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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 17 |
NetGPI | no | yes: 0, no: 17 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 16 |
GO:0110165 | cellular anatomical entity | 1 | 16 |
Related structures:
AlphaFold database: E9B4G6
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 18 |
GO:0008152 | metabolic process | 1 | 18 |
GO:0044238 | primary metabolic process | 2 | 18 |
GO:0071704 | organic substance metabolic process | 2 | 18 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004768 | stearoyl-CoA 9-desaturase activity | 6 | 6 |
GO:0016215 | acyl-CoA desaturase activity | 5 | 6 |
GO:0016491 | oxidoreductase activity | 2 | 7 |
GO:0016705 | oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen | 3 | 6 |
GO:0016717 | oxidoreductase activity, acting on paired donors, with oxidation of a pair of donors resulting in the reduction of molecular oxygen to two molecules of water | 4 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.553 |
CLV_NRD_NRD_1 | 215 | 217 | PF00675 | 0.337 |
CLV_NRD_NRD_1 | 227 | 229 | PF00675 | 0.290 |
CLV_NRD_NRD_1 | 360 | 362 | PF00675 | 0.357 |
CLV_PCSK_KEX2_1 | 215 | 217 | PF00082 | 0.337 |
CLV_PCSK_KEX2_1 | 360 | 362 | PF00082 | 0.323 |
CLV_PCSK_KEX2_1 | 392 | 394 | PF00082 | 0.464 |
CLV_PCSK_PC1ET2_1 | 392 | 394 | PF00082 | 0.464 |
CLV_PCSK_SKI1_1 | 2 | 6 | PF00082 | 0.349 |
CLV_PCSK_SKI1_1 | 349 | 353 | PF00082 | 0.206 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.669 |
DOC_MAPK_gen_1 | 10 | 17 | PF00069 | 0.504 |
DOC_MAPK_gen_1 | 172 | 180 | PF00069 | 0.322 |
DOC_MAPK_MEF2A_6 | 10 | 17 | PF00069 | 0.575 |
DOC_PP4_FxxP_1 | 198 | 201 | PF00568 | 0.301 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.496 |
DOC_USP7_MATH_1 | 145 | 149 | PF00917 | 0.301 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.221 |
DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.331 |
DOC_USP7_MATH_2 | 379 | 385 | PF00917 | 0.606 |
DOC_USP7_UBL2_3 | 2 | 6 | PF12436 | 0.560 |
DOC_WW_Pin1_4 | 122 | 127 | PF00397 | 0.432 |
DOC_WW_Pin1_4 | 181 | 186 | PF00397 | 0.297 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.521 |
LIG_14-3-3_CanoR_1 | 16 | 24 | PF00244 | 0.421 |
LIG_BRCT_BRCA1_1 | 223 | 227 | PF00533 | 0.519 |
LIG_BRCT_BRCA1_2 | 223 | 229 | PF00533 | 0.548 |
LIG_deltaCOP1_diTrp_1 | 295 | 299 | PF00928 | 0.446 |
LIG_EH1_1 | 345 | 353 | PF00400 | 0.553 |
LIG_FHA_1 | 158 | 164 | PF00498 | 0.260 |
LIG_FHA_1 | 165 | 171 | PF00498 | 0.319 |
LIG_FHA_1 | 182 | 188 | PF00498 | 0.369 |
LIG_GBD_Chelix_1 | 327 | 335 | PF00786 | 0.280 |
LIG_LIR_Apic_2 | 373 | 379 | PF02991 | 0.498 |
LIG_LIR_Gen_1 | 295 | 305 | PF02991 | 0.432 |
LIG_LIR_Gen_1 | 39 | 48 | PF02991 | 0.512 |
LIG_LIR_Gen_1 | 85 | 95 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 125 | 130 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 295 | 300 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 308 | 314 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 384 | 389 | PF02991 | 0.590 |
LIG_LIR_Nem_3 | 39 | 45 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 85 | 90 | PF02991 | 0.387 |
LIG_LYPXL_SIV_4 | 268 | 276 | PF13949 | 0.212 |
LIG_Pex14_1 | 42 | 46 | PF04695 | 0.568 |
LIG_Pex14_2 | 196 | 200 | PF04695 | 0.317 |
LIG_SH2_CRK | 127 | 131 | PF00017 | 0.547 |
LIG_SH2_CRK | 311 | 315 | PF00017 | 0.482 |
LIG_SH2_CRK | 62 | 66 | PF00017 | 0.350 |
LIG_SH2_NCK_1 | 77 | 81 | PF00017 | 0.284 |
LIG_SH2_PTP2 | 265 | 268 | PF00017 | 0.432 |
LIG_SH2_PTP2 | 376 | 379 | PF00017 | 0.502 |
LIG_SH2_SRC | 254 | 257 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 265 | 268 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 278 | 281 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 35 | 38 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 356 | 359 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 376 | 379 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 46 | 49 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 58 | 61 | PF00017 | 0.365 |
LIG_SH3_3 | 12 | 18 | PF00018 | 0.514 |
LIG_SH3_3 | 139 | 145 | PF00018 | 0.365 |
LIG_SH3_3 | 165 | 171 | PF00018 | 0.243 |
LIG_SH3_3 | 219 | 225 | PF00018 | 0.460 |
LIG_SUMO_SIM_par_1 | 174 | 184 | PF11976 | 0.253 |
LIG_SUMO_SIM_par_1 | 185 | 190 | PF11976 | 0.348 |
LIG_TRAF2_1 | 209 | 212 | PF00917 | 0.366 |
LIG_TYR_ITIM | 267 | 272 | PF00017 | 0.244 |
LIG_TYR_ITIM | 60 | 65 | PF00017 | 0.360 |
LIG_UBA3_1 | 363 | 372 | PF00899 | 0.589 |
MOD_CDC14_SPxK_1 | 125 | 128 | PF00782 | 0.432 |
MOD_CDK_SPxK_1 | 122 | 128 | PF00069 | 0.432 |
MOD_CDK_SPxxK_3 | 221 | 228 | PF00069 | 0.467 |
MOD_CK1_1 | 20 | 26 | PF00069 | 0.430 |
MOD_CK1_1 | 83 | 89 | PF00069 | 0.216 |
MOD_CK2_1 | 367 | 373 | PF00069 | 0.517 |
MOD_CMANNOS | 84 | 87 | PF00535 | 0.475 |
MOD_Cter_Amidation | 213 | 216 | PF01082 | 0.348 |
MOD_GlcNHglycan | 37 | 41 | PF01048 | 0.422 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.563 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.463 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.301 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.254 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.517 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.478 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.578 |
MOD_N-GLC_1 | 107 | 112 | PF02516 | 0.229 |
MOD_N-GLC_1 | 322 | 327 | PF02516 | 0.247 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.246 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.417 |
MOD_NEK2_1 | 277 | 282 | PF00069 | 0.427 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.366 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.521 |
MOD_NEK2_1 | 367 | 372 | PF00069 | 0.543 |
MOD_NEK2_2 | 40 | 45 | PF00069 | 0.424 |
MOD_PIKK_1 | 207 | 213 | PF00454 | 0.548 |
MOD_PIKK_1 | 330 | 336 | PF00454 | 0.497 |
MOD_PKA_1 | 172 | 178 | PF00069 | 0.311 |
MOD_PKA_2 | 149 | 155 | PF00069 | 0.254 |
MOD_Plk_1 | 20 | 26 | PF00069 | 0.605 |
MOD_Plk_1 | 322 | 328 | PF00069 | 0.447 |
MOD_Plk_1 | 36 | 42 | PF00069 | 0.520 |
MOD_Plk_4 | 138 | 144 | PF00069 | 0.280 |
MOD_Plk_4 | 164 | 170 | PF00069 | 0.296 |
MOD_Plk_4 | 314 | 320 | PF00069 | 0.365 |
MOD_Plk_4 | 381 | 387 | PF00069 | 0.559 |
MOD_ProDKin_1 | 122 | 128 | PF00069 | 0.432 |
MOD_ProDKin_1 | 181 | 187 | PF00069 | 0.297 |
MOD_ProDKin_1 | 221 | 227 | PF00069 | 0.521 |
TRG_DiLeu_BaEn_1 | 85 | 90 | PF01217 | 0.188 |
TRG_DiLeu_BaEn_2 | 294 | 300 | PF01217 | 0.488 |
TRG_DiLeu_BaLyEn_6 | 359 | 364 | PF01217 | 0.558 |
TRG_ENDOCYTIC_2 | 127 | 130 | PF00928 | 0.548 |
TRG_ENDOCYTIC_2 | 203 | 206 | PF00928 | 0.421 |
TRG_ENDOCYTIC_2 | 269 | 272 | PF00928 | 0.255 |
TRG_ENDOCYTIC_2 | 311 | 314 | PF00928 | 0.480 |
TRG_ENDOCYTIC_2 | 338 | 341 | PF00928 | 0.454 |
TRG_ENDOCYTIC_2 | 58 | 61 | PF00928 | 0.302 |
TRG_ENDOCYTIC_2 | 62 | 65 | PF00928 | 0.302 |
TRG_ER_diArg_1 | 215 | 217 | PF00400 | 0.434 |
TRG_ER_diArg_1 | 360 | 362 | PF00400 | 0.619 |
TRG_ER_diLys_1 | 391 | 394 | PF00400 | 0.662 |
TRG_Pf-PMV_PEXEL_1 | 361 | 365 | PF00026 | 0.402 |
TRG_Pf-PMV_PEXEL_1 | 49 | 53 | PF00026 | 0.266 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5L0 | Leptomonas seymouri | 79% | 100% |
A0A0S4IVK0 | Bodo saltans | 56% | 94% |
A0A1X0NKF1 | Trypanosomatidae | 48% | 85% |
A0A3Q8I8P6 | Leishmania donovani | 75% | 100% |
A0A3S7X797 | Leishmania donovani | 95% | 100% |
A0A422MYL0 | Trypanosoma rangeli | 60% | 94% |
A3F5L2 | Sorghum bicolor | 35% | 100% |
A3F5L3 | Sorghum bicolor | 38% | 100% |
A4H5Y3 | Leishmania braziliensis | 74% | 100% |
A4H6C4 | Leishmania braziliensis | 74% | 100% |
A4HM35 | Leishmania braziliensis | 82% | 100% |
A4HUP7 | Leishmania infantum | 75% | 100% |
A4I9G8 | Leishmania infantum | 95% | 100% |
B4YQU1 | Claviceps purpurea | 36% | 83% |
C9ZJ57 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 57% | 97% |
E9ANE6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 100% |
G5EGA5 | Caenorhabditis elegans | 28% | 100% |
O81931 | Crepis alpina | 37% | 100% |
P32291 | Vigna radiata var. radiata | 34% | 100% |
P46310 | Arabidopsis thaliana | 32% | 88% |
P46313 | Arabidopsis thaliana | 38% | 100% |
P48618 | Brassica napus | 34% | 98% |
P48619 | Ricinus communis | 33% | 86% |
P48620 | Sesamum indicum | 32% | 88% |
P48621 | Glycine max | 36% | 87% |
P48622 | Arabidopsis thaliana | 31% | 91% |
P48623 | Arabidopsis thaliana | 32% | 100% |
P48624 | Brassica napus | 33% | 100% |
P48625 | Glycine max | 32% | 100% |
P48626 | Nicotiana tabacum | 37% | 100% |
P48627 | Brassica napus | 25% | 89% |
P48630 | Glycine max | 39% | 100% |
P48631 | Glycine max | 38% | 100% |
P59668 | Mortierella isabellina | 43% | 98% |
Q39287 | Brassica juncea | 40% | 100% |
Q41131 | Ricinus communis | 38% | 100% |
Q4Q3K9 | Leishmania major | 95% | 100% |
Q4QH80 | Leishmania major | 75% | 100% |
Q56VS4 | Helianthus annuus | 36% | 89% |
Q594P3 | Sorghum bicolor | 38% | 100% |
Q59J82 | Mortierella alpina | 37% | 98% |
Q6RS95 | Dimorphotheca sinuata | 35% | 100% |
Q6RS96 | Dimorphotheca sinuata | 32% | 100% |
Q84UB8 | Punica granatum | 37% | 100% |
Q84UB9 | Trichosanthes kirilowii | 38% | 100% |
Q84UC0 | Trichosanthes kirilowii | 37% | 100% |
Q84VT2 | Punica granatum | 40% | 100% |
Q8GZC2 | Vernicia fordii | 40% | 100% |
Q8GZC3 | Vernicia fordii | 39% | 100% |
Q9AT72 | Calendula officinalis | 38% | 100% |
Q9FPP7 | Calendula officinalis | 34% | 100% |
Q9FPP8 | Calendula officinalis | 34% | 100% |
Q9NEQ0 | Caenorhabditis elegans | 31% | 98% |
Q9SCG2 | Calendula officinalis | 38% | 100% |
Q9SP61 | Momordica charantia | 36% | 99% |
Q9SP62 | Impatiens balsamina | 35% | 100% |
Q9Y8H5 | Mortierella alpina | 43% | 98% |
V5BA48 | Trypanosoma cruzi | 60% | 96% |