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: A0A3S7X1C6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 195 | 197 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 249 | 251 | PF00675 | 0.395 |
CLV_NRD_NRD_1 | 332 | 334 | PF00675 | 0.365 |
CLV_NRD_NRD_1 | 82 | 84 | PF00675 | 0.586 |
CLV_PCSK_KEX2_1 | 195 | 197 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 249 | 251 | PF00082 | 0.395 |
CLV_PCSK_KEX2_1 | 331 | 333 | PF00082 | 0.608 |
DEG_APCC_DBOX_1 | 180 | 188 | PF00400 | 0.374 |
DEG_APCC_DBOX_1 | 82 | 90 | PF00400 | 0.424 |
DEG_SPOP_SBC_1 | 134 | 138 | PF00917 | 0.613 |
DOC_MAPK_RevD_3 | 182 | 196 | PF00069 | 0.390 |
DOC_PP1_RVXF_1 | 285 | 291 | PF00149 | 0.351 |
DOC_PP2B_LxvP_1 | 378 | 381 | PF13499 | 0.328 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.521 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.495 |
DOC_USP7_MATH_1 | 396 | 400 | PF00917 | 0.471 |
DOC_USP7_MATH_2 | 128 | 134 | PF00917 | 0.585 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 114 | 119 | PF00397 | 0.539 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.537 |
DOC_WW_Pin1_4 | 225 | 230 | PF00397 | 0.594 |
DOC_WW_Pin1_4 | 293 | 298 | PF00397 | 0.431 |
DOC_WW_Pin1_4 | 345 | 350 | PF00397 | 0.406 |
DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.642 |
LIG_14-3-3_CanoR_1 | 216 | 225 | PF00244 | 0.534 |
LIG_14-3-3_CanoR_1 | 249 | 259 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 331 | 336 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 386 | 394 | PF00244 | 0.389 |
LIG_14-3-3_CanoR_1 | 400 | 404 | PF00244 | 0.435 |
LIG_14-3-3_CanoR_1 | 9 | 16 | PF00244 | 0.626 |
LIG_AP2alpha_2 | 45 | 47 | PF02296 | 0.527 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.659 |
LIG_BIR_III_2 | 205 | 209 | PF00653 | 0.638 |
LIG_BRCT_BRCA1_1 | 218 | 222 | PF00533 | 0.697 |
LIG_BRCT_BRCA1_1 | 314 | 318 | PF00533 | 0.400 |
LIG_DLG_GKlike_1 | 331 | 338 | PF00625 | 0.451 |
LIG_FHA_2 | 166 | 172 | PF00498 | 0.434 |
LIG_LIR_Apic_2 | 265 | 271 | PF02991 | 0.441 |
LIG_LIR_Gen_1 | 219 | 229 | PF02991 | 0.695 |
LIG_LIR_Nem_3 | 219 | 225 | PF02991 | 0.697 |
LIG_LIR_Nem_3 | 334 | 338 | PF02991 | 0.433 |
LIG_NRBOX | 222 | 228 | PF00104 | 0.539 |
LIG_RPA_C_Fungi | 326 | 338 | PF08784 | 0.437 |
LIG_RPA_C_Fungi | 395 | 407 | PF08784 | 0.419 |
LIG_SH2_NCK_1 | 51 | 55 | PF00017 | 0.523 |
LIG_SH2_PTP2 | 268 | 271 | PF00017 | 0.450 |
LIG_SH2_SRC | 150 | 153 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 102 | 105 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 150 | 153 | PF00017 | 0.367 |
LIG_SH2_STAT5 | 268 | 271 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 358 | 361 | PF00017 | 0.365 |
LIG_SH3_2 | 101 | 106 | PF14604 | 0.453 |
LIG_SH3_3 | 150 | 156 | PF00018 | 0.344 |
LIG_SH3_3 | 98 | 104 | PF00018 | 0.453 |
LIG_SUMO_SIM_anti_2 | 399 | 405 | PF11976 | 0.407 |
LIG_WRC_WIRS_1 | 244 | 249 | PF05994 | 0.306 |
MOD_CDK_SPxxK_3 | 54 | 61 | PF00069 | 0.555 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.572 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.549 |
MOD_CK1_1 | 399 | 405 | PF00069 | 0.454 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.579 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.725 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.379 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.411 |
MOD_GlcNHglycan | 388 | 391 | PF01048 | 0.457 |
MOD_GlcNHglycan | 404 | 407 | PF01048 | 0.431 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.448 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.697 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.666 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.553 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.342 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.335 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.634 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.355 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.581 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.425 |
MOD_N-GLC_1 | 113 | 118 | PF02516 | 0.520 |
MOD_N-GLC_1 | 396 | 401 | PF02516 | 0.458 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.560 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.416 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.480 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.381 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.528 |
MOD_PIKK_1 | 239 | 245 | PF00454 | 0.434 |
MOD_PKA_1 | 331 | 337 | PF00069 | 0.563 |
MOD_PKA_2 | 331 | 337 | PF00069 | 0.563 |
MOD_PKA_2 | 399 | 405 | PF00069 | 0.448 |
MOD_PKA_2 | 8 | 14 | PF00069 | 0.660 |
MOD_Plk_4 | 243 | 249 | PF00069 | 0.310 |
MOD_Plk_4 | 380 | 386 | PF00069 | 0.513 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.588 |
MOD_ProDKin_1 | 114 | 120 | PF00069 | 0.546 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.537 |
MOD_ProDKin_1 | 225 | 231 | PF00069 | 0.589 |
MOD_ProDKin_1 | 293 | 299 | PF00069 | 0.427 |
MOD_ProDKin_1 | 345 | 351 | PF00069 | 0.400 |
MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.639 |
TRG_DiLeu_BaLyEn_6 | 153 | 158 | PF01217 | 0.445 |
TRG_DiLeu_BaLyEn_6 | 373 | 378 | PF01217 | 0.477 |
TRG_ENDOCYTIC_2 | 102 | 105 | PF00928 | 0.412 |
TRG_ENDOCYTIC_2 | 150 | 153 | PF00928 | 0.392 |
TRG_ER_diArg_1 | 194 | 196 | PF00400 | 0.516 |
TRG_ER_diArg_1 | 248 | 250 | PF00400 | 0.394 |
TRG_ER_diArg_1 | 287 | 290 | PF00400 | 0.378 |
TRG_ER_diArg_1 | 331 | 333 | PF00400 | 0.432 |
TRG_Pf-PMV_PEXEL_1 | 167 | 171 | PF00026 | 0.440 |
TRG_Pf-PMV_PEXEL_1 | 61 | 65 | PF00026 | 0.514 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0NYD6 | Trypanosomatidae | 34% | 83% |
A4HGE9 | Leishmania braziliensis | 70% | 100% |
A4I3I0 | Leishmania infantum | 98% | 100% |
E9AZS2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4Q8G2 | Leishmania major | 89% | 100% |