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:0032865 | ERMES complex | 3 | 11 |
GO:0032991 | protein-containing complex | 1 | 11 |
GO:0098796 | membrane protein complex | 2 | 11 |
GO:0098798 | mitochondrial protein-containing complex | 2 | 11 |
GO:0098799 | outer mitochondrial membrane protein complex | 3 | 11 |
GO:0140534 | endoplasmic reticulum protein-containing complex | 2 | 11 |
Related structures:
AlphaFold database: E9AQX0
Term | Name | Level | Count |
---|---|---|---|
GO:0006996 | organelle organization | 4 | 11 |
GO:0007005 | mitochondrion organization | 5 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016043 | cellular component organization | 3 | 11 |
GO:0071840 | cellular component organization or biogenesis | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 213 | 215 | PF00675 | 0.630 |
CLV_NRD_NRD_1 | 285 | 287 | PF00675 | 0.457 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.618 |
CLV_PCSK_KEX2_1 | 278 | 280 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 284 | 286 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 297 | 299 | PF00082 | 0.355 |
CLV_PCSK_PC1ET2_1 | 278 | 280 | PF00082 | 0.528 |
CLV_PCSK_PC1ET2_1 | 284 | 286 | PF00082 | 0.476 |
CLV_PCSK_PC1ET2_1 | 297 | 299 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 19 | 23 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 285 | 289 | PF00082 | 0.419 |
DEG_APCC_DBOX_1 | 268 | 276 | PF00400 | 0.612 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.478 |
DOC_ANK_TNKS_1 | 328 | 335 | PF00023 | 0.594 |
DOC_CYCLIN_yCln2_LP_2 | 234 | 237 | PF00134 | 0.494 |
DOC_MAPK_gen_1 | 283 | 291 | PF00069 | 0.437 |
DOC_MAPK_gen_1 | 36 | 46 | PF00069 | 0.557 |
DOC_MAPK_gen_1 | 84 | 92 | PF00069 | 0.463 |
DOC_MAPK_MEF2A_6 | 15 | 22 | PF00069 | 0.482 |
DOC_MAPK_MEF2A_6 | 283 | 291 | PF00069 | 0.436 |
DOC_MAPK_MEF2A_6 | 39 | 46 | PF00069 | 0.548 |
DOC_MAPK_MEF2A_6 | 84 | 92 | PF00069 | 0.439 |
DOC_PP2B_LxvP_1 | 107 | 110 | PF13499 | 0.626 |
DOC_PP2B_LxvP_1 | 234 | 237 | PF13499 | 0.620 |
DOC_PP4_FxxP_1 | 111 | 114 | PF00568 | 0.437 |
DOC_PP4_FxxP_1 | 292 | 295 | PF00568 | 0.454 |
DOC_PP4_MxPP_1 | 216 | 219 | PF00568 | 0.638 |
DOC_USP7_MATH_1 | 185 | 189 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.607 |
DOC_USP7_UBL2_3 | 284 | 288 | PF12436 | 0.471 |
DOC_USP7_UBL2_3 | 32 | 36 | PF12436 | 0.616 |
DOC_WW_Pin1_4 | 146 | 151 | PF00397 | 0.656 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.506 |
LIG_14-3-3_CanoR_1 | 173 | 183 | PF00244 | 0.669 |
LIG_14-3-3_CanoR_1 | 269 | 273 | PF00244 | 0.569 |
LIG_APCC_ABBA_1 | 130 | 135 | PF00400 | 0.445 |
LIG_APCC_ABBA_1 | 289 | 294 | PF00400 | 0.448 |
LIG_APCC_ABBAyCdc20_2 | 288 | 294 | PF00400 | 0.462 |
LIG_APCC_ABBAyCdc20_2 | 39 | 45 | PF00400 | 0.582 |
LIG_Clathr_ClatBox_1 | 41 | 45 | PF01394 | 0.571 |
LIG_CtBP_PxDLS_1 | 114 | 118 | PF00389 | 0.521 |
LIG_CtBP_PxDLS_1 | 218 | 222 | PF00389 | 0.705 |
LIG_deltaCOP1_diTrp_1 | 5 | 10 | PF00928 | 0.454 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.742 |
LIG_FHA_1 | 334 | 340 | PF00498 | 0.535 |
LIG_FHA_1 | 7 | 13 | PF00498 | 0.586 |
LIG_FHA_2 | 116 | 122 | PF00498 | 0.425 |
LIG_FHA_2 | 138 | 144 | PF00498 | 0.387 |
LIG_LIR_Gen_1 | 131 | 139 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 131 | 136 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 201 | 207 | PF02991 | 0.670 |
LIG_MYND_1 | 232 | 236 | PF01753 | 0.487 |
LIG_SH2_CRK | 204 | 208 | PF00017 | 0.617 |
LIG_SH2_STAT5 | 112 | 115 | PF00017 | 0.519 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.686 |
LIG_SH3_3 | 225 | 231 | PF00018 | 0.788 |
LIG_SH3_3 | 303 | 309 | PF00018 | 0.630 |
LIG_SH3_3 | 41 | 47 | PF00018 | 0.532 |
LIG_SUMO_SIM_par_1 | 271 | 277 | PF11976 | 0.638 |
LIG_SUMO_SIM_par_1 | 335 | 340 | PF11976 | 0.599 |
LIG_UBA3_1 | 272 | 278 | PF00899 | 0.609 |
MOD_CDK_SPK_2 | 156 | 161 | PF00069 | 0.755 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.698 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.726 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.623 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.686 |
MOD_CK1_1 | 241 | 247 | PF00069 | 0.712 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.576 |
MOD_CK1_1 | 268 | 274 | PF00069 | 0.428 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.701 |
MOD_CK2_1 | 137 | 143 | PF00069 | 0.369 |
MOD_Cter_Amidation | 211 | 214 | PF01082 | 0.612 |
MOD_Cter_Amidation | 311 | 314 | PF01082 | 0.630 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.722 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.716 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.713 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.595 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.718 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.703 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.690 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.671 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.608 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.720 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.631 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.598 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.581 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.429 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.620 |
MOD_N-GLC_1 | 97 | 102 | PF02516 | 0.589 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.397 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.799 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.706 |
MOD_NEK2_1 | 22 | 27 | PF00069 | 0.487 |
MOD_NEK2_1 | 66 | 71 | PF00069 | 0.514 |
MOD_NEK2_2 | 79 | 84 | PF00069 | 0.417 |
MOD_PIKK_1 | 183 | 189 | PF00454 | 0.614 |
MOD_PIKK_1 | 263 | 269 | PF00454 | 0.709 |
MOD_PKA_2 | 250 | 256 | PF00069 | 0.662 |
MOD_PKA_2 | 268 | 274 | PF00069 | 0.549 |
MOD_Plk_1 | 115 | 121 | PF00069 | 0.297 |
MOD_Plk_1 | 150 | 156 | PF00069 | 0.755 |
MOD_Plk_1 | 22 | 28 | PF00069 | 0.489 |
MOD_Plk_1 | 245 | 251 | PF00069 | 0.773 |
MOD_Plk_1 | 62 | 68 | PF00069 | 0.464 |
MOD_Plk_1 | 79 | 85 | PF00069 | 0.314 |
MOD_Plk_1 | 97 | 103 | PF00069 | 0.560 |
MOD_Plk_2-3 | 333 | 339 | PF00069 | 0.588 |
MOD_Plk_4 | 268 | 274 | PF00069 | 0.575 |
MOD_ProDKin_1 | 146 | 152 | PF00069 | 0.657 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.503 |
MOD_SUMO_for_1 | 31 | 34 | PF00179 | 0.609 |
TRG_DiLeu_BaEn_1 | 143 | 148 | PF01217 | 0.756 |
TRG_DiLeu_BaEn_1 | 67 | 72 | PF01217 | 0.544 |
TRG_DiLeu_BaLyEn_6 | 322 | 327 | PF01217 | 0.603 |
TRG_ENDOCYTIC_2 | 112 | 115 | PF00928 | 0.498 |
TRG_ENDOCYTIC_2 | 204 | 207 | PF00928 | 0.617 |
TRG_ER_diArg_1 | 285 | 287 | PF00400 | 0.459 |
TRG_NES_CRM1_1 | 55 | 67 | PF08389 | 0.553 |
TRG_NLS_Bipartite_1 | 283 | 301 | PF00514 | 0.556 |
TRG_NLS_MonoCore_2 | 282 | 287 | PF00514 | 0.552 |
TRG_NLS_MonoExtC_3 | 283 | 288 | PF00514 | 0.551 |
TRG_NLS_MonoExtC_3 | 296 | 302 | PF00514 | 0.567 |
TRG_NLS_MonoExtN_4 | 283 | 288 | PF00514 | 0.534 |
TRG_NLS_MonoExtN_4 | 295 | 301 | PF00514 | 0.476 |
TRG_Pf-PMV_PEXEL_1 | 62 | 67 | PF00026 | 0.460 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKY6 | Leptomonas seymouri | 65% | 100% |
A0A0S4IYB8 | Bodo saltans | 35% | 93% |
A0A1X0NYR1 | Trypanosomatidae | 42% | 100% |
A0A3R7LUZ6 | Trypanosoma rangeli | 42% | 100% |
A0A3S7WU79 | Leishmania donovani | 96% | 100% |
A4H8T6 | Leishmania braziliensis | 85% | 100% |
A4HX55 | Leishmania infantum | 96% | 100% |
Q4QEK8 | Leishmania major | 96% | 100% |
V5BSA1 | Trypanosoma cruzi | 41% | 100% |