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 | yes | 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: A0A3Q8IMB7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 171 | 175 | PF00656 | 0.355 |
CLV_MEL_PAP_1 | 337 | 343 | PF00089 | 0.374 |
CLV_NRD_NRD_1 | 147 | 149 | PF00675 | 0.652 |
CLV_NRD_NRD_1 | 186 | 188 | PF00675 | 0.613 |
CLV_NRD_NRD_1 | 233 | 235 | PF00675 | 0.368 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.682 |
CLV_NRD_NRD_1 | 326 | 328 | PF00675 | 0.327 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.660 |
CLV_PCSK_FUR_1 | 324 | 328 | PF00082 | 0.383 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.682 |
CLV_PCSK_KEX2_1 | 326 | 328 | PF00082 | 0.327 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.686 |
CLV_PCSK_SKI1_1 | 187 | 191 | PF00082 | 0.663 |
CLV_PCSK_SKI1_1 | 235 | 239 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 288 | 292 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 364 | 368 | PF00082 | 0.530 |
DEG_SPOP_SBC_1 | 10 | 14 | PF00917 | 0.726 |
DOC_CKS1_1 | 274 | 279 | PF01111 | 0.663 |
DOC_PP1_RVXF_1 | 367 | 373 | PF00149 | 0.728 |
DOC_PP2B_LxvP_1 | 7 | 10 | PF13499 | 0.557 |
DOC_PP4_FxxP_1 | 257 | 260 | PF00568 | 0.640 |
DOC_PP4_FxxP_1 | 274 | 277 | PF00568 | 0.633 |
DOC_PP4_FxxP_1 | 33 | 36 | PF00568 | 0.518 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.730 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.681 |
DOC_USP7_MATH_1 | 336 | 340 | PF00917 | 0.681 |
DOC_USP7_MATH_1 | 355 | 359 | PF00917 | 0.628 |
DOC_USP7_UBL2_3 | 122 | 126 | PF12436 | 0.402 |
DOC_WW_Pin1_4 | 102 | 107 | PF00397 | 0.490 |
DOC_WW_Pin1_4 | 273 | 278 | PF00397 | 0.609 |
LIG_14-3-3_CanoR_1 | 3 | 8 | PF00244 | 0.638 |
LIG_14-3-3_CanoR_1 | 340 | 344 | PF00244 | 0.734 |
LIG_14-3-3_CanoR_1 | 42 | 47 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 57 | 63 | PF00244 | 0.356 |
LIG_APCC_ABBA_1 | 317 | 322 | PF00400 | 0.662 |
LIG_BRCT_BRCA1_1 | 249 | 253 | PF00533 | 0.646 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.657 |
LIG_FHA_1 | 164 | 170 | PF00498 | 0.428 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.640 |
LIG_FHA_1 | 398 | 404 | PF00498 | 0.713 |
LIG_FHA_2 | 139 | 145 | PF00498 | 0.442 |
LIG_FHA_2 | 236 | 242 | PF00498 | 0.581 |
LIG_FHA_2 | 363 | 369 | PF00498 | 0.713 |
LIG_FHA_2 | 47 | 53 | PF00498 | 0.484 |
LIG_Integrin_isoDGR_2 | 286 | 288 | PF01839 | 0.438 |
LIG_LIR_Apic_2 | 256 | 260 | PF02991 | 0.697 |
LIG_LIR_Apic_2 | 271 | 277 | PF02991 | 0.704 |
LIG_LIR_Gen_1 | 107 | 115 | PF02991 | 0.493 |
LIG_LIR_Gen_1 | 365 | 375 | PF02991 | 0.651 |
LIG_LIR_Gen_1 | 387 | 395 | PF02991 | 0.636 |
LIG_LIR_Gen_1 | 83 | 94 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 107 | 112 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 365 | 370 | PF02991 | 0.654 |
LIG_LIR_Nem_3 | 371 | 375 | PF02991 | 0.600 |
LIG_LIR_Nem_3 | 387 | 392 | PF02991 | 0.615 |
LIG_LIR_Nem_3 | 83 | 89 | PF02991 | 0.403 |
LIG_MLH1_MIPbox_1 | 249 | 253 | PF16413 | 0.646 |
LIG_NBox_RRM_1 | 216 | 226 | PF00076 | 0.449 |
LIG_Pex14_2 | 253 | 257 | PF04695 | 0.677 |
LIG_SH2_GRB2like | 273 | 276 | PF00017 | 0.708 |
LIG_SH2_SRC | 172 | 175 | PF00017 | 0.355 |
LIG_SH2_STAP1 | 232 | 236 | PF00017 | 0.657 |
LIG_SH2_STAP1 | 289 | 293 | PF00017 | 0.617 |
LIG_SH2_STAT3 | 289 | 292 | PF00017 | 0.707 |
LIG_SH2_STAT3 | 308 | 311 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 172 | 175 | PF00017 | 0.355 |
LIG_SH2_STAT5 | 178 | 181 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 236 | 239 | PF00017 | 0.613 |
LIG_SH2_STAT5 | 252 | 255 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.650 |
LIG_SH2_STAT5 | 308 | 311 | PF00017 | 0.613 |
LIG_SH2_STAT5 | 344 | 347 | PF00017 | 0.712 |
LIG_SH3_3 | 24 | 30 | PF00018 | 0.728 |
LIG_SH3_3 | 340 | 346 | PF00018 | 0.709 |
LIG_SH3_5 | 265 | 269 | PF00018 | 0.626 |
LIG_TRAF2_1 | 157 | 160 | PF00917 | 0.458 |
LIG_TRAF2_1 | 295 | 298 | PF00917 | 0.649 |
LIG_TRAF2_1 | 371 | 374 | PF00917 | 0.666 |
LIG_UBA3_1 | 55 | 63 | PF00899 | 0.534 |
LIG_WRC_WIRS_1 | 254 | 259 | PF05994 | 0.687 |
LIG_WRC_WIRS_1 | 86 | 91 | PF05994 | 0.447 |
MOD_CK1_1 | 339 | 345 | PF00069 | 0.736 |
MOD_CK1_1 | 358 | 364 | PF00069 | 0.719 |
MOD_CK1_1 | 397 | 403 | PF00069 | 0.705 |
MOD_CK2_1 | 138 | 144 | PF00069 | 0.380 |
MOD_CK2_1 | 275 | 281 | PF00069 | 0.661 |
MOD_CK2_1 | 292 | 298 | PF00069 | 0.572 |
MOD_CK2_1 | 362 | 368 | PF00069 | 0.731 |
MOD_CK2_1 | 395 | 401 | PF00069 | 0.724 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.437 |
MOD_GlcNHglycan | 303 | 307 | PF01048 | 0.442 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.764 |
MOD_GlcNHglycan | 374 | 378 | PF01048 | 0.483 |
MOD_GlcNHglycan | 411 | 414 | PF01048 | 0.551 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.745 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.765 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.710 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.483 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.567 |
MOD_N-GLC_1 | 208 | 213 | PF02516 | 0.653 |
MOD_NEK2_1 | 11 | 16 | PF00069 | 0.663 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.476 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.458 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.629 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.608 |
MOD_NEK2_1 | 46 | 51 | PF00069 | 0.474 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.512 |
MOD_PKA_1 | 100 | 106 | PF00069 | 0.512 |
MOD_PKA_1 | 3 | 9 | PF00069 | 0.689 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.680 |
MOD_PKA_2 | 339 | 345 | PF00069 | 0.646 |
MOD_PKA_2 | 358 | 364 | PF00069 | 0.777 |
MOD_PKA_2 | 390 | 396 | PF00069 | 0.645 |
MOD_PKB_1 | 206 | 214 | PF00069 | 0.456 |
MOD_PKB_1 | 357 | 365 | PF00069 | 0.620 |
MOD_PKB_1 | 407 | 415 | PF00069 | 0.692 |
MOD_Plk_1 | 173 | 179 | PF00069 | 0.387 |
MOD_Plk_1 | 208 | 214 | PF00069 | 0.359 |
MOD_Plk_1 | 362 | 368 | PF00069 | 0.690 |
MOD_Plk_1 | 51 | 57 | PF00069 | 0.518 |
MOD_Plk_2-3 | 368 | 374 | PF00069 | 0.706 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.439 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.330 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.649 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.731 |
MOD_Plk_4 | 339 | 345 | PF00069 | 0.712 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.493 |
MOD_Plk_4 | 85 | 91 | PF00069 | 0.450 |
MOD_ProDKin_1 | 102 | 108 | PF00069 | 0.487 |
MOD_ProDKin_1 | 273 | 279 | PF00069 | 0.608 |
MOD_SUMO_for_1 | 130 | 133 | PF00179 | 0.465 |
MOD_SUMO_for_1 | 309 | 312 | PF00179 | 0.517 |
MOD_SUMO_rev_2 | 114 | 124 | PF00179 | 0.429 |
MOD_SUMO_rev_2 | 330 | 337 | PF00179 | 0.668 |
TRG_DiLeu_BaEn_4 | 133 | 139 | PF01217 | 0.460 |
TRG_DiLeu_BaEn_4 | 312 | 318 | PF01217 | 0.582 |
TRG_ENDOCYTIC_2 | 186 | 189 | PF00928 | 0.449 |
TRG_ENDOCYTIC_2 | 252 | 255 | PF00928 | 0.566 |
TRG_ER_diArg_1 | 326 | 329 | PF00400 | 0.526 |
TRG_ER_diArg_1 | 98 | 100 | PF00400 | 0.563 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4S8 | Leptomonas seymouri | 66% | 98% |
A0A0S4IRC9 | Bodo saltans | 36% | 100% |
A0A1X0NWQ4 | Trypanosomatidae | 45% | 97% |
A0A422NXY7 | Trypanosoma rangeli | 44% | 100% |
A4HD09 | Leishmania braziliensis | 78% | 100% |
A4I0J5 | Leishmania infantum | 100% | 100% |
C9ZVC2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
E9AWF6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4QB16 | Leishmania major | 94% | 100% |
V5BJ93 | Trypanosoma cruzi | 43% | 99% |