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: 2 |
NetGPI | no | yes: 0, no: 2 |
Related structures:
AlphaFold database: A0A3S7X2I2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 321 | 325 | PF00656 | 0.678 |
CLV_NRD_NRD_1 | 62 | 64 | PF00675 | 0.732 |
CLV_PCSK_KEX2_1 | 446 | 448 | PF00082 | 0.574 |
CLV_PCSK_KEX2_1 | 62 | 64 | PF00082 | 0.732 |
CLV_PCSK_PC1ET2_1 | 446 | 448 | PF00082 | 0.644 |
CLV_PCSK_SKI1_1 | 232 | 236 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 323 | 327 | PF00082 | 0.579 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.671 |
DOC_CKS1_1 | 38 | 43 | PF01111 | 0.693 |
DOC_MAPK_gen_1 | 230 | 239 | PF00069 | 0.493 |
DOC_MAPK_gen_1 | 79 | 87 | PF00069 | 0.625 |
DOC_PP1_RVXF_1 | 233 | 240 | PF00149 | 0.482 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 123 | 127 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 140 | 144 | PF00917 | 0.704 |
DOC_USP7_MATH_1 | 173 | 177 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 358 | 362 | PF00917 | 0.285 |
DOC_USP7_MATH_1 | 419 | 423 | PF00917 | 0.538 |
DOC_WW_Pin1_4 | 143 | 148 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 169 | 174 | PF00397 | 0.666 |
DOC_WW_Pin1_4 | 186 | 191 | PF00397 | 0.699 |
DOC_WW_Pin1_4 | 195 | 200 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 209 | 214 | PF00397 | 0.591 |
DOC_WW_Pin1_4 | 288 | 293 | PF00397 | 0.610 |
DOC_WW_Pin1_4 | 303 | 308 | PF00397 | 0.595 |
DOC_WW_Pin1_4 | 37 | 42 | PF00397 | 0.694 |
DOC_WW_Pin1_4 | 423 | 428 | PF00397 | 0.714 |
DOC_WW_Pin1_4 | 430 | 435 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 89 | 94 | PF00397 | 0.661 |
DOC_WW_Pin1_4 | 95 | 100 | PF00397 | 0.623 |
LIG_14-3-3_CanoR_1 | 101 | 107 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 110 | 118 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 25 | 31 | PF00244 | 0.780 |
LIG_14-3-3_CanoR_1 | 39 | 45 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 425 | 434 | PF00244 | 0.592 |
LIG_14-3-3_CanoR_1 | 54 | 60 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 81 | 86 | PF00244 | 0.556 |
LIG_BRCT_BRCA1_1 | 175 | 179 | PF00533 | 0.636 |
LIG_Clathr_ClatBox_1 | 368 | 372 | PF01394 | 0.363 |
LIG_FHA_1 | 204 | 210 | PF00498 | 0.810 |
LIG_FHA_1 | 330 | 336 | PF00498 | 0.666 |
LIG_FHA_1 | 337 | 343 | PF00498 | 0.600 |
LIG_FHA_2 | 103 | 109 | PF00498 | 0.568 |
LIG_FHA_2 | 144 | 150 | PF00498 | 0.517 |
LIG_FHA_2 | 273 | 279 | PF00498 | 0.654 |
LIG_FHA_2 | 339 | 345 | PF00498 | 0.663 |
LIG_FHA_2 | 54 | 60 | PF00498 | 0.637 |
LIG_FHA_2 | 69 | 75 | PF00498 | 0.583 |
LIG_LIR_Gen_1 | 176 | 183 | PF02991 | 0.564 |
LIG_LIR_Gen_1 | 3 | 14 | PF02991 | 0.501 |
LIG_LIR_Nem_3 | 3 | 9 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 390 | 394 | PF02991 | 0.433 |
LIG_MYND_1 | 199 | 203 | PF01753 | 0.553 |
LIG_NRBOX | 413 | 419 | PF00104 | 0.550 |
LIG_REV1ctd_RIR_1 | 237 | 246 | PF16727 | 0.484 |
LIG_SH2_SRC | 319 | 322 | PF00017 | 0.606 |
LIG_SH2_STAT3 | 296 | 299 | PF00017 | 0.538 |
LIG_SH2_STAT5 | 2 | 5 | PF00017 | 0.585 |
LIG_SH2_STAT5 | 296 | 299 | PF00017 | 0.547 |
LIG_SH3_3 | 196 | 202 | PF00018 | 0.707 |
LIG_SH3_3 | 210 | 216 | PF00018 | 0.631 |
LIG_SH3_3 | 28 | 34 | PF00018 | 0.622 |
LIG_SH3_3 | 301 | 307 | PF00018 | 0.580 |
LIG_SH3_5 | 292 | 296 | PF00018 | 0.515 |
LIG_SUMO_SIM_anti_2 | 365 | 370 | PF11976 | 0.433 |
LIG_SUMO_SIM_par_1 | 365 | 370 | PF11976 | 0.423 |
LIG_TRAF2_1 | 438 | 441 | PF00917 | 0.563 |
LIG_WRC_WIRS_1 | 217 | 222 | PF05994 | 0.576 |
LIG_WRC_WIRS_1 | 388 | 393 | PF05994 | 0.433 |
LIG_WW_2 | 199 | 202 | PF00397 | 0.550 |
MOD_CDC14_SPxK_1 | 98 | 101 | PF00782 | 0.585 |
MOD_CDK_SPxK_1 | 95 | 101 | PF00069 | 0.578 |
MOD_CK1_1 | 126 | 132 | PF00069 | 0.595 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.584 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.666 |
MOD_CK1_1 | 160 | 166 | PF00069 | 0.654 |
MOD_CK1_1 | 267 | 273 | PF00069 | 0.576 |
MOD_CK1_1 | 387 | 393 | PF00069 | 0.433 |
MOD_CK1_1 | 426 | 432 | PF00069 | 0.733 |
MOD_CK2_1 | 102 | 108 | PF00069 | 0.521 |
MOD_CK2_1 | 201 | 207 | PF00069 | 0.726 |
MOD_CK2_1 | 272 | 278 | PF00069 | 0.653 |
MOD_CK2_1 | 89 | 95 | PF00069 | 0.561 |
MOD_Cter_Amidation | 60 | 63 | PF01082 | 0.636 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.525 |
MOD_GlcNHglycan | 174 | 178 | PF01048 | 0.704 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.653 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.673 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.734 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.730 |
MOD_GlcNHglycan | 448 | 451 | PF01048 | 0.700 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.722 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.656 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.723 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.711 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.269 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.648 |
MOD_GSK3_1 | 442 | 449 | PF00069 | 0.783 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.567 |
MOD_N-GLC_1 | 420 | 425 | PF02516 | 0.574 |
MOD_N-GLC_1 | 430 | 435 | PF02516 | 0.632 |
MOD_N-GLC_2 | 396 | 398 | PF02516 | 0.433 |
MOD_NEK2_1 | 362 | 367 | PF00069 | 0.489 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.640 |
MOD_NEK2_2 | 216 | 221 | PF00069 | 0.584 |
MOD_NEK2_2 | 4 | 9 | PF00069 | 0.564 |
MOD_PIKK_1 | 157 | 163 | PF00454 | 0.632 |
MOD_PIKK_1 | 403 | 409 | PF00454 | 0.395 |
MOD_PK_1 | 83 | 89 | PF00069 | 0.558 |
MOD_PKA_2 | 109 | 115 | PF00069 | 0.622 |
MOD_PKA_2 | 53 | 59 | PF00069 | 0.719 |
MOD_PKB_1 | 79 | 87 | PF00069 | 0.625 |
MOD_Plk_1 | 377 | 383 | PF00069 | 0.433 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.715 |
MOD_Plk_4 | 362 | 368 | PF00069 | 0.433 |
MOD_Plk_4 | 387 | 393 | PF00069 | 0.433 |
MOD_ProDKin_1 | 143 | 149 | PF00069 | 0.572 |
MOD_ProDKin_1 | 169 | 175 | PF00069 | 0.743 |
MOD_ProDKin_1 | 186 | 192 | PF00069 | 0.701 |
MOD_ProDKin_1 | 195 | 201 | PF00069 | 0.643 |
MOD_ProDKin_1 | 209 | 215 | PF00069 | 0.576 |
MOD_ProDKin_1 | 288 | 294 | PF00069 | 0.613 |
MOD_ProDKin_1 | 303 | 309 | PF00069 | 0.597 |
MOD_ProDKin_1 | 37 | 43 | PF00069 | 0.694 |
MOD_ProDKin_1 | 423 | 429 | PF00069 | 0.715 |
MOD_ProDKin_1 | 430 | 436 | PF00069 | 0.643 |
MOD_ProDKin_1 | 89 | 95 | PF00069 | 0.661 |
MOD_SUMO_rev_2 | 321 | 328 | PF00179 | 0.601 |
MOD_SUMO_rev_2 | 343 | 347 | PF00179 | 0.616 |
TRG_DiLeu_BaEn_1 | 410 | 415 | PF01217 | 0.433 |
TRG_DiLeu_BaLyEn_6 | 289 | 294 | PF01217 | 0.611 |
TRG_DiLeu_BaLyEn_6 | 86 | 91 | PF01217 | 0.722 |
TRG_ER_diArg_1 | 130 | 133 | PF00400 | 0.620 |
TRG_ER_diArg_1 | 22 | 25 | PF00400 | 0.695 |
TRG_ER_diArg_1 | 80 | 83 | PF00400 | 0.559 |
TRG_Pf-PMV_PEXEL_1 | 353 | 357 | PF00026 | 0.474 |
TRG_Pf-PMV_PEXEL_1 | 83 | 88 | PF00026 | 0.557 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A4HHH9 | Leishmania braziliensis | 62% | 100% |