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. | yes | yes: 25 |
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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005739 | mitochondrion | 5 | 1 |
GO:0005829 | cytosol | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AQ96
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0032446 | protein modification by small protein conjugation | 6 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 1 |
GO:0071569 | protein ufmylation | 7 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 11 |
GO:0008641 | ubiquitin-like modifier activating enzyme activity | 2 | 12 |
GO:0016874 | ligase activity | 2 | 12 |
GO:0016877 | ligase activity, forming carbon-sulfur bonds | 3 | 12 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043169 | cation binding | 3 | 11 |
GO:0046872 | metal ion binding | 4 | 11 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 12 |
GO:0140657 | ATP-dependent activity | 1 | 12 |
GO:0005515 | protein binding | 2 | 1 |
GO:0032182 | ubiquitin-like protein binding | 3 | 1 |
GO:0071566 | UFM1 activating enzyme activity | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 332 | 336 | PF00656 | 0.714 |
CLV_NRD_NRD_1 | 286 | 288 | PF00675 | 0.474 |
CLV_NRD_NRD_1 | 299 | 301 | PF00675 | 0.519 |
CLV_PCSK_KEX2_1 | 212 | 214 | PF00082 | 0.358 |
CLV_PCSK_PC1ET2_1 | 212 | 214 | PF00082 | 0.358 |
CLV_PCSK_SKI1_1 | 238 | 242 | PF00082 | 0.327 |
CLV_PCSK_SKI1_1 | 271 | 275 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 380 | 384 | PF00082 | 0.754 |
CLV_PCSK_SKI1_1 | 68 | 72 | PF00082 | 0.374 |
DEG_SCF_FBW7_2 | 190 | 197 | PF00400 | 0.374 |
DEG_SPOP_SBC_1 | 2 | 6 | PF00917 | 0.692 |
DOC_CYCLIN_RxL_1 | 235 | 245 | PF00134 | 0.327 |
DOC_CYCLIN_RxL_1 | 63 | 76 | PF00134 | 0.358 |
DOC_MAPK_MEF2A_6 | 256 | 264 | PF00069 | 0.374 |
DOC_PP1_RVXF_1 | 66 | 73 | PF00149 | 0.358 |
DOC_PP2B_LxvP_1 | 187 | 190 | PF13499 | 0.358 |
DOC_PP4_FxxP_1 | 86 | 89 | PF00568 | 0.358 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 338 | 342 | PF00917 | 0.673 |
DOC_WW_Pin1_4 | 136 | 141 | PF00397 | 0.405 |
DOC_WW_Pin1_4 | 190 | 195 | PF00397 | 0.358 |
LIG_14-3-3_CanoR_1 | 157 | 161 | PF00244 | 0.358 |
LIG_Clathr_ClatBox_1 | 69 | 73 | PF01394 | 0.443 |
LIG_deltaCOP1_diTrp_1 | 124 | 129 | PF00928 | 0.358 |
LIG_FHA_1 | 157 | 163 | PF00498 | 0.438 |
LIG_FHA_1 | 164 | 170 | PF00498 | 0.443 |
LIG_FHA_1 | 222 | 228 | PF00498 | 0.358 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.379 |
LIG_FHA_2 | 109 | 115 | PF00498 | 0.374 |
LIG_FHA_2 | 119 | 125 | PF00498 | 0.293 |
LIG_FHA_2 | 366 | 372 | PF00498 | 0.712 |
LIG_FHA_2 | 93 | 99 | PF00498 | 0.213 |
LIG_IBAR_NPY_1 | 20 | 22 | PF08397 | 0.470 |
LIG_LIR_Apic_2 | 166 | 170 | PF02991 | 0.443 |
LIG_LIR_Gen_1 | 123 | 133 | PF02991 | 0.358 |
LIG_LIR_Gen_1 | 19 | 28 | PF02991 | 0.374 |
LIG_LIR_Gen_1 | 35 | 45 | PF02991 | 0.374 |
LIG_LIR_Gen_1 | 73 | 82 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 123 | 129 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 19 | 25 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 247 | 252 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 257 | 262 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 35 | 40 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 73 | 77 | PF02991 | 0.346 |
LIG_NRBOX | 236 | 242 | PF00104 | 0.327 |
LIG_PCNA_PIPBox_1 | 225 | 234 | PF02747 | 0.392 |
LIG_SH2_CRK | 22 | 26 | PF00017 | 0.374 |
LIG_SH2_NCK_1 | 74 | 78 | PF00017 | 0.358 |
LIG_SH2_SRC | 363 | 366 | PF00017 | 0.613 |
LIG_SH2_STAP1 | 22 | 26 | PF00017 | 0.374 |
LIG_SH2_STAP1 | 282 | 286 | PF00017 | 0.537 |
LIG_SH2_STAT3 | 239 | 242 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 239 | 242 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 249 | 252 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 381 | 384 | PF00017 | 0.754 |
LIG_SH3_2 | 295 | 300 | PF14604 | 0.339 |
LIG_SH3_3 | 109 | 115 | PF00018 | 0.478 |
LIG_SH3_3 | 137 | 143 | PF00018 | 0.415 |
LIG_SH3_3 | 292 | 298 | PF00018 | 0.321 |
LIG_SUMO_SIM_anti_2 | 142 | 148 | PF11976 | 0.374 |
LIG_SUMO_SIM_par_1 | 200 | 206 | PF11976 | 0.358 |
LIG_TRAF2_1 | 388 | 391 | PF00917 | 0.675 |
LIG_TYR_ITAM | 19 | 40 | PF00017 | 0.392 |
LIG_UBA3_1 | 392 | 397 | PF00899 | 0.583 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.505 |
MOD_CK1_1 | 220 | 226 | PF00069 | 0.358 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.528 |
MOD_CK2_1 | 108 | 114 | PF00069 | 0.428 |
MOD_CK2_1 | 118 | 124 | PF00069 | 0.344 |
MOD_CK2_1 | 356 | 362 | PF00069 | 0.712 |
MOD_CK2_1 | 385 | 391 | PF00069 | 0.649 |
MOD_CK2_1 | 92 | 98 | PF00069 | 0.327 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.609 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.358 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.358 |
MOD_GlcNHglycan | 340 | 343 | PF01048 | 0.710 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.642 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.453 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.358 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.615 |
MOD_N-GLC_1 | 118 | 123 | PF02516 | 0.443 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.591 |
MOD_NEK2_2 | 233 | 238 | PF00069 | 0.392 |
MOD_PKA_1 | 10 | 16 | PF00069 | 0.590 |
MOD_PKA_2 | 127 | 133 | PF00069 | 0.505 |
MOD_PKA_2 | 156 | 162 | PF00069 | 0.358 |
MOD_Plk_2-3 | 36 | 42 | PF00069 | 0.505 |
MOD_Plk_2-3 | 73 | 79 | PF00069 | 0.478 |
MOD_Plk_4 | 108 | 114 | PF00069 | 0.478 |
MOD_Plk_4 | 52 | 58 | PF00069 | 0.374 |
MOD_ProDKin_1 | 136 | 142 | PF00069 | 0.405 |
MOD_ProDKin_1 | 190 | 196 | PF00069 | 0.358 |
MOD_SUMO_for_1 | 211 | 214 | PF00179 | 0.374 |
MOD_SUMO_rev_2 | 257 | 266 | PF00179 | 0.487 |
MOD_SUMO_rev_2 | 330 | 336 | PF00179 | 0.678 |
MOD_SUMO_rev_2 | 376 | 382 | PF00179 | 0.739 |
TRG_ENDOCYTIC_2 | 22 | 25 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 252 | 255 | PF00928 | 0.358 |
TRG_ENDOCYTIC_2 | 37 | 40 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 74 | 77 | PF00928 | 0.348 |
TRG_NLS_Bipartite_1 | 287 | 304 | PF00514 | 0.456 |
TRG_NLS_MonoExtC_3 | 299 | 305 | PF00514 | 0.628 |
TRG_NLS_MonoExtN_4 | 298 | 304 | PF00514 | 0.362 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2F3 | Leptomonas seymouri | 76% | 94% |
A0A0N0P8E8 | Leptomonas seymouri | 25% | 88% |
A0A0S4JGN9 | Bodo saltans | 72% | 96% |
A0A1X0NTY2 | Trypanosomatidae | 71% | 99% |
A0A3R7JZ58 | Trypanosoma rangeli | 73% | 100% |
A0A3S5H6V3 | Leishmania donovani | 95% | 100% |
A0A422NC72 | Trypanosoma rangeli | 28% | 81% |
A1A4L8 | Bos taurus | 28% | 88% |
A2BDX3 | Mus musculus | 28% | 87% |
A4H870 | Leishmania braziliensis | 87% | 100% |
A4HWJ5 | Leishmania infantum | 96% | 100% |
A5DSR2 | Lodderomyces elongisporus (strain ATCC 11503 / CBS 2605 / JCM 1781 / NBRC 1676 / NRRL YB-4239) | 24% | 88% |
A6ZT19 | Saccharomyces cerevisiae (strain YJM789) | 23% | 91% |
A7MAZ3 | Bos taurus | 50% | 99% |
A7THV5 | Vanderwaltozyma polyspora (strain ATCC 22028 / DSM 70294 / BCRC 21397 / CBS 2163 / NBRC 10782 / NRRL Y-8283 / UCD 57-17) | 22% | 92% |
A8XEQ8 | Caenorhabditis briggsae | 63% | 93% |
B0WQV1 | Culex quinquefasciatus | 49% | 100% |
B3LSM6 | Saccharomyces cerevisiae (strain RM11-1a) | 23% | 91% |
B3NUC9 | Drosophila erecta | 51% | 100% |
B4GKQ3 | Drosophila persimilis | 29% | 89% |
B4GYC7 | Drosophila persimilis | 49% | 100% |
B4IK21 | Drosophila sechellia | 52% | 99% |
B4JIY0 | Drosophila grimshawi | 49% | 100% |
B4KI53 | Drosophila mojavensis | 27% | 88% |
B4L1K2 | Drosophila mojavensis | 52% | 100% |
B4M357 | Drosophila virilis | 50% | 100% |
B4NDE5 | Drosophila willistoni | 51% | 99% |
B4PYA4 | Drosophila yakuba | 52% | 99% |
B4R345 | Drosophila simulans | 51% | 99% |
B5DS72 | Drosophila pseudoobscura pseudoobscura | 29% | 89% |
B5VK45 | Saccharomyces cerevisiae (strain AWRI1631) | 23% | 91% |
B9VJ80 | Bombyx mori | 61% | 100% |
C3YZ51 | Branchiostoma floridae | 51% | 99% |
C9ZXU3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 70% | 100% |
D0A640 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 79% |
D1GY43 | Drosophila ananassae | 50% | 100% |
O23034 | Arabidopsis thaliana | 62% | 93% |
P38820 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 23% | 91% |
P91430 | Caenorhabditis elegans | 63% | 95% |
Q17DT0 | Aedes aegypti | 62% | 100% |
Q29HT0 | Drosophila pseudoobscura pseudoobscura | 50% | 100% |
Q29PG5 | Drosophila pseudoobscura pseudoobscura | 29% | 89% |
Q3KQ23 | Xenopus laevis | 61% | 100% |
Q4QF87 | Leishmania major | 92% | 100% |
Q54C02 | Dictyostelium discoideum | 62% | 100% |
Q5M7A4 | Rattus norvegicus | 50% | 99% |
Q5R8X4 | Pongo abelii | 51% | 99% |
Q6BHZ2 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 21% | 89% |
Q6GLG7 | Xenopus tropicalis | 50% | 100% |
Q6IVA4 | Gallus gallus | 49% | 100% |
Q6K6K7 | Oryza sativa subsp. japonica | 62% | 95% |
Q8AWD2 | Danio rerio | 24% | 87% |
Q8VE47 | Mus musculus | 50% | 99% |
Q9GZZ9 | Homo sapiens | 62% | 99% |
Q9VYY3 | Drosophila melanogaster | 51% | 99% |
V5BPQ6 | Trypanosoma cruzi | 69% | 100% |
X1WER2 | Danio rerio | 51% | 100% |