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 | yes | yes: 10, no: 0 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
Related structures:
AlphaFold database: Q4Q7Z3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 137 | 141 | PF00656 | 0.333 |
CLV_C14_Caspase3-7 | 172 | 176 | PF00656 | 0.352 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.662 |
CLV_NRD_NRD_1 | 307 | 309 | PF00675 | 0.408 |
CLV_NRD_NRD_1 | 323 | 325 | PF00675 | 0.434 |
CLV_NRD_NRD_1 | 335 | 337 | PF00675 | 0.404 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.691 |
CLV_PCSK_KEX2_1 | 323 | 325 | PF00082 | 0.492 |
CLV_PCSK_KEX2_1 | 334 | 336 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 189 | 193 | PF00082 | 0.538 |
CLV_PCSK_SKI1_1 | 349 | 353 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 354 | 358 | PF00082 | 0.467 |
CLV_PCSK_SKI1_1 | 6 | 10 | PF00082 | 0.619 |
DEG_APCC_DBOX_1 | 323 | 331 | PF00400 | 0.690 |
DEG_SPOP_SBC_1 | 117 | 121 | PF00917 | 0.439 |
DEG_SPOP_SBC_1 | 229 | 233 | PF00917 | 0.442 |
DOC_CYCLIN_RxL_1 | 3 | 11 | PF00134 | 0.463 |
DOC_MAPK_DCC_7 | 271 | 279 | PF00069 | 0.358 |
DOC_MAPK_gen_1 | 271 | 279 | PF00069 | 0.358 |
DOC_MAPK_MEF2A_6 | 273 | 281 | PF00069 | 0.405 |
DOC_PP4_FxxP_1 | 356 | 359 | PF00568 | 0.714 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.390 |
DOC_USP7_MATH_1 | 229 | 233 | PF00917 | 0.443 |
DOC_USP7_MATH_1 | 243 | 247 | PF00917 | 0.415 |
DOC_USP7_MATH_1 | 293 | 297 | PF00917 | 0.306 |
DOC_USP7_MATH_1 | 350 | 354 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.459 |
DOC_WW_Pin1_4 | 110 | 115 | PF00397 | 0.389 |
DOC_WW_Pin1_4 | 289 | 294 | PF00397 | 0.385 |
DOC_WW_Pin1_4 | 84 | 89 | PF00397 | 0.383 |
LIG_14-3-3_CanoR_1 | 106 | 116 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 170 | 180 | PF00244 | 0.264 |
LIG_14-3-3_CanoR_1 | 308 | 317 | PF00244 | 0.534 |
LIG_14-3-3_CanoR_1 | 324 | 332 | PF00244 | 0.706 |
LIG_14-3-3_CanoR_1 | 335 | 341 | PF00244 | 0.706 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.661 |
LIG_BRCT_BRCA1_1 | 295 | 299 | PF00533 | 0.306 |
LIG_BRCT_BRCA1_1 | 352 | 356 | PF00533 | 0.631 |
LIG_BRCT_BRCA1_1 | 64 | 68 | PF00533 | 0.416 |
LIG_deltaCOP1_diTrp_1 | 101 | 108 | PF00928 | 0.420 |
LIG_deltaCOP1_diTrp_1 | 46 | 52 | PF00928 | 0.351 |
LIG_FHA_1 | 185 | 191 | PF00498 | 0.329 |
LIG_FHA_1 | 204 | 210 | PF00498 | 0.251 |
LIG_FHA_1 | 233 | 239 | PF00498 | 0.399 |
LIG_FHA_2 | 170 | 176 | PF00498 | 0.421 |
LIG_FHA_2 | 194 | 200 | PF00498 | 0.388 |
LIG_IRF3_LxIS_1 | 76 | 82 | PF10401 | 0.251 |
LIG_LIR_Apic_2 | 353 | 359 | PF02991 | 0.712 |
LIG_LIR_Gen_1 | 287 | 295 | PF02991 | 0.281 |
LIG_LIR_Gen_1 | 296 | 307 | PF02991 | 0.283 |
LIG_LIR_Gen_1 | 66 | 77 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 128 | 134 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 178 | 184 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 287 | 291 | PF02991 | 0.281 |
LIG_LIR_Nem_3 | 296 | 302 | PF02991 | 0.283 |
LIG_LIR_Nem_3 | 66 | 72 | PF02991 | 0.347 |
LIG_Pex14_1 | 131 | 135 | PF04695 | 0.317 |
LIG_Pex14_1 | 64 | 68 | PF04695 | 0.335 |
LIG_SH2_CRK | 10 | 14 | PF00017 | 0.331 |
LIG_SH2_CRK | 181 | 185 | PF00017 | 0.352 |
LIG_SH2_SRC | 263 | 266 | PF00017 | 0.373 |
LIG_SH2_STAP1 | 10 | 14 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 10 | 13 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 205 | 208 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 263 | 266 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 345 | 348 | PF00017 | 0.606 |
LIG_SH3_1 | 344 | 350 | PF00018 | 0.599 |
LIG_SH3_2 | 347 | 352 | PF14604 | 0.660 |
LIG_SH3_3 | 154 | 160 | PF00018 | 0.418 |
LIG_SH3_3 | 344 | 350 | PF00018 | 0.610 |
LIG_SH3_3 | 356 | 362 | PF00018 | 0.637 |
LIG_SUMO_SIM_anti_2 | 15 | 21 | PF11976 | 0.445 |
LIG_SUMO_SIM_par_1 | 77 | 82 | PF11976 | 0.373 |
LIG_TYR_ITIM | 179 | 184 | PF00017 | 0.297 |
LIG_TYR_ITIM | 8 | 13 | PF00017 | 0.343 |
LIG_UBA3_1 | 190 | 195 | PF00899 | 0.309 |
LIG_UBA3_1 | 280 | 286 | PF00899 | 0.444 |
LIG_UBA3_1 | 303 | 309 | PF00899 | 0.469 |
LIG_WW_1 | 367 | 370 | PF00397 | 0.630 |
MOD_CK1_1 | 119 | 125 | PF00069 | 0.489 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.439 |
MOD_CK1_1 | 230 | 236 | PF00069 | 0.492 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.454 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.517 |
MOD_CK2_1 | 95 | 101 | PF00069 | 0.416 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.710 |
MOD_GlcNHglycan | 215 | 219 | PF01048 | 0.538 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.655 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.541 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.585 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.529 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.372 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.343 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.274 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.405 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.440 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.378 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.285 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.678 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.579 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.554 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.394 |
MOD_N-GLC_1 | 153 | 158 | PF02516 | 0.537 |
MOD_N-GLC_1 | 175 | 180 | PF02516 | 0.519 |
MOD_N-GLC_1 | 193 | 198 | PF02516 | 0.503 |
MOD_N-GLC_1 | 243 | 248 | PF02516 | 0.587 |
MOD_N-GLC_1 | 293 | 298 | PF02516 | 0.306 |
MOD_N-GLC_1 | 310 | 315 | PF02516 | 0.478 |
MOD_N-GLC_1 | 325 | 330 | PF02516 | 0.486 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.456 |
MOD_NEK2_1 | 134 | 139 | PF00069 | 0.340 |
MOD_NEK2_1 | 162 | 167 | PF00069 | 0.454 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.254 |
MOD_NEK2_1 | 280 | 285 | PF00069 | 0.428 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.459 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.604 |
MOD_NEK2_1 | 340 | 345 | PF00069 | 0.634 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.341 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.533 |
MOD_PIKK_1 | 107 | 113 | PF00454 | 0.449 |
MOD_PIKK_1 | 162 | 168 | PF00454 | 0.376 |
MOD_PKA_2 | 169 | 175 | PF00069 | 0.273 |
MOD_PKA_2 | 82 | 88 | PF00069 | 0.470 |
MOD_PKB_1 | 334 | 342 | PF00069 | 0.696 |
MOD_Plk_1 | 153 | 159 | PF00069 | 0.376 |
MOD_Plk_1 | 293 | 299 | PF00069 | 0.355 |
MOD_Plk_1 | 325 | 331 | PF00069 | 0.655 |
MOD_Plk_4 | 153 | 159 | PF00069 | 0.394 |
MOD_Plk_4 | 175 | 181 | PF00069 | 0.394 |
MOD_Plk_4 | 293 | 299 | PF00069 | 0.374 |
MOD_Plk_4 | 336 | 342 | PF00069 | 0.696 |
MOD_Plk_4 | 8 | 14 | PF00069 | 0.437 |
MOD_ProDKin_1 | 110 | 116 | PF00069 | 0.389 |
MOD_ProDKin_1 | 289 | 295 | PF00069 | 0.385 |
MOD_ProDKin_1 | 84 | 90 | PF00069 | 0.390 |
TRG_ENDOCYTIC_2 | 10 | 13 | PF00928 | 0.440 |
TRG_ENDOCYTIC_2 | 181 | 184 | PF00928 | 0.319 |
TRG_ENDOCYTIC_2 | 345 | 348 | PF00928 | 0.695 |
TRG_ER_diArg_1 | 3 | 6 | PF00400 | 0.621 |
TRG_ER_diArg_1 | 322 | 324 | PF00400 | 0.694 |
TRG_ER_diArg_1 | 334 | 336 | PF00400 | 0.661 |
TRG_ER_diArg_1 | 362 | 365 | PF00400 | 0.732 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3M3 | Leptomonas seymouri | 47% | 98% |
A0A1X0NQJ6 | Trypanosomatidae | 36% | 100% |
A0A3S7X1V5 | Leishmania donovani | 87% | 99% |
A0A422MSP0 | Trypanosoma rangeli | 38% | 100% |
A4HGX2 | Leishmania braziliensis | 66% | 94% |
A4I402 | Leishmania infantum | 88% | 99% |
D0A972 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9B092 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 99% |
V5AWR0 | Trypanosoma cruzi | 35% | 100% |