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:0005737 | cytoplasm | 2 | 1 |
GO:0005930 | axoneme | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HB14
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 12 |
GO:0005509 | calcium ion binding | 5 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043169 | cation binding | 3 | 12 |
GO:0046872 | metal ion binding | 4 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 309 | 313 | PF00656 | 0.328 |
CLV_NRD_NRD_1 | 103 | 105 | PF00675 | 0.414 |
CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.566 |
CLV_NRD_NRD_1 | 237 | 239 | PF00675 | 0.413 |
CLV_NRD_NRD_1 | 359 | 361 | PF00675 | 0.608 |
CLV_NRD_NRD_1 | 57 | 59 | PF00675 | 0.262 |
CLV_PCSK_KEX2_1 | 19 | 21 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 57 | 59 | PF00082 | 0.262 |
CLV_PCSK_PC1ET2_1 | 19 | 21 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 19 | 23 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 239 | 243 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 332 | 336 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 370 | 374 | PF00082 | 0.469 |
CLV_PCSK_SKI1_1 | 57 | 61 | PF00082 | 0.390 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.658 |
DOC_CYCLIN_RxL_1 | 16 | 26 | PF00134 | 0.434 |
DOC_CYCLIN_RxL_1 | 262 | 270 | PF00134 | 0.433 |
DOC_MAPK_gen_1 | 17 | 24 | PF00069 | 0.431 |
DOC_PP1_RVXF_1 | 17 | 24 | PF00149 | 0.443 |
DOC_PP2B_LxvP_1 | 296 | 299 | PF13499 | 0.505 |
DOC_PP2B_LxvP_1 | 323 | 326 | PF13499 | 0.459 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.461 |
DOC_USP7_MATH_1 | 202 | 206 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 263 | 267 | PF00917 | 0.461 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 299 | 303 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 326 | 330 | PF00917 | 0.428 |
DOC_WW_Pin1_4 | 23 | 28 | PF00397 | 0.608 |
DOC_WW_Pin1_4 | 324 | 329 | PF00397 | 0.491 |
DOC_WW_Pin1_4 | 363 | 368 | PF00397 | 0.601 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.389 |
LIG_Actin_WH2_2 | 88 | 106 | PF00022 | 0.486 |
LIG_BRCT_BRCA1_1 | 340 | 344 | PF00533 | 0.513 |
LIG_eIF4E_1 | 319 | 325 | PF01652 | 0.490 |
LIG_FHA_1 | 16 | 22 | PF00498 | 0.393 |
LIG_FHA_1 | 88 | 94 | PF00498 | 0.382 |
LIG_FHA_2 | 145 | 151 | PF00498 | 0.544 |
LIG_FHA_2 | 156 | 162 | PF00498 | 0.556 |
LIG_FHA_2 | 307 | 313 | PF00498 | 0.331 |
LIG_FHA_2 | 373 | 379 | PF00498 | 0.487 |
LIG_FHA_2 | 75 | 81 | PF00498 | 0.449 |
LIG_LIR_Apic_2 | 348 | 354 | PF02991 | 0.515 |
LIG_LIR_Gen_1 | 157 | 165 | PF02991 | 0.330 |
LIG_LIR_Gen_1 | 188 | 198 | PF02991 | 0.417 |
LIG_LIR_Gen_1 | 406 | 413 | PF02991 | 0.454 |
LIG_LIR_Gen_1 | 90 | 100 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 157 | 162 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 173 | 178 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 188 | 194 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 406 | 412 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 90 | 95 | PF02991 | 0.470 |
LIG_Pex14_1 | 340 | 344 | PF04695 | 0.486 |
LIG_Pex14_2 | 155 | 159 | PF04695 | 0.408 |
LIG_Pex14_2 | 373 | 377 | PF04695 | 0.404 |
LIG_RPA_C_Fungi | 233 | 245 | PF08784 | 0.536 |
LIG_SH2_CRK | 178 | 182 | PF00017 | 0.375 |
LIG_SH2_CRK | 351 | 355 | PF00017 | 0.505 |
LIG_SH2_STAP1 | 320 | 324 | PF00017 | 0.490 |
LIG_SH2_STAT3 | 396 | 399 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 297 | 300 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 396 | 399 | PF00017 | 0.428 |
LIG_SH3_1 | 361 | 367 | PF00018 | 0.337 |
LIG_SH3_3 | 295 | 301 | PF00018 | 0.307 |
LIG_SH3_3 | 361 | 367 | PF00018 | 0.337 |
LIG_SUMO_SIM_anti_2 | 187 | 196 | PF11976 | 0.392 |
LIG_SUMO_SIM_anti_2 | 90 | 97 | PF11976 | 0.475 |
LIG_SUMO_SIM_par_1 | 254 | 260 | PF11976 | 0.496 |
LIG_TRAF2_1 | 170 | 173 | PF00917 | 0.383 |
LIG_TRAF2_1 | 354 | 357 | PF00917 | 0.442 |
LIG_TRAF2_1 | 66 | 69 | PF00917 | 0.377 |
LIG_UBA3_1 | 75 | 84 | PF00899 | 0.475 |
LIG_WRC_WIRS_1 | 33 | 38 | PF05994 | 0.538 |
MOD_CDC14_SPxK_1 | 101 | 104 | PF00782 | 0.481 |
MOD_CDK_SPxK_1 | 98 | 104 | PF00069 | 0.383 |
MOD_CDK_SPxxK_3 | 363 | 370 | PF00069 | 0.593 |
MOD_CDK_SPxxK_3 | 98 | 105 | PF00069 | 0.425 |
MOD_CK1_1 | 157 | 163 | PF00069 | 0.466 |
MOD_CK1_1 | 222 | 228 | PF00069 | 0.603 |
MOD_CK2_1 | 144 | 150 | PF00069 | 0.535 |
MOD_CK2_1 | 155 | 161 | PF00069 | 0.484 |
MOD_CK2_1 | 167 | 173 | PF00069 | 0.393 |
MOD_CK2_1 | 225 | 231 | PF00069 | 0.544 |
MOD_CK2_1 | 299 | 305 | PF00069 | 0.539 |
MOD_CK2_1 | 49 | 55 | PF00069 | 0.396 |
MOD_CK2_1 | 63 | 69 | PF00069 | 0.308 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.484 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.548 |
MOD_GlcNHglycan | 259 | 262 | PF01048 | 0.378 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.448 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.524 |
MOD_GlcNHglycan | 399 | 402 | PF01048 | 0.493 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.392 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.423 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.482 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.496 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.470 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.479 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.444 |
MOD_N-GLC_1 | 63 | 68 | PF02516 | 0.437 |
MOD_N-GLC_1 | 98 | 103 | PF02516 | 0.472 |
MOD_NEK2_1 | 11 | 16 | PF00069 | 0.459 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.414 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.484 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.492 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.519 |
MOD_NEK2_1 | 46 | 51 | PF00069 | 0.458 |
MOD_PIKK_1 | 46 | 52 | PF00454 | 0.584 |
MOD_Plk_1 | 187 | 193 | PF00069 | 0.393 |
MOD_Plk_1 | 225 | 231 | PF00069 | 0.543 |
MOD_Plk_1 | 63 | 69 | PF00069 | 0.421 |
MOD_Plk_2-3 | 120 | 126 | PF00069 | 0.306 |
MOD_Plk_4 | 187 | 193 | PF00069 | 0.391 |
MOD_Plk_4 | 244 | 250 | PF00069 | 0.444 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.505 |
MOD_ProDKin_1 | 23 | 29 | PF00069 | 0.603 |
MOD_ProDKin_1 | 324 | 330 | PF00069 | 0.490 |
MOD_ProDKin_1 | 363 | 369 | PF00069 | 0.594 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.383 |
MOD_SUMO_rev_2 | 160 | 170 | PF00179 | 0.552 |
MOD_SUMO_rev_2 | 341 | 349 | PF00179 | 0.424 |
TRG_DiLeu_BaLyEn_6 | 17 | 22 | PF01217 | 0.403 |
TRG_ENDOCYTIC_2 | 178 | 181 | PF00928 | 0.375 |
TRG_ENDOCYTIC_2 | 320 | 323 | PF00928 | 0.372 |
TRG_ER_diArg_1 | 56 | 58 | PF00400 | 0.262 |
TRG_Pf-PMV_PEXEL_1 | 127 | 132 | PF00026 | 0.323 |
TRG_Pf-PMV_PEXEL_1 | 58 | 62 | PF00026 | 0.461 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2R2 | Leptomonas seymouri | 66% | 100% |
A0A0S4J207 | Bodo saltans | 33% | 97% |
A0A1X0PAP2 | Trypanosomatidae | 40% | 100% |
A0A3Q8IHP2 | Leishmania donovani | 84% | 100% |
A0A422N4H8 | Trypanosoma rangeli | 42% | 100% |
A4IA71 | Leishmania infantum | 84% | 100% |
C9ZM35 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
E9B584 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q4Q2P9 | Leishmania major | 83% | 100% |
V5B5A3 | Trypanosoma cruzi | 42% | 100% |