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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: A0A3Q8IBV5
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0016746 | acyltransferase activity | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 336 | 340 | PF00656 | 0.711 |
CLV_NRD_NRD_1 | 188 | 190 | PF00675 | 0.473 |
CLV_NRD_NRD_1 | 209 | 211 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 380 | 382 | PF00675 | 0.428 |
CLV_PCSK_KEX2_1 | 188 | 190 | PF00082 | 0.471 |
CLV_PCSK_KEX2_1 | 380 | 382 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 246 | 250 | PF00082 | 0.371 |
CLV_PCSK_SKI1_1 | 38 | 42 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 399 | 403 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 69 | 73 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 81 | 85 | PF00082 | 0.308 |
DEG_APCC_DBOX_1 | 37 | 45 | PF00400 | 0.475 |
DEG_APCC_DBOX_1 | 68 | 76 | PF00400 | 0.376 |
DEG_APCC_DBOX_1 | 80 | 88 | PF00400 | 0.503 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.663 |
DEG_ODPH_VHL_1 | 72 | 85 | PF01847 | 0.446 |
DEG_SIAH_1 | 94 | 102 | PF03145 | 0.660 |
DOC_CYCLIN_RxL_1 | 35 | 42 | PF00134 | 0.433 |
DOC_CYCLIN_yCln2_LP_2 | 138 | 144 | PF00134 | 0.562 |
DOC_CYCLIN_yCln2_LP_2 | 351 | 357 | PF00134 | 0.612 |
DOC_MAPK_gen_1 | 113 | 122 | PF00069 | 0.569 |
DOC_MAPK_gen_1 | 188 | 195 | PF00069 | 0.661 |
DOC_MAPK_gen_1 | 380 | 388 | PF00069 | 0.600 |
DOC_MAPK_MEF2A_6 | 380 | 388 | PF00069 | 0.600 |
DOC_PP1_RVXF_1 | 169 | 175 | PF00149 | 0.582 |
DOC_PP1_RVXF_1 | 79 | 86 | PF00149 | 0.560 |
DOC_PP2B_LxvP_1 | 249 | 252 | PF13499 | 0.601 |
DOC_PP2B_LxvP_1 | 351 | 354 | PF13499 | 0.582 |
DOC_PP2B_LxvP_1 | 71 | 74 | PF13499 | 0.363 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.757 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.693 |
DOC_USP7_MATH_1 | 332 | 336 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 337 | 341 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 407 | 411 | PF00917 | 0.603 |
DOC_WW_Pin1_4 | 276 | 281 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 311 | 316 | PF00397 | 0.623 |
DOC_WW_Pin1_4 | 330 | 335 | PF00397 | 0.575 |
DOC_WW_Pin1_4 | 405 | 410 | PF00397 | 0.683 |
LIG_14-3-3_CanoR_1 | 188 | 194 | PF00244 | 0.565 |
LIG_14-3-3_CanoR_1 | 210 | 219 | PF00244 | 0.642 |
LIG_14-3-3_CanoR_1 | 346 | 352 | PF00244 | 0.640 |
LIG_14-3-3_CanoR_1 | 38 | 48 | PF00244 | 0.420 |
LIG_14-3-3_CanoR_1 | 381 | 387 | PF00244 | 0.670 |
LIG_BRCT_BRCA1_1 | 191 | 195 | PF00533 | 0.616 |
LIG_BRCT_BRCA1_1 | 313 | 317 | PF00533 | 0.700 |
LIG_BRCT_BRCA1_1 | 41 | 45 | PF00533 | 0.433 |
LIG_DLG_GKlike_1 | 189 | 196 | PF00625 | 0.658 |
LIG_EH1_1 | 84 | 92 | PF00400 | 0.607 |
LIG_FHA_1 | 188 | 194 | PF00498 | 0.582 |
LIG_FHA_1 | 298 | 304 | PF00498 | 0.699 |
LIG_FHA_1 | 311 | 317 | PF00498 | 0.594 |
LIG_FHA_1 | 50 | 56 | PF00498 | 0.394 |
LIG_FHA_2 | 334 | 340 | PF00498 | 0.673 |
LIG_Integrin_isoDGR_2 | 244 | 246 | PF01839 | 0.451 |
LIG_LIR_Apic_2 | 274 | 280 | PF02991 | 0.642 |
LIG_LIR_Gen_1 | 127 | 137 | PF02991 | 0.582 |
LIG_LIR_Gen_1 | 291 | 302 | PF02991 | 0.717 |
LIG_LIR_Gen_1 | 42 | 51 | PF02991 | 0.484 |
LIG_LIR_LC3C_4 | 119 | 122 | PF02991 | 0.600 |
LIG_LIR_Nem_3 | 127 | 132 | PF02991 | 0.586 |
LIG_LIR_Nem_3 | 2 | 7 | PF02991 | 0.654 |
LIG_LIR_Nem_3 | 291 | 297 | PF02991 | 0.714 |
LIG_LIR_Nem_3 | 42 | 48 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 54 | 60 | PF02991 | 0.344 |
LIG_NRBOX | 66 | 72 | PF00104 | 0.404 |
LIG_NRBOX | 79 | 85 | PF00104 | 0.464 |
LIG_Pex14_2 | 294 | 298 | PF04695 | 0.721 |
LIG_SH2_CRK | 142 | 146 | PF00017 | 0.579 |
LIG_SH2_CRK | 277 | 281 | PF00017 | 0.679 |
LIG_SH2_NCK_1 | 277 | 281 | PF00017 | 0.653 |
LIG_SH2_STAT3 | 221 | 224 | PF00017 | 0.578 |
LIG_SH2_STAT5 | 186 | 189 | PF00017 | 0.621 |
LIG_SH2_STAT5 | 60 | 63 | PF00017 | 0.373 |
LIG_SH3_3 | 169 | 175 | PF00018 | 0.554 |
LIG_SH3_3 | 17 | 23 | PF00018 | 0.682 |
LIG_SH3_3 | 312 | 318 | PF00018 | 0.612 |
LIG_SH3_3 | 89 | 95 | PF00018 | 0.628 |
LIG_SH3_4 | 100 | 107 | PF00018 | 0.781 |
LIG_SUMO_SIM_par_1 | 46 | 54 | PF11976 | 0.388 |
LIG_TYR_ITIM | 61 | 66 | PF00017 | 0.262 |
LIG_Vh1_VBS_1 | 40 | 58 | PF01044 | 0.449 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.715 |
MOD_CK1_1 | 158 | 164 | PF00069 | 0.727 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.659 |
MOD_CK1_1 | 335 | 341 | PF00069 | 0.614 |
MOD_CK1_1 | 342 | 348 | PF00069 | 0.686 |
MOD_CK2_1 | 157 | 163 | PF00069 | 0.740 |
MOD_CK2_1 | 285 | 291 | PF00069 | 0.581 |
MOD_CMANNOS | 181 | 184 | PF00535 | 0.374 |
MOD_GlcNHglycan | 107 | 111 | PF01048 | 0.592 |
MOD_GlcNHglycan | 155 | 160 | PF01048 | 0.501 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.434 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.404 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.442 |
MOD_GlcNHglycan | 263 | 267 | PF01048 | 0.324 |
MOD_GlcNHglycan | 341 | 344 | PF01048 | 0.503 |
MOD_GlcNHglycan | 351 | 354 | PF01048 | 0.367 |
MOD_GlcNHglycan | 372 | 375 | PF01048 | 0.531 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.421 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.588 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.625 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.616 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.626 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.550 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.655 |
MOD_N-GLC_1 | 289 | 294 | PF02516 | 0.371 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.635 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.630 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.755 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.383 |
MOD_NEK2_1 | 401 | 406 | PF00069 | 0.673 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.582 |
MOD_PIKK_1 | 175 | 181 | PF00454 | 0.558 |
MOD_PK_1 | 28 | 34 | PF00069 | 0.581 |
MOD_PKA_1 | 188 | 194 | PF00069 | 0.565 |
MOD_PKA_1 | 210 | 216 | PF00069 | 0.668 |
MOD_PKA_2 | 187 | 193 | PF00069 | 0.633 |
MOD_PKA_2 | 324 | 330 | PF00069 | 0.625 |
MOD_Plk_1 | 148 | 154 | PF00069 | 0.627 |
MOD_Plk_1 | 289 | 295 | PF00069 | 0.629 |
MOD_Plk_1 | 320 | 326 | PF00069 | 0.605 |
MOD_Plk_4 | 124 | 130 | PF00069 | 0.520 |
MOD_Plk_4 | 289 | 295 | PF00069 | 0.601 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.398 |
MOD_ProDKin_1 | 276 | 282 | PF00069 | 0.660 |
MOD_ProDKin_1 | 311 | 317 | PF00069 | 0.622 |
MOD_ProDKin_1 | 330 | 336 | PF00069 | 0.583 |
MOD_ProDKin_1 | 405 | 411 | PF00069 | 0.690 |
MOD_SUMO_rev_2 | 335 | 343 | PF00179 | 0.720 |
MOD_SUMO_rev_2 | 385 | 394 | PF00179 | 0.677 |
TRG_DiLeu_BaEn_2 | 389 | 395 | PF01217 | 0.610 |
TRG_DiLeu_BaLyEn_6 | 35 | 40 | PF01217 | 0.410 |
TRG_DiLeu_BaLyEn_6 | 66 | 71 | PF01217 | 0.397 |
TRG_ENDOCYTIC_2 | 142 | 145 | PF00928 | 0.579 |
TRG_ENDOCYTIC_2 | 398 | 401 | PF00928 | 0.656 |
TRG_ENDOCYTIC_2 | 63 | 66 | PF00928 | 0.359 |
TRG_ER_diArg_1 | 379 | 381 | PF00400 | 0.628 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IK56 | Leptomonas seymouri | 63% | 100% |
A0A0S4IZ96 | Bodo saltans | 30% | 100% |
A0A1X0NMQ7 | Trypanosomatidae | 30% | 97% |
A0A3S5IRZ0 | Trypanosoma rangeli | 33% | 100% |
A4H5M6 | Leishmania braziliensis | 78% | 98% |
A4HTW3 | Leishmania infantum | 99% | 100% |
D0A9C7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9AMQ0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4QHX5 | Leishmania major | 92% | 100% |
V5BIH4 | Trypanosoma cruzi | 32% | 100% |