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: A4I5W6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 11 | 15 | PF00656 | 0.607 |
CLV_C14_Caspase3-7 | 358 | 362 | PF00656 | 0.565 |
CLV_NRD_NRD_1 | 228 | 230 | PF00675 | 0.567 |
CLV_NRD_NRD_1 | 298 | 300 | PF00675 | 0.541 |
CLV_NRD_NRD_1 | 317 | 319 | PF00675 | 0.576 |
CLV_PCSK_SKI1_1 | 379 | 383 | PF00082 | 0.521 |
DEG_COP1_1 | 54 | 62 | PF00400 | 0.476 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.555 |
DOC_MAPK_gen_1 | 297 | 304 | PF00069 | 0.521 |
DOC_PP2B_LxvP_1 | 115 | 118 | PF13499 | 0.662 |
DOC_PP2B_LxvP_1 | 126 | 129 | PF13499 | 0.698 |
DOC_PP2B_LxvP_1 | 57 | 60 | PF13499 | 0.528 |
DOC_PP4_MxPP_1 | 63 | 66 | PF00568 | 0.544 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 238 | 242 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 35 | 39 | PF00917 | 0.468 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 390 | 394 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 440 | 444 | PF00917 | 0.761 |
DOC_USP7_MATH_1 | 452 | 456 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 99 | 103 | PF00917 | 0.385 |
DOC_USP7_UBL2_3 | 268 | 272 | PF12436 | 0.591 |
DOC_WW_Pin1_4 | 127 | 132 | PF00397 | 0.742 |
DOC_WW_Pin1_4 | 152 | 157 | PF00397 | 0.518 |
DOC_WW_Pin1_4 | 392 | 397 | PF00397 | 0.763 |
DOC_WW_Pin1_4 | 399 | 404 | PF00397 | 0.724 |
DOC_WW_Pin1_4 | 412 | 417 | PF00397 | 0.715 |
DOC_WW_Pin1_4 | 429 | 434 | PF00397 | 0.742 |
DOC_WW_Pin1_4 | 90 | 95 | PF00397 | 0.493 |
LIG_14-3-3_CanoR_1 | 180 | 189 | PF00244 | 0.444 |
LIG_14-3-3_CanoR_1 | 437 | 445 | PF00244 | 0.785 |
LIG_CtBP_PxDLS_1 | 433 | 437 | PF00389 | 0.761 |
LIG_deltaCOP1_diTrp_1 | 184 | 193 | PF00928 | 0.385 |
LIG_deltaCOP1_diTrp_1 | 74 | 78 | PF00928 | 0.469 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.544 |
LIG_FHA_1 | 54 | 60 | PF00498 | 0.496 |
LIG_FHA_1 | 87 | 93 | PF00498 | 0.470 |
LIG_FHA_2 | 180 | 186 | PF00498 | 0.535 |
LIG_FHA_2 | 356 | 362 | PF00498 | 0.577 |
LIG_LIR_Apic_2 | 175 | 179 | PF02991 | 0.536 |
LIG_LIR_Gen_1 | 102 | 112 | PF02991 | 0.494 |
LIG_LIR_Gen_1 | 185 | 195 | PF02991 | 0.397 |
LIG_LIR_Gen_1 | 286 | 295 | PF02991 | 0.511 |
LIG_LIR_Gen_1 | 332 | 343 | PF02991 | 0.501 |
LIG_LIR_Gen_1 | 366 | 372 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 166 | 171 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 185 | 191 | PF02991 | 0.219 |
LIG_LIR_Nem_3 | 286 | 291 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 332 | 338 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 366 | 371 | PF02991 | 0.412 |
LIG_SH2_CRK | 335 | 339 | PF00017 | 0.505 |
LIG_SH2_NCK_1 | 154 | 158 | PF00017 | 0.572 |
LIG_SH2_NCK_1 | 281 | 285 | PF00017 | 0.538 |
LIG_SH2_PTP2 | 176 | 179 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 154 | 157 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 163 | 166 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 377 | 380 | PF00017 | 0.487 |
LIG_SH3_2 | 118 | 123 | PF14604 | 0.740 |
LIG_SH3_3 | 115 | 121 | PF00018 | 0.640 |
LIG_SH3_3 | 228 | 234 | PF00018 | 0.619 |
LIG_SH3_3 | 397 | 403 | PF00018 | 0.749 |
LIG_SUMO_SIM_par_1 | 54 | 61 | PF11976 | 0.615 |
LIG_TRAF2_1 | 455 | 458 | PF00917 | 0.679 |
LIG_TRAF2_1 | 51 | 54 | PF00917 | 0.675 |
LIG_TRAF2_1 | 72 | 75 | PF00917 | 0.458 |
LIG_UBA3_1 | 311 | 319 | PF00899 | 0.442 |
LIG_UBA3_1 | 367 | 373 | PF00899 | 0.447 |
MOD_CDK_SPK_2 | 392 | 397 | PF00069 | 0.759 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.690 |
MOD_CK1_1 | 18 | 24 | PF00069 | 0.654 |
MOD_CK1_1 | 355 | 361 | PF00069 | 0.556 |
MOD_CK1_1 | 401 | 407 | PF00069 | 0.726 |
MOD_CK1_1 | 441 | 447 | PF00069 | 0.771 |
MOD_CK2_1 | 179 | 185 | PF00069 | 0.490 |
MOD_CK2_1 | 429 | 435 | PF00069 | 0.725 |
MOD_CK2_1 | 452 | 458 | PF00069 | 0.692 |
MOD_CK2_1 | 69 | 75 | PF00069 | 0.450 |
MOD_CK2_1 | 99 | 105 | PF00069 | 0.549 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.576 |
MOD_GlcNHglycan | 125 | 129 | PF01048 | 0.720 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.760 |
MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.547 |
MOD_GlcNHglycan | 390 | 393 | PF01048 | 0.631 |
MOD_GlcNHglycan | 404 | 407 | PF01048 | 0.661 |
MOD_GlcNHglycan | 409 | 412 | PF01048 | 0.780 |
MOD_GlcNHglycan | 438 | 441 | PF01048 | 0.717 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.708 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.760 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.499 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.412 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.580 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.608 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.641 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.710 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.739 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.532 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.474 |
MOD_N-GLC_1 | 133 | 138 | PF02516 | 0.633 |
MOD_N-GLC_2 | 276 | 278 | PF02516 | 0.343 |
MOD_N-GLC_2 | 88 | 90 | PF02516 | 0.417 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.472 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.522 |
MOD_NEK2_1 | 311 | 316 | PF00069 | 0.443 |
MOD_NEK2_1 | 325 | 330 | PF00069 | 0.282 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.524 |
MOD_NEK2_1 | 436 | 441 | PF00069 | 0.773 |
MOD_PK_1 | 55 | 61 | PF00069 | 0.604 |
MOD_PKA_2 | 179 | 185 | PF00069 | 0.480 |
MOD_PKA_2 | 27 | 33 | PF00069 | 0.616 |
MOD_PKA_2 | 436 | 442 | PF00069 | 0.756 |
MOD_Plk_1 | 53 | 59 | PF00069 | 0.585 |
MOD_Plk_1 | 99 | 105 | PF00069 | 0.529 |
MOD_Plk_4 | 206 | 212 | PF00069 | 0.510 |
MOD_Plk_4 | 311 | 317 | PF00069 | 0.517 |
MOD_Plk_4 | 325 | 331 | PF00069 | 0.354 |
MOD_Plk_4 | 355 | 361 | PF00069 | 0.445 |
MOD_Plk_4 | 363 | 369 | PF00069 | 0.394 |
MOD_Plk_4 | 99 | 105 | PF00069 | 0.473 |
MOD_ProDKin_1 | 127 | 133 | PF00069 | 0.740 |
MOD_ProDKin_1 | 152 | 158 | PF00069 | 0.523 |
MOD_ProDKin_1 | 392 | 398 | PF00069 | 0.764 |
MOD_ProDKin_1 | 399 | 405 | PF00069 | 0.723 |
MOD_ProDKin_1 | 412 | 418 | PF00069 | 0.717 |
MOD_ProDKin_1 | 429 | 435 | PF00069 | 0.742 |
MOD_ProDKin_1 | 90 | 96 | PF00069 | 0.495 |
MOD_SUMO_for_1 | 234 | 237 | PF00179 | 0.652 |
MOD_SUMO_rev_2 | 100 | 110 | PF00179 | 0.549 |
MOD_SUMO_rev_2 | 455 | 465 | PF00179 | 0.717 |
TRG_DiLeu_BaEn_4 | 262 | 268 | PF01217 | 0.553 |
TRG_DiLeu_BaLyEn_6 | 339 | 344 | PF01217 | 0.458 |
TRG_ENDOCYTIC_2 | 281 | 284 | PF00928 | 0.560 |
TRG_ENDOCYTIC_2 | 335 | 338 | PF00928 | 0.488 |
TRG_Pf-PMV_PEXEL_1 | 342 | 346 | PF00026 | 0.519 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4Q4 | Leptomonas seymouri | 46% | 97% |
A0A1X0P2L0 | Trypanosomatidae | 30% | 100% |
A0A3Q8IC68 | Leishmania donovani | 99% | 100% |
A0A422N306 | Trypanosoma rangeli | 28% | 100% |
A4HIM1 | Leishmania braziliensis | 69% | 100% |
C9ZR88 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
Q4Q705 | Leishmania major | 88% | 100% |
V5DNX2 | Trypanosoma cruzi | 27% | 100% |