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: 21 |
NetGPI | no | yes: 0, no: 21 |
Related structures:
AlphaFold database: E9AW61
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 21 |
GO:0005488 | binding | 1 | 21 |
GO:0036094 | small molecule binding | 2 | 21 |
GO:0097159 | organic cyclic compound binding | 2 | 21 |
GO:1901265 | nucleoside phosphate binding | 3 | 21 |
GO:1901363 | heterocyclic compound binding | 2 | 21 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 395 | 399 | PF00656 | 0.546 |
CLV_MEL_PAP_1 | 72 | 78 | PF00089 | 0.174 |
CLV_NRD_NRD_1 | 1 | 3 | PF00675 | 0.640 |
CLV_NRD_NRD_1 | 17 | 19 | PF00675 | 0.267 |
CLV_NRD_NRD_1 | 265 | 267 | PF00675 | 0.537 |
CLV_NRD_NRD_1 | 59 | 61 | PF00675 | 0.249 |
CLV_PCSK_KEX2_1 | 265 | 267 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.408 |
CLV_PCSK_PC1ET2_1 | 99 | 101 | PF00082 | 0.408 |
CLV_PCSK_SKI1_1 | 138 | 142 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 207 | 211 | PF00082 | 0.334 |
CLV_PCSK_SKI1_1 | 347 | 351 | PF00082 | 0.406 |
DEG_APCC_DBOX_1 | 206 | 214 | PF00400 | 0.345 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.610 |
DEG_SPOP_SBC_1 | 389 | 393 | PF00917 | 0.445 |
DOC_CKS1_1 | 268 | 273 | PF01111 | 0.412 |
DOC_CYCLIN_yClb1_LxF_4 | 136 | 141 | PF00134 | 0.299 |
DOC_CYCLIN_yCln2_LP_2 | 163 | 169 | PF00134 | 0.478 |
DOC_CYCLIN_yCln2_LP_2 | 191 | 197 | PF00134 | 0.255 |
DOC_MAPK_gen_1 | 18 | 24 | PF00069 | 0.277 |
DOC_MAPK_gen_1 | 2 | 10 | PF00069 | 0.319 |
DOC_MAPK_gen_1 | 99 | 106 | PF00069 | 0.408 |
DOC_MAPK_MEF2A_6 | 2 | 10 | PF00069 | 0.319 |
DOC_MAPK_MEF2A_6 | 250 | 259 | PF00069 | 0.525 |
DOC_PP1_RVXF_1 | 136 | 142 | PF00149 | 0.441 |
DOC_PP1_RVXF_1 | 5 | 11 | PF00149 | 0.393 |
DOC_PP4_FxxP_1 | 215 | 218 | PF00568 | 0.388 |
DOC_PP4_FxxP_1 | 285 | 288 | PF00568 | 0.514 |
DOC_PP4_FxxP_1 | 71 | 74 | PF00568 | 0.408 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.275 |
DOC_USP7_MATH_1 | 171 | 175 | PF00917 | 0.408 |
DOC_USP7_MATH_1 | 290 | 294 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 356 | 360 | PF00917 | 0.517 |
DOC_USP7_MATH_2 | 394 | 400 | PF00917 | 0.390 |
DOC_WW_Pin1_4 | 175 | 180 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 267 | 272 | PF00397 | 0.673 |
DOC_WW_Pin1_4 | 390 | 395 | PF00397 | 0.523 |
LIG_14-3-3_CanoR_1 | 224 | 232 | PF00244 | 0.540 |
LIG_14-3-3_CanoR_1 | 347 | 355 | PF00244 | 0.456 |
LIG_BRCT_BRCA1_1 | 177 | 181 | PF00533 | 0.417 |
LIG_Clathr_ClatBox_1 | 139 | 143 | PF01394 | 0.354 |
LIG_deltaCOP1_diTrp_1 | 200 | 208 | PF00928 | 0.336 |
LIG_FHA_1 | 320 | 326 | PF00498 | 0.430 |
LIG_FHA_1 | 329 | 335 | PF00498 | 0.405 |
LIG_FHA_1 | 438 | 444 | PF00498 | 0.380 |
LIG_FHA_2 | 224 | 230 | PF00498 | 0.470 |
LIG_FHA_2 | 275 | 281 | PF00498 | 0.472 |
LIG_FHA_2 | 339 | 345 | PF00498 | 0.505 |
LIG_FHA_2 | 390 | 396 | PF00498 | 0.578 |
LIG_LIR_Apic_2 | 214 | 218 | PF02991 | 0.430 |
LIG_LIR_Apic_2 | 284 | 288 | PF02991 | 0.518 |
LIG_LIR_Apic_2 | 291 | 297 | PF02991 | 0.657 |
LIG_LIR_Gen_1 | 434 | 444 | PF02991 | 0.379 |
LIG_LIR_Gen_1 | 78 | 85 | PF02991 | 0.319 |
LIG_LIR_Gen_1 | 89 | 96 | PF02991 | 0.302 |
LIG_LIR_Nem_3 | 193 | 198 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 200 | 206 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 373 | 379 | PF02991 | 0.547 |
LIG_LIR_Nem_3 | 404 | 410 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 434 | 439 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 78 | 82 | PF02991 | 0.319 |
LIG_LIR_Nem_3 | 89 | 95 | PF02991 | 0.302 |
LIG_MYND_1 | 190 | 194 | PF01753 | 0.414 |
LIG_Pex14_2 | 311 | 315 | PF04695 | 0.426 |
LIG_SH2_CRK | 195 | 199 | PF00017 | 0.226 |
LIG_SH2_PTP2 | 294 | 297 | PF00017 | 0.418 |
LIG_SH2_PTP2 | 92 | 95 | PF00017 | 0.306 |
LIG_SH2_STAT3 | 438 | 441 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 204 | 207 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 294 | 297 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 438 | 441 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 92 | 95 | PF00017 | 0.306 |
LIG_SH3_1 | 265 | 271 | PF00018 | 0.474 |
LIG_SH3_3 | 173 | 179 | PF00018 | 0.326 |
LIG_SH3_3 | 265 | 271 | PF00018 | 0.474 |
LIG_SUMO_SIM_anti_2 | 86 | 92 | PF11976 | 0.361 |
LIG_TRAF2_1 | 393 | 396 | PF00917 | 0.421 |
LIG_TYR_ITIM | 90 | 95 | PF00017 | 0.312 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.329 |
MOD_CK2_1 | 120 | 126 | PF00069 | 0.374 |
MOD_CK2_1 | 274 | 280 | PF00069 | 0.486 |
MOD_CK2_1 | 389 | 395 | PF00069 | 0.691 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.353 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.720 |
MOD_GlcNHglycan | 365 | 370 | PF01048 | 0.676 |
MOD_GlcNHglycan | 398 | 401 | PF01048 | 0.513 |
MOD_GlcNHglycan | 461 | 464 | PF01048 | 0.661 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.438 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.505 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.530 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.426 |
MOD_N-GLC_1 | 242 | 247 | PF02516 | 0.492 |
MOD_N-GLC_1 | 328 | 333 | PF02516 | 0.295 |
MOD_N-GLC_1 | 370 | 375 | PF02516 | 0.435 |
MOD_N-GLC_1 | 56 | 61 | PF02516 | 0.400 |
MOD_NEK2_1 | 11 | 16 | PF00069 | 0.317 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.402 |
MOD_NEK2_1 | 283 | 288 | PF00069 | 0.477 |
MOD_NEK2_2 | 330 | 335 | PF00069 | 0.261 |
MOD_PIKK_1 | 147 | 153 | PF00454 | 0.325 |
MOD_PIKK_1 | 347 | 353 | PF00454 | 0.345 |
MOD_PIKK_1 | 437 | 443 | PF00454 | 0.351 |
MOD_PKA_1 | 431 | 437 | PF00069 | 0.475 |
MOD_PKA_2 | 223 | 229 | PF00069 | 0.506 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.370 |
MOD_PKB_1 | 345 | 353 | PF00069 | 0.349 |
MOD_Plk_1 | 283 | 289 | PF00069 | 0.451 |
MOD_Plk_1 | 319 | 325 | PF00069 | 0.419 |
MOD_Plk_1 | 444 | 450 | PF00069 | 0.429 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.505 |
MOD_Plk_4 | 290 | 296 | PF00069 | 0.444 |
MOD_Plk_4 | 410 | 416 | PF00069 | 0.432 |
MOD_Plk_4 | 75 | 81 | PF00069 | 0.358 |
MOD_ProDKin_1 | 175 | 181 | PF00069 | 0.543 |
MOD_ProDKin_1 | 267 | 273 | PF00069 | 0.663 |
MOD_ProDKin_1 | 390 | 396 | PF00069 | 0.515 |
MOD_SUMO_rev_2 | 52 | 59 | PF00179 | 0.409 |
TRG_DiLeu_BaLyEn_6 | 135 | 140 | PF01217 | 0.316 |
TRG_DiLeu_BaLyEn_6 | 187 | 192 | PF01217 | 0.340 |
TRG_DiLeu_BaLyEn_6 | 419 | 424 | PF01217 | 0.549 |
TRG_ENDOCYTIC_2 | 195 | 198 | PF00928 | 0.227 |
TRG_ENDOCYTIC_2 | 379 | 382 | PF00928 | 0.585 |
TRG_ENDOCYTIC_2 | 79 | 82 | PF00928 | 0.319 |
TRG_ENDOCYTIC_2 | 92 | 95 | PF00928 | 0.294 |
TRG_ER_diArg_1 | 345 | 348 | PF00400 | 0.551 |
TRG_Pf-PMV_PEXEL_1 | 138 | 143 | PF00026 | 0.376 |
TRG_Pf-PMV_PEXEL_1 | 347 | 351 | PF00026 | 0.339 |
TRG_Pf-PMV_PEXEL_1 | 43 | 47 | PF00026 | 0.198 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P740 | Leptomonas seymouri | 63% | 100% |
A0A0N1I5Z7 | Leptomonas seymouri | 31% | 100% |
A0A0N1I7E8 | Leptomonas seymouri | 32% | 100% |
A0A1X0NX10 | Trypanosomatidae | 32% | 100% |
A0A1X0NX22 | Trypanosomatidae | 37% | 100% |
A0A1X0NXP4 | Trypanosomatidae | 29% | 100% |
A0A3Q8IM07 | Leishmania donovani | 31% | 100% |
A0A3S7WXP2 | Leishmania donovani | 92% | 100% |
A0A3S7WXT7 | Leishmania donovani | 32% | 100% |
A4HCS3 | Leishmania braziliensis | 79% | 100% |
A4I097 | Leishmania infantum | 92% | 100% |
A4I0B8 | Leishmania infantum | 32% | 100% |
E9AH12 | Leishmania infantum | 31% | 100% |
E9AW62 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9AW82 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
Q4QBB6 | Leishmania major | 31% | 82% |
Q4QBB7 | Leishmania major | 90% | 100% |
Q9U0V7 | Leishmania major | 32% | 82% |
V5BB31 | Trypanosoma cruzi | 24% | 100% |
V5BH08 | Trypanosoma cruzi | 36% | 100% |