424 |
TRG_ENDOCYTIC_2 | 94 | 97 | PF00928 | 0.393 |
TRG_ER_diArg_1 | 17 | 19 | PF00400 | 0.616 |
TRG_ER_diArg_1 | 271 | 273 | PF00400 | 0.476 |
TRG_ER_diArg_1 | 28 | 31 | PF00400 | 0.434 |
TRG_ER_diArg_1 | 443 | 446 | PF00400 | 0.519 |
TRG_ER_diArg_1 | 98 | 101 | PF00400 | 0.389 |
TRG_NLS_Bipartite_1 | 412 | 430 | PF00514 | 0.463 |
TRG_NLS_MonoExtC_3 | 411 | 417 | PF00514 | 0.474 |
TRG_NLS_MonoExtC_3 | 424 | 429 | PF00514 | 0.461 |
TRG_NLS_MonoExtN_4 | 411 | 416 | PF00514 | 0.493 |
TRG_NLS_MonoExtN_4 | 425 | 430 | PF00514 | 0.442 |
TRG_NLS_MonoExtN_4 | 434 | 440 | PF00514 | 0.483 |
TRG_NLS_MonoExtN_4 | 461 | 467 | PF00514 | 0.628 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAL5 | Leptomonas seymouri | 91% | 100% |
A0A0S4IMW0 | Bodo saltans | 78% | 100% |
A0A1X0NZZ6 | Trypanosomatidae | 90% | 99% |
A0A3Q8IR02 | Leishmania donovani | 97% | 100% |
A0A422NUY5 | Trypanosoma rangeli | 90% | 99% |
A4HH11 | Leishmania braziliensis | 94% | 100% |
A4I440 | Leishmania infantum | 97% | 100% |
C9ZKS2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 88% | 99% |
E9ADK5 | Leishmania major | 98% | 100% |
V5BPV7 | Trypanosoma cruzi | 90% | 88% |