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: A4HGH9
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 | 0.204 |
CLV_NRD_NRD_1 | 272 | 274 | PF00675 | 0.242 |
CLV_NRD_NRD_1 | 289 | 291 | PF00675 | 0.159 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.401 |
CLV_NRD_NRD_1 | 445 | 447 | PF00675 | 0.525 |
CLV_NRD_NRD_1 | 71 | 73 | PF00675 | 0.317 |
CLV_PCSK_KEX2_1 | 215 | 217 | PF00082 | 0.218 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.292 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.401 |
CLV_PCSK_KEX2_1 | 445 | 447 | PF00082 | 0.525 |
CLV_PCSK_PC1ET2_1 | 215 | 217 | PF00082 | 0.218 |
CLV_PCSK_SKI1_1 | 215 | 219 | PF00082 | 0.218 |
CLV_PCSK_SKI1_1 | 291 | 295 | PF00082 | 0.232 |
CLV_PCSK_SKI1_1 | 394 | 398 | PF00082 | 0.576 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.592 |
DEG_SPOP_SBC_1 | 469 | 473 | PF00917 | 0.249 |
DOC_CDC14_PxL_1 | 217 | 225 | PF14671 | 0.411 |
DOC_CYCLIN_RxL_1 | 388 | 402 | PF00134 | 0.365 |
DOC_CYCLIN_yCln2_LP_2 | 118 | 124 | PF00134 | 0.204 |
DOC_MAPK_gen_1 | 350 | 360 | PF00069 | 0.452 |
DOC_MAPK_HePTP_8 | 213 | 225 | PF00069 | 0.413 |
DOC_MAPK_HePTP_8 | 240 | 252 | PF00069 | 0.238 |
DOC_MAPK_MEF2A_6 | 216 | 225 | PF00069 | 0.413 |
DOC_MAPK_MEF2A_6 | 243 | 252 | PF00069 | 0.204 |
DOC_MAPK_MEF2A_6 | 353 | 362 | PF00069 | 0.302 |
DOC_PP1_RVXF_1 | 104 | 111 | PF00149 | 0.238 |
DOC_PP1_RVXF_1 | 83 | 90 | PF00149 | 0.548 |
DOC_PP2B_LxvP_1 | 118 | 121 | PF13499 | 0.204 |
DOC_PP2B_LxvP_1 | 92 | 95 | PF13499 | 0.257 |
DOC_PP4_FxxP_1 | 418 | 421 | PF00568 | 0.350 |
DOC_PP4_FxxP_1 | 83 | 86 | PF00568 | 0.567 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.250 |
DOC_USP7_MATH_1 | 35 | 39 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.384 |
DOC_USP7_MATH_1 | 387 | 391 | PF00917 | 0.308 |
DOC_USP7_UBL2_3 | 277 | 281 | PF12436 | 0.423 |
DOC_WW_Pin1_4 | 191 | 196 | PF00397 | 0.204 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 202 | 207 | PF00397 | 0.238 |
LIG_14-3-3_CanoR_1 | 216 | 224 | PF00244 | 0.404 |
LIG_14-3-3_CanoR_1 | 381 | 387 | PF00244 | 0.522 |
LIG_BRCT_BRCA1_1 | 473 | 477 | PF00533 | 0.264 |
LIG_Clathr_ClatBox_1 | 80 | 84 | PF01394 | 0.457 |
LIG_deltaCOP1_diTrp_1 | 147 | 153 | PF00928 | 0.460 |
LIG_deltaCOP1_diTrp_1 | 340 | 348 | PF00928 | 0.460 |
LIG_EH1_1 | 317 | 325 | PF00400 | 0.183 |
LIG_FHA_1 | 103 | 109 | PF00498 | 0.297 |
LIG_FHA_1 | 347 | 353 | PF00498 | 0.535 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.523 |
LIG_FHA_2 | 411 | 417 | PF00498 | 0.261 |
LIG_FHA_2 | 474 | 480 | PF00498 | 0.268 |
LIG_LIR_Apic_2 | 416 | 421 | PF02991 | 0.344 |
LIG_LIR_Gen_1 | 150 | 161 | PF02991 | 0.404 |
LIG_LIR_Gen_1 | 260 | 269 | PF02991 | 0.242 |
LIG_LIR_Gen_1 | 393 | 401 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 472 | 483 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 205 | 211 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 260 | 266 | PF02991 | 0.282 |
LIG_LIR_Nem_3 | 393 | 398 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 479 | 484 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 5 | 11 | PF02991 | 0.672 |
LIG_LYPXL_S_1 | 210 | 214 | PF13949 | 0.286 |
LIG_LYPXL_S_1 | 7 | 11 | PF13949 | 0.322 |
LIG_LYPXL_yS_3 | 211 | 214 | PF13949 | 0.438 |
LIG_LYPXL_yS_3 | 8 | 11 | PF13949 | 0.523 |
LIG_PCNA_PIPBox_1 | 130 | 139 | PF02747 | 0.303 |
LIG_PCNA_yPIPBox_3 | 130 | 139 | PF02747 | 0.303 |
LIG_PDZ_Class_2 | 484 | 489 | PF00595 | 0.334 |
LIG_Pex14_1 | 149 | 153 | PF04695 | 0.434 |
LIG_Pex14_1 | 259 | 263 | PF04695 | 0.238 |
LIG_Pex14_1 | 414 | 418 | PF04695 | 0.348 |
LIG_SH2_CRK | 237 | 241 | PF00017 | 0.258 |
LIG_SH2_CRK | 263 | 267 | PF00017 | 0.238 |
LIG_SH2_CRK | 77 | 81 | PF00017 | 0.384 |
LIG_SH2_NCK_1 | 263 | 267 | PF00017 | 0.238 |
LIG_SH2_PTP2 | 319 | 322 | PF00017 | 0.257 |
LIG_SH2_PTP2 | 357 | 360 | PF00017 | 0.311 |
LIG_SH2_STAP1 | 237 | 241 | PF00017 | 0.238 |
LIG_SH2_STAP1 | 263 | 267 | PF00017 | 0.247 |
LIG_SH2_STAT3 | 267 | 270 | PF00017 | 0.404 |
LIG_SH2_STAT3 | 448 | 451 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 136 | 139 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 253 | 256 | PF00017 | 0.183 |
LIG_SH2_STAT5 | 292 | 295 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 319 | 322 | PF00017 | 0.238 |
LIG_SH2_STAT5 | 357 | 360 | PF00017 | 0.330 |
LIG_SH2_STAT5 | 407 | 410 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 448 | 451 | PF00017 | 0.294 |
LIG_SH2_STAT5 | 475 | 478 | PF00017 | 0.273 |
LIG_SH3_1 | 3 | 9 | PF00018 | 0.662 |
LIG_SH3_3 | 118 | 124 | PF00018 | 0.228 |
LIG_SH3_3 | 245 | 251 | PF00018 | 0.217 |
LIG_SH3_3 | 3 | 9 | PF00018 | 0.667 |
LIG_SH3_3 | 435 | 441 | PF00018 | 0.412 |
LIG_TRAF2_1 | 45 | 48 | PF00917 | 0.526 |
LIG_TYR_ITIM | 235 | 240 | PF00017 | 0.238 |
LIG_TYR_ITIM | 261 | 266 | PF00017 | 0.238 |
LIG_UBA3_1 | 209 | 215 | PF00899 | 0.260 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.574 |
MOD_CK1_1 | 390 | 396 | PF00069 | 0.372 |
MOD_CK1_1 | 463 | 469 | PF00069 | 0.396 |
MOD_CK1_1 | 471 | 477 | PF00069 | 0.461 |
MOD_CK2_1 | 168 | 174 | PF00069 | 0.417 |
MOD_CK2_1 | 370 | 376 | PF00069 | 0.498 |
MOD_CK2_1 | 41 | 47 | PF00069 | 0.597 |
MOD_GlcNHglycan | 174 | 178 | PF01048 | 0.296 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.373 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.229 |
MOD_GlcNHglycan | 307 | 310 | PF01048 | 0.225 |
MOD_GlcNHglycan | 384 | 387 | PF01048 | 0.570 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.409 |
MOD_GlcNHglycan | 427 | 430 | PF01048 | 0.576 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.419 |
MOD_GlcNHglycan | 453 | 456 | PF01048 | 0.550 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.282 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.599 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.420 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.431 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.266 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.213 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.613 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.276 |
MOD_N-GLC_1 | 191 | 196 | PF02516 | 0.410 |
MOD_N-GLC_1 | 451 | 456 | PF02516 | 0.602 |
MOD_N-GLC_2 | 366 | 368 | PF02516 | 0.303 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.238 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.265 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.426 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.326 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.254 |
MOD_PIKK_1 | 310 | 316 | PF00454 | 0.238 |
MOD_PIKK_1 | 447 | 453 | PF00454 | 0.438 |
MOD_PIKK_1 | 482 | 488 | PF00454 | 0.298 |
MOD_PK_1 | 328 | 334 | PF00069 | 0.161 |
MOD_PKA_1 | 215 | 221 | PF00069 | 0.404 |
MOD_PKA_2 | 215 | 221 | PF00069 | 0.404 |
MOD_PKA_2 | 380 | 386 | PF00069 | 0.523 |
MOD_Plk_1 | 173 | 179 | PF00069 | 0.328 |
MOD_Plk_1 | 403 | 409 | PF00069 | 0.415 |
MOD_Plk_1 | 451 | 457 | PF00069 | 0.396 |
MOD_Plk_1 | 463 | 469 | PF00069 | 0.389 |
MOD_Plk_1 | 47 | 53 | PF00069 | 0.664 |
MOD_Plk_1 | 54 | 60 | PF00069 | 0.657 |
MOD_Plk_4 | 262 | 268 | PF00069 | 0.278 |
MOD_Plk_4 | 328 | 334 | PF00069 | 0.422 |
MOD_Plk_4 | 387 | 393 | PF00069 | 0.379 |
MOD_Plk_4 | 473 | 479 | PF00069 | 0.264 |
MOD_ProDKin_1 | 191 | 197 | PF00069 | 0.204 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.669 |
MOD_ProDKin_1 | 202 | 208 | PF00069 | 0.238 |
MOD_SUMO_for_1 | 45 | 48 | PF00179 | 0.536 |
MOD_SUMO_for_1 | 58 | 61 | PF00179 | 0.562 |
MOD_SUMO_rev_2 | 147 | 153 | PF00179 | 0.417 |
TRG_ENDOCYTIC_2 | 211 | 214 | PF00928 | 0.438 |
TRG_ENDOCYTIC_2 | 237 | 240 | PF00928 | 0.258 |
TRG_ENDOCYTIC_2 | 263 | 266 | PF00928 | 0.238 |
TRG_ENDOCYTIC_2 | 319 | 322 | PF00928 | 0.257 |
TRG_ENDOCYTIC_2 | 357 | 360 | PF00928 | 0.330 |
TRG_ENDOCYTIC_2 | 475 | 478 | PF00928 | 0.332 |
TRG_ENDOCYTIC_2 | 481 | 484 | PF00928 | 0.342 |
TRG_ENDOCYTIC_2 | 77 | 80 | PF00928 | 0.538 |
TRG_ENDOCYTIC_2 | 8 | 11 | PF00928 | 0.548 |
TRG_ER_diArg_1 | 2 | 4 | PF00400 | 0.605 |
TRG_ER_diArg_1 | 444 | 446 | PF00400 | 0.330 |
TRG_Pf-PMV_PEXEL_1 | 106 | 111 | PF00026 | 0.499 |
TRG_Pf-PMV_PEXEL_1 | 394 | 399 | PF00026 | 0.650 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDG5 | Leptomonas seymouri | 75% | 100% |
A0A1X0NRA0 | Trypanosomatidae | 62% | 100% |
A0A3Q8II29 | Leishmania donovani | 86% | 100% |
A0A3R7KN50 | Trypanosoma rangeli | 59% | 100% |
A4I3L1 | Leishmania infantum | 86% | 100% |
D0A8C8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 57% | 100% |
E9AZV1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q10252 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 33% | 100% |
Q298G6 | Drosophila pseudoobscura pseudoobscura | 35% | 100% |
Q4Q8D4 | Leishmania major | 87% | 100% |
Q93YP7 | Arabidopsis thaliana | 32% | 100% |
V5BFC2 | Trypanosoma cruzi | 57% | 100% |