Uncharacterized Protein, Uncharacterized
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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: A4I5M2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 144 | 146 | PF00675 | 0.633 |
CLV_NRD_NRD_1 | 241 | 243 | PF00675 | 0.506 |
CLV_NRD_NRD_1 | 344 | 346 | PF00675 | 0.558 |
CLV_NRD_NRD_1 | 395 | 397 | PF00675 | 0.510 |
CLV_PCSK_KEX2_1 | 144 | 146 | PF00082 | 0.726 |
CLV_PCSK_KEX2_1 | 241 | 243 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 288 | 290 | PF00082 | 0.547 |
CLV_PCSK_PC1ET2_1 | 288 | 290 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 201 | 205 | PF00082 | 0.564 |
CLV_PCSK_SKI1_1 | 24 | 28 | PF00082 | 0.483 |
CLV_PCSK_SKI1_1 | 365 | 369 | PF00082 | 0.670 |
CLV_PCSK_SKI1_1 | 423 | 427 | PF00082 | 0.555 |
CLV_PCSK_SKI1_1 | 47 | 51 | PF00082 | 0.505 |
CLV_PCSK_SKI1_1 | 64 | 68 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 73 | 77 | PF00082 | 0.436 |
DEG_APCC_DBOX_1 | 340 | 348 | PF00400 | 0.612 |
DOC_CDC14_PxL_1 | 33 | 41 | PF14671 | 0.489 |
DOC_CYCLIN_RxL_1 | 420 | 429 | PF00134 | 0.671 |
DOC_MAPK_gen_1 | 226 | 233 | PF00069 | 0.477 |
DOC_MAPK_gen_1 | 288 | 296 | PF00069 | 0.447 |
DOC_MAPK_MEF2A_6 | 376 | 384 | PF00069 | 0.640 |
DOC_MAPK_MEF2A_6 | 423 | 432 | PF00069 | 0.698 |
DOC_PP1_RVXF_1 | 22 | 28 | PF00149 | 0.510 |
DOC_USP7_MATH_1 | 287 | 291 | PF00917 | 0.471 |
DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.598 |
DOC_USP7_UBL2_3 | 184 | 188 | PF12436 | 0.394 |
DOC_WW_Pin1_4 | 147 | 152 | PF00397 | 0.702 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.755 |
DOC_WW_Pin1_4 | 352 | 357 | PF00397 | 0.612 |
LIG_14-3-3_CanoR_1 | 144 | 151 | PF00244 | 0.699 |
LIG_14-3-3_CanoR_1 | 201 | 210 | PF00244 | 0.589 |
LIG_14-3-3_CanoR_1 | 242 | 252 | PF00244 | 0.587 |
LIG_14-3-3_CanoR_1 | 365 | 375 | PF00244 | 0.649 |
LIG_14-3-3_CanoR_1 | 388 | 392 | PF00244 | 0.524 |
LIG_14-3-3_CanoR_1 | 396 | 400 | PF00244 | 0.590 |
LIG_14-3-3_CanoR_1 | 73 | 79 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 89 | 93 | PF00244 | 0.470 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.643 |
LIG_BRCT_BRCA1_1 | 260 | 264 | PF00533 | 0.293 |
LIG_deltaCOP1_diTrp_1 | 209 | 214 | PF00928 | 0.588 |
LIG_FHA_1 | 202 | 208 | PF00498 | 0.462 |
LIG_FHA_1 | 244 | 250 | PF00498 | 0.596 |
LIG_FHA_1 | 296 | 302 | PF00498 | 0.523 |
LIG_FHA_1 | 349 | 355 | PF00498 | 0.699 |
LIG_FHA_1 | 95 | 101 | PF00498 | 0.511 |
LIG_FHA_2 | 107 | 113 | PF00498 | 0.577 |
LIG_FHA_2 | 124 | 130 | PF00498 | 0.600 |
LIG_FHA_2 | 137 | 143 | PF00498 | 0.697 |
LIG_FHA_2 | 422 | 428 | PF00498 | 0.583 |
LIG_FHA_2 | 55 | 61 | PF00498 | 0.583 |
LIG_LIR_Gen_1 | 176 | 185 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 45 | 53 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 176 | 182 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 261 | 267 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 45 | 51 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 74 | 78 | PF02991 | 0.487 |
LIG_SH2_CRK | 48 | 52 | PF00017 | 0.530 |
LIG_SH2_NCK_1 | 179 | 183 | PF00017 | 0.553 |
LIG_SH2_SRC | 179 | 182 | PF00017 | 0.397 |
LIG_SH2_SRC | 28 | 31 | PF00017 | 0.615 |
LIG_SH2_SRC | 299 | 302 | PF00017 | 0.445 |
LIG_SH2_STAP1 | 179 | 183 | PF00017 | 0.433 |
LIG_SH2_STAP1 | 28 | 32 | PF00017 | 0.538 |
LIG_SH2_STAP1 | 292 | 296 | PF00017 | 0.541 |
LIG_SH2_STAT3 | 303 | 306 | PF00017 | 0.482 |
LIG_SUMO_SIM_anti_2 | 152 | 161 | PF11976 | 0.576 |
LIG_SUMO_SIM_anti_2 | 326 | 331 | PF11976 | 0.492 |
LIG_SUMO_SIM_par_1 | 152 | 161 | PF11976 | 0.555 |
LIG_SUMO_SIM_par_1 | 350 | 355 | PF11976 | 0.665 |
LIG_TRAF2_1 | 254 | 257 | PF00917 | 0.492 |
LIG_TRAF2_1 | 91 | 94 | PF00917 | 0.543 |
LIG_UBA3_1 | 249 | 253 | PF00899 | 0.375 |
LIG_UBA3_1 | 39 | 47 | PF00899 | 0.535 |
LIG_WRC_WIRS_1 | 50 | 55 | PF05994 | 0.558 |
MOD_CDK_SPK_2 | 3 | 8 | PF00069 | 0.677 |
MOD_CDK_SPxK_1 | 352 | 358 | PF00069 | 0.691 |
MOD_CK1_1 | 147 | 153 | PF00069 | 0.603 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.734 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.528 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.549 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.715 |
MOD_CK2_1 | 106 | 112 | PF00069 | 0.496 |
MOD_CK2_1 | 123 | 129 | PF00069 | 0.645 |
MOD_CK2_1 | 136 | 142 | PF00069 | 0.590 |
MOD_CK2_1 | 287 | 293 | PF00069 | 0.501 |
MOD_CK2_1 | 309 | 315 | PF00069 | 0.504 |
MOD_CK2_1 | 387 | 393 | PF00069 | 0.635 |
MOD_CK2_1 | 421 | 427 | PF00069 | 0.607 |
MOD_CK2_1 | 49 | 55 | PF00069 | 0.571 |
MOD_CK2_1 | 88 | 94 | PF00069 | 0.510 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.553 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.562 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.657 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.527 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.607 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.412 |
MOD_GlcNHglycan | 404 | 407 | PF01048 | 0.690 |
MOD_GlcNHglycan | 414 | 418 | PF01048 | 0.560 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.481 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.289 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.598 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.702 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.763 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.573 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.577 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.565 |
MOD_N-GLC_1 | 132 | 137 | PF02516 | 0.708 |
MOD_N-GLC_1 | 79 | 84 | PF02516 | 0.584 |
MOD_NEK2_1 | 11 | 16 | PF00069 | 0.688 |
MOD_NEK2_1 | 114 | 119 | PF00069 | 0.621 |
MOD_NEK2_1 | 319 | 324 | PF00069 | 0.592 |
MOD_NEK2_1 | 348 | 353 | PF00069 | 0.499 |
MOD_NEK2_1 | 380 | 385 | PF00069 | 0.617 |
MOD_NEK2_1 | 402 | 407 | PF00069 | 0.586 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.595 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.486 |
MOD_PIKK_1 | 258 | 264 | PF00454 | 0.374 |
MOD_PKA_1 | 144 | 150 | PF00069 | 0.626 |
MOD_PKA_2 | 144 | 150 | PF00069 | 0.670 |
MOD_PKA_2 | 387 | 393 | PF00069 | 0.597 |
MOD_PKA_2 | 395 | 401 | PF00069 | 0.566 |
MOD_PKA_2 | 88 | 94 | PF00069 | 0.567 |
MOD_Plk_1 | 20 | 26 | PF00069 | 0.559 |
MOD_Plk_1 | 363 | 369 | PF00069 | 0.693 |
MOD_Plk_1 | 54 | 60 | PF00069 | 0.409 |
MOD_Plk_1 | 9 | 15 | PF00069 | 0.575 |
MOD_Plk_2-3 | 309 | 315 | PF00069 | 0.504 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.614 |
MOD_Plk_4 | 35 | 41 | PF00069 | 0.463 |
MOD_Plk_4 | 380 | 386 | PF00069 | 0.528 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.617 |
MOD_ProDKin_1 | 147 | 153 | PF00069 | 0.699 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.754 |
MOD_ProDKin_1 | 352 | 358 | PF00069 | 0.616 |
MOD_SUMO_for_1 | 281 | 284 | PF00179 | 0.602 |
MOD_SUMO_rev_2 | 91 | 100 | PF00179 | 0.552 |
TRG_DiLeu_BaEn_1 | 315 | 320 | PF01217 | 0.607 |
TRG_ENDOCYTIC_2 | 179 | 182 | PF00928 | 0.556 |
TRG_ENDOCYTIC_2 | 28 | 31 | PF00928 | 0.573 |
TRG_ENDOCYTIC_2 | 48 | 51 | PF00928 | 0.507 |
TRG_ER_diArg_1 | 143 | 145 | PF00400 | 0.649 |
TRG_ER_diArg_1 | 289 | 292 | PF00400 | 0.588 |
TRG_NLS_MonoExtC_3 | 287 | 293 | PF00514 | 0.587 |
TRG_Pf-PMV_PEXEL_1 | 365 | 370 | PF00026 | 0.695 |
TRG_Pf-PMV_PEXEL_1 | 423 | 427 | PF00026 | 0.630 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDD9 | Leptomonas seymouri | 59% | 100% |
A0A1X0P1Q4 | Trypanosomatidae | 37% | 95% |
A0A3S5H7N1 | Leishmania donovani | 99% | 100% |
A0A3S5ISM8 | Trypanosoma rangeli | 34% | 93% |
A4HIC9 | Leishmania braziliensis | 76% | 100% |
E9B0W7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4Q799 | Leishmania major | 91% | 100% |
V5B8X3 | Trypanosoma cruzi | 34% | 93% |