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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000315 | organellar large ribosomal subunit | 5 | 2 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0005762 | mitochondrial large ribosomal subunit | 3 | 2 |
GO:0015934 | large ribosomal subunit | 4 | 11 |
GO:0032991 | protein-containing complex | 1 | 11 |
GO:0044391 | ribosomal subunit | 3 | 11 |
GO:0098798 | mitochondrial protein-containing complex | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:1990904 | ribonucleoprotein complex | 2 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0006412 | translation | 4 | 11 |
GO:0006518 | peptide metabolic process | 4 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009058 | biosynthetic process | 2 | 11 |
GO:0009059 | macromolecule biosynthetic process | 4 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0019538 | protein metabolic process | 3 | 11 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
GO:0034645 | obsolete cellular macromolecule biosynthetic process | 4 | 11 |
GO:0043043 | peptide biosynthetic process | 5 | 11 |
GO:0043170 | macromolecule metabolic process | 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:0071704 | organic substance metabolic process | 2 | 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:0003735 | structural constituent of ribosome | 2 | 11 |
GO:0005198 | structural molecule activity | 1 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 129 | 133 | PF00656 | 0.535 |
CLV_MEL_PAP_1 | 153 | 159 | PF00089 | 0.335 |
CLV_NRD_NRD_1 | 134 | 136 | PF00675 | 0.346 |
CLV_NRD_NRD_1 | 144 | 146 | PF00675 | 0.321 |
CLV_NRD_NRD_1 | 281 | 283 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 292 | 294 | PF00675 | 0.448 |
CLV_NRD_NRD_1 | 315 | 317 | PF00675 | 0.452 |
CLV_NRD_NRD_1 | 368 | 370 | PF00675 | 0.564 |
CLV_NRD_NRD_1 | 53 | 55 | PF00675 | 0.463 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.568 |
CLV_PCSK_KEX2_1 | 134 | 136 | PF00082 | 0.339 |
CLV_PCSK_KEX2_1 | 294 | 296 | PF00082 | 0.423 |
CLV_PCSK_KEX2_1 | 315 | 317 | PF00082 | 0.452 |
CLV_PCSK_KEX2_1 | 368 | 370 | PF00082 | 0.491 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.568 |
CLV_PCSK_PC1ET2_1 | 294 | 296 | PF00082 | 0.412 |
CLV_PCSK_SKI1_1 | 145 | 149 | PF00082 | 0.363 |
CLV_PCSK_SKI1_1 | 150 | 154 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 201 | 205 | PF00082 | 0.447 |
DEG_APCC_DBOX_1 | 173 | 181 | PF00400 | 0.378 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.578 |
DOC_MAPK_MEF2A_6 | 225 | 234 | PF00069 | 0.378 |
DOC_PP1_RVXF_1 | 177 | 183 | PF00149 | 0.335 |
DOC_PP1_RVXF_1 | 207 | 214 | PF00149 | 0.372 |
DOC_PP1_RVXF_1 | 43 | 49 | PF00149 | 0.593 |
DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.378 |
DOC_USP7_MATH_1 | 248 | 252 | PF00917 | 0.331 |
DOC_USP7_MATH_1 | 27 | 31 | PF00917 | 0.462 |
DOC_USP7_MATH_1 | 289 | 293 | PF00917 | 0.484 |
DOC_USP7_MATH_1 | 357 | 361 | PF00917 | 0.491 |
DOC_USP7_MATH_1 | 367 | 371 | PF00917 | 0.487 |
DOC_USP7_UBL2_3 | 340 | 344 | PF12436 | 0.455 |
DOC_WW_Pin1_4 | 145 | 150 | PF00397 | 0.335 |
DOC_WW_Pin1_4 | 97 | 102 | PF00397 | 0.483 |
LIG_14-3-3_CanoR_1 | 156 | 162 | PF00244 | 0.378 |
LIG_14-3-3_CanoR_1 | 174 | 178 | PF00244 | 0.410 |
LIG_14-3-3_CanoR_1 | 315 | 323 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 368 | 374 | PF00244 | 0.577 |
LIG_14-3-3_CanoR_1 | 45 | 49 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 73 | 82 | PF00244 | 0.484 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.643 |
LIG_FHA_1 | 184 | 190 | PF00498 | 0.389 |
LIG_FHA_1 | 192 | 198 | PF00498 | 0.362 |
LIG_FHA_2 | 271 | 277 | PF00498 | 0.591 |
LIG_FHA_2 | 323 | 329 | PF00498 | 0.494 |
LIG_FHA_2 | 330 | 336 | PF00498 | 0.471 |
LIG_LIR_Apic_2 | 100 | 106 | PF02991 | 0.571 |
LIG_LIR_Apic_2 | 305 | 311 | PF02991 | 0.467 |
LIG_LIR_Apic_2 | 317 | 323 | PF02991 | 0.530 |
LIG_LIR_Apic_2 | 83 | 88 | PF02991 | 0.441 |
LIG_LIR_Gen_1 | 171 | 180 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 251 | 257 | PF02991 | 0.436 |
LIG_LIR_Gen_1 | 260 | 271 | PF02991 | 0.413 |
LIG_LIR_Gen_1 | 91 | 101 | PF02991 | 0.542 |
LIG_LIR_Nem_3 | 171 | 175 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 251 | 255 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 260 | 266 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 269 | 274 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 30 | 35 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 47 | 51 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 80 | 85 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 91 | 97 | PF02991 | 0.480 |
LIG_NRBOX | 176 | 182 | PF00104 | 0.355 |
LIG_SH2_GRB2like | 36 | 39 | PF00017 | 0.553 |
LIG_SH2_GRB2like | 85 | 88 | PF00017 | 0.451 |
LIG_SH2_NCK_1 | 308 | 312 | PF00017 | 0.474 |
LIG_SH2_PTP2 | 103 | 106 | PF00017 | 0.599 |
LIG_SH2_PTP2 | 320 | 323 | PF00017 | 0.511 |
LIG_SH2_PTP2 | 85 | 88 | PF00017 | 0.576 |
LIG_SH2_SRC | 308 | 311 | PF00017 | 0.477 |
LIG_SH2_SRC | 85 | 88 | PF00017 | 0.451 |
LIG_SH2_STAP1 | 126 | 130 | PF00017 | 0.535 |
LIG_SH2_STAP1 | 36 | 40 | PF00017 | 0.552 |
LIG_SH2_STAT3 | 96 | 99 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 103 | 106 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 320 | 323 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 96 | 99 | PF00017 | 0.477 |
LIG_SH3_3 | 208 | 214 | PF00018 | 0.394 |
LIG_SH3_3 | 223 | 229 | PF00018 | 0.276 |
LIG_TRAF2_1 | 332 | 335 | PF00917 | 0.499 |
LIG_TRFH_1 | 151 | 155 | PF08558 | 0.335 |
LIG_WRC_WIRS_1 | 271 | 276 | PF05994 | 0.593 |
MOD_CDK_SPK_2 | 145 | 150 | PF00069 | 0.335 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.424 |
MOD_CK1_1 | 360 | 366 | PF00069 | 0.473 |
MOD_CK2_1 | 270 | 276 | PF00069 | 0.590 |
MOD_CK2_1 | 329 | 335 | PF00069 | 0.472 |
MOD_CMANNOS | 79 | 82 | PF00535 | 0.464 |
MOD_Cter_Amidation | 313 | 316 | PF01082 | 0.450 |
MOD_Cter_Amidation | 52 | 55 | PF01082 | 0.469 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.452 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.358 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.360 |
MOD_GlcNHglycan | 351 | 354 | PF01048 | 0.517 |
MOD_GlcNHglycan | 369 | 372 | PF01048 | 0.385 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.666 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.470 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.552 |
MOD_N-GLC_1 | 191 | 196 | PF02516 | 0.437 |
MOD_N-GLC_1 | 235 | 240 | PF02516 | 0.355 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.423 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.572 |
MOD_NEK2_1 | 95 | 100 | PF00069 | 0.536 |
MOD_NEK2_2 | 27 | 32 | PF00069 | 0.434 |
MOD_PIKK_1 | 88 | 94 | PF00454 | 0.519 |
MOD_PIKK_1 | 95 | 101 | PF00454 | 0.493 |
MOD_PKA_2 | 155 | 161 | PF00069 | 0.355 |
MOD_PKA_2 | 173 | 179 | PF00069 | 0.380 |
MOD_PKA_2 | 314 | 320 | PF00069 | 0.523 |
MOD_PKA_2 | 367 | 373 | PF00069 | 0.537 |
MOD_PKA_2 | 44 | 50 | PF00069 | 0.523 |
MOD_PKA_2 | 72 | 78 | PF00069 | 0.495 |
MOD_Plk_1 | 191 | 197 | PF00069 | 0.447 |
MOD_Plk_1 | 303 | 309 | PF00069 | 0.560 |
MOD_Plk_2-3 | 270 | 276 | PF00069 | 0.623 |
MOD_Plk_4 | 27 | 33 | PF00069 | 0.434 |
MOD_Plk_4 | 270 | 276 | PF00069 | 0.590 |
MOD_Plk_4 | 351 | 357 | PF00069 | 0.459 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.503 |
MOD_ProDKin_1 | 145 | 151 | PF00069 | 0.335 |
MOD_ProDKin_1 | 97 | 103 | PF00069 | 0.481 |
MOD_SUMO_rev_2 | 276 | 285 | PF00179 | 0.499 |
TRG_DiLeu_BaEn_3 | 269 | 275 | PF01217 | 0.584 |
TRG_DiLeu_BaLyEn_6 | 30 | 35 | PF01217 | 0.406 |
TRG_ENDOCYTIC_2 | 11 | 14 | PF00928 | 0.472 |
TRG_ENDOCYTIC_2 | 263 | 266 | PF00928 | 0.430 |
TRG_ER_diArg_1 | 162 | 165 | PF00400 | 0.355 |
TRG_ER_diArg_1 | 9 | 11 | PF00400 | 0.552 |
TRG_NLS_Bipartite_1 | 282 | 297 | PF00514 | 0.537 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PET7 | Leptomonas seymouri | 90% | 100% |
A0A0S4JQJ9 | Bodo saltans | 59% | 100% |
A0A1X0NZG0 | Trypanosomatidae | 74% | 100% |
A0A3Q8IA98 | Leishmania donovani | 98% | 100% |
A4H8C8 | Leishmania braziliensis | 92% | 100% |
A4HWQ0 | Leishmania infantum | 98% | 100% |
C9ZPT1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 75% | 100% |
E9AQF7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
V5BFU8 | Trypanosoma cruzi | 74% | 100% |