Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 1 |
Forrest at al. (metacyclic) | no | yes: 1 |
Forrest at al. (procyclic) | no | yes: 1 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 4 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 4 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H7V6
Term | Name | Level | Count |
---|---|---|---|
GO:0005975 | carbohydrate metabolic process | 3 | 11 |
GO:0006020 | inositol metabolic process | 4 | 11 |
GO:0006021 | inositol biosynthetic process | 5 | 11 |
GO:0006066 | alcohol metabolic process | 3 | 11 |
GO:0006629 | lipid metabolic process | 3 | 11 |
GO:0006644 | phospholipid metabolic process | 4 | 11 |
GO:0006793 | phosphorus metabolic process | 3 | 11 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0008610 | lipid biosynthetic process | 4 | 11 |
GO:0008654 | phospholipid biosynthetic process | 5 | 11 |
GO:0009058 | biosynthetic process | 2 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016051 | carbohydrate biosynthetic process | 4 | 11 |
GO:0019637 | organophosphate metabolic process | 3 | 11 |
GO:0019751 | polyol metabolic process | 4 | 11 |
GO:0034637 | obsolete cellular carbohydrate 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:0044262 | obsolete cellular carbohydrate metabolic process | 3 | 11 |
GO:0044281 | small molecule metabolic process | 2 | 11 |
GO:0044283 | small molecule biosynthetic process | 3 | 11 |
GO:0046165 | alcohol biosynthetic process | 4 | 11 |
GO:0046173 | polyol biosynthetic process | 5 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0090407 | organophosphate biosynthetic process | 4 | 11 |
GO:1901576 | organic substance biosynthetic process | 3 | 11 |
GO:1901615 | organic hydroxy compound metabolic process | 3 | 11 |
GO:1901617 | organic hydroxy compound biosynthetic process | 4 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004512 | inositol-3-phosphate synthase activity | 4 | 11 |
GO:0016853 | isomerase activity | 2 | 11 |
GO:0016872 | intramolecular lyase activity | 3 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 235 | 239 | PF00656 | 0.529 |
CLV_C14_Caspase3-7 | 242 | 246 | PF00656 | 0.492 |
CLV_C14_Caspase3-7 | 444 | 448 | PF00656 | 0.422 |
CLV_NRD_NRD_1 | 150 | 152 | PF00675 | 0.310 |
CLV_NRD_NRD_1 | 51 | 53 | PF00675 | 0.331 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.301 |
CLV_PCSK_FUR_1 | 86 | 90 | PF00082 | 0.301 |
CLV_PCSK_KEX2_1 | 150 | 152 | PF00082 | 0.313 |
CLV_PCSK_KEX2_1 | 252 | 254 | PF00082 | 0.313 |
CLV_PCSK_KEX2_1 | 394 | 396 | PF00082 | 0.299 |
CLV_PCSK_KEX2_1 | 88 | 90 | PF00082 | 0.301 |
CLV_PCSK_PC1ET2_1 | 252 | 254 | PF00082 | 0.313 |
CLV_PCSK_PC1ET2_1 | 394 | 396 | PF00082 | 0.299 |
CLV_PCSK_SKI1_1 | 211 | 215 | PF00082 | 0.307 |
CLV_PCSK_SKI1_1 | 312 | 316 | PF00082 | 0.225 |
CLV_PCSK_SKI1_1 | 352 | 356 | PF00082 | 0.299 |
CLV_PCSK_SKI1_1 | 45 | 49 | PF00082 | 0.421 |
DOC_CYCLIN_yCln2_LP_2 | 423 | 429 | PF00134 | 0.499 |
DOC_CYCLIN_yCln2_LP_2 | 471 | 477 | PF00134 | 0.551 |
DOC_MAPK_DCC_7 | 49 | 59 | PF00069 | 0.516 |
DOC_MAPK_gen_1 | 150 | 157 | PF00069 | 0.504 |
DOC_MAPK_gen_1 | 187 | 196 | PF00069 | 0.466 |
DOC_MAPK_gen_1 | 310 | 318 | PF00069 | 0.541 |
DOC_MAPK_gen_1 | 49 | 59 | PF00069 | 0.424 |
DOC_MAPK_MEF2A_6 | 150 | 159 | PF00069 | 0.500 |
DOC_MAPK_MEF2A_6 | 52 | 61 | PF00069 | 0.509 |
DOC_PP1_RVXF_1 | 43 | 49 | PF00149 | 0.490 |
DOC_PP2B_LxvP_1 | 423 | 426 | PF13499 | 0.530 |
DOC_PP2B_LxvP_1 | 471 | 474 | PF13499 | 0.491 |
DOC_USP7_MATH_1 | 504 | 508 | PF00917 | 0.368 |
DOC_USP7_UBL2_3 | 352 | 356 | PF12436 | 0.499 |
DOC_USP7_UBL2_3 | 373 | 377 | PF12436 | 0.422 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.512 |
DOC_WW_Pin1_4 | 126 | 131 | PF00397 | 0.579 |
DOC_WW_Pin1_4 | 342 | 347 | PF00397 | 0.422 |
DOC_WW_Pin1_4 | 372 | 377 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 448 | 453 | PF00397 | 0.572 |
DOC_WW_Pin1_4 | 477 | 482 | PF00397 | 0.499 |
LIG_14-3-3_CanoR_1 | 232 | 240 | PF00244 | 0.513 |
LIG_14-3-3_CanoR_1 | 28 | 36 | PF00244 | 0.626 |
LIG_14-3-3_CanoR_1 | 365 | 370 | PF00244 | 0.512 |
LIG_14-3-3_CanoR_1 | 440 | 449 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 5 | 13 | PF00244 | 0.586 |
LIG_14-3-3_CanoR_1 | 89 | 97 | PF00244 | 0.569 |
LIG_BIR_III_4 | 32 | 36 | PF00653 | 0.372 |
LIG_BRCT_BRCA1_1 | 367 | 371 | PF00533 | 0.533 |
LIG_BRCT_BRCA1_1 | 93 | 97 | PF00533 | 0.509 |
LIG_BRCT_BRCA1_2 | 367 | 373 | PF00533 | 0.422 |
LIG_EH1_1 | 263 | 271 | PF00400 | 0.443 |
LIG_EVH1_2 | 453 | 457 | PF00568 | 0.491 |
LIG_FHA_1 | 103 | 109 | PF00498 | 0.515 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.488 |
LIG_FHA_1 | 292 | 298 | PF00498 | 0.422 |
LIG_FHA_1 | 399 | 405 | PF00498 | 0.513 |
LIG_FHA_1 | 409 | 415 | PF00498 | 0.478 |
LIG_FHA_1 | 478 | 484 | PF00498 | 0.499 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.487 |
LIG_FHA_2 | 18 | 24 | PF00498 | 0.325 |
LIG_FHA_2 | 415 | 421 | PF00498 | 0.499 |
LIG_LIR_Gen_1 | 161 | 172 | PF02991 | 0.513 |
LIG_LIR_Gen_1 | 198 | 206 | PF02991 | 0.602 |
LIG_LIR_Gen_1 | 331 | 339 | PF02991 | 0.499 |
LIG_LIR_Gen_1 | 399 | 406 | PF02991 | 0.499 |
LIG_LIR_Gen_1 | 456 | 464 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 116 | 121 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 198 | 203 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 230 | 236 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 331 | 335 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 399 | 405 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 94 | 100 | PF02991 | 0.509 |
LIG_MLH1_MIPbox_1 | 93 | 97 | PF16413 | 0.509 |
LIG_NRBOX | 466 | 472 | PF00104 | 0.499 |
LIG_Pex14_2 | 177 | 181 | PF04695 | 0.499 |
LIG_SH2_NCK_1 | 264 | 268 | PF00017 | 0.499 |
LIG_SH2_SRC | 264 | 267 | PF00017 | 0.473 |
LIG_SH2_STAP1 | 264 | 268 | PF00017 | 0.513 |
LIG_SH2_STAP1 | 400 | 404 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 13 | 16 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 386 | 389 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 400 | 403 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 469 | 472 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 96 | 99 | PF00017 | 0.486 |
LIG_SH3_3 | 366 | 372 | PF00018 | 0.579 |
LIG_SH3_3 | 471 | 477 | PF00018 | 0.499 |
LIG_SUMO_SIM_anti_2 | 220 | 227 | PF11976 | 0.499 |
LIG_SUMO_SIM_anti_2 | 430 | 436 | PF11976 | 0.499 |
LIG_SUMO_SIM_anti_2 | 461 | 468 | PF11976 | 0.499 |
LIG_SUMO_SIM_par_1 | 192 | 198 | PF11976 | 0.422 |
LIG_SUMO_SIM_par_1 | 220 | 227 | PF11976 | 0.499 |
LIG_SUMO_SIM_par_1 | 425 | 430 | PF11976 | 0.499 |
LIG_SUMO_SIM_par_1 | 461 | 468 | PF11976 | 0.499 |
LIG_UBA3_1 | 466 | 472 | PF00899 | 0.352 |
MOD_CDK_SPK_2 | 342 | 347 | PF00069 | 0.244 |
MOD_CDK_SPK_2 | 372 | 377 | PF00069 | 0.366 |
MOD_CK1_1 | 306 | 312 | PF00069 | 0.352 |
MOD_CK1_1 | 465 | 471 | PF00069 | 0.348 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.286 |
MOD_CK2_1 | 347 | 353 | PF00069 | 0.244 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.240 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.320 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.361 |
MOD_GlcNHglycan | 443 | 446 | PF01048 | 0.458 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.371 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.449 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.352 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.352 |
MOD_GSK3_1 | 414 | 421 | PF00069 | 0.352 |
MOD_GSK3_1 | 439 | 446 | PF00069 | 0.441 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.336 |
MOD_N-GLC_1 | 253 | 258 | PF02516 | 0.464 |
MOD_N-GLC_1 | 341 | 346 | PF02516 | 0.425 |
MOD_N-GLC_1 | 67 | 72 | PF02516 | 0.335 |
MOD_N-GLC_2 | 416 | 418 | PF02516 | 0.352 |
MOD_NEK2_1 | 114 | 119 | PF00069 | 0.380 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.244 |
MOD_NEK2_1 | 363 | 368 | PF00069 | 0.395 |
MOD_NEK2_1 | 81 | 86 | PF00069 | 0.366 |
MOD_NEK2_1 | 91 | 96 | PF00069 | 0.366 |
MOD_NEK2_2 | 400 | 405 | PF00069 | 0.352 |
MOD_PIKK_1 | 17 | 23 | PF00454 | 0.439 |
MOD_PIKK_1 | 98 | 104 | PF00454 | 0.335 |
MOD_PK_1 | 365 | 371 | PF00069 | 0.283 |
MOD_PKA_2 | 231 | 237 | PF00069 | 0.371 |
MOD_PKA_2 | 27 | 33 | PF00069 | 0.493 |
MOD_PKA_2 | 439 | 445 | PF00069 | 0.395 |
MOD_Plk_1 | 398 | 404 | PF00069 | 0.352 |
MOD_Plk_1 | 418 | 424 | PF00069 | 0.166 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.320 |
MOD_Plk_4 | 271 | 277 | PF00069 | 0.304 |
MOD_Plk_4 | 365 | 371 | PF00069 | 0.341 |
MOD_Plk_4 | 408 | 414 | PF00069 | 0.352 |
MOD_Plk_4 | 418 | 424 | PF00069 | 0.352 |
MOD_Plk_4 | 459 | 465 | PF00069 | 0.346 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.504 |
MOD_ProDKin_1 | 126 | 132 | PF00069 | 0.464 |
MOD_ProDKin_1 | 342 | 348 | PF00069 | 0.244 |
MOD_ProDKin_1 | 372 | 378 | PF00069 | 0.366 |
MOD_ProDKin_1 | 448 | 454 | PF00069 | 0.454 |
MOD_ProDKin_1 | 477 | 483 | PF00069 | 0.352 |
MOD_SUMO_for_1 | 324 | 327 | PF00179 | 0.352 |
MOD_SUMO_rev_2 | 30 | 36 | PF00179 | 0.366 |
MOD_SUMO_rev_2 | 302 | 306 | PF00179 | 0.301 |
TRG_DiLeu_BaEn_1 | 506 | 511 | PF01217 | 0.355 |
TRG_DiLeu_BaEn_2 | 270 | 276 | PF01217 | 0.464 |
TRG_DiLeu_BaLyEn_6 | 423 | 428 | PF01217 | 0.352 |
TRG_ENDOCYTIC_2 | 164 | 167 | PF00928 | 0.371 |
TRG_ENDOCYTIC_2 | 332 | 335 | PF00928 | 0.352 |
TRG_ER_diArg_1 | 149 | 151 | PF00400 | 0.371 |
TRG_ER_diArg_1 | 4 | 7 | PF00400 | 0.374 |
TRG_ER_diArg_1 | 85 | 88 | PF00400 | 0.411 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I042 | Leptomonas seymouri | 86% | 100% |
A0A0S4JLI5 | Bodo saltans | 67% | 100% |
A0A1X0P7U4 | Trypanosomatidae | 71% | 99% |
A0A3R7LTQ6 | Trypanosoma rangeli | 68% | 100% |
A0A3S5H6T1 | Leishmania donovani | 84% | 100% |
A4HW82 | Leishmania infantum | 86% | 100% |
E9APY4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
O64437 | Oryza sativa subsp. japonica | 55% | 100% |
O65195 | Hordeum vulgare | 56% | 100% |
O97477 | Drosophila melanogaster | 54% | 93% |
P11986 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 49% | 99% |
P42800 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 50% | 100% |
P42801 | Arabidopsis thaliana | 54% | 100% |
P42802 | Citrus paradisi | 52% | 100% |
P42803 | Spirodela polyrhiza | 55% | 100% |
Q2NL29 | Bos taurus | 56% | 94% |
Q38862 | Arabidopsis thaliana | 55% | 100% |
Q40271 | Mesembryanthemum crystallinum | 54% | 100% |
Q41107 | Phaseolus vulgaris | 54% | 100% |
Q4QFJ8 | Leishmania major | 84% | 100% |
Q4R6E3 | Macaca fascicularis | 57% | 94% |
Q54N49 | Dictyostelium discoideum | 57% | 100% |
Q6AYK3 | Rattus norvegicus | 56% | 94% |
Q6DDT1 | Xenopus laevis | 57% | 93% |
Q6FQI1 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 51% | 98% |
Q7ZXY0 | Xenopus laevis | 56% | 93% |
Q8A7J8 | Bacteroides thetaiotaomicron (strain ATCC 29148 / DSM 2079 / JCM 5827 / CCUG 10774 / NCTC 10582 / VPI-5482 / E50) | 33% | 100% |
Q8I3Y8 | Plasmodium falciparum (isolate 3D7) | 37% | 87% |
Q8S5N2 | Oryza sativa subsp. japonica | 57% | 100% |
Q96348 | Brassica napus | 55% | 100% |
Q9FPK7 | Zea mays | 55% | 100% |
Q9FYV1 | Sesamum indicum | 54% | 100% |
Q9JHU9 | Mus musculus | 57% | 94% |
Q9LW96 | Nicotiana tabacum | 55% | 100% |
Q9LX12 | Arabidopsis thaliana | 54% | 100% |
Q9NPH2 | Homo sapiens | 57% | 94% |
Q9S7U0 | Triticum aestivum | 55% | 100% |
Q9SSV4 | Nicotiana paniculata | 55% | 100% |
V5B836 | Trypanosoma cruzi | 70% | 99% |