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: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
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: 15 |
NetGPI | no | yes: 0, no: 15 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: E9AKE5
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 16 |
GO:0006793 | phosphorus metabolic process | 3 | 16 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 16 |
GO:0006807 | nitrogen compound metabolic process | 2 | 16 |
GO:0008152 | metabolic process | 1 | 16 |
GO:0009987 | cellular process | 1 | 16 |
GO:0016310 | phosphorylation | 5 | 16 |
GO:0019538 | protein metabolic process | 3 | 16 |
GO:0036211 | protein modification process | 4 | 16 |
GO:0043170 | macromolecule metabolic process | 3 | 16 |
GO:0043412 | macromolecule modification | 4 | 16 |
GO:0044237 | cellular metabolic process | 2 | 16 |
GO:0044238 | primary metabolic process | 2 | 16 |
GO:0071704 | organic substance metabolic process | 2 | 16 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 16 |
GO:0007165 | signal transduction | 2 | 1 |
GO:0018105 | peptidyl-serine phosphorylation | 6 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018209 | peptidyl-serine modification | 6 | 1 |
GO:0035556 | intracellular signal transduction | 3 | 1 |
GO:0046777 | protein autophosphorylation | 6 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 16 |
GO:0003824 | catalytic activity | 1 | 16 |
GO:0004672 | protein kinase activity | 3 | 16 |
GO:0005488 | binding | 1 | 16 |
GO:0005524 | ATP binding | 5 | 16 |
GO:0016301 | kinase activity | 4 | 16 |
GO:0016740 | transferase activity | 2 | 16 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 16 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 16 |
GO:0017076 | purine nucleotide binding | 4 | 16 |
GO:0030554 | adenyl nucleotide binding | 5 | 16 |
GO:0032553 | ribonucleotide binding | 3 | 16 |
GO:0032555 | purine ribonucleotide binding | 4 | 16 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 16 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 16 |
GO:0036094 | small molecule binding | 2 | 16 |
GO:0043167 | ion binding | 2 | 16 |
GO:0043168 | anion binding | 3 | 16 |
GO:0097159 | organic cyclic compound binding | 2 | 16 |
GO:0097367 | carbohydrate derivative binding | 2 | 16 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 16 |
GO:1901265 | nucleoside phosphate binding | 3 | 16 |
GO:1901363 | heterocyclic compound binding | 2 | 16 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 4 |
GO:0004683 | calmodulin-dependent protein kinase activity | 5 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0005516 | calmodulin binding | 3 | 1 |
GO:0009931 | calcium-dependent protein serine/threonine kinase activity | 5 | 1 |
GO:0010857 | calcium-dependent protein kinase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 168 | 172 | PF00656 | 0.304 |
CLV_C14_Caspase3-7 | 189 | 193 | PF00656 | 0.465 |
CLV_C14_Caspase3-7 | 260 | 264 | PF00656 | 0.427 |
CLV_C14_Caspase3-7 | 321 | 325 | PF00656 | 0.497 |
CLV_C14_Caspase3-7 | 338 | 342 | PF00656 | 0.482 |
CLV_C14_Caspase3-7 | 93 | 97 | PF00656 | 0.618 |
CLV_NRD_NRD_1 | 382 | 384 | PF00675 | 0.667 |
CLV_NRD_NRD_1 | 409 | 411 | PF00675 | 0.703 |
CLV_NRD_NRD_1 | 506 | 508 | PF00675 | 0.427 |
CLV_NRD_NRD_1 | 731 | 733 | PF00675 | 0.669 |
CLV_PCSK_KEX2_1 | 382 | 384 | PF00082 | 0.667 |
CLV_PCSK_KEX2_1 | 506 | 508 | PF00082 | 0.323 |
CLV_PCSK_KEX2_1 | 731 | 733 | PF00082 | 0.615 |
CLV_PCSK_SKI1_1 | 191 | 195 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 577 | 581 | PF00082 | 0.323 |
DEG_SCF_FBW7_1 | 334 | 340 | PF00400 | 0.588 |
DOC_CKS1_1 | 334 | 339 | PF01111 | 0.588 |
DOC_CKS1_1 | 617 | 622 | PF01111 | 0.276 |
DOC_CYCLIN_yCln2_LP_2 | 235 | 241 | PF00134 | 0.456 |
DOC_CYCLIN_yCln2_LP_2 | 711 | 717 | PF00134 | 0.334 |
DOC_MAPK_gen_1 | 497 | 504 | PF00069 | 0.276 |
DOC_MAPK_gen_1 | 523 | 530 | PF00069 | 0.257 |
DOC_MAPK_gen_1 | 577 | 586 | PF00069 | 0.323 |
DOC_MAPK_HePTP_8 | 520 | 532 | PF00069 | 0.370 |
DOC_MAPK_MEF2A_6 | 523 | 532 | PF00069 | 0.276 |
DOC_MAPK_MEF2A_6 | 580 | 588 | PF00069 | 0.323 |
DOC_PP2B_LxvP_1 | 439 | 442 | PF13499 | 0.643 |
DOC_USP7_MATH_1 | 21 | 25 | PF00917 | 0.706 |
DOC_USP7_MATH_1 | 337 | 341 | PF00917 | 0.603 |
DOC_USP7_MATH_1 | 401 | 405 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.786 |
DOC_USP7_UBL2_3 | 295 | 299 | PF12436 | 0.309 |
DOC_USP7_UBL2_3 | 458 | 462 | PF12436 | 0.323 |
DOC_WW_Pin1_4 | 333 | 338 | PF00397 | 0.581 |
DOC_WW_Pin1_4 | 395 | 400 | PF00397 | 0.745 |
DOC_WW_Pin1_4 | 430 | 435 | PF00397 | 0.547 |
DOC_WW_Pin1_4 | 452 | 457 | PF00397 | 0.531 |
DOC_WW_Pin1_4 | 48 | 53 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 616 | 621 | PF00397 | 0.316 |
DOC_WW_Pin1_4 | 722 | 727 | PF00397 | 0.539 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.693 |
LIG_14-3-3_CanoR_1 | 329 | 335 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 406 | 410 | PF00244 | 0.596 |
LIG_14-3-3_CanoR_1 | 45 | 50 | PF00244 | 0.770 |
LIG_14-3-3_CanoR_1 | 474 | 480 | PF00244 | 0.433 |
LIG_14-3-3_CanoR_1 | 59 | 65 | PF00244 | 0.755 |
LIG_Actin_WH2_2 | 461 | 476 | PF00022 | 0.422 |
LIG_APCC_ABBA_1 | 291 | 296 | PF00400 | 0.422 |
LIG_APCC_ABBA_1 | 528 | 533 | PF00400 | 0.276 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.513 |
LIG_BIR_III_4 | 192 | 196 | PF00653 | 0.334 |
LIG_BIR_III_4 | 341 | 345 | PF00653 | 0.602 |
LIG_BRCT_BRCA1_1 | 431 | 435 | PF00533 | 0.480 |
LIG_BRCT_BRCA1_1 | 50 | 54 | PF00533 | 0.468 |
LIG_BRCT_BRCA1_1 | 711 | 715 | PF00533 | 0.293 |
LIG_Clathr_ClatBox_1 | 585 | 589 | PF01394 | 0.276 |
LIG_deltaCOP1_diTrp_1 | 305 | 312 | PF00928 | 0.279 |
LIG_eIF4E_1 | 109 | 115 | PF01652 | 0.649 |
LIG_FHA_1 | 468 | 474 | PF00498 | 0.437 |
LIG_FHA_1 | 525 | 531 | PF00498 | 0.287 |
LIG_FHA_1 | 539 | 545 | PF00498 | 0.276 |
LIG_FHA_1 | 718 | 724 | PF00498 | 0.545 |
LIG_FHA_2 | 100 | 106 | PF00498 | 0.736 |
LIG_FHA_2 | 129 | 135 | PF00498 | 0.365 |
LIG_FHA_2 | 166 | 172 | PF00498 | 0.316 |
LIG_FHA_2 | 258 | 264 | PF00498 | 0.316 |
LIG_FHA_2 | 425 | 431 | PF00498 | 0.686 |
LIG_FHA_2 | 645 | 651 | PF00498 | 0.284 |
LIG_FHA_2 | 704 | 710 | PF00498 | 0.417 |
LIG_FHA_2 | 87 | 93 | PF00498 | 0.637 |
LIG_Integrin_isoDGR_2 | 277 | 279 | PF01839 | 0.422 |
LIG_Integrin_isoDGR_2 | 475 | 477 | PF01839 | 0.370 |
LIG_LIR_Apic_2 | 48 | 52 | PF02991 | 0.476 |
LIG_LIR_Apic_2 | 619 | 625 | PF02991 | 0.323 |
LIG_LIR_Gen_1 | 414 | 423 | PF02991 | 0.568 |
LIG_LIR_Gen_1 | 663 | 672 | PF02991 | 0.276 |
LIG_LIR_Nem_3 | 108 | 112 | PF02991 | 0.661 |
LIG_LIR_Nem_3 | 414 | 420 | PF02991 | 0.697 |
LIG_LIR_Nem_3 | 452 | 457 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 464 | 468 | PF02991 | 0.259 |
LIG_LIR_Nem_3 | 663 | 668 | PF02991 | 0.276 |
LIG_MYND_1 | 701 | 705 | PF01753 | 0.422 |
LIG_NRBOX | 688 | 694 | PF00104 | 0.422 |
LIG_Pex14_1 | 665 | 669 | PF04695 | 0.276 |
LIG_Pex14_2 | 543 | 547 | PF04695 | 0.276 |
LIG_SH2_CRK | 109 | 113 | PF00017 | 0.659 |
LIG_SH2_CRK | 469 | 473 | PF00017 | 0.378 |
LIG_SH2_CRK | 560 | 564 | PF00017 | 0.334 |
LIG_SH2_STAP1 | 469 | 473 | PF00017 | 0.283 |
LIG_SH2_STAT5 | 109 | 112 | PF00017 | 0.619 |
LIG_SH2_STAT5 | 128 | 131 | PF00017 | 0.278 |
LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.347 |
LIG_SH2_STAT5 | 179 | 182 | PF00017 | 0.278 |
LIG_SH2_STAT5 | 197 | 200 | PF00017 | 0.232 |
LIG_SH2_STAT5 | 282 | 285 | PF00017 | 0.290 |
LIG_SH2_STAT5 | 290 | 293 | PF00017 | 0.290 |
LIG_SH2_STAT5 | 469 | 472 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 534 | 537 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 568 | 571 | PF00017 | 0.323 |
LIG_SH3_3 | 100 | 106 | PF00018 | 0.584 |
LIG_SH3_3 | 331 | 337 | PF00018 | 0.558 |
LIG_SH3_3 | 369 | 375 | PF00018 | 0.684 |
LIG_SH3_3 | 385 | 391 | PF00018 | 0.764 |
LIG_SH3_3 | 614 | 620 | PF00018 | 0.276 |
LIG_SH3_3 | 653 | 659 | PF00018 | 0.279 |
LIG_SH3_3 | 720 | 726 | PF00018 | 0.517 |
LIG_SH3_3 | 76 | 82 | PF00018 | 0.671 |
LIG_SUMO_SIM_anti_2 | 501 | 506 | PF11976 | 0.276 |
LIG_SUMO_SIM_par_1 | 584 | 589 | PF11976 | 0.290 |
LIG_TRAF2_1 | 345 | 348 | PF00917 | 0.608 |
LIG_TRAF2_1 | 491 | 494 | PF00917 | 0.422 |
LIG_TYR_ITIM | 107 | 112 | PF00017 | 0.656 |
LIG_UBA3_1 | 689 | 695 | PF00899 | 0.391 |
LIG_WRC_WIRS_1 | 540 | 545 | PF05994 | 0.290 |
MOD_CDK_SPxK_1 | 452 | 458 | PF00069 | 0.533 |
MOD_CDK_SPxxK_3 | 430 | 437 | PF00069 | 0.477 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.741 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.643 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.531 |
MOD_CK1_1 | 365 | 371 | PF00069 | 0.712 |
MOD_CK1_1 | 404 | 410 | PF00069 | 0.615 |
MOD_CK1_1 | 412 | 418 | PF00069 | 0.708 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.634 |
MOD_CK1_1 | 536 | 542 | PF00069 | 0.284 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.644 |
MOD_CK2_1 | 128 | 134 | PF00069 | 0.290 |
MOD_CK2_1 | 446 | 452 | PF00069 | 0.531 |
MOD_CK2_1 | 488 | 494 | PF00069 | 0.295 |
MOD_CK2_1 | 50 | 56 | PF00069 | 0.531 |
MOD_CK2_1 | 644 | 650 | PF00069 | 0.276 |
MOD_CK2_1 | 703 | 709 | PF00069 | 0.464 |
MOD_CK2_1 | 722 | 728 | PF00069 | 0.756 |
MOD_CK2_1 | 99 | 105 | PF00069 | 0.515 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.747 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.361 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.428 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.643 |
MOD_GlcNHglycan | 535 | 538 | PF01048 | 0.276 |
MOD_GlcNHglycan | 607 | 610 | PF01048 | 0.422 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.577 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.300 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.803 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.721 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.733 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.765 |
MOD_GSK3_1 | 391 | 398 | PF00069 | 0.658 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.632 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.616 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.482 |
MOD_GSK3_1 | 607 | 614 | PF00069 | 0.336 |
MOD_GSK3_1 | 636 | 643 | PF00069 | 0.276 |
MOD_GSK3_1 | 672 | 679 | PF00069 | 0.277 |
MOD_GSK3_1 | 717 | 724 | PF00069 | 0.566 |
MOD_N-GLC_1 | 395 | 400 | PF02516 | 0.624 |
MOD_N-GLC_1 | 672 | 677 | PF02516 | 0.370 |
MOD_N-GLC_1 | 8 | 13 | PF02516 | 0.689 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.736 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.708 |
MOD_NEK2_1 | 405 | 410 | PF00069 | 0.617 |
MOD_NEK2_1 | 435 | 440 | PF00069 | 0.562 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.546 |
MOD_NEK2_1 | 597 | 602 | PF00069 | 0.276 |
MOD_NEK2_1 | 727 | 732 | PF00069 | 0.762 |
MOD_NEK2_2 | 401 | 406 | PF00069 | 0.739 |
MOD_NEK2_2 | 551 | 556 | PF00069 | 0.422 |
MOD_PIKK_1 | 322 | 328 | PF00454 | 0.580 |
MOD_PK_1 | 546 | 552 | PF00069 | 0.422 |
MOD_PKA_1 | 410 | 416 | PF00069 | 0.574 |
MOD_PKA_2 | 278 | 284 | PF00069 | 0.422 |
MOD_PKA_2 | 358 | 364 | PF00069 | 0.707 |
MOD_PKA_2 | 405 | 411 | PF00069 | 0.727 |
MOD_PKA_2 | 58 | 64 | PF00069 | 0.578 |
MOD_PKA_2 | 703 | 709 | PF00069 | 0.339 |
MOD_Plk_1 | 418 | 424 | PF00069 | 0.511 |
MOD_Plk_2-3 | 343 | 349 | PF00069 | 0.624 |
MOD_Plk_4 | 278 | 284 | PF00069 | 0.318 |
MOD_Plk_4 | 330 | 336 | PF00069 | 0.693 |
MOD_Plk_4 | 539 | 545 | PF00069 | 0.290 |
MOD_Plk_4 | 612 | 618 | PF00069 | 0.314 |
MOD_Plk_4 | 644 | 650 | PF00069 | 0.276 |
MOD_Plk_4 | 660 | 666 | PF00069 | 0.276 |
MOD_Plk_4 | 80 | 86 | PF00069 | 0.635 |
MOD_ProDKin_1 | 333 | 339 | PF00069 | 0.584 |
MOD_ProDKin_1 | 395 | 401 | PF00069 | 0.746 |
MOD_ProDKin_1 | 430 | 436 | PF00069 | 0.545 |
MOD_ProDKin_1 | 452 | 458 | PF00069 | 0.533 |
MOD_ProDKin_1 | 48 | 54 | PF00069 | 0.510 |
MOD_ProDKin_1 | 616 | 622 | PF00069 | 0.316 |
MOD_ProDKin_1 | 722 | 728 | PF00069 | 0.543 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.695 |
MOD_SUMO_for_1 | 628 | 631 | PF00179 | 0.290 |
MOD_SUMO_rev_2 | 185 | 193 | PF00179 | 0.428 |
MOD_SUMO_rev_2 | 519 | 524 | PF00179 | 0.403 |
TRG_DiLeu_BaEn_1 | 688 | 693 | PF01217 | 0.439 |
TRG_DiLeu_BaEn_4 | 493 | 499 | PF01217 | 0.334 |
TRG_ENDOCYTIC_2 | 109 | 112 | PF00928 | 0.661 |
TRG_ENDOCYTIC_2 | 209 | 212 | PF00928 | 0.403 |
TRG_ENDOCYTIC_2 | 290 | 293 | PF00928 | 0.422 |
TRG_ENDOCYTIC_2 | 417 | 420 | PF00928 | 0.703 |
TRG_ENDOCYTIC_2 | 469 | 472 | PF00928 | 0.294 |
TRG_ENDOCYTIC_2 | 517 | 520 | PF00928 | 0.441 |
TRG_ENDOCYTIC_2 | 560 | 563 | PF00928 | 0.334 |
TRG_ER_diArg_1 | 180 | 183 | PF00400 | 0.334 |
TRG_ER_diArg_1 | 381 | 383 | PF00400 | 0.653 |
TRG_ER_diArg_1 | 505 | 507 | PF00400 | 0.427 |
TRG_Pf-PMV_PEXEL_1 | 382 | 386 | PF00026 | 0.549 |
TRG_Pf-PMV_PEXEL_1 | 567 | 571 | PF00026 | 0.334 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZR8 | Leptomonas seymouri | 71% | 92% |
A0A0S4J7Q1 | Bodo saltans | 54% | 100% |
A0A1X0P0R3 | Trypanosomatidae | 64% | 100% |
A0A3S7WP16 | Leishmania donovani | 93% | 93% |
A0A3S7X8Z8 | Leishmania donovani | 26% | 100% |
A0A422N0Q9 | Trypanosoma rangeli | 60% | 100% |
A4H485 | Leishmania braziliensis | 82% | 100% |
A4HSG1 | Leishmania infantum | 93% | 93% |
A4IB02 | Leishmania infantum | 26% | 100% |
D0A4H1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 57% | 100% |
E9AET0 | Leishmania major | 27% | 100% |
E9B5Y5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
Q4QJG3 | Leishmania major | 93% | 100% |
V5D179 | Trypanosoma cruzi | 62% | 100% |