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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005840 | ribosome | 5 | 7 |
GO:0032991 | protein-containing complex | 1 | 7 |
GO:0043226 | organelle | 2 | 7 |
GO:0043228 | non-membrane-bounded organelle | 3 | 7 |
GO:0043229 | intracellular organelle | 3 | 7 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
GO:1990904 | ribonucleoprotein complex | 2 | 7 |
Related structures:
AlphaFold database: E9AGZ5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 282 | 286 | PF00656 | 0.651 |
CLV_NRD_NRD_1 | 325 | 327 | PF00675 | 0.683 |
CLV_NRD_NRD_1 | 94 | 96 | PF00675 | 0.427 |
CLV_PCSK_KEX2_1 | 325 | 327 | PF00082 | 0.683 |
CLV_PCSK_KEX2_1 | 94 | 96 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 325 | 329 | PF00082 | 0.623 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 406 | 410 | PF00082 | 0.390 |
CLV_PCSK_SKI1_1 | 424 | 428 | PF00082 | 0.396 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.462 |
DEG_SPOP_SBC_1 | 181 | 185 | PF00917 | 0.383 |
DOC_ANK_TNKS_1 | 258 | 265 | PF00023 | 0.568 |
DOC_CYCLIN_RxL_1 | 109 | 120 | PF00134 | 0.398 |
DOC_CYCLIN_RxL_1 | 370 | 382 | PF00134 | 0.392 |
DOC_PP1_RVXF_1 | 373 | 380 | PF00149 | 0.373 |
DOC_PP2B_LxvP_1 | 114 | 117 | PF13499 | 0.398 |
DOC_PP2B_LxvP_1 | 252 | 255 | PF13499 | 0.558 |
DOC_PP4_FxxP_1 | 238 | 241 | PF00568 | 0.411 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 207 | 211 | PF00917 | 0.362 |
DOC_USP7_MATH_1 | 255 | 259 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 287 | 291 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 342 | 346 | PF00917 | 0.356 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.612 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.391 |
DOC_WW_Pin1_4 | 418 | 423 | PF00397 | 0.390 |
LIG_14-3-3_CanoR_1 | 180 | 190 | PF00244 | 0.409 |
LIG_14-3-3_CanoR_1 | 209 | 214 | PF00244 | 0.404 |
LIG_14-3-3_CanoR_1 | 230 | 236 | PF00244 | 0.490 |
LIG_BRCT_BRCA1_1 | 14 | 18 | PF00533 | 0.380 |
LIG_BRCT_BRCA1_1 | 289 | 293 | PF00533 | 0.549 |
LIG_CSL_BTD_1 | 114 | 117 | PF09270 | 0.404 |
LIG_DLG_GKlike_1 | 209 | 217 | PF00625 | 0.481 |
LIG_FHA_1 | 164 | 170 | PF00498 | 0.445 |
LIG_FHA_1 | 181 | 187 | PF00498 | 0.412 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.380 |
LIG_FHA_1 | 400 | 406 | PF00498 | 0.443 |
LIG_FHA_1 | 443 | 449 | PF00498 | 0.535 |
LIG_FHA_1 | 8 | 14 | PF00498 | 0.401 |
LIG_FHA_2 | 160 | 166 | PF00498 | 0.508 |
LIG_FHA_2 | 183 | 189 | PF00498 | 0.361 |
LIG_FHA_2 | 199 | 205 | PF00498 | 0.351 |
LIG_FHA_2 | 22 | 28 | PF00498 | 0.495 |
LIG_FHA_2 | 232 | 238 | PF00498 | 0.491 |
LIG_FHA_2 | 32 | 38 | PF00498 | 0.375 |
LIG_FHA_2 | 385 | 391 | PF00498 | 0.362 |
LIG_FHA_2 | 427 | 433 | PF00498 | 0.373 |
LIG_FHA_2 | 79 | 85 | PF00498 | 0.493 |
LIG_LIR_Apic_2 | 236 | 241 | PF02991 | 0.422 |
LIG_LIR_Gen_1 | 74 | 82 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 74 | 80 | PF02991 | 0.482 |
LIG_Pex14_1 | 439 | 443 | PF04695 | 0.403 |
LIG_Pex14_2 | 349 | 353 | PF04695 | 0.351 |
LIG_SH2_CRK | 297 | 301 | PF00017 | 0.531 |
LIG_SH2_CRK | 77 | 81 | PF00017 | 0.490 |
LIG_SH2_SRC | 147 | 150 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 147 | 150 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 373 | 376 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 77 | 80 | PF00017 | 0.490 |
LIG_SH3_3 | 14 | 20 | PF00018 | 0.399 |
LIG_SH3_3 | 187 | 193 | PF00018 | 0.402 |
LIG_SH3_3 | 243 | 249 | PF00018 | 0.399 |
LIG_SUMO_SIM_anti_2 | 195 | 201 | PF11976 | 0.320 |
LIG_SUMO_SIM_par_1 | 244 | 250 | PF11976 | 0.447 |
LIG_SUMO_SIM_par_1 | 384 | 393 | PF11976 | 0.367 |
MOD_CDC14_SPxK_1 | 421 | 424 | PF00782 | 0.499 |
MOD_CDK_SPxK_1 | 418 | 424 | PF00069 | 0.477 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.382 |
MOD_CK1_1 | 267 | 273 | PF00069 | 0.714 |
MOD_CK1_1 | 288 | 294 | PF00069 | 0.490 |
MOD_CK1_1 | 389 | 395 | PF00069 | 0.399 |
MOD_CK1_1 | 418 | 424 | PF00069 | 0.396 |
MOD_CK2_1 | 153 | 159 | PF00069 | 0.600 |
MOD_CK2_1 | 198 | 204 | PF00069 | 0.350 |
MOD_CK2_1 | 21 | 27 | PF00069 | 0.493 |
MOD_CK2_1 | 231 | 237 | PF00069 | 0.495 |
MOD_CK2_1 | 390 | 396 | PF00069 | 0.369 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.379 |
MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.559 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.391 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.559 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.580 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.747 |
MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.627 |
MOD_GlcNHglycan | 317 | 320 | PF01048 | 0.702 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.439 |
MOD_GlcNHglycan | 417 | 420 | PF01048 | 0.364 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.387 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.594 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.478 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.615 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.401 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.462 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.729 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.375 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.450 |
MOD_GSK3_1 | 414 | 421 | PF00069 | 0.372 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.530 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.471 |
MOD_N-GLC_1 | 220 | 225 | PF02516 | 0.549 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.458 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.389 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.581 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.373 |
MOD_NEK2_1 | 414 | 419 | PF00069 | 0.371 |
MOD_NEK2_1 | 426 | 431 | PF00069 | 0.365 |
MOD_PIKK_1 | 49 | 55 | PF00454 | 0.498 |
MOD_PKA_1 | 325 | 331 | PF00069 | 0.607 |
MOD_PKA_2 | 123 | 129 | PF00069 | 0.594 |
MOD_PKA_2 | 179 | 185 | PF00069 | 0.404 |
MOD_PKA_2 | 325 | 331 | PF00069 | 0.607 |
MOD_Plk_1 | 220 | 226 | PF00069 | 0.549 |
MOD_Plk_1 | 37 | 43 | PF00069 | 0.411 |
MOD_Plk_1 | 390 | 396 | PF00069 | 0.369 |
MOD_Plk_1 | 84 | 90 | PF00069 | 0.477 |
MOD_Plk_2-3 | 159 | 165 | PF00069 | 0.514 |
MOD_Plk_4 | 12 | 18 | PF00069 | 0.406 |
MOD_Plk_4 | 75 | 81 | PF00069 | 0.603 |
MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.393 |
MOD_ProDKin_1 | 418 | 424 | PF00069 | 0.398 |
MOD_SUMO_rev_2 | 378 | 386 | PF00179 | 0.479 |
TRG_DiLeu_BaLyEn_6 | 227 | 232 | PF01217 | 0.503 |
TRG_ENDOCYTIC_2 | 297 | 300 | PF00928 | 0.532 |
TRG_ENDOCYTIC_2 | 77 | 80 | PF00928 | 0.490 |
TRG_ER_diArg_1 | 324 | 326 | PF00400 | 0.698 |
TRG_ER_diArg_1 | 93 | 95 | PF00400 | 0.422 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IM43 | Leptomonas seymouri | 68% | 100% |
A0A3S7WX82 | Leishmania donovani | 100% | 100% |
A4HCG2 | Leishmania braziliensis | 83% | 100% |
E9AVV7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4QBM2 | Leishmania major | 94% | 100% |