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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: E9AZS2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 195 | 197 | PF00675 | 0.549 |
CLV_NRD_NRD_1 | 249 | 251 | PF00675 | 0.415 |
CLV_NRD_NRD_1 | 286 | 288 | PF00675 | 0.307 |
CLV_NRD_NRD_1 | 82 | 84 | PF00675 | 0.467 |
CLV_PCSK_KEX2_1 | 195 | 197 | PF00082 | 0.549 |
CLV_PCSK_KEX2_1 | 249 | 251 | PF00082 | 0.415 |
CLV_PCSK_KEX2_1 | 286 | 288 | PF00082 | 0.307 |
CLV_PCSK_SKI1_1 | 195 | 199 | PF00082 | 0.396 |
DEG_APCC_DBOX_1 | 180 | 188 | PF00400 | 0.401 |
DEG_APCC_DBOX_1 | 82 | 90 | PF00400 | 0.427 |
DEG_SCF_FBW7_1 | 10 | 17 | PF00400 | 0.497 |
DEG_SPOP_SBC_1 | 134 | 138 | PF00917 | 0.625 |
DEG_SPOP_SBC_1 | 54 | 58 | PF00917 | 0.473 |
DOC_CYCLIN_RxL_1 | 283 | 294 | PF00134 | 0.334 |
DOC_MAPK_RevD_3 | 182 | 196 | PF00069 | 0.411 |
DOC_PP1_RVXF_1 | 284 | 291 | PF00149 | 0.367 |
DOC_PP2B_LxvP_1 | 378 | 381 | PF13499 | 0.343 |
DOC_PP4_FxxP_1 | 20 | 23 | PF00568 | 0.509 |
DOC_PP4_FxxP_1 | 226 | 229 | PF00568 | 0.457 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 159 | 163 | PF00917 | 0.348 |
DOC_USP7_MATH_1 | 239 | 243 | PF00917 | 0.418 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.519 |
DOC_USP7_MATH_1 | 396 | 400 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 54 | 58 | PF00917 | 0.516 |
DOC_USP7_MATH_2 | 128 | 134 | PF00917 | 0.583 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.587 |
DOC_WW_Pin1_4 | 225 | 230 | PF00397 | 0.733 |
DOC_WW_Pin1_4 | 293 | 298 | PF00397 | 0.459 |
DOC_WW_Pin1_4 | 326 | 331 | PF00397 | 0.445 |
DOC_WW_Pin1_4 | 345 | 350 | PF00397 | 0.397 |
LIG_14-3-3_CanoR_1 | 331 | 336 | PF00244 | 0.591 |
LIG_14-3-3_CanoR_1 | 386 | 394 | PF00244 | 0.422 |
LIG_14-3-3_CanoR_1 | 400 | 404 | PF00244 | 0.362 |
LIG_14-3-3_CanoR_1 | 9 | 16 | PF00244 | 0.711 |
LIG_AP2alpha_1 | 222 | 226 | PF02296 | 0.472 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.680 |
LIG_BIR_III_4 | 49 | 53 | PF00653 | 0.551 |
LIG_BRCT_BRCA1_1 | 16 | 20 | PF00533 | 0.506 |
LIG_BRCT_BRCA1_1 | 218 | 222 | PF00533 | 0.598 |
LIG_BRCT_BRCA1_1 | 314 | 318 | PF00533 | 0.432 |
LIG_BRCT_BRCA1_1 | 331 | 335 | PF00533 | 0.343 |
LIG_DLG_GKlike_1 | 331 | 338 | PF00625 | 0.488 |
LIG_FHA_1 | 135 | 141 | PF00498 | 0.474 |
LIG_FHA_2 | 166 | 172 | PF00498 | 0.460 |
LIG_FHA_2 | 228 | 234 | PF00498 | 0.430 |
LIG_LIR_Apic_2 | 17 | 23 | PF02991 | 0.506 |
LIG_LIR_Apic_2 | 202 | 208 | PF02991 | 0.483 |
LIG_LIR_Apic_2 | 224 | 229 | PF02991 | 0.464 |
LIG_LIR_Apic_2 | 265 | 271 | PF02991 | 0.465 |
LIG_LIR_Gen_1 | 219 | 229 | PF02991 | 0.600 |
LIG_LIR_Nem_3 | 115 | 119 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 219 | 225 | PF02991 | 0.604 |
LIG_LIR_Nem_3 | 332 | 338 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 97 | 102 | PF02991 | 0.313 |
LIG_Pex14_2 | 222 | 226 | PF04695 | 0.472 |
LIG_RPA_C_Fungi | 395 | 407 | PF08784 | 0.446 |
LIG_SH2_CRK | 205 | 209 | PF00017 | 0.490 |
LIG_SH2_NCK_1 | 205 | 209 | PF00017 | 0.490 |
LIG_SH2_PTP2 | 268 | 271 | PF00017 | 0.471 |
LIG_SH2_SRC | 150 | 153 | PF00017 | 0.375 |
LIG_SH2_STAP1 | 70 | 74 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 102 | 105 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 150 | 153 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 268 | 271 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 358 | 361 | PF00017 | 0.383 |
LIG_SH3_2 | 101 | 106 | PF14604 | 0.473 |
LIG_SH3_3 | 150 | 156 | PF00018 | 0.377 |
LIG_SH3_3 | 98 | 104 | PF00018 | 0.479 |
LIG_SUMO_SIM_anti_2 | 399 | 405 | PF11976 | 0.434 |
LIG_SUMO_SIM_par_1 | 118 | 124 | PF11976 | 0.459 |
LIG_TRAF2_1 | 230 | 233 | PF00917 | 0.427 |
MOD_CDK_SPK_2 | 326 | 331 | PF00069 | 0.438 |
MOD_CDK_SPxxK_3 | 326 | 333 | PF00069 | 0.411 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.657 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.677 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.469 |
MOD_CK1_1 | 329 | 335 | PF00069 | 0.493 |
MOD_CK1_1 | 399 | 405 | PF00069 | 0.480 |
MOD_CK1_1 | 57 | 63 | PF00069 | 0.467 |
MOD_CK2_1 | 227 | 233 | PF00069 | 0.438 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.582 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.424 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.687 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.326 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.389 |
MOD_GlcNHglycan | 388 | 391 | PF01048 | 0.364 |
MOD_GlcNHglycan | 404 | 407 | PF01048 | 0.377 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.499 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.652 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.601 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.624 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.391 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.659 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.283 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.514 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.439 |
MOD_N-GLC_1 | 396 | 401 | PF02516 | 0.488 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.440 |
MOD_NEK2_1 | 313 | 318 | PF00069 | 0.501 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.325 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.550 |
MOD_NEK2_2 | 281 | 286 | PF00069 | 0.368 |
MOD_NEK2_2 | 94 | 99 | PF00069 | 0.293 |
MOD_PIKK_1 | 239 | 245 | PF00454 | 0.476 |
MOD_PKA_2 | 206 | 212 | PF00069 | 0.485 |
MOD_PKA_2 | 399 | 405 | PF00069 | 0.448 |
MOD_PKA_2 | 8 | 14 | PF00069 | 0.753 |
MOD_Plk_4 | 112 | 118 | PF00069 | 0.423 |
MOD_Plk_4 | 136 | 142 | PF00069 | 0.556 |
MOD_Plk_4 | 380 | 386 | PF00069 | 0.522 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.297 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.588 |
MOD_ProDKin_1 | 225 | 231 | PF00069 | 0.729 |
MOD_ProDKin_1 | 293 | 299 | PF00069 | 0.454 |
MOD_ProDKin_1 | 326 | 332 | PF00069 | 0.434 |
MOD_ProDKin_1 | 345 | 351 | PF00069 | 0.391 |
TRG_DiLeu_BaLyEn_6 | 153 | 158 | PF01217 | 0.470 |
TRG_DiLeu_BaLyEn_6 | 373 | 378 | PF01217 | 0.492 |
TRG_ENDOCYTIC_2 | 102 | 105 | PF00928 | 0.372 |
TRG_ENDOCYTIC_2 | 150 | 153 | PF00928 | 0.375 |
TRG_ER_diArg_1 | 194 | 196 | PF00400 | 0.515 |
TRG_ER_diArg_1 | 248 | 250 | PF00400 | 0.415 |
TRG_ER_diArg_1 | 285 | 287 | PF00400 | 0.392 |
TRG_ER_diArg_1 | 330 | 333 | PF00400 | 0.514 |
TRG_Pf-PMV_PEXEL_1 | 167 | 171 | PF00026 | 0.467 |
TRG_Pf-PMV_PEXEL_1 | 286 | 291 | PF00026 | 0.325 |
TRG_Pf-PMV_PEXEL_1 | 61 | 65 | PF00026 | 0.522 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0NYD6 | Trypanosomatidae | 32% | 83% |
A0A3S7X1C6 | Leishmania donovani | 88% | 100% |
A4HGE9 | Leishmania braziliensis | 70% | 100% |
A4I3I0 | Leishmania infantum | 87% | 100% |
Q4Q8G2 | Leishmania major | 85% | 100% |