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: E9B3J2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 339 | 343 | PF00656 | 0.640 |
CLV_NRD_NRD_1 | 377 | 379 | PF00675 | 0.560 |
CLV_NRD_NRD_1 | 384 | 386 | PF00675 | 0.587 |
CLV_NRD_NRD_1 | 388 | 390 | PF00675 | 0.607 |
CLV_PCSK_KEX2_1 | 365 | 367 | PF00082 | 0.432 |
CLV_PCSK_KEX2_1 | 377 | 379 | PF00082 | 0.555 |
CLV_PCSK_KEX2_1 | 384 | 386 | PF00082 | 0.585 |
CLV_PCSK_PC1ET2_1 | 365 | 367 | PF00082 | 0.353 |
CLV_PCSK_SKI1_1 | 21 | 25 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 272 | 276 | PF00082 | 0.588 |
DEG_APCC_DBOX_1 | 20 | 28 | PF00400 | 0.521 |
DOC_CYCLIN_yCln2_LP_2 | 193 | 199 | PF00134 | 0.493 |
DOC_MAPK_MEF2A_6 | 225 | 233 | PF00069 | 0.483 |
DOC_PP2B_LxvP_1 | 193 | 196 | PF13499 | 0.569 |
DOC_USP7_MATH_1 | 334 | 338 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 364 | 368 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 9 | 13 | PF00917 | 0.465 |
DOC_WW_Pin1_4 | 398 | 403 | PF00397 | 0.590 |
DOC_WW_Pin1_4 | 45 | 50 | PF00397 | 0.630 |
LIG_14-3-3_CanoR_1 | 207 | 215 | PF00244 | 0.622 |
LIG_14-3-3_CanoR_1 | 306 | 316 | PF00244 | 0.585 |
LIG_14-3-3_CanoR_1 | 377 | 382 | PF00244 | 0.648 |
LIG_14-3-3_CanoR_1 | 384 | 388 | PF00244 | 0.515 |
LIG_14-3-3_CterR_2 | 404 | 408 | PF00244 | 0.777 |
LIG_APCC_ABBA_1 | 195 | 200 | PF00400 | 0.588 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.720 |
LIG_BIR_III_4 | 92 | 96 | PF00653 | 0.513 |
LIG_BRCT_BRCA1_1 | 246 | 250 | PF00533 | 0.694 |
LIG_Clathr_ClatBox_1 | 279 | 283 | PF01394 | 0.384 |
LIG_EH_1 | 42 | 46 | PF12763 | 0.609 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.550 |
LIG_FHA_1 | 2 | 8 | PF00498 | 0.497 |
LIG_FHA_1 | 209 | 215 | PF00498 | 0.354 |
LIG_FHA_1 | 27 | 33 | PF00498 | 0.535 |
LIG_FHA_1 | 292 | 298 | PF00498 | 0.641 |
LIG_FHA_1 | 308 | 314 | PF00498 | 0.432 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.485 |
LIG_FHA_2 | 208 | 214 | PF00498 | 0.622 |
LIG_FHA_2 | 237 | 243 | PF00498 | 0.384 |
LIG_FHA_2 | 260 | 266 | PF00498 | 0.295 |
LIG_FHA_2 | 300 | 306 | PF00498 | 0.493 |
LIG_Integrin_RGD_1 | 340 | 342 | PF01839 | 0.651 |
LIG_Integrin_RGD_1 | 40 | 42 | PF01839 | 0.577 |
LIG_LIR_Apic_2 | 159 | 164 | PF02991 | 0.516 |
LIG_LIR_Gen_1 | 254 | 264 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 254 | 260 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 386 | 391 | PF02991 | 0.536 |
LIG_NRBOX | 226 | 232 | PF00104 | 0.452 |
LIG_PCNA_yPIPBox_3 | 17 | 27 | PF02747 | 0.653 |
LIG_Pex14_2 | 180 | 184 | PF04695 | 0.369 |
LIG_PTAP_UEV_1 | 10 | 15 | PF05743 | 0.457 |
LIG_SH2_CRK | 16 | 20 | PF00017 | 0.697 |
LIG_SH2_STAT5 | 290 | 293 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 358 | 361 | PF00017 | 0.592 |
LIG_SH2_STAT5 | 368 | 371 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 73 | 76 | PF00017 | 0.724 |
LIG_SH3_3 | 152 | 158 | PF00018 | 0.513 |
LIG_SH3_3 | 2 | 8 | PF00018 | 0.750 |
LIG_SUMO_SIM_anti_2 | 22 | 29 | PF11976 | 0.556 |
LIG_SUMO_SIM_anti_2 | 226 | 232 | PF11976 | 0.554 |
LIG_SUMO_SIM_anti_2 | 239 | 245 | PF11976 | 0.534 |
LIG_SUMO_SIM_anti_2 | 34 | 40 | PF11976 | 0.478 |
LIG_SUMO_SIM_par_1 | 228 | 235 | PF11976 | 0.506 |
LIG_SUMO_SIM_par_1 | 244 | 249 | PF11976 | 0.489 |
MOD_CDC14_SPxK_1 | 401 | 404 | PF00782 | 0.729 |
MOD_CDK_SPxK_1 | 398 | 404 | PF00069 | 0.704 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.513 |
MOD_CK1_1 | 299 | 305 | PF00069 | 0.549 |
MOD_CK1_1 | 376 | 382 | PF00069 | 0.371 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.513 |
MOD_CK2_1 | 207 | 213 | PF00069 | 0.633 |
MOD_CK2_1 | 259 | 265 | PF00069 | 0.569 |
MOD_CK2_1 | 299 | 305 | PF00069 | 0.538 |
MOD_CK2_1 | 341 | 347 | PF00069 | 0.617 |
MOD_CK2_1 | 364 | 370 | PF00069 | 0.636 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.545 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.478 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.587 |
MOD_GlcNHglycan | 92 | 96 | PF01048 | 0.513 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.410 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.523 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.521 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.504 |
MOD_GSK3_1 | 373 | 380 | PF00069 | 0.389 |
MOD_LATS_1 | 375 | 381 | PF00433 | 0.596 |
MOD_N-GLC_1 | 125 | 130 | PF02516 | 0.513 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.411 |
MOD_NEK2_1 | 201 | 206 | PF00069 | 0.466 |
MOD_NEK2_2 | 129 | 134 | PF00069 | 0.222 |
MOD_NEK2_2 | 175 | 180 | PF00069 | 0.454 |
MOD_PKA_1 | 377 | 383 | PF00069 | 0.649 |
MOD_PKA_2 | 376 | 382 | PF00069 | 0.659 |
MOD_PKA_2 | 383 | 389 | PF00069 | 0.534 |
MOD_PKB_1 | 89 | 97 | PF00069 | 0.436 |
MOD_Plk_1 | 291 | 297 | PF00069 | 0.616 |
MOD_Plk_4 | 175 | 181 | PF00069 | 0.461 |
MOD_Plk_4 | 225 | 231 | PF00069 | 0.412 |
MOD_Plk_4 | 236 | 242 | PF00069 | 0.476 |
MOD_Plk_4 | 259 | 265 | PF00069 | 0.527 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.571 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.481 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.512 |
MOD_Plk_4 | 377 | 383 | PF00069 | 0.596 |
MOD_ProDKin_1 | 398 | 404 | PF00069 | 0.602 |
MOD_ProDKin_1 | 45 | 51 | PF00069 | 0.624 |
MOD_SUMO_rev_2 | 353 | 357 | PF00179 | 0.588 |
TRG_DiLeu_BaEn_1 | 347 | 352 | PF01217 | 0.506 |
TRG_DiLeu_BaLyEn_6 | 143 | 148 | PF01217 | 0.436 |
TRG_ENDOCYTIC_2 | 198 | 201 | PF00928 | 0.429 |
TRG_ER_diArg_1 | 88 | 91 | PF00400 | 0.527 |
TRG_NES_CRM1_1 | 278 | 292 | PF08389 | 0.383 |
TRG_Pf-PMV_PEXEL_1 | 146 | 150 | PF00026 | 0.409 |
TRG_Pf-PMV_PEXEL_1 | 21 | 25 | PF00026 | 0.546 |
TRG_Pf-PMV_PEXEL_1 | 317 | 321 | PF00026 | 0.489 |
TRG_Pf-PMV_PEXEL_1 | 389 | 394 | PF00026 | 0.348 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBF8 | Leptomonas seymouri | 52% | 100% |
A0A3Q8IHJ7 | Leishmania donovani | 88% | 100% |
A4HL51 | Leishmania braziliensis | 73% | 100% |
A4I8N0 | Leishmania infantum | 88% | 100% |
Q4Q4K9 | Leishmania major | 87% | 100% |