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 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: A4H8D6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 227 | 229 | PF00675 | 0.356 |
CLV_NRD_NRD_1 | 236 | 238 | PF00675 | 0.434 |
CLV_NRD_NRD_1 | 296 | 298 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 369 | 371 | PF00675 | 0.573 |
CLV_NRD_NRD_1 | 62 | 64 | PF00675 | 0.757 |
CLV_PCSK_KEX2_1 | 227 | 229 | PF00082 | 0.428 |
CLV_PCSK_KEX2_1 | 236 | 238 | PF00082 | 0.434 |
CLV_PCSK_KEX2_1 | 296 | 298 | PF00082 | 0.488 |
CLV_PCSK_KEX2_1 | 369 | 371 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 62 | 64 | PF00082 | 0.658 |
CLV_PCSK_SKI1_1 | 194 | 198 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 336 | 340 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 390 | 394 | PF00082 | 0.624 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.506 |
DEG_ODPH_VHL_1 | 348 | 361 | PF01847 | 0.306 |
DOC_CKS1_1 | 249 | 254 | PF01111 | 0.363 |
DOC_CYCLIN_RxL_1 | 268 | 282 | PF00134 | 0.217 |
DOC_CYCLIN_yCln2_LP_2 | 272 | 278 | PF00134 | 0.443 |
DOC_CYCLIN_yCln2_LP_2 | 405 | 408 | PF00134 | 0.416 |
DOC_MAPK_gen_1 | 336 | 344 | PF00069 | 0.446 |
DOC_MAPK_gen_1 | 40 | 50 | PF00069 | 0.481 |
DOC_MAPK_MEF2A_6 | 129 | 136 | PF00069 | 0.499 |
DOC_MAPK_MEF2A_6 | 309 | 316 | PF00069 | 0.513 |
DOC_MAPK_MEF2A_6 | 336 | 344 | PF00069 | 0.519 |
DOC_MAPK_MEF2A_6 | 355 | 364 | PF00069 | 0.434 |
DOC_PP2B_LxvP_1 | 404 | 407 | PF13499 | 0.609 |
DOC_PP2B_LxvP_1 | 50 | 53 | PF13499 | 0.487 |
DOC_PP2B_LxvP_1 | 70 | 73 | PF13499 | 0.476 |
DOC_PP4_FxxP_1 | 169 | 172 | PF00568 | 0.511 |
DOC_PP4_FxxP_1 | 307 | 310 | PF00568 | 0.581 |
DOC_USP7_MATH_1 | 386 | 390 | PF00917 | 0.463 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.771 |
DOC_WW_Pin1_4 | 248 | 253 | PF00397 | 0.253 |
DOC_WW_Pin1_4 | 354 | 359 | PF00397 | 0.442 |
DOC_WW_Pin1_4 | 369 | 374 | PF00397 | 0.650 |
LIG_14-3-3_CanoR_1 | 153 | 162 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 237 | 247 | PF00244 | 0.441 |
LIG_14-3-3_CanoR_1 | 250 | 258 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 369 | 373 | PF00244 | 0.631 |
LIG_ActinCP_TwfCPI_2 | 307 | 317 | PF01115 | 0.550 |
LIG_BIR_III_2 | 206 | 210 | PF00653 | 0.545 |
LIG_BRCT_BRCA1_1 | 165 | 169 | PF00533 | 0.519 |
LIG_CSL_BTD_1 | 130 | 133 | PF09270 | 0.378 |
LIG_deltaCOP1_diTrp_1 | 244 | 253 | PF00928 | 0.484 |
LIG_EVH1_1 | 17 | 21 | PF00568 | 0.426 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.438 |
LIG_FHA_1 | 20 | 26 | PF00498 | 0.401 |
LIG_FHA_1 | 355 | 361 | PF00498 | 0.439 |
LIG_FHA_1 | 372 | 378 | PF00498 | 0.569 |
LIG_FHA_1 | 95 | 101 | PF00498 | 0.474 |
LIG_FHA_2 | 210 | 216 | PF00498 | 0.363 |
LIG_FHA_2 | 239 | 245 | PF00498 | 0.344 |
LIG_IRF3_LxIS_1 | 358 | 363 | PF10401 | 0.276 |
LIG_LIR_Apic_2 | 166 | 172 | PF02991 | 0.542 |
LIG_LIR_Gen_1 | 22 | 32 | PF02991 | 0.606 |
LIG_LIR_Gen_1 | 328 | 338 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 22 | 27 | PF02991 | 0.600 |
LIG_LIR_Nem_3 | 328 | 334 | PF02991 | 0.379 |
LIG_Pex14_2 | 20 | 24 | PF04695 | 0.544 |
LIG_REV1ctd_RIR_1 | 351 | 357 | PF16727 | 0.326 |
LIG_SH2_CRK | 14 | 18 | PF00017 | 0.424 |
LIG_SH2_CRK | 249 | 253 | PF00017 | 0.443 |
LIG_SH2_CRK | 298 | 302 | PF00017 | 0.384 |
LIG_SH2_CRK | 323 | 327 | PF00017 | 0.563 |
LIG_SH2_CRK | 71 | 75 | PF00017 | 0.476 |
LIG_SH2_NCK_1 | 298 | 302 | PF00017 | 0.425 |
LIG_SH2_SRC | 298 | 301 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 14 | 17 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 257 | 260 | PF00017 | 0.313 |
LIG_SH3_3 | 127 | 133 | PF00018 | 0.407 |
LIG_SH3_3 | 13 | 19 | PF00018 | 0.504 |
LIG_SH3_3 | 39 | 45 | PF00018 | 0.661 |
LIG_SUMO_SIM_anti_2 | 357 | 363 | PF11976 | 0.286 |
LIG_SUMO_SIM_par_1 | 132 | 138 | PF11976 | 0.316 |
LIG_SUMO_SIM_par_1 | 357 | 363 | PF11976 | 0.286 |
LIG_TRAF2_1 | 220 | 223 | PF00917 | 0.484 |
LIG_TRFH_1 | 142 | 146 | PF08558 | 0.293 |
LIG_TYR_ITIM | 321 | 326 | PF00017 | 0.536 |
LIG_WRC_WIRS_1 | 139 | 144 | PF05994 | 0.290 |
MOD_CK1_1 | 157 | 163 | PF00069 | 0.507 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.392 |
MOD_CK1_1 | 371 | 377 | PF00069 | 0.688 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.460 |
MOD_CK2_1 | 132 | 138 | PF00069 | 0.358 |
MOD_CK2_1 | 209 | 215 | PF00069 | 0.344 |
MOD_CK2_1 | 216 | 222 | PF00069 | 0.344 |
MOD_CK2_1 | 238 | 244 | PF00069 | 0.344 |
MOD_CK2_1 | 391 | 397 | PF00069 | 0.489 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.493 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.393 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.477 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.695 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.574 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.481 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.561 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.541 |
MOD_GSK3_1 | 368 | 375 | PF00069 | 0.596 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.464 |
MOD_N-GLC_1 | 157 | 162 | PF02516 | 0.492 |
MOD_N-GLC_2 | 147 | 149 | PF02516 | 0.323 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.341 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.398 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.558 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.645 |
MOD_NEK2_1 | 340 | 345 | PF00069 | 0.468 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.459 |
MOD_NEK2_1 | 74 | 79 | PF00069 | 0.474 |
MOD_PIKK_1 | 164 | 170 | PF00454 | 0.412 |
MOD_PIKK_1 | 198 | 204 | PF00454 | 0.524 |
MOD_PIKK_1 | 364 | 370 | PF00454 | 0.530 |
MOD_PIKK_1 | 74 | 80 | PF00454 | 0.474 |
MOD_PKA_2 | 288 | 294 | PF00069 | 0.412 |
MOD_PKA_2 | 368 | 374 | PF00069 | 0.654 |
MOD_PKB_1 | 122 | 130 | PF00069 | 0.309 |
MOD_Plk_1 | 157 | 163 | PF00069 | 0.422 |
MOD_Plk_1 | 194 | 200 | PF00069 | 0.403 |
MOD_Plk_1 | 4 | 10 | PF00069 | 0.574 |
MOD_Plk_1 | 400 | 406 | PF00069 | 0.333 |
MOD_Plk_2-3 | 218 | 224 | PF00069 | 0.443 |
MOD_Plk_2-3 | 391 | 397 | PF00069 | 0.421 |
MOD_Plk_4 | 132 | 138 | PF00069 | 0.355 |
MOD_Plk_4 | 157 | 163 | PF00069 | 0.441 |
MOD_Plk_4 | 171 | 177 | PF00069 | 0.301 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.406 |
MOD_Plk_4 | 194 | 200 | PF00069 | 0.403 |
MOD_Plk_4 | 340 | 346 | PF00069 | 0.509 |
MOD_Plk_4 | 349 | 355 | PF00069 | 0.478 |
MOD_Plk_4 | 400 | 406 | PF00069 | 0.466 |
MOD_ProDKin_1 | 248 | 254 | PF00069 | 0.253 |
MOD_ProDKin_1 | 354 | 360 | PF00069 | 0.436 |
MOD_ProDKin_1 | 369 | 375 | PF00069 | 0.658 |
MOD_SUMO_rev_2 | 56 | 61 | PF00179 | 0.508 |
TRG_DiLeu_BaEn_1 | 112 | 117 | PF01217 | 0.401 |
TRG_DiLeu_BaEn_1 | 401 | 406 | PF01217 | 0.605 |
TRG_DiLeu_LyEn_5 | 112 | 117 | PF01217 | 0.299 |
TRG_ENDOCYTIC_2 | 14 | 17 | PF00928 | 0.422 |
TRG_ENDOCYTIC_2 | 298 | 301 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 323 | 326 | PF00928 | 0.452 |
TRG_ENDOCYTIC_2 | 71 | 74 | PF00928 | 0.474 |
TRG_ER_diArg_1 | 226 | 228 | PF00400 | 0.350 |
TRG_ER_diArg_1 | 236 | 238 | PF00400 | 0.428 |
TRG_ER_diArg_1 | 296 | 298 | PF00400 | 0.508 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMA4 | Leptomonas seymouri | 50% | 100% |
A0A1X0P0E9 | Trypanosomatidae | 32% | 100% |
A0A3Q8ICF1 | Leishmania donovani | 69% | 100% |
A4HWQ8 | Leishmania infantum | 69% | 100% |
C9ZPS2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9AQG5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 65% | 100% |
Q4QF11 | Leishmania major | 70% | 100% |
V5ARD2 | Trypanosoma cruzi | 34% | 100% |