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: Q4QH80
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 | 8 |
GO:0004768 | stearoyl-CoA 9-desaturase activity | 6 | 7 |
GO:0016215 | acyl-CoA desaturase activity | 5 | 7 |
GO:0016491 | oxidoreductase activity | 2 | 8 |
GO:0016705 | oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen | 3 | 7 |
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 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.528 |
CLV_NRD_NRD_1 | 215 | 217 | PF00675 | 0.333 |
CLV_PCSK_KEX2_1 | 215 | 217 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 2 | 6 | PF00082 | 0.374 |
CLV_PCSK_SKI1_1 | 20 | 24 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 49 | 53 | PF00082 | 0.236 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.642 |
DOC_AGCK_PIF_1 | 193 | 198 | PF00069 | 0.228 |
DOC_MAPK_gen_1 | 172 | 180 | PF00069 | 0.317 |
DOC_MAPK_gen_1 | 6 | 15 | PF00069 | 0.544 |
DOC_MAPK_MEF2A_6 | 229 | 237 | PF00069 | 0.508 |
DOC_MAPK_MEF2A_6 | 9 | 17 | PF00069 | 0.596 |
DOC_PP2B_LxvP_1 | 287 | 290 | PF13499 | 0.452 |
DOC_PP4_FxxP_1 | 198 | 201 | PF00568 | 0.291 |
DOC_USP7_MATH_1 | 123 | 127 | PF00917 | 0.495 |
DOC_USP7_MATH_1 | 145 | 149 | PF00917 | 0.279 |
DOC_USP7_MATH_2 | 379 | 385 | PF00917 | 0.606 |
DOC_USP7_UBL2_3 | 2 | 6 | PF12436 | 0.574 |
DOC_WW_Pin1_4 | 181 | 186 | PF00397 | 0.291 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.514 |
LIG_AP2alpha_1 | 48 | 52 | PF02296 | 0.421 |
LIG_BRCT_BRCA1_1 | 223 | 227 | PF00533 | 0.514 |
LIG_BRCT_BRCA1_2 | 223 | 229 | PF00533 | 0.545 |
LIG_EH1_1 | 345 | 353 | PF00400 | 0.528 |
LIG_FHA_1 | 158 | 164 | PF00498 | 0.259 |
LIG_FHA_1 | 165 | 171 | PF00498 | 0.248 |
LIG_FHA_1 | 182 | 188 | PF00498 | 0.368 |
LIG_FHA_2 | 368 | 374 | PF00498 | 0.523 |
LIG_GBD_Chelix_1 | 327 | 335 | PF00786 | 0.273 |
LIG_HP1_1 | 185 | 189 | PF01393 | 0.268 |
LIG_LIR_Apic_2 | 197 | 201 | PF02991 | 0.253 |
LIG_LIR_Apic_2 | 373 | 379 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 50 | 60 | PF02991 | 0.300 |
LIG_LIR_Gen_1 | 86 | 95 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 125 | 130 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 197 | 203 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 253 | 259 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 272 | 278 | PF02991 | 0.240 |
LIG_LIR_Nem_3 | 308 | 314 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 317 | 321 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 384 | 389 | PF02991 | 0.589 |
LIG_LIR_Nem_3 | 39 | 45 | PF02991 | 0.541 |
LIG_LIR_Nem_3 | 50 | 55 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 86 | 90 | PF02991 | 0.386 |
LIG_Pex14_1 | 42 | 46 | PF04695 | 0.562 |
LIG_Pex14_2 | 196 | 200 | PF04695 | 0.306 |
LIG_Pex14_2 | 48 | 52 | PF04695 | 0.421 |
LIG_SH2_CRK | 127 | 131 | PF00017 | 0.543 |
LIG_SH2_CRK | 311 | 315 | PF00017 | 0.473 |
LIG_SH2_CRK | 62 | 66 | PF00017 | 0.338 |
LIG_SH2_GRB2like | 321 | 324 | PF00017 | 0.452 |
LIG_SH2_PTP2 | 265 | 268 | PF00017 | 0.427 |
LIG_SH2_PTP2 | 376 | 379 | PF00017 | 0.505 |
LIG_SH2_SRC | 254 | 257 | PF00017 | 0.459 |
LIG_SH2_SRC | 376 | 379 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 265 | 268 | PF00017 | 0.296 |
LIG_SH2_STAT5 | 269 | 272 | PF00017 | 0.290 |
LIG_SH2_STAT5 | 278 | 281 | PF00017 | 0.289 |
LIG_SH2_STAT5 | 292 | 295 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 321 | 324 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 35 | 38 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 356 | 359 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 376 | 379 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 46 | 49 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 58 | 61 | PF00017 | 0.326 |
LIG_SH3_3 | 12 | 18 | PF00018 | 0.512 |
LIG_SH3_3 | 165 | 171 | PF00018 | 0.237 |
LIG_SH3_3 | 219 | 225 | PF00018 | 0.448 |
LIG_SUMO_SIM_anti_2 | 12 | 17 | PF11976 | 0.579 |
LIG_SUMO_SIM_anti_2 | 139 | 145 | PF11976 | 0.185 |
LIG_TYR_ITIM | 60 | 65 | PF00017 | 0.351 |
LIG_WRC_WIRS_1 | 195 | 200 | PF05994 | 0.403 |
LIG_WRC_WIRS_1 | 386 | 391 | PF05994 | 0.481 |
MOD_CK2_1 | 359 | 365 | PF00069 | 0.535 |
MOD_CK2_1 | 367 | 373 | PF00069 | 0.510 |
MOD_Cter_Amidation | 213 | 216 | PF01082 | 0.345 |
MOD_GlcNHglycan | 37 | 41 | PF01048 | 0.350 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.414 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.291 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.248 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.472 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.578 |
MOD_N-GLC_1 | 322 | 327 | PF02516 | 0.240 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.403 |
MOD_NEK2_1 | 277 | 282 | PF00069 | 0.422 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.514 |
MOD_NEK2_1 | 367 | 372 | PF00069 | 0.538 |
MOD_NEK2_2 | 96 | 101 | PF00069 | 0.278 |
MOD_PIKK_1 | 207 | 213 | PF00454 | 0.545 |
MOD_PIKK_1 | 330 | 336 | PF00454 | 0.491 |
MOD_PKA_2 | 149 | 155 | PF00069 | 0.248 |
MOD_PKA_2 | 214 | 220 | PF00069 | 0.502 |
MOD_Plk_1 | 20 | 26 | PF00069 | 0.600 |
MOD_Plk_1 | 322 | 328 | PF00069 | 0.440 |
MOD_Plk_1 | 36 | 42 | PF00069 | 0.385 |
MOD_Plk_2-3 | 359 | 365 | PF00069 | 0.500 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.262 |
MOD_Plk_4 | 164 | 170 | PF00069 | 0.290 |
MOD_Plk_4 | 277 | 283 | PF00069 | 0.297 |
MOD_ProDKin_1 | 181 | 187 | PF00069 | 0.291 |
MOD_ProDKin_1 | 221 | 227 | PF00069 | 0.514 |
TRG_DiLeu_BaLyEn_6 | 125 | 130 | PF01217 | 0.412 |
TRG_ENDOCYTIC_2 | 127 | 130 | PF00928 | 0.545 |
TRG_ENDOCYTIC_2 | 259 | 262 | PF00928 | 0.277 |
TRG_ENDOCYTIC_2 | 311 | 314 | PF00928 | 0.473 |
TRG_ENDOCYTIC_2 | 338 | 341 | PF00928 | 0.448 |
TRG_ENDOCYTIC_2 | 45 | 48 | PF00928 | 0.535 |
TRG_ENDOCYTIC_2 | 58 | 61 | PF00928 | 0.252 |
TRG_ENDOCYTIC_2 | 62 | 65 | PF00928 | 0.232 |
TRG_NES_CRM1_1 | 105 | 118 | PF08389 | 0.297 |
TRG_Pf-PMV_PEXEL_1 | 361 | 365 | PF00026 | 0.394 |
TRG_Pf-PMV_PEXEL_1 | 49 | 53 | PF00026 | 0.259 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5L0 | Leptomonas seymouri | 69% | 100% |
A0A0S4IVK0 | Bodo saltans | 51% | 94% |
A0A1X0NKF1 | Trypanosomatidae | 44% | 85% |
A0A3Q8I8P6 | Leishmania donovani | 98% | 100% |
A0A3S7X797 | Leishmania donovani | 75% | 100% |
A0A422MYL0 | Trypanosoma rangeli | 54% | 94% |
A3F5L2 | Sorghum bicolor | 37% | 100% |
A3F5L3 | Sorghum bicolor | 38% | 100% |
A4H5Y3 | Leishmania braziliensis | 90% | 100% |
A4H6C4 | Leishmania braziliensis | 90% | 100% |
A4HM35 | Leishmania braziliensis | 74% | 100% |
A4HUP7 | Leishmania infantum | 98% | 100% |
A4I9G8 | Leishmania infantum | 75% | 100% |
B4YQU1 | Claviceps purpurea | 35% | 83% |
C9ZJ57 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 97% |
E9ANE6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
E9B4G6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 100% |
G5EGA5 | Caenorhabditis elegans | 29% | 100% |
O34653 | Bacillus subtilis (strain 168) | 24% | 100% |
O81931 | Crepis alpina | 35% | 100% |
P20388 | Synechocystis sp. (strain PCC 6803 / Kazusa) | 23% | 100% |
P32291 | Vigna radiata var. radiata | 34% | 100% |
P46310 | Arabidopsis thaliana | 32% | 88% |
P46312 | Arabidopsis thaliana | 24% | 88% |
P46313 | Arabidopsis thaliana | 35% | 100% |
P48618 | Brassica napus | 32% | 98% |
P48619 | Ricinus communis | 32% | 86% |
P48620 | Sesamum indicum | 32% | 88% |
P48621 | Glycine max | 33% | 87% |
P48622 | Arabidopsis thaliana | 31% | 91% |
P48623 | Arabidopsis thaliana | 36% | 100% |
P48624 | Brassica napus | 34% | 100% |
P48625 | Glycine max | 32% | 100% |
P48626 | Nicotiana tabacum | 33% | 100% |
P48627 | Brassica napus | 25% | 89% |
P48630 | Glycine max | 36% | 100% |
P48631 | Glycine max | 36% | 100% |
P59668 | Mortierella isabellina | 42% | 98% |
Q39287 | Brassica juncea | 36% | 100% |
Q41131 | Ricinus communis | 35% | 100% |
Q4Q3K9 | Leishmania major | 75% | 100% |
Q54794 | Arthrospira platensis | 28% | 100% |
Q56VS4 | Helianthus annuus | 33% | 89% |
Q594P3 | Sorghum bicolor | 37% | 100% |
Q59J82 | Mortierella alpina | 35% | 98% |
Q6RS95 | Dimorphotheca sinuata | 34% | 100% |
Q6RS96 | Dimorphotheca sinuata | 31% | 100% |
Q84UB8 | Punica granatum | 35% | 100% |
Q84UB9 | Trichosanthes kirilowii | 35% | 100% |
Q84UC0 | Trichosanthes kirilowii | 35% | 100% |
Q84VT2 | Punica granatum | 37% | 100% |
Q8GZC2 | Vernicia fordii | 35% | 100% |
Q8GZC3 | Vernicia fordii | 36% | 100% |
Q9AT72 | Calendula officinalis | 37% | 100% |
Q9FPP7 | Calendula officinalis | 32% | 100% |
Q9FPP8 | Calendula officinalis | 31% | 100% |
Q9NEQ0 | Caenorhabditis elegans | 32% | 98% |
Q9SCG2 | Calendula officinalis | 33% | 100% |
Q9SP61 | Momordica charantia | 34% | 99% |
Q9SP62 | Impatiens balsamina | 32% | 100% |
Q9Y8H5 | Mortierella alpina | 42% | 98% |
V5BA48 | Trypanosoma cruzi | 55% | 96% |