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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9B368
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 198 | 202 | PF00656 | 0.721 |
CLV_C14_Caspase3-7 | 217 | 221 | PF00656 | 0.673 |
CLV_NRD_NRD_1 | 326 | 328 | PF00675 | 0.563 |
CLV_NRD_NRD_1 | 346 | 348 | PF00675 | 0.616 |
CLV_NRD_NRD_1 | 349 | 351 | PF00675 | 0.598 |
CLV_PCSK_FUR_1 | 324 | 328 | PF00082 | 0.612 |
CLV_PCSK_FUR_1 | 347 | 351 | PF00082 | 0.626 |
CLV_PCSK_KEX2_1 | 326 | 328 | PF00082 | 0.556 |
CLV_PCSK_KEX2_1 | 348 | 350 | PF00082 | 0.631 |
CLV_PCSK_PC1ET2_1 | 348 | 350 | PF00082 | 0.631 |
CLV_PCSK_PC7_1 | 322 | 328 | PF00082 | 0.615 |
CLV_PCSK_SKI1_1 | 365 | 369 | PF00082 | 0.545 |
CLV_PCSK_SKI1_1 | 55 | 59 | PF00082 | 0.467 |
DEG_APCC_DBOX_1 | 298 | 306 | PF00400 | 0.504 |
DOC_ANK_TNKS_1 | 196 | 203 | PF00023 | 0.588 |
DOC_PP1_RVXF_1 | 101 | 108 | PF00149 | 0.642 |
DOC_PP2B_PxIxI_1 | 43 | 49 | PF00149 | 0.491 |
DOC_PP4_FxxP_1 | 50 | 53 | PF00568 | 0.490 |
DOC_USP7_MATH_1 | 141 | 145 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 156 | 160 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.588 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 221 | 225 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 287 | 291 | PF00917 | 0.441 |
DOC_USP7_MATH_1 | 314 | 318 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 357 | 361 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 375 | 379 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 434 | 438 | PF00917 | 0.608 |
DOC_USP7_MATH_1 | 85 | 89 | PF00917 | 0.671 |
DOC_WW_Pin1_4 | 112 | 117 | PF00397 | 0.545 |
DOC_WW_Pin1_4 | 158 | 163 | PF00397 | 0.734 |
DOC_WW_Pin1_4 | 88 | 93 | PF00397 | 0.696 |
LIG_14-3-3_CanoR_1 | 299 | 303 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 329 | 338 | PF00244 | 0.611 |
LIG_14-3-3_CanoR_1 | 74 | 80 | PF00244 | 0.693 |
LIG_APCC_ABBA_1 | 234 | 239 | PF00400 | 0.411 |
LIG_BIR_III_4 | 84 | 88 | PF00653 | 0.664 |
LIG_BRCT_BRCA1_1 | 188 | 192 | PF00533 | 0.642 |
LIG_FHA_1 | 15 | 21 | PF00498 | 0.544 |
LIG_FHA_1 | 240 | 246 | PF00498 | 0.380 |
LIG_FHA_1 | 408 | 414 | PF00498 | 0.647 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.686 |
LIG_FHA_1 | 84 | 90 | PF00498 | 0.633 |
LIG_FHA_2 | 215 | 221 | PF00498 | 0.521 |
LIG_GBD_Chelix_1 | 173 | 181 | PF00786 | 0.476 |
LIG_LIR_Gen_1 | 104 | 113 | PF02991 | 0.629 |
LIG_LIR_Gen_1 | 3 | 9 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 104 | 110 | PF02991 | 0.635 |
LIG_LIR_Nem_3 | 3 | 8 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 361 | 367 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 78 | 82 | PF02991 | 0.627 |
LIG_LYPXL_yS_3 | 79 | 82 | PF13949 | 0.645 |
LIG_NRBOX | 304 | 310 | PF00104 | 0.527 |
LIG_PDZ_Class_1 | 434 | 439 | PF00595 | 0.550 |
LIG_Pex14_2 | 107 | 111 | PF04695 | 0.627 |
LIG_PTAP_UEV_1 | 152 | 157 | PF05743 | 0.492 |
LIG_SH2_PTP2 | 5 | 8 | PF00017 | 0.463 |
LIG_SH2_SRC | 59 | 62 | PF00017 | 0.299 |
LIG_SH2_STAP1 | 16 | 20 | PF00017 | 0.512 |
LIG_SH2_STAP1 | 61 | 65 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 16 | 19 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 183 | 186 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 334 | 337 | PF00017 | 0.483 |
LIG_SH2_STAT5 | 435 | 438 | PF00017 | 0.485 |
LIG_SH2_STAT5 | 5 | 8 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 59 | 62 | PF00017 | 0.306 |
LIG_SH3_1 | 150 | 156 | PF00018 | 0.487 |
LIG_SH3_2 | 342 | 347 | PF14604 | 0.661 |
LIG_SH3_3 | 150 | 156 | PF00018 | 0.523 |
LIG_SH3_3 | 339 | 345 | PF00018 | 0.570 |
LIG_SH3_3 | 428 | 434 | PF00018 | 0.631 |
LIG_SH3_3 | 86 | 92 | PF00018 | 0.703 |
LIG_SUMO_SIM_par_1 | 284 | 291 | PF11976 | 0.486 |
LIG_TRAF2_1 | 126 | 129 | PF00917 | 0.572 |
LIG_TRAF2_1 | 91 | 94 | PF00917 | 0.542 |
LIG_WW_3 | 226 | 230 | PF00397 | 0.680 |
MOD_CK1_1 | 161 | 167 | PF00069 | 0.704 |
MOD_CK1_1 | 216 | 222 | PF00069 | 0.721 |
MOD_CK1_1 | 230 | 236 | PF00069 | 0.552 |
MOD_CK1_1 | 83 | 89 | PF00069 | 0.734 |
MOD_CK2_1 | 88 | 94 | PF00069 | 0.671 |
MOD_GlcNHglycan | 156 | 159 | PF01048 | 0.735 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.672 |
MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.721 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.539 |
MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.266 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.615 |
MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.592 |
MOD_GlcNHglycan | 422 | 425 | PF01048 | 0.726 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.645 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.603 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.762 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.364 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.561 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.569 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.572 |
MOD_N-GLC_1 | 130 | 135 | PF02516 | 0.610 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.482 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.340 |
MOD_NEK2_1 | 264 | 269 | PF00069 | 0.417 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.400 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.413 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.507 |
MOD_NEK2_1 | 9 | 14 | PF00069 | 0.367 |
MOD_NEK2_2 | 298 | 303 | PF00069 | 0.518 |
MOD_NEK2_2 | 85 | 90 | PF00069 | 0.637 |
MOD_PIKK_1 | 329 | 335 | PF00454 | 0.590 |
MOD_PKA_1 | 365 | 371 | PF00069 | 0.550 |
MOD_PKA_2 | 298 | 304 | PF00069 | 0.493 |
MOD_PKA_2 | 401 | 407 | PF00069 | 0.692 |
MOD_PKB_1 | 327 | 335 | PF00069 | 0.595 |
MOD_Plk_1 | 101 | 107 | PF00069 | 0.644 |
MOD_Plk_1 | 130 | 136 | PF00069 | 0.661 |
MOD_Plk_1 | 141 | 147 | PF00069 | 0.711 |
MOD_Plk_4 | 1 | 7 | PF00069 | 0.505 |
MOD_Plk_4 | 230 | 236 | PF00069 | 0.523 |
MOD_Plk_4 | 314 | 320 | PF00069 | 0.693 |
MOD_Plk_4 | 336 | 342 | PF00069 | 0.616 |
MOD_Plk_4 | 384 | 390 | PF00069 | 0.594 |
MOD_Plk_4 | 85 | 91 | PF00069 | 0.731 |
MOD_ProDKin_1 | 112 | 118 | PF00069 | 0.539 |
MOD_ProDKin_1 | 158 | 164 | PF00069 | 0.727 |
MOD_ProDKin_1 | 88 | 94 | PF00069 | 0.702 |
MOD_SUMO_rev_2 | 233 | 243 | PF00179 | 0.449 |
MOD_SUMO_rev_2 | 358 | 367 | PF00179 | 0.600 |
TRG_DiLeu_BaEn_2 | 383 | 389 | PF01217 | 0.404 |
TRG_ENDOCYTIC_2 | 5 | 8 | PF00928 | 0.463 |
TRG_ENDOCYTIC_2 | 79 | 82 | PF00928 | 0.666 |
TRG_ER_diArg_1 | 111 | 114 | PF00400 | 0.558 |
TRG_ER_diArg_1 | 324 | 327 | PF00400 | 0.612 |
TRG_ER_diArg_1 | 346 | 349 | PF00400 | 0.621 |
TRG_NLS_MonoCore_2 | 346 | 351 | PF00514 | 0.622 |
TRG_NLS_MonoExtC_3 | 347 | 353 | PF00514 | 0.545 |
TRG_NLS_MonoExtN_4 | 345 | 352 | PF00514 | 0.620 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IME3 | Leptomonas seymouri | 53% | 100% |
A0A1X0NTD1 | Trypanosomatidae | 28% | 100% |
A0A3S7X601 | Leishmania donovani | 87% | 99% |
A0A422NZX0 | Trypanosoma rangeli | 31% | 100% |
A4HKT0 | Leishmania braziliensis | 79% | 99% |
A4I8A9 | Leishmania infantum | 88% | 99% |
D0AAI0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
Q4Q4Y6 | Leishmania major | 87% | 100% |
V5DE70 | Trypanosoma cruzi | 28% | 100% |