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: 0, no: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: A4H8A9
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 1 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009057 | macromolecule catabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 1 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 2 |
GO:0004842 | ubiquitin-protein transferase activity | 4 | 2 |
GO:0016740 | transferase activity | 2 | 2 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 2 |
GO:0061630 | ubiquitin protein ligase activity | 5 | 1 |
GO:0061659 | ubiquitin-like protein ligase activity | 4 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 2 |
GO:0016746 | acyltransferase activity | 3 | 1 |
GO:0061631 | ubiquitin conjugating enzyme activity | 5 | 1 |
GO:0061650 | ubiquitin-like protein conjugating enzyme activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 269 | 271 | PF00675 | 0.364 |
CLV_NRD_NRD_1 | 4 | 6 | PF00675 | 0.340 |
CLV_NRD_NRD_1 | 428 | 430 | PF00675 | 0.422 |
CLV_NRD_NRD_1 | 466 | 468 | PF00675 | 0.385 |
CLV_PCSK_KEX2_1 | 269 | 271 | PF00082 | 0.383 |
CLV_PCSK_KEX2_1 | 303 | 305 | PF00082 | 0.326 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.261 |
CLV_PCSK_KEX2_1 | 428 | 430 | PF00082 | 0.422 |
CLV_PCSK_KEX2_1 | 468 | 470 | PF00082 | 0.446 |
CLV_PCSK_PC1ET2_1 | 303 | 305 | PF00082 | 0.336 |
CLV_PCSK_PC1ET2_1 | 468 | 470 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 443 | 447 | PF00082 | 0.544 |
CLV_PCSK_SKI1_1 | 478 | 482 | PF00082 | 0.344 |
DEG_MDM2_SWIB_1 | 112 | 119 | PF02201 | 0.418 |
DEG_SPOP_SBC_1 | 40 | 44 | PF00917 | 0.394 |
DOC_CYCLIN_yCln2_LP_2 | 400 | 406 | PF00134 | 0.578 |
DOC_MAPK_gen_1 | 475 | 483 | PF00069 | 0.498 |
DOC_MAPK_MEF2A_6 | 475 | 483 | PF00069 | 0.679 |
DOC_USP7_MATH_1 | 101 | 105 | PF00917 | 0.207 |
DOC_USP7_MATH_1 | 216 | 220 | PF00917 | 0.423 |
DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.459 |
DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.394 |
DOC_USP7_MATH_1 | 449 | 453 | PF00917 | 0.691 |
DOC_WW_Pin1_4 | 363 | 368 | PF00397 | 0.740 |
DOC_WW_Pin1_4 | 378 | 383 | PF00397 | 0.768 |
DOC_WW_Pin1_4 | 399 | 404 | PF00397 | 0.569 |
DOC_WW_Pin1_4 | 423 | 428 | PF00397 | 0.752 |
DOC_WW_Pin1_4 | 429 | 434 | PF00397 | 0.755 |
LIG_14-3-3_CanoR_1 | 126 | 131 | PF00244 | 0.312 |
LIG_14-3-3_CanoR_1 | 192 | 196 | PF00244 | 0.429 |
LIG_14-3-3_CanoR_1 | 204 | 210 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 4 | 8 | PF00244 | 0.566 |
LIG_14-3-3_CanoR_1 | 428 | 433 | PF00244 | 0.714 |
LIG_Actin_WH2_2 | 177 | 194 | PF00022 | 0.418 |
LIG_APCC_ABBA_1 | 94 | 99 | PF00400 | 0.630 |
LIG_BRCT_BRCA1_1 | 106 | 110 | PF00533 | 0.437 |
LIG_BRCT_BRCA1_1 | 222 | 226 | PF00533 | 0.365 |
LIG_BRCT_BRCA1_1 | 41 | 45 | PF00533 | 0.265 |
LIG_EH1_1 | 195 | 203 | PF00400 | 0.286 |
LIG_EH1_1 | 86 | 94 | PF00400 | 0.504 |
LIG_FHA_1 | 157 | 163 | PF00498 | 0.504 |
LIG_FHA_1 | 300 | 306 | PF00498 | 0.566 |
LIG_FHA_1 | 440 | 446 | PF00498 | 0.787 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.583 |
LIG_FHA_2 | 162 | 168 | PF00498 | 0.621 |
LIG_FHA_2 | 26 | 32 | PF00498 | 0.539 |
LIG_FHA_2 | 277 | 283 | PF00498 | 0.594 |
LIG_FHA_2 | 366 | 372 | PF00498 | 0.730 |
LIG_GBD_Chelix_1 | 12 | 20 | PF00786 | 0.207 |
LIG_LIR_Gen_1 | 174 | 185 | PF02991 | 0.522 |
LIG_LIR_Gen_1 | 194 | 203 | PF02991 | 0.413 |
LIG_LIR_Gen_1 | 263 | 271 | PF02991 | 0.555 |
LIG_LIR_Gen_1 | 290 | 298 | PF02991 | 0.522 |
LIG_LIR_Gen_1 | 31 | 40 | PF02991 | 0.264 |
LIG_LIR_Gen_1 | 63 | 74 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 106 | 112 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 113 | 119 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 174 | 180 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 194 | 200 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 223 | 229 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 263 | 267 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 28 | 32 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 391 | 396 | PF02991 | 0.716 |
LIG_LIR_Nem_3 | 42 | 48 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 461 | 466 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 63 | 69 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 82 | 87 | PF02991 | 0.611 |
LIG_MLH1_MIPbox_1 | 106 | 110 | PF16413 | 0.460 |
LIG_PCNA_yPIPBox_3 | 204 | 213 | PF02747 | 0.266 |
LIG_Pex14_2 | 112 | 116 | PF04695 | 0.410 |
LIG_Pex14_2 | 15 | 19 | PF04695 | 0.246 |
LIG_SH2_CRK | 177 | 181 | PF00017 | 0.413 |
LIG_SH2_CRK | 183 | 187 | PF00017 | 0.389 |
LIG_SH2_CRK | 230 | 234 | PF00017 | 0.460 |
LIG_SH2_GRB2like | 25 | 28 | PF00017 | 0.546 |
LIG_SH2_SRC | 230 | 233 | PF00017 | 0.469 |
LIG_SH2_STAP1 | 177 | 181 | PF00017 | 0.355 |
LIG_SH2_STAP1 | 230 | 234 | PF00017 | 0.469 |
LIG_SH2_STAP1 | 25 | 29 | PF00017 | 0.434 |
LIG_SH2_STAP1 | 293 | 297 | PF00017 | 0.536 |
LIG_SH2_STAP1 | 33 | 37 | PF00017 | 0.308 |
LIG_SH2_STAT3 | 396 | 399 | PF00017 | 0.726 |
LIG_SH2_STAT3 | 97 | 100 | PF00017 | 0.640 |
LIG_SH2_STAT5 | 10 | 13 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 146 | 149 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 232 | 235 | PF00017 | 0.341 |
LIG_SH2_STAT5 | 328 | 331 | PF00017 | 0.471 |
LIG_SH3_3 | 427 | 433 | PF00018 | 0.785 |
LIG_SUMO_SIM_anti_2 | 199 | 204 | PF11976 | 0.257 |
LIG_SUMO_SIM_par_1 | 183 | 190 | PF11976 | 0.460 |
LIG_SUMO_SIM_par_1 | 46 | 52 | PF11976 | 0.379 |
LIG_TRAF2_1 | 368 | 371 | PF00917 | 0.632 |
LIG_TRAF2_1 | 74 | 77 | PF00917 | 0.619 |
LIG_TYR_ITIM | 181 | 186 | PF00017 | 0.434 |
LIG_UBA3_1 | 157 | 163 | PF00899 | 0.533 |
LIG_Vh1_VBS_1 | 49 | 67 | PF01044 | 0.207 |
LIG_WRC_WIRS_1 | 12 | 17 | PF05994 | 0.440 |
LIG_WRC_WIRS_1 | 209 | 214 | PF05994 | 0.318 |
LIG_WRC_WIRS_1 | 81 | 86 | PF05994 | 0.595 |
MOD_CDC14_SPxK_1 | 426 | 429 | PF00782 | 0.763 |
MOD_CDK_SPK_2 | 423 | 428 | PF00069 | 0.608 |
MOD_CDK_SPxK_1 | 423 | 429 | PF00069 | 0.763 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.393 |
MOD_CK1_1 | 138 | 144 | PF00069 | 0.344 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.377 |
MOD_CK1_1 | 402 | 408 | PF00069 | 0.636 |
MOD_CK1_1 | 432 | 438 | PF00069 | 0.711 |
MOD_CK1_1 | 439 | 445 | PF00069 | 0.738 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.583 |
MOD_CK2_1 | 161 | 167 | PF00069 | 0.622 |
MOD_CK2_1 | 216 | 222 | PF00069 | 0.397 |
MOD_CK2_1 | 25 | 31 | PF00069 | 0.531 |
MOD_CK2_1 | 365 | 371 | PF00069 | 0.680 |
MOD_CK2_1 | 470 | 476 | PF00069 | 0.604 |
MOD_DYRK1A_RPxSP_1 | 429 | 433 | PF00069 | 0.621 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.421 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.431 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.405 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.399 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.438 |
MOD_GlcNHglycan | 404 | 407 | PF01048 | 0.514 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.436 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.369 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.568 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.350 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.324 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.704 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.691 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.570 |
MOD_LATS_1 | 441 | 447 | PF00433 | 0.618 |
MOD_N-GLC_1 | 40 | 45 | PF02516 | 0.558 |
MOD_N-GLC_1 | 72 | 77 | PF02516 | 0.360 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.317 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.385 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.326 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.553 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.302 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.309 |
MOD_NEK2_1 | 191 | 196 | PF00069 | 0.267 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.370 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.358 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.242 |
MOD_NEK2_1 | 80 | 85 | PF00069 | 0.524 |
MOD_PKA_1 | 428 | 434 | PF00069 | 0.622 |
MOD_PKA_2 | 125 | 131 | PF00069 | 0.311 |
MOD_PKA_2 | 191 | 197 | PF00069 | 0.460 |
MOD_PKA_2 | 287 | 293 | PF00069 | 0.427 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.566 |
MOD_PKA_2 | 428 | 434 | PF00069 | 0.784 |
MOD_PKA_2 | 470 | 476 | PF00069 | 0.604 |
MOD_Plk_1 | 40 | 46 | PF00069 | 0.305 |
MOD_Plk_1 | 75 | 81 | PF00069 | 0.583 |
MOD_Plk_4 | 104 | 110 | PF00069 | 0.339 |
MOD_Plk_4 | 11 | 17 | PF00069 | 0.299 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.471 |
MOD_Plk_4 | 175 | 181 | PF00069 | 0.180 |
MOD_Plk_4 | 196 | 202 | PF00069 | 0.371 |
MOD_Plk_4 | 205 | 211 | PF00069 | 0.402 |
MOD_Plk_4 | 220 | 226 | PF00069 | 0.303 |
MOD_Plk_4 | 54 | 60 | PF00069 | 0.281 |
MOD_ProDKin_1 | 363 | 369 | PF00069 | 0.741 |
MOD_ProDKin_1 | 378 | 384 | PF00069 | 0.765 |
MOD_ProDKin_1 | 399 | 405 | PF00069 | 0.572 |
MOD_ProDKin_1 | 423 | 429 | PF00069 | 0.754 |
MOD_SUMO_for_1 | 458 | 461 | PF00179 | 0.586 |
MOD_SUMO_rev_2 | 167 | 174 | PF00179 | 0.669 |
TRG_DiLeu_BaEn_1 | 76 | 81 | PF01217 | 0.580 |
TRG_DiLeu_BaEn_2 | 221 | 227 | PF01217 | 0.418 |
TRG_DiLeu_BaEn_4 | 76 | 82 | PF01217 | 0.613 |
TRG_DiLeu_BaLyEn_6 | 237 | 242 | PF01217 | 0.354 |
TRG_ENDOCYTIC_2 | 146 | 149 | PF00928 | 0.345 |
TRG_ENDOCYTIC_2 | 177 | 180 | PF00928 | 0.331 |
TRG_ENDOCYTIC_2 | 183 | 186 | PF00928 | 0.303 |
TRG_ENDOCYTIC_2 | 230 | 233 | PF00928 | 0.408 |
TRG_ENDOCYTIC_2 | 29 | 32 | PF00928 | 0.389 |
TRG_ENDOCYTIC_2 | 293 | 296 | PF00928 | 0.505 |
TRG_ENDOCYTIC_2 | 33 | 36 | PF00928 | 0.340 |
TRG_ER_diArg_1 | 269 | 272 | PF00400 | 0.595 |
TRG_ER_diArg_1 | 427 | 429 | PF00400 | 0.612 |
TRG_ER_diArg_1 | 466 | 469 | PF00400 | 0.585 |
TRG_NLS_MonoExtC_3 | 466 | 471 | PF00514 | 0.499 |
TRG_NLS_MonoExtN_4 | 465 | 471 | PF00514 | 0.500 |
TRG_Pf-PMV_PEXEL_1 | 468 | 472 | PF00026 | 0.448 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I9A3 | Leptomonas seymouri | 49% | 91% |
A0A1X0NU29 | Trypanosomatidae | 33% | 93% |
A0A3R7MBX1 | Trypanosoma rangeli | 32% | 92% |
A0A3S5H6W0 | Leishmania donovani | 78% | 100% |
A4HWM9 | Leishmania infantum | 78% | 100% |
C9ZXQ9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9AQD6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
O74757 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 26% | 73% |
Q4QF39 | Leishmania major | 77% | 97% |
Q5Z880 | Oryza sativa subsp. japonica | 31% | 98% |
Q6NPT7 | Arabidopsis thaliana | 26% | 100% |
Q95SP2 | Drosophila melanogaster | 28% | 78% |
Q9LW77 | Arabidopsis thaliana | 26% | 100% |
V5BUE9 | Trypanosoma cruzi | 29% | 92% |