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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0005829 | cytosol | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QBW3
Term | Name | Level | Count |
---|---|---|---|
GO:0000045 | autophagosome assembly | 6 | 2 |
GO:0006508 | proteolysis | 4 | 2 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0006996 | organelle organization | 4 | 2 |
GO:0007030 | Golgi organization | 5 | 2 |
GO:0007033 | vacuole organization | 5 | 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:0010498 | proteasomal protein catabolic process | 5 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 2 |
GO:0022607 | cellular component assembly | 4 | 2 |
GO:0030163 | protein catabolic process | 4 | 2 |
GO:0031468 | nuclear membrane reassembly | 6 | 2 |
GO:0043161 | proteasome-mediated ubiquitin-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:0061024 | membrane organization | 4 | 2 |
GO:0061025 | membrane fusion | 5 | 2 |
GO:0070925 | organelle assembly | 5 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0071709 | membrane assembly | 5 | 2 |
GO:0071763 | nuclear membrane organization | 5 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 2 |
GO:1901575 | organic substance catabolic process | 3 | 2 |
GO:1905037 | autophagosome organization | 6 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 2 |
GO:0005515 | protein binding | 2 | 2 |
GO:0032182 | ubiquitin-like protein binding | 3 | 2 |
GO:0043130 | ubiquitin binding | 4 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 116 | 120 | PF00656 | 0.695 |
CLV_C14_Caspase3-7 | 26 | 30 | PF00656 | 0.582 |
CLV_C14_Caspase3-7 | 56 | 60 | PF00656 | 0.464 |
CLV_NRD_NRD_1 | 105 | 107 | PF00675 | 0.579 |
CLV_NRD_NRD_1 | 292 | 294 | PF00675 | 0.490 |
CLV_NRD_NRD_1 | 331 | 333 | PF00675 | 0.566 |
CLV_PCSK_KEX2_1 | 292 | 294 | PF00082 | 0.561 |
CLV_PCSK_KEX2_1 | 331 | 333 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 31 | 35 | PF00082 | 0.534 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.695 |
DEG_SPOP_SBC_1 | 237 | 241 | PF00917 | 0.626 |
DOC_ANK_TNKS_1 | 3 | 10 | PF00023 | 0.431 |
DOC_MAPK_gen_1 | 154 | 163 | PF00069 | 0.448 |
DOC_MAPK_gen_1 | 19 | 27 | PF00069 | 0.544 |
DOC_MAPK_gen_1 | 289 | 297 | PF00069 | 0.605 |
DOC_MAPK_gen_1 | 346 | 354 | PF00069 | 0.495 |
DOC_MAPK_MEF2A_6 | 154 | 163 | PF00069 | 0.447 |
DOC_MAPK_MEF2A_6 | 19 | 27 | PF00069 | 0.566 |
DOC_PP2B_LxvP_1 | 235 | 238 | PF13499 | 0.691 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 177 | 181 | PF00917 | 0.499 |
DOC_USP7_MATH_1 | 236 | 240 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 242 | 246 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 258 | 262 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 92 | 96 | PF00917 | 0.569 |
DOC_WW_Pin1_4 | 143 | 148 | PF00397 | 0.495 |
DOC_WW_Pin1_4 | 251 | 256 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 260 | 265 | PF00397 | 0.660 |
LIG_14-3-3_CanoR_1 | 13 | 19 | PF00244 | 0.348 |
LIG_14-3-3_CanoR_1 | 138 | 148 | PF00244 | 0.520 |
LIG_14-3-3_CanoR_1 | 301 | 305 | PF00244 | 0.418 |
LIG_APCC_ABBA_1 | 161 | 166 | PF00400 | 0.426 |
LIG_BRCT_BRCA1_1 | 171 | 175 | PF00533 | 0.549 |
LIG_CaM_NSCaTE_8 | 39 | 46 | PF13499 | 0.559 |
LIG_CtBP_PxDLS_1 | 196 | 200 | PF00389 | 0.560 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.536 |
LIG_FHA_1 | 269 | 275 | PF00498 | 0.564 |
LIG_FHA_1 | 278 | 284 | PF00498 | 0.490 |
LIG_FHA_2 | 24 | 30 | PF00498 | 0.548 |
LIG_FHA_2 | 286 | 292 | PF00498 | 0.519 |
LIG_FHA_2 | 301 | 307 | PF00498 | 0.311 |
LIG_FHA_2 | 54 | 60 | PF00498 | 0.462 |
LIG_LIR_Apic_2 | 191 | 197 | PF02991 | 0.560 |
LIG_LIR_Apic_2 | 219 | 223 | PF02991 | 0.518 |
LIG_LIR_Gen_1 | 224 | 231 | PF02991 | 0.398 |
LIG_LIR_Gen_1 | 280 | 286 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 10 | 15 | PF02991 | 0.577 |
LIG_LIR_Nem_3 | 172 | 178 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 20 | 25 | PF02991 | 0.561 |
LIG_LIR_Nem_3 | 224 | 228 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 280 | 285 | PF02991 | 0.513 |
LIG_PCNA_yPIPBox_3 | 315 | 326 | PF02747 | 0.514 |
LIG_SH2_PTP2 | 194 | 197 | PF00017 | 0.515 |
LIG_SH2_PTP2 | 220 | 223 | PF00017 | 0.515 |
LIG_SH2_SRC | 194 | 197 | PF00017 | 0.515 |
LIG_SH2_SRC | 220 | 223 | PF00017 | 0.515 |
LIG_SH2_SRC | 266 | 269 | PF00017 | 0.582 |
LIG_SH2_STAT5 | 141 | 144 | PF00017 | 0.580 |
LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.596 |
LIG_SH2_STAT5 | 194 | 197 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 220 | 223 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 225 | 228 | PF00017 | 0.521 |
LIG_SH2_STAT5 | 63 | 66 | PF00017 | 0.547 |
LIG_SH3_3 | 73 | 79 | PF00018 | 0.607 |
LIG_SUMO_SIM_anti_2 | 280 | 288 | PF11976 | 0.449 |
LIG_SUMO_SIM_par_1 | 269 | 278 | PF11976 | 0.635 |
LIG_SUMO_SIM_par_1 | 280 | 288 | PF11976 | 0.512 |
LIG_UBA3_1 | 100 | 107 | PF00899 | 0.544 |
LIG_WW_1 | 222 | 225 | PF00397 | 0.516 |
LIG_WW_3 | 328 | 332 | PF00397 | 0.481 |
MOD_CK1_1 | 14 | 20 | PF00069 | 0.510 |
MOD_CK1_1 | 254 | 260 | PF00069 | 0.729 |
MOD_CK1_1 | 336 | 342 | PF00069 | 0.519 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.703 |
MOD_CK2_1 | 119 | 125 | PF00069 | 0.733 |
MOD_CK2_1 | 285 | 291 | PF00069 | 0.547 |
MOD_DYRK1A_RPxSP_1 | 260 | 264 | PF00069 | 0.553 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.685 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.690 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.694 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.592 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.564 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.511 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.517 |
MOD_GlcNHglycan | 86 | 90 | PF01048 | 0.622 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.604 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.490 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.363 |
MOD_GSK3_1 | 237 | 244 | PF00069 | 0.582 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.616 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.525 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.557 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.554 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.573 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.499 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.543 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.593 |
MOD_PIKK_1 | 336 | 342 | PF00454 | 0.495 |
MOD_PK_1 | 11 | 17 | PF00069 | 0.563 |
MOD_PKA_2 | 300 | 306 | PF00069 | 0.427 |
MOD_Plk_1 | 155 | 161 | PF00069 | 0.420 |
MOD_Plk_1 | 206 | 212 | PF00069 | 0.498 |
MOD_Plk_1 | 277 | 283 | PF00069 | 0.562 |
MOD_Plk_2-3 | 273 | 279 | PF00069 | 0.620 |
MOD_Plk_2-3 | 300 | 306 | PF00069 | 0.573 |
MOD_Plk_4 | 221 | 227 | PF00069 | 0.531 |
MOD_Plk_4 | 278 | 284 | PF00069 | 0.539 |
MOD_Plk_4 | 96 | 102 | PF00069 | 0.460 |
MOD_ProDKin_1 | 143 | 149 | PF00069 | 0.497 |
MOD_ProDKin_1 | 251 | 257 | PF00069 | 0.680 |
MOD_ProDKin_1 | 260 | 266 | PF00069 | 0.644 |
TRG_DiLeu_BaEn_2 | 181 | 187 | PF01217 | 0.541 |
TRG_DiLeu_BaEn_2 | 277 | 283 | PF01217 | 0.551 |
TRG_DiLeu_BaEn_2 | 316 | 322 | PF01217 | 0.547 |
TRG_ENDOCYTIC_2 | 225 | 228 | PF00928 | 0.516 |
TRG_ER_diArg_1 | 18 | 21 | PF00400 | 0.530 |
TRG_ER_diArg_1 | 330 | 332 | PF00400 | 0.587 |
TRG_NES_CRM1_1 | 207 | 219 | PF08389 | 0.541 |
TRG_Pf-PMV_PEXEL_1 | 31 | 35 | PF00026 | 0.532 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P591 | Leptomonas seymouri | 67% | 100% |
A0A0S4JV00 | Bodo saltans | 34% | 96% |
A0A1X0NTT3 | Trypanosomatidae | 39% | 100% |
A0A3Q8IAL1 | Leishmania donovani | 93% | 100% |
A0A422NSS0 | Trypanosoma rangeli | 37% | 100% |
A4HC82 | Leishmania braziliensis | 78% | 83% |
A4HZR0 | Leishmania infantum | 94% | 100% |
C9ZRJ0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
E9AVL6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
O35987 | Rattus norvegicus | 24% | 96% |
P0C627 | Rattus norvegicus | 21% | 100% |
Q0KL01 | Mus musculus | 23% | 100% |
Q14CS0 | Homo sapiens | 21% | 100% |
Q3SZC4 | Bos taurus | 24% | 96% |
Q5RBG3 | Pongo abelii | 26% | 96% |
Q5ZK10 | Gallus gallus | 26% | 97% |
Q9CZ44 | Mus musculus | 24% | 96% |
Q9N2W5 | Caenorhabditis elegans | 21% | 100% |
Q9SUG6 | Arabidopsis thaliana | 25% | 100% |
Q9UNZ2 | Homo sapiens | 26% | 96% |
V5AVR5 | Trypanosoma cruzi | 39% | 100% |