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: A4HD60
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 | 0.401 |
CLV_C14_Caspase3-7 | 129 | 133 | PF00656 | 0.343 |
CLV_C14_Caspase3-7 | 344 | 348 | PF00656 | 0.717 |
CLV_NRD_NRD_1 | 161 | 163 | PF00675 | 0.383 |
CLV_NRD_NRD_1 | 247 | 249 | PF00675 | 0.352 |
CLV_NRD_NRD_1 | 254 | 256 | PF00675 | 0.322 |
CLV_PCSK_FUR_1 | 159 | 163 | PF00082 | 0.165 |
CLV_PCSK_KEX2_1 | 120 | 122 | PF00082 | 0.406 |
CLV_PCSK_KEX2_1 | 161 | 163 | PF00082 | 0.370 |
CLV_PCSK_KEX2_1 | 221 | 223 | PF00082 | 0.305 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.369 |
CLV_PCSK_KEX2_1 | 246 | 248 | PF00082 | 0.243 |
CLV_PCSK_KEX2_1 | 254 | 256 | PF00082 | 0.318 |
CLV_PCSK_KEX2_1 | 80 | 82 | PF00082 | 0.243 |
CLV_PCSK_PC1ET2_1 | 120 | 122 | PF00082 | 0.406 |
CLV_PCSK_PC1ET2_1 | 221 | 223 | PF00082 | 0.305 |
CLV_PCSK_PC1ET2_1 | 229 | 231 | PF00082 | 0.369 |
CLV_PCSK_PC1ET2_1 | 246 | 248 | PF00082 | 0.388 |
CLV_PCSK_PC1ET2_1 | 80 | 82 | PF00082 | 0.243 |
CLV_PCSK_PC7_1 | 76 | 82 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 116 | 120 | PF00082 | 0.326 |
CLV_PCSK_SKI1_1 | 221 | 225 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 230 | 234 | PF00082 | 0.217 |
CLV_PCSK_SKI1_1 | 31 | 35 | PF00082 | 0.388 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.511 |
DOC_MAPK_DCC_7 | 189 | 199 | PF00069 | 0.165 |
DOC_MAPK_gen_1 | 14 | 21 | PF00069 | 0.373 |
DOC_MAPK_gen_1 | 246 | 252 | PF00069 | 0.249 |
DOC_PP1_RVXF_1 | 227 | 234 | PF00149 | 0.280 |
DOC_PP2B_LxvP_1 | 41 | 44 | PF13499 | 0.258 |
DOC_PP2B_LxvP_1 | 463 | 466 | PF13499 | 0.463 |
DOC_PP4_FxxP_1 | 241 | 244 | PF00568 | 0.412 |
DOC_PP4_FxxP_1 | 277 | 280 | PF00568 | 0.277 |
DOC_USP7_MATH_1 | 104 | 108 | PF00917 | 0.242 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.446 |
DOC_USP7_MATH_1 | 335 | 339 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 390 | 394 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 464 | 468 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.448 |
DOC_USP7_UBL2_3 | 116 | 120 | PF12436 | 0.249 |
DOC_USP7_UBL2_3 | 31 | 35 | PF12436 | 0.388 |
DOC_USP7_UBL2_3 | 47 | 51 | PF12436 | 0.388 |
DOC_WW_Pin1_4 | 350 | 355 | PF00397 | 0.675 |
DOC_WW_Pin1_4 | 458 | 463 | PF00397 | 0.658 |
LIG_14-3-3_CanoR_1 | 254 | 263 | PF00244 | 0.337 |
LIG_14-3-3_CanoR_1 | 81 | 90 | PF00244 | 0.260 |
LIG_AP2alpha_2 | 472 | 474 | PF02296 | 0.545 |
LIG_APCC_ABBA_1 | 471 | 476 | PF00400 | 0.510 |
LIG_BRCT_BRCA1_1 | 273 | 277 | PF00533 | 0.337 |
LIG_FHA_1 | 16 | 22 | PF00498 | 0.534 |
LIG_FHA_1 | 172 | 178 | PF00498 | 0.360 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.131 |
LIG_FHA_1 | 424 | 430 | PF00498 | 0.610 |
LIG_FHA_2 | 303 | 309 | PF00498 | 0.548 |
LIG_FHA_2 | 325 | 331 | PF00498 | 0.621 |
LIG_LIR_Apic_2 | 239 | 244 | PF02991 | 0.412 |
LIG_LIR_Apic_2 | 274 | 280 | PF02991 | 0.337 |
LIG_LIR_Gen_1 | 167 | 175 | PF02991 | 0.367 |
LIG_LIR_Gen_1 | 181 | 191 | PF02991 | 0.305 |
LIG_LIR_Gen_1 | 211 | 217 | PF02991 | 0.261 |
LIG_LIR_Gen_1 | 236 | 244 | PF02991 | 0.313 |
LIG_LIR_Gen_1 | 258 | 267 | PF02991 | 0.311 |
LIG_LIR_Gen_1 | 84 | 95 | PF02991 | 0.243 |
LIG_LIR_Gen_1 | 96 | 104 | PF02991 | 0.243 |
LIG_LIR_Nem_3 | 141 | 146 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 167 | 171 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 181 | 187 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 211 | 216 | PF02991 | 0.252 |
LIG_LIR_Nem_3 | 236 | 241 | PF02991 | 0.295 |
LIG_LIR_Nem_3 | 251 | 256 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 258 | 263 | PF02991 | 0.270 |
LIG_LIR_Nem_3 | 472 | 477 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 56 | 60 | PF02991 | 0.260 |
LIG_LIR_Nem_3 | 84 | 90 | PF02991 | 0.243 |
LIG_LIR_Nem_3 | 96 | 100 | PF02991 | 0.243 |
LIG_MYND_1 | 282 | 286 | PF01753 | 0.277 |
LIG_NRBOX | 186 | 192 | PF00104 | 0.291 |
LIG_PCNA_yPIPBox_3 | 27 | 35 | PF02747 | 0.165 |
LIG_Pex14_1 | 249 | 253 | PF04695 | 0.243 |
LIG_Rb_LxCxE_1 | 313 | 330 | PF01857 | 0.412 |
LIG_SH2_CRK | 115 | 119 | PF00017 | 0.307 |
LIG_SH2_CRK | 213 | 217 | PF00017 | 0.251 |
LIG_SH2_NCK_1 | 256 | 260 | PF00017 | 0.302 |
LIG_SH2_STAP1 | 256 | 260 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 12 | 15 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 146 | 149 | PF00017 | 0.254 |
LIG_SH2_STAT5 | 266 | 269 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 48 | 51 | PF00017 | 0.271 |
LIG_SH3_1 | 368 | 374 | PF00018 | 0.598 |
LIG_SH3_2 | 470 | 475 | PF14604 | 0.545 |
LIG_SH3_3 | 351 | 357 | PF00018 | 0.541 |
LIG_SH3_3 | 368 | 374 | PF00018 | 0.556 |
LIG_SH3_3 | 379 | 385 | PF00018 | 0.585 |
LIG_SH3_3 | 467 | 473 | PF00018 | 0.587 |
LIG_SUMO_SIM_par_1 | 87 | 93 | PF11976 | 0.258 |
LIG_TRAF2_1 | 327 | 330 | PF00917 | 0.501 |
LIG_TRAF2_1 | 367 | 370 | PF00917 | 0.560 |
LIG_UBA3_1 | 223 | 229 | PF00899 | 0.388 |
LIG_WRC_WIRS_1 | 21 | 26 | PF05994 | 0.435 |
LIG_WRC_WIRS_1 | 403 | 408 | PF05994 | 0.459 |
LIG_WRC_WIRS_1 | 94 | 99 | PF05994 | 0.306 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.503 |
MOD_CK1_1 | 302 | 308 | PF00069 | 0.561 |
MOD_CK1_1 | 383 | 389 | PF00069 | 0.707 |
MOD_CK1_1 | 458 | 464 | PF00069 | 0.581 |
MOD_CK2_1 | 104 | 110 | PF00069 | 0.463 |
MOD_CK2_1 | 239 | 245 | PF00069 | 0.380 |
MOD_CK2_1 | 302 | 308 | PF00069 | 0.577 |
MOD_CK2_1 | 324 | 330 | PF00069 | 0.657 |
MOD_CK2_1 | 364 | 370 | PF00069 | 0.451 |
MOD_Cter_Amidation | 159 | 162 | PF01082 | 0.388 |
MOD_Cter_Amidation | 219 | 222 | PF01082 | 0.217 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.241 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.308 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.521 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.334 |
MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.633 |
MOD_GlcNHglycan | 438 | 441 | PF01048 | 0.658 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.552 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.346 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.413 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.319 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.296 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.639 |
MOD_GSK3_1 | 418 | 425 | PF00069 | 0.629 |
MOD_N-GLC_1 | 1 | 6 | PF02516 | 0.593 |
MOD_N-GLC_1 | 409 | 414 | PF02516 | 0.476 |
MOD_N-GLC_1 | 447 | 452 | PF02516 | 0.524 |
MOD_N-GLC_2 | 206 | 208 | PF02516 | 0.258 |
MOD_NEK2_1 | 108 | 113 | PF00069 | 0.360 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.316 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.423 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.430 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.334 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.275 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.424 |
MOD_NEK2_1 | 427 | 432 | PF00069 | 0.672 |
MOD_NEK2_2 | 114 | 119 | PF00069 | 0.165 |
MOD_NEK2_2 | 259 | 264 | PF00069 | 0.388 |
MOD_PIKK_1 | 138 | 144 | PF00454 | 0.274 |
MOD_PKA_2 | 299 | 305 | PF00069 | 0.405 |
MOD_Plk_1 | 239 | 245 | PF00069 | 0.284 |
MOD_Plk_1 | 478 | 484 | PF00069 | 0.395 |
MOD_Plk_2-3 | 239 | 245 | PF00069 | 0.285 |
MOD_Plk_2-3 | 308 | 314 | PF00069 | 0.504 |
MOD_Plk_4 | 104 | 110 | PF00069 | 0.258 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.182 |
MOD_Plk_4 | 266 | 272 | PF00069 | 0.329 |
MOD_Plk_4 | 287 | 293 | PF00069 | 0.277 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.258 |
MOD_ProDKin_1 | 350 | 356 | PF00069 | 0.671 |
MOD_ProDKin_1 | 458 | 464 | PF00069 | 0.656 |
MOD_SUMO_rev_2 | 326 | 333 | PF00179 | 0.652 |
TRG_DiLeu_BaEn_1 | 211 | 216 | PF01217 | 0.388 |
TRG_DiLeu_BaEn_2 | 166 | 172 | PF01217 | 0.388 |
TRG_DiLeu_BaLyEn_6 | 186 | 191 | PF01217 | 0.279 |
TRG_DiLeu_BaLyEn_6 | 96 | 101 | PF01217 | 0.307 |
TRG_ENDOCYTIC_2 | 115 | 118 | PF00928 | 0.388 |
TRG_ENDOCYTIC_2 | 213 | 216 | PF00928 | 0.301 |
TRG_ER_diArg_1 | 121 | 124 | PF00400 | 0.165 |
TRG_ER_diArg_1 | 159 | 162 | PF00400 | 0.416 |
TRG_ER_diArg_1 | 247 | 249 | PF00400 | 0.325 |
TRG_ER_diArg_1 | 253 | 255 | PF00400 | 0.284 |
TRG_NES_CRM1_1 | 178 | 192 | PF08389 | 0.192 |
TRG_Pf-PMV_PEXEL_1 | 99 | 103 | PF00026 | 0.307 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1II26 | Leptomonas seymouri | 59% | 100% |
A0A0S4J0L1 | Bodo saltans | 35% | 100% |
A0A1X0NIY0 | Trypanosomatidae | 40% | 97% |
A0A3S5H7C6 | Leishmania donovani | 72% | 100% |
A0A422P449 | Trypanosoma rangeli | 42% | 97% |
A4I0M5 | Leishmania infantum | 72% | 100% |
D0A6X3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 99% |
E9AWJ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 100% |
P94017 | Arabidopsis thaliana | 24% | 70% |
Q4QAX8 | Leishmania major | 70% | 98% |
Q8LBH2 | Arabidopsis thaliana | 25% | 85% |
Q9LHS0 | Arabidopsis thaliana | 23% | 89% |
V5DSQ8 | Trypanosoma cruzi | 42% | 97% |