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: 18 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 15 |
NetGPI | no | yes: 0, no: 15 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 16 |
GO:0110165 | cellular anatomical entity | 1 | 16 |
GO:0005789 | endoplasmic reticulum membrane | 4 | 2 |
GO:0031090 | organelle membrane | 3 | 2 |
Related structures:
AlphaFold database: A4H6I1
Term | Name | Level | Count |
---|---|---|---|
GO:0006082 | organic acid metabolic process | 3 | 16 |
GO:0006629 | lipid metabolic process | 3 | 16 |
GO:0006631 | fatty acid metabolic process | 4 | 16 |
GO:0006633 | fatty acid biosynthetic process | 5 | 16 |
GO:0006636 | unsaturated fatty acid biosynthetic process | 6 | 16 |
GO:0008152 | metabolic process | 1 | 16 |
GO:0008610 | lipid biosynthetic process | 4 | 16 |
GO:0009058 | biosynthetic process | 2 | 16 |
GO:0009987 | cellular process | 1 | 16 |
GO:0016053 | organic acid biosynthetic process | 4 | 16 |
GO:0019752 | carboxylic acid metabolic process | 5 | 16 |
GO:0032787 | monocarboxylic acid metabolic process | 6 | 16 |
GO:0033559 | unsaturated fatty acid metabolic process | 5 | 16 |
GO:0043436 | oxoacid metabolic process | 4 | 16 |
GO:0044237 | cellular metabolic process | 2 | 16 |
GO:0044238 | primary metabolic process | 2 | 16 |
GO:0044249 | cellular biosynthetic process | 3 | 16 |
GO:0044255 | cellular lipid metabolic process | 3 | 16 |
GO:0044281 | small molecule metabolic process | 2 | 16 |
GO:0044283 | small molecule biosynthetic process | 3 | 16 |
GO:0046394 | carboxylic acid biosynthetic process | 5 | 16 |
GO:0071704 | organic substance metabolic process | 2 | 16 |
GO:0072330 | monocarboxylic acid biosynthetic process | 6 | 16 |
GO:1901576 | organic substance biosynthetic process | 3 | 16 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 16 |
GO:0004768 | stearoyl-CoA 9-desaturase activity | 6 | 16 |
GO:0005488 | binding | 1 | 7 |
GO:0016215 | acyl-CoA desaturase activity | 5 | 16 |
GO:0016491 | oxidoreductase activity | 2 | 16 |
GO:0016705 | oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen | 3 | 16 |
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 | 16 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043169 | cation binding | 3 | 7 |
GO:0046872 | metal ion binding | 4 | 7 |
GO:0005506 | iron ion binding | 6 | 2 |
GO:0046914 | transition metal ion binding | 5 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 168 | 172 | PF00656 | 0.428 |
CLV_NRD_NRD_1 | 178 | 180 | PF00675 | 0.228 |
CLV_NRD_NRD_1 | 334 | 336 | PF00675 | 0.320 |
CLV_NRD_NRD_1 | 356 | 358 | PF00675 | 0.328 |
CLV_PCSK_KEX2_1 | 334 | 336 | PF00082 | 0.289 |
CLV_PCSK_SKI1_1 | 142 | 146 | PF00082 | 0.159 |
CLV_PCSK_SKI1_1 | 216 | 220 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 395 | 399 | PF00082 | 0.256 |
CLV_PCSK_SKI1_1 | 404 | 408 | PF00082 | 0.268 |
DEG_APCC_DBOX_1 | 421 | 429 | PF00400 | 0.392 |
DEG_MDM2_SWIB_1 | 210 | 217 | PF02201 | 0.264 |
DEG_MDM2_SWIB_1 | 35 | 42 | PF02201 | 0.473 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.675 |
DEG_SCF_FBW7_1 | 246 | 251 | PF00400 | 0.361 |
DOC_CDC14_PxL_1 | 44 | 52 | PF14671 | 0.390 |
DOC_CYCLIN_yCln2_LP_2 | 336 | 342 | PF00134 | 0.583 |
DOC_CYCLIN_yCln2_LP_2 | 58 | 64 | PF00134 | 0.489 |
DOC_MAPK_DCC_7 | 422 | 430 | PF00069 | 0.415 |
DOC_MAPK_MEF2A_6 | 170 | 177 | PF00069 | 0.477 |
DOC_MAPK_MEF2A_6 | 422 | 430 | PF00069 | 0.415 |
DOC_PP1_RVXF_1 | 382 | 388 | PF00149 | 0.545 |
DOC_PP2B_LxvP_1 | 336 | 339 | PF13499 | 0.569 |
DOC_PP2B_LxvP_1 | 58 | 61 | PF13499 | 0.428 |
DOC_USP7_MATH_1 | 164 | 168 | PF00917 | 0.428 |
DOC_USP7_MATH_1 | 248 | 252 | PF00917 | 0.493 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 439 | 443 | PF00917 | 0.613 |
DOC_WW_Pin1_4 | 244 | 249 | PF00397 | 0.500 |
DOC_WW_Pin1_4 | 60 | 65 | PF00397 | 0.202 |
LIG_14-3-3_CanoR_1 | 240 | 248 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 88 | 95 | PF00244 | 0.461 |
LIG_Clathr_ClatBox_1 | 359 | 363 | PF01394 | 0.462 |
LIG_deltaCOP1_diTrp_1 | 204 | 211 | PF00928 | 0.257 |
LIG_FHA_1 | 187 | 193 | PF00498 | 0.328 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.516 |
LIG_FHA_1 | 47 | 53 | PF00498 | 0.338 |
LIG_FHA_1 | 75 | 81 | PF00498 | 0.339 |
LIG_FHA_1 | 8 | 14 | PF00498 | 0.698 |
LIG_FHA_2 | 131 | 137 | PF00498 | 0.443 |
LIG_FHA_2 | 199 | 205 | PF00498 | 0.264 |
LIG_FHA_2 | 245 | 251 | PF00498 | 0.444 |
LIG_FHA_2 | 343 | 349 | PF00498 | 0.471 |
LIG_LIR_Gen_1 | 157 | 166 | PF02991 | 0.459 |
LIG_LIR_Gen_1 | 261 | 271 | PF02991 | 0.438 |
LIG_LIR_Gen_1 | 286 | 296 | PF02991 | 0.559 |
LIG_LIR_Gen_1 | 343 | 353 | PF02991 | 0.523 |
LIG_LIR_Gen_1 | 49 | 58 | PF02991 | 0.391 |
LIG_LIR_Gen_1 | 83 | 94 | PF02991 | 0.246 |
LIG_LIR_LC3C_4 | 171 | 175 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 147 | 152 | PF02991 | 0.501 |
LIG_LIR_Nem_3 | 157 | 161 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 261 | 266 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 286 | 292 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 294 | 298 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 343 | 349 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 49 | 54 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 83 | 89 | PF02991 | 0.265 |
LIG_NRBOX | 49 | 55 | PF00104 | 0.264 |
LIG_PDZ_Class_1 | 455 | 460 | PF00595 | 0.538 |
LIG_Pex14_1 | 103 | 107 | PF04695 | 0.457 |
LIG_Pex14_1 | 205 | 209 | PF04695 | 0.243 |
LIG_Pex14_1 | 214 | 218 | PF04695 | 0.285 |
LIG_Pex14_1 | 39 | 43 | PF04695 | 0.264 |
LIG_Pex14_1 | 69 | 73 | PF04695 | 0.264 |
LIG_Pex14_2 | 145 | 149 | PF04695 | 0.361 |
LIG_Pex14_2 | 210 | 214 | PF04695 | 0.411 |
LIG_Pex14_2 | 266 | 270 | PF04695 | 0.416 |
LIG_Pex14_2 | 291 | 295 | PF04695 | 0.471 |
LIG_Pex14_2 | 35 | 39 | PF04695 | 0.478 |
LIG_SH2_CRK | 86 | 90 | PF00017 | 0.457 |
LIG_SH2_GRB2like | 263 | 266 | PF00017 | 0.443 |
LIG_SH2_PTP2 | 289 | 292 | PF00017 | 0.404 |
LIG_SH2_SRC | 43 | 46 | PF00017 | 0.278 |
LIG_SH2_SRC | 57 | 60 | PF00017 | 0.247 |
LIG_SH2_STAP1 | 242 | 246 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 289 | 292 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 344 | 347 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 365 | 368 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 401 | 404 | PF00017 | 0.433 |
LIG_SH2_STAT5 | 424 | 427 | PF00017 | 0.521 |
LIG_SH2_STAT5 | 43 | 46 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 457 | 460 | PF00017 | 0.558 |
LIG_SH2_STAT5 | 57 | 60 | PF00017 | 0.399 |
LIG_SH3_3 | 15 | 21 | PF00018 | 0.591 |
LIG_SH3_3 | 371 | 377 | PF00018 | 0.536 |
LIG_SH3_3 | 433 | 439 | PF00018 | 0.541 |
LIG_SH3_3 | 58 | 64 | PF00018 | 0.233 |
LIG_SUMO_SIM_anti_2 | 250 | 258 | PF11976 | 0.361 |
LIG_SUMO_SIM_par_1 | 365 | 370 | PF11976 | 0.553 |
LIG_TRAF2_1 | 21 | 24 | PF00917 | 0.605 |
LIG_WRC_WIRS_1 | 292 | 297 | PF05994 | 0.475 |
MOD_CK1_1 | 442 | 448 | PF00069 | 0.611 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.591 |
MOD_CK2_1 | 198 | 204 | PF00069 | 0.264 |
MOD_CMANNOS | 211 | 214 | PF00535 | 0.314 |
MOD_Cter_Amidation | 355 | 358 | PF01082 | 0.337 |
MOD_GlcNHglycan | 441 | 444 | PF01048 | 0.421 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.381 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.169 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.313 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.440 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.397 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.512 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.440 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.447 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.443 |
MOD_NEK2_1 | 226 | 231 | PF00069 | 0.308 |
MOD_NEK2_1 | 236 | 241 | PF00069 | 0.443 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.473 |
MOD_NEK2_1 | 9 | 14 | PF00069 | 0.688 |
MOD_NEK2_2 | 130 | 135 | PF00069 | 0.413 |
MOD_NEK2_2 | 4 | 9 | PF00069 | 0.505 |
MOD_Plk_1 | 249 | 255 | PF00069 | 0.361 |
MOD_Plk_1 | 342 | 348 | PF00069 | 0.530 |
MOD_Plk_4 | 249 | 255 | PF00069 | 0.449 |
MOD_Plk_4 | 291 | 297 | PF00069 | 0.564 |
MOD_Plk_4 | 4 | 10 | PF00069 | 0.630 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.312 |
MOD_Plk_4 | 62 | 68 | PF00069 | 0.212 |
MOD_ProDKin_1 | 244 | 250 | PF00069 | 0.500 |
MOD_ProDKin_1 | 60 | 66 | PF00069 | 0.196 |
MOD_SUMO_for_1 | 21 | 24 | PF00179 | 0.591 |
TRG_ENDOCYTIC_2 | 158 | 161 | PF00928 | 0.480 |
TRG_ENDOCYTIC_2 | 181 | 184 | PF00928 | 0.424 |
TRG_ENDOCYTIC_2 | 263 | 266 | PF00928 | 0.440 |
TRG_ENDOCYTIC_2 | 289 | 292 | PF00928 | 0.462 |
TRG_ENDOCYTIC_2 | 37 | 40 | PF00928 | 0.605 |
TRG_ENDOCYTIC_2 | 57 | 60 | PF00928 | 0.533 |
TRG_ENDOCYTIC_2 | 86 | 89 | PF00928 | 0.444 |
TRG_ER_diArg_1 | 333 | 335 | PF00400 | 0.458 |
TRG_Pf-PMV_PEXEL_1 | 324 | 328 | PF00026 | 0.343 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCI5 | Leptomonas seymouri | 46% | 100% |
A0A0S4KNP4 | Bodo saltans | 44% | 100% |
A0A1X0NW01 | Trypanosomatidae | 48% | 100% |
A0A3Q8I9W7 | Leishmania donovani | 84% | 99% |
A0A3Q8IBJ0 | Leishmania donovani | 46% | 100% |
A0A3R7MEL0 | Trypanosoma rangeli | 47% | 100% |
A4HDT6 | Leishmania braziliensis | 47% | 100% |
A4HVZ3 | Leishmania infantum | 84% | 99% |
A4I134 | Leishmania infantum | 46% | 100% |
C9ZW73 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
E9APP5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
E9AX71 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 46% | 100% |
G5ED44 | Caenorhabditis elegans | 28% | 100% |
G5EGH6 | Caenorhabditis elegans | 30% | 100% |
G5EGN2 | Caenorhabditis elegans | 30% | 100% |
O94523 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 35% | 96% |
P0DOW2 | Anemone leveillei | 28% | 100% |
P0DOW3 | Anemone leveillei | 27% | 100% |
P21147 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 32% | 90% |
Q12618 | Ajellomyces capsulatus | 37% | 97% |
Q4QAA5 | Leishmania major | 45% | 100% |
Q4QFT4 | Leishmania major | 83% | 100% |
Q6US81 | Spodoptera littoralis | 32% | 100% |
Q95MI7 | Capra hircus | 30% | 100% |
Q9FV68 | Limnanthes douglasii | 27% | 100% |
Q9SID2 | Arabidopsis thaliana | 26% | 100% |