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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 10 |
GO:0005814 | centriole | 5 | 10 |
GO:0043226 | organelle | 2 | 10 |
GO:0043228 | non-membrane-bounded organelle | 3 | 10 |
GO:0043229 | intracellular organelle | 3 | 10 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:0005813 | centrosome | 3 | 1 |
GO:0005815 | microtubule organizing center | 2 | 1 |
Related structures:
AlphaFold database: E9AT47
Term | Name | Level | Count |
---|---|---|---|
GO:0007049 | cell cycle | 2 | 10 |
GO:0009987 | cellular process | 1 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 218 | 222 | PF00656 | 0.541 |
CLV_NRD_NRD_1 | 110 | 112 | PF00675 | 0.432 |
CLV_NRD_NRD_1 | 116 | 118 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 120 | 122 | PF00675 | 0.420 |
CLV_NRD_NRD_1 | 41 | 43 | PF00675 | 0.476 |
CLV_NRD_NRD_1 | 63 | 65 | PF00675 | 0.456 |
CLV_PCSK_FUR_1 | 117 | 121 | PF00082 | 0.525 |
CLV_PCSK_FUR_1 | 150 | 154 | PF00082 | 0.426 |
CLV_PCSK_KEX2_1 | 110 | 112 | PF00082 | 0.421 |
CLV_PCSK_KEX2_1 | 116 | 118 | PF00082 | 0.428 |
CLV_PCSK_KEX2_1 | 119 | 121 | PF00082 | 0.405 |
CLV_PCSK_KEX2_1 | 152 | 154 | PF00082 | 0.459 |
CLV_PCSK_KEX2_1 | 161 | 163 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 40 | 42 | PF00082 | 0.490 |
CLV_PCSK_KEX2_1 | 63 | 65 | PF00082 | 0.433 |
CLV_PCSK_PC1ET2_1 | 152 | 154 | PF00082 | 0.432 |
CLV_PCSK_PC1ET2_1 | 161 | 163 | PF00082 | 0.535 |
CLV_PCSK_PC7_1 | 116 | 122 | PF00082 | 0.585 |
CLV_PCSK_SKI1_1 | 195 | 199 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 240 | 244 | PF00082 | 0.684 |
DOC_MAPK_MEF2A_6 | 26 | 35 | PF00069 | 0.500 |
DOC_PP4_FxxP_1 | 272 | 275 | PF00568 | 0.655 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.631 |
DOC_USP7_UBL2_3 | 157 | 161 | PF12436 | 0.493 |
DOC_WW_Pin1_4 | 240 | 245 | PF00397 | 0.603 |
DOC_WW_Pin1_4 | 248 | 253 | PF00397 | 0.670 |
DOC_WW_Pin1_4 | 275 | 280 | PF00397 | 0.634 |
DOC_WW_Pin1_4 | 318 | 323 | PF00397 | 0.621 |
LIG_14-3-3_CanoR_1 | 132 | 136 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 238 | 243 | PF00244 | 0.684 |
LIG_14-3-3_CanoR_1 | 291 | 300 | PF00244 | 0.716 |
LIG_BIR_III_4 | 267 | 271 | PF00653 | 0.545 |
LIG_BRCT_BRCA1_1 | 302 | 306 | PF00533 | 0.631 |
LIG_eIF4E_1 | 139 | 145 | PF01652 | 0.365 |
LIG_EVH1_2 | 322 | 326 | PF00568 | 0.713 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.432 |
LIG_LIR_Nem_3 | 134 | 139 | PF02991 | 0.364 |
LIG_SH2_STAT3 | 176 | 179 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 129 | 132 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 38 | 41 | PF00017 | 0.497 |
LIG_SH3_2 | 322 | 327 | PF14604 | 0.633 |
LIG_SH3_3 | 319 | 325 | PF00018 | 0.686 |
LIG_SUMO_SIM_anti_2 | 29 | 37 | PF11976 | 0.494 |
LIG_TRAF2_1 | 50 | 53 | PF00917 | 0.433 |
LIG_TRAF2_1 | 73 | 76 | PF00917 | 0.527 |
MOD_CK1_1 | 232 | 238 | PF00069 | 0.714 |
MOD_CK1_1 | 250 | 256 | PF00069 | 0.648 |
MOD_CK1_1 | 314 | 320 | PF00069 | 0.650 |
MOD_CK1_1 | 330 | 336 | PF00069 | 0.685 |
MOD_CK2_1 | 186 | 192 | PF00069 | 0.446 |
MOD_DYRK1A_RPxSP_1 | 240 | 244 | PF00069 | 0.617 |
MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.663 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.779 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.731 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.592 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.603 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.645 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.668 |
MOD_LATS_1 | 236 | 242 | PF00433 | 0.606 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.695 |
MOD_NEK2_1 | 329 | 334 | PF00069 | 0.620 |
MOD_NEK2_2 | 131 | 136 | PF00069 | 0.322 |
MOD_PIKK_1 | 332 | 338 | PF00454 | 0.627 |
MOD_PIKK_1 | 40 | 46 | PF00454 | 0.430 |
MOD_PK_1 | 238 | 244 | PF00069 | 0.704 |
MOD_PKA_1 | 40 | 46 | PF00069 | 0.430 |
MOD_PKA_2 | 131 | 137 | PF00069 | 0.541 |
MOD_PKA_2 | 232 | 238 | PF00069 | 0.661 |
MOD_PKA_2 | 285 | 291 | PF00069 | 0.564 |
MOD_PKA_2 | 40 | 46 | PF00069 | 0.525 |
MOD_Plk_1 | 186 | 192 | PF00069 | 0.444 |
MOD_Plk_1 | 8 | 14 | PF00069 | 0.509 |
MOD_Plk_4 | 131 | 137 | PF00069 | 0.322 |
MOD_Plk_4 | 8 | 14 | PF00069 | 0.577 |
MOD_ProDKin_1 | 240 | 246 | PF00069 | 0.603 |
MOD_ProDKin_1 | 248 | 254 | PF00069 | 0.666 |
MOD_ProDKin_1 | 275 | 281 | PF00069 | 0.636 |
MOD_ProDKin_1 | 318 | 324 | PF00069 | 0.621 |
MOD_SUMO_for_1 | 4 | 7 | PF00179 | 0.635 |
MOD_SUMO_for_1 | 50 | 53 | PF00179 | 0.488 |
TRG_ER_diArg_1 | 109 | 111 | PF00400 | 0.477 |
TRG_ER_diArg_1 | 115 | 117 | PF00400 | 0.458 |
TRG_ER_diArg_1 | 119 | 121 | PF00400 | 0.427 |
TRG_ER_diArg_1 | 39 | 42 | PF00400 | 0.515 |
TRG_ER_diArg_1 | 63 | 65 | PF00400 | 0.529 |
TRG_NES_CRM1_1 | 92 | 103 | PF08389 | 0.415 |
TRG_NLS_Bipartite_1 | 63 | 85 | PF00514 | 0.530 |
TRG_NLS_MonoExtN_4 | 78 | 85 | PF00514 | 0.452 |
TRG_Pf-PMV_PEXEL_1 | 120 | 124 | PF00026 | 0.450 |
TRG_Pf-PMV_PEXEL_1 | 178 | 182 | PF00026 | 0.610 |
TRG_Pf-PMV_PEXEL_1 | 63 | 67 | PF00026 | 0.533 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2V9 | Leptomonas seymouri | 49% | 99% |
A0A1X0NKY4 | Trypanosomatidae | 27% | 82% |
A0A3Q8IKC6 | Leishmania donovani | 94% | 100% |
A4HPD7 | Leishmania braziliensis | 81% | 100% |
A4ICH6 | Leishmania infantum | 94% | 100% |
D0A3J5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 93% |
Q4Q1F1 | Leishmania major | 91% | 100% |
V5BK99 | Trypanosoma cruzi | 28% | 90% |