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: A0A3Q8IC33
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 294 | 298 | PF00656 | 0.632 |
CLV_C14_Caspase3-7 | 35 | 39 | PF00656 | 0.546 |
CLV_C14_Caspase3-7 | 444 | 448 | PF00656 | 0.495 |
CLV_C14_Caspase3-7 | 459 | 463 | PF00656 | 0.435 |
CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.554 |
CLV_NRD_NRD_1 | 272 | 274 | PF00675 | 0.387 |
CLV_NRD_NRD_1 | 316 | 318 | PF00675 | 0.592 |
CLV_NRD_NRD_1 | 398 | 400 | PF00675 | 0.468 |
CLV_NRD_NRD_1 | 460 | 462 | PF00675 | 0.479 |
CLV_NRD_NRD_1 | 49 | 51 | PF00675 | 0.603 |
CLV_NRD_NRD_1 | 89 | 91 | PF00675 | 0.646 |
CLV_PCSK_FUR_1 | 224 | 228 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 223 | 225 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 226 | 228 | PF00082 | 0.580 |
CLV_PCSK_KEX2_1 | 316 | 318 | PF00082 | 0.628 |
CLV_PCSK_KEX2_1 | 398 | 400 | PF00082 | 0.468 |
CLV_PCSK_KEX2_1 | 460 | 462 | PF00082 | 0.489 |
CLV_PCSK_KEX2_1 | 49 | 51 | PF00082 | 0.605 |
CLV_PCSK_KEX2_1 | 89 | 91 | PF00082 | 0.688 |
CLV_PCSK_PC1ET2_1 | 223 | 225 | PF00082 | 0.587 |
CLV_PCSK_PC1ET2_1 | 226 | 228 | PF00082 | 0.580 |
CLV_PCSK_SKI1_1 | 273 | 277 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 344 | 348 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 488 | 492 | PF00082 | 0.418 |
DEG_APCC_DBOX_1 | 272 | 280 | PF00400 | 0.443 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.562 |
DEG_SPOP_SBC_1 | 327 | 331 | PF00917 | 0.515 |
DOC_CYCLIN_RxL_1 | 355 | 366 | PF00134 | 0.268 |
DOC_MAPK_gen_1 | 11 | 19 | PF00069 | 0.531 |
DOC_MAPK_gen_1 | 223 | 233 | PF00069 | 0.638 |
DOC_MAPK_gen_1 | 273 | 281 | PF00069 | 0.445 |
DOC_MAPK_gen_1 | 460 | 468 | PF00069 | 0.398 |
DOC_MAPK_MEF2A_6 | 224 | 233 | PF00069 | 0.667 |
DOC_MAPK_MEF2A_6 | 460 | 468 | PF00069 | 0.469 |
DOC_PP1_RVXF_1 | 272 | 279 | PF00149 | 0.441 |
DOC_PP2B_LxvP_1 | 336 | 339 | PF13499 | 0.443 |
DOC_USP7_MATH_1 | 142 | 146 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 180 | 184 | PF00917 | 0.634 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 238 | 242 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 248 | 252 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.797 |
DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.423 |
DOC_USP7_MATH_1 | 438 | 442 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.749 |
DOC_WW_Pin1_4 | 110 | 115 | PF00397 | 0.666 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.562 |
DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.548 |
DOC_WW_Pin1_4 | 172 | 177 | PF00397 | 0.626 |
DOC_WW_Pin1_4 | 234 | 239 | PF00397 | 0.612 |
DOC_WW_Pin1_4 | 285 | 290 | PF00397 | 0.615 |
DOC_WW_Pin1_4 | 318 | 323 | PF00397 | 0.558 |
LIG_14-3-3_CanoR_1 | 23 | 31 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 32 | 37 | PF00244 | 0.577 |
LIG_14-3-3_CanoR_1 | 358 | 363 | PF00244 | 0.268 |
LIG_14-3-3_CanoR_1 | 371 | 377 | PF00244 | 0.268 |
LIG_14-3-3_CanoR_1 | 413 | 422 | PF00244 | 0.504 |
LIG_14-3-3_CanoR_1 | 56 | 60 | PF00244 | 0.640 |
LIG_14-3-3_CanoR_1 | 94 | 102 | PF00244 | 0.658 |
LIG_Actin_WH2_2 | 10 | 25 | PF00022 | 0.527 |
LIG_APCC_ABBAyCdc20_2 | 226 | 232 | PF00400 | 0.559 |
LIG_BIR_III_4 | 199 | 203 | PF00653 | 0.541 |
LIG_BRCT_BRCA1_1 | 464 | 468 | PF00533 | 0.416 |
LIG_FHA_1 | 226 | 232 | PF00498 | 0.620 |
LIG_FHA_1 | 286 | 292 | PF00498 | 0.530 |
LIG_FHA_1 | 401 | 407 | PF00498 | 0.313 |
LIG_FHA_2 | 33 | 39 | PF00498 | 0.613 |
LIG_FHA_2 | 374 | 380 | PF00498 | 0.268 |
LIG_FHA_2 | 442 | 448 | PF00498 | 0.601 |
LIG_FHA_2 | 93 | 99 | PF00498 | 0.614 |
LIG_LIR_Gen_1 | 366 | 375 | PF02991 | 0.268 |
LIG_LIR_Gen_1 | 5 | 13 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 182 | 187 | PF02991 | 0.723 |
LIG_LIR_Nem_3 | 198 | 204 | PF02991 | 0.553 |
LIG_LIR_Nem_3 | 366 | 370 | PF02991 | 0.268 |
LIG_LIR_Nem_3 | 5 | 10 | PF02991 | 0.527 |
LIG_SH2_CRK | 184 | 188 | PF00017 | 0.550 |
LIG_SH2_CRK | 33 | 37 | PF00017 | 0.579 |
LIG_SH2_NCK_1 | 33 | 37 | PF00017 | 0.537 |
LIG_SH2_STAP1 | 148 | 152 | PF00017 | 0.458 |
LIG_SH3_3 | 170 | 176 | PF00018 | 0.588 |
LIG_SUMO_SIM_par_1 | 138 | 145 | PF11976 | 0.416 |
LIG_WRC_WIRS_1 | 261 | 266 | PF05994 | 0.521 |
MOD_CDK_SPxK_1 | 110 | 116 | PF00069 | 0.627 |
MOD_CDK_SPxK_1 | 17 | 23 | PF00069 | 0.510 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.614 |
MOD_CK1_1 | 241 | 247 | PF00069 | 0.711 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.585 |
MOD_CK1_1 | 283 | 289 | PF00069 | 0.485 |
MOD_CK1_1 | 323 | 329 | PF00069 | 0.578 |
MOD_CK1_1 | 373 | 379 | PF00069 | 0.268 |
MOD_CK1_1 | 415 | 421 | PF00069 | 0.470 |
MOD_CK1_1 | 441 | 447 | PF00069 | 0.536 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.599 |
MOD_CK2_1 | 124 | 130 | PF00069 | 0.730 |
MOD_CK2_1 | 38 | 44 | PF00069 | 0.676 |
MOD_CK2_1 | 92 | 98 | PF00069 | 0.616 |
MOD_Cter_Amidation | 87 | 90 | PF01082 | 0.641 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.489 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.754 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.474 |
MOD_GlcNHglycan | 291 | 294 | PF01048 | 0.579 |
MOD_GlcNHglycan | 322 | 325 | PF01048 | 0.602 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.366 |
MOD_GlcNHglycan | 496 | 499 | PF01048 | 0.503 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.628 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.650 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.643 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.646 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.616 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.615 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.558 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.558 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.552 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.483 |
MOD_GSK3_1 | 490 | 497 | PF00069 | 0.492 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.754 |
MOD_LATS_1 | 356 | 362 | PF00433 | 0.268 |
MOD_N-GLC_1 | 283 | 288 | PF02516 | 0.487 |
MOD_N-GLC_1 | 400 | 405 | PF02516 | 0.513 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.613 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.419 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.499 |
MOD_NEK2_1 | 22 | 27 | PF00069 | 0.565 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.522 |
MOD_NEK2_1 | 382 | 387 | PF00069 | 0.313 |
MOD_NEK2_1 | 416 | 421 | PF00069 | 0.386 |
MOD_NEK2_1 | 478 | 483 | PF00069 | 0.386 |
MOD_PIKK_1 | 297 | 303 | PF00454 | 0.655 |
MOD_PIKK_1 | 478 | 484 | PF00454 | 0.441 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.618 |
MOD_PKA_2 | 115 | 121 | PF00069 | 0.559 |
MOD_PKA_2 | 22 | 28 | PF00069 | 0.588 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.522 |
MOD_PKA_2 | 31 | 37 | PF00069 | 0.569 |
MOD_PKA_2 | 370 | 376 | PF00069 | 0.268 |
MOD_PKA_2 | 412 | 418 | PF00069 | 0.512 |
MOD_PKA_2 | 441 | 447 | PF00069 | 0.506 |
MOD_PKA_2 | 55 | 61 | PF00069 | 0.683 |
MOD_Plk_1 | 103 | 109 | PF00069 | 0.595 |
MOD_Plk_1 | 365 | 371 | PF00069 | 0.268 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.512 |
MOD_Plk_4 | 358 | 364 | PF00069 | 0.293 |
MOD_Plk_4 | 391 | 397 | PF00069 | 0.283 |
MOD_ProDKin_1 | 110 | 116 | PF00069 | 0.667 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.557 |
MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.548 |
MOD_ProDKin_1 | 172 | 178 | PF00069 | 0.625 |
MOD_ProDKin_1 | 234 | 240 | PF00069 | 0.613 |
MOD_ProDKin_1 | 285 | 291 | PF00069 | 0.624 |
MOD_ProDKin_1 | 318 | 324 | PF00069 | 0.555 |
MOD_SUMO_rev_2 | 268 | 276 | PF00179 | 0.398 |
TRG_ENDOCYTIC_2 | 184 | 187 | PF00928 | 0.701 |
TRG_ENDOCYTIC_2 | 201 | 204 | PF00928 | 0.558 |
TRG_ENDOCYTIC_2 | 33 | 36 | PF00928 | 0.605 |
TRG_ER_diArg_1 | 10 | 12 | PF00400 | 0.528 |
TRG_ER_diArg_1 | 397 | 399 | PF00400 | 0.268 |
TRG_ER_diArg_1 | 48 | 50 | PF00400 | 0.591 |
TRG_ER_diArg_1 | 503 | 506 | PF00400 | 0.539 |
TRG_Pf-PMV_PEXEL_1 | 185 | 189 | PF00026 | 0.540 |
TRG_Pf-PMV_PEXEL_1 | 227 | 232 | PF00026 | 0.682 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I5M8 | Leptomonas seymouri | 41% | 100% |
A4HES5 | Leishmania braziliensis | 65% | 100% |
A4I202 | Leishmania infantum | 100% | 100% |
E9AY49 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 99% |
Q4Q9C4 | Leishmania major | 86% | 100% |