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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A4IAI0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 14 | 18 | PF00656 | 0.688 |
CLV_C14_Caspase3-7 | 277 | 281 | PF00656 | 0.637 |
CLV_C14_Caspase3-7 | 373 | 377 | PF00656 | 0.684 |
CLV_NRD_NRD_1 | 202 | 204 | PF00675 | 0.549 |
CLV_NRD_NRD_1 | 398 | 400 | PF00675 | 0.547 |
CLV_NRD_NRD_1 | 418 | 420 | PF00675 | 0.498 |
CLV_NRD_NRD_1 | 425 | 427 | PF00675 | 0.679 |
CLV_PCSK_KEX2_1 | 177 | 179 | PF00082 | 0.600 |
CLV_PCSK_KEX2_1 | 201 | 203 | PF00082 | 0.543 |
CLV_PCSK_KEX2_1 | 398 | 400 | PF00082 | 0.608 |
CLV_PCSK_KEX2_1 | 418 | 420 | PF00082 | 0.387 |
CLV_PCSK_KEX2_1 | 425 | 427 | PF00082 | 0.567 |
CLV_PCSK_PC1ET2_1 | 177 | 179 | PF00082 | 0.587 |
CLV_PCSK_SKI1_1 | 160 | 164 | PF00082 | 0.626 |
CLV_PCSK_SKI1_1 | 462 | 466 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 484 | 488 | PF00082 | 0.597 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.603 |
DEG_APCC_DBOX_1 | 200 | 208 | PF00400 | 0.403 |
DEG_APCC_DBOX_1 | 461 | 469 | PF00400 | 0.410 |
DOC_CYCLIN_RxL_1 | 459 | 469 | PF00134 | 0.408 |
DOC_CYCLIN_RxL_1 | 81 | 90 | PF00134 | 0.559 |
DOC_MAPK_DCC_7 | 462 | 470 | PF00069 | 0.434 |
DOC_MAPK_DCC_7 | 93 | 102 | PF00069 | 0.631 |
DOC_MAPK_gen_1 | 418 | 424 | PF00069 | 0.601 |
DOC_MAPK_gen_1 | 459 | 467 | PF00069 | 0.442 |
DOC_MAPK_MEF2A_6 | 462 | 470 | PF00069 | 0.434 |
DOC_MAPK_MEF2A_6 | 93 | 102 | PF00069 | 0.631 |
DOC_MIT_MIM_1 | 199 | 207 | PF04212 | 0.573 |
DOC_PP1_RVXF_1 | 402 | 408 | PF00149 | 0.541 |
DOC_USP7_MATH_1 | 11 | 15 | PF00917 | 0.764 |
DOC_USP7_UBL2_3 | 56 | 60 | PF12436 | 0.520 |
DOC_WW_Pin1_4 | 140 | 145 | PF00397 | 0.759 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.495 |
DOC_WW_Pin1_4 | 291 | 296 | PF00397 | 0.673 |
LIG_14-3-3_CanoR_1 | 404 | 408 | PF00244 | 0.541 |
LIG_Actin_WH2_2 | 155 | 172 | PF00022 | 0.612 |
LIG_Actin_WH2_2 | 457 | 475 | PF00022 | 0.420 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.661 |
LIG_BRCT_BRCA1_1 | 104 | 108 | PF00533 | 0.634 |
LIG_CaM_IQ_9 | 155 | 170 | PF13499 | 0.647 |
LIG_CaM_IQ_9 | 271 | 286 | PF13499 | 0.525 |
LIG_FHA_1 | 121 | 127 | PF00498 | 0.527 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.555 |
LIG_FHA_1 | 185 | 191 | PF00498 | 0.556 |
LIG_FHA_1 | 20 | 26 | PF00498 | 0.512 |
LIG_FHA_1 | 33 | 39 | PF00498 | 0.353 |
LIG_FHA_1 | 367 | 373 | PF00498 | 0.689 |
LIG_FHA_1 | 388 | 394 | PF00498 | 0.661 |
LIG_FHA_1 | 72 | 78 | PF00498 | 0.542 |
LIG_FHA_2 | 151 | 157 | PF00498 | 0.691 |
LIG_FHA_2 | 159 | 165 | PF00498 | 0.513 |
LIG_FHA_2 | 239 | 245 | PF00498 | 0.604 |
LIG_FHA_2 | 305 | 311 | PF00498 | 0.566 |
LIG_FHA_2 | 371 | 377 | PF00498 | 0.721 |
LIG_FHA_2 | 473 | 479 | PF00498 | 0.451 |
LIG_FHA_2 | 59 | 65 | PF00498 | 0.577 |
LIG_GBD_Chelix_1 | 447 | 455 | PF00786 | 0.480 |
LIG_LIR_Gen_1 | 310 | 320 | PF02991 | 0.544 |
LIG_LIR_Gen_1 | 381 | 391 | PF02991 | 0.566 |
LIG_LIR_Gen_1 | 406 | 415 | PF02991 | 0.547 |
LIG_LIR_Nem_3 | 310 | 316 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 381 | 387 | PF02991 | 0.589 |
LIG_LIR_Nem_3 | 406 | 410 | PF02991 | 0.618 |
LIG_NRBOX | 347 | 353 | PF00104 | 0.569 |
LIG_NRBOX | 467 | 473 | PF00104 | 0.335 |
LIG_RPA_C_Fungi | 413 | 425 | PF08784 | 0.563 |
LIG_SH2_STAT3 | 101 | 104 | PF00017 | 0.649 |
LIG_SH2_STAT5 | 101 | 104 | PF00017 | 0.628 |
LIG_SH2_STAT5 | 313 | 316 | PF00017 | 0.619 |
LIG_SH2_STAT5 | 443 | 446 | PF00017 | 0.335 |
LIG_SUMO_SIM_par_1 | 122 | 127 | PF11976 | 0.430 |
LIG_SUMO_SIM_par_1 | 69 | 74 | PF11976 | 0.538 |
LIG_TRAF2_1 | 230 | 233 | PF00917 | 0.582 |
LIG_TRAF2_1 | 330 | 333 | PF00917 | 0.630 |
LIG_TRAF2_2 | 133 | 138 | PF00917 | 0.636 |
LIG_UBA3_1 | 464 | 473 | PF00899 | 0.447 |
MOD_CDC14_SPxK_1 | 143 | 146 | PF00782 | 0.624 |
MOD_CDK_SPxK_1 | 140 | 146 | PF00069 | 0.626 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.664 |
MOD_CK1_1 | 247 | 253 | PF00069 | 0.575 |
MOD_CK2_1 | 150 | 156 | PF00069 | 0.703 |
MOD_CK2_1 | 238 | 244 | PF00069 | 0.549 |
MOD_CK2_1 | 414 | 420 | PF00069 | 0.627 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.578 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.641 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.636 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.658 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.743 |
MOD_GlcNHglycan | 436 | 439 | PF01048 | 0.658 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.671 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.538 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.743 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.619 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.463 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.564 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.678 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.434 |
MOD_N-GLC_1 | 210 | 215 | PF02516 | 0.585 |
MOD_N-GLC_1 | 291 | 296 | PF02516 | 0.523 |
MOD_N-GLC_1 | 364 | 369 | PF02516 | 0.636 |
MOD_N-GLC_1 | 5 | 10 | PF02516 | 0.541 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.502 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.468 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.550 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.684 |
MOD_NEK2_1 | 158 | 163 | PF00069 | 0.558 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.588 |
MOD_NEK2_1 | 351 | 356 | PF00069 | 0.603 |
MOD_NEK2_1 | 387 | 392 | PF00069 | 0.586 |
MOD_NEK2_1 | 414 | 419 | PF00069 | 0.498 |
MOD_NEK2_1 | 451 | 456 | PF00069 | 0.420 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.496 |
MOD_NEK2_1 | 87 | 92 | PF00069 | 0.536 |
MOD_NEK2_2 | 210 | 215 | PF00069 | 0.571 |
MOD_PIKK_1 | 102 | 108 | PF00454 | 0.553 |
MOD_PIKK_1 | 247 | 253 | PF00454 | 0.621 |
MOD_PIKK_1 | 328 | 334 | PF00454 | 0.523 |
MOD_PKA_1 | 177 | 183 | PF00069 | 0.622 |
MOD_PKA_2 | 177 | 183 | PF00069 | 0.591 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.504 |
MOD_PKA_2 | 333 | 339 | PF00069 | 0.472 |
MOD_PKA_2 | 403 | 409 | PF00069 | 0.473 |
MOD_Plk_1 | 210 | 216 | PF00069 | 0.512 |
MOD_Plk_1 | 87 | 93 | PF00069 | 0.624 |
MOD_Plk_4 | 120 | 126 | PF00069 | 0.508 |
MOD_Plk_4 | 293 | 299 | PF00069 | 0.694 |
MOD_Plk_4 | 466 | 472 | PF00069 | 0.358 |
MOD_ProDKin_1 | 140 | 146 | PF00069 | 0.760 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.492 |
MOD_ProDKin_1 | 291 | 297 | PF00069 | 0.680 |
MOD_SUMO_rev_2 | 220 | 230 | PF00179 | 0.619 |
MOD_SUMO_rev_2 | 315 | 323 | PF00179 | 0.505 |
TRG_DiLeu_BaEn_1 | 340 | 345 | PF01217 | 0.593 |
TRG_DiLeu_BaEn_1 | 347 | 352 | PF01217 | 0.598 |
TRG_ENDOCYTIC_2 | 313 | 316 | PF00928 | 0.507 |
TRG_ENDOCYTIC_2 | 320 | 323 | PF00928 | 0.470 |
TRG_ER_diArg_1 | 200 | 203 | PF00400 | 0.533 |
TRG_ER_diArg_1 | 240 | 243 | PF00400 | 0.574 |
TRG_ER_diArg_1 | 397 | 399 | PF00400 | 0.596 |
TRG_ER_diArg_1 | 424 | 426 | PF00400 | 0.678 |
TRG_Pf-PMV_PEXEL_1 | 202 | 206 | PF00026 | 0.535 |
TRG_Pf-PMV_PEXEL_1 | 346 | 350 | PF00026 | 0.566 |
TRG_Pf-PMV_PEXEL_1 | 398 | 402 | PF00026 | 0.584 |
TRG_Pf-PMV_PEXEL_1 | 84 | 88 | PF00026 | 0.632 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PF68 | Leptomonas seymouri | 41% | 100% |
A0A0S4KIU3 | Bodo saltans | 27% | 100% |
A0A1X0PB65 | Trypanosomatidae | 25% | 100% |
A0A3S7X8J7 | Leishmania donovani | 99% | 100% |
A4HBD2 | Leishmania braziliensis | 66% | 100% |
C9ZLQ9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
E9B5K4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q4Q2D2 | Leishmania major | 85% | 100% |
V5BW28 | Trypanosoma cruzi | 27% | 100% |