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: 2, no: 9 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
Related structures:
AlphaFold database: E9AWF6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 171 | 175 | PF00656 | 0.347 |
CLV_NRD_NRD_1 | 148 | 150 | PF00675 | 0.628 |
CLV_NRD_NRD_1 | 186 | 188 | PF00675 | 0.607 |
CLV_NRD_NRD_1 | 233 | 235 | PF00675 | 0.394 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.654 |
CLV_PCSK_KEX2_1 | 148 | 150 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.680 |
CLV_PCSK_SKI1_1 | 187 | 191 | PF00082 | 0.656 |
CLV_PCSK_SKI1_1 | 235 | 239 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 291 | 295 | PF00082 | 0.508 |
CLV_PCSK_SKI1_1 | 364 | 368 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 70 | 74 | PF00082 | 0.654 |
CLV_Separin_Metazoa | 315 | 319 | PF03568 | 0.496 |
DEG_SPOP_SBC_1 | 10 | 14 | PF00917 | 0.435 |
DOC_CKS1_1 | 274 | 279 | PF01111 | 0.664 |
DOC_MAPK_gen_1 | 335 | 343 | PF00069 | 0.650 |
DOC_MAPK_MEF2A_6 | 337 | 345 | PF00069 | 0.696 |
DOC_PP1_RVXF_1 | 367 | 373 | PF00149 | 0.711 |
DOC_PP2B_LxvP_1 | 7 | 10 | PF13499 | 0.300 |
DOC_PP4_FxxP_1 | 257 | 260 | PF00568 | 0.646 |
DOC_PP4_FxxP_1 | 274 | 277 | PF00568 | 0.632 |
DOC_PP4_FxxP_1 | 33 | 36 | PF00568 | 0.518 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 16 | 20 | PF00917 | 0.368 |
DOC_USP7_MATH_1 | 247 | 251 | PF00917 | 0.576 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 336 | 340 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 355 | 359 | PF00917 | 0.773 |
DOC_USP7_UBL2_3 | 122 | 126 | PF12436 | 0.393 |
DOC_WW_Pin1_4 | 102 | 107 | PF00397 | 0.474 |
DOC_WW_Pin1_4 | 273 | 278 | PF00397 | 0.608 |
LIG_14-3-3_CanoR_1 | 340 | 344 | PF00244 | 0.750 |
LIG_14-3-3_CanoR_1 | 369 | 373 | PF00244 | 0.663 |
LIG_14-3-3_CanoR_1 | 4 | 8 | PF00244 | 0.697 |
LIG_14-3-3_CanoR_1 | 42 | 47 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 57 | 63 | PF00244 | 0.475 |
LIG_APCC_ABBA_1 | 317 | 322 | PF00400 | 0.671 |
LIG_BRCT_BRCA1_1 | 249 | 253 | PF00533 | 0.652 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.390 |
LIG_FHA_1 | 164 | 170 | PF00498 | 0.425 |
LIG_FHA_1 | 294 | 300 | PF00498 | 0.605 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.702 |
LIG_FHA_1 | 398 | 404 | PF00498 | 0.705 |
LIG_FHA_2 | 140 | 146 | PF00498 | 0.426 |
LIG_FHA_2 | 200 | 206 | PF00498 | 0.395 |
LIG_FHA_2 | 236 | 242 | PF00498 | 0.584 |
LIG_FHA_2 | 363 | 369 | PF00498 | 0.708 |
LIG_FHA_2 | 47 | 53 | PF00498 | 0.454 |
LIG_Integrin_isoDGR_2 | 286 | 288 | PF01839 | 0.449 |
LIG_LIR_Apic_2 | 256 | 260 | PF02991 | 0.703 |
LIG_LIR_Apic_2 | 271 | 277 | PF02991 | 0.704 |
LIG_LIR_Gen_1 | 365 | 375 | PF02991 | 0.653 |
LIG_LIR_Gen_1 | 387 | 395 | PF02991 | 0.631 |
LIG_LIR_Gen_1 | 83 | 94 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 107 | 112 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 365 | 370 | PF02991 | 0.662 |
LIG_LIR_Nem_3 | 371 | 375 | PF02991 | 0.599 |
LIG_LIR_Nem_3 | 387 | 392 | PF02991 | 0.614 |
LIG_LIR_Nem_3 | 83 | 89 | PF02991 | 0.400 |
LIG_MLH1_MIPbox_1 | 249 | 253 | PF16413 | 0.652 |
LIG_NBox_RRM_1 | 216 | 226 | PF00076 | 0.449 |
LIG_Pex14_2 | 253 | 257 | PF04695 | 0.679 |
LIG_Pex14_2 | 86 | 90 | PF04695 | 0.291 |
LIG_REV1ctd_RIR_1 | 87 | 96 | PF16727 | 0.304 |
LIG_SH2_GRB2like | 273 | 276 | PF00017 | 0.707 |
LIG_SH2_SRC | 172 | 175 | PF00017 | 0.348 |
LIG_SH2_STAP1 | 232 | 236 | PF00017 | 0.671 |
LIG_SH2_STAT3 | 289 | 292 | PF00017 | 0.709 |
LIG_SH2_STAT3 | 308 | 311 | PF00017 | 0.629 |
LIG_SH2_STAT5 | 172 | 175 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 236 | 239 | PF00017 | 0.632 |
LIG_SH2_STAT5 | 252 | 255 | PF00017 | 0.596 |
LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.648 |
LIG_SH2_STAT5 | 344 | 347 | PF00017 | 0.721 |
LIG_SH3_3 | 24 | 30 | PF00018 | 0.536 |
LIG_SH3_5 | 265 | 269 | PF00018 | 0.630 |
LIG_TRAF2_1 | 157 | 160 | PF00917 | 0.460 |
LIG_TRAF2_1 | 307 | 310 | PF00917 | 0.599 |
LIG_TRAF2_1 | 371 | 374 | PF00917 | 0.662 |
LIG_UBA3_1 | 55 | 63 | PF00899 | 0.501 |
LIG_WRC_WIRS_1 | 254 | 259 | PF05994 | 0.671 |
LIG_WRC_WIRS_1 | 86 | 91 | PF05994 | 0.446 |
MOD_CK1_1 | 339 | 345 | PF00069 | 0.751 |
MOD_CK1_1 | 358 | 364 | PF00069 | 0.733 |
MOD_CK1_1 | 397 | 403 | PF00069 | 0.695 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.419 |
MOD_CK2_1 | 199 | 205 | PF00069 | 0.341 |
MOD_CK2_1 | 275 | 281 | PF00069 | 0.654 |
MOD_CK2_1 | 292 | 298 | PF00069 | 0.576 |
MOD_CK2_1 | 362 | 368 | PF00069 | 0.741 |
MOD_CK2_1 | 395 | 401 | PF00069 | 0.721 |
MOD_GlcNHglycan | 303 | 307 | PF01048 | 0.456 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.745 |
MOD_GlcNHglycan | 374 | 378 | PF01048 | 0.455 |
MOD_GlcNHglycan | 411 | 414 | PF01048 | 0.528 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.745 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.419 |
MOD_GSK3_1 | 237 | 244 | PF00069 | 0.677 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.671 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.758 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.680 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.467 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.551 |
MOD_N-GLC_1 | 208 | 213 | PF02516 | 0.654 |
MOD_NEK2_1 | 11 | 16 | PF00069 | 0.382 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.350 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.459 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.475 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.631 |
MOD_NEK2_1 | 46 | 51 | PF00069 | 0.446 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.458 |
MOD_PK_1 | 324 | 330 | PF00069 | 0.616 |
MOD_PKA_1 | 100 | 106 | PF00069 | 0.502 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.726 |
MOD_PKA_2 | 336 | 342 | PF00069 | 0.624 |
MOD_PKA_2 | 358 | 364 | PF00069 | 0.776 |
MOD_PKA_2 | 368 | 374 | PF00069 | 0.663 |
MOD_PKA_2 | 390 | 396 | PF00069 | 0.639 |
MOD_PKB_1 | 206 | 214 | PF00069 | 0.456 |
MOD_PKB_1 | 407 | 415 | PF00069 | 0.688 |
MOD_Plk_1 | 173 | 179 | PF00069 | 0.381 |
MOD_Plk_1 | 208 | 214 | PF00069 | 0.359 |
MOD_Plk_1 | 324 | 330 | PF00069 | 0.699 |
MOD_Plk_1 | 362 | 368 | PF00069 | 0.696 |
MOD_Plk_1 | 51 | 57 | PF00069 | 0.486 |
MOD_Plk_2-3 | 368 | 374 | PF00069 | 0.705 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.428 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.337 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.647 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.767 |
MOD_Plk_4 | 339 | 345 | PF00069 | 0.736 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.468 |
MOD_Plk_4 | 85 | 91 | PF00069 | 0.449 |
MOD_ProDKin_1 | 102 | 108 | PF00069 | 0.473 |
MOD_ProDKin_1 | 273 | 279 | PF00069 | 0.609 |
MOD_SUMO_for_1 | 130 | 133 | PF00179 | 0.459 |
MOD_SUMO_rev_2 | 114 | 124 | PF00179 | 0.422 |
MOD_SUMO_rev_2 | 327 | 336 | PF00179 | 0.668 |
TRG_DiLeu_BaEn_4 | 312 | 318 | PF01217 | 0.598 |
TRG_ENDOCYTIC_2 | 186 | 189 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 252 | 255 | PF00928 | 0.596 |
TRG_ER_diArg_1 | 147 | 149 | PF00400 | 0.336 |
TRG_ER_diArg_1 | 98 | 100 | PF00400 | 0.552 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4S8 | Leptomonas seymouri | 66% | 98% |
A0A0S4IRC9 | Bodo saltans | 35% | 100% |
A0A1X0NWQ4 | Trypanosomatidae | 44% | 97% |
A0A3Q8IMB7 | Leishmania donovani | 90% | 100% |
A0A422NXY7 | Trypanosoma rangeli | 43% | 100% |
A4HD09 | Leishmania braziliensis | 76% | 100% |
A4I0J5 | Leishmania infantum | 90% | 100% |
C9ZVC2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
Q4QB16 | Leishmania major | 88% | 100% |
V5BJ93 | Trypanosoma cruzi | 44% | 99% |