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: A4HW27
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 11 |
GO:0006793 | phosphorus metabolic process | 3 | 11 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016310 | phosphorylation | 5 | 11 |
GO:0019538 | protein metabolic process | 3 | 11 |
GO:0036211 | protein modification process | 4 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0043412 | macromolecule modification | 4 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 11 |
GO:0051301 | cell division | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004672 | protein kinase activity | 3 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0016301 | kinase activity | 4 | 11 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 11 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0030554 | adenyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 3 |
GO:0004707 | MAP kinase activity | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 130 | 132 | PF00675 | 0.229 |
CLV_NRD_NRD_1 | 168 | 170 | PF00675 | 0.398 |
CLV_NRD_NRD_1 | 335 | 337 | PF00675 | 0.704 |
CLV_NRD_NRD_1 | 44 | 46 | PF00675 | 0.450 |
CLV_NRD_NRD_1 | 538 | 540 | PF00675 | 0.462 |
CLV_PCSK_KEX2_1 | 335 | 337 | PF00082 | 0.691 |
CLV_PCSK_KEX2_1 | 413 | 415 | PF00082 | 0.426 |
CLV_PCSK_KEX2_1 | 540 | 542 | PF00082 | 0.351 |
CLV_PCSK_PC1ET2_1 | 413 | 415 | PF00082 | 0.369 |
CLV_PCSK_PC1ET2_1 | 540 | 542 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 131 | 135 | PF00082 | 0.369 |
CLV_PCSK_SKI1_1 | 153 | 157 | PF00082 | 0.382 |
CLV_PCSK_SKI1_1 | 177 | 181 | PF00082 | 0.251 |
CLV_PCSK_SKI1_1 | 32 | 36 | PF00082 | 0.545 |
CLV_PCSK_SKI1_1 | 557 | 561 | PF00082 | 0.458 |
DEG_SCF_FBW7_1 | 451 | 458 | PF00400 | 0.406 |
DEG_SPOP_SBC_1 | 287 | 291 | PF00917 | 0.475 |
DOC_ANK_TNKS_1 | 473 | 480 | PF00023 | 0.163 |
DOC_CYCLIN_RxL_1 | 174 | 183 | PF00134 | 0.369 |
DOC_CYCLIN_RxL_1 | 29 | 37 | PF00134 | 0.367 |
DOC_CYCLIN_yCln2_LP_2 | 36 | 42 | PF00134 | 0.419 |
DOC_MAPK_gen_1 | 348 | 357 | PF00069 | 0.268 |
DOC_MAPK_HePTP_8 | 345 | 357 | PF00069 | 0.222 |
DOC_MAPK_HePTP_8 | 84 | 96 | PF00069 | 0.229 |
DOC_MAPK_MEF2A_6 | 137 | 144 | PF00069 | 0.229 |
DOC_MAPK_MEF2A_6 | 159 | 167 | PF00069 | 0.229 |
DOC_MAPK_MEF2A_6 | 348 | 357 | PF00069 | 0.222 |
DOC_MAPK_MEF2A_6 | 87 | 96 | PF00069 | 0.229 |
DOC_MAPK_NFAT4_5 | 137 | 145 | PF00069 | 0.229 |
DOC_PP1_RVXF_1 | 208 | 215 | PF00149 | 0.229 |
DOC_PP2B_LxvP_1 | 36 | 39 | PF13499 | 0.401 |
DOC_PP2B_LxvP_1 | 470 | 473 | PF13499 | 0.229 |
DOC_PP4_FxxP_1 | 552 | 555 | PF00568 | 0.324 |
DOC_USP7_MATH_1 | 204 | 208 | PF00917 | 0.314 |
DOC_USP7_MATH_1 | 246 | 250 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 297 | 301 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 455 | 459 | PF00917 | 0.319 |
DOC_USP7_MATH_1 | 558 | 562 | PF00917 | 0.539 |
DOC_WW_Pin1_4 | 223 | 228 | PF00397 | 0.330 |
DOC_WW_Pin1_4 | 235 | 240 | PF00397 | 0.416 |
DOC_WW_Pin1_4 | 271 | 276 | PF00397 | 0.764 |
DOC_WW_Pin1_4 | 349 | 354 | PF00397 | 0.318 |
DOC_WW_Pin1_4 | 408 | 413 | PF00397 | 0.362 |
DOC_WW_Pin1_4 | 451 | 456 | PF00397 | 0.397 |
DOC_WW_Pin1_4 | 463 | 468 | PF00397 | 0.411 |
DOC_WW_Pin1_4 | 489 | 494 | PF00397 | 0.417 |
LIG_14-3-3_CanoR_1 | 153 | 158 | PF00244 | 0.382 |
LIG_14-3-3_CanoR_1 | 367 | 371 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 539 | 548 | PF00244 | 0.229 |
LIG_BIR_III_2 | 318 | 322 | PF00653 | 0.462 |
LIG_BIR_III_2 | 448 | 452 | PF00653 | 0.229 |
LIG_BIR_III_4 | 49 | 53 | PF00653 | 0.253 |
LIG_BRCT_BRCA1_1 | 465 | 469 | PF00533 | 0.229 |
LIG_Clathr_ClatBox_1 | 179 | 183 | PF01394 | 0.328 |
LIG_deltaCOP1_diTrp_1 | 366 | 373 | PF00928 | 0.212 |
LIG_eIF4E_1 | 29 | 35 | PF01652 | 0.364 |
LIG_EVH1_1 | 588 | 592 | PF00568 | 0.482 |
LIG_FHA_1 | 289 | 295 | PF00498 | 0.599 |
LIG_FHA_1 | 360 | 366 | PF00498 | 0.402 |
LIG_FHA_1 | 395 | 401 | PF00498 | 0.257 |
LIG_FHA_1 | 8 | 14 | PF00498 | 0.384 |
LIG_FHA_2 | 361 | 367 | PF00498 | 0.254 |
LIG_Integrin_RGD_1 | 336 | 338 | PF01839 | 0.510 |
LIG_LIR_Apic_2 | 347 | 353 | PF02991 | 0.265 |
LIG_LIR_Gen_1 | 19 | 29 | PF02991 | 0.573 |
LIG_LIR_Gen_1 | 520 | 530 | PF02991 | 0.229 |
LIG_LIR_Nem_3 | 148 | 152 | PF02991 | 0.316 |
LIG_LIR_Nem_3 | 158 | 163 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 19 | 24 | PF02991 | 0.570 |
LIG_LIR_Nem_3 | 520 | 526 | PF02991 | 0.229 |
LIG_LIR_Nem_3 | 76 | 80 | PF02991 | 0.247 |
LIG_MLH1_MIPbox_1 | 465 | 469 | PF16413 | 0.229 |
LIG_MYND_1 | 451 | 455 | PF01753 | 0.229 |
LIG_MYND_1 | 551 | 555 | PF01753 | 0.242 |
LIG_REV1ctd_RIR_1 | 466 | 472 | PF16727 | 0.229 |
LIG_SH2_CRK | 152 | 156 | PF00017 | 0.383 |
LIG_SH2_CRK | 160 | 164 | PF00017 | 0.359 |
LIG_SH2_CRK | 173 | 177 | PF00017 | 0.369 |
LIG_SH2_NCK_1 | 21 | 25 | PF00017 | 0.557 |
LIG_SH2_NCK_1 | 47 | 51 | PF00017 | 0.328 |
LIG_SH2_SRC | 47 | 50 | PF00017 | 0.470 |
LIG_SH2_STAP1 | 361 | 365 | PF00017 | 0.229 |
LIG_SH2_STAP1 | 47 | 51 | PF00017 | 0.403 |
LIG_SH2_STAT3 | 219 | 222 | PF00017 | 0.229 |
LIG_SH2_STAT5 | 102 | 105 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 344 | 347 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 361 | 364 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 395 | 398 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 419 | 422 | PF00017 | 0.262 |
LIG_SH2_STAT5 | 54 | 57 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 66 | 69 | PF00017 | 0.272 |
LIG_SH3_2 | 272 | 277 | PF14604 | 0.506 |
LIG_SH3_2 | 382 | 387 | PF14604 | 0.369 |
LIG_SH3_3 | 140 | 146 | PF00018 | 0.229 |
LIG_SH3_3 | 229 | 235 | PF00018 | 0.418 |
LIG_SH3_3 | 240 | 246 | PF00018 | 0.424 |
LIG_SH3_3 | 269 | 275 | PF00018 | 0.664 |
LIG_SH3_3 | 299 | 305 | PF00018 | 0.554 |
LIG_SH3_3 | 379 | 385 | PF00018 | 0.314 |
LIG_SH3_3 | 581 | 587 | PF00018 | 0.487 |
LIG_SH3_5 | 402 | 406 | PF00018 | 0.229 |
LIG_SUMO_SIM_par_1 | 139 | 145 | PF11976 | 0.314 |
LIG_SUMO_SIM_par_1 | 153 | 158 | PF11976 | 0.186 |
LIG_SUMO_SIM_par_1 | 177 | 183 | PF11976 | 0.229 |
LIG_SUMO_SIM_par_1 | 492 | 499 | PF11976 | 0.229 |
LIG_SUMO_SIM_par_1 | 9 | 14 | PF11976 | 0.511 |
LIG_TRAF2_1 | 496 | 499 | PF00917 | 0.438 |
LIG_TRAF2_1 | 58 | 61 | PF00917 | 0.316 |
LIG_TYR_ITSM | 156 | 163 | PF00017 | 0.229 |
LIG_UBA3_1 | 154 | 159 | PF00899 | 0.328 |
LIG_WW_2 | 586 | 589 | PF00397 | 0.486 |
MOD_CDC14_SPxK_1 | 274 | 277 | PF00782 | 0.638 |
MOD_CDC14_SPxK_1 | 411 | 414 | PF00782 | 0.229 |
MOD_CDK_SPK_2 | 408 | 413 | PF00069 | 0.229 |
MOD_CDK_SPxK_1 | 271 | 277 | PF00069 | 0.640 |
MOD_CDK_SPxK_1 | 408 | 414 | PF00069 | 0.229 |
MOD_CK1_1 | 238 | 244 | PF00069 | 0.658 |
MOD_CK1_1 | 423 | 429 | PF00069 | 0.256 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.295 |
MOD_CK2_1 | 16 | 22 | PF00069 | 0.523 |
MOD_CK2_1 | 202 | 208 | PF00069 | 0.377 |
MOD_CK2_1 | 246 | 252 | PF00069 | 0.601 |
MOD_CK2_1 | 493 | 499 | PF00069 | 0.443 |
MOD_CK2_1 | 518 | 524 | PF00069 | 0.325 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.406 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.644 |
MOD_GlcNHglycan | 266 | 272 | PF01048 | 0.542 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.705 |
MOD_GlcNHglycan | 428 | 431 | PF01048 | 0.348 |
MOD_GlcNHglycan | 457 | 460 | PF01048 | 0.398 |
MOD_GlcNHglycan | 487 | 490 | PF01048 | 0.312 |
MOD_GlcNHglycan | 519 | 523 | PF01048 | 0.295 |
MOD_GlcNHglycan | 562 | 565 | PF01048 | 0.668 |
MOD_GlcNHglycan | 567 | 570 | PF01048 | 0.640 |
MOD_GlcNHglycan | 581 | 584 | PF01048 | 0.771 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.293 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.440 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.553 |
MOD_GSK3_1 | 267 | 274 | PF00069 | 0.658 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.646 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.430 |
MOD_GSK3_1 | 420 | 427 | PF00069 | 0.365 |
MOD_GSK3_1 | 451 | 458 | PF00069 | 0.334 |
MOD_GSK3_1 | 485 | 492 | PF00069 | 0.315 |
MOD_GSK3_1 | 575 | 582 | PF00069 | 0.716 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.514 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.365 |
MOD_NEK2_1 | 165 | 170 | PF00069 | 0.245 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.395 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.298 |
MOD_NEK2_1 | 417 | 422 | PF00069 | 0.229 |
MOD_NEK2_2 | 23 | 28 | PF00069 | 0.342 |
MOD_PIKK_1 | 102 | 108 | PF00454 | 0.377 |
MOD_PIKK_1 | 11 | 17 | PF00454 | 0.458 |
MOD_PIKK_1 | 412 | 418 | PF00454 | 0.326 |
MOD_PKA_1 | 540 | 546 | PF00069 | 0.366 |
MOD_PKA_2 | 366 | 372 | PF00069 | 0.229 |
MOD_PKA_2 | 540 | 546 | PF00069 | 0.263 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.370 |
MOD_Plk_1 | 518 | 524 | PF00069 | 0.299 |
MOD_Plk_4 | 16 | 22 | PF00069 | 0.551 |
MOD_Plk_4 | 23 | 29 | PF00069 | 0.568 |
MOD_Plk_4 | 395 | 401 | PF00069 | 0.314 |
MOD_Plk_4 | 76 | 82 | PF00069 | 0.254 |
MOD_ProDKin_1 | 223 | 229 | PF00069 | 0.337 |
MOD_ProDKin_1 | 235 | 241 | PF00069 | 0.421 |
MOD_ProDKin_1 | 271 | 277 | PF00069 | 0.766 |
MOD_ProDKin_1 | 349 | 355 | PF00069 | 0.318 |
MOD_ProDKin_1 | 408 | 414 | PF00069 | 0.362 |
MOD_ProDKin_1 | 451 | 457 | PF00069 | 0.397 |
MOD_ProDKin_1 | 463 | 469 | PF00069 | 0.411 |
MOD_ProDKin_1 | 489 | 495 | PF00069 | 0.417 |
MOD_SUMO_for_1 | 194 | 197 | PF00179 | 0.222 |
TRG_DiLeu_BaEn_1 | 31 | 36 | PF01217 | 0.366 |
TRG_DiLeu_BaLyEn_6 | 150 | 155 | PF01217 | 0.456 |
TRG_ENDOCYTIC_2 | 152 | 155 | PF00928 | 0.383 |
TRG_ENDOCYTIC_2 | 160 | 163 | PF00928 | 0.359 |
TRG_ENDOCYTIC_2 | 173 | 176 | PF00928 | 0.369 |
TRG_ENDOCYTIC_2 | 21 | 24 | PF00928 | 0.567 |
TRG_ENDOCYTIC_2 | 523 | 526 | PF00928 | 0.393 |
TRG_ER_diArg_1 | 538 | 541 | PF00400 | 0.298 |
TRG_NLS_MonoExtN_4 | 538 | 543 | PF00514 | 0.229 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1H8 | Leptomonas seymouri | 26% | 81% |
A0A0S4JMD1 | Bodo saltans | 28% | 77% |
A0A0S4KIN4 | Bodo saltans | 25% | 87% |
A0A1X0NZD5 | Trypanosomatidae | 24% | 100% |
A0A1X0P1B0 | Trypanosomatidae | 25% | 82% |
A4H7N7 | Leishmania braziliensis | 83% | 100% |
C9ZW07 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
V5BPV5 | Trypanosoma cruzi | 26% | 68% |
V5DTK9 | Trypanosoma cruzi | 24% | 74% |