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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A4I3L1
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 11 |
GO:0006720 | isoprenoid metabolic process | 4 | 11 |
GO:0006743 | ubiquinone metabolic process | 5 | 11 |
GO:0006744 | ubiquinone biosynthetic process | 6 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0008299 | isoprenoid biosynthetic process | 4 | 11 |
GO:0008610 | lipid biosynthetic process | 4 | 11 |
GO:0009058 | biosynthetic process | 2 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0042180 | cellular ketone metabolic process | 3 | 11 |
GO:0042181 | ketone biosynthetic process | 4 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0044249 | cellular biosynthetic process | 3 | 11 |
GO:0044255 | cellular lipid metabolic process | 3 | 11 |
GO:0044281 | small molecule metabolic process | 2 | 11 |
GO:0044283 | small molecule biosynthetic process | 3 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:1901576 | organic substance biosynthetic process | 3 | 11 |
GO:1901661 | quinone metabolic process | 4 | 11 |
GO:1901663 | quinone biosynthetic process | 5 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0002083 | 4-hydroxybenzoate decaprenyltransferase activity | 6 | 11 |
GO:0002094 | polyprenyltransferase activity | 5 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004659 | prenyltransferase activity | 4 | 11 |
GO:0008412 | 4-hydroxybenzoate octaprenyltransferase activity | 6 | 11 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0016765 | transferase activity, transferring alkyl or aryl (other than methyl) groups | 3 | 11 |
GO:0047293 | 4-hydroxybenzoate nonaprenyltransferase activity | 6 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 150 | 152 | PF00675 | 0.202 |
CLV_NRD_NRD_1 | 272 | 274 | PF00675 | 0.240 |
CLV_NRD_NRD_1 | 289 | 291 | PF00675 | 0.158 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.377 |
CLV_NRD_NRD_1 | 445 | 447 | PF00675 | 0.507 |
CLV_NRD_NRD_1 | 71 | 73 | PF00675 | 0.334 |
CLV_PCSK_KEX2_1 | 215 | 217 | PF00082 | 0.216 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.290 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.377 |
CLV_PCSK_KEX2_1 | 349 | 351 | PF00082 | 0.255 |
CLV_PCSK_KEX2_1 | 445 | 447 | PF00082 | 0.507 |
CLV_PCSK_PC1ET2_1 | 215 | 217 | PF00082 | 0.216 |
CLV_PCSK_PC1ET2_1 | 349 | 351 | PF00082 | 0.326 |
CLV_PCSK_SKI1_1 | 215 | 219 | PF00082 | 0.216 |
CLV_PCSK_SKI1_1 | 291 | 295 | PF00082 | 0.231 |
CLV_PCSK_SKI1_1 | 394 | 398 | PF00082 | 0.545 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.577 |
DOC_CDC14_PxL_1 | 217 | 225 | PF14671 | 0.409 |
DOC_CYCLIN_RxL_1 | 388 | 402 | PF00134 | 0.349 |
DOC_CYCLIN_yCln2_LP_2 | 118 | 124 | PF00134 | 0.202 |
DOC_MAPK_gen_1 | 349 | 358 | PF00069 | 0.450 |
DOC_MAPK_HePTP_8 | 240 | 252 | PF00069 | 0.236 |
DOC_MAPK_MEF2A_6 | 216 | 225 | PF00069 | 0.411 |
DOC_MAPK_MEF2A_6 | 243 | 252 | PF00069 | 0.202 |
DOC_MAPK_MEF2A_6 | 349 | 356 | PF00069 | 0.479 |
DOC_PP1_RVXF_1 | 104 | 111 | PF00149 | 0.236 |
DOC_PP1_RVXF_1 | 83 | 90 | PF00149 | 0.545 |
DOC_PP2B_LxvP_1 | 118 | 121 | PF13499 | 0.202 |
DOC_PP2B_LxvP_1 | 92 | 95 | PF13499 | 0.255 |
DOC_PP4_FxxP_1 | 418 | 421 | PF00568 | 0.348 |
DOC_PP4_FxxP_1 | 83 | 86 | PF00568 | 0.565 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.248 |
DOC_USP7_MATH_1 | 35 | 39 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.387 |
DOC_USP7_MATH_1 | 387 | 391 | PF00917 | 0.298 |
DOC_USP7_MATH_1 | 45 | 49 | PF00917 | 0.575 |
DOC_USP7_UBL2_3 | 277 | 281 | PF12436 | 0.421 |
DOC_WW_Pin1_4 | 191 | 196 | PF00397 | 0.202 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 202 | 207 | PF00397 | 0.236 |
LIG_14-3-3_CanoR_1 | 13 | 20 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 216 | 220 | PF00244 | 0.402 |
LIG_14-3-3_CanoR_1 | 381 | 387 | PF00244 | 0.513 |
LIG_APCC_ABBA_1 | 74 | 79 | PF00400 | 0.471 |
LIG_APCC_ABBAyCdc20_2 | 73 | 79 | PF00400 | 0.540 |
LIG_deltaCOP1_diTrp_1 | 147 | 153 | PF00928 | 0.458 |
LIG_deltaCOP1_diTrp_1 | 340 | 348 | PF00928 | 0.415 |
LIG_deltaCOP1_diTrp_1 | 476 | 484 | PF00928 | 0.443 |
LIG_FHA_1 | 103 | 109 | PF00498 | 0.296 |
LIG_FHA_1 | 15 | 21 | PF00498 | 0.552 |
LIG_GBD_Chelix_1 | 185 | 193 | PF00786 | 0.290 |
LIG_HOMEOBOX | 475 | 478 | PF00046 | 0.318 |
LIG_IRF3_LxIS_1 | 301 | 308 | PF10401 | 0.181 |
LIG_LIR_Apic_2 | 416 | 421 | PF02991 | 0.342 |
LIG_LIR_Gen_1 | 150 | 161 | PF02991 | 0.402 |
LIG_LIR_Gen_1 | 260 | 269 | PF02991 | 0.240 |
LIG_LIR_Gen_1 | 393 | 401 | PF02991 | 0.445 |
LIG_LIR_Gen_1 | 447 | 458 | PF02991 | 0.277 |
LIG_LIR_Gen_1 | 472 | 483 | PF02991 | 0.313 |
LIG_LIR_Nem_3 | 205 | 211 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 260 | 266 | PF02991 | 0.280 |
LIG_LIR_Nem_3 | 393 | 398 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 447 | 453 | PF02991 | 0.277 |
LIG_LIR_Nem_3 | 479 | 484 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 5 | 11 | PF02991 | 0.651 |
LIG_LYPXL_S_1 | 210 | 214 | PF13949 | 0.284 |
LIG_LYPXL_yS_3 | 211 | 214 | PF13949 | 0.436 |
LIG_PCNA_PIPBox_1 | 130 | 139 | PF02747 | 0.301 |
LIG_PCNA_yPIPBox_3 | 130 | 139 | PF02747 | 0.301 |
LIG_Pex14_1 | 149 | 153 | PF04695 | 0.433 |
LIG_Pex14_1 | 259 | 263 | PF04695 | 0.236 |
LIG_Pex14_1 | 414 | 418 | PF04695 | 0.337 |
LIG_Pex14_1 | 477 | 481 | PF04695 | 0.391 |
LIG_Pex14_2 | 473 | 477 | PF04695 | 0.397 |
LIG_SH2_CRK | 237 | 241 | PF00017 | 0.256 |
LIG_SH2_CRK | 263 | 267 | PF00017 | 0.236 |
LIG_SH2_NCK_1 | 263 | 267 | PF00017 | 0.236 |
LIG_SH2_PTP2 | 319 | 322 | PF00017 | 0.255 |
LIG_SH2_STAP1 | 237 | 241 | PF00017 | 0.236 |
LIG_SH2_STAP1 | 263 | 267 | PF00017 | 0.245 |
LIG_SH2_STAT3 | 219 | 222 | PF00017 | 0.387 |
LIG_SH2_STAT3 | 267 | 270 | PF00017 | 0.402 |
LIG_SH2_STAT3 | 448 | 451 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 136 | 139 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 292 | 295 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 319 | 322 | PF00017 | 0.236 |
LIG_SH2_STAT5 | 357 | 360 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 407 | 410 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 448 | 451 | PF00017 | 0.266 |
LIG_SH3_1 | 3 | 9 | PF00018 | 0.639 |
LIG_SH3_3 | 118 | 124 | PF00018 | 0.226 |
LIG_SH3_3 | 245 | 251 | PF00018 | 0.215 |
LIG_SH3_3 | 3 | 9 | PF00018 | 0.644 |
LIG_SH3_3 | 435 | 441 | PF00018 | 0.403 |
LIG_SUMO_SIM_anti_2 | 176 | 182 | PF11976 | 0.350 |
LIG_TYR_ITIM | 235 | 240 | PF00017 | 0.236 |
LIG_TYR_ITIM | 261 | 266 | PF00017 | 0.236 |
MOD_CK1_1 | 14 | 20 | PF00069 | 0.582 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.575 |
MOD_CK1_1 | 37 | 43 | PF00069 | 0.664 |
MOD_CK1_1 | 390 | 396 | PF00069 | 0.338 |
MOD_CK1_1 | 405 | 411 | PF00069 | 0.414 |
MOD_CK1_1 | 471 | 477 | PF00069 | 0.433 |
MOD_CK2_1 | 168 | 174 | PF00069 | 0.415 |
MOD_CK2_1 | 370 | 376 | PF00069 | 0.496 |
MOD_CK2_1 | 41 | 47 | PF00069 | 0.585 |
MOD_GlcNHglycan | 174 | 178 | PF01048 | 0.294 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.371 |
MOD_GlcNHglycan | 307 | 310 | PF01048 | 0.223 |
MOD_GlcNHglycan | 384 | 387 | PF01048 | 0.559 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.519 |
MOD_GlcNHglycan | 427 | 430 | PF01048 | 0.561 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.404 |
MOD_GlcNHglycan | 453 | 456 | PF01048 | 0.507 |
MOD_GSK3_1 | 301 | 308 | PF00069 | 0.235 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.602 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.412 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.605 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.274 |
MOD_N-GLC_1 | 191 | 196 | PF02516 | 0.408 |
MOD_N-GLC_1 | 451 | 456 | PF02516 | 0.561 |
MOD_N-GLC_2 | 366 | 368 | PF02516 | 0.301 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.236 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.264 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.228 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.324 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.252 |
MOD_NEK2_2 | 54 | 59 | PF00069 | 0.569 |
MOD_PIKK_1 | 310 | 316 | PF00454 | 0.236 |
MOD_PKA_1 | 215 | 221 | PF00069 | 0.402 |
MOD_PKA_2 | 215 | 221 | PF00069 | 0.402 |
MOD_PKA_2 | 380 | 386 | PF00069 | 0.513 |
MOD_PKA_2 | 81 | 87 | PF00069 | 0.534 |
MOD_Plk_1 | 173 | 179 | PF00069 | 0.326 |
MOD_Plk_1 | 451 | 457 | PF00069 | 0.353 |
MOD_Plk_1 | 463 | 469 | PF00069 | 0.362 |
MOD_Plk_1 | 54 | 60 | PF00069 | 0.657 |
MOD_Plk_4 | 262 | 268 | PF00069 | 0.276 |
MOD_Plk_4 | 301 | 307 | PF00069 | 0.382 |
MOD_Plk_4 | 328 | 334 | PF00069 | 0.420 |
MOD_Plk_4 | 402 | 408 | PF00069 | 0.450 |
MOD_ProDKin_1 | 191 | 197 | PF00069 | 0.202 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.645 |
MOD_ProDKin_1 | 202 | 208 | PF00069 | 0.236 |
MOD_SUMO_for_1 | 58 | 61 | PF00179 | 0.562 |
MOD_SUMO_rev_2 | 147 | 153 | PF00179 | 0.415 |
TRG_ENDOCYTIC_2 | 211 | 214 | PF00928 | 0.436 |
TRG_ENDOCYTIC_2 | 237 | 240 | PF00928 | 0.256 |
TRG_ENDOCYTIC_2 | 263 | 266 | PF00928 | 0.236 |
TRG_ENDOCYTIC_2 | 319 | 322 | PF00928 | 0.255 |
TRG_ENDOCYTIC_2 | 357 | 360 | PF00928 | 0.328 |
TRG_ENDOCYTIC_2 | 475 | 478 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 481 | 484 | PF00928 | 0.324 |
TRG_ENDOCYTIC_2 | 77 | 80 | PF00928 | 0.536 |
TRG_ER_diArg_1 | 2 | 4 | PF00400 | 0.587 |
TRG_ER_diArg_1 | 444 | 446 | PF00400 | 0.318 |
TRG_Pf-PMV_PEXEL_1 | 106 | 111 | PF00026 | 0.497 |
TRG_Pf-PMV_PEXEL_1 | 394 | 399 | PF00026 | 0.618 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDG5 | Leptomonas seymouri | 76% | 100% |
A0A1X0NRA0 | Trypanosomatidae | 62% | 100% |
A0A3Q8II29 | Leishmania donovani | 100% | 100% |
A0A3R7KN50 | Trypanosoma rangeli | 58% | 100% |
A4HGH9 | Leishmania braziliensis | 86% | 100% |
D0A8C8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 58% | 100% |
E9AZV1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
Q10252 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 34% | 100% |
Q298G6 | Drosophila pseudoobscura pseudoobscura | 34% | 100% |
Q2KIQ4 | Bos taurus | 36% | 100% |
Q499N4 | Rattus norvegicus | 39% | 100% |
Q4Q8D4 | Leishmania major | 96% | 100% |
Q66JT7 | Mus musculus | 38% | 100% |
Q8I7J4 | Caenorhabditis elegans | 36% | 100% |
Q9VHS7 | Drosophila melanogaster | 36% | 100% |
V5BFC2 | Trypanosoma cruzi | 56% | 100% |