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:0005840 | ribosome | 5 | 10 |
GO:0032991 | protein-containing complex | 1 | 10 |
GO:0043226 | organelle | 2 | 10 |
GO:0043228 | non-membrane-bounded organelle | 3 | 10 |
GO:0043229 | intracellular organelle | 3 | 10 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:1990904 | ribonucleoprotein complex | 2 | 10 |
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 |
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 |
GO:0032543 | mitochondrial translation | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003735 | structural constituent of ribosome | 2 | 11 |
GO:0005198 | structural molecule activity | 1 | 11 |
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 181 | 183 | PF00675 | 0.506 |
CLV_NRD_NRD_1 | 213 | 215 | PF00675 | 0.454 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.529 |
CLV_NRD_NRD_1 | 324 | 326 | PF00675 | 0.248 |
CLV_NRD_NRD_1 | 58 | 60 | PF00675 | 0.515 |
CLV_PCSK_KEX2_1 | 181 | 183 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 200 | 202 | PF00082 | 0.564 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.435 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.529 |
CLV_PCSK_KEX2_1 | 324 | 326 | PF00082 | 0.248 |
CLV_PCSK_KEX2_1 | 338 | 340 | PF00082 | 0.248 |
CLV_PCSK_KEX2_1 | 356 | 358 | PF00082 | 0.187 |
CLV_PCSK_KEX2_1 | 58 | 60 | PF00082 | 0.489 |
CLV_PCSK_PC1ET2_1 | 200 | 202 | PF00082 | 0.483 |
CLV_PCSK_PC1ET2_1 | 338 | 340 | PF00082 | 0.285 |
CLV_PCSK_PC1ET2_1 | 356 | 358 | PF00082 | 0.176 |
CLV_PCSK_PC7_1 | 334 | 340 | PF00082 | 0.280 |
CLV_PCSK_SKI1_1 | 174 | 178 | PF00082 | 0.569 |
CLV_PCSK_SKI1_1 | 216 | 220 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.561 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.508 |
DOC_CKS1_1 | 373 | 378 | PF01111 | 0.606 |
DOC_CYCLIN_RxL_1 | 1 | 10 | PF00134 | 0.600 |
DOC_MAPK_gen_1 | 213 | 221 | PF00069 | 0.392 |
DOC_MAPK_MEF2A_6 | 106 | 115 | PF00069 | 0.605 |
DOC_PP1_RVXF_1 | 2 | 9 | PF00149 | 0.453 |
DOC_PP2B_LxvP_1 | 304 | 307 | PF13499 | 0.462 |
DOC_PP2B_LxvP_1 | 54 | 57 | PF13499 | 0.629 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.604 |
DOC_USP7_UBL2_3 | 200 | 204 | PF12436 | 0.402 |
DOC_USP7_UBL2_3 | 350 | 354 | PF12436 | 0.480 |
DOC_WW_Pin1_4 | 117 | 122 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 133 | 138 | PF00397 | 0.529 |
DOC_WW_Pin1_4 | 145 | 150 | PF00397 | 0.545 |
DOC_WW_Pin1_4 | 367 | 372 | PF00397 | 0.505 |
DOC_WW_Pin1_4 | 38 | 43 | PF00397 | 0.674 |
LIG_14-3-3_CanoR_1 | 213 | 219 | PF00244 | 0.458 |
LIG_14-3-3_CanoR_1 | 357 | 362 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 405 | 410 | PF00244 | 0.620 |
LIG_APCC_ABBA_1 | 102 | 107 | PF00400 | 0.515 |
LIG_CSL_BTD_1 | 134 | 137 | PF09270 | 0.531 |
LIG_deltaCOP1_diTrp_1 | 133 | 138 | PF00928 | 0.529 |
LIG_deltaCOP1_diTrp_1 | 153 | 157 | PF00928 | 0.545 |
LIG_FHA_1 | 110 | 116 | PF00498 | 0.570 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.467 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.462 |
LIG_FHA_1 | 353 | 359 | PF00498 | 0.462 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.659 |
LIG_FHA_2 | 373 | 379 | PF00498 | 0.607 |
LIG_FHA_2 | 406 | 412 | PF00498 | 0.520 |
LIG_HCF-1_HBM_1 | 122 | 125 | PF13415 | 0.627 |
LIG_LIR_Nem_3 | 133 | 138 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 146 | 150 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 153 | 157 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 217 | 221 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 235 | 239 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 92 | 98 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 99 | 105 | PF02991 | 0.517 |
LIG_MYND_1 | 299 | 303 | PF01753 | 0.448 |
LIG_Pex14_1 | 392 | 396 | PF04695 | 0.425 |
LIG_Pex14_2 | 218 | 222 | PF04695 | 0.364 |
LIG_PTB_Apo_2 | 223 | 230 | PF02174 | 0.387 |
LIG_PTB_Apo_2 | 242 | 249 | PF02174 | 0.496 |
LIG_PTB_Phospho_1 | 223 | 229 | PF10480 | 0.390 |
LIG_SH2_CRK | 147 | 151 | PF00017 | 0.537 |
LIG_SH2_CRK | 236 | 240 | PF00017 | 0.407 |
LIG_SH2_GRB2like | 224 | 227 | PF00017 | 0.396 |
LIG_SH2_NCK_1 | 244 | 248 | PF00017 | 0.438 |
LIG_SH2_SRC | 224 | 227 | PF00017 | 0.396 |
LIG_SH2_STAP1 | 125 | 129 | PF00017 | 0.586 |
LIG_SH2_STAP1 | 98 | 102 | PF00017 | 0.514 |
LIG_SH2_STAT3 | 330 | 333 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 117 | 120 | PF00017 | 0.570 |
LIG_SH2_STAT5 | 147 | 150 | PF00017 | 0.556 |
LIG_SH2_STAT5 | 162 | 165 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 229 | 232 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 396 | 399 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 98 | 101 | PF00017 | 0.506 |
LIG_SH3_3 | 115 | 121 | PF00018 | 0.587 |
LIG_SH3_3 | 343 | 349 | PF00018 | 0.448 |
LIG_SUMO_SIM_anti_2 | 43 | 49 | PF11976 | 0.617 |
LIG_SUMO_SIM_par_1 | 257 | 263 | PF11976 | 0.448 |
LIG_SUMO_SIM_par_1 | 302 | 308 | PF11976 | 0.448 |
LIG_TRAF2_1 | 340 | 343 | PF00917 | 0.513 |
LIG_TRFH_1 | 75 | 79 | PF08558 | 0.708 |
LIG_TYR_ITIM | 234 | 239 | PF00017 | 0.374 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.537 |
MOD_CK1_1 | 337 | 343 | PF00069 | 0.505 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.565 |
MOD_CK2_1 | 15 | 21 | PF00069 | 0.657 |
MOD_CK2_1 | 257 | 263 | PF00069 | 0.462 |
MOD_CK2_1 | 337 | 343 | PF00069 | 0.513 |
MOD_Cter_Amidation | 322 | 325 | PF01082 | 0.248 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.565 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.462 |
MOD_GlcNHglycan | 286 | 289 | PF01048 | 0.248 |
MOD_GlcNHglycan | 393 | 396 | PF01048 | 0.415 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.561 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.501 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.393 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.448 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.654 |
MOD_GSK3_1 | 411 | 418 | PF00069 | 0.528 |
MOD_N-GLC_1 | 334 | 339 | PF02516 | 0.305 |
MOD_N-GLC_1 | 405 | 410 | PF02516 | 0.573 |
MOD_NEK2_1 | 313 | 318 | PF00069 | 0.483 |
MOD_PIKK_1 | 123 | 129 | PF00454 | 0.543 |
MOD_PIKK_1 | 69 | 75 | PF00454 | 0.578 |
MOD_PIKK_1 | 84 | 90 | PF00454 | 0.540 |
MOD_PKA_1 | 214 | 220 | PF00069 | 0.425 |
MOD_PKA_1 | 356 | 362 | PF00069 | 0.448 |
MOD_PKA_2 | 284 | 290 | PF00069 | 0.448 |
MOD_PKA_2 | 294 | 300 | PF00069 | 0.448 |
MOD_PKA_2 | 356 | 362 | PF00069 | 0.461 |
MOD_Plk_1 | 184 | 190 | PF00069 | 0.452 |
MOD_Plk_1 | 262 | 268 | PF00069 | 0.448 |
MOD_Plk_1 | 405 | 411 | PF00069 | 0.652 |
MOD_Plk_2-3 | 269 | 275 | PF00069 | 0.448 |
MOD_Plk_2-3 | 96 | 102 | PF00069 | 0.511 |
MOD_Plk_4 | 214 | 220 | PF00069 | 0.400 |
MOD_Plk_4 | 43 | 49 | PF00069 | 0.668 |
MOD_ProDKin_1 | 117 | 123 | PF00069 | 0.562 |
MOD_ProDKin_1 | 133 | 139 | PF00069 | 0.530 |
MOD_ProDKin_1 | 145 | 151 | PF00069 | 0.549 |
MOD_ProDKin_1 | 367 | 373 | PF00069 | 0.505 |
MOD_ProDKin_1 | 38 | 44 | PF00069 | 0.674 |
MOD_SUMO_for_1 | 79 | 82 | PF00179 | 0.608 |
MOD_SUMO_rev_2 | 72 | 81 | PF00179 | 0.596 |
TRG_DiLeu_BaLyEn_6 | 300 | 305 | PF01217 | 0.480 |
TRG_ENDOCYTIC_2 | 147 | 150 | PF00928 | 0.556 |
TRG_ENDOCYTIC_2 | 190 | 193 | PF00928 | 0.548 |
TRG_ENDOCYTIC_2 | 236 | 239 | PF00928 | 0.397 |
TRG_ER_diArg_1 | 180 | 182 | PF00400 | 0.501 |
TRG_ER_diArg_1 | 2 | 4 | PF00400 | 0.487 |
TRG_ER_diArg_1 | 398 | 401 | PF00400 | 0.403 |
TRG_ER_diArg_1 | 57 | 59 | PF00400 | 0.467 |
TRG_NLS_Bipartite_1 | 200 | 218 | PF00514 | 0.422 |
TRG_NLS_MonoExtN_4 | 213 | 218 | PF00514 | 0.426 |
TRG_Pf-PMV_PEXEL_1 | 339 | 343 | PF00026 | 0.236 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEP9 | Leptomonas seymouri | 83% | 100% |
A0A0S4KG37 | Bodo saltans | 77% | 100% |
A0A1X0NNZ0 | Trypanosomatidae | 87% | 100% |
A0A3R7NN14 | Trypanosoma rangeli | 88% | 100% |
A0A3S5H640 | Leishmania donovani | 97% | 100% |
A4HTH9 | Leishmania infantum | 97% | 100% |
C9ZPK6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 83% | 100% |
E9AMA7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
Q4QIE1 | Leishmania major | 96% | 100% |