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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A4H7N7
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 7 |
GO:0006793 | phosphorus metabolic process | 3 | 7 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016310 | phosphorylation | 5 | 7 |
GO:0019538 | protein metabolic process | 3 | 7 |
GO:0036211 | protein modification process | 4 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0043412 | macromolecule modification | 4 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 7 |
GO:0051301 | cell division | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 7 |
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004672 | protein kinase activity | 3 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0005524 | ATP binding | 5 | 7 |
GO:0016301 | kinase activity | 4 | 7 |
GO:0016740 | transferase activity | 2 | 7 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 7 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 7 |
GO:0017076 | purine nucleotide binding | 4 | 7 |
GO:0030554 | adenyl nucleotide binding | 5 | 7 |
GO:0032553 | ribonucleotide binding | 3 | 7 |
GO:0032555 | purine ribonucleotide binding | 4 | 7 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 7 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 7 |
GO:0036094 | small molecule binding | 2 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043168 | anion binding | 3 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:0097367 | carbohydrate derivative binding | 2 | 7 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 7 |
GO:1901265 | nucleoside phosphate binding | 3 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 3 |
GO:0004707 | MAP kinase activity | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 512 | 516 | PF00656 | 0.320 |
CLV_NRD_NRD_1 | 173 | 175 | PF00675 | 0.460 |
CLV_NRD_NRD_1 | 211 | 213 | PF00675 | 0.428 |
CLV_NRD_NRD_1 | 564 | 566 | PF00675 | 0.381 |
CLV_NRD_NRD_1 | 87 | 89 | PF00675 | 0.631 |
CLV_PCSK_KEX2_1 | 440 | 442 | PF00082 | 0.428 |
CLV_PCSK_KEX2_1 | 566 | 568 | PF00082 | 0.373 |
CLV_PCSK_PC1ET2_1 | 440 | 442 | PF00082 | 0.460 |
CLV_PCSK_PC1ET2_1 | 566 | 568 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 174 | 178 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 196 | 200 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 220 | 224 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 583 | 587 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 75 | 79 | PF00082 | 0.595 |
DEG_SCF_FBW7_1 | 476 | 483 | PF00400 | 0.419 |
DOC_CYCLIN_RxL_1 | 217 | 226 | PF00134 | 0.373 |
DOC_CYCLIN_RxL_1 | 72 | 80 | PF00134 | 0.603 |
DOC_CYCLIN_yCln2_LP_2 | 79 | 85 | PF00134 | 0.645 |
DOC_MAPK_gen_1 | 375 | 384 | PF00069 | 0.360 |
DOC_MAPK_HePTP_8 | 127 | 139 | PF00069 | 0.460 |
DOC_MAPK_HePTP_8 | 372 | 384 | PF00069 | 0.360 |
DOC_MAPK_MEF2A_6 | 130 | 139 | PF00069 | 0.460 |
DOC_MAPK_MEF2A_6 | 180 | 187 | PF00069 | 0.460 |
DOC_MAPK_MEF2A_6 | 202 | 210 | PF00069 | 0.460 |
DOC_MAPK_MEF2A_6 | 375 | 384 | PF00069 | 0.360 |
DOC_MAPK_NFAT4_5 | 180 | 188 | PF00069 | 0.460 |
DOC_PP1_RVXF_1 | 251 | 258 | PF00149 | 0.460 |
DOC_PP2B_LxvP_1 | 495 | 498 | PF13499 | 0.460 |
DOC_PP2B_LxvP_1 | 614 | 617 | PF13499 | 0.616 |
DOC_PP2B_LxvP_1 | 79 | 82 | PF13499 | 0.621 |
DOC_PP4_FxxP_1 | 578 | 581 | PF00568 | 0.488 |
DOC_PP4_MxPP_1 | 1 | 4 | PF00568 | 0.634 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 247 | 251 | PF00917 | 0.431 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.401 |
DOC_USP7_MATH_1 | 289 | 293 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.681 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.354 |
DOC_USP7_MATH_1 | 455 | 459 | PF00917 | 0.320 |
DOC_USP7_MATH_1 | 462 | 466 | PF00917 | 0.225 |
DOC_USP7_MATH_1 | 480 | 484 | PF00917 | 0.460 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 584 | 588 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 591 | 595 | PF00917 | 0.627 |
DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.628 |
DOC_WW_Pin1_4 | 278 | 283 | PF00397 | 0.580 |
DOC_WW_Pin1_4 | 313 | 318 | PF00397 | 0.715 |
DOC_WW_Pin1_4 | 376 | 381 | PF00397 | 0.402 |
DOC_WW_Pin1_4 | 435 | 440 | PF00397 | 0.367 |
DOC_WW_Pin1_4 | 476 | 481 | PF00397 | 0.402 |
DOC_WW_Pin1_4 | 488 | 493 | PF00397 | 0.443 |
DOC_WW_Pin1_4 | 515 | 520 | PF00397 | 0.390 |
LIG_14-3-3_CanoR_1 | 196 | 201 | PF00244 | 0.431 |
LIG_14-3-3_CanoR_1 | 394 | 398 | PF00244 | 0.412 |
LIG_14-3-3_CanoR_1 | 565 | 574 | PF00244 | 0.336 |
LIG_14-3-3_CanoR_1 | 588 | 596 | PF00244 | 0.592 |
LIG_BIR_III_2 | 473 | 477 | PF00653 | 0.460 |
LIG_BRCT_BRCA1_1 | 490 | 494 | PF00533 | 0.460 |
LIG_Clathr_ClatBox_1 | 222 | 226 | PF01394 | 0.460 |
LIG_deltaCOP1_diTrp_1 | 393 | 400 | PF00928 | 0.329 |
LIG_eIF4E_1 | 72 | 78 | PF01652 | 0.601 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.591 |
LIG_FHA_1 | 317 | 323 | PF00498 | 0.665 |
LIG_FHA_1 | 325 | 331 | PF00498 | 0.669 |
LIG_FHA_1 | 387 | 393 | PF00498 | 0.460 |
LIG_FHA_1 | 422 | 428 | PF00498 | 0.339 |
LIG_FHA_1 | 445 | 451 | PF00498 | 0.320 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.622 |
LIG_FHA_1 | 595 | 601 | PF00498 | 0.659 |
LIG_FHA_2 | 388 | 394 | PF00498 | 0.460 |
LIG_FHA_2 | 510 | 516 | PF00498 | 0.454 |
LIG_LIR_Apic_2 | 374 | 380 | PF02991 | 0.304 |
LIG_LIR_Gen_1 | 546 | 556 | PF02991 | 0.460 |
LIG_LIR_Gen_1 | 62 | 72 | PF02991 | 0.579 |
LIG_LIR_Nem_3 | 119 | 123 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 191 | 195 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 201 | 206 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 546 | 552 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 62 | 67 | PF02991 | 0.580 |
LIG_LIR_Nem_3 | 94 | 100 | PF02991 | 0.492 |
LIG_MLH1_MIPbox_1 | 490 | 494 | PF16413 | 0.460 |
LIG_MYND_1 | 476 | 480 | PF01753 | 0.460 |
LIG_MYND_1 | 577 | 581 | PF01753 | 0.460 |
LIG_REV1ctd_RIR_1 | 491 | 497 | PF16727 | 0.460 |
LIG_SH2_CRK | 195 | 199 | PF00017 | 0.460 |
LIG_SH2_CRK | 203 | 207 | PF00017 | 0.402 |
LIG_SH2_CRK | 216 | 220 | PF00017 | 0.333 |
LIG_SH2_CRK | 446 | 450 | PF00017 | 0.320 |
LIG_SH2_NCK_1 | 64 | 68 | PF00017 | 0.581 |
LIG_SH2_NCK_1 | 90 | 94 | PF00017 | 0.565 |
LIG_SH2_SRC | 90 | 93 | PF00017 | 0.563 |
LIG_SH2_STAP1 | 388 | 392 | PF00017 | 0.460 |
LIG_SH2_STAT3 | 262 | 265 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 109 | 112 | PF00017 | 0.250 |
LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 371 | 374 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 388 | 391 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 422 | 425 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 446 | 449 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 97 | 100 | PF00017 | 0.531 |
LIG_SH3_1 | 446 | 452 | PF00018 | 0.320 |
LIG_SH3_2 | 409 | 414 | PF14604 | 0.402 |
LIG_SH3_3 | 183 | 189 | PF00018 | 0.460 |
LIG_SH3_3 | 272 | 278 | PF00018 | 0.607 |
LIG_SH3_3 | 311 | 317 | PF00018 | 0.767 |
LIG_SH3_3 | 327 | 333 | PF00018 | 0.754 |
LIG_SH3_3 | 406 | 412 | PF00018 | 0.360 |
LIG_SH3_3 | 423 | 429 | PF00018 | 0.360 |
LIG_SH3_3 | 446 | 452 | PF00018 | 0.369 |
LIG_SH3_5 | 429 | 433 | PF00018 | 0.460 |
LIG_SUMO_SIM_anti_2 | 362 | 368 | PF11976 | 0.549 |
LIG_SUMO_SIM_par_1 | 182 | 188 | PF11976 | 0.460 |
LIG_SUMO_SIM_par_1 | 196 | 201 | PF11976 | 0.215 |
LIG_SUMO_SIM_par_1 | 220 | 226 | PF11976 | 0.460 |
LIG_SUMO_SIM_par_1 | 518 | 525 | PF11976 | 0.460 |
LIG_SUMO_SIM_par_1 | 52 | 57 | PF11976 | 0.621 |
LIG_TRAF2_1 | 101 | 104 | PF00917 | 0.546 |
LIG_TRAF2_1 | 522 | 525 | PF00917 | 0.443 |
LIG_TYR_ITSM | 199 | 206 | PF00017 | 0.460 |
LIG_UBA3_1 | 197 | 202 | PF00899 | 0.460 |
MOD_CDC14_SPxK_1 | 438 | 441 | PF00782 | 0.460 |
MOD_CDK_SPK_2 | 435 | 440 | PF00069 | 0.460 |
MOD_CDK_SPxK_1 | 435 | 441 | PF00069 | 0.431 |
MOD_CDK_SPxxK_3 | 17 | 24 | PF00069 | 0.628 |
MOD_CK1_1 | 119 | 125 | PF00069 | 0.460 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.672 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.693 |
MOD_CK1_1 | 347 | 353 | PF00069 | 0.686 |
MOD_CK1_1 | 37 | 43 | PF00069 | 0.533 |
MOD_CK1_1 | 589 | 595 | PF00069 | 0.598 |
MOD_CK1_1 | 612 | 618 | PF00069 | 0.620 |
MOD_CK2_1 | 245 | 251 | PF00069 | 0.379 |
MOD_CK2_1 | 455 | 461 | PF00069 | 0.414 |
MOD_CK2_1 | 519 | 525 | PF00069 | 0.443 |
MOD_CK2_1 | 59 | 65 | PF00069 | 0.586 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.675 |
MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.460 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.678 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.406 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.631 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.669 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.742 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.341 |
MOD_GlcNHglycan | 457 | 460 | PF01048 | 0.395 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.325 |
MOD_GlcNHglycan | 482 | 485 | PF01048 | 0.460 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.678 |
MOD_GlcNHglycan | 593 | 596 | PF01048 | 0.640 |
MOD_GlcNHglycan | 607 | 610 | PF01048 | 0.722 |
MOD_GlcNHglycan | 91 | 96 | PF01048 | 0.411 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.629 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.440 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.600 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.553 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.714 |
MOD_GSK3_1 | 435 | 442 | PF00069 | 0.443 |
MOD_GSK3_1 | 451 | 458 | PF00069 | 0.351 |
MOD_GSK3_1 | 476 | 483 | PF00069 | 0.406 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.624 |
MOD_GSK3_1 | 509 | 516 | PF00069 | 0.383 |
MOD_GSK3_1 | 605 | 612 | PF00069 | 0.719 |
MOD_N-GLC_1 | 455 | 460 | PF02516 | 0.419 |
MOD_N-GLC_1 | 513 | 518 | PF02516 | 0.366 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.460 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.379 |
MOD_NEK2_1 | 386 | 391 | PF00069 | 0.346 |
MOD_NEK2_1 | 444 | 449 | PF00069 | 0.460 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.621 |
MOD_NEK2_2 | 66 | 71 | PF00069 | 0.582 |
MOD_PIKK_1 | 145 | 151 | PF00454 | 0.460 |
MOD_PIKK_1 | 19 | 25 | PF00454 | 0.705 |
MOD_PIKK_1 | 439 | 445 | PF00454 | 0.402 |
MOD_PIKK_1 | 54 | 60 | PF00454 | 0.604 |
MOD_PIKK_1 | 589 | 595 | PF00454 | 0.574 |
MOD_PK_1 | 586 | 592 | PF00069 | 0.494 |
MOD_PKA_1 | 566 | 572 | PF00069 | 0.402 |
MOD_PKA_2 | 393 | 399 | PF00069 | 0.417 |
MOD_PKA_2 | 50 | 56 | PF00069 | 0.624 |
MOD_PKA_2 | 566 | 572 | PF00069 | 0.304 |
MOD_Plk_4 | 119 | 125 | PF00069 | 0.460 |
MOD_Plk_4 | 422 | 428 | PF00069 | 0.379 |
MOD_Plk_4 | 59 | 65 | PF00069 | 0.586 |
MOD_Plk_4 | 609 | 615 | PF00069 | 0.615 |
MOD_Plk_4 | 66 | 72 | PF00069 | 0.458 |
MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.628 |
MOD_ProDKin_1 | 278 | 284 | PF00069 | 0.587 |
MOD_ProDKin_1 | 313 | 319 | PF00069 | 0.715 |
MOD_ProDKin_1 | 376 | 382 | PF00069 | 0.402 |
MOD_ProDKin_1 | 435 | 441 | PF00069 | 0.367 |
MOD_ProDKin_1 | 476 | 482 | PF00069 | 0.402 |
MOD_ProDKin_1 | 488 | 494 | PF00069 | 0.443 |
MOD_ProDKin_1 | 515 | 521 | PF00069 | 0.390 |
MOD_SUMO_for_1 | 237 | 240 | PF00179 | 0.360 |
TRG_DiLeu_BaEn_1 | 74 | 79 | PF01217 | 0.602 |
TRG_DiLeu_BaLyEn_6 | 193 | 198 | PF01217 | 0.460 |
TRG_DiLeu_BaLyEn_6 | 39 | 44 | PF01217 | 0.525 |
TRG_ENDOCYTIC_2 | 195 | 198 | PF00928 | 0.428 |
TRG_ENDOCYTIC_2 | 203 | 206 | PF00928 | 0.402 |
TRG_ENDOCYTIC_2 | 216 | 219 | PF00928 | 0.333 |
TRG_ENDOCYTIC_2 | 549 | 552 | PF00928 | 0.412 |
TRG_ENDOCYTIC_2 | 64 | 67 | PF00928 | 0.588 |
TRG_ENDOCYTIC_2 | 90 | 93 | PF00928 | 0.557 |
TRG_ER_diArg_1 | 564 | 567 | PF00400 | 0.422 |
TRG_NLS_MonoExtN_4 | 564 | 569 | PF00514 | 0.460 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4J5U4 | Bodo saltans | 25% | 100% |
A0A0S4KIN4 | Bodo saltans | 25% | 91% |
A0A1X0NZD5 | Trypanosomatidae | 23% | 100% |
A0A3S5IQV1 | Trypanosoma rangeli | 24% | 100% |
A4HW27 | Leishmania infantum | 83% | 100% |
C9ZW07 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
Q01917 | Crithidia fasciculata | 23% | 100% |