A large and apprently artificial collection of diverse kinetoplastid protein kinases. A subfamily has 2TM regions, but the majority is cytoplasmic.
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:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QJG3
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 12 |
GO:0006793 | phosphorus metabolic process | 3 | 12 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016310 | phosphorylation | 5 | 12 |
GO:0019538 | protein metabolic process | 3 | 12 |
GO:0036211 | protein modification process | 4 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004672 | protein kinase activity | 3 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0016301 | kinase activity | 4 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 12 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 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:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140096 | catalytic activity, acting on a protein | 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 | 163 | 167 | PF00656 | 0.350 |
CLV_C14_Caspase3-7 | 184 | 188 | PF00656 | 0.473 |
CLV_C14_Caspase3-7 | 255 | 259 | PF00656 | 0.449 |
CLV_C14_Caspase3-7 | 316 | 320 | PF00656 | 0.653 |
CLV_C14_Caspase3-7 | 333 | 337 | PF00656 | 0.500 |
CLV_NRD_NRD_1 | 377 | 379 | PF00675 | 0.704 |
CLV_NRD_NRD_1 | 404 | 406 | PF00675 | 0.740 |
CLV_NRD_NRD_1 | 501 | 503 | PF00675 | 0.398 |
CLV_PCSK_KEX2_1 | 377 | 379 | PF00082 | 0.704 |
CLV_PCSK_KEX2_1 | 501 | 503 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 186 | 190 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 572 | 576 | PF00082 | 0.328 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.496 |
DEG_SCF_FBW7_1 | 329 | 335 | PF00400 | 0.698 |
DOC_CKS1_1 | 329 | 334 | PF01111 | 0.699 |
DOC_CKS1_1 | 612 | 617 | PF01111 | 0.328 |
DOC_CYCLIN_yCln2_LP_2 | 230 | 236 | PF00134 | 0.590 |
DOC_CYCLIN_yCln2_LP_2 | 706 | 712 | PF00134 | 0.385 |
DOC_MAPK_gen_1 | 492 | 499 | PF00069 | 0.328 |
DOC_MAPK_gen_1 | 518 | 525 | PF00069 | 0.306 |
DOC_MAPK_gen_1 | 572 | 581 | PF00069 | 0.328 |
DOC_MAPK_HePTP_8 | 515 | 527 | PF00069 | 0.413 |
DOC_MAPK_MEF2A_6 | 518 | 527 | PF00069 | 0.328 |
DOC_MAPK_MEF2A_6 | 575 | 583 | PF00069 | 0.328 |
DOC_PP2B_LxvP_1 | 434 | 437 | PF13499 | 0.678 |
DOC_USP7_MATH_1 | 332 | 336 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.798 |
DOC_USP7_MATH_1 | 396 | 400 | PF00917 | 0.746 |
DOC_USP7_MATH_1 | 426 | 430 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.612 |
DOC_USP7_UBL2_3 | 290 | 294 | PF12436 | 0.413 |
DOC_USP7_UBL2_3 | 453 | 457 | PF12436 | 0.328 |
DOC_WW_Pin1_4 | 328 | 333 | PF00397 | 0.700 |
DOC_WW_Pin1_4 | 447 | 452 | PF00397 | 0.579 |
DOC_WW_Pin1_4 | 611 | 616 | PF00397 | 0.328 |
LIG_14-3-3_CanoR_1 | 401 | 405 | PF00244 | 0.692 |
LIG_14-3-3_CanoR_1 | 469 | 475 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 54 | 62 | PF00244 | 0.785 |
LIG_Actin_WH2_2 | 456 | 471 | PF00022 | 0.449 |
LIG_APCC_ABBA_1 | 286 | 291 | PF00400 | 0.449 |
LIG_APCC_ABBA_1 | 523 | 528 | PF00400 | 0.328 |
LIG_BIR_III_4 | 187 | 191 | PF00653 | 0.385 |
LIG_BIR_III_4 | 336 | 340 | PF00653 | 0.701 |
LIG_BRCT_BRCA1_1 | 426 | 430 | PF00533 | 0.592 |
LIG_BRCT_BRCA1_1 | 706 | 710 | PF00533 | 0.398 |
LIG_Clathr_ClatBox_1 | 580 | 584 | PF01394 | 0.328 |
LIG_deltaCOP1_diTrp_1 | 300 | 307 | PF00928 | 0.331 |
LIG_eIF4E_1 | 104 | 110 | PF01652 | 0.573 |
LIG_FHA_1 | 15 | 21 | PF00498 | 0.719 |
LIG_FHA_1 | 463 | 469 | PF00498 | 0.449 |
LIG_FHA_1 | 520 | 526 | PF00498 | 0.341 |
LIG_FHA_1 | 534 | 540 | PF00498 | 0.307 |
LIG_FHA_1 | 57 | 63 | PF00498 | 0.558 |
LIG_FHA_1 | 713 | 719 | PF00498 | 0.713 |
LIG_FHA_2 | 124 | 130 | PF00498 | 0.381 |
LIG_FHA_2 | 161 | 167 | PF00498 | 0.363 |
LIG_FHA_2 | 253 | 259 | PF00498 | 0.363 |
LIG_FHA_2 | 420 | 426 | PF00498 | 0.698 |
LIG_FHA_2 | 640 | 646 | PF00498 | 0.328 |
LIG_FHA_2 | 82 | 88 | PF00498 | 0.706 |
LIG_Integrin_isoDGR_2 | 272 | 274 | PF01839 | 0.449 |
LIG_Integrin_isoDGR_2 | 470 | 472 | PF01839 | 0.413 |
LIG_LIR_Apic_2 | 614 | 620 | PF02991 | 0.328 |
LIG_LIR_Gen_1 | 409 | 418 | PF02991 | 0.686 |
LIG_LIR_Gen_1 | 658 | 667 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 103 | 107 | PF02991 | 0.586 |
LIG_LIR_Nem_3 | 409 | 415 | PF02991 | 0.737 |
LIG_LIR_Nem_3 | 447 | 452 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 459 | 463 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 540 | 545 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 658 | 663 | PF02991 | 0.328 |
LIG_MYND_1 | 696 | 700 | PF01753 | 0.449 |
LIG_NRBOX | 683 | 689 | PF00104 | 0.449 |
LIG_Pex14_1 | 660 | 664 | PF04695 | 0.328 |
LIG_Pex14_2 | 538 | 542 | PF04695 | 0.328 |
LIG_PTB_Apo_2 | 43 | 50 | PF02174 | 0.666 |
LIG_SH2_CRK | 104 | 108 | PF00017 | 0.580 |
LIG_SH2_CRK | 464 | 468 | PF00017 | 0.420 |
LIG_SH2_CRK | 555 | 559 | PF00017 | 0.385 |
LIG_SH2_STAP1 | 464 | 468 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 104 | 107 | PF00017 | 0.543 |
LIG_SH2_STAT5 | 123 | 126 | PF00017 | 0.166 |
LIG_SH2_STAT5 | 162 | 165 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 174 | 177 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 192 | 195 | PF00017 | 0.218 |
LIG_SH2_STAT5 | 277 | 280 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 285 | 288 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 464 | 467 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 529 | 532 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 563 | 566 | PF00017 | 0.315 |
LIG_SH3_3 | 326 | 332 | PF00018 | 0.691 |
LIG_SH3_3 | 364 | 370 | PF00018 | 0.702 |
LIG_SH3_3 | 380 | 386 | PF00018 | 0.683 |
LIG_SH3_3 | 47 | 53 | PF00018 | 0.546 |
LIG_SH3_3 | 609 | 615 | PF00018 | 0.328 |
LIG_SH3_3 | 648 | 654 | PF00018 | 0.328 |
LIG_SH3_3 | 71 | 77 | PF00018 | 0.799 |
LIG_SH3_3 | 95 | 101 | PF00018 | 0.651 |
LIG_SUMO_SIM_anti_2 | 496 | 501 | PF11976 | 0.328 |
LIG_SUMO_SIM_par_1 | 477 | 483 | PF11976 | 0.333 |
LIG_SUMO_SIM_par_1 | 579 | 584 | PF11976 | 0.344 |
LIG_SUMO_SIM_par_1 | 75 | 81 | PF11976 | 0.571 |
LIG_TRAF2_1 | 422 | 425 | PF00917 | 0.594 |
LIG_TRAF2_1 | 486 | 489 | PF00917 | 0.449 |
LIG_TYR_ITIM | 102 | 107 | PF00017 | 0.593 |
LIG_UBA3_1 | 684 | 690 | PF00899 | 0.428 |
LIG_WRC_WIRS_1 | 535 | 540 | PF05994 | 0.344 |
MOD_CDK_SPxK_1 | 447 | 453 | PF00069 | 0.582 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.376 |
MOD_CK1_1 | 320 | 326 | PF00069 | 0.718 |
MOD_CK1_1 | 353 | 359 | PF00069 | 0.753 |
MOD_CK1_1 | 360 | 366 | PF00069 | 0.693 |
MOD_CK1_1 | 399 | 405 | PF00069 | 0.694 |
MOD_CK1_1 | 531 | 537 | PF00069 | 0.337 |
MOD_CK1_1 | 56 | 62 | PF00069 | 0.803 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.789 |
MOD_CK2_1 | 123 | 129 | PF00069 | 0.344 |
MOD_CK2_1 | 419 | 425 | PF00069 | 0.622 |
MOD_CK2_1 | 441 | 447 | PF00069 | 0.570 |
MOD_CK2_1 | 483 | 489 | PF00069 | 0.348 |
MOD_CK2_1 | 639 | 645 | PF00069 | 0.328 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.762 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.395 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.452 |
MOD_GlcNHglycan | 392 | 395 | PF01048 | 0.738 |
MOD_GlcNHglycan | 414 | 418 | PF01048 | 0.670 |
MOD_GlcNHglycan | 530 | 533 | PF01048 | 0.328 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.583 |
MOD_GlcNHglycan | 602 | 605 | PF01048 | 0.449 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.344 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.792 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.754 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.761 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.676 |
MOD_GSK3_1 | 396 | 403 | PF00069 | 0.665 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.766 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.552 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.624 |
MOD_GSK3_1 | 533 | 540 | PF00069 | 0.242 |
MOD_GSK3_1 | 602 | 609 | PF00069 | 0.348 |
MOD_GSK3_1 | 631 | 638 | PF00069 | 0.328 |
MOD_GSK3_1 | 667 | 674 | PF00069 | 0.328 |
MOD_N-GLC_1 | 1 | 6 | PF02516 | 0.759 |
MOD_N-GLC_1 | 390 | 395 | PF02516 | 0.677 |
MOD_N-GLC_1 | 406 | 411 | PF02516 | 0.681 |
MOD_N-GLC_1 | 54 | 59 | PF02516 | 0.765 |
MOD_N-GLC_1 | 667 | 672 | PF02516 | 0.413 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.757 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.720 |
MOD_NEK2_1 | 400 | 405 | PF00069 | 0.662 |
MOD_NEK2_1 | 430 | 435 | PF00069 | 0.623 |
MOD_NEK2_1 | 592 | 597 | PF00069 | 0.328 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.571 |
MOD_NEK2_2 | 396 | 401 | PF00069 | 0.756 |
MOD_NEK2_2 | 546 | 551 | PF00069 | 0.449 |
MOD_PIKK_1 | 317 | 323 | PF00454 | 0.642 |
MOD_PK_1 | 541 | 547 | PF00069 | 0.427 |
MOD_PKA_1 | 405 | 411 | PF00069 | 0.684 |
MOD_PKA_2 | 273 | 279 | PF00069 | 0.449 |
MOD_PKA_2 | 353 | 359 | PF00069 | 0.749 |
MOD_PKA_2 | 400 | 406 | PF00069 | 0.742 |
MOD_PKA_2 | 53 | 59 | PF00069 | 0.795 |
MOD_PKA_2 | 698 | 704 | PF00069 | 0.344 |
MOD_Plk_1 | 1 | 7 | PF00069 | 0.749 |
MOD_Plk_2-3 | 338 | 344 | PF00069 | 0.728 |
MOD_Plk_2-3 | 480 | 486 | PF00069 | 0.370 |
MOD_Plk_4 | 273 | 279 | PF00069 | 0.363 |
MOD_Plk_4 | 325 | 331 | PF00069 | 0.745 |
MOD_Plk_4 | 426 | 432 | PF00069 | 0.587 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.548 |
MOD_Plk_4 | 534 | 540 | PF00069 | 0.344 |
MOD_Plk_4 | 607 | 613 | PF00069 | 0.327 |
MOD_Plk_4 | 639 | 645 | PF00069 | 0.324 |
MOD_Plk_4 | 655 | 661 | PF00069 | 0.328 |
MOD_ProDKin_1 | 328 | 334 | PF00069 | 0.699 |
MOD_ProDKin_1 | 447 | 453 | PF00069 | 0.582 |
MOD_ProDKin_1 | 611 | 617 | PF00069 | 0.328 |
MOD_SUMO_for_1 | 623 | 626 | PF00179 | 0.344 |
MOD_SUMO_rev_2 | 180 | 188 | PF00179 | 0.449 |
MOD_SUMO_rev_2 | 514 | 519 | PF00179 | 0.421 |
MOD_SUMO_rev_2 | 675 | 685 | PF00179 | 0.283 |
MOD_SUMO_rev_2 | 693 | 698 | PF00179 | 0.283 |
TRG_DiLeu_BaEn_4 | 488 | 494 | PF01217 | 0.385 |
TRG_DiLeu_BaLyEn_6 | 105 | 110 | PF01217 | 0.486 |
TRG_DiLeu_BaLyEn_6 | 74 | 79 | PF01217 | 0.570 |
TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.579 |
TRG_ENDOCYTIC_2 | 204 | 207 | PF00928 | 0.437 |
TRG_ENDOCYTIC_2 | 285 | 288 | PF00928 | 0.449 |
TRG_ENDOCYTIC_2 | 412 | 415 | PF00928 | 0.742 |
TRG_ENDOCYTIC_2 | 464 | 467 | PF00928 | 0.348 |
TRG_ENDOCYTIC_2 | 512 | 515 | PF00928 | 0.449 |
TRG_ENDOCYTIC_2 | 555 | 558 | PF00928 | 0.385 |
TRG_ER_diArg_1 | 175 | 178 | PF00400 | 0.475 |
TRG_ER_diArg_1 | 376 | 378 | PF00400 | 0.700 |
TRG_ER_diArg_1 | 500 | 502 | PF00400 | 0.398 |
TRG_Pf-PMV_PEXEL_1 | 377 | 381 | PF00026 | 0.621 |
TRG_Pf-PMV_PEXEL_1 | 562 | 566 | PF00026 | 0.475 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZR8 | Leptomonas seymouri | 73% | 90% |
A0A0S4J7Q1 | Bodo saltans | 55% | 100% |
A0A1X0P0R3 | Trypanosomatidae | 64% | 100% |
A0A3S7WP16 | Leishmania donovani | 95% | 91% |
A0A422N0Q9 | Trypanosoma rangeli | 62% | 100% |
A4H485 | Leishmania braziliensis | 83% | 98% |
A4HSG1 | Leishmania infantum | 95% | 91% |
D0A4H1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 59% | 100% |
E9AKE5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 98% |
V5D179 | Trypanosoma cruzi | 64% | 100% |