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:0032865 | ERMES complex | 3 | 12 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0098796 | membrane protein complex | 2 | 12 |
GO:0098798 | mitochondrial protein-containing complex | 2 | 12 |
GO:0098799 | outer mitochondrial membrane protein complex | 3 | 12 |
GO:0140534 | endoplasmic reticulum protein-containing complex | 2 | 12 |
Related structures:
AlphaFold database: A0A3S7WU79
Term | Name | Level | Count |
---|---|---|---|
GO:0006996 | organelle organization | 4 | 12 |
GO:0007005 | mitochondrion organization | 5 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016043 | cellular component organization | 3 | 12 |
GO:0071840 | cellular component organization or biogenesis | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 213 | 215 | PF00675 | 0.573 |
CLV_NRD_NRD_1 | 285 | 287 | PF00675 | 0.415 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.573 |
CLV_PCSK_KEX2_1 | 278 | 280 | PF00082 | 0.471 |
CLV_PCSK_KEX2_1 | 284 | 286 | PF00082 | 0.400 |
CLV_PCSK_KEX2_1 | 297 | 299 | PF00082 | 0.321 |
CLV_PCSK_PC1ET2_1 | 278 | 280 | PF00082 | 0.494 |
CLV_PCSK_PC1ET2_1 | 284 | 286 | PF00082 | 0.427 |
CLV_PCSK_PC1ET2_1 | 297 | 299 | PF00082 | 0.340 |
CLV_PCSK_SKI1_1 | 19 | 23 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 285 | 289 | PF00082 | 0.369 |
DEG_APCC_DBOX_1 | 268 | 276 | PF00400 | 0.589 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.432 |
DEG_SPOP_SBC_1 | 186 | 190 | PF00917 | 0.645 |
DOC_ANK_TNKS_1 | 328 | 335 | PF00023 | 0.598 |
DOC_MAPK_gen_1 | 283 | 291 | PF00069 | 0.374 |
DOC_MAPK_gen_1 | 36 | 46 | PF00069 | 0.527 |
DOC_MAPK_gen_1 | 84 | 92 | PF00069 | 0.417 |
DOC_MAPK_MEF2A_6 | 15 | 22 | PF00069 | 0.442 |
DOC_MAPK_MEF2A_6 | 283 | 291 | PF00069 | 0.388 |
DOC_MAPK_MEF2A_6 | 39 | 46 | PF00069 | 0.520 |
DOC_MAPK_MEF2A_6 | 84 | 92 | PF00069 | 0.388 |
DOC_PP2B_LxvP_1 | 107 | 110 | PF13499 | 0.588 |
DOC_PP4_FxxP_1 | 111 | 114 | PF00568 | 0.386 |
DOC_PP4_FxxP_1 | 292 | 295 | PF00568 | 0.391 |
DOC_PP4_MxPP_1 | 216 | 219 | PF00568 | 0.584 |
DOC_USP7_MATH_1 | 100 | 104 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 185 | 189 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 268 | 272 | PF00917 | 0.499 |
DOC_USP7_UBL2_3 | 284 | 288 | PF12436 | 0.406 |
DOC_USP7_UBL2_3 | 32 | 36 | PF12436 | 0.592 |
DOC_WW_Pin1_4 | 146 | 151 | PF00397 | 0.634 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.544 |
DOC_WW_Pin1_4 | 233 | 238 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.505 |
LIG_14-3-3_CanoR_1 | 173 | 183 | PF00244 | 0.622 |
LIG_14-3-3_CanoR_1 | 269 | 273 | PF00244 | 0.508 |
LIG_APCC_ABBA_1 | 130 | 135 | PF00400 | 0.390 |
LIG_APCC_ABBA_1 | 289 | 294 | PF00400 | 0.384 |
LIG_APCC_ABBAyCdc20_2 | 288 | 294 | PF00400 | 0.394 |
LIG_APCC_ABBAyCdc20_2 | 39 | 45 | PF00400 | 0.445 |
LIG_Clathr_ClatBox_1 | 41 | 45 | PF01394 | 0.433 |
LIG_CtBP_PxDLS_1 | 114 | 118 | PF00389 | 0.492 |
LIG_CtBP_PxDLS_1 | 218 | 222 | PF00389 | 0.591 |
LIG_deltaCOP1_diTrp_1 | 5 | 10 | PF00928 | 0.410 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.719 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.772 |
LIG_FHA_1 | 334 | 340 | PF00498 | 0.528 |
LIG_FHA_1 | 7 | 13 | PF00498 | 0.571 |
LIG_FHA_1 | 80 | 86 | PF00498 | 0.434 |
LIG_FHA_2 | 116 | 122 | PF00498 | 0.354 |
LIG_LIR_Gen_1 | 131 | 140 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 131 | 136 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 201 | 207 | PF02991 | 0.624 |
LIG_SH2_CRK | 204 | 208 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 112 | 115 | PF00017 | 0.483 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.568 |
LIG_SH3_3 | 225 | 231 | PF00018 | 0.760 |
LIG_SH3_3 | 262 | 268 | PF00018 | 0.692 |
LIG_SH3_3 | 303 | 309 | PF00018 | 0.598 |
LIG_SH3_3 | 41 | 47 | PF00018 | 0.504 |
LIG_SUMO_SIM_par_1 | 271 | 277 | PF11976 | 0.508 |
LIG_SUMO_SIM_par_1 | 335 | 340 | PF11976 | 0.462 |
LIG_UBA3_1 | 272 | 278 | PF00899 | 0.588 |
MOD_CDK_SPK_2 | 156 | 161 | PF00069 | 0.663 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.670 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.698 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.598 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.626 |
MOD_CK1_1 | 241 | 247 | PF00069 | 0.650 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.565 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.548 |
MOD_Cter_Amidation | 211 | 214 | PF01082 | 0.557 |
MOD_Cter_Amidation | 311 | 314 | PF01082 | 0.605 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.687 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.669 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.542 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.543 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.675 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.520 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.641 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.692 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.543 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.665 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.585 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.591 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.573 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.363 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.560 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.339 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.702 |
MOD_NEK2_1 | 22 | 27 | PF00069 | 0.434 |
MOD_NEK2_1 | 66 | 71 | PF00069 | 0.487 |
MOD_NEK2_2 | 79 | 84 | PF00069 | 0.370 |
MOD_PIKK_1 | 263 | 269 | PF00454 | 0.678 |
MOD_PKA_2 | 268 | 274 | PF00069 | 0.497 |
MOD_Plk_1 | 103 | 109 | PF00069 | 0.520 |
MOD_Plk_1 | 115 | 121 | PF00069 | 0.255 |
MOD_Plk_1 | 150 | 156 | PF00069 | 0.722 |
MOD_Plk_1 | 22 | 28 | PF00069 | 0.452 |
MOD_Plk_1 | 245 | 251 | PF00069 | 0.635 |
MOD_Plk_1 | 62 | 68 | PF00069 | 0.404 |
MOD_Plk_1 | 79 | 85 | PF00069 | 0.271 |
MOD_Plk_2-3 | 333 | 339 | PF00069 | 0.451 |
MOD_Plk_4 | 268 | 274 | PF00069 | 0.540 |
MOD_ProDKin_1 | 146 | 152 | PF00069 | 0.639 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.546 |
MOD_ProDKin_1 | 233 | 239 | PF00069 | 0.692 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.508 |
MOD_SUMO_for_1 | 31 | 34 | PF00179 | 0.588 |
TRG_DiLeu_BaEn_1 | 143 | 148 | PF01217 | 0.733 |
TRG_DiLeu_BaEn_1 | 67 | 72 | PF01217 | 0.402 |
TRG_DiLeu_BaLyEn_6 | 322 | 327 | PF01217 | 0.582 |
TRG_ENDOCYTIC_2 | 112 | 115 | PF00928 | 0.498 |
TRG_ENDOCYTIC_2 | 204 | 207 | PF00928 | 0.547 |
TRG_ER_diArg_1 | 285 | 287 | PF00400 | 0.414 |
TRG_NES_CRM1_1 | 55 | 67 | PF08389 | 0.524 |
TRG_NLS_Bipartite_1 | 283 | 301 | PF00514 | 0.524 |
TRG_NLS_MonoCore_2 | 282 | 287 | PF00514 | 0.522 |
TRG_NLS_MonoExtC_3 | 283 | 288 | PF00514 | 0.522 |
TRG_NLS_MonoExtC_3 | 296 | 302 | PF00514 | 0.531 |
TRG_NLS_MonoExtN_4 | 283 | 288 | PF00514 | 0.499 |
TRG_NLS_MonoExtN_4 | 295 | 301 | PF00514 | 0.423 |
TRG_Pf-PMV_PEXEL_1 | 62 | 67 | PF00026 | 0.390 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKY6 | Leptomonas seymouri | 66% | 100% |
A0A0S4IYB8 | Bodo saltans | 33% | 93% |
A0A1X0NYR1 | Trypanosomatidae | 43% | 100% |
A0A3R7LUZ6 | Trypanosoma rangeli | 42% | 100% |
A4H8T6 | Leishmania braziliensis | 86% | 100% |
A4HX55 | Leishmania infantum | 100% | 100% |
C9ZVT6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
E9AQX0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
Q4QEK8 | Leishmania major | 96% | 100% |
V5BSA1 | Trypanosoma cruzi | 41% | 100% |