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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
Related structures:
AlphaFold database: E9ALC8
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 8 |
GO:0008152 | metabolic process | 1 | 8 |
GO:0044238 | primary metabolic process | 2 | 8 |
GO:0071704 | organic substance metabolic process | 2 | 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 8 |
GO:0016491 | oxidoreductase activity | 2 | 8 |
GO:0016705 | oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen | 3 | 1 |
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 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 110 | 116 | PF00089 | 0.327 |
CLV_NRD_NRD_1 | 221 | 223 | PF00675 | 0.434 |
CLV_NRD_NRD_1 | 379 | 381 | PF00675 | 0.310 |
CLV_NRD_NRD_1 | 81 | 83 | PF00675 | 0.261 |
CLV_PCSK_FUR_1 | 222 | 226 | PF00082 | 0.495 |
CLV_PCSK_KEX2_1 | 221 | 223 | PF00082 | 0.455 |
CLV_PCSK_KEX2_1 | 224 | 226 | PF00082 | 0.467 |
CLV_PCSK_KEX2_1 | 62 | 64 | PF00082 | 0.472 |
CLV_PCSK_KEX2_1 | 81 | 83 | PF00082 | 0.272 |
CLV_PCSK_PC1ET2_1 | 224 | 226 | PF00082 | 0.503 |
CLV_PCSK_PC1ET2_1 | 62 | 64 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 380 | 384 | PF00082 | 0.297 |
CLV_PCSK_SKI1_1 | 401 | 405 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.326 |
CLV_PCSK_SKI1_1 | 82 | 86 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 88 | 92 | PF00082 | 0.317 |
DOC_CDC14_PxL_1 | 128 | 136 | PF14671 | 0.314 |
DOC_CYCLIN_RxL_1 | 377 | 385 | PF00134 | 0.493 |
DOC_MAPK_DCC_7 | 130 | 139 | PF00069 | 0.326 |
DOC_MAPK_FxFP_2 | 370 | 373 | PF00069 | 0.366 |
DOC_MAPK_gen_1 | 200 | 207 | PF00069 | 0.226 |
DOC_MAPK_MEF2A_6 | 230 | 237 | PF00069 | 0.267 |
DOC_MAPK_NFAT4_5 | 230 | 238 | PF00069 | 0.267 |
DOC_PP1_SILK_1 | 31 | 36 | PF00149 | 0.545 |
DOC_PP2B_LxvP_1 | 52 | 55 | PF13499 | 0.527 |
DOC_PP4_FxxP_1 | 129 | 132 | PF00568 | 0.314 |
DOC_PP4_FxxP_1 | 26 | 29 | PF00568 | 0.506 |
DOC_PP4_FxxP_1 | 370 | 373 | PF00568 | 0.366 |
DOC_USP7_MATH_1 | 68 | 72 | PF00917 | 0.550 |
DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.283 |
DOC_WW_Pin1_4 | 340 | 345 | PF00397 | 0.483 |
LIG_14-3-3_CanoR_1 | 113 | 120 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 230 | 236 | PF00244 | 0.248 |
LIG_14-3-3_CanoR_1 | 266 | 274 | PF00244 | 0.445 |
LIG_BRCT_BRCA1_1 | 300 | 304 | PF00533 | 0.337 |
LIG_BRCT_BRCA1_1 | 86 | 90 | PF00533 | 0.482 |
LIG_eIF4E_1 | 112 | 118 | PF01652 | 0.527 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.258 |
LIG_FHA_1 | 242 | 248 | PF00498 | 0.281 |
LIG_FHA_1 | 337 | 343 | PF00498 | 0.460 |
LIG_LIR_Apic_2 | 24 | 29 | PF02991 | 0.497 |
LIG_LIR_Gen_1 | 305 | 315 | PF02991 | 0.305 |
LIG_LIR_Gen_1 | 333 | 342 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 106 | 110 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 290 | 295 | PF02991 | 0.311 |
LIG_LIR_Nem_3 | 305 | 311 | PF02991 | 0.220 |
LIG_LIR_Nem_3 | 333 | 337 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 349 | 354 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 402 | 406 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 44 | 50 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 87 | 93 | PF02991 | 0.486 |
LIG_MYND_1 | 132 | 136 | PF01753 | 0.314 |
LIG_MYND_1 | 373 | 377 | PF01753 | 0.366 |
LIG_PCNA_yPIPBox_3 | 221 | 233 | PF02747 | 0.250 |
LIG_Pex14_1 | 350 | 354 | PF04695 | 0.441 |
LIG_Pex14_2 | 103 | 107 | PF04695 | 0.538 |
LIG_Pex14_2 | 300 | 304 | PF04695 | 0.278 |
LIG_Pex14_2 | 347 | 351 | PF04695 | 0.467 |
LIG_SH2_CRK | 334 | 338 | PF00017 | 0.483 |
LIG_SH2_GRB2like | 354 | 357 | PF00017 | 0.441 |
LIG_SH2_NCK_1 | 334 | 338 | PF00017 | 0.483 |
LIG_SH2_PTP2 | 308 | 311 | PF00017 | 0.278 |
LIG_SH2_STAP1 | 334 | 338 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 238 | 241 | PF00017 | 0.209 |
LIG_SH2_STAT5 | 267 | 270 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 308 | 311 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 338 | 341 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 354 | 357 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 37 | 40 | PF00017 | 0.545 |
LIG_SH2_STAT5 | 60 | 63 | PF00017 | 0.567 |
LIG_SH3_1 | 62 | 68 | PF00018 | 0.573 |
LIG_SH3_3 | 318 | 324 | PF00018 | 0.506 |
LIG_SH3_3 | 362 | 368 | PF00018 | 0.441 |
LIG_SH3_3 | 5 | 11 | PF00018 | 0.594 |
LIG_SH3_3 | 62 | 68 | PF00018 | 0.573 |
LIG_SUMO_SIM_anti_2 | 115 | 121 | PF11976 | 0.483 |
LIG_TYR_ITIM | 332 | 337 | PF00017 | 0.483 |
MOD_CDK_SPxK_1 | 194 | 200 | PF00069 | 0.283 |
MOD_CK1_1 | 71 | 77 | PF00069 | 0.507 |
MOD_Cter_Amidation | 222 | 225 | PF01082 | 0.483 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.442 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.480 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.332 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.381 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.447 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.351 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.483 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.497 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.573 |
MOD_N-GLC_1 | 103 | 108 | PF02516 | 0.305 |
MOD_N-GLC_1 | 315 | 320 | PF02516 | 0.283 |
MOD_N-GLC_1 | 340 | 345 | PF02516 | 0.283 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.511 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.295 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.278 |
MOD_NEK2_1 | 315 | 320 | PF00069 | 0.469 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.486 |
MOD_PIKK_1 | 186 | 192 | PF00454 | 0.283 |
MOD_PIKK_1 | 261 | 267 | PF00454 | 0.461 |
MOD_PIKK_1 | 298 | 304 | PF00454 | 0.337 |
MOD_PIKK_1 | 68 | 74 | PF00454 | 0.510 |
MOD_PKA_2 | 112 | 118 | PF00069 | 0.527 |
MOD_PKA_2 | 265 | 271 | PF00069 | 0.483 |
MOD_Plk_1 | 103 | 109 | PF00069 | 0.502 |
MOD_Plk_1 | 315 | 321 | PF00069 | 0.484 |
MOD_Plk_4 | 182 | 188 | PF00069 | 0.381 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.521 |
MOD_Plk_4 | 243 | 249 | PF00069 | 0.278 |
MOD_Plk_4 | 287 | 293 | PF00069 | 0.471 |
MOD_Plk_4 | 342 | 348 | PF00069 | 0.456 |
MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.283 |
MOD_ProDKin_1 | 340 | 346 | PF00069 | 0.483 |
MOD_SUMO_rev_2 | 87 | 93 | PF00179 | 0.527 |
TRG_DiLeu_BaEn_2 | 326 | 332 | PF01217 | 0.461 |
TRG_ENDOCYTIC_2 | 126 | 129 | PF00928 | 0.354 |
TRG_ENDOCYTIC_2 | 251 | 254 | PF00928 | 0.278 |
TRG_ENDOCYTIC_2 | 308 | 311 | PF00928 | 0.302 |
TRG_ENDOCYTIC_2 | 334 | 337 | PF00928 | 0.483 |
TRG_ENDOCYTIC_2 | 354 | 357 | PF00928 | 0.349 |
TRG_ENDOCYTIC_2 | 47 | 50 | PF00928 | 0.526 |
TRG_ER_diArg_1 | 377 | 380 | PF00400 | 0.460 |
TRG_ER_diArg_1 | 81 | 83 | PF00400 | 0.428 |
TRG_Pf-PMV_PEXEL_1 | 380 | 384 | PF00026 | 0.311 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0C5PRW9 | Tachysurus fulvidraco | 28% | 94% |
A0A0N1HZP4 | Leptomonas seymouri | 24% | 100% |
A0A0N1IMB2 | Leptomonas seymouri | 27% | 100% |
A0A0N1PAQ6 | Leptomonas seymouri | 78% | 100% |
A0A0S4KLP1 | Bodo saltans | 24% | 100% |
A0A1X0NMZ1 | Trypanosomatidae | 25% | 100% |
A0A1X0NPK3 | Trypanosomatidae | 60% | 99% |
A0A3Q8I9Z6 | Leishmania donovani | 24% | 100% |
A0A3Q8IK71 | Leishmania donovani | 25% | 100% |
A0A3S5H618 | Leishmania donovani | 93% | 100% |
A0A422NCE1 | Trypanosoma rangeli | 23% | 98% |
A4FV48 | Bos taurus | 27% | 94% |
A4H558 | Leishmania braziliensis | 86% | 100% |
A4H7V4 | Leishmania braziliensis | 22% | 100% |
A4HQL7 | Leishmania braziliensis | 25% | 97% |
A4HTD5 | Leishmania infantum | 92% | 100% |
A4HW80 | Leishmania infantum | 24% | 100% |
A4IFP3 | Bos taurus | 27% | 94% |
A4KDP0 | Rebecca salina | 49% | 98% |
A4KDP1 | Rebecca salina | 25% | 98% |
A4UVI1 | Papio anubis | 27% | 94% |
A8MWK0 | Homo sapiens | 24% | 87% |
B2KKL4 | Siganus canaliculatus | 28% | 94% |
B8R1K0 | Papio anubis | 27% | 94% |
C4QVU3 | Komagataella phaffii (strain GS115 / ATCC 20864) | 22% | 77% |
D0A3D4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 22% | 100% |
D8X2C5 | Siganus canaliculatus | 28% | 94% |
E9AI08 | Leishmania infantum | 25% | 100% |
E9APY2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9AUD2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
G5EG11 | Caenorhabditis elegans | 25% | 93% |
O04353 | Borago officinalis | 23% | 93% |
O60427 | Homo sapiens | 26% | 94% |
O95864 | Homo sapiens | 26% | 94% |
Q0VAX3 | Mus musculus | 27% | 86% |
Q23221 | Caenorhabditis elegans | 25% | 94% |
Q3EBF7 | Arabidopsis thaliana | 28% | 93% |
Q43469 | Helianthus annuus | 25% | 91% |
Q4Q058 | Leishmania major | 25% | 100% |
Q4QFK0 | Leishmania major | 25% | 100% |
Q4QIH7 | Leishmania major | 94% | 100% |
Q4R749 | Macaca fascicularis | 27% | 94% |
Q5AEK8 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 23% | 71% |
Q5REA7 | Pongo abelii | 26% | 94% |
Q6CMK7 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 24% | 73% |
Q6DDK2 | Xenopus laevis | 27% | 93% |
Q8K1P9 | Rattus norvegicus | 27% | 93% |
Q8NKG8 | Kluyveromyces lactis | 24% | 73% |
Q8NKG9 | Lachancea kluyveri (strain ATCC 58438 / CBS 3082 / BCRC 21498 / NBRC 1685 / JCM 7257 / NCYC 543 / NRRL Y-12651) | 24% | 73% |
Q8S3C1 | Thraustochytrium sp. | 44% | 95% |
Q920L1 | Mus musculus | 26% | 93% |
Q920R3 | Rattus norvegicus | 28% | 93% |
Q9DEX7 | Danio rerio | 29% | 94% |
Q9FR82 | Borago officinalis | 25% | 93% |
Q9JJE7 | Mus musculus | 28% | 93% |
Q9LEM9 | Ceratodon purpureus | 25% | 80% |
Q9LEN0 | Ceratodon purpureus | 25% | 86% |
Q9SWQ9 | Euglena gracilis | 27% | 100% |
Q9Y1W0 | Dictyostelium discoideum | 23% | 90% |
Q9Y5Q0 | Homo sapiens | 28% | 94% |
Q9Z0R9 | Mus musculus | 27% | 94% |
Q9Z122 | Rattus norvegicus | 27% | 94% |
Q9ZNW2 | Physcomitrium patens | 25% | 79% |
Q9ZRP7 | Arabidopsis thaliana | 25% | 93% |