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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
GO:0005737 | cytoplasm | 2 | 1 |
Related structures:
AlphaFold database: A0A3Q8IJ09
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 145 | 149 | PF00656 | 0.724 |
CLV_C14_Caspase3-7 | 290 | 294 | PF00656 | 0.702 |
CLV_C14_Caspase3-7 | 386 | 390 | PF00656 | 0.651 |
CLV_NRD_NRD_1 | 119 | 121 | PF00675 | 0.450 |
CLV_NRD_NRD_1 | 15 | 17 | PF00675 | 0.505 |
CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.452 |
CLV_NRD_NRD_1 | 215 | 217 | PF00675 | 0.523 |
CLV_NRD_NRD_1 | 252 | 254 | PF00675 | 0.619 |
CLV_NRD_NRD_1 | 329 | 331 | PF00675 | 0.525 |
CLV_PCSK_KEX2_1 | 119 | 121 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 15 | 17 | PF00082 | 0.505 |
CLV_PCSK_KEX2_1 | 171 | 173 | PF00082 | 0.432 |
CLV_PCSK_KEX2_1 | 176 | 178 | PF00082 | 0.414 |
CLV_PCSK_KEX2_1 | 215 | 217 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 252 | 254 | PF00082 | 0.597 |
CLV_PCSK_KEX2_1 | 329 | 331 | PF00082 | 0.514 |
CLV_PCSK_PC1ET2_1 | 176 | 178 | PF00082 | 0.418 |
CLV_PCSK_PC7_1 | 172 | 178 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 103 | 107 | PF00082 | 0.307 |
CLV_PCSK_SKI1_1 | 308 | 312 | PF00082 | 0.494 |
CLV_PCSK_SKI1_1 | 376 | 380 | PF00082 | 0.468 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.680 |
DOC_CYCLIN_RxL_1 | 304 | 315 | PF00134 | 0.702 |
DOC_CYCLIN_RxL_1 | 372 | 380 | PF00134 | 0.644 |
DOC_MAPK_gen_1 | 176 | 182 | PF00069 | 0.549 |
DOC_PP2B_LxvP_1 | 336 | 339 | PF13499 | 0.776 |
DOC_PP4_FxxP_1 | 446 | 449 | PF00568 | 0.646 |
DOC_USP7_MATH_1 | 14 | 18 | PF00917 | 0.696 |
DOC_USP7_MATH_1 | 287 | 291 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.656 |
DOC_WW_Pin1_4 | 257 | 262 | PF00397 | 0.758 |
DOC_WW_Pin1_4 | 74 | 79 | PF00397 | 0.636 |
LIG_14-3-3_CanoR_1 | 15 | 21 | PF00244 | 0.756 |
LIG_14-3-3_CanoR_1 | 163 | 173 | PF00244 | 0.621 |
LIG_14-3-3_CanoR_1 | 24 | 28 | PF00244 | 0.748 |
LIG_14-3-3_CanoR_1 | 252 | 261 | PF00244 | 0.810 |
LIG_14-3-3_CanoR_1 | 61 | 69 | PF00244 | 0.580 |
LIG_CaM_NSCaTE_8 | 121 | 128 | PF13499 | 0.600 |
LIG_eIF4E_1 | 5 | 11 | PF01652 | 0.707 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.573 |
LIG_FHA_1 | 268 | 274 | PF00498 | 0.705 |
LIG_FHA_1 | 313 | 319 | PF00498 | 0.706 |
LIG_FHA_1 | 39 | 45 | PF00498 | 0.667 |
LIG_FHA_1 | 448 | 454 | PF00498 | 0.575 |
LIG_FHA_1 | 61 | 67 | PF00498 | 0.651 |
LIG_FHA_2 | 131 | 137 | PF00498 | 0.774 |
LIG_FHA_2 | 218 | 224 | PF00498 | 0.652 |
LIG_FHA_2 | 32 | 38 | PF00498 | 0.693 |
LIG_FHA_2 | 362 | 368 | PF00498 | 0.655 |
LIG_GBD_Chelix_1 | 209 | 217 | PF00786 | 0.366 |
LIG_GBD_Chelix_1 | 453 | 461 | PF00786 | 0.484 |
LIG_LIR_Apic_2 | 444 | 449 | PF02991 | 0.673 |
LIG_LIR_Gen_1 | 415 | 422 | PF02991 | 0.581 |
LIG_LIR_Nem_3 | 269 | 274 | PF02991 | 0.713 |
LIG_LIR_Nem_3 | 415 | 421 | PF02991 | 0.566 |
LIG_MYND_1 | 356 | 360 | PF01753 | 0.731 |
LIG_Pex14_2 | 267 | 271 | PF04695 | 0.743 |
LIG_SH2_STAT5 | 370 | 373 | PF00017 | 0.682 |
LIG_SH3_3 | 141 | 147 | PF00018 | 0.788 |
LIG_SH3_3 | 350 | 356 | PF00018 | 0.754 |
LIG_SH3_3 | 436 | 442 | PF00018 | 0.630 |
LIG_SH3_4 | 146 | 153 | PF00018 | 0.722 |
LIG_SUMO_SIM_par_1 | 94 | 101 | PF11976 | 0.609 |
LIG_TRAF2_1 | 183 | 186 | PF00917 | 0.614 |
LIG_TRAF2_1 | 364 | 367 | PF00917 | 0.603 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.769 |
MOD_CK1_1 | 257 | 263 | PF00069 | 0.744 |
MOD_CK1_1 | 401 | 407 | PF00069 | 0.574 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.599 |
MOD_CK2_1 | 217 | 223 | PF00069 | 0.709 |
MOD_CK2_1 | 31 | 37 | PF00069 | 0.688 |
MOD_CK2_1 | 314 | 320 | PF00069 | 0.714 |
MOD_CK2_1 | 361 | 367 | PF00069 | 0.611 |
MOD_CK2_1 | 434 | 440 | PF00069 | 0.569 |
MOD_CK2_1 | 6 | 12 | PF00069 | 0.648 |
MOD_CK2_1 | 88 | 94 | PF00069 | 0.562 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.471 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.440 |
MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.379 |
MOD_GlcNHglycan | 443 | 446 | PF01048 | 0.471 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.424 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.497 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.661 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.800 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.676 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.669 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.571 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.607 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.573 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.413 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.582 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.531 |
MOD_N-GLC_1 | 334 | 339 | PF02516 | 0.537 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.667 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.517 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.637 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.741 |
MOD_NEK2_1 | 344 | 349 | PF00069 | 0.736 |
MOD_NEK2_1 | 44 | 49 | PF00069 | 0.605 |
MOD_NEK2_1 | 84 | 89 | PF00069 | 0.567 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.527 |
MOD_NEK2_2 | 281 | 286 | PF00069 | 0.692 |
MOD_PIKK_1 | 35 | 41 | PF00454 | 0.641 |
MOD_PIKK_1 | 398 | 404 | PF00454 | 0.571 |
MOD_PIKK_1 | 45 | 51 | PF00454 | 0.552 |
MOD_PKA_1 | 15 | 21 | PF00069 | 0.638 |
MOD_PKA_2 | 123 | 129 | PF00069 | 0.612 |
MOD_PKA_2 | 14 | 20 | PF00069 | 0.748 |
MOD_PKA_2 | 23 | 29 | PF00069 | 0.732 |
MOD_PKA_2 | 60 | 66 | PF00069 | 0.553 |
MOD_Plk_1 | 1 | 7 | PF00069 | 0.732 |
MOD_Plk_1 | 334 | 340 | PF00069 | 0.663 |
MOD_Plk_1 | 398 | 404 | PF00069 | 0.586 |
MOD_Plk_4 | 40 | 46 | PF00069 | 0.635 |
MOD_Plk_4 | 402 | 408 | PF00069 | 0.572 |
MOD_Plk_4 | 84 | 90 | PF00069 | 0.577 |
MOD_ProDKin_1 | 257 | 263 | PF00069 | 0.757 |
MOD_ProDKin_1 | 74 | 80 | PF00069 | 0.632 |
MOD_SUMO_for_1 | 183 | 186 | PF00179 | 0.609 |
MOD_SUMO_rev_2 | 145 | 154 | PF00179 | 0.692 |
MOD_SUMO_rev_2 | 386 | 393 | PF00179 | 0.581 |
TRG_DiLeu_BaEn_1 | 416 | 421 | PF01217 | 0.635 |
TRG_DiLeu_BaEn_4 | 366 | 372 | PF01217 | 0.588 |
TRG_ER_diArg_1 | 119 | 121 | PF00400 | 0.705 |
TRG_ER_diArg_1 | 122 | 125 | PF00400 | 0.711 |
TRG_ER_diArg_1 | 171 | 173 | PF00400 | 0.557 |
TRG_ER_diArg_1 | 215 | 217 | PF00400 | 0.573 |
TRG_Pf-PMV_PEXEL_1 | 376 | 380 | PF00026 | 0.468 |
TRG_Pf-PMV_PEXEL_1 | 398 | 402 | PF00026 | 0.370 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCQ6 | Leptomonas seymouri | 52% | 100% |
A0A422P578 | Trypanosoma rangeli | 30% | 100% |
A4HPX8 | Leishmania braziliensis | 72% | 100% |
A4IDP0 | Leishmania infantum | 100% | 100% |
D0A4C6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9ATP5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
Q4Q0V3 | Leishmania major | 89% | 100% |
V5BUS9 | Trypanosoma cruzi | 35% | 100% |