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:0016020 | membrane | 2 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0000331 | contractile vacuole | 6 | 1 |
GO:0005739 | mitochondrion | 5 | 1 |
GO:0005741 | mitochondrial outer membrane | 5 | 1 |
GO:0005773 | vacuole | 5 | 1 |
GO:0019867 | outer membrane | 3 | 1 |
GO:0031090 | organelle membrane | 3 | 1 |
GO:0031410 | cytoplasmic vesicle | 6 | 1 |
GO:0031966 | mitochondrial membrane | 4 | 1 |
GO:0031968 | organelle outer membrane | 4 | 1 |
GO:0031982 | vesicle | 4 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0097708 | intracellular vesicle | 5 | 1 |
GO:0098588 | bounding membrane of organelle | 4 | 1 |
Related structures:
AlphaFold database: A4HLV8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 314 | 316 | PF00675 | 0.630 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.461 |
CLV_PCSK_KEX2_1 | 314 | 316 | PF00082 | 0.630 |
CLV_PCSK_KEX2_1 | 81 | 83 | PF00082 | 0.391 |
CLV_PCSK_PC1ET2_1 | 138 | 140 | PF00082 | 0.435 |
CLV_PCSK_PC1ET2_1 | 81 | 83 | PF00082 | 0.447 |
CLV_PCSK_PC7_1 | 310 | 316 | PF00082 | 0.645 |
CLV_PCSK_SKI1_1 | 139 | 143 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 237 | 241 | PF00082 | 0.672 |
CLV_PCSK_SKI1_1 | 288 | 292 | PF00082 | 0.596 |
CLV_PCSK_SKI1_1 | 82 | 86 | PF00082 | 0.387 |
DEG_SCF_FBW7_1 | 214 | 221 | PF00400 | 0.371 |
DOC_CKS1_1 | 215 | 220 | PF01111 | 0.508 |
DOC_CYCLIN_yCln2_LP_2 | 127 | 133 | PF00134 | 0.223 |
DOC_MAPK_gen_1 | 27 | 37 | PF00069 | 0.381 |
DOC_MAPK_gen_1 | 303 | 313 | PF00069 | 0.456 |
DOC_MAPK_HePTP_8 | 109 | 121 | PF00069 | 0.223 |
DOC_MAPK_MEF2A_6 | 112 | 121 | PF00069 | 0.313 |
DOC_MAPK_MEF2A_6 | 231 | 240 | PF00069 | 0.407 |
DOC_MAPK_MEF2A_6 | 384 | 392 | PF00069 | 0.479 |
DOC_PP1_RVXF_1 | 144 | 151 | PF00149 | 0.546 |
DOC_PP1_RVXF_1 | 301 | 308 | PF00149 | 0.451 |
DOC_PP2B_LxvP_1 | 134 | 137 | PF13499 | 0.462 |
DOC_PP2B_LxvP_1 | 140 | 143 | PF13499 | 0.563 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.511 |
DOC_USP7_MATH_1 | 218 | 222 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 226 | 230 | PF00917 | 0.418 |
DOC_USP7_MATH_1 | 318 | 322 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.651 |
DOC_WW_Pin1_4 | 214 | 219 | PF00397 | 0.421 |
DOC_WW_Pin1_4 | 222 | 227 | PF00397 | 0.492 |
DOC_WW_Pin1_4 | 383 | 388 | PF00397 | 0.398 |
LIG_14-3-3_CanoR_1 | 194 | 200 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 361 | 366 | PF00244 | 0.405 |
LIG_14-3-3_CanoR_1 | 87 | 96 | PF00244 | 0.508 |
LIG_Actin_WH2_2 | 14 | 32 | PF00022 | 0.450 |
LIG_DLG_GKlike_1 | 30 | 37 | PF00625 | 0.362 |
LIG_FHA_1 | 103 | 109 | PF00498 | 0.377 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.396 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.272 |
LIG_FHA_1 | 247 | 253 | PF00498 | 0.379 |
LIG_FHA_1 | 261 | 267 | PF00498 | 0.369 |
LIG_FHA_1 | 72 | 78 | PF00498 | 0.624 |
LIG_FHA_1 | 91 | 97 | PF00498 | 0.194 |
LIG_LIR_Gen_1 | 224 | 232 | PF02991 | 0.339 |
LIG_LIR_Gen_1 | 332 | 341 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 224 | 230 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 298 | 302 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 332 | 336 | PF02991 | 0.468 |
LIG_MAD2 | 379 | 387 | PF02301 | 0.322 |
LIG_SH2_CRK | 302 | 306 | PF00017 | 0.454 |
LIG_SH2_CRK | 31 | 35 | PF00017 | 0.449 |
LIG_SH2_NCK_1 | 94 | 98 | PF00017 | 0.388 |
LIG_SH2_SRC | 113 | 116 | PF00017 | 0.286 |
LIG_SH2_STAP1 | 339 | 343 | PF00017 | 0.458 |
LIG_SH2_STAP1 | 40 | 44 | PF00017 | 0.464 |
LIG_SH2_STAP1 | 94 | 98 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 191 | 194 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.307 |
LIG_SH2_STAT5 | 299 | 302 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 359 | 362 | PF00017 | 0.376 |
LIG_SH3_1 | 112 | 118 | PF00018 | 0.467 |
LIG_SH3_3 | 112 | 118 | PF00018 | 0.362 |
LIG_SH3_3 | 212 | 218 | PF00018 | 0.449 |
LIG_SH3_3 | 220 | 226 | PF00018 | 0.427 |
LIG_Sin3_3 | 124 | 131 | PF02671 | 0.223 |
LIG_SUMO_SIM_anti_2 | 211 | 217 | PF11976 | 0.449 |
LIG_SUMO_SIM_anti_2 | 33 | 38 | PF11976 | 0.413 |
LIG_SUMO_SIM_anti_2 | 64 | 72 | PF11976 | 0.505 |
LIG_SUMO_SIM_par_1 | 99 | 106 | PF11976 | 0.475 |
LIG_TRFH_1 | 159 | 163 | PF08558 | 0.449 |
LIG_TYR_ITIM | 29 | 34 | PF00017 | 0.449 |
LIG_TYR_ITIM | 300 | 305 | PF00017 | 0.595 |
LIG_UBA3_1 | 132 | 138 | PF00899 | 0.405 |
MOD_CDK_SPK_2 | 214 | 219 | PF00069 | 0.353 |
MOD_CK1_1 | 153 | 159 | PF00069 | 0.453 |
MOD_CK1_1 | 221 | 227 | PF00069 | 0.528 |
MOD_CK1_1 | 337 | 343 | PF00069 | 0.625 |
MOD_CK1_1 | 386 | 392 | PF00069 | 0.570 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.692 |
MOD_CK1_1 | 88 | 94 | PF00069 | 0.391 |
MOD_CK2_1 | 17 | 23 | PF00069 | 0.646 |
MOD_CK2_1 | 226 | 232 | PF00069 | 0.544 |
MOD_CK2_1 | 62 | 68 | PF00069 | 0.503 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.449 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.384 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.423 |
MOD_GlcNHglycan | 232 | 236 | PF01048 | 0.521 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.563 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.672 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.612 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.449 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.584 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.396 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.324 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.300 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.377 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.586 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.566 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.409 |
MOD_N-GLC_1 | 337 | 342 | PF02516 | 0.671 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.255 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.339 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.463 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.539 |
MOD_NEK2_1 | 391 | 396 | PF00069 | 0.667 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.455 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.326 |
MOD_NEK2_2 | 226 | 231 | PF00069 | 0.409 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.515 |
MOD_PIKK_1 | 318 | 324 | PF00454 | 0.609 |
MOD_PIKK_1 | 71 | 77 | PF00454 | 0.618 |
MOD_PKA_2 | 280 | 286 | PF00069 | 0.474 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.657 |
MOD_Plk_1 | 337 | 343 | PF00069 | 0.643 |
MOD_Plk_4 | 150 | 156 | PF00069 | 0.434 |
MOD_Plk_4 | 168 | 174 | PF00069 | 0.316 |
MOD_Plk_4 | 295 | 301 | PF00069 | 0.567 |
MOD_Plk_4 | 30 | 36 | PF00069 | 0.251 |
MOD_Plk_4 | 329 | 335 | PF00069 | 0.623 |
MOD_Plk_4 | 349 | 355 | PF00069 | 0.311 |
MOD_Plk_4 | 361 | 367 | PF00069 | 0.457 |
MOD_Plk_4 | 370 | 376 | PF00069 | 0.580 |
MOD_Plk_4 | 386 | 392 | PF00069 | 0.517 |
MOD_ProDKin_1 | 214 | 220 | PF00069 | 0.435 |
MOD_ProDKin_1 | 222 | 228 | PF00069 | 0.622 |
MOD_ProDKin_1 | 383 | 389 | PF00069 | 0.502 |
TRG_DiLeu_BaLyEn_6 | 143 | 148 | PF01217 | 0.529 |
TRG_DiLeu_BaLyEn_6 | 307 | 312 | PF01217 | 0.565 |
TRG_ENDOCYTIC_2 | 302 | 305 | PF00928 | 0.573 |
TRG_ENDOCYTIC_2 | 31 | 34 | PF00928 | 0.425 |
TRG_ER_diArg_1 | 313 | 315 | PF00400 | 0.541 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2S4 | Leptomonas seymouri | 68% | 100% |
A0A0S4KLU0 | Bodo saltans | 32% | 100% |
A0A1X0P431 | Trypanosomatidae | 42% | 100% |
A0A3Q8IMM4 | Leishmania donovani | 80% | 100% |
A0A422P095 | Trypanosoma rangeli | 43% | 100% |
D0A664 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9AHR5 | Leishmania infantum | 80% | 100% |
E9B486 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
Q4Q3U0 | Leishmania major | 80% | 100% |
V5B8N1 | Trypanosoma cruzi | 44% | 100% |