| 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: 20 |
| NetGPI | no | yes: 0, no: 20 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005737 | cytoplasm | 2 | 2 |
| GO:0031974 | membrane-enclosed lumen | 2 | 2 |
| GO:0031981 | nuclear lumen | 5 | 2 |
| GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 2 |
| GO:0043233 | organelle lumen | 3 | 2 |
| GO:0070013 | intracellular organelle lumen | 4 | 2 |
| GO:0097014 | ciliary plasm | 5 | 2 |
| GO:0099568 | cytoplasmic region | 3 | 2 |
| GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: A4HDK4
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
| GO:0008152 | metabolic process | 1 | 2 |
| GO:0016567 | protein ubiquitination | 7 | 2 |
| GO:0019538 | protein metabolic process | 3 | 2 |
| GO:0032446 | protein modification by small protein conjugation | 6 | 2 |
| GO:0036211 | protein modification process | 4 | 2 |
| GO:0043170 | macromolecule metabolic process | 3 | 2 |
| GO:0043412 | macromolecule modification | 4 | 2 |
| GO:0044238 | primary metabolic process | 2 | 2 |
| GO:0070647 | protein modification by small protein conjugation or removal | 5 | 2 |
| GO:0071704 | organic substance metabolic process | 2 | 2 |
| GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005488 | binding | 1 | 20 |
| GO:0005509 | calcium ion binding | 5 | 17 |
| GO:0043167 | ion binding | 2 | 20 |
| GO:0043169 | cation binding | 3 | 20 |
| GO:0046872 | metal ion binding | 4 | 20 |
| 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 | 2 |
| GO:0061659 | ubiquitin-like protein ligase activity | 4 | 2 |
| GO:0140096 | catalytic activity, acting on a protein | 2 | 2 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 340 | 344 | PF00656 | 0.396 |
| CLV_NRD_NRD_1 | 50 | 52 | PF00675 | 0.194 |
| CLV_PCSK_SKI1_1 | 287 | 291 | PF00082 | 0.414 |
| DEG_SCF_FBW7_1 | 56 | 63 | PF00400 | 0.312 |
| DOC_CKS1_1 | 57 | 62 | PF01111 | 0.460 |
| DOC_CYCLIN_RxL_1 | 272 | 282 | PF00134 | 0.341 |
| DOC_MAPK_gen_1 | 376 | 384 | PF00069 | 0.267 |
| DOC_PP1_RVXF_1 | 273 | 280 | PF00149 | 0.347 |
| DOC_PP4_FxxP_1 | 123 | 126 | PF00568 | 0.563 |
| DOC_USP7_MATH_1 | 163 | 167 | PF00917 | 0.755 |
| DOC_USP7_MATH_1 | 180 | 184 | PF00917 | 0.526 |
| DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.708 |
| DOC_USP7_UBL2_3 | 314 | 318 | PF12436 | 0.465 |
| DOC_WW_Pin1_4 | 101 | 106 | PF00397 | 0.618 |
| DOC_WW_Pin1_4 | 122 | 127 | PF00397 | 0.575 |
| DOC_WW_Pin1_4 | 135 | 140 | PF00397 | 0.622 |
| DOC_WW_Pin1_4 | 218 | 223 | PF00397 | 0.668 |
| DOC_WW_Pin1_4 | 27 | 32 | PF00397 | 0.194 |
| DOC_WW_Pin1_4 | 279 | 284 | PF00397 | 0.376 |
| DOC_WW_Pin1_4 | 56 | 61 | PF00397 | 0.453 |
| LIG_14-3-3_CanoR_1 | 235 | 240 | PF00244 | 0.573 |
| LIG_14-3-3_CanoR_1 | 300 | 304 | PF00244 | 0.384 |
| LIG_APCC_ABBA_1 | 253 | 258 | PF00400 | 0.397 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.565 |
| LIG_CtBP_PxDLS_1 | 26 | 30 | PF00389 | 0.354 |
| LIG_FHA_1 | 126 | 132 | PF00498 | 0.732 |
| LIG_FHA_1 | 13 | 19 | PF00498 | 0.416 |
| LIG_FHA_1 | 350 | 356 | PF00498 | 0.270 |
| LIG_FHA_2 | 338 | 344 | PF00498 | 0.326 |
| LIG_LIR_Apic_2 | 134 | 139 | PF02991 | 0.511 |
| LIG_LIR_Apic_2 | 21 | 26 | PF02991 | 0.353 |
| LIG_LIR_Gen_1 | 224 | 234 | PF02991 | 0.400 |
| LIG_LIR_Gen_1 | 246 | 255 | PF02991 | 0.322 |
| LIG_LIR_Gen_1 | 326 | 335 | PF02991 | 0.367 |
| LIG_LIR_Gen_1 | 350 | 358 | PF02991 | 0.319 |
| LIG_LIR_Gen_1 | 386 | 392 | PF02991 | 0.398 |
| LIG_LIR_Nem_3 | 206 | 212 | PF02991 | 0.501 |
| LIG_LIR_Nem_3 | 224 | 229 | PF02991 | 0.573 |
| LIG_LIR_Nem_3 | 246 | 250 | PF02991 | 0.483 |
| LIG_LIR_Nem_3 | 252 | 257 | PF02991 | 0.335 |
| LIG_LIR_Nem_3 | 326 | 331 | PF02991 | 0.413 |
| LIG_LIR_Nem_3 | 350 | 354 | PF02991 | 0.332 |
| LIG_LIR_Nem_3 | 386 | 390 | PF02991 | 0.355 |
| LIG_Pex14_2 | 10 | 14 | PF04695 | 0.283 |
| LIG_SH2_CRK | 136 | 140 | PF00017 | 0.522 |
| LIG_SH2_CRK | 247 | 251 | PF00017 | 0.365 |
| LIG_SH2_CRK | 328 | 332 | PF00017 | 0.250 |
| LIG_SH2_STAP1 | 127 | 131 | PF00017 | 0.634 |
| LIG_SH2_STAP1 | 247 | 251 | PF00017 | 0.365 |
| LIG_SH2_STAT3 | 127 | 130 | PF00017 | 0.629 |
| LIG_SH2_STAT3 | 201 | 204 | PF00017 | 0.711 |
| LIG_SH2_STAT3 | 212 | 215 | PF00017 | 0.596 |
| LIG_SH2_STAT5 | 127 | 130 | PF00017 | 0.617 |
| LIG_SH2_STAT5 | 209 | 212 | PF00017 | 0.524 |
| LIG_SH3_3 | 156 | 162 | PF00018 | 0.818 |
| LIG_SH3_3 | 225 | 231 | PF00018 | 0.597 |
| LIG_SH3_3 | 97 | 103 | PF00018 | 0.555 |
| LIG_SH3_4 | 314 | 321 | PF00018 | 0.579 |
| LIG_SUMO_SIM_par_1 | 25 | 30 | PF11976 | 0.255 |
| LIG_TYR_ITSM | 222 | 229 | PF00017 | 0.445 |
| MOD_CDK_SPxK_1 | 56 | 62 | PF00069 | 0.460 |
| MOD_CDK_SPxxK_3 | 218 | 225 | PF00069 | 0.495 |
| MOD_CK1_1 | 107 | 113 | PF00069 | 0.724 |
| MOD_CK1_1 | 125 | 131 | PF00069 | 0.704 |
| MOD_CK1_1 | 149 | 155 | PF00069 | 0.658 |
| MOD_CK1_1 | 183 | 189 | PF00069 | 0.637 |
| MOD_CK1_1 | 221 | 227 | PF00069 | 0.563 |
| MOD_CK1_1 | 98 | 104 | PF00069 | 0.554 |
| MOD_CK2_1 | 200 | 206 | PF00069 | 0.495 |
| MOD_CK2_1 | 299 | 305 | PF00069 | 0.339 |
| MOD_CK2_1 | 380 | 386 | PF00069 | 0.399 |
| MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.632 |
| MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.668 |
| MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.674 |
| MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.582 |
| MOD_GlcNHglycan | 258 | 264 | PF01048 | 0.334 |
| MOD_GlcNHglycan | 296 | 300 | PF01048 | 0.341 |
| MOD_GlcNHglycan | 95 | 98 | PF01048 | 0.572 |
| MOD_GSK3_1 | 101 | 108 | PF00069 | 0.642 |
| MOD_GSK3_1 | 131 | 138 | PF00069 | 0.692 |
| MOD_GSK3_1 | 149 | 156 | PF00069 | 0.573 |
| MOD_GSK3_1 | 163 | 170 | PF00069 | 0.735 |
| MOD_GSK3_1 | 295 | 302 | PF00069 | 0.311 |
| MOD_GSK3_1 | 323 | 330 | PF00069 | 0.530 |
| MOD_GSK3_1 | 56 | 63 | PF00069 | 0.608 |
| MOD_N-GLC_1 | 149 | 154 | PF02516 | 0.515 |
| MOD_N-GLC_1 | 60 | 65 | PF02516 | 0.530 |
| MOD_N-GLC_1 | 93 | 98 | PF02516 | 0.605 |
| MOD_NEK2_1 | 153 | 158 | PF00069 | 0.706 |
| MOD_NEK2_1 | 295 | 300 | PF00069 | 0.288 |
| MOD_NEK2_1 | 323 | 328 | PF00069 | 0.566 |
| MOD_NEK2_1 | 337 | 342 | PF00069 | 0.414 |
| MOD_NEK2_2 | 380 | 385 | PF00069 | 0.415 |
| MOD_OFUCOSY | 11 | 16 | PF10250 | 0.194 |
| MOD_PIKK_1 | 108 | 114 | PF00454 | 0.796 |
| MOD_PIKK_1 | 125 | 131 | PF00454 | 0.504 |
| MOD_PIKK_1 | 157 | 163 | PF00454 | 0.626 |
| MOD_PIKK_1 | 200 | 206 | PF00454 | 0.530 |
| MOD_PIKK_1 | 321 | 327 | PF00454 | 0.497 |
| MOD_PIKK_1 | 98 | 104 | PF00454 | 0.507 |
| MOD_PKA_2 | 299 | 305 | PF00069 | 0.199 |
| MOD_PKA_2 | 361 | 367 | PF00069 | 0.206 |
| MOD_Plk_1 | 149 | 155 | PF00069 | 0.518 |
| MOD_Plk_1 | 205 | 211 | PF00069 | 0.780 |
| MOD_Plk_1 | 349 | 355 | PF00069 | 0.356 |
| MOD_Plk_1 | 60 | 66 | PF00069 | 0.510 |
| MOD_Plk_4 | 149 | 155 | PF00069 | 0.559 |
| MOD_Plk_4 | 249 | 255 | PF00069 | 0.314 |
| MOD_Plk_4 | 305 | 311 | PF00069 | 0.339 |
| MOD_Plk_4 | 316 | 322 | PF00069 | 0.525 |
| MOD_Plk_4 | 327 | 333 | PF00069 | 0.325 |
| MOD_ProDKin_1 | 101 | 107 | PF00069 | 0.622 |
| MOD_ProDKin_1 | 122 | 128 | PF00069 | 0.585 |
| MOD_ProDKin_1 | 135 | 141 | PF00069 | 0.626 |
| MOD_ProDKin_1 | 218 | 224 | PF00069 | 0.667 |
| MOD_ProDKin_1 | 27 | 33 | PF00069 | 0.194 |
| MOD_ProDKin_1 | 279 | 285 | PF00069 | 0.376 |
| MOD_ProDKin_1 | 56 | 62 | PF00069 | 0.460 |
| TRG_DiLeu_BaEn_1 | 350 | 355 | PF01217 | 0.394 |
| TRG_ENDOCYTIC_2 | 226 | 229 | PF00928 | 0.556 |
| TRG_ENDOCYTIC_2 | 247 | 250 | PF00928 | 0.511 |
| TRG_ENDOCYTIC_2 | 328 | 331 | PF00928 | 0.451 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P229 | Leptomonas seymouri | 57% | 100% |
| A0A0N1ILD7 | Leptomonas seymouri | 22% | 87% |
| A0A0S4JBP2 | Bodo saltans | 23% | 88% |
| A0A1X0NCU6 | Trypanosomatidae | 33% | 100% |
| A0A3Q8IMS6 | Leishmania donovani | 75% | 100% |
| A0A3S5H5B1 | Leishmania donovani | 27% | 67% |
| A0A3S7WWY0 | Leishmania donovani | 24% | 88% |
| A0A3S7WYG1 | Leishmania donovani | 61% | 85% |
| A4HDK3 | Leishmania braziliensis | 100% | 100% |
| A4HS49 | Leishmania infantum | 27% | 67% |
| A4HZP7 | Leishmania infantum | 24% | 88% |
| A4I0X7 | Leishmania infantum | 75% | 100% |
| A4I0X8 | Leishmania infantum | 60% | 100% |
| E9AK36 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 68% |
| E9AWY1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 100% |
| E9AWY2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 58% | 100% |
| O97201 | Leishmania major | 29% | 100% |
| Q4QAJ2 | Leishmania major | 59% | 85% |
| Q4QAJ3 | Leishmania major | 73% | 100% |
| Q8HZJ4 | Bos taurus | 21% | 100% |