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: A4HPC7
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 | 141 | 145 | PF00656 | 0.386 |
CLV_C14_Caspase3-7 | 55 | 59 | PF00656 | 0.477 |
CLV_NRD_NRD_1 | 322 | 324 | PF00675 | 0.349 |
CLV_NRD_NRD_1 | 395 | 397 | PF00675 | 0.328 |
CLV_NRD_NRD_1 | 527 | 529 | PF00675 | 0.554 |
CLV_NRD_NRD_1 | 69 | 71 | PF00675 | 0.631 |
CLV_PCSK_KEX2_1 | 322 | 324 | PF00082 | 0.349 |
CLV_PCSK_KEX2_1 | 395 | 397 | PF00082 | 0.336 |
CLV_PCSK_KEX2_1 | 526 | 528 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 69 | 71 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 82 | 84 | PF00082 | 0.511 |
CLV_PCSK_PC1ET2_1 | 82 | 84 | PF00082 | 0.409 |
CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.323 |
CLV_PCSK_SKI1_1 | 273 | 277 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.285 |
CLV_PCSK_SKI1_1 | 338 | 342 | PF00082 | 0.326 |
CLV_PCSK_SKI1_1 | 395 | 399 | PF00082 | 0.375 |
CLV_PCSK_SKI1_1 | 407 | 411 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 466 | 470 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 54 | 58 | PF00082 | 0.529 |
CLV_PCSK_SKI1_1 | 64 | 68 | PF00082 | 0.426 |
DEG_SCF_TRCP1_1 | 356 | 362 | PF00400 | 0.290 |
DOC_ANK_TNKS_1 | 139 | 146 | PF00023 | 0.431 |
DOC_CDC14_PxL_1 | 88 | 96 | PF14671 | 0.387 |
DOC_CKS1_1 | 283 | 288 | PF01111 | 0.388 |
DOC_CYCLIN_RxL_1 | 390 | 403 | PF00134 | 0.379 |
DOC_MAPK_DCC_7 | 323 | 333 | PF00069 | 0.397 |
DOC_MAPK_gen_1 | 54 | 62 | PF00069 | 0.553 |
DOC_MAPK_gen_1 | 82 | 90 | PF00069 | 0.469 |
DOC_MAPK_MEF2A_6 | 188 | 197 | PF00069 | 0.353 |
DOC_MAPK_MEF2A_6 | 281 | 290 | PF00069 | 0.360 |
DOC_PP1_RVXF_1 | 85 | 91 | PF00149 | 0.374 |
DOC_PP1_RVXF_1 | 94 | 100 | PF00149 | 0.278 |
DOC_PP1_SILK_1 | 407 | 412 | PF00149 | 0.230 |
DOC_PP2B_LxvP_1 | 486 | 489 | PF13499 | 0.487 |
DOC_PP4_FxxP_1 | 129 | 132 | PF00568 | 0.293 |
DOC_PP4_FxxP_1 | 262 | 265 | PF00568 | 0.408 |
DOC_USP7_MATH_1 | 249 | 253 | PF00917 | 0.172 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 347 | 351 | PF00917 | 0.364 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.414 |
DOC_USP7_MATH_1 | 415 | 419 | PF00917 | 0.418 |
DOC_USP7_MATH_1 | 426 | 430 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 489 | 493 | PF00917 | 0.528 |
DOC_USP7_UBL2_3 | 407 | 411 | PF12436 | 0.458 |
DOC_WW_Pin1_4 | 128 | 133 | PF00397 | 0.295 |
DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.712 |
DOC_WW_Pin1_4 | 177 | 182 | PF00397 | 0.560 |
DOC_WW_Pin1_4 | 282 | 287 | PF00397 | 0.333 |
DOC_WW_Pin1_4 | 39 | 44 | PF00397 | 0.733 |
DOC_WW_Pin1_4 | 390 | 395 | PF00397 | 0.415 |
LIG_14-3-3_CanoR_1 | 432 | 440 | PF00244 | 0.573 |
LIG_14-3-3_CanoR_1 | 453 | 461 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 475 | 484 | PF00244 | 0.514 |
LIG_Clathr_ClatBox_1 | 287 | 291 | PF01394 | 0.409 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.291 |
LIG_FHA_1 | 270 | 276 | PF00498 | 0.378 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.419 |
LIG_FHA_1 | 360 | 366 | PF00498 | 0.354 |
LIG_FHA_2 | 139 | 145 | PF00498 | 0.395 |
LIG_FHA_2 | 241 | 247 | PF00498 | 0.284 |
LIG_FHA_2 | 400 | 406 | PF00498 | 0.414 |
LIG_FHA_2 | 439 | 445 | PF00498 | 0.468 |
LIG_HP1_1 | 286 | 290 | PF01393 | 0.389 |
LIG_LIR_Gen_1 | 231 | 240 | PF02991 | 0.322 |
LIG_LIR_Gen_1 | 378 | 387 | PF02991 | 0.410 |
LIG_LIR_Gen_1 | 418 | 428 | PF02991 | 0.399 |
LIG_LIR_LC3C_4 | 485 | 488 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 162 | 167 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 299 | 303 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 378 | 384 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 418 | 423 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 463 | 468 | PF02991 | 0.277 |
LIG_LIR_Nem_3 | 508 | 512 | PF02991 | 0.332 |
LIG_Pex14_1 | 461 | 465 | PF04695 | 0.327 |
LIG_Pex14_2 | 187 | 191 | PF04695 | 0.272 |
LIG_REV1ctd_RIR_1 | 184 | 192 | PF16727 | 0.348 |
LIG_SH2_SRC | 364 | 367 | PF00017 | 0.343 |
LIG_SH2_STAP1 | 153 | 157 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 114 | 117 | PF00017 | 0.271 |
LIG_SH2_STAT5 | 196 | 199 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 364 | 367 | PF00017 | 0.299 |
LIG_SH2_STAT5 | 401 | 404 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 416 | 419 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 84 | 87 | PF00017 | 0.410 |
LIG_SH3_3 | 280 | 286 | PF00018 | 0.351 |
LIG_SH3_3 | 326 | 332 | PF00018 | 0.400 |
LIG_SH3_3 | 425 | 431 | PF00018 | 0.328 |
LIG_SH3_3 | 43 | 49 | PF00018 | 0.564 |
LIG_SUMO_SIM_anti_2 | 204 | 209 | PF11976 | 0.244 |
LIG_SUMO_SIM_anti_2 | 224 | 231 | PF11976 | 0.288 |
LIG_SUMO_SIM_anti_2 | 285 | 291 | PF11976 | 0.472 |
LIG_SUMO_SIM_anti_2 | 314 | 320 | PF11976 | 0.297 |
LIG_SUMO_SIM_anti_2 | 481 | 488 | PF11976 | 0.418 |
LIG_SUMO_SIM_par_1 | 285 | 291 | PF11976 | 0.399 |
LIG_SUMO_SIM_par_1 | 396 | 403 | PF11976 | 0.241 |
LIG_TRAF2_1 | 243 | 246 | PF00917 | 0.249 |
LIG_UBA3_1 | 330 | 338 | PF00899 | 0.491 |
LIG_WRC_WIRS_1 | 53 | 58 | PF05994 | 0.281 |
MOD_CDC14_SPxK_1 | 393 | 396 | PF00782 | 0.380 |
MOD_CDK_SPK_2 | 390 | 395 | PF00069 | 0.415 |
MOD_CDK_SPxK_1 | 390 | 396 | PF00069 | 0.407 |
MOD_CK1_1 | 179 | 185 | PF00069 | 0.379 |
MOD_CK1_1 | 218 | 224 | PF00069 | 0.363 |
MOD_CK1_1 | 227 | 233 | PF00069 | 0.314 |
MOD_CK1_1 | 373 | 379 | PF00069 | 0.461 |
MOD_CK2_1 | 240 | 246 | PF00069 | 0.249 |
MOD_CK2_1 | 438 | 444 | PF00069 | 0.536 |
MOD_CK2_1 | 475 | 481 | PF00069 | 0.347 |
MOD_CK2_1 | 489 | 495 | PF00069 | 0.369 |
MOD_Cter_Amidation | 524 | 527 | PF01082 | 0.535 |
MOD_Cter_Amidation | 67 | 70 | PF01082 | 0.509 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.357 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.705 |
MOD_GlcNHglycan | 250 | 254 | PF01048 | 0.407 |
MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.350 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.424 |
MOD_GlcNHglycan | 383 | 387 | PF01048 | 0.443 |
MOD_GlcNHglycan | 436 | 439 | PF01048 | 0.654 |
MOD_GlcNHglycan | 477 | 480 | PF01048 | 0.487 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.710 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.470 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.335 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.396 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.531 |
MOD_N-GLC_1 | 359 | 364 | PF02516 | 0.392 |
MOD_N-GLC_2 | 72 | 74 | PF02516 | 0.603 |
MOD_NEK2_1 | 148 | 153 | PF00069 | 0.342 |
MOD_NEK2_1 | 191 | 196 | PF00069 | 0.285 |
MOD_NEK2_1 | 240 | 245 | PF00069 | 0.393 |
MOD_NEK2_1 | 382 | 387 | PF00069 | 0.409 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.260 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.352 |
MOD_NEK2_2 | 2 | 7 | PF00069 | 0.700 |
MOD_NEK2_2 | 359 | 364 | PF00069 | 0.367 |
MOD_NEK2_2 | 460 | 465 | PF00069 | 0.233 |
MOD_NEK2_2 | 52 | 57 | PF00069 | 0.498 |
MOD_PIKK_1 | 169 | 175 | PF00454 | 0.481 |
MOD_PIKK_1 | 179 | 185 | PF00454 | 0.424 |
MOD_PIKK_1 | 347 | 353 | PF00454 | 0.330 |
MOD_PIKK_1 | 375 | 381 | PF00454 | 0.448 |
MOD_PK_1 | 323 | 329 | PF00069 | 0.304 |
MOD_PKA_1 | 64 | 70 | PF00069 | 0.347 |
MOD_PKA_2 | 431 | 437 | PF00069 | 0.555 |
MOD_Plk_1 | 138 | 144 | PF00069 | 0.492 |
MOD_Plk_1 | 148 | 154 | PF00069 | 0.407 |
MOD_Plk_1 | 224 | 230 | PF00069 | 0.284 |
MOD_Plk_1 | 336 | 342 | PF00069 | 0.395 |
MOD_Plk_1 | 359 | 365 | PF00069 | 0.445 |
MOD_Plk_1 | 466 | 472 | PF00069 | 0.394 |
MOD_Plk_4 | 191 | 197 | PF00069 | 0.309 |
MOD_Plk_4 | 224 | 230 | PF00069 | 0.284 |
MOD_Plk_4 | 336 | 342 | PF00069 | 0.441 |
MOD_Plk_4 | 405 | 411 | PF00069 | 0.384 |
MOD_Plk_4 | 415 | 421 | PF00069 | 0.304 |
MOD_Plk_4 | 505 | 511 | PF00069 | 0.319 |
MOD_ProDKin_1 | 128 | 134 | PF00069 | 0.297 |
MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.710 |
MOD_ProDKin_1 | 177 | 183 | PF00069 | 0.559 |
MOD_ProDKin_1 | 282 | 288 | PF00069 | 0.333 |
MOD_ProDKin_1 | 39 | 45 | PF00069 | 0.732 |
MOD_ProDKin_1 | 390 | 396 | PF00069 | 0.407 |
MOD_SUMO_rev_2 | 403 | 409 | PF00179 | 0.474 |
MOD_SUMO_rev_2 | 439 | 448 | PF00179 | 0.610 |
TRG_DiLeu_BaEn_2 | 94 | 100 | PF01217 | 0.396 |
TRG_DiLeu_BaLyEn_6 | 143 | 148 | PF01217 | 0.400 |
TRG_ENDOCYTIC_2 | 164 | 167 | PF00928 | 0.451 |
TRG_ENDOCYTIC_2 | 234 | 237 | PF00928 | 0.393 |
TRG_ENDOCYTIC_2 | 465 | 468 | PF00928 | 0.358 |
TRG_ENDOCYTIC_2 | 53 | 56 | PF00928 | 0.347 |
TRG_ER_diArg_1 | 322 | 324 | PF00400 | 0.349 |
TRG_ER_diArg_1 | 394 | 396 | PF00400 | 0.361 |
TRG_ER_diArg_1 | 526 | 528 | PF00400 | 0.475 |
TRG_ER_diArg_1 | 69 | 71 | PF00400 | 0.532 |
TRG_ER_diArg_1 | 96 | 99 | PF00400 | 0.368 |
TRG_Pf-PMV_PEXEL_1 | 146 | 150 | PF00026 | 0.440 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6C4 | Leptomonas seymouri | 72% | 81% |
A0A0S4KJ93 | Bodo saltans | 47% | 100% |
A0A1X0NM42 | Trypanosomatidae | 54% | 100% |
A0A3Q8IJ59 | Leishmania donovani | 85% | 98% |
A0A3R7RIQ8 | Trypanosoma rangeli | 53% | 100% |
A4ICG7 | Leishmania infantum | 85% | 98% |
A6H751 | Bos taurus | 32% | 91% |
A6ZP80 | Saccharomyces cerevisiae (strain YJM789) | 30% | 97% |
B3LJR0 | Saccharomyces cerevisiae (strain RM11-1a) | 30% | 97% |
B5VSC3 | Saccharomyces cerevisiae (strain AWRI1631) | 30% | 97% |
C8ZGZ3 | Saccharomyces cerevisiae (strain Lalvin EC1118 / Prise de mousse) | 30% | 97% |
D0A3I6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
E7KIA3 | Saccharomyces cerevisiae (strain AWRI796) | 30% | 97% |
E7KUJ4 | Saccharomyces cerevisiae (strain Lalvin QA23) | 30% | 97% |
E7NMM0 | Saccharomyces cerevisiae (strain FostersO) | 30% | 97% |
E7Q9C7 | Saccharomyces cerevisiae (strain FostersB) | 30% | 97% |
E7QKX4 | Saccharomyces cerevisiae (strain Zymaflore VL3) | 30% | 97% |
E9AT38 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 99% |
F4J2K2 | Arabidopsis thaliana | 30% | 85% |
F4K2A1 | Arabidopsis thaliana | 29% | 93% |
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 | 31% | 90% |
Q05932 | Homo sapiens | 31% | 90% |
Q08645 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 30% | 97% |
Q09509 | Caenorhabditis elegans | 29% | 100% |
Q12676 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 23% | 100% |
Q4Q1G0 | Leishmania major | 85% | 100% |
Q54CY5 | Dictyostelium discoideum | 29% | 85% |
Q8W035 | Arabidopsis thaliana | 31% | 100% |
Q924L9 | Cricetulus griseus | 29% | 90% |
Q9UTD0 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 27% | 100% |
Q9Y893 | Candida albicans | 31% | 100% |
V5BKB0 | Trypanosoma cruzi | 51% | 100% |