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: 10, no: 0 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
Related structures:
AlphaFold database: A4I402
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.702 |
CLV_NRD_NRD_1 | 310 | 312 | PF00675 | 0.429 |
CLV_NRD_NRD_1 | 326 | 328 | PF00675 | 0.448 |
CLV_NRD_NRD_1 | 338 | 340 | PF00675 | 0.301 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.722 |
CLV_PCSK_KEX2_1 | 326 | 328 | PF00082 | 0.504 |
CLV_PCSK_KEX2_1 | 337 | 339 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 192 | 196 | PF00082 | 0.637 |
CLV_PCSK_SKI1_1 | 352 | 356 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 357 | 361 | PF00082 | 0.373 |
CLV_PCSK_SKI1_1 | 6 | 10 | PF00082 | 0.667 |
DEG_APCC_DBOX_1 | 326 | 334 | PF00400 | 0.707 |
DEG_SPOP_SBC_1 | 118 | 122 | PF00917 | 0.542 |
DEG_SPOP_SBC_1 | 232 | 236 | PF00917 | 0.495 |
DOC_CYCLIN_RxL_1 | 3 | 11 | PF00134 | 0.568 |
DOC_MAPK_DCC_7 | 274 | 282 | PF00069 | 0.432 |
DOC_MAPK_gen_1 | 274 | 282 | PF00069 | 0.432 |
DOC_MAPK_MEF2A_6 | 276 | 284 | PF00069 | 0.447 |
DOC_PP1_RVXF_1 | 131 | 138 | PF00149 | 0.313 |
DOC_PP4_FxxP_1 | 137 | 140 | PF00568 | 0.299 |
DOC_PP4_FxxP_1 | 359 | 362 | PF00568 | 0.762 |
DOC_USP7_MATH_1 | 232 | 236 | PF00917 | 0.419 |
DOC_USP7_MATH_1 | 260 | 264 | PF00917 | 0.358 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.473 |
DOC_USP7_MATH_1 | 353 | 357 | PF00917 | 0.681 |
DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.548 |
DOC_WW_Pin1_4 | 136 | 141 | PF00397 | 0.372 |
DOC_WW_Pin1_4 | 292 | 297 | PF00397 | 0.480 |
DOC_WW_Pin1_4 | 93 | 98 | PF00397 | 0.504 |
LIG_14-3-3_CanoR_1 | 106 | 116 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 206 | 215 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 327 | 335 | PF00244 | 0.675 |
LIG_14-3-3_CanoR_1 | 338 | 344 | PF00244 | 0.691 |
LIG_APCC_ABBA_1 | 138 | 143 | PF00400 | 0.396 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.683 |
LIG_BRCT_BRCA1_1 | 298 | 302 | PF00533 | 0.402 |
LIG_BRCT_BRCA1_1 | 355 | 359 | PF00533 | 0.678 |
LIG_BRCT_BRCA1_1 | 64 | 68 | PF00533 | 0.436 |
LIG_deltaCOP1_diTrp_1 | 46 | 52 | PF00928 | 0.393 |
LIG_FHA_1 | 188 | 194 | PF00498 | 0.369 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.224 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.464 |
LIG_FHA_2 | 173 | 179 | PF00498 | 0.458 |
LIG_FHA_2 | 197 | 203 | PF00498 | 0.424 |
LIG_FHA_2 | 205 | 211 | PF00498 | 0.382 |
LIG_LIR_Apic_2 | 356 | 362 | PF02991 | 0.747 |
LIG_LIR_Gen_1 | 290 | 298 | PF02991 | 0.284 |
LIG_LIR_Gen_1 | 299 | 310 | PF02991 | 0.340 |
LIG_LIR_Gen_1 | 66 | 77 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 131 | 137 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 181 | 187 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 290 | 294 | PF02991 | 0.284 |
LIG_LIR_Nem_3 | 299 | 305 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 66 | 72 | PF02991 | 0.381 |
LIG_Pex14_1 | 134 | 138 | PF04695 | 0.329 |
LIG_Pex14_1 | 64 | 68 | PF04695 | 0.420 |
LIG_SH2_CRK | 184 | 188 | PF00017 | 0.390 |
LIG_SH2_SRC | 266 | 269 | PF00017 | 0.413 |
LIG_SH2_STAP1 | 130 | 134 | PF00017 | 0.357 |
LIG_SH2_STAP1 | 208 | 212 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 184 | 187 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 208 | 211 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 266 | 269 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 348 | 351 | PF00017 | 0.665 |
LIG_SH3_1 | 347 | 353 | PF00018 | 0.654 |
LIG_SH3_2 | 350 | 355 | PF14604 | 0.711 |
LIG_SH3_3 | 157 | 163 | PF00018 | 0.451 |
LIG_SH3_3 | 347 | 353 | PF00018 | 0.651 |
LIG_SH3_3 | 359 | 365 | PF00018 | 0.748 |
LIG_SUMO_SIM_anti_2 | 15 | 21 | PF11976 | 0.559 |
LIG_SUMO_SIM_par_1 | 77 | 82 | PF11976 | 0.399 |
LIG_TYR_ITIM | 182 | 187 | PF00017 | 0.373 |
LIG_UBA3_1 | 283 | 289 | PF00899 | 0.476 |
LIG_UBA3_1 | 306 | 312 | PF00899 | 0.441 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.502 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.502 |
MOD_CK2_1 | 172 | 178 | PF00069 | 0.408 |
MOD_CK2_1 | 204 | 210 | PF00069 | 0.378 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.691 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.550 |
MOD_GlcNHglycan | 218 | 222 | PF01048 | 0.597 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.643 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.607 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.619 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.530 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.581 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.447 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.412 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.366 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.305 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.436 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.444 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.416 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.342 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.747 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.565 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.657 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.565 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.520 |
MOD_N-GLC_1 | 156 | 161 | PF02516 | 0.582 |
MOD_N-GLC_1 | 196 | 201 | PF02516 | 0.545 |
MOD_N-GLC_1 | 246 | 251 | PF02516 | 0.647 |
MOD_N-GLC_1 | 296 | 301 | PF02516 | 0.402 |
MOD_N-GLC_1 | 313 | 318 | PF02516 | 0.498 |
MOD_N-GLC_1 | 328 | 333 | PF02516 | 0.502 |
MOD_NEK2_1 | 112 | 117 | PF00069 | 0.527 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.578 |
MOD_NEK2_1 | 165 | 170 | PF00069 | 0.472 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.346 |
MOD_NEK2_1 | 283 | 288 | PF00069 | 0.500 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.486 |
MOD_NEK2_1 | 320 | 325 | PF00069 | 0.654 |
MOD_NEK2_1 | 343 | 348 | PF00069 | 0.683 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.380 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.571 |
MOD_NEK2_2 | 128 | 133 | PF00069 | 0.323 |
MOD_NEK2_2 | 64 | 69 | PF00069 | 0.330 |
MOD_PIKK_1 | 107 | 113 | PF00454 | 0.516 |
MOD_PIKK_1 | 165 | 171 | PF00454 | 0.432 |
MOD_PKB_1 | 337 | 345 | PF00069 | 0.722 |
MOD_Plk_1 | 156 | 162 | PF00069 | 0.412 |
MOD_Plk_1 | 296 | 302 | PF00069 | 0.402 |
MOD_Plk_1 | 328 | 334 | PF00069 | 0.702 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.433 |
MOD_Plk_4 | 178 | 184 | PF00069 | 0.404 |
MOD_Plk_4 | 296 | 302 | PF00069 | 0.402 |
MOD_Plk_4 | 339 | 345 | PF00069 | 0.721 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.376 |
MOD_Plk_4 | 8 | 14 | PF00069 | 0.552 |
MOD_ProDKin_1 | 136 | 142 | PF00069 | 0.376 |
MOD_ProDKin_1 | 292 | 298 | PF00069 | 0.480 |
MOD_ProDKin_1 | 93 | 99 | PF00069 | 0.504 |
TRG_DiLeu_BaEn_1 | 178 | 183 | PF01217 | 0.321 |
TRG_DiLeu_BaLyEn_6 | 75 | 80 | PF01217 | 0.291 |
TRG_ENDOCYTIC_2 | 184 | 187 | PF00928 | 0.365 |
TRG_ENDOCYTIC_2 | 348 | 351 | PF00928 | 0.731 |
TRG_ER_diArg_1 | 3 | 6 | PF00400 | 0.665 |
TRG_ER_diArg_1 | 325 | 327 | PF00400 | 0.702 |
TRG_ER_diArg_1 | 337 | 339 | PF00400 | 0.504 |
TRG_ER_diArg_1 | 365 | 368 | PF00400 | 0.782 |
TRG_Pf-PMV_PEXEL_1 | 106 | 111 | PF00026 | 0.620 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3M3 | Leptomonas seymouri | 48% | 99% |
A0A1X0NQJ6 | Trypanosomatidae | 35% | 100% |
A0A3S7X1V5 | Leishmania donovani | 99% | 100% |
A0A422MSP0 | Trypanosoma rangeli | 36% | 100% |
A4HGX2 | Leishmania braziliensis | 70% | 100% |
D0A972 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9B092 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4Q7Z3 | Leishmania major | 88% | 99% |
V5AWR0 | Trypanosoma cruzi | 36% | 100% |