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:0005789 | endoplasmic reticulum membrane | 4 | 3 |
GO:0016020 | membrane | 2 | 16 |
GO:0031090 | organelle membrane | 3 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 16 |
Related structures:
AlphaFold database: Q4QFT4
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:0005506 | iron ion binding | 6 | 3 |
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:0046914 | transition metal ion binding | 5 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 168 | 172 | PF00656 | 0.429 |
CLV_NRD_NRD_1 | 141 | 143 | PF00675 | 0.208 |
CLV_NRD_NRD_1 | 178 | 180 | PF00675 | 0.229 |
CLV_NRD_NRD_1 | 323 | 325 | PF00675 | 0.404 |
CLV_NRD_NRD_1 | 356 | 358 | PF00675 | 0.331 |
CLV_NRD_NRD_1 | 461 | 463 | PF00675 | 0.414 |
CLV_PCSK_KEX2_1 | 141 | 143 | PF00082 | 0.286 |
CLV_PCSK_KEX2_1 | 461 | 463 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 216 | 220 | PF00082 | 0.305 |
CLV_PCSK_SKI1_1 | 357 | 361 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 396 | 400 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 405 | 409 | PF00082 | 0.260 |
DEG_MDM2_SWIB_1 | 210 | 217 | PF02201 | 0.277 |
DEG_MDM2_SWIB_1 | 35 | 42 | PF02201 | 0.477 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.668 |
DOC_CDC14_PxL_1 | 44 | 52 | PF14671 | 0.471 |
DOC_CYCLIN_RxL_1 | 354 | 363 | PF00134 | 0.461 |
DOC_CYCLIN_yCln2_LP_2 | 369 | 375 | PF00134 | 0.483 |
DOC_CYCLIN_yCln2_LP_2 | 58 | 64 | PF00134 | 0.538 |
DOC_MAPK_gen_1 | 461 | 467 | PF00069 | 0.576 |
DOC_MAPK_MEF2A_6 | 170 | 177 | PF00069 | 0.429 |
DOC_PP1_RVXF_1 | 382 | 389 | PF00149 | 0.566 |
DOC_PP2B_LxvP_1 | 336 | 339 | PF13499 | 0.575 |
DOC_PP2B_LxvP_1 | 58 | 61 | PF13499 | 0.526 |
DOC_USP7_MATH_1 | 164 | 168 | PF00917 | 0.477 |
DOC_USP7_MATH_1 | 248 | 252 | PF00917 | 0.498 |
DOC_USP7_MATH_1 | 438 | 442 | PF00917 | 0.610 |
DOC_WW_Pin1_4 | 244 | 249 | PF00397 | 0.500 |
LIG_14-3-3_CanoR_1 | 304 | 310 | PF00244 | 0.585 |
LIG_14-3-3_CanoR_1 | 59 | 65 | PF00244 | 0.255 |
LIG_14-3-3_CanoR_1 | 88 | 95 | PF00244 | 0.463 |
LIG_BRCT_BRCA1_1 | 250 | 254 | PF00533 | 0.408 |
LIG_Clathr_ClatBox_1 | 359 | 363 | PF01394 | 0.465 |
LIG_deltaCOP1_diTrp_1 | 204 | 211 | PF00928 | 0.258 |
LIG_FHA_1 | 187 | 193 | PF00498 | 0.265 |
LIG_FHA_1 | 75 | 81 | PF00498 | 0.356 |
LIG_FHA_1 | 8 | 14 | PF00498 | 0.664 |
LIG_FHA_2 | 131 | 137 | PF00498 | 0.444 |
LIG_FHA_2 | 199 | 205 | PF00498 | 0.265 |
LIG_FHA_2 | 245 | 251 | PF00498 | 0.450 |
LIG_FHA_2 | 306 | 312 | PF00498 | 0.527 |
LIG_LIR_Gen_1 | 157 | 166 | PF02991 | 0.464 |
LIG_LIR_Gen_1 | 251 | 259 | PF02991 | 0.434 |
LIG_LIR_Gen_1 | 286 | 296 | PF02991 | 0.561 |
LIG_LIR_Gen_1 | 343 | 353 | PF02991 | 0.527 |
LIG_LIR_Gen_1 | 387 | 393 | PF02991 | 0.413 |
LIG_LIR_Gen_1 | 63 | 72 | PF02991 | 0.208 |
LIG_LIR_Gen_1 | 83 | 94 | PF02991 | 0.292 |
LIG_LIR_LC3C_4 | 171 | 175 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 147 | 152 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 157 | 161 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 251 | 257 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 261 | 266 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 286 | 291 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 294 | 298 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 343 | 349 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 63 | 67 | PF02991 | 0.216 |
LIG_LIR_Nem_3 | 83 | 89 | PF02991 | 0.313 |
LIG_NRBOX | 49 | 55 | PF00104 | 0.265 |
LIG_PDZ_Class_2 | 462 | 467 | PF00595 | 0.577 |
LIG_Pex14_1 | 103 | 107 | PF04695 | 0.458 |
LIG_Pex14_1 | 205 | 209 | PF04695 | 0.244 |
LIG_Pex14_1 | 214 | 218 | PF04695 | 0.286 |
LIG_Pex14_1 | 39 | 43 | PF04695 | 0.265 |
LIG_Pex14_1 | 69 | 73 | PF04695 | 0.265 |
LIG_Pex14_2 | 210 | 214 | PF04695 | 0.416 |
LIG_Pex14_2 | 291 | 295 | PF04695 | 0.472 |
LIG_Pex14_2 | 35 | 39 | PF04695 | 0.485 |
LIG_SH2_CRK | 158 | 162 | PF00017 | 0.468 |
LIG_SH2_CRK | 86 | 90 | PF00017 | 0.458 |
LIG_SH2_GRB2like | 263 | 266 | PF00017 | 0.444 |
LIG_SH2_SRC | 43 | 46 | PF00017 | 0.474 |
LIG_SH2_STAT3 | 266 | 269 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 289 | 292 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 365 | 368 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 402 | 405 | PF00017 | 0.433 |
LIG_SH2_STAT5 | 425 | 428 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 43 | 46 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 57 | 60 | PF00017 | 0.213 |
LIG_SH3_1 | 371 | 377 | PF00018 | 0.535 |
LIG_SH3_3 | 371 | 377 | PF00018 | 0.574 |
LIG_SH3_3 | 454 | 460 | PF00018 | 0.546 |
LIG_Sin3_3 | 72 | 79 | PF02671 | 0.176 |
LIG_SUMO_SIM_par_1 | 365 | 370 | PF11976 | 0.523 |
LIG_TRAF2_1 | 443 | 446 | PF00917 | 0.575 |
LIG_WRC_WIRS_1 | 292 | 297 | PF05994 | 0.478 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.615 |
MOD_CK1_1 | 440 | 446 | PF00069 | 0.623 |
MOD_CK2_1 | 12 | 18 | PF00069 | 0.644 |
MOD_CK2_1 | 198 | 204 | PF00069 | 0.265 |
MOD_CK2_1 | 440 | 446 | PF00069 | 0.604 |
MOD_CMANNOS | 211 | 214 | PF00535 | 0.315 |
MOD_Cter_Amidation | 322 | 325 | PF01082 | 0.277 |
MOD_Cter_Amidation | 355 | 358 | PF01082 | 0.339 |
MOD_GlcNHglycan | 440 | 443 | PF01048 | 0.468 |
MOD_GlcNHglycan | 445 | 450 | PF01048 | 0.448 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.301 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.339 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.662 |
MOD_N-GLC_1 | 244 | 249 | PF02516 | 0.235 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.450 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.457 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.440 |
MOD_NEK2_1 | 226 | 231 | PF00069 | 0.319 |
MOD_NEK2_1 | 236 | 241 | PF00069 | 0.466 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.475 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.282 |
MOD_NEK2_1 | 9 | 14 | PF00069 | 0.646 |
MOD_PKA_1 | 384 | 390 | PF00069 | 0.398 |
MOD_Plk_4 | 169 | 175 | PF00069 | 0.556 |
MOD_Plk_4 | 248 | 254 | PF00069 | 0.449 |
MOD_Plk_4 | 291 | 297 | PF00069 | 0.602 |
MOD_Plk_4 | 9 | 15 | PF00069 | 0.632 |
MOD_ProDKin_1 | 244 | 250 | PF00069 | 0.500 |
MOD_SUMO_for_1 | 21 | 24 | PF00179 | 0.591 |
MOD_SUMO_rev_2 | 12 | 21 | PF00179 | 0.566 |
MOD_SUMO_rev_2 | 163 | 172 | PF00179 | 0.408 |
TRG_DiLeu_BaLyEn_6 | 45 | 50 | PF01217 | 0.455 |
TRG_ENDOCYTIC_2 | 158 | 161 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 289 | 292 | PF00928 | 0.493 |
TRG_ENDOCYTIC_2 | 37 | 40 | PF00928 | 0.591 |
TRG_ENDOCYTIC_2 | 57 | 60 | PF00928 | 0.279 |
TRG_ENDOCYTIC_2 | 86 | 89 | PF00928 | 0.449 |
TRG_ER_diArg_1 | 460 | 462 | PF00400 | 0.621 |
TRG_Pf-PMV_PEXEL_1 | 324 | 328 | PF00026 | 0.369 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCI5 | Leptomonas seymouri | 46% | 100% |
A0A0S4KNP4 | Bodo saltans | 42% | 100% |
A0A1X0NW01 | Trypanosomatidae | 45% | 100% |
A0A3Q8I9W7 | Leishmania donovani | 96% | 100% |
A0A3Q8IBJ0 | Leishmania donovani | 46% | 100% |
A0A3R7MEL0 | Trypanosoma rangeli | 47% | 100% |
A4H6I1 | Leishmania braziliensis | 83% | 100% |
A4HDT6 | Leishmania braziliensis | 47% | 100% |
A4HVZ3 | Leishmania infantum | 96% | 100% |
A4I134 | Leishmania infantum | 46% | 100% |
C9ZW73 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
E9APP5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
E9AX71 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 46% | 100% |
G5ED44 | Caenorhabditis elegans | 29% | 100% |
O00767 | Homo sapiens | 30% | 100% |
O44390 | Trichoplusia ni | 31% | 100% |
O94523 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 35% | 97% |
P0DOW2 | Anemone leveillei | 27% | 100% |
P21147 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 32% | 92% |
Q12618 | Ajellomyces capsulatus | 37% | 98% |
Q4QAA5 | Leishmania major | 45% | 100% |
Q64420 | Mesocricetus auratus | 31% | 100% |
Q6US81 | Spodoptera littoralis | 32% | 100% |
Q99PL7 | Mus musculus | 29% | 100% |
Q9BH41 | Acheta domesticus | 27% | 100% |
Q9FV68 | Limnanthes douglasii | 27% | 100% |