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:0030135 | coated vesicle | 7 | 12 |
GO:0030136 | clathrin-coated vesicle | 8 | 12 |
GO:0031410 | cytoplasmic vesicle | 6 | 12 |
GO:0031982 | vesicle | 4 | 12 |
GO:0043226 | organelle | 2 | 12 |
GO:0043227 | membrane-bounded organelle | 3 | 12 |
GO:0043229 | intracellular organelle | 3 | 12 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 12 |
GO:0097708 | intracellular vesicle | 5 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0000331 | contractile vacuole | 6 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005773 | vacuole | 5 | 1 |
GO:0005905 | clathrin-coated pit | 4 | 1 |
GO:0016020 | membrane | 2 | 1 |
GO:0098590 | plasma membrane region | 3 | 1 |
Related structures:
AlphaFold database: A0A3S5H7C6
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 12 |
GO:0006897 | endocytosis | 5 | 12 |
GO:0006898 | receptor-mediated endocytosis | 6 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016043 | cellular component organization | 3 | 12 |
GO:0016192 | vesicle-mediated transport | 4 | 12 |
GO:0022607 | cellular component assembly | 4 | 12 |
GO:0043933 | protein-containing complex organization | 4 | 12 |
GO:0048268 | clathrin coat assembly | 6 | 12 |
GO:0051179 | localization | 1 | 12 |
GO:0051234 | establishment of localization | 2 | 12 |
GO:0065003 | protein-containing complex assembly | 5 | 12 |
GO:0071840 | cellular component organization or biogenesis | 2 | 12 |
GO:0072583 | clathrin-dependent endocytosis | 7 | 12 |
GO:0006900 | vesicle budding from membrane | 5 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0016050 | vesicle organization | 5 | 1 |
GO:0061024 | membrane organization | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 12 |
GO:0005515 | protein binding | 2 | 12 |
GO:0005543 | phospholipid binding | 3 | 12 |
GO:0005545 | 1-phosphatidylinositol binding | 5 | 12 |
GO:0008289 | lipid binding | 2 | 12 |
GO:0030276 | clathrin binding | 3 | 12 |
GO:0035091 | phosphatidylinositol binding | 4 | 12 |
GO:0000149 | SNARE binding | 3 | 1 |
GO:0005546 | phosphatidylinositol-4,5-bisphosphate binding | 4 | 1 |
GO:0032050 | clathrin heavy chain binding | 4 | 1 |
GO:0043167 | ion binding | 2 | 1 |
GO:0043168 | anion binding | 3 | 1 |
GO:1901981 | phosphatidylinositol phosphate binding | 5 | 1 |
GO:1902936 | phosphatidylinositol bisphosphate binding | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 103 | 107 | PF00656 | 0.436 |
CLV_C14_Caspase3-7 | 129 | 133 | PF00656 | 0.397 |
CLV_NRD_NRD_1 | 161 | 163 | PF00675 | 0.404 |
CLV_NRD_NRD_1 | 254 | 256 | PF00675 | 0.381 |
CLV_PCSK_KEX2_1 | 161 | 163 | PF00082 | 0.392 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.415 |
CLV_PCSK_KEX2_1 | 246 | 248 | PF00082 | 0.277 |
CLV_PCSK_KEX2_1 | 254 | 256 | PF00082 | 0.378 |
CLV_PCSK_KEX2_1 | 80 | 82 | PF00082 | 0.307 |
CLV_PCSK_PC1ET2_1 | 229 | 231 | PF00082 | 0.415 |
CLV_PCSK_PC1ET2_1 | 246 | 248 | PF00082 | 0.428 |
CLV_PCSK_PC1ET2_1 | 80 | 82 | PF00082 | 0.307 |
CLV_PCSK_PC7_1 | 76 | 82 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 116 | 120 | PF00082 | 0.372 |
CLV_PCSK_SKI1_1 | 181 | 185 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 221 | 225 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 230 | 234 | PF00082 | 0.278 |
CLV_PCSK_SKI1_1 | 275 | 279 | PF00082 | 0.407 |
CLV_PCSK_SKI1_1 | 31 | 35 | PF00082 | 0.428 |
DEG_APCC_DBOX_1 | 274 | 282 | PF00400 | 0.377 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.583 |
DEG_SPOP_SBC_1 | 348 | 352 | PF00917 | 0.552 |
DOC_CDC14_PxL_1 | 278 | 286 | PF14671 | 0.377 |
DOC_MAPK_DCC_7 | 456 | 464 | PF00069 | 0.668 |
DOC_MAPK_gen_1 | 14 | 21 | PF00069 | 0.440 |
DOC_MAPK_MEF2A_6 | 181 | 190 | PF00069 | 0.240 |
DOC_MAPK_MEF2A_6 | 456 | 464 | PF00069 | 0.668 |
DOC_PP1_RVXF_1 | 227 | 234 | PF00149 | 0.345 |
DOC_PP2B_LxvP_1 | 364 | 367 | PF13499 | 0.625 |
DOC_PP2B_LxvP_1 | 41 | 44 | PF13499 | 0.323 |
DOC_PP4_FxxP_1 | 241 | 244 | PF00568 | 0.422 |
DOC_PP4_FxxP_1 | 277 | 280 | PF00568 | 0.342 |
DOC_PP4_FxxP_1 | 464 | 467 | PF00568 | 0.666 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.436 |
DOC_USP7_MATH_1 | 348 | 352 | PF00917 | 0.777 |
DOC_USP7_MATH_1 | 357 | 361 | PF00917 | 0.588 |
DOC_USP7_MATH_1 | 390 | 394 | PF00917 | 0.749 |
DOC_USP7_UBL2_3 | 31 | 35 | PF12436 | 0.428 |
DOC_USP7_UBL2_3 | 47 | 51 | PF12436 | 0.428 |
DOC_WW_Pin1_4 | 350 | 355 | PF00397 | 0.731 |
DOC_WW_Pin1_4 | 382 | 387 | PF00397 | 0.713 |
DOC_WW_Pin1_4 | 421 | 426 | PF00397 | 0.690 |
DOC_WW_Pin1_4 | 450 | 455 | PF00397 | 0.704 |
LIG_14-3-3_CanoR_1 | 254 | 263 | PF00244 | 0.392 |
LIG_14-3-3_CanoR_1 | 308 | 313 | PF00244 | 0.607 |
LIG_14-3-3_CanoR_1 | 81 | 90 | PF00244 | 0.325 |
LIG_Actin_WH2_2 | 165 | 183 | PF00022 | 0.240 |
LIG_ActinCP_TwfCPI_2 | 464 | 472 | PF01115 | 0.630 |
LIG_AP2alpha_2 | 469 | 471 | PF02296 | 0.592 |
LIG_BRCT_BRCA1_1 | 273 | 277 | PF00533 | 0.392 |
LIG_BRCT_BRCA1_1 | 397 | 401 | PF00533 | 0.699 |
LIG_EVH1_2 | 430 | 434 | PF00568 | 0.608 |
LIG_EVH1_2 | 460 | 464 | PF00568 | 0.671 |
LIG_FHA_1 | 16 | 22 | PF00498 | 0.559 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.140 |
LIG_FHA_1 | 370 | 376 | PF00498 | 0.686 |
LIG_FHA_2 | 143 | 149 | PF00498 | 0.428 |
LIG_FHA_2 | 291 | 297 | PF00498 | 0.471 |
LIG_FHA_2 | 325 | 331 | PF00498 | 0.709 |
LIG_LIR_Apic_2 | 239 | 244 | PF02991 | 0.422 |
LIG_LIR_Apic_2 | 274 | 280 | PF02991 | 0.392 |
LIG_LIR_Gen_1 | 211 | 217 | PF02991 | 0.326 |
LIG_LIR_Gen_1 | 236 | 244 | PF02991 | 0.342 |
LIG_LIR_Gen_1 | 258 | 267 | PF02991 | 0.341 |
LIG_LIR_Gen_1 | 84 | 95 | PF02991 | 0.307 |
LIG_LIR_Gen_1 | 96 | 104 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 141 | 146 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 167 | 171 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 211 | 216 | PF02991 | 0.316 |
LIG_LIR_Nem_3 | 236 | 241 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 251 | 256 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 258 | 263 | PF02991 | 0.297 |
LIG_LIR_Nem_3 | 469 | 474 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 56 | 60 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 84 | 90 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 96 | 100 | PF02991 | 0.307 |
LIG_LYPXL_S_1 | 447 | 451 | PF13949 | 0.662 |
LIG_LYPXL_yS_3 | 448 | 451 | PF13949 | 0.699 |
LIG_MYND_1 | 282 | 286 | PF01753 | 0.342 |
LIG_Pex14_1 | 249 | 253 | PF04695 | 0.307 |
LIG_SH2_CRK | 213 | 217 | PF00017 | 0.316 |
LIG_SH2_NCK_1 | 256 | 260 | PF00017 | 0.364 |
LIG_SH2_STAP1 | 256 | 260 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 12 | 15 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 138 | 141 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 146 | 149 | PF00017 | 0.275 |
LIG_SH2_STAT5 | 171 | 174 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 266 | 269 | PF00017 | 0.449 |
LIG_SH3_1 | 331 | 337 | PF00018 | 0.698 |
LIG_SH3_2 | 467 | 472 | PF14604 | 0.671 |
LIG_SH3_3 | 115 | 121 | PF00018 | 0.468 |
LIG_SH3_3 | 331 | 337 | PF00018 | 0.602 |
LIG_SH3_3 | 340 | 346 | PF00018 | 0.612 |
LIG_SH3_3 | 351 | 357 | PF00018 | 0.626 |
LIG_SH3_3 | 368 | 374 | PF00018 | 0.639 |
LIG_SH3_3 | 383 | 389 | PF00018 | 0.606 |
LIG_SH3_3 | 420 | 426 | PF00018 | 0.690 |
LIG_SH3_3 | 448 | 454 | PF00018 | 0.633 |
LIG_SH3_3 | 455 | 461 | PF00018 | 0.730 |
LIG_SH3_3 | 464 | 470 | PF00018 | 0.643 |
LIG_SUMO_SIM_par_1 | 87 | 93 | PF11976 | 0.323 |
LIG_TRAF2_1 | 367 | 370 | PF00917 | 0.714 |
LIG_UBA3_1 | 223 | 229 | PF00899 | 0.428 |
LIG_WRC_WIRS_1 | 21 | 26 | PF05994 | 0.580 |
LIG_WRC_WIRS_1 | 94 | 99 | PF05994 | 0.368 |
LIG_WW_3 | 333 | 337 | PF00397 | 0.728 |
MOD_CDC14_SPxK_1 | 453 | 456 | PF00782 | 0.581 |
MOD_CDK_SPxK_1 | 450 | 456 | PF00069 | 0.720 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.538 |
MOD_CK1_1 | 290 | 296 | PF00069 | 0.443 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.592 |
MOD_CK1_1 | 320 | 326 | PF00069 | 0.617 |
MOD_CK1_1 | 421 | 427 | PF00069 | 0.698 |
MOD_CK2_1 | 142 | 148 | PF00069 | 0.338 |
MOD_CK2_1 | 22 | 28 | PF00069 | 0.410 |
MOD_CK2_1 | 239 | 245 | PF00069 | 0.422 |
MOD_CK2_1 | 290 | 296 | PF00069 | 0.373 |
MOD_CK2_1 | 324 | 330 | PF00069 | 0.702 |
MOD_Cter_Amidation | 159 | 162 | PF01082 | 0.428 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.454 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.555 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.392 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.706 |
MOD_GlcNHglycan | 434 | 437 | PF01048 | 0.756 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.416 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.592 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.446 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.560 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.359 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.279 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.566 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.700 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.708 |
MOD_GSK3_1 | 410 | 417 | PF00069 | 0.703 |
MOD_N-GLC_1 | 1 | 6 | PF02516 | 0.637 |
MOD_N-GLC_1 | 421 | 426 | PF02516 | 0.568 |
MOD_N-GLC_2 | 206 | 208 | PF02516 | 0.323 |
MOD_NEK2_1 | 108 | 113 | PF00069 | 0.409 |
MOD_NEK2_1 | 152 | 157 | PF00069 | 0.331 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.361 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.340 |
MOD_NEK2_1 | 474 | 479 | PF00069 | 0.636 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.169 |
MOD_NEK2_2 | 259 | 264 | PF00069 | 0.428 |
MOD_PIKK_1 | 138 | 144 | PF00454 | 0.391 |
MOD_PIKK_1 | 365 | 371 | PF00454 | 0.618 |
MOD_PKA_2 | 299 | 305 | PF00069 | 0.470 |
MOD_Plk_1 | 239 | 245 | PF00069 | 0.350 |
MOD_Plk_1 | 320 | 326 | PF00069 | 0.695 |
MOD_Plk_2-3 | 239 | 245 | PF00069 | 0.415 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.334 |
MOD_Plk_4 | 266 | 272 | PF00069 | 0.346 |
MOD_Plk_4 | 287 | 293 | PF00069 | 0.342 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.323 |
MOD_ProDKin_1 | 350 | 356 | PF00069 | 0.727 |
MOD_ProDKin_1 | 382 | 388 | PF00069 | 0.710 |
MOD_ProDKin_1 | 421 | 427 | PF00069 | 0.688 |
MOD_ProDKin_1 | 450 | 456 | PF00069 | 0.703 |
MOD_SUMO_rev_2 | 3 | 9 | PF00179 | 0.537 |
MOD_SUMO_rev_2 | 323 | 333 | PF00179 | 0.714 |
TRG_DiLeu_BaEn_1 | 148 | 153 | PF01217 | 0.240 |
TRG_DiLeu_BaEn_1 | 211 | 216 | PF01217 | 0.428 |
TRG_ENDOCYTIC_2 | 115 | 118 | PF00928 | 0.428 |
TRG_ENDOCYTIC_2 | 213 | 216 | PF00928 | 0.330 |
TRG_ENDOCYTIC_2 | 448 | 451 | PF00928 | 0.699 |
TRG_ER_diArg_1 | 161 | 163 | PF00400 | 0.427 |
TRG_ER_diArg_1 | 253 | 255 | PF00400 | 0.349 |
TRG_Pf-PMV_PEXEL_1 | 150 | 154 | PF00026 | 0.306 |
TRG_Pf-PMV_PEXEL_1 | 285 | 289 | PF00026 | 0.394 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1II26 | Leptomonas seymouri | 58% | 100% |
A0A0S4J0L1 | Bodo saltans | 38% | 100% |
A0A1X0NIY0 | Trypanosomatidae | 42% | 97% |
A0A422P449 | Trypanosoma rangeli | 44% | 96% |
A4HD60 | Leishmania braziliensis | 72% | 99% |
A4I0M5 | Leishmania infantum | 98% | 100% |
D0A6X3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 98% |
E9AWJ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
P94017 | Arabidopsis thaliana | 23% | 70% |
Q4QAX8 | Leishmania major | 89% | 100% |
Q8LBH2 | Arabidopsis thaliana | 24% | 85% |
Q8VYT2 | Arabidopsis thaliana | 21% | 80% |
Q9LHS0 | Arabidopsis thaliana | 23% | 89% |
Q9LVD8 | Arabidopsis thaliana | 24% | 82% |
V5DSQ8 | Trypanosoma cruzi | 44% | 97% |