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:0043226 | organelle | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:0005869 | dynactin complex | 3 | 1 |
GO:0005875 | microtubule associated complex | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
Related structures:
AlphaFold database: A4HHT1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 189 | 193 | PF00656 | 0.413 |
CLV_NRD_NRD_1 | 23 | 25 | PF00675 | 0.537 |
CLV_NRD_NRD_1 | 34 | 36 | PF00675 | 0.314 |
CLV_PCSK_KEX2_1 | 202 | 204 | PF00082 | 0.157 |
CLV_PCSK_KEX2_1 | 21 | 23 | PF00082 | 0.510 |
CLV_PCSK_KEX2_1 | 34 | 36 | PF00082 | 0.533 |
CLV_PCSK_PC1ET2_1 | 202 | 204 | PF00082 | 0.157 |
CLV_PCSK_PC1ET2_1 | 21 | 23 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 169 | 173 | PF00082 | 0.253 |
CLV_PCSK_SKI1_1 | 211 | 215 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 277 | 281 | PF00082 | 0.308 |
DEG_APCC_DBOX_1 | 202 | 210 | PF00400 | 0.349 |
DEG_COP1_1 | 179 | 188 | PF00400 | 0.454 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.349 |
DOC_CYCLIN_RxL_1 | 207 | 218 | PF00134 | 0.357 |
DOC_MAPK_DCC_7 | 181 | 190 | PF00069 | 0.459 |
DOC_MAPK_gen_1 | 21 | 31 | PF00069 | 0.509 |
DOC_MAPK_HePTP_8 | 178 | 190 | PF00069 | 0.459 |
DOC_MAPK_HePTP_8 | 19 | 31 | PF00069 | 0.429 |
DOC_MAPK_MEF2A_6 | 181 | 190 | PF00069 | 0.459 |
DOC_MAPK_MEF2A_6 | 22 | 31 | PF00069 | 0.505 |
DOC_MAPK_MEF2A_6 | 61 | 70 | PF00069 | 0.508 |
DOC_PP2B_LxvP_1 | 188 | 191 | PF13499 | 0.469 |
DOC_USP7_MATH_1 | 191 | 195 | PF00917 | 0.477 |
DOC_USP7_UBL2_3 | 21 | 25 | PF12436 | 0.516 |
LIG_14-3-3_CanoR_1 | 142 | 147 | PF00244 | 0.460 |
LIG_14-3-3_CanoR_1 | 169 | 178 | PF00244 | 0.414 |
LIG_14-3-3_CanoR_1 | 235 | 243 | PF00244 | 0.357 |
LIG_14-3-3_CanoR_1 | 268 | 276 | PF00244 | 0.436 |
LIG_14-3-3_CanoR_1 | 34 | 42 | PF00244 | 0.523 |
LIG_APCC_ABBA_1 | 195 | 200 | PF00400 | 0.459 |
LIG_BRCT_BRCA1_1 | 232 | 236 | PF00533 | 0.459 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.426 |
LIG_FHA_1 | 146 | 152 | PF00498 | 0.439 |
LIG_FHA_1 | 165 | 171 | PF00498 | 0.412 |
LIG_FHA_1 | 2 | 8 | PF00498 | 0.281 |
LIG_FHA_1 | 208 | 214 | PF00498 | 0.500 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.482 |
LIG_FHA_1 | 238 | 244 | PF00498 | 0.494 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.426 |
LIG_FHA_2 | 177 | 183 | PF00498 | 0.441 |
LIG_FHA_2 | 187 | 193 | PF00498 | 0.418 |
LIG_FHA_2 | 41 | 47 | PF00498 | 0.447 |
LIG_LIR_Gen_1 | 239 | 250 | PF02991 | 0.480 |
LIG_LIR_Gen_1 | 83 | 92 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 119 | 125 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 13 | 19 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 239 | 245 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 305 | 309 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 83 | 89 | PF02991 | 0.472 |
LIG_NRBOX | 154 | 160 | PF00104 | 0.508 |
LIG_NRBOX | 67 | 73 | PF00104 | 0.490 |
LIG_SH2_CRK | 122 | 126 | PF00017 | 0.365 |
LIG_SH2_CRK | 16 | 20 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 101 | 104 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 41 | 44 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 5 | 8 | PF00017 | 0.406 |
LIG_SUMO_SIM_anti_2 | 62 | 70 | PF11976 | 0.452 |
LIG_SUMO_SIM_par_1 | 67 | 74 | PF11976 | 0.470 |
LIG_TRAF2_1 | 163 | 166 | PF00917 | 0.357 |
LIG_TRAF2_1 | 43 | 46 | PF00917 | 0.357 |
LIG_TYR_ITIM | 120 | 125 | PF00017 | 0.365 |
LIG_TYR_ITIM | 14 | 19 | PF00017 | 0.429 |
LIG_UBA3_1 | 289 | 297 | PF00899 | 0.426 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.506 |
MOD_CK1_1 | 216 | 222 | PF00069 | 0.508 |
MOD_CK1_1 | 237 | 243 | PF00069 | 0.379 |
MOD_CK1_1 | 249 | 255 | PF00069 | 0.513 |
MOD_CK1_1 | 77 | 83 | PF00069 | 0.472 |
MOD_CK2_1 | 159 | 165 | PF00069 | 0.436 |
MOD_CK2_1 | 174 | 180 | PF00069 | 0.493 |
MOD_CK2_1 | 217 | 223 | PF00069 | 0.560 |
MOD_CK2_1 | 40 | 46 | PF00069 | 0.438 |
MOD_GlcNHglycan | 112 | 116 | PF01048 | 0.224 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.220 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.252 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.301 |
MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.223 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.243 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.506 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.540 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.476 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.528 |
MOD_LATS_1 | 275 | 281 | PF00433 | 0.508 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.304 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.451 |
MOD_NEK2_1 | 170 | 175 | PF00069 | 0.405 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.492 |
MOD_NEK2_1 | 236 | 241 | PF00069 | 0.519 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.438 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.410 |
MOD_NEK2_2 | 10 | 15 | PF00069 | 0.316 |
MOD_NEK2_2 | 191 | 196 | PF00069 | 0.508 |
MOD_PIKK_1 | 288 | 294 | PF00454 | 0.419 |
MOD_PIKK_1 | 74 | 80 | PF00454 | 0.459 |
MOD_PK_1 | 142 | 148 | PF00069 | 0.508 |
MOD_PKA_2 | 141 | 147 | PF00069 | 0.494 |
MOD_PKA_2 | 207 | 213 | PF00069 | 0.509 |
MOD_PKA_2 | 234 | 240 | PF00069 | 0.528 |
MOD_PKA_2 | 267 | 273 | PF00069 | 0.557 |
MOD_PKA_2 | 33 | 39 | PF00069 | 0.350 |
MOD_Plk_1 | 1 | 7 | PF00069 | 0.299 |
MOD_Plk_1 | 164 | 170 | PF00069 | 0.518 |
MOD_Plk_1 | 186 | 192 | PF00069 | 0.512 |
MOD_Plk_1 | 237 | 243 | PF00069 | 0.473 |
MOD_Plk_1 | 64 | 70 | PF00069 | 0.472 |
MOD_Plk_2-3 | 59 | 65 | PF00069 | 0.422 |
MOD_Plk_4 | 1 | 7 | PF00069 | 0.377 |
MOD_Plk_4 | 191 | 197 | PF00069 | 0.477 |
MOD_Plk_4 | 238 | 244 | PF00069 | 0.461 |
MOD_Plk_4 | 246 | 252 | PF00069 | 0.489 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.421 |
MOD_Plk_4 | 80 | 86 | PF00069 | 0.387 |
TRG_DiLeu_BaEn_1 | 154 | 159 | PF01217 | 0.508 |
TRG_DiLeu_BaEn_1 | 166 | 171 | PF01217 | 0.508 |
TRG_DiLeu_BaEn_1 | 64 | 69 | PF01217 | 0.508 |
TRG_DiLeu_LyEn_5 | 154 | 159 | PF01217 | 0.459 |
TRG_ENDOCYTIC_2 | 122 | 125 | PF00928 | 0.365 |
TRG_ENDOCYTIC_2 | 16 | 19 | PF00928 | 0.380 |
TRG_ENDOCYTIC_2 | 86 | 89 | PF00928 | 0.508 |
TRG_NES_CRM1_1 | 292 | 305 | PF08389 | 0.426 |
TRG_NLS_MonoExtC_3 | 20 | 25 | PF00514 | 0.447 |
TRG_Pf-PMV_PEXEL_1 | 149 | 153 | PF00026 | 0.229 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6Y8 | Leptomonas seymouri | 76% | 100% |
A0A0S4KG45 | Bodo saltans | 26% | 89% |
A0A0S4KJ86 | Bodo saltans | 27% | 100% |
A0A1X0NRG7 | Trypanosomatidae | 25% | 83% |
A0A1X0P9A3 | Trypanosomatidae | 37% | 99% |
A0A3S5IR27 | Trypanosoma rangeli | 38% | 95% |
A0A3S7X2U7 | Leishmania donovani | 84% | 100% |
A4I4Z1 | Leishmania infantum | 85% | 100% |
C9ZKK7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 99% |
E9AKA4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 90% |
E9ALF0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
P11426 | Entamoeba histolytica | 26% | 86% |
P12432 | Trypanosoma brucei brucei | 24% | 86% |
P42023 | Pneumocystis carinii | 26% | 84% |
P45889 | Drosophila melanogaster | 25% | 86% |
P53473 | Strongylocentrotus purpuratus | 24% | 86% |
P61162 | Canis lupus familiaris | 26% | 86% |
P61163 | Homo sapiens | 26% | 86% |
P61164 | Mus musculus | 26% | 86% |
P69004 | Mesocentrotus franciscanus | 24% | 86% |
P69005 | Strongylocentrotus purpuratus | 24% | 86% |
P85515 | Rattus norvegicus | 26% | 86% |
Q2U7A3 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 25% | 86% |
Q4FXC8 | Leishmania major | 85% | 100% |
Q4R6J9 | Macaca fascicularis | 26% | 86% |
Q54I79 | Dictyostelium discoideum | 27% | 84% |
Q55CU2 | Dictyostelium discoideum | 23% | 86% |
Q8R5C5 | Mus musculus | 26% | 86% |
V5BDL0 | Trypanosoma cruzi | 24% | 86% |
V5C0Q2 | Trypanosoma cruzi | 23% | 83% |
V5DTX0 | Trypanosoma cruzi | 37% | 99% |