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:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AM48
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 236 | 240 | PF00656 | 0.173 |
CLV_C14_Caspase3-7 | 315 | 319 | PF00656 | 0.306 |
CLV_C14_Caspase3-7 | 62 | 66 | PF00656 | 0.580 |
CLV_NRD_NRD_1 | 173 | 175 | PF00675 | 0.463 |
CLV_NRD_NRD_1 | 328 | 330 | PF00675 | 0.414 |
CLV_NRD_NRD_1 | 56 | 58 | PF00675 | 0.573 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.390 |
CLV_PCSK_KEX2_1 | 56 | 58 | PF00082 | 0.573 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 216 | 220 | PF00082 | 0.410 |
CLV_PCSK_SKI1_1 | 25 | 29 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 257 | 261 | PF00082 | 0.288 |
CLV_PCSK_SKI1_1 | 36 | 40 | PF00082 | 0.414 |
CLV_PCSK_SKI1_1 | 86 | 90 | PF00082 | 0.433 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.596 |
DEG_SIAH_1 | 245 | 253 | PF03145 | 0.246 |
DOC_CDC14_PxL_1 | 38 | 46 | PF14671 | 0.333 |
DOC_CYCLIN_RxL_1 | 22 | 32 | PF00134 | 0.518 |
DOC_PP1_RVXF_1 | 34 | 41 | PF00149 | 0.528 |
DOC_PP2B_LxvP_1 | 243 | 246 | PF13499 | 0.173 |
DOC_PP2B_LxvP_1 | 26 | 29 | PF13499 | 0.567 |
DOC_PP2B_LxvP_1 | 45 | 48 | PF13499 | 0.353 |
DOC_PP4_FxxP_1 | 160 | 163 | PF00568 | 0.481 |
DOC_PP4_FxxP_1 | 76 | 79 | PF00568 | 0.297 |
DOC_PP4_MxPP_1 | 242 | 245 | PF00568 | 0.173 |
DOC_USP7_MATH_1 | 151 | 155 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 204 | 208 | PF00917 | 0.297 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.355 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.201 |
DOC_USP7_MATH_1 | 29 | 33 | PF00917 | 0.696 |
DOC_USP7_MATH_2 | 200 | 206 | PF00917 | 0.391 |
DOC_USP7_UBL2_3 | 171 | 175 | PF12436 | 0.461 |
DOC_WW_Pin1_4 | 103 | 108 | PF00397 | 0.387 |
LIG_14-3-3_CanoR_1 | 109 | 116 | PF00244 | 0.685 |
LIG_14-3-3_CanoR_1 | 216 | 225 | PF00244 | 0.255 |
LIG_14-3-3_CanoR_1 | 261 | 271 | PF00244 | 0.222 |
LIG_14-3-3_CanoR_1 | 72 | 76 | PF00244 | 0.362 |
LIG_14-3-3_CanoR_1 | 86 | 91 | PF00244 | 0.209 |
LIG_BRCT_BRCA1_1 | 156 | 160 | PF00533 | 0.496 |
LIG_eIF4E_1 | 6 | 12 | PF01652 | 0.628 |
LIG_FHA_1 | 109 | 115 | PF00498 | 0.636 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.243 |
LIG_FHA_1 | 157 | 163 | PF00498 | 0.452 |
LIG_FHA_1 | 228 | 234 | PF00498 | 0.391 |
LIG_FHA_1 | 285 | 291 | PF00498 | 0.410 |
LIG_FHA_1 | 312 | 318 | PF00498 | 0.297 |
LIG_FHA_1 | 7 | 13 | PF00498 | 0.503 |
LIG_FHA_2 | 234 | 240 | PF00498 | 0.259 |
LIG_FHA_2 | 313 | 319 | PF00498 | 0.279 |
LIG_FHA_2 | 87 | 93 | PF00498 | 0.432 |
LIG_LIR_Apic_2 | 157 | 163 | PF02991 | 0.521 |
LIG_LIR_Apic_2 | 73 | 79 | PF02991 | 0.329 |
LIG_LIR_Gen_1 | 125 | 132 | PF02991 | 0.409 |
LIG_LIR_Gen_1 | 178 | 187 | PF02991 | 0.429 |
LIG_LIR_Gen_1 | 265 | 275 | PF02991 | 0.347 |
LIG_LIR_Gen_1 | 328 | 337 | PF02991 | 0.360 |
LIG_LIR_Gen_1 | 83 | 91 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 125 | 131 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 178 | 182 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 183 | 187 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 222 | 228 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 265 | 271 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 83 | 87 | PF02991 | 0.409 |
LIG_LYPXL_yS_3 | 41 | 44 | PF13949 | 0.516 |
LIG_MLH1_MIPbox_1 | 157 | 161 | PF16413 | 0.479 |
LIG_SH2_CRK | 165 | 169 | PF00017 | 0.427 |
LIG_SH2_CRK | 179 | 183 | PF00017 | 0.358 |
LIG_SH2_GRB2like | 179 | 182 | PF00017 | 0.485 |
LIG_SH2_STAP1 | 128 | 132 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 128 | 131 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 228 | 231 | PF00017 | 0.355 |
LIG_SH2_STAT5 | 331 | 334 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 84 | 87 | PF00017 | 0.450 |
LIG_SH3_3 | 113 | 119 | PF00018 | 0.505 |
LIG_SH3_3 | 18 | 24 | PF00018 | 0.601 |
LIG_SUMO_SIM_par_1 | 291 | 298 | PF11976 | 0.279 |
LIG_TRAF2_2 | 48 | 53 | PF00917 | 0.510 |
LIG_TYR_ITIM | 82 | 87 | PF00017 | 0.455 |
LIG_UBA3_1 | 167 | 175 | PF00899 | 0.484 |
MOD_CDC14_SPxK_1 | 106 | 109 | PF00782 | 0.412 |
MOD_CDK_SPxK_1 | 103 | 109 | PF00069 | 0.371 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.619 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.575 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.355 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.522 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.361 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.483 |
MOD_CK2_1 | 86 | 92 | PF00069 | 0.433 |
MOD_CMANNOS | 98 | 101 | PF00535 | 0.419 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.585 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.546 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.602 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.258 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.545 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.653 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.512 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.517 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.649 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.457 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.346 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.234 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.150 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.611 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.615 |
MOD_N-GLC_1 | 180 | 185 | PF02516 | 0.488 |
MOD_N-GLC_1 | 233 | 238 | PF02516 | 0.455 |
MOD_N-GLC_1 | 298 | 303 | PF02516 | 0.279 |
MOD_NEK2_1 | 11 | 16 | PF00069 | 0.606 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.355 |
MOD_NEK2_1 | 295 | 300 | PF00069 | 0.279 |
MOD_NEK2_1 | 311 | 316 | PF00069 | 0.292 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.285 |
MOD_PKA_2 | 108 | 114 | PF00069 | 0.642 |
MOD_PKA_2 | 71 | 77 | PF00069 | 0.370 |
MOD_Plk_1 | 180 | 186 | PF00069 | 0.429 |
MOD_Plk_1 | 280 | 286 | PF00069 | 0.373 |
MOD_Plk_1 | 311 | 317 | PF00069 | 0.433 |
MOD_Plk_2-3 | 312 | 318 | PF00069 | 0.357 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.537 |
MOD_Plk_4 | 280 | 286 | PF00069 | 0.241 |
MOD_Plk_4 | 312 | 318 | PF00069 | 0.279 |
MOD_Plk_4 | 40 | 46 | PF00069 | 0.378 |
MOD_Plk_4 | 71 | 77 | PF00069 | 0.484 |
MOD_ProDKin_1 | 103 | 109 | PF00069 | 0.400 |
MOD_SUMO_rev_2 | 172 | 177 | PF00179 | 0.324 |
TRG_DiLeu_BaLyEn_6 | 22 | 27 | PF01217 | 0.696 |
TRG_DiLeu_BaLyEn_6 | 33 | 38 | PF01217 | 0.545 |
TRG_ENDOCYTIC_2 | 128 | 131 | PF00928 | 0.442 |
TRG_ENDOCYTIC_2 | 165 | 168 | PF00928 | 0.432 |
TRG_ENDOCYTIC_2 | 179 | 182 | PF00928 | 0.365 |
TRG_ENDOCYTIC_2 | 331 | 334 | PF00928 | 0.320 |
TRG_ENDOCYTIC_2 | 41 | 44 | PF00928 | 0.516 |
TRG_ENDOCYTIC_2 | 84 | 87 | PF00928 | 0.364 |
TRG_ER_diArg_1 | 23 | 26 | PF00400 | 0.548 |
TRG_ER_diArg_1 | 55 | 57 | PF00400 | 0.554 |
TRG_ER_diArg_1 | 98 | 100 | PF00400 | 0.407 |
TRG_Pf-PMV_PEXEL_1 | 261 | 266 | PF00026 | 0.239 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I9L3 | Leptomonas seymouri | 56% | 99% |
A0A1X0NZG4 | Trypanosomatidae | 36% | 100% |
A0A3S7X221 | Leishmania donovani | 88% | 100% |
A0A422N067 | Trypanosoma rangeli | 36% | 100% |
A4HH57 | Leishmania braziliensis | 81% | 100% |
A4I483 | Leishmania infantum | 89% | 100% |
C9ZKP7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9ADN2 | Leishmania major | 90% | 100% |
V5BPX7 | Trypanosoma cruzi | 34% | 100% |