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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005739 | mitochondrion | 5 | 1 |
GO:0005829 | cytosol | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4ICG7
Term | Name | Level | Count |
---|---|---|---|
GO:0006575 | cellular modified amino acid metabolic process | 3 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006760 | folic acid-containing compound metabolic process | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009396 | folic acid-containing compound biosynthetic process | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0018130 | heterocycle biosynthetic process | 4 | 1 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0042398 | cellular modified amino acid biosynthetic process | 4 | 1 |
GO:0042558 | pteridine-containing compound metabolic process | 4 | 1 |
GO:0042559 | pteridine-containing compound biosynthetic process | 5 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0046900 | tetrahydrofolylpolyglutamate metabolic process | 5 | 1 |
GO:0046901 | tetrahydrofolylpolyglutamate biosynthetic process | 6 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004326 | tetrahydrofolylpolyglutamate synthase activity | 5 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0016874 | ligase activity | 2 | 12 |
GO:0016879 | ligase activity, forming carbon-nitrogen bonds | 3 | 12 |
GO:0016881 | acid-amino acid ligase activity | 4 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0043169 | cation binding | 3 | 12 |
GO:0046872 | metal ion binding | 4 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 151 | 155 | PF00656 | 0.388 |
CLV_C14_Caspase3-7 | 65 | 69 | PF00656 | 0.499 |
CLV_NRD_NRD_1 | 290 | 292 | PF00675 | 0.432 |
CLV_NRD_NRD_1 | 405 | 407 | PF00675 | 0.315 |
CLV_NRD_NRD_1 | 537 | 539 | PF00675 | 0.537 |
CLV_NRD_NRD_1 | 61 | 63 | PF00675 | 0.596 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.655 |
CLV_PCSK_KEX2_1 | 405 | 407 | PF00082 | 0.323 |
CLV_PCSK_KEX2_1 | 417 | 419 | PF00082 | 0.336 |
CLV_PCSK_KEX2_1 | 537 | 539 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 60 | 62 | PF00082 | 0.579 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.610 |
CLV_PCSK_KEX2_1 | 92 | 94 | PF00082 | 0.512 |
CLV_PCSK_PC1ET2_1 | 417 | 419 | PF00082 | 0.446 |
CLV_PCSK_PC1ET2_1 | 60 | 62 | PF00082 | 0.631 |
CLV_PCSK_PC1ET2_1 | 92 | 94 | PF00082 | 0.411 |
CLV_PCSK_PC7_1 | 75 | 81 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 198 | 202 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 283 | 287 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 325 | 329 | PF00082 | 0.272 |
CLV_PCSK_SKI1_1 | 348 | 352 | PF00082 | 0.325 |
CLV_PCSK_SKI1_1 | 405 | 409 | PF00082 | 0.363 |
CLV_PCSK_SKI1_1 | 417 | 421 | PF00082 | 0.318 |
CLV_PCSK_SKI1_1 | 463 | 467 | PF00082 | 0.372 |
CLV_PCSK_SKI1_1 | 476 | 480 | PF00082 | 0.318 |
CLV_PCSK_SKI1_1 | 527 | 531 | PF00082 | 0.340 |
CLV_PCSK_SKI1_1 | 64 | 68 | PF00082 | 0.547 |
DOC_CDC14_PxL_1 | 98 | 106 | PF14671 | 0.384 |
DOC_CYCLIN_RxL_1 | 400 | 413 | PF00134 | 0.362 |
DOC_MAPK_gen_1 | 291 | 299 | PF00069 | 0.438 |
DOC_MAPK_gen_1 | 64 | 72 | PF00069 | 0.571 |
DOC_MAPK_gen_1 | 92 | 100 | PF00069 | 0.469 |
DOC_MAPK_MEF2A_6 | 198 | 207 | PF00069 | 0.349 |
DOC_MAPK_MEF2A_6 | 291 | 300 | PF00069 | 0.347 |
DOC_MAPK_MEF2A_6 | 308 | 315 | PF00069 | 0.364 |
DOC_PP1_RVXF_1 | 104 | 110 | PF00149 | 0.281 |
DOC_PP1_RVXF_1 | 404 | 411 | PF00149 | 0.313 |
DOC_PP1_RVXF_1 | 95 | 101 | PF00149 | 0.374 |
DOC_PP2B_LxvP_1 | 496 | 499 | PF13499 | 0.477 |
DOC_PP4_FxxP_1 | 139 | 142 | PF00568 | 0.290 |
DOC_PP4_FxxP_1 | 272 | 275 | PF00568 | 0.402 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 189 | 193 | PF00917 | 0.432 |
DOC_USP7_MATH_1 | 306 | 310 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 357 | 361 | PF00917 | 0.376 |
DOC_USP7_MATH_1 | 425 | 429 | PF00917 | 0.414 |
DOC_USP7_MATH_1 | 499 | 503 | PF00917 | 0.515 |
DOC_USP7_UBL2_3 | 288 | 292 | PF12436 | 0.354 |
DOC_USP7_UBL2_3 | 417 | 421 | PF12436 | 0.460 |
DOC_WW_Pin1_4 | 138 | 143 | PF00397 | 0.291 |
DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.730 |
DOC_WW_Pin1_4 | 187 | 192 | PF00397 | 0.497 |
LIG_14-3-3_CanoR_1 | 442 | 450 | PF00244 | 0.561 |
LIG_14-3-3_CanoR_1 | 463 | 471 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 485 | 494 | PF00244 | 0.505 |
LIG_14-3-3_CanoR_1 | 61 | 67 | PF00244 | 0.483 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.541 |
LIG_Clathr_ClatBox_1 | 297 | 301 | PF01394 | 0.394 |
LIG_DLG_GKlike_1 | 62 | 70 | PF00625 | 0.401 |
LIG_EH1_1 | 519 | 527 | PF00400 | 0.274 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.257 |
LIG_FHA_1 | 227 | 233 | PF00498 | 0.291 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.365 |
LIG_FHA_1 | 370 | 376 | PF00498 | 0.353 |
LIG_FHA_2 | 149 | 155 | PF00498 | 0.397 |
LIG_FHA_2 | 251 | 257 | PF00498 | 0.284 |
LIG_FHA_2 | 362 | 368 | PF00498 | 0.311 |
LIG_FHA_2 | 410 | 416 | PF00498 | 0.400 |
LIG_GBD_Chelix_1 | 521 | 529 | PF00786 | 0.275 |
LIG_HP1_1 | 296 | 300 | PF01393 | 0.373 |
LIG_LIR_Gen_1 | 172 | 179 | PF02991 | 0.368 |
LIG_LIR_Gen_1 | 241 | 250 | PF02991 | 0.322 |
LIG_LIR_Gen_1 | 388 | 397 | PF02991 | 0.402 |
LIG_LIR_Gen_1 | 428 | 438 | PF02991 | 0.397 |
LIG_LIR_LC3C_4 | 495 | 498 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 160 | 166 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 172 | 177 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 309 | 313 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 388 | 394 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 428 | 433 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 518 | 522 | PF02991 | 0.322 |
LIG_Pex14_1 | 471 | 475 | PF04695 | 0.339 |
LIG_Pex14_2 | 197 | 201 | PF04695 | 0.263 |
LIG_PROFILIN_1 | 21 | 27 | PF00235 | 0.496 |
LIG_REV1ctd_RIR_1 | 194 | 202 | PF16727 | 0.330 |
LIG_SH2_SRC | 374 | 377 | PF00017 | 0.344 |
LIG_SH2_STAP1 | 124 | 128 | PF00017 | 0.258 |
LIG_SH2_STAP1 | 163 | 167 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 124 | 127 | PF00017 | 0.284 |
LIG_SH2_STAT5 | 166 | 169 | PF00017 | 0.284 |
LIG_SH2_STAT5 | 206 | 209 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 374 | 377 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 411 | 414 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 426 | 429 | PF00017 | 0.364 |
LIG_SH3_1 | 18 | 24 | PF00018 | 0.572 |
LIG_SH3_3 | 16 | 22 | PF00018 | 0.590 |
LIG_SH3_3 | 23 | 29 | PF00018 | 0.546 |
LIG_SH3_3 | 290 | 296 | PF00018 | 0.339 |
LIG_SH3_3 | 336 | 342 | PF00018 | 0.388 |
LIG_SH3_3 | 435 | 441 | PF00018 | 0.327 |
LIG_SUMO_SIM_anti_2 | 214 | 219 | PF11976 | 0.244 |
LIG_SUMO_SIM_anti_2 | 234 | 241 | PF11976 | 0.288 |
LIG_SUMO_SIM_anti_2 | 322 | 330 | PF11976 | 0.292 |
LIG_SUMO_SIM_anti_2 | 491 | 498 | PF11976 | 0.403 |
LIG_SUMO_SIM_par_1 | 295 | 301 | PF11976 | 0.384 |
LIG_TRAF2_1 | 253 | 256 | PF00917 | 0.249 |
LIG_UBA3_1 | 340 | 348 | PF00899 | 0.485 |
MOD_CDC14_SPxK_1 | 190 | 193 | PF00782 | 0.472 |
MOD_CDK_SPxK_1 | 187 | 193 | PF00069 | 0.477 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.352 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.737 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.363 |
MOD_CK1_1 | 237 | 243 | PF00069 | 0.314 |
MOD_CK1_1 | 383 | 389 | PF00069 | 0.454 |
MOD_CK2_1 | 250 | 256 | PF00069 | 0.249 |
MOD_CK2_1 | 485 | 491 | PF00069 | 0.342 |
MOD_CK2_1 | 499 | 505 | PF00069 | 0.356 |
MOD_Cter_Amidation | 535 | 538 | PF01082 | 0.513 |
MOD_Cter_Amidation | 77 | 80 | PF01082 | 0.517 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.371 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.750 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.456 |
MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.418 |
MOD_GlcNHglycan | 393 | 397 | PF01048 | 0.434 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.658 |
MOD_GlcNHglycan | 487 | 490 | PF01048 | 0.489 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.693 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.273 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.464 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.335 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.428 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.494 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.383 |
MOD_N-GLC_1 | 369 | 374 | PF02516 | 0.389 |
MOD_N-GLC_2 | 82 | 84 | PF02516 | 0.583 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.556 |
MOD_NEK2_1 | 201 | 206 | PF00069 | 0.283 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.393 |
MOD_NEK2_1 | 392 | 397 | PF00069 | 0.400 |
MOD_NEK2_1 | 464 | 469 | PF00069 | 0.286 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.350 |
MOD_NEK2_2 | 369 | 374 | PF00069 | 0.364 |
MOD_PIKK_1 | 179 | 185 | PF00454 | 0.406 |
MOD_PIKK_1 | 357 | 363 | PF00454 | 0.340 |
MOD_PIKK_1 | 385 | 391 | PF00454 | 0.441 |
MOD_PIKK_1 | 465 | 471 | PF00454 | 0.441 |
MOD_PKA_2 | 441 | 447 | PF00069 | 0.540 |
MOD_PKA_2 | 74 | 80 | PF00069 | 0.533 |
MOD_PKB_1 | 461 | 469 | PF00069 | 0.355 |
MOD_Plk_1 | 148 | 154 | PF00069 | 0.488 |
MOD_Plk_1 | 159 | 165 | PF00069 | 0.403 |
MOD_Plk_1 | 234 | 240 | PF00069 | 0.284 |
MOD_Plk_1 | 346 | 352 | PF00069 | 0.394 |
MOD_Plk_1 | 369 | 375 | PF00069 | 0.442 |
MOD_Plk_1 | 476 | 482 | PF00069 | 0.397 |
MOD_Plk_4 | 201 | 207 | PF00069 | 0.309 |
MOD_Plk_4 | 234 | 240 | PF00069 | 0.284 |
MOD_Plk_4 | 346 | 352 | PF00069 | 0.440 |
MOD_Plk_4 | 515 | 521 | PF00069 | 0.312 |
MOD_ProDKin_1 | 138 | 144 | PF00069 | 0.292 |
MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.729 |
MOD_ProDKin_1 | 187 | 193 | PF00069 | 0.496 |
MOD_SUMO_rev_2 | 322 | 327 | PF00179 | 0.318 |
MOD_SUMO_rev_2 | 413 | 419 | PF00179 | 0.466 |
MOD_SUMO_rev_2 | 449 | 458 | PF00179 | 0.611 |
TRG_DiLeu_BaEn_2 | 104 | 110 | PF01217 | 0.399 |
TRG_DiLeu_BaLyEn_6 | 153 | 158 | PF01217 | 0.400 |
TRG_ENDOCYTIC_2 | 174 | 177 | PF00928 | 0.430 |
TRG_ENDOCYTIC_2 | 244 | 247 | PF00928 | 0.393 |
TRG_ENDOCYTIC_2 | 475 | 478 | PF00928 | 0.365 |
TRG_ER_diArg_1 | 106 | 109 | PF00400 | 0.375 |
TRG_ER_diArg_1 | 33 | 36 | PF00400 | 0.558 |
TRG_ER_diArg_1 | 404 | 406 | PF00400 | 0.347 |
TRG_ER_diArg_1 | 537 | 539 | PF00400 | 0.463 |
TRG_ER_diArg_1 | 61 | 64 | PF00400 | 0.569 |
TRG_ER_diArg_1 | 79 | 81 | PF00400 | 0.556 |
TRG_NLS_MonoExtC_3 | 59 | 64 | PF00514 | 0.492 |
TRG_NLS_MonoExtN_4 | 59 | 64 | PF00514 | 0.417 |
TRG_Pf-PMV_PEXEL_1 | 156 | 160 | PF00026 | 0.433 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6C4 | Leptomonas seymouri | 74% | 82% |
A0A0S4KJ93 | Bodo saltans | 49% | 100% |
A0A1X0NM42 | Trypanosomatidae | 56% | 100% |
A0A3Q8IJ59 | Leishmania donovani | 100% | 100% |
A0A3R7RIQ8 | Trypanosoma rangeli | 52% | 100% |
A4HPC7 | Leishmania braziliensis | 85% | 98% |
A6H751 | Bos taurus | 31% | 92% |
A6ZP80 | Saccharomyces cerevisiae (strain YJM789) | 31% | 99% |
B3LJR0 | Saccharomyces cerevisiae (strain RM11-1a) | 31% | 99% |
B5VSC3 | Saccharomyces cerevisiae (strain AWRI1631) | 31% | 99% |
C8ZGZ3 | Saccharomyces cerevisiae (strain Lalvin EC1118 / Prise de mousse) | 31% | 99% |
D0A3I6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
E7KIA3 | Saccharomyces cerevisiae (strain AWRI796) | 31% | 99% |
E7KUJ4 | Saccharomyces cerevisiae (strain Lalvin QA23) | 31% | 99% |
E7NMM0 | Saccharomyces cerevisiae (strain FostersO) | 31% | 99% |
E7Q9C7 | Saccharomyces cerevisiae (strain FostersB) | 30% | 99% |
E7QKX4 | Saccharomyces cerevisiae (strain Zymaflore VL3) | 31% | 99% |
E9AT38 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 99% |
F4J2K2 | Arabidopsis thaliana | 30% | 86% |
F4JYE9 | Arabidopsis thaliana | 27% | 100% |
F4K2A1 | Arabidopsis thaliana | 29% | 95% |
O13492 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 29% | 100% |
O74742 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 32% | 100% |
P48760 | Mus musculus | 32% | 92% |
Q05932 | Homo sapiens | 32% | 92% |
Q08645 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 31% | 99% |
Q09509 | Caenorhabditis elegans | 29% | 100% |
Q12676 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 23% | 100% |
Q4Q1G0 | Leishmania major | 95% | 99% |
Q54CY5 | Dictyostelium discoideum | 29% | 86% |
Q8W035 | Arabidopsis thaliana | 32% | 100% |
Q924L9 | Cricetulus griseus | 27% | 92% |
Q9UTD0 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 26% | 100% |
Q9Y893 | Candida albicans | 30% | 100% |
V5BKB0 | Trypanosoma cruzi | 53% | 100% |