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: 15 |
NetGPI | no | yes: 0, no: 15 |
Related structures:
AlphaFold database: E9AH12
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 16 |
GO:0005488 | binding | 1 | 16 |
GO:0036094 | small molecule binding | 2 | 16 |
GO:0097159 | organic cyclic compound binding | 2 | 16 |
GO:1901265 | nucleoside phosphate binding | 3 | 16 |
GO:1901363 | heterocyclic compound binding | 2 | 16 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 123 | 125 | PF00675 | 0.283 |
CLV_NRD_NRD_1 | 219 | 221 | PF00675 | 0.363 |
CLV_NRD_NRD_1 | 412 | 414 | PF00675 | 0.404 |
CLV_PCSK_KEX2_1 | 219 | 221 | PF00082 | 0.363 |
CLV_PCSK_SKI1_1 | 102 | 106 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 189 | 193 | PF00082 | 0.292 |
CLV_PCSK_SKI1_1 | 219 | 223 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 22 | 26 | PF00082 | 0.407 |
CLV_PCSK_SKI1_1 | 259 | 263 | PF00082 | 0.325 |
CLV_PCSK_SKI1_1 | 347 | 351 | PF00082 | 0.471 |
DEG_APCC_DBOX_1 | 258 | 266 | PF00400 | 0.338 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.395 |
DOC_MAPK_gen_1 | 22 | 32 | PF00069 | 0.409 |
DOC_MAPK_MEF2A_6 | 25 | 32 | PF00069 | 0.412 |
DOC_PP1_RVXF_1 | 69 | 75 | PF00149 | 0.360 |
DOC_PP4_FxxP_1 | 267 | 270 | PF00568 | 0.382 |
DOC_PP4_FxxP_1 | 353 | 356 | PF00568 | 0.432 |
DOC_USP7_MATH_1 | 285 | 289 | PF00917 | 0.461 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.362 |
DOC_USP7_MATH_1 | 356 | 360 | PF00917 | 0.596 |
DOC_USP7_MATH_1 | 412 | 416 | PF00917 | 0.490 |
DOC_USP7_UBL2_3 | 105 | 109 | PF12436 | 0.195 |
DOC_WW_Pin1_4 | 172 | 177 | PF00397 | 0.396 |
DOC_WW_Pin1_4 | 227 | 232 | PF00397 | 0.470 |
DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.408 |
DOC_WW_Pin1_4 | 333 | 338 | PF00397 | 0.393 |
DOC_WW_Pin1_4 | 58 | 63 | PF00397 | 0.518 |
LIG_14-3-3_CanoR_1 | 219 | 224 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 233 | 242 | PF00244 | 0.214 |
LIG_14-3-3_CanoR_1 | 413 | 417 | PF00244 | 0.433 |
LIG_APCC_ABBAyCdc20_2 | 189 | 195 | PF00400 | 0.254 |
LIG_Clathr_ClatBox_1 | 191 | 195 | PF01394 | 0.300 |
LIG_deltaCOP1_diTrp_1 | 252 | 261 | PF00928 | 0.302 |
LIG_deltaCOP1_diTrp_1 | 410 | 416 | PF00928 | 0.475 |
LIG_FHA_1 | 113 | 119 | PF00498 | 0.334 |
LIG_FHA_1 | 333 | 339 | PF00498 | 0.389 |
LIG_FHA_1 | 416 | 422 | PF00498 | 0.363 |
LIG_FHA_1 | 67 | 73 | PF00498 | 0.436 |
LIG_FHA_2 | 128 | 134 | PF00498 | 0.308 |
LIG_FHA_2 | 149 | 155 | PF00498 | 0.338 |
LIG_GBD_Chelix_1 | 273 | 281 | PF00786 | 0.369 |
LIG_LIR_Apic_2 | 266 | 270 | PF02991 | 0.427 |
LIG_LIR_Apic_2 | 352 | 356 | PF02991 | 0.364 |
LIG_LIR_Gen_1 | 130 | 135 | PF02991 | 0.315 |
LIG_LIR_Gen_1 | 141 | 149 | PF02991 | 0.274 |
LIG_LIR_Gen_1 | 260 | 269 | PF02991 | 0.370 |
LIG_LIR_Gen_1 | 27 | 37 | PF02991 | 0.570 |
LIG_LIR_Gen_1 | 302 | 313 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 130 | 134 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 141 | 147 | PF02991 | 0.274 |
LIG_LIR_Nem_3 | 252 | 258 | PF02991 | 0.311 |
LIG_LIR_Nem_3 | 27 | 32 | PF02991 | 0.572 |
LIG_LIR_Nem_3 | 302 | 308 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 383 | 389 | PF02991 | 0.377 |
LIG_MYND_1 | 242 | 246 | PF01753 | 0.406 |
LIG_Pex14_2 | 223 | 227 | PF04695 | 0.314 |
LIG_Pex14_2 | 308 | 312 | PF04695 | 0.366 |
LIG_SH2_CRK | 144 | 148 | PF00017 | 0.386 |
LIG_SH2_SRC | 131 | 134 | PF00017 | 0.268 |
LIG_SH2_STAP1 | 131 | 135 | PF00017 | 0.300 |
LIG_SH2_STAP1 | 305 | 309 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 204 | 207 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 307 | 310 | PF00017 | 0.397 |
LIG_SH3_3 | 368 | 374 | PF00018 | 0.524 |
LIG_SUMO_SIM_anti_2 | 137 | 144 | PF11976 | 0.348 |
LIG_SUMO_SIM_par_1 | 29 | 36 | PF11976 | 0.410 |
LIG_SUMO_SIM_par_1 | 8 | 14 | PF11976 | 0.609 |
LIG_TYR_ITIM | 142 | 147 | PF00017 | 0.300 |
LIG_WRC_WIRS_1 | 224 | 229 | PF05994 | 0.330 |
LIG_WRC_WIRS_1 | 258 | 263 | PF05994 | 0.406 |
LIG_WRC_WIRS_1 | 286 | 291 | PF05994 | 0.517 |
LIG_WRC_WIRS_1 | 309 | 314 | PF05994 | 0.348 |
MOD_CDC14_SPxK_1 | 230 | 233 | PF00782 | 0.373 |
MOD_CDK_SPxK_1 | 227 | 233 | PF00069 | 0.361 |
MOD_CK1_1 | 311 | 317 | PF00069 | 0.323 |
MOD_CK1_1 | 336 | 342 | PF00069 | 0.456 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.530 |
MOD_CK1_1 | 415 | 421 | PF00069 | 0.449 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.495 |
MOD_CK2_1 | 127 | 133 | PF00069 | 0.336 |
MOD_CK2_1 | 148 | 154 | PF00069 | 0.399 |
MOD_CK2_1 | 178 | 184 | PF00069 | 0.364 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.374 |
MOD_GlcNHglycan | 322 | 325 | PF01048 | 0.402 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.563 |
MOD_GlcNHglycan | 396 | 400 | PF01048 | 0.528 |
MOD_GlcNHglycan | 427 | 430 | PF01048 | 0.412 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.120 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.352 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.404 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.378 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.287 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.351 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.311 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.317 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.496 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.427 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.310 |
MOD_NEK2_1 | 194 | 199 | PF00069 | 0.306 |
MOD_NEK2_1 | 223 | 228 | PF00069 | 0.363 |
MOD_NEK2_1 | 308 | 313 | PF00069 | 0.346 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.395 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.406 |
MOD_NEK2_1 | 380 | 385 | PF00069 | 0.366 |
MOD_NEK2_1 | 425 | 430 | PF00069 | 0.397 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.348 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.358 |
MOD_NEK2_2 | 100 | 105 | PF00069 | 0.203 |
MOD_NEK2_2 | 114 | 119 | PF00069 | 0.168 |
MOD_NEK2_2 | 285 | 290 | PF00069 | 0.460 |
MOD_NEK2_2 | 300 | 305 | PF00069 | 0.453 |
MOD_PIKK_1 | 380 | 386 | PF00454 | 0.481 |
MOD_PKA_1 | 219 | 225 | PF00069 | 0.436 |
MOD_PKA_2 | 219 | 225 | PF00069 | 0.436 |
MOD_PKA_2 | 412 | 418 | PF00069 | 0.416 |
MOD_Plk_1 | 20 | 26 | PF00069 | 0.404 |
MOD_Plk_1 | 265 | 271 | PF00069 | 0.405 |
MOD_Plk_1 | 291 | 297 | PF00069 | 0.413 |
MOD_Plk_1 | 300 | 306 | PF00069 | 0.413 |
MOD_Plk_1 | 360 | 366 | PF00069 | 0.540 |
MOD_Plk_4 | 178 | 184 | PF00069 | 0.300 |
MOD_Plk_4 | 194 | 200 | PF00069 | 0.316 |
MOD_Plk_4 | 219 | 225 | PF00069 | 0.428 |
MOD_Plk_4 | 300 | 306 | PF00069 | 0.383 |
MOD_Plk_4 | 308 | 314 | PF00069 | 0.340 |
MOD_Plk_4 | 316 | 322 | PF00069 | 0.342 |
MOD_Plk_4 | 33 | 39 | PF00069 | 0.406 |
MOD_Plk_4 | 412 | 418 | PF00069 | 0.420 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.307 |
MOD_ProDKin_1 | 172 | 178 | PF00069 | 0.396 |
MOD_ProDKin_1 | 227 | 233 | PF00069 | 0.474 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.410 |
MOD_ProDKin_1 | 333 | 339 | PF00069 | 0.393 |
MOD_ProDKin_1 | 58 | 64 | PF00069 | 0.516 |
MOD_SUMO_for_1 | 289 | 292 | PF00179 | 0.483 |
MOD_SUMO_rev_2 | 117 | 127 | PF00179 | 0.404 |
TRG_DiLeu_BaEn_1 | 397 | 402 | PF01217 | 0.402 |
TRG_DiLeu_LyEn_5 | 397 | 402 | PF01217 | 0.402 |
TRG_ENDOCYTIC_2 | 131 | 134 | PF00928 | 0.313 |
TRG_ENDOCYTIC_2 | 144 | 147 | PF00928 | 0.231 |
TRG_ENDOCYTIC_2 | 305 | 308 | PF00928 | 0.422 |
TRG_ENDOCYTIC_2 | 309 | 312 | PF00928 | 0.359 |
TRG_ER_diArg_1 | 218 | 220 | PF00400 | 0.367 |
TRG_Pf-PMV_PEXEL_1 | 276 | 280 | PF00026 | 0.522 |
TRG_Pf-PMV_PEXEL_1 | 400 | 404 | PF00026 | 0.524 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P740 | Leptomonas seymouri | 29% | 94% |
A0A0N1I5Z7 | Leptomonas seymouri | 69% | 100% |
A0A0N1I7E8 | Leptomonas seymouri | 38% | 100% |
A0A0S4IRH3 | Bodo saltans | 38% | 100% |
A0A0S4JVB2 | Bodo saltans | 22% | 100% |
A0A1X0NWZ0 | Trypanosomatidae | 26% | 89% |
A0A1X0NX10 | Trypanosomatidae | 43% | 100% |
A0A1X0NX22 | Trypanosomatidae | 41% | 93% |
A0A1X0NXP4 | Trypanosomatidae | 50% | 100% |
A0A3Q8IM07 | Leishmania donovani | 100% | 100% |
A0A3S7WXP2 | Leishmania donovani | 31% | 100% |
A0A3S7WXT7 | Leishmania donovani | 38% | 100% |
A4HCS3 | Leishmania braziliensis | 30% | 100% |
A4I097 | Leishmania infantum | 31% | 100% |
A4I0B8 | Leishmania infantum | 39% | 100% |
E9AW61 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9AW62 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
E9AW82 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 100% |
Q4QBB6 | Leishmania major | 95% | 100% |
Q4QBB7 | Leishmania major | 31% | 100% |
Q9SZ83 | Arabidopsis thaliana | 32% | 100% |
Q9U0V7 | Leishmania major | 39% | 100% |
V5BB31 | Trypanosoma cruzi | 25% | 99% |
V5BH08 | Trypanosoma cruzi | 41% | 100% |