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:0005762 | mitochondrial large ribosomal subunit | 3 | 2 |
GO:0015934 | large ribosomal subunit | 4 | 2 |
GO:0032991 | protein-containing complex | 1 | 10 |
GO:0044391 | ribosomal subunit | 3 | 2 |
GO:0098798 | mitochondrial protein-containing complex | 2 | 2 |
GO:1990904 | ribonucleoprotein complex | 2 | 10 |
GO:0005840 | ribosome | 5 | 9 |
GO:0043226 | organelle | 2 | 9 |
GO:0043228 | non-membrane-bounded organelle | 3 | 9 |
GO:0043229 | intracellular organelle | 3 | 9 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
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:0032543 | mitochondrial translation | 5 | 2 |
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:0003676 | nucleic acid binding | 3 | 2 |
GO:0003723 | RNA binding | 4 | 2 |
GO:0003735 | structural constituent of ribosome | 2 | 11 |
GO:0005198 | structural molecule activity | 1 | 11 |
GO:0005488 | binding | 1 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 134 | 136 | PF00675 | 0.488 |
CLV_NRD_NRD_1 | 166 | 168 | PF00675 | 0.459 |
CLV_NRD_NRD_1 | 277 | 279 | PF00675 | 0.237 |
CLV_PCSK_KEX2_1 | 134 | 136 | PF00082 | 0.443 |
CLV_PCSK_KEX2_1 | 153 | 155 | PF00082 | 0.417 |
CLV_PCSK_KEX2_1 | 277 | 279 | PF00082 | 0.237 |
CLV_PCSK_KEX2_1 | 291 | 293 | PF00082 | 0.237 |
CLV_PCSK_KEX2_1 | 309 | 311 | PF00082 | 0.170 |
CLV_PCSK_PC1ET2_1 | 153 | 155 | PF00082 | 0.458 |
CLV_PCSK_PC1ET2_1 | 291 | 293 | PF00082 | 0.274 |
CLV_PCSK_PC1ET2_1 | 309 | 311 | PF00082 | 0.157 |
CLV_PCSK_PC7_1 | 287 | 293 | PF00082 | 0.268 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.552 |
CLV_PCSK_SKI1_1 | 127 | 131 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 169 | 173 | PF00082 | 0.487 |
DOC_CKS1_1 | 326 | 331 | PF01111 | 0.626 |
DOC_MAPK_gen_1 | 167 | 174 | PF00069 | 0.381 |
DOC_MAPK_MEF2A_6 | 59 | 68 | PF00069 | 0.578 |
DOC_PP2B_LxvP_1 | 257 | 260 | PF13499 | 0.450 |
DOC_PP2B_LxvP_1 | 7 | 10 | PF13499 | 0.661 |
DOC_USP7_UBL2_3 | 153 | 157 | PF12436 | 0.394 |
DOC_USP7_UBL2_3 | 303 | 307 | PF12436 | 0.468 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.657 |
DOC_WW_Pin1_4 | 320 | 325 | PF00397 | 0.496 |
DOC_WW_Pin1_4 | 70 | 75 | PF00397 | 0.541 |
DOC_WW_Pin1_4 | 86 | 91 | PF00397 | 0.512 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.505 |
LIG_14-3-3_CanoR_1 | 167 | 172 | PF00244 | 0.437 |
LIG_14-3-3_CanoR_1 | 310 | 315 | PF00244 | 0.450 |
LIG_14-3-3_CanoR_1 | 358 | 363 | PF00244 | 0.603 |
LIG_APCC_ABBA_1 | 55 | 60 | PF00400 | 0.495 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.542 |
LIG_CSL_BTD_1 | 87 | 90 | PF09270 | 0.512 |
LIG_deltaCOP1_diTrp_1 | 106 | 110 | PF00928 | 0.549 |
LIG_deltaCOP1_diTrp_1 | 86 | 91 | PF00928 | 0.512 |
LIG_FHA_1 | 209 | 215 | PF00498 | 0.437 |
LIG_FHA_1 | 240 | 246 | PF00498 | 0.456 |
LIG_FHA_1 | 306 | 312 | PF00498 | 0.457 |
LIG_FHA_1 | 63 | 69 | PF00498 | 0.543 |
LIG_FHA_2 | 326 | 332 | PF00498 | 0.644 |
LIG_FHA_2 | 359 | 365 | PF00498 | 0.503 |
LIG_HCF-1_HBM_1 | 75 | 78 | PF13415 | 0.598 |
LIG_LIR_Nem_3 | 106 | 110 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 170 | 174 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 188 | 192 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 45 | 51 | PF02991 | 0.520 |
LIG_LIR_Nem_3 | 52 | 58 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 86 | 91 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 99 | 103 | PF02991 | 0.528 |
LIG_MYND_1 | 252 | 256 | PF01753 | 0.437 |
LIG_MYND_1 | 6 | 10 | PF01753 | 0.593 |
LIG_Pex14_1 | 345 | 349 | PF04695 | 0.459 |
LIG_Pex14_2 | 171 | 175 | PF04695 | 0.349 |
LIG_PTB_Apo_2 | 176 | 183 | PF02174 | 0.388 |
LIG_PTB_Apo_2 | 195 | 202 | PF02174 | 0.399 |
LIG_PTB_Phospho_1 | 176 | 182 | PF10480 | 0.393 |
LIG_SH2_CRK | 100 | 104 | PF00017 | 0.504 |
LIG_SH2_CRK | 189 | 193 | PF00017 | 0.399 |
LIG_SH2_GRB2like | 177 | 180 | PF00017 | 0.394 |
LIG_SH2_NCK_1 | 197 | 201 | PF00017 | 0.412 |
LIG_SH2_SRC | 177 | 180 | PF00017 | 0.394 |
LIG_SH2_STAP1 | 51 | 55 | PF00017 | 0.514 |
LIG_SH2_STAP1 | 78 | 82 | PF00017 | 0.555 |
LIG_SH2_STAT3 | 283 | 286 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 100 | 103 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 115 | 118 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 182 | 185 | PF00017 | 0.381 |
LIG_SH2_STAT5 | 349 | 352 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 51 | 54 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 70 | 73 | PF00017 | 0.540 |
LIG_SH3_3 | 160 | 166 | PF00018 | 0.427 |
LIG_SH3_3 | 296 | 302 | PF00018 | 0.437 |
LIG_SH3_3 | 68 | 74 | PF00018 | 0.564 |
LIG_SUMO_SIM_par_1 | 210 | 216 | PF11976 | 0.437 |
LIG_SUMO_SIM_par_1 | 255 | 261 | PF11976 | 0.437 |
LIG_TRAF2_1 | 293 | 296 | PF00917 | 0.527 |
LIG_TRFH_1 | 28 | 32 | PF08558 | 0.699 |
LIG_TYR_ITIM | 187 | 192 | PF00017 | 0.368 |
MOD_CK1_1 | 290 | 296 | PF00069 | 0.492 |
MOD_CK2_1 | 210 | 216 | PF00069 | 0.455 |
MOD_CK2_1 | 290 | 296 | PF00069 | 0.527 |
MOD_Cter_Amidation | 275 | 278 | PF01082 | 0.237 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.439 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.237 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.447 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.454 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.366 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.437 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.513 |
MOD_N-GLC_1 | 287 | 292 | PF02516 | 0.292 |
MOD_N-GLC_1 | 358 | 363 | PF02516 | 0.559 |
MOD_N-GLC_2 | 269 | 271 | PF02516 | 0.196 |
MOD_PIKK_1 | 22 | 28 | PF00454 | 0.577 |
MOD_PIKK_1 | 37 | 43 | PF00454 | 0.526 |
MOD_PIKK_1 | 76 | 82 | PF00454 | 0.512 |
MOD_PKA_1 | 167 | 173 | PF00069 | 0.430 |
MOD_PKA_1 | 309 | 315 | PF00069 | 0.437 |
MOD_PKA_2 | 237 | 243 | PF00069 | 0.437 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.437 |
MOD_PKA_2 | 309 | 315 | PF00069 | 0.450 |
MOD_PKA_2 | 37 | 43 | PF00069 | 0.680 |
MOD_Plk_1 | 215 | 221 | PF00069 | 0.437 |
MOD_Plk_1 | 358 | 364 | PF00069 | 0.632 |
MOD_Plk_2-3 | 222 | 228 | PF00069 | 0.437 |
MOD_Plk_2-3 | 49 | 55 | PF00069 | 0.497 |
MOD_Plk_4 | 167 | 173 | PF00069 | 0.407 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.658 |
MOD_ProDKin_1 | 320 | 326 | PF00069 | 0.496 |
MOD_ProDKin_1 | 70 | 76 | PF00069 | 0.535 |
MOD_ProDKin_1 | 86 | 92 | PF00069 | 0.513 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.505 |
MOD_SUMO_for_1 | 32 | 35 | PF00179 | 0.600 |
MOD_SUMO_rev_2 | 25 | 34 | PF00179 | 0.591 |
TRG_DiLeu_BaLyEn_6 | 253 | 258 | PF01217 | 0.468 |
TRG_DiLeu_BaLyEn_6 | 3 | 8 | PF01217 | 0.720 |
TRG_ENDOCYTIC_2 | 100 | 103 | PF00928 | 0.504 |
TRG_ENDOCYTIC_2 | 143 | 146 | PF00928 | 0.548 |
TRG_ENDOCYTIC_2 | 189 | 192 | PF00928 | 0.389 |
TRG_ER_diArg_1 | 133 | 135 | PF00400 | 0.485 |
TRG_ER_diArg_1 | 351 | 354 | PF00400 | 0.416 |
TRG_NLS_Bipartite_1 | 153 | 171 | PF00514 | 0.420 |
TRG_NLS_MonoExtN_4 | 166 | 171 | PF00514 | 0.429 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEP9 | Leptomonas seymouri | 92% | 95% |
A0A0S4KG37 | Bodo saltans | 78% | 92% |
A0A1X0NNZ0 | Trypanosomatidae | 89% | 89% |
A0A3R7NN14 | Trypanosoma rangeli | 88% | 89% |
A0A3S5H640 | Leishmania donovani | 99% | 100% |
A4GGF8 | Phaseolus vulgaris | 27% | 100% |
A4H598 | Leishmania braziliensis | 96% | 89% |
A4HTH9 | Leishmania infantum | 99% | 100% |
A5IYY3 | Mycoplasmopsis agalactiae (strain NCTC 10123 / CIP 59.7 / PG2) | 26% | 100% |
A6MMG4 | Chloranthus spicatus | 27% | 100% |
A6MMI6 | Chloranthus spicatus | 26% | 100% |
A6MMY6 | Illicium oligandrum | 26% | 100% |
A9L9D7 | Lemna minor | 26% | 100% |
B3PMP4 | Metamycoplasma arthritidis (strain 158L3-1) | 26% | 100% |
C1A6Q8 | Gemmatimonas aurantiaca (strain T-27 / DSM 14586 / JCM 11422 / NBRC 100505) | 27% | 100% |
C9ZPK6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 86% | 92% |
E9AMA7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 99% | 100% |
P18663 | Glycine max | 27% | 100% |
Q03ZP2 | Leuconostoc mesenteroides subsp. mesenteroides (strain ATCC 8293 / DSM 20343 / BCRC 11652 / CCM 1803 / JCM 6124 / NCDO 523 / NBRC 100496 / NCIMB 8023 / NCTC 12954 / NRRL B-1118 / 37Y) | 25% | 100% |
Q06GT2 | Drimys granadensis | 27% | 100% |
Q09FY3 | Platanus occidentalis | 27% | 100% |
Q0G9F5 | Liriodendron tulipifera | 26% | 100% |
Q0G9H8 | Liriodendron tulipifera | 26% | 100% |
Q23888 | Dictyostelium discoideum | 26% | 100% |
Q2PMM3 | Glycine max | 27% | 100% |
Q49KT4 | Eucalyptus globulus subsp. globulus | 27% | 100% |
Q4A5C4 | Mycoplasmopsis synoviae (strain 53) | 26% | 100% |
Q8LVH2 | Phaseolus angularis | 27% | 100% |
Q9B1H9 | Lotus japonicus | 27% | 100% |