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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: Q4QF39
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 2 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009056 | catabolic process | 2 | 2 |
GO:0009057 | macromolecule catabolic process | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044248 | cellular catabolic process | 3 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 2 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
GO:1901575 | organic substance catabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 3 |
GO:0004842 | ubiquitin-protein transferase activity | 4 | 3 |
GO:0016740 | transferase activity | 2 | 3 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 3 |
GO:0061630 | ubiquitin protein ligase activity | 5 | 2 |
GO:0061659 | ubiquitin-like protein ligase activity | 4 | 2 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 3 |
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_C14_Caspase3-7 | 274 | 278 | PF00656 | 0.584 |
CLV_C14_Caspase3-7 | 418 | 422 | PF00656 | 0.636 |
CLV_NRD_NRD_1 | 269 | 271 | PF00675 | 0.365 |
CLV_PCSK_KEX2_1 | 269 | 271 | PF00082 | 0.386 |
CLV_PCSK_KEX2_1 | 303 | 305 | PF00082 | 0.323 |
CLV_PCSK_KEX2_1 | 455 | 457 | PF00082 | 0.441 |
CLV_PCSK_PC1ET2_1 | 303 | 305 | PF00082 | 0.338 |
CLV_PCSK_PC1ET2_1 | 455 | 457 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 236 | 240 | PF00082 | 0.436 |
DEG_MDM2_SWIB_1 | 112 | 119 | PF02201 | 0.423 |
DEG_SPOP_SBC_1 | 40 | 44 | PF00917 | 0.396 |
DOC_CKS1_1 | 436 | 441 | PF01111 | 0.714 |
DOC_MAPK_DCC_7 | 236 | 244 | PF00069 | 0.409 |
DOC_MAPK_MEF2A_6 | 236 | 244 | PF00069 | 0.409 |
DOC_MAPK_MEF2A_6 | 462 | 470 | PF00069 | 0.691 |
DOC_MAPK_NFAT4_5 | 236 | 244 | PF00069 | 0.409 |
DOC_PP2B_LxvP_1 | 398 | 401 | PF13499 | 0.689 |
DOC_USP7_MATH_1 | 216 | 220 | PF00917 | 0.469 |
DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.396 |
DOC_USP7_MATH_1 | 404 | 408 | PF00917 | 0.744 |
DOC_USP7_MATH_1 | 410 | 414 | PF00917 | 0.705 |
DOC_USP7_UBL2_3 | 448 | 452 | PF12436 | 0.570 |
DOC_WW_Pin1_4 | 367 | 372 | PF00397 | 0.778 |
DOC_WW_Pin1_4 | 421 | 426 | PF00397 | 0.788 |
DOC_WW_Pin1_4 | 435 | 440 | PF00397 | 0.725 |
LIG_14-3-3_CanoR_1 | 126 | 131 | PF00244 | 0.296 |
LIG_14-3-3_CanoR_1 | 192 | 196 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 204 | 210 | PF00244 | 0.344 |
LIG_14-3-3_CanoR_1 | 270 | 276 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 4 | 8 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 427 | 431 | PF00244 | 0.782 |
LIG_Actin_WH2_2 | 177 | 194 | PF00022 | 0.423 |
LIG_APCC_ABBA_1 | 94 | 99 | PF00400 | 0.625 |
LIG_BRCT_BRCA1_1 | 106 | 110 | PF00533 | 0.408 |
LIG_BRCT_BRCA1_1 | 222 | 226 | PF00533 | 0.354 |
LIG_BRCT_BRCA1_1 | 41 | 45 | PF00533 | 0.246 |
LIG_FHA_1 | 157 | 163 | PF00498 | 0.537 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.574 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.534 |
LIG_FHA_1 | 300 | 306 | PF00498 | 0.561 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.366 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.585 |
LIG_FHA_2 | 162 | 168 | PF00498 | 0.600 |
LIG_FHA_2 | 26 | 32 | PF00498 | 0.513 |
LIG_FHA_2 | 277 | 283 | PF00498 | 0.593 |
LIG_FHA_2 | 377 | 383 | PF00498 | 0.754 |
LIG_FHA_2 | 416 | 422 | PF00498 | 0.744 |
LIG_LIR_Gen_1 | 194 | 203 | PF02991 | 0.491 |
LIG_LIR_Gen_1 | 223 | 234 | PF02991 | 0.316 |
LIG_LIR_Gen_1 | 263 | 271 | PF02991 | 0.524 |
LIG_LIR_Gen_1 | 290 | 298 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 107 | 112 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 113 | 119 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 194 | 200 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 223 | 229 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 263 | 267 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 28 | 32 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 389 | 394 | PF02991 | 0.713 |
LIG_LIR_Nem_3 | 42 | 48 | PF02991 | 0.262 |
LIG_LIR_Nem_3 | 82 | 87 | PF02991 | 0.619 |
LIG_LYPXL_S_1 | 32 | 36 | PF13949 | 0.565 |
LIG_LYPXL_yS_3 | 33 | 36 | PF13949 | 0.360 |
LIG_MLH1_MIPbox_1 | 106 | 110 | PF16413 | 0.456 |
LIG_Pex14_2 | 108 | 112 | PF04695 | 0.430 |
LIG_Pex14_2 | 197 | 201 | PF04695 | 0.344 |
LIG_SH2_CRK | 177 | 181 | PF00017 | 0.398 |
LIG_SH2_CRK | 183 | 187 | PF00017 | 0.363 |
LIG_SH2_CRK | 230 | 234 | PF00017 | 0.456 |
LIG_SH2_GRB2like | 25 | 28 | PF00017 | 0.509 |
LIG_SH2_SRC | 230 | 233 | PF00017 | 0.456 |
LIG_SH2_STAP1 | 177 | 181 | PF00017 | 0.339 |
LIG_SH2_STAP1 | 230 | 234 | PF00017 | 0.456 |
LIG_SH2_STAP1 | 25 | 29 | PF00017 | 0.402 |
LIG_SH2_STAP1 | 293 | 297 | PF00017 | 0.538 |
LIG_SH2_STAT3 | 394 | 397 | PF00017 | 0.731 |
LIG_SH2_STAT3 | 97 | 100 | PF00017 | 0.635 |
LIG_SH2_STAT5 | 10 | 13 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 146 | 149 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 232 | 235 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 328 | 331 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 87 | 90 | PF00017 | 0.498 |
LIG_SH3_3 | 340 | 346 | PF00018 | 0.661 |
LIG_SH3_3 | 89 | 95 | PF00018 | 0.533 |
LIG_SUMO_SIM_par_1 | 183 | 190 | PF11976 | 0.456 |
LIG_SUMO_SIM_par_1 | 46 | 52 | PF11976 | 0.374 |
LIG_TRAF2_1 | 74 | 77 | PF00917 | 0.599 |
LIG_TYR_ITIM | 181 | 186 | PF00017 | 0.442 |
LIG_UBA3_1 | 157 | 163 | PF00899 | 0.527 |
LIG_Vh1_VBS_1 | 247 | 265 | PF01044 | 0.536 |
LIG_WRC_WIRS_1 | 12 | 17 | PF05994 | 0.414 |
LIG_WRC_WIRS_1 | 81 | 86 | PF05994 | 0.595 |
MOD_CDC14_SPxK_1 | 424 | 427 | PF00782 | 0.767 |
MOD_CDK_SPxK_1 | 421 | 427 | PF00069 | 0.771 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.389 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.385 |
MOD_CK1_1 | 403 | 409 | PF00069 | 0.729 |
MOD_CK1_1 | 415 | 421 | PF00069 | 0.700 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.557 |
MOD_CK2_1 | 161 | 167 | PF00069 | 0.586 |
MOD_CK2_1 | 216 | 222 | PF00069 | 0.389 |
MOD_CK2_1 | 25 | 31 | PF00069 | 0.505 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.418 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.402 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.409 |
MOD_GlcNHglycan | 340 | 343 | PF01048 | 0.534 |
MOD_GlcNHglycan | 402 | 405 | PF01048 | 0.500 |
MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.511 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.483 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.511 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.414 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.355 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.274 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.333 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.693 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.709 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.755 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.553 |
MOD_N-GLC_1 | 40 | 45 | PF02516 | 0.541 |
MOD_N-GLC_1 | 72 | 77 | PF02516 | 0.341 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.378 |
MOD_NEK2_1 | 16 | 21 | PF00069 | 0.325 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.544 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.327 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.297 |
MOD_NEK2_1 | 191 | 196 | PF00069 | 0.209 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.333 |
MOD_NEK2_1 | 255 | 260 | PF00069 | 0.544 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.343 |
MOD_NEK2_1 | 80 | 85 | PF00069 | 0.538 |
MOD_PKA_2 | 125 | 131 | PF00069 | 0.299 |
MOD_PKA_2 | 191 | 197 | PF00069 | 0.456 |
MOD_PKA_2 | 271 | 277 | PF00069 | 0.593 |
MOD_PKA_2 | 287 | 293 | PF00069 | 0.418 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.546 |
MOD_PKA_2 | 426 | 432 | PF00069 | 0.745 |
MOD_Plk_1 | 40 | 46 | PF00069 | 0.284 |
MOD_Plk_1 | 75 | 81 | PF00069 | 0.584 |
MOD_Plk_4 | 104 | 110 | PF00069 | 0.331 |
MOD_Plk_4 | 11 | 17 | PF00069 | 0.255 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.367 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.522 |
MOD_Plk_4 | 175 | 181 | PF00069 | 0.398 |
MOD_Plk_4 | 196 | 202 | PF00069 | 0.355 |
MOD_Plk_4 | 205 | 211 | PF00069 | 0.390 |
MOD_Plk_4 | 220 | 226 | PF00069 | 0.361 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.492 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.284 |
MOD_ProDKin_1 | 367 | 373 | PF00069 | 0.778 |
MOD_ProDKin_1 | 421 | 427 | PF00069 | 0.790 |
MOD_ProDKin_1 | 435 | 441 | PF00069 | 0.718 |
MOD_SUMO_rev_2 | 167 | 174 | PF00179 | 0.646 |
TRG_DiLeu_BaEn_1 | 76 | 81 | PF01217 | 0.581 |
TRG_DiLeu_BaEn_2 | 221 | 227 | PF01217 | 0.423 |
TRG_DiLeu_BaEn_4 | 76 | 82 | PF01217 | 0.608 |
TRG_DiLeu_BaLyEn_6 | 237 | 242 | PF01217 | 0.320 |
TRG_DiLeu_BaLyEn_6 | 43 | 48 | PF01217 | 0.332 |
TRG_ENDOCYTIC_2 | 146 | 149 | PF00928 | 0.346 |
TRG_ENDOCYTIC_2 | 177 | 180 | PF00928 | 0.320 |
TRG_ENDOCYTIC_2 | 183 | 186 | PF00928 | 0.276 |
TRG_ENDOCYTIC_2 | 230 | 233 | PF00928 | 0.427 |
TRG_ENDOCYTIC_2 | 29 | 32 | PF00928 | 0.394 |
TRG_ENDOCYTIC_2 | 293 | 296 | PF00928 | 0.510 |
TRG_ENDOCYTIC_2 | 33 | 36 | PF00928 | 0.348 |
TRG_ER_diArg_1 | 269 | 272 | PF00400 | 0.592 |
TRG_Pf-PMV_PEXEL_1 | 455 | 459 | PF00026 | 0.461 |
TRG_Pf-PMV_PEXEL_1 | 462 | 467 | PF00026 | 0.425 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I9A3 | Leptomonas seymouri | 48% | 89% |
A0A1X0NU29 | Trypanosomatidae | 33% | 91% |
A0A3R7MBX1 | Trypanosoma rangeli | 37% | 89% |
A0A3S5H6W0 | Leishmania donovani | 95% | 100% |
A4H8A9 | Leishmania braziliensis | 77% | 97% |
A4HWM9 | Leishmania infantum | 95% | 100% |
A8Y4B2 | Caenorhabditis briggsae | 27% | 77% |
C9ZXQ9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 98% |
E9AQD6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
O74757 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 24% | 71% |
Q20798 | Caenorhabditis elegans | 28% | 78% |
Q5XHH7 | Xenopus laevis | 27% | 80% |
Q5Z880 | Oryza sativa subsp. japonica | 25% | 96% |
Q6NPT7 | Arabidopsis thaliana | 27% | 100% |
Q6NRL6 | Xenopus laevis | 28% | 79% |
Q803I8 | Danio rerio | 27% | 76% |
Q86TM6 | Homo sapiens | 27% | 77% |
Q95SP2 | Drosophila melanogaster | 29% | 76% |
Q9DBY1 | Mus musculus | 27% | 78% |
Q9LW77 | Arabidopsis thaliana | 26% | 97% |
V5BUE9 | Trypanosoma cruzi | 30% | 90% |