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: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 1, no: 8 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005654 | nucleoplasm | 2 | 3 |
GO:0005730 | nucleolus | 5 | 1 |
GO:0005829 | cytosol | 2 | 3 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
Related structures:
AlphaFold database: E9ALR5
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 10 |
GO:0006259 | DNA metabolic process | 4 | 10 |
GO:0006281 | DNA repair | 5 | 10 |
GO:0006289 | nucleotide-excision repair | 6 | 10 |
GO:0006508 | proteolysis | 4 | 10 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 10 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0006950 | response to stress | 2 | 10 |
GO:0006974 | DNA damage response | 4 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009056 | catabolic process | 2 | 10 |
GO:0009057 | macromolecule catabolic process | 4 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0010498 | proteasomal protein catabolic process | 5 | 10 |
GO:0019538 | protein metabolic process | 3 | 10 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 10 |
GO:0030163 | protein catabolic process | 4 | 10 |
GO:0033554 | cellular response to stress | 3 | 10 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 10 |
GO:0043161 | proteasome-mediated ubiquitin-dependent protein catabolic process | 6 | 10 |
GO:0043170 | macromolecule metabolic process | 3 | 10 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
GO:0044248 | cellular catabolic process | 3 | 10 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 10 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 10 |
GO:0046483 | heterocycle metabolic process | 3 | 10 |
GO:0050896 | response to stimulus | 1 | 10 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 10 |
GO:0051716 | cellular response to stimulus | 2 | 10 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:0090304 | nucleic acid metabolic process | 4 | 10 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 10 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 10 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 10 |
GO:1901575 | organic substance catabolic process | 3 | 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 10 |
GO:0003677 | DNA binding | 4 | 10 |
GO:0003684 | damaged DNA binding | 5 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
GO:0005515 | protein binding | 2 | 3 |
GO:0031593 | polyubiquitin modification-dependent protein binding | 4 | 3 |
GO:0032182 | ubiquitin-like protein binding | 3 | 3 |
GO:0043130 | ubiquitin binding | 4 | 3 |
GO:0044877 | protein-containing complex binding | 2 | 1 |
GO:0070628 | proteasome binding | 3 | 1 |
GO:0140030 | modification-dependent protein binding | 3 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 175 | 179 | PF00656 | 0.743 |
CLV_C14_Caspase3-7 | 321 | 325 | PF00656 | 0.755 |
CLV_C14_Caspase3-7 | 65 | 69 | PF00656 | 0.785 |
CLV_NRD_NRD_1 | 60 | 62 | PF00675 | 0.420 |
CLV_PCSK_KEX2_1 | 135 | 137 | PF00082 | 0.806 |
CLV_PCSK_KEX2_1 | 340 | 342 | PF00082 | 0.625 |
CLV_PCSK_KEX2_1 | 60 | 62 | PF00082 | 0.420 |
CLV_PCSK_PC1ET2_1 | 135 | 137 | PF00082 | 0.806 |
CLV_PCSK_PC1ET2_1 | 340 | 342 | PF00082 | 0.625 |
CLV_PCSK_SKI1_1 | 25 | 29 | PF00082 | 0.609 |
CLV_PCSK_SKI1_1 | 375 | 379 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 89 | 93 | PF00082 | 0.494 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.424 |
DEG_SPOP_SBC_1 | 71 | 75 | PF00917 | 0.729 |
DOC_MAPK_MEF2A_6 | 40 | 47 | PF00069 | 0.422 |
DOC_PP1_RVXF_1 | 373 | 379 | PF00149 | 0.344 |
DOC_PP1_RVXF_1 | 48 | 55 | PF00149 | 0.499 |
DOC_PP4_FxxP_1 | 393 | 396 | PF00568 | 0.512 |
DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.715 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 330 | 334 | PF00917 | 0.754 |
DOC_USP7_MATH_1 | 70 | 74 | PF00917 | 0.713 |
DOC_USP7_UBL2_3 | 104 | 108 | PF12436 | 0.503 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.803 |
DOC_WW_Pin1_4 | 72 | 77 | PF00397 | 0.783 |
LIG_14-3-3_CanoR_1 | 33 | 37 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 341 | 349 | PF00244 | 0.586 |
LIG_14-3-3_CanoR_1 | 40 | 44 | PF00244 | 0.453 |
LIG_Actin_WH2_2 | 36 | 52 | PF00022 | 0.496 |
LIG_Actin_WH2_2 | 99 | 116 | PF00022 | 0.356 |
LIG_BIR_III_4 | 178 | 182 | PF00653 | 0.646 |
LIG_BRCT_BRCA1_1 | 285 | 289 | PF00533 | 0.560 |
LIG_BRCT_BRCA1_1 | 301 | 305 | PF00533 | 0.466 |
LIG_EH1_1 | 2 | 10 | PF00400 | 0.506 |
LIG_FHA_1 | 132 | 138 | PF00498 | 0.673 |
LIG_FHA_1 | 22 | 28 | PF00498 | 0.349 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.494 |
LIG_FHA_1 | 40 | 46 | PF00498 | 0.377 |
LIG_FHA_2 | 207 | 213 | PF00498 | 0.383 |
LIG_FHA_2 | 63 | 69 | PF00498 | 0.692 |
LIG_LIR_Gen_1 | 184 | 194 | PF02991 | 0.596 |
LIG_LIR_Gen_1 | 220 | 226 | PF02991 | 0.522 |
LIG_LIR_Gen_1 | 230 | 236 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 184 | 189 | PF02991 | 0.588 |
LIG_LIR_Nem_3 | 220 | 225 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 230 | 235 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 286 | 292 | PF02991 | 0.633 |
LIG_Pex14_2 | 54 | 58 | PF04695 | 0.524 |
LIG_SH2_CRK | 110 | 114 | PF00017 | 0.642 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 292 | 295 | PF00017 | 0.603 |
LIG_SH2_STAT5 | 379 | 382 | PF00017 | 0.408 |
LIG_SH3_3 | 142 | 148 | PF00018 | 0.751 |
LIG_SH3_3 | 26 | 32 | PF00018 | 0.582 |
LIG_SUMO_SIM_anti_2 | 195 | 200 | PF11976 | 0.561 |
LIG_SUMO_SIM_anti_2 | 230 | 237 | PF11976 | 0.511 |
LIG_TRAF2_1 | 158 | 161 | PF00917 | 0.721 |
LIG_TRAF2_1 | 188 | 191 | PF00917 | 0.422 |
LIG_TRAF2_1 | 353 | 356 | PF00917 | 0.520 |
MOD_CK1_1 | 11 | 17 | PF00069 | 0.563 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.577 |
MOD_CK1_1 | 299 | 305 | PF00069 | 0.562 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.774 |
MOD_CK2_1 | 124 | 130 | PF00069 | 0.807 |
MOD_CK2_1 | 150 | 156 | PF00069 | 0.629 |
MOD_CK2_1 | 206 | 212 | PF00069 | 0.383 |
MOD_CK2_1 | 266 | 272 | PF00069 | 0.784 |
MOD_CK2_1 | 340 | 346 | PF00069 | 0.622 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.625 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.607 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.659 |
MOD_GlcNHglycan | 314 | 318 | PF01048 | 0.407 |
MOD_GlcNHglycan | 327 | 331 | PF01048 | 0.730 |
MOD_GlcNHglycan | 332 | 335 | PF01048 | 0.734 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.796 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.586 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.538 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.755 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.565 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.432 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.483 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.611 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.706 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.523 |
MOD_N-GLC_1 | 108 | 113 | PF02516 | 0.681 |
MOD_N-GLC_1 | 12 | 17 | PF02516 | 0.557 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.436 |
MOD_NEK2_1 | 266 | 271 | PF00069 | 0.783 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.589 |
MOD_NEK2_1 | 313 | 318 | PF00069 | 0.693 |
MOD_NEK2_1 | 347 | 352 | PF00069 | 0.622 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.507 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.484 |
MOD_PKA_1 | 340 | 346 | PF00069 | 0.599 |
MOD_PKA_2 | 123 | 129 | PF00069 | 0.498 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.563 |
MOD_PKA_2 | 340 | 346 | PF00069 | 0.599 |
MOD_PKA_2 | 386 | 392 | PF00069 | 0.444 |
MOD_PKA_2 | 39 | 45 | PF00069 | 0.528 |
MOD_Plk_1 | 108 | 114 | PF00069 | 0.689 |
MOD_Plk_1 | 12 | 18 | PF00069 | 0.558 |
MOD_Plk_1 | 194 | 200 | PF00069 | 0.561 |
MOD_Plk_1 | 25 | 31 | PF00069 | 0.583 |
MOD_Plk_1 | 266 | 272 | PF00069 | 0.704 |
MOD_Plk_2-3 | 159 | 165 | PF00069 | 0.748 |
MOD_Plk_2-3 | 262 | 268 | PF00069 | 0.720 |
MOD_Plk_2-3 | 62 | 68 | PF00069 | 0.595 |
MOD_Plk_4 | 12 | 18 | PF00069 | 0.587 |
MOD_Plk_4 | 194 | 200 | PF00069 | 0.561 |
MOD_Plk_4 | 206 | 212 | PF00069 | 0.534 |
MOD_Plk_4 | 217 | 223 | PF00069 | 0.530 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.525 |
MOD_Plk_4 | 288 | 294 | PF00069 | 0.517 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.804 |
MOD_ProDKin_1 | 72 | 78 | PF00069 | 0.782 |
MOD_SUMO_rev_2 | 354 | 361 | PF00179 | 0.345 |
MOD_SUMO_rev_2 | 84 | 92 | PF00179 | 0.564 |
TRG_DiLeu_BaEn_2 | 145 | 151 | PF01217 | 0.731 |
TRG_DiLeu_BaEn_4 | 159 | 165 | PF01217 | 0.743 |
TRG_ENDOCYTIC_2 | 110 | 113 | PF00928 | 0.610 |
TRG_ER_diArg_1 | 136 | 139 | PF00400 | 0.795 |
TRG_NLS_MonoExtC_3 | 134 | 140 | PF00514 | 0.750 |
TRG_NLS_MonoExtN_4 | 132 | 139 | PF00514 | 0.752 |
TRG_Pf-PMV_PEXEL_1 | 90 | 94 | PF00026 | 0.530 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I958 | Leptomonas seymouri | 61% | 100% |
A0A1X0NZX2 | Trypanosomatidae | 28% | 100% |
A0A3Q8IFF1 | Leishmania donovani | 90% | 100% |
A0A422NEC4 | Trypanosoma rangeli | 29% | 100% |
A4HHH1 | Leishmania braziliensis | 79% | 100% |
A4I4M0 | Leishmania infantum | 90% | 100% |
E9AE18 | Leishmania major | 89% | 98% |
V5B988 | Trypanosoma cruzi | 28% | 100% |