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 | 2 |
GO:0005739 | mitochondrion | 5 | 2 |
GO:0005829 | cytosol | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q1G0
Term | Name | Level | Count |
---|---|---|---|
GO:0006575 | cellular modified amino acid metabolic process | 3 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006760 | folic acid-containing compound metabolic process | 4 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009058 | biosynthetic process | 2 | 2 |
GO:0009396 | folic acid-containing compound biosynthetic process | 5 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0018130 | heterocycle biosynthetic process | 4 | 2 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0042398 | cellular modified amino acid biosynthetic process | 4 | 2 |
GO:0042558 | pteridine-containing compound metabolic process | 4 | 2 |
GO:0042559 | pteridine-containing compound biosynthetic process | 5 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044249 | cellular biosynthetic process | 3 | 2 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0046900 | tetrahydrofolylpolyglutamate metabolic process | 5 | 2 |
GO:0046901 | tetrahydrofolylpolyglutamate biosynthetic process | 6 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 2 |
GO:1901576 | organic substance biosynthetic process | 3 | 2 |
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 | 148 | 152 | PF00656 | 0.506 |
CLV_C14_Caspase3-7 | 62 | 66 | PF00656 | 0.530 |
CLV_NRD_NRD_1 | 287 | 289 | PF00675 | 0.466 |
CLV_NRD_NRD_1 | 329 | 331 | PF00675 | 0.402 |
CLV_NRD_NRD_1 | 402 | 404 | PF00675 | 0.383 |
CLV_NRD_NRD_1 | 534 | 536 | PF00675 | 0.570 |
CLV_NRD_NRD_1 | 58 | 60 | PF00675 | 0.596 |
CLV_NRD_NRD_1 | 76 | 78 | PF00675 | 0.624 |
CLV_PCSK_KEX2_1 | 329 | 331 | PF00082 | 0.402 |
CLV_PCSK_KEX2_1 | 402 | 404 | PF00082 | 0.391 |
CLV_PCSK_KEX2_1 | 414 | 416 | PF00082 | 0.421 |
CLV_PCSK_KEX2_1 | 534 | 536 | PF00082 | 0.571 |
CLV_PCSK_KEX2_1 | 57 | 59 | PF00082 | 0.628 |
CLV_PCSK_KEX2_1 | 76 | 78 | PF00082 | 0.571 |
CLV_PCSK_KEX2_1 | 89 | 91 | PF00082 | 0.528 |
CLV_PCSK_PC1ET2_1 | 414 | 416 | PF00082 | 0.494 |
CLV_PCSK_PC1ET2_1 | 57 | 59 | PF00082 | 0.665 |
CLV_PCSK_PC1ET2_1 | 89 | 91 | PF00082 | 0.542 |
CLV_PCSK_PC7_1 | 72 | 78 | PF00082 | 0.559 |
CLV_PCSK_SKI1_1 | 195 | 199 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 280 | 284 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 322 | 326 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 345 | 349 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 402 | 406 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 414 | 418 | PF00082 | 0.366 |
CLV_PCSK_SKI1_1 | 460 | 464 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 473 | 477 | PF00082 | 0.407 |
CLV_PCSK_SKI1_1 | 524 | 528 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 61 | 65 | PF00082 | 0.543 |
DOC_ANK_TNKS_1 | 146 | 153 | PF00023 | 0.467 |
DOC_CDC14_PxL_1 | 95 | 103 | PF14671 | 0.512 |
DOC_CYCLIN_RxL_1 | 397 | 410 | PF00134 | 0.424 |
DOC_MAPK_DCC_7 | 330 | 340 | PF00069 | 0.446 |
DOC_MAPK_gen_1 | 288 | 296 | PF00069 | 0.454 |
DOC_MAPK_gen_1 | 61 | 69 | PF00069 | 0.530 |
DOC_MAPK_gen_1 | 89 | 97 | PF00069 | 0.496 |
DOC_MAPK_MEF2A_6 | 195 | 204 | PF00069 | 0.400 |
DOC_MAPK_MEF2A_6 | 288 | 297 | PF00069 | 0.393 |
DOC_MAPK_MEF2A_6 | 305 | 312 | PF00069 | 0.365 |
DOC_PP1_RVXF_1 | 101 | 107 | PF00149 | 0.332 |
DOC_PP1_RVXF_1 | 401 | 408 | PF00149 | 0.379 |
DOC_PP1_RVXF_1 | 92 | 98 | PF00149 | 0.427 |
DOC_PP2B_LxvP_1 | 493 | 496 | PF13499 | 0.538 |
DOC_PP4_FxxP_1 | 136 | 139 | PF00568 | 0.350 |
DOC_PP4_FxxP_1 | 269 | 272 | PF00568 | 0.447 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.521 |
DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.423 |
DOC_USP7_MATH_1 | 496 | 500 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.722 |
DOC_USP7_UBL2_3 | 285 | 289 | PF12436 | 0.462 |
DOC_USP7_UBL2_3 | 414 | 418 | PF12436 | 0.500 |
DOC_WW_Pin1_4 | 135 | 140 | PF00397 | 0.352 |
DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.782 |
DOC_WW_Pin1_4 | 184 | 189 | PF00397 | 0.575 |
LIG_14-3-3_CanoR_1 | 439 | 447 | PF00244 | 0.623 |
LIG_14-3-3_CanoR_1 | 460 | 468 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 482 | 491 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 58 | 64 | PF00244 | 0.529 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.598 |
LIG_Clathr_ClatBox_1 | 294 | 298 | PF01394 | 0.439 |
LIG_DLG_GKlike_1 | 59 | 67 | PF00625 | 0.498 |
LIG_EH1_1 | 516 | 524 | PF00400 | 0.335 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.306 |
LIG_FHA_1 | 224 | 230 | PF00498 | 0.292 |
LIG_FHA_1 | 277 | 283 | PF00498 | 0.411 |
LIG_FHA_1 | 367 | 373 | PF00498 | 0.398 |
LIG_FHA_2 | 146 | 152 | PF00498 | 0.508 |
LIG_FHA_2 | 248 | 254 | PF00498 | 0.341 |
LIG_FHA_2 | 407 | 413 | PF00498 | 0.457 |
LIG_FHA_2 | 461 | 467 | PF00498 | 0.490 |
LIG_GBD_Chelix_1 | 518 | 526 | PF00786 | 0.358 |
LIG_HP1_1 | 293 | 297 | PF01393 | 0.496 |
LIG_LIR_Gen_1 | 169 | 176 | PF02991 | 0.441 |
LIG_LIR_Gen_1 | 238 | 247 | PF02991 | 0.452 |
LIG_LIR_Gen_1 | 385 | 393 | PF02991 | 0.455 |
LIG_LIR_LC3C_4 | 492 | 495 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 157 | 163 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 169 | 174 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 306 | 310 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 385 | 391 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 515 | 519 | PF02991 | 0.348 |
LIG_Pex14_1 | 468 | 472 | PF04695 | 0.403 |
LIG_Pex14_2 | 194 | 198 | PF04695 | 0.325 |
LIG_REV1ctd_RIR_1 | 191 | 199 | PF16727 | 0.400 |
LIG_SH2_SRC | 371 | 374 | PF00017 | 0.405 |
LIG_SH2_SRC | 423 | 426 | PF00017 | 0.305 |
LIG_SH2_STAP1 | 121 | 125 | PF00017 | 0.307 |
LIG_SH2_STAP1 | 160 | 164 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 121 | 124 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 163 | 166 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 371 | 374 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 408 | 411 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 423 | 426 | PF00017 | 0.422 |
LIG_SH3_1 | 18 | 24 | PF00018 | 0.646 |
LIG_SH3_3 | 18 | 24 | PF00018 | 0.673 |
LIG_SH3_3 | 287 | 293 | PF00018 | 0.400 |
LIG_SH3_3 | 333 | 339 | PF00018 | 0.429 |
LIG_SH3_3 | 419 | 425 | PF00018 | 0.305 |
LIG_SH3_3 | 432 | 438 | PF00018 | 0.392 |
LIG_SUMO_SIM_anti_2 | 231 | 238 | PF11976 | 0.367 |
LIG_SUMO_SIM_anti_2 | 319 | 327 | PF11976 | 0.364 |
LIG_SUMO_SIM_anti_2 | 488 | 495 | PF11976 | 0.476 |
LIG_SUMO_SIM_par_1 | 292 | 298 | PF11976 | 0.429 |
LIG_TRAF2_1 | 250 | 253 | PF00917 | 0.306 |
LIG_UBA3_1 | 337 | 345 | PF00899 | 0.521 |
LIG_UBA3_1 | 522 | 527 | PF00899 | 0.297 |
MOD_CDC14_SPxK_1 | 187 | 190 | PF00782 | 0.552 |
MOD_CDK_SPxK_1 | 184 | 190 | PF00069 | 0.563 |
MOD_CK1_1 | 119 | 125 | PF00069 | 0.400 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.665 |
MOD_CK1_1 | 225 | 231 | PF00069 | 0.406 |
MOD_CK1_1 | 234 | 240 | PF00069 | 0.368 |
MOD_CK1_1 | 380 | 386 | PF00069 | 0.448 |
MOD_CK2_1 | 247 | 253 | PF00069 | 0.306 |
MOD_CK2_1 | 278 | 284 | PF00069 | 0.444 |
MOD_CK2_1 | 460 | 466 | PF00069 | 0.496 |
MOD_CK2_1 | 482 | 488 | PF00069 | 0.403 |
MOD_CK2_1 | 496 | 502 | PF00069 | 0.447 |
MOD_Cter_Amidation | 532 | 535 | PF01082 | 0.543 |
MOD_Cter_Amidation | 74 | 77 | PF01082 | 0.649 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.414 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.739 |
MOD_GlcNHglycan | 382 | 385 | PF01048 | 0.457 |
MOD_GlcNHglycan | 390 | 394 | PF01048 | 0.382 |
MOD_GlcNHglycan | 443 | 446 | PF01048 | 0.683 |
MOD_GlcNHglycan | 484 | 487 | PF01048 | 0.502 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.675 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.323 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.470 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.385 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.452 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.424 |
MOD_N-GLC_1 | 366 | 371 | PF02516 | 0.529 |
MOD_N-GLC_2 | 79 | 81 | PF02516 | 0.656 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.679 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.327 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.427 |
MOD_NEK2_1 | 389 | 394 | PF00069 | 0.452 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.411 |
MOD_PIKK_1 | 176 | 182 | PF00454 | 0.513 |
MOD_PIKK_1 | 354 | 360 | PF00454 | 0.381 |
MOD_PIKK_1 | 382 | 388 | PF00454 | 0.489 |
MOD_PK_1 | 330 | 336 | PF00069 | 0.365 |
MOD_PKA_2 | 438 | 444 | PF00069 | 0.601 |
MOD_PKA_2 | 71 | 77 | PF00069 | 0.579 |
MOD_PKB_1 | 458 | 466 | PF00069 | 0.441 |
MOD_Plk_1 | 145 | 151 | PF00069 | 0.502 |
MOD_Plk_1 | 231 | 237 | PF00069 | 0.341 |
MOD_Plk_1 | 343 | 349 | PF00069 | 0.502 |
MOD_Plk_1 | 366 | 372 | PF00069 | 0.490 |
MOD_Plk_1 | 473 | 479 | PF00069 | 0.539 |
MOD_Plk_2-3 | 278 | 284 | PF00069 | 0.308 |
MOD_Plk_4 | 198 | 204 | PF00069 | 0.391 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.341 |
MOD_Plk_4 | 343 | 349 | PF00069 | 0.455 |
MOD_Plk_4 | 512 | 518 | PF00069 | 0.335 |
MOD_ProDKin_1 | 135 | 141 | PF00069 | 0.354 |
MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.781 |
MOD_ProDKin_1 | 184 | 190 | PF00069 | 0.575 |
MOD_SUMO_rev_2 | 319 | 324 | PF00179 | 0.392 |
MOD_SUMO_rev_2 | 410 | 416 | PF00179 | 0.475 |
MOD_SUMO_rev_2 | 446 | 455 | PF00179 | 0.647 |
TRG_DiLeu_BaEn_2 | 101 | 107 | PF01217 | 0.445 |
TRG_DiLeu_BaLyEn_6 | 150 | 155 | PF01217 | 0.519 |
TRG_ENDOCYTIC_2 | 171 | 174 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 241 | 244 | PF00928 | 0.427 |
TRG_ENDOCYTIC_2 | 472 | 475 | PF00928 | 0.431 |
TRG_ER_diArg_1 | 103 | 106 | PF00400 | 0.424 |
TRG_ER_diArg_1 | 329 | 331 | PF00400 | 0.402 |
TRG_ER_diArg_1 | 401 | 403 | PF00400 | 0.398 |
TRG_ER_diArg_1 | 534 | 536 | PF00400 | 0.591 |
TRG_ER_diArg_1 | 58 | 61 | PF00400 | 0.602 |
TRG_ER_diArg_1 | 76 | 78 | PF00400 | 0.560 |
TRG_NLS_MonoExtC_3 | 56 | 61 | PF00514 | 0.585 |
TRG_Pf-PMV_PEXEL_1 | 153 | 157 | PF00026 | 0.475 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6C4 | Leptomonas seymouri | 75% | 82% |
A0A0S4KJ93 | Bodo saltans | 48% | 100% |
A0A1X0NM42 | Trypanosomatidae | 57% | 100% |
A0A3Q8IJ59 | Leishmania donovani | 95% | 99% |
A0A3R7RIQ8 | Trypanosoma rangeli | 53% | 100% |
A4HPC7 | Leishmania braziliensis | 85% | 100% |
A4ICG7 | Leishmania infantum | 95% | 99% |
A6H751 | Bos taurus | 30% | 92% |
A6ZP80 | Saccharomyces cerevisiae (strain YJM789) | 30% | 98% |
B3LJR0 | Saccharomyces cerevisiae (strain RM11-1a) | 30% | 98% |
B5VSC3 | Saccharomyces cerevisiae (strain AWRI1631) | 30% | 98% |
C8ZGZ3 | Saccharomyces cerevisiae (strain Lalvin EC1118 / Prise de mousse) | 30% | 98% |
D0A3I6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
E7KIA3 | Saccharomyces cerevisiae (strain AWRI796) | 30% | 98% |
E7KUJ4 | Saccharomyces cerevisiae (strain Lalvin QA23) | 30% | 98% |
E7NMM0 | Saccharomyces cerevisiae (strain FostersO) | 30% | 98% |
E7Q9C7 | Saccharomyces cerevisiae (strain FostersB) | 30% | 98% |
E7QKX4 | Saccharomyces cerevisiae (strain Zymaflore VL3) | 30% | 98% |
E9AT38 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
F4J2K2 | Arabidopsis thaliana | 30% | 86% |
F4JYE9 | Arabidopsis thaliana | 26% | 100% |
F4K2A1 | Arabidopsis thaliana | 28% | 94% |
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% | 91% |
Q05932 | Homo sapiens | 32% | 91% |
Q08645 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 30% | 98% |
Q09509 | Caenorhabditis elegans | 29% | 100% |
Q12676 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 22% | 100% |
Q54CY5 | Dictyostelium discoideum | 29% | 86% |
Q8W035 | Arabidopsis thaliana | 31% | 100% |
Q924L9 | Cricetulus griseus | 29% | 91% |
Q9UTD0 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 100% |
Q9Y893 | Candida albicans | 29% | 100% |
V5BKB0 | Trypanosoma cruzi | 54% | 100% |