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:0016020 | membrane | 2 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0005737 | cytoplasm | 2 | 1 |
Related structures:
AlphaFold database: E9AYU3
Term | Name | Level | Count |
---|---|---|---|
GO:0006457 | protein folding | 2 | 1 |
GO:0006458 | 'de novo' protein folding | 3 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0042026 | protein refolding | 3 | 1 |
GO:0051084 | 'de novo' post-translational protein folding | 4 | 1 |
GO:0051085 | chaperone cofactor-dependent protein refolding | 4 | 1 |
GO:0061077 | chaperone-mediated protein folding | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0051082 | unfolded protein binding | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 224 | 228 | PF00656 | 0.639 |
CLV_C14_Caspase3-7 | 258 | 262 | PF00656 | 0.583 |
CLV_NRD_NRD_1 | 130 | 132 | PF00675 | 0.266 |
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.457 |
CLV_NRD_NRD_1 | 270 | 272 | PF00675 | 0.432 |
CLV_NRD_NRD_1 | 42 | 44 | PF00675 | 0.436 |
CLV_NRD_NRD_1 | 62 | 64 | PF00675 | 0.474 |
CLV_PCSK_FUR_1 | 127 | 131 | PF00082 | 0.274 |
CLV_PCSK_FUR_1 | 263 | 267 | PF00082 | 0.422 |
CLV_PCSK_KEX2_1 | 129 | 131 | PF00082 | 0.266 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 265 | 267 | PF00082 | 0.486 |
CLV_PCSK_KEX2_1 | 270 | 272 | PF00082 | 0.470 |
CLV_PCSK_KEX2_1 | 42 | 44 | PF00082 | 0.439 |
CLV_PCSK_KEX2_1 | 62 | 64 | PF00082 | 0.432 |
CLV_PCSK_PC1ET2_1 | 129 | 131 | PF00082 | 0.318 |
CLV_PCSK_PC1ET2_1 | 265 | 267 | PF00082 | 0.414 |
CLV_PCSK_PC7_1 | 266 | 272 | PF00082 | 0.461 |
CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.340 |
CLV_PCSK_SKI1_1 | 2 | 6 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 233 | 237 | PF00082 | 0.415 |
CLV_PCSK_SKI1_1 | 265 | 269 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 95 | 99 | PF00082 | 0.238 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.675 |
DEG_SPOP_SBC_1 | 238 | 242 | PF00917 | 0.562 |
DOC_CYCLIN_RxL_1 | 90 | 99 | PF00134 | 0.450 |
DOC_PP4_FxxP_1 | 309 | 312 | PF00568 | 0.690 |
DOC_SPAK_OSR1_1 | 266 | 270 | PF12202 | 0.670 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 277 | 281 | PF00917 | 0.617 |
DOC_USP7_UBL2_3 | 90 | 94 | PF12436 | 0.430 |
DOC_WW_Pin1_4 | 326 | 331 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 78 | 83 | PF00397 | 0.360 |
LIG_14-3-3_CanoR_1 | 233 | 239 | PF00244 | 0.752 |
LIG_14-3-3_CanoR_1 | 266 | 270 | PF00244 | 0.590 |
LIG_14-3-3_CanoR_1 | 271 | 277 | PF00244 | 0.610 |
LIG_14-3-3_CanoR_1 | 28 | 34 | PF00244 | 0.659 |
LIG_14-3-3_CanoR_1 | 50 | 58 | PF00244 | 0.720 |
LIG_14-3-3_CanoR_1 | 7 | 16 | PF00244 | 0.567 |
LIG_BRCT_BRCA1_1 | 160 | 164 | PF00533 | 0.703 |
LIG_BRCT_BRCA1_1 | 22 | 26 | PF00533 | 0.728 |
LIG_BRCT_BRCA1_1 | 305 | 309 | PF00533 | 0.662 |
LIG_BRCT_BRCA1_1 | 53 | 57 | PF00533 | 0.630 |
LIG_FHA_1 | 240 | 246 | PF00498 | 0.683 |
LIG_FHA_1 | 339 | 345 | PF00498 | 0.296 |
LIG_FHA_2 | 256 | 262 | PF00498 | 0.599 |
LIG_FHA_2 | 282 | 288 | PF00498 | 0.631 |
LIG_FHA_2 | 83 | 89 | PF00498 | 0.534 |
LIG_LIR_Apic_2 | 306 | 312 | PF02991 | 0.684 |
LIG_LIR_Gen_1 | 118 | 128 | PF02991 | 0.464 |
LIG_LIR_Gen_1 | 73 | 82 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 111 | 117 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 118 | 124 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 184 | 190 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 197 | 203 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 229 | 235 | PF02991 | 0.644 |
LIG_LIR_Nem_3 | 73 | 78 | PF02991 | 0.431 |
LIG_NRBOX | 343 | 349 | PF00104 | 0.357 |
LIG_Pex14_2 | 187 | 191 | PF04695 | 0.526 |
LIG_Pex14_2 | 232 | 236 | PF04695 | 0.625 |
LIG_Pex14_2 | 40 | 44 | PF04695 | 0.779 |
LIG_REV1ctd_RIR_1 | 38 | 46 | PF16727 | 0.576 |
LIG_SH2_CRK | 121 | 125 | PF00017 | 0.430 |
LIG_SH2_CRK | 75 | 79 | PF00017 | 0.407 |
LIG_SH2_CRK | 93 | 97 | PF00017 | 0.390 |
LIG_SH2_NCK_1 | 121 | 125 | PF00017 | 0.472 |
LIG_SH2_SRC | 173 | 176 | PF00017 | 0.695 |
LIG_SH2_STAT3 | 133 | 136 | PF00017 | 0.603 |
LIG_SH2_STAT5 | 259 | 262 | PF00017 | 0.624 |
LIG_SUMO_SIM_anti_2 | 364 | 370 | PF11976 | 0.362 |
LIG_SUMO_SIM_par_1 | 340 | 346 | PF11976 | 0.409 |
LIG_TRAF2_1 | 179 | 182 | PF00917 | 0.549 |
LIG_WRPW_2 | 232 | 235 | PF00400 | 0.550 |
MOD_CK1_1 | 147 | 153 | PF00069 | 0.569 |
MOD_CK1_1 | 158 | 164 | PF00069 | 0.628 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.567 |
MOD_CK1_1 | 237 | 243 | PF00069 | 0.568 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.491 |
MOD_CK2_1 | 176 | 182 | PF00069 | 0.442 |
MOD_CK2_1 | 281 | 287 | PF00069 | 0.610 |
MOD_CK2_1 | 82 | 88 | PF00069 | 0.264 |
MOD_Cter_Amidation | 263 | 266 | PF01082 | 0.541 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.400 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.575 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.583 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.428 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.598 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.556 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.553 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.367 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.521 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.532 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.609 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.465 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.602 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.553 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.570 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.581 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.245 |
MOD_N-GLC_1 | 277 | 282 | PF02516 | 0.523 |
MOD_N-GLC_1 | 303 | 308 | PF02516 | 0.509 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.488 |
MOD_NEK2_1 | 27 | 32 | PF00069 | 0.673 |
MOD_NEK2_1 | 361 | 366 | PF00069 | 0.304 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.584 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.568 |
MOD_NEK2_2 | 20 | 25 | PF00069 | 0.507 |
MOD_PIKK_1 | 314 | 320 | PF00454 | 0.568 |
MOD_PIKK_1 | 82 | 88 | PF00454 | 0.357 |
MOD_PK_1 | 113 | 119 | PF00069 | 0.344 |
MOD_PK_1 | 271 | 277 | PF00069 | 0.391 |
MOD_PKA_1 | 265 | 271 | PF00069 | 0.575 |
MOD_PKA_2 | 265 | 271 | PF00069 | 0.502 |
MOD_PKA_2 | 27 | 33 | PF00069 | 0.664 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.648 |
MOD_Plk_1 | 228 | 234 | PF00069 | 0.524 |
MOD_Plk_1 | 254 | 260 | PF00069 | 0.498 |
MOD_Plk_1 | 277 | 283 | PF00069 | 0.580 |
MOD_Plk_2-3 | 255 | 261 | PF00069 | 0.494 |
MOD_Plk_4 | 119 | 125 | PF00069 | 0.357 |
MOD_Plk_4 | 343 | 349 | PF00069 | 0.264 |
MOD_Plk_4 | 361 | 367 | PF00069 | 0.264 |
MOD_ProDKin_1 | 326 | 332 | PF00069 | 0.558 |
MOD_ProDKin_1 | 78 | 84 | PF00069 | 0.166 |
MOD_SUMO_rev_2 | 83 | 92 | PF00179 | 0.264 |
TRG_ENDOCYTIC_2 | 121 | 124 | PF00928 | 0.264 |
TRG_ENDOCYTIC_2 | 175 | 178 | PF00928 | 0.477 |
TRG_ENDOCYTIC_2 | 75 | 78 | PF00928 | 0.266 |
TRG_ENDOCYTIC_2 | 93 | 96 | PF00928 | 0.145 |
TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.616 |
TRG_ER_diArg_1 | 269 | 271 | PF00400 | 0.584 |
TRG_ER_diArg_1 | 289 | 292 | PF00400 | 0.438 |
TRG_ER_diArg_1 | 41 | 43 | PF00400 | 0.590 |
TRG_ER_diArg_1 | 62 | 64 | PF00400 | 0.607 |
TRG_NES_CRM1_1 | 184 | 197 | PF08389 | 0.437 |
TRG_Pf-PMV_PEXEL_1 | 201 | 205 | PF00026 | 0.523 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PD75 | Leptomonas seymouri | 69% | 100% |
A0A0S4JV26 | Bodo saltans | 41% | 100% |
A0A1X0P3X0 | Trypanosomatidae | 56% | 100% |
A0A3S5IRT6 | Trypanosoma rangeli | 53% | 100% |
A0A3S7X0F2 | Leishmania donovani | 93% | 79% |
A4HFG5 | Leishmania braziliensis | 81% | 100% |
A4I2M7 | Leishmania infantum | 93% | 100% |
D0A5P1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
E9AD18 | Leishmania major | 92% | 100% |
V5BN28 | Trypanosoma cruzi | 52% | 92% |