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 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S7WP16
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 | 149 | 153 | PF00656 | 0.689 |
CLV_C14_Caspase3-7 | 224 | 228 | PF00656 | 0.350 |
CLV_C14_Caspase3-7 | 245 | 249 | PF00656 | 0.473 |
CLV_C14_Caspase3-7 | 316 | 320 | PF00656 | 0.449 |
CLV_C14_Caspase3-7 | 377 | 381 | PF00656 | 0.661 |
CLV_C14_Caspase3-7 | 394 | 398 | PF00656 | 0.456 |
CLV_NRD_NRD_1 | 438 | 440 | PF00675 | 0.684 |
CLV_NRD_NRD_1 | 465 | 467 | PF00675 | 0.742 |
CLV_NRD_NRD_1 | 562 | 564 | PF00675 | 0.452 |
CLV_NRD_NRD_1 | 787 | 789 | PF00675 | 0.596 |
CLV_PCSK_KEX2_1 | 438 | 440 | PF00082 | 0.684 |
CLV_PCSK_KEX2_1 | 562 | 564 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 247 | 251 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 633 | 637 | PF00082 | 0.328 |
DEG_SCF_FBW7_1 | 390 | 396 | PF00400 | 0.706 |
DOC_CKS1_1 | 390 | 395 | PF01111 | 0.705 |
DOC_CKS1_1 | 673 | 678 | PF01111 | 0.328 |
DOC_CYCLIN_yCln2_LP_2 | 291 | 297 | PF00134 | 0.598 |
DOC_CYCLIN_yCln2_LP_2 | 767 | 773 | PF00134 | 0.385 |
DOC_MAPK_gen_1 | 553 | 560 | PF00069 | 0.328 |
DOC_MAPK_gen_1 | 633 | 642 | PF00069 | 0.328 |
DOC_MAPK_HePTP_8 | 576 | 588 | PF00069 | 0.413 |
DOC_MAPK_MEF2A_6 | 579 | 588 | PF00069 | 0.328 |
DOC_MAPK_MEF2A_6 | 636 | 644 | PF00069 | 0.328 |
DOC_PP2B_LxvP_1 | 495 | 498 | PF13499 | 0.665 |
DOC_PP4_FxxP_1 | 476 | 479 | PF00568 | 0.564 |
DOC_USP7_MATH_1 | 393 | 397 | PF00917 | 0.710 |
DOC_USP7_MATH_1 | 411 | 415 | PF00917 | 0.687 |
DOC_USP7_MATH_1 | 457 | 461 | PF00917 | 0.743 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.739 |
DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.751 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.777 |
DOC_USP7_UBL2_3 | 351 | 355 | PF12436 | 0.413 |
DOC_USP7_UBL2_3 | 514 | 518 | PF12436 | 0.328 |
DOC_USP7_UBL2_3 | 785 | 789 | PF12436 | 0.557 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.762 |
DOC_WW_Pin1_4 | 389 | 394 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 486 | 491 | PF00397 | 0.550 |
DOC_WW_Pin1_4 | 508 | 513 | PF00397 | 0.568 |
DOC_WW_Pin1_4 | 672 | 677 | PF00397 | 0.328 |
DOC_WW_Pin1_4 | 778 | 783 | PF00397 | 0.632 |
LIG_14-3-3_CanoR_1 | 115 | 123 | PF00244 | 0.783 |
LIG_14-3-3_CanoR_1 | 385 | 391 | PF00244 | 0.578 |
LIG_14-3-3_CanoR_1 | 462 | 466 | PF00244 | 0.694 |
LIG_14-3-3_CanoR_1 | 530 | 536 | PF00244 | 0.449 |
LIG_Actin_WH2_2 | 446 | 464 | PF00022 | 0.548 |
LIG_Actin_WH2_2 | 517 | 532 | PF00022 | 0.449 |
LIG_APCC_ABBA_1 | 347 | 352 | PF00400 | 0.449 |
LIG_APCC_ABBA_1 | 584 | 589 | PF00400 | 0.328 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.715 |
LIG_BIR_III_4 | 248 | 252 | PF00653 | 0.385 |
LIG_BIR_III_4 | 397 | 401 | PF00653 | 0.703 |
LIG_BRCT_BRCA1_1 | 487 | 491 | PF00533 | 0.601 |
LIG_BRCT_BRCA1_1 | 767 | 771 | PF00533 | 0.398 |
LIG_Clathr_ClatBox_1 | 641 | 645 | PF01394 | 0.328 |
LIG_deltaCOP1_diTrp_1 | 361 | 368 | PF00928 | 0.331 |
LIG_eIF4E_1 | 165 | 171 | PF01652 | 0.570 |
LIG_FHA_1 | 10 | 16 | PF00498 | 0.629 |
LIG_FHA_1 | 17 | 23 | PF00498 | 0.787 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.805 |
LIG_FHA_1 | 524 | 530 | PF00498 | 0.441 |
LIG_FHA_1 | 581 | 587 | PF00498 | 0.341 |
LIG_FHA_1 | 595 | 601 | PF00498 | 0.328 |
LIG_FHA_1 | 774 | 780 | PF00498 | 0.657 |
LIG_FHA_2 | 143 | 149 | PF00498 | 0.722 |
LIG_FHA_2 | 185 | 191 | PF00498 | 0.381 |
LIG_FHA_2 | 222 | 228 | PF00498 | 0.363 |
LIG_FHA_2 | 314 | 320 | PF00498 | 0.363 |
LIG_FHA_2 | 481 | 487 | PF00498 | 0.745 |
LIG_FHA_2 | 701 | 707 | PF00498 | 0.328 |
LIG_FHA_2 | 760 | 766 | PF00498 | 0.378 |
LIG_Integrin_isoDGR_2 | 333 | 335 | PF01839 | 0.449 |
LIG_Integrin_isoDGR_2 | 531 | 533 | PF01839 | 0.413 |
LIG_LIR_Apic_2 | 475 | 479 | PF02991 | 0.565 |
LIG_LIR_Apic_2 | 675 | 681 | PF02991 | 0.328 |
LIG_LIR_Gen_1 | 470 | 479 | PF02991 | 0.700 |
LIG_LIR_Gen_1 | 719 | 728 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 164 | 168 | PF02991 | 0.585 |
LIG_LIR_Nem_3 | 470 | 476 | PF02991 | 0.753 |
LIG_LIR_Nem_3 | 508 | 513 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 520 | 524 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 719 | 724 | PF02991 | 0.328 |
LIG_MYND_1 | 757 | 761 | PF01753 | 0.449 |
LIG_NRBOX | 744 | 750 | PF00104 | 0.449 |
LIG_Pex14_1 | 721 | 725 | PF04695 | 0.328 |
LIG_Pex14_2 | 599 | 603 | PF04695 | 0.328 |
LIG_PTB_Apo_2 | 104 | 111 | PF02174 | 0.666 |
LIG_SH2_CRK | 165 | 169 | PF00017 | 0.578 |
LIG_SH2_CRK | 525 | 529 | PF00017 | 0.420 |
LIG_SH2_CRK | 616 | 620 | PF00017 | 0.385 |
LIG_SH2_STAP1 | 525 | 529 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 165 | 168 | PF00017 | 0.540 |
LIG_SH2_STAT5 | 184 | 187 | PF00017 | 0.166 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 253 | 256 | PF00017 | 0.218 |
LIG_SH2_STAT5 | 338 | 341 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 346 | 349 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 525 | 528 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 590 | 593 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 624 | 627 | PF00017 | 0.328 |
LIG_SH3_3 | 132 | 138 | PF00018 | 0.800 |
LIG_SH3_3 | 156 | 162 | PF00018 | 0.655 |
LIG_SH3_3 | 387 | 393 | PF00018 | 0.694 |
LIG_SH3_3 | 425 | 431 | PF00018 | 0.684 |
LIG_SH3_3 | 441 | 447 | PF00018 | 0.745 |
LIG_SH3_3 | 670 | 676 | PF00018 | 0.328 |
LIG_SH3_3 | 709 | 715 | PF00018 | 0.328 |
LIG_SH3_3 | 776 | 782 | PF00018 | 0.607 |
LIG_SUMO_SIM_anti_2 | 557 | 562 | PF11976 | 0.319 |
LIG_SUMO_SIM_par_1 | 18 | 24 | PF11976 | 0.579 |
LIG_SUMO_SIM_par_1 | 538 | 544 | PF11976 | 0.328 |
LIG_SUMO_SIM_par_1 | 640 | 645 | PF11976 | 0.344 |
LIG_TRAF2_1 | 483 | 486 | PF00917 | 0.632 |
LIG_TRAF2_1 | 547 | 550 | PF00917 | 0.447 |
LIG_TYR_ITIM | 163 | 168 | PF00017 | 0.591 |
LIG_WRC_WIRS_1 | 596 | 601 | PF05994 | 0.344 |
MOD_CDK_SPxK_1 | 508 | 514 | PF00069 | 0.571 |
MOD_CDK_SPxxK_3 | 486 | 493 | PF00069 | 0.587 |
MOD_CDK_SPxxK_3 | 778 | 785 | PF00069 | 0.525 |
MOD_CK1_1 | 10 | 16 | PF00069 | 0.554 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.800 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.762 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.626 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.376 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.483 |
MOD_CK1_1 | 34 | 40 | PF00069 | 0.816 |
MOD_CK1_1 | 381 | 387 | PF00069 | 0.718 |
MOD_CK1_1 | 414 | 420 | PF00069 | 0.737 |
MOD_CK1_1 | 421 | 427 | PF00069 | 0.684 |
MOD_CK1_1 | 460 | 466 | PF00069 | 0.696 |
MOD_CK1_1 | 592 | 598 | PF00069 | 0.337 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.772 |
MOD_CK2_1 | 184 | 190 | PF00069 | 0.344 |
MOD_CK2_1 | 20 | 26 | PF00069 | 0.651 |
MOD_CK2_1 | 32 | 38 | PF00069 | 0.824 |
MOD_CK2_1 | 480 | 486 | PF00069 | 0.658 |
MOD_CK2_1 | 502 | 508 | PF00069 | 0.568 |
MOD_CK2_1 | 544 | 550 | PF00069 | 0.348 |
MOD_CK2_1 | 700 | 706 | PF00069 | 0.328 |
MOD_CK2_1 | 778 | 784 | PF00069 | 0.746 |
MOD_CK2_1 | 95 | 101 | PF00069 | 0.627 |
MOD_Cter_Amidation | 786 | 789 | PF01082 | 0.555 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.582 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.395 |
MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.452 |
MOD_GlcNHglycan | 453 | 456 | PF01048 | 0.744 |
MOD_GlcNHglycan | 475 | 479 | PF01048 | 0.683 |
MOD_GlcNHglycan | 591 | 594 | PF01048 | 0.328 |
MOD_GlcNHglycan | 663 | 666 | PF01048 | 0.449 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.728 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.782 |
MOD_GlcNHglycan | 784 | 788 | PF01048 | 0.552 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.782 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.675 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.344 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.757 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.759 |
MOD_GSK3_1 | 414 | 421 | PF00069 | 0.747 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.677 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.655 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.751 |
MOD_GSK3_1 | 508 | 515 | PF00069 | 0.559 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.756 |
MOD_GSK3_1 | 663 | 670 | PF00069 | 0.348 |
MOD_GSK3_1 | 692 | 699 | PF00069 | 0.328 |
MOD_GSK3_1 | 728 | 735 | PF00069 | 0.328 |
MOD_N-GLC_1 | 115 | 120 | PF02516 | 0.763 |
MOD_N-GLC_1 | 451 | 456 | PF02516 | 0.676 |
MOD_N-GLC_1 | 467 | 472 | PF02516 | 0.695 |
MOD_N-GLC_1 | 61 | 66 | PF02516 | 0.768 |
MOD_N-GLC_1 | 728 | 733 | PF02516 | 0.413 |
MOD_NEK2_1 | 114 | 119 | PF00069 | 0.604 |
MOD_NEK2_1 | 420 | 425 | PF00069 | 0.701 |
MOD_NEK2_1 | 451 | 456 | PF00069 | 0.739 |
MOD_NEK2_1 | 461 | 466 | PF00069 | 0.663 |
MOD_NEK2_1 | 491 | 496 | PF00069 | 0.600 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.766 |
MOD_NEK2_1 | 653 | 658 | PF00069 | 0.328 |
MOD_NEK2_1 | 783 | 788 | PF00069 | 0.762 |
MOD_NEK2_2 | 457 | 462 | PF00069 | 0.754 |
MOD_NEK2_2 | 607 | 612 | PF00069 | 0.449 |
MOD_PIKK_1 | 27 | 33 | PF00454 | 0.654 |
MOD_PIKK_1 | 378 | 384 | PF00454 | 0.643 |
MOD_PK_1 | 602 | 608 | PF00069 | 0.449 |
MOD_PKA_1 | 466 | 472 | PF00069 | 0.697 |
MOD_PKA_2 | 114 | 120 | PF00069 | 0.796 |
MOD_PKA_2 | 334 | 340 | PF00069 | 0.449 |
MOD_PKA_2 | 414 | 420 | PF00069 | 0.735 |
MOD_PKA_2 | 461 | 467 | PF00069 | 0.745 |
MOD_PKA_2 | 759 | 765 | PF00069 | 0.344 |
MOD_Plk_1 | 46 | 52 | PF00069 | 0.748 |
MOD_Plk_1 | 61 | 67 | PF00069 | 0.760 |
MOD_Plk_2-3 | 399 | 405 | PF00069 | 0.727 |
MOD_Plk_2-3 | 541 | 547 | PF00069 | 0.376 |
MOD_Plk_4 | 136 | 142 | PF00069 | 0.706 |
MOD_Plk_4 | 334 | 340 | PF00069 | 0.363 |
MOD_Plk_4 | 386 | 392 | PF00069 | 0.752 |
MOD_Plk_4 | 595 | 601 | PF00069 | 0.344 |
MOD_Plk_4 | 668 | 674 | PF00069 | 0.328 |
MOD_Plk_4 | 700 | 706 | PF00069 | 0.328 |
MOD_Plk_4 | 716 | 722 | PF00069 | 0.328 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.764 |
MOD_ProDKin_1 | 389 | 395 | PF00069 | 0.704 |
MOD_ProDKin_1 | 486 | 492 | PF00069 | 0.547 |
MOD_ProDKin_1 | 508 | 514 | PF00069 | 0.571 |
MOD_ProDKin_1 | 672 | 678 | PF00069 | 0.328 |
MOD_ProDKin_1 | 778 | 784 | PF00069 | 0.636 |
MOD_SUMO_for_1 | 684 | 687 | PF00179 | 0.344 |
MOD_SUMO_rev_2 | 241 | 249 | PF00179 | 0.449 |
MOD_SUMO_rev_2 | 575 | 580 | PF00179 | 0.437 |
TRG_DiLeu_BaEn_1 | 744 | 749 | PF01217 | 0.428 |
TRG_DiLeu_BaEn_4 | 549 | 555 | PF01217 | 0.385 |
TRG_DiLeu_BaLyEn_6 | 166 | 171 | PF01217 | 0.484 |
TRG_ENDOCYTIC_2 | 165 | 168 | PF00928 | 0.577 |
TRG_ENDOCYTIC_2 | 265 | 268 | PF00928 | 0.437 |
TRG_ENDOCYTIC_2 | 346 | 349 | PF00928 | 0.449 |
TRG_ENDOCYTIC_2 | 473 | 476 | PF00928 | 0.755 |
TRG_ENDOCYTIC_2 | 525 | 528 | PF00928 | 0.348 |
TRG_ENDOCYTIC_2 | 573 | 576 | PF00928 | 0.413 |
TRG_ENDOCYTIC_2 | 616 | 619 | PF00928 | 0.385 |
TRG_ER_diArg_1 | 236 | 239 | PF00400 | 0.475 |
TRG_ER_diArg_1 | 437 | 439 | PF00400 | 0.684 |
TRG_ER_diArg_1 | 561 | 563 | PF00400 | 0.398 |
TRG_Pf-PMV_PEXEL_1 | 438 | 442 | PF00026 | 0.599 |
TRG_Pf-PMV_PEXEL_1 | 623 | 627 | PF00026 | 0.475 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZR8 | Leptomonas seymouri | 64% | 99% |
A0A0S4J7Q1 | Bodo saltans | 54% | 100% |
A0A1X0P0R3 | Trypanosomatidae | 64% | 100% |
A0A422N0Q9 | Trypanosoma rangeli | 61% | 100% |
A4H485 | Leishmania braziliensis | 84% | 100% |
A4HSG1 | Leishmania infantum | 100% | 100% |
D0A4H1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 58% | 100% |
E9AKE5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q4QJG3 | Leishmania major | 95% | 100% |
V5D179 | Trypanosoma cruzi | 62% | 100% |