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: 20 |
NetGPI | no | yes: 0, no: 20 |
Related structures:
AlphaFold database: A4HCS3
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 | 409 | 413 | PF00656 | 0.542 |
CLV_C14_Caspase3-7 | 461 | 465 | PF00656 | 0.630 |
CLV_NRD_NRD_1 | 1 | 3 | PF00675 | 0.616 |
CLV_NRD_NRD_1 | 17 | 19 | PF00675 | 0.313 |
CLV_NRD_NRD_1 | 265 | 267 | PF00675 | 0.560 |
CLV_NRD_NRD_1 | 289 | 291 | PF00675 | 0.370 |
CLV_PCSK_KEX2_1 | 136 | 138 | PF00082 | 0.268 |
CLV_PCSK_KEX2_1 | 265 | 267 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 98 | 100 | PF00082 | 0.401 |
CLV_PCSK_PC1ET2_1 | 136 | 138 | PF00082 | 0.268 |
CLV_PCSK_PC1ET2_1 | 98 | 100 | PF00082 | 0.401 |
CLV_PCSK_SKI1_1 | 136 | 140 | PF00082 | 0.310 |
CLV_PCSK_SKI1_1 | 206 | 210 | PF00082 | 0.323 |
CLV_PCSK_SKI1_1 | 43 | 47 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 57 | 61 | PF00082 | 0.229 |
DEG_APCC_DBOX_1 | 205 | 213 | PF00400 | 0.335 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.598 |
DEG_SPOP_SBC_1 | 458 | 462 | PF00917 | 0.682 |
DOC_CYCLIN_RxL_1 | 131 | 144 | PF00134 | 0.235 |
DOC_CYCLIN_yCln2_LP_2 | 162 | 168 | PF00134 | 0.455 |
DOC_MAPK_gen_1 | 18 | 24 | PF00069 | 0.373 |
DOC_MAPK_gen_1 | 2 | 10 | PF00069 | 0.401 |
DOC_MAPK_gen_1 | 98 | 105 | PF00069 | 0.401 |
DOC_MAPK_MEF2A_6 | 2 | 10 | PF00069 | 0.401 |
DOC_PP1_RVXF_1 | 134 | 141 | PF00149 | 0.306 |
DOC_PP1_RVXF_1 | 28 | 34 | PF00149 | 0.357 |
DOC_PP1_RVXF_1 | 5 | 11 | PF00149 | 0.369 |
DOC_PP4_FxxP_1 | 214 | 217 | PF00568 | 0.372 |
DOC_PP4_FxxP_1 | 285 | 288 | PF00568 | 0.497 |
DOC_PP4_FxxP_1 | 70 | 73 | PF00568 | 0.401 |
DOC_SPAK_OSR1_1 | 347 | 351 | PF12202 | 0.350 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.285 |
DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.395 |
DOC_USP7_MATH_1 | 458 | 462 | PF00917 | 0.589 |
DOC_WW_Pin1_4 | 174 | 179 | PF00397 | 0.543 |
DOC_WW_Pin1_4 | 246 | 251 | PF00397 | 0.567 |
LIG_14-3-3_CanoR_1 | 223 | 230 | PF00244 | 0.541 |
LIG_14-3-3_CanoR_1 | 30 | 34 | PF00244 | 0.328 |
LIG_14-3-3_CanoR_1 | 352 | 356 | PF00244 | 0.488 |
LIG_APCC_ABBAyCdc20_2 | 136 | 142 | PF00400 | 0.313 |
LIG_BRCT_BRCA1_1 | 176 | 180 | PF00533 | 0.404 |
LIG_Clathr_ClatBox_1 | 138 | 142 | PF01394 | 0.343 |
LIG_deltaCOP1_diTrp_1 | 199 | 207 | PF00928 | 0.325 |
LIG_FHA_1 | 239 | 245 | PF00498 | 0.535 |
LIG_FHA_1 | 320 | 326 | PF00498 | 0.417 |
LIG_FHA_1 | 329 | 335 | PF00498 | 0.406 |
LIG_FHA_1 | 395 | 401 | PF00498 | 0.426 |
LIG_FHA_1 | 438 | 444 | PF00498 | 0.366 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.396 |
LIG_FHA_2 | 223 | 229 | PF00498 | 0.475 |
LIG_FHA_2 | 275 | 281 | PF00498 | 0.462 |
LIG_FHA_2 | 312 | 318 | PF00498 | 0.429 |
LIG_FHA_2 | 339 | 345 | PF00498 | 0.469 |
LIG_LIR_Apic_2 | 213 | 217 | PF02991 | 0.414 |
LIG_LIR_Apic_2 | 284 | 288 | PF02991 | 0.504 |
LIG_LIR_Gen_1 | 377 | 385 | PF02991 | 0.388 |
LIG_LIR_Gen_1 | 434 | 444 | PF02991 | 0.367 |
LIG_LIR_Gen_1 | 77 | 84 | PF02991 | 0.323 |
LIG_LIR_Gen_1 | 88 | 95 | PF02991 | 0.303 |
LIG_LIR_Nem_3 | 199 | 205 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 373 | 379 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 404 | 410 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 434 | 439 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 77 | 81 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 88 | 94 | PF02991 | 0.303 |
LIG_MYND_1 | 189 | 193 | PF01753 | 0.418 |
LIG_Pex14_2 | 311 | 315 | PF04695 | 0.410 |
LIG_SH2_NCK_1 | 391 | 395 | PF00017 | 0.577 |
LIG_SH2_PTP2 | 91 | 94 | PF00017 | 0.313 |
LIG_SH2_STAT3 | 438 | 441 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.301 |
LIG_SH2_STAT5 | 243 | 246 | PF00017 | 0.483 |
LIG_SH2_STAT5 | 438 | 441 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 91 | 94 | PF00017 | 0.313 |
LIG_SUMO_SIM_anti_2 | 85 | 91 | PF11976 | 0.373 |
LIG_TYR_ITIM | 89 | 94 | PF00017 | 0.315 |
MOD_CK1_1 | 242 | 248 | PF00069 | 0.478 |
MOD_CK1_1 | 93 | 99 | PF00069 | 0.320 |
MOD_CK2_1 | 119 | 125 | PF00069 | 0.365 |
MOD_CK2_1 | 274 | 280 | PF00069 | 0.477 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.373 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.304 |
MOD_GlcNHglycan | 270 | 273 | PF01048 | 0.464 |
MOD_GlcNHglycan | 449 | 452 | PF01048 | 0.442 |
MOD_GlcNHglycan | 461 | 464 | PF01048 | 0.637 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.426 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.521 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.595 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.470 |
MOD_GSK3_1 | 458 | 465 | PF00069 | 0.624 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.420 |
MOD_NEK2_1 | 11 | 16 | PF00069 | 0.325 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.401 |
MOD_NEK2_1 | 172 | 177 | PF00069 | 0.461 |
MOD_NEK2_1 | 283 | 288 | PF00069 | 0.463 |
MOD_NEK2_1 | 311 | 316 | PF00069 | 0.381 |
MOD_PIKK_1 | 146 | 152 | PF00454 | 0.320 |
MOD_PIKK_1 | 260 | 266 | PF00454 | 0.488 |
MOD_PIKK_1 | 437 | 443 | PF00454 | 0.339 |
MOD_PKA_1 | 2 | 8 | PF00069 | 0.301 |
MOD_PKA_1 | 431 | 437 | PF00069 | 0.466 |
MOD_PKA_2 | 222 | 228 | PF00069 | 0.506 |
MOD_PKA_2 | 289 | 295 | PF00069 | 0.398 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.362 |
MOD_PKA_2 | 351 | 357 | PF00069 | 0.435 |
MOD_Plk_1 | 238 | 244 | PF00069 | 0.487 |
MOD_Plk_1 | 283 | 289 | PF00069 | 0.449 |
MOD_Plk_1 | 319 | 325 | PF00069 | 0.421 |
MOD_Plk_1 | 444 | 450 | PF00069 | 0.277 |
MOD_Plk_4 | 176 | 182 | PF00069 | 0.495 |
MOD_Plk_4 | 239 | 245 | PF00069 | 0.529 |
MOD_Plk_4 | 29 | 35 | PF00069 | 0.283 |
MOD_Plk_4 | 328 | 334 | PF00069 | 0.463 |
MOD_Plk_4 | 74 | 80 | PF00069 | 0.350 |
MOD_ProDKin_1 | 174 | 180 | PF00069 | 0.537 |
MOD_ProDKin_1 | 246 | 252 | PF00069 | 0.565 |
TRG_DiLeu_BaEn_3 | 384 | 390 | PF01217 | 0.391 |
TRG_DiLeu_BaLyEn_6 | 134 | 139 | PF01217 | 0.308 |
TRG_DiLeu_BaLyEn_6 | 186 | 191 | PF01217 | 0.356 |
TRG_DiLeu_BaLyEn_6 | 419 | 424 | PF01217 | 0.543 |
TRG_ENDOCYTIC_2 | 379 | 382 | PF00928 | 0.598 |
TRG_ENDOCYTIC_2 | 78 | 81 | PF00928 | 0.323 |
TRG_ENDOCYTIC_2 | 91 | 94 | PF00928 | 0.295 |
TRG_ER_diArg_1 | 265 | 267 | PF00400 | 0.481 |
TRG_ER_diArg_1 | 345 | 348 | PF00400 | 0.558 |
TRG_Pf-PMV_PEXEL_1 | 137 | 142 | PF00026 | 0.365 |
TRG_Pf-PMV_PEXEL_1 | 43 | 47 | PF00026 | 0.201 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P740 | Leptomonas seymouri | 62% | 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 | 30% | 100% |
A0A3S7WXP2 | Leishmania donovani | 78% | 100% |
A0A3S7WXT7 | Leishmania donovani | 32% | 100% |
A4I097 | Leishmania infantum | 78% | 100% |
A4I0B8 | Leishmania infantum | 32% | 100% |
E9AH12 | Leishmania infantum | 30% | 100% |
E9AW61 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |
E9AW62 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9AW82 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
Q4QBB6 | Leishmania major | 30% | 81% |
Q4QBB7 | Leishmania major | 77% | 100% |
Q9U0V7 | Leishmania major | 32% | 82% |
V5BH08 | Trypanosoma cruzi | 35% | 100% |