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: 18 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 1 |
GO:0097014 | ciliary plasm | 5 | 1 |
GO:0099568 | cytoplasmic region | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H8F5
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 13 |
GO:0006793 | phosphorus metabolic process | 3 | 13 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 13 |
GO:0006807 | nitrogen compound metabolic process | 2 | 13 |
GO:0008152 | metabolic process | 1 | 13 |
GO:0009987 | cellular process | 1 | 13 |
GO:0016310 | phosphorylation | 5 | 13 |
GO:0019538 | protein metabolic process | 3 | 13 |
GO:0036211 | protein modification process | 4 | 13 |
GO:0043170 | macromolecule metabolic process | 3 | 13 |
GO:0043412 | macromolecule modification | 4 | 13 |
GO:0044237 | cellular metabolic process | 2 | 13 |
GO:0044238 | primary metabolic process | 2 | 13 |
GO:0071704 | organic substance metabolic process | 2 | 13 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 13 |
GO:0007165 | signal transduction | 2 | 2 |
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 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0009966 | regulation of signal transduction | 4 | 1 |
GO:0010646 | regulation of cell communication | 4 | 1 |
GO:0023051 | regulation of signaling | 3 | 1 |
GO:0043408 | regulation of MAPK cascade | 6 | 1 |
GO:0048583 | regulation of response to stimulus | 3 | 1 |
GO:1902531 | regulation of intracellular signal transduction | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 13 |
GO:0003824 | catalytic activity | 1 | 13 |
GO:0004672 | protein kinase activity | 3 | 13 |
GO:0005488 | binding | 1 | 13 |
GO:0005524 | ATP binding | 5 | 13 |
GO:0016301 | kinase activity | 4 | 13 |
GO:0016740 | transferase activity | 2 | 13 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 13 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 13 |
GO:0017076 | purine nucleotide binding | 4 | 13 |
GO:0030554 | adenyl nucleotide binding | 5 | 13 |
GO:0032553 | ribonucleotide binding | 3 | 13 |
GO:0032555 | purine ribonucleotide binding | 4 | 13 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 13 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 13 |
GO:0036094 | small molecule binding | 2 | 13 |
GO:0043167 | ion binding | 2 | 13 |
GO:0043168 | anion binding | 3 | 13 |
GO:0097159 | organic cyclic compound binding | 2 | 13 |
GO:0097367 | carbohydrate derivative binding | 2 | 13 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 13 |
GO:1901265 | nucleoside phosphate binding | 3 | 13 |
GO:1901363 | heterocyclic compound binding | 2 | 13 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 303 | 307 | PF00656 | 0.579 |
CLV_C14_Caspase3-7 | 308 | 312 | PF00656 | 0.574 |
CLV_NRD_NRD_1 | 113 | 115 | PF00675 | 0.368 |
CLV_NRD_NRD_1 | 175 | 177 | PF00675 | 0.306 |
CLV_NRD_NRD_1 | 254 | 256 | PF00675 | 0.317 |
CLV_NRD_NRD_1 | 298 | 300 | PF00675 | 0.482 |
CLV_NRD_NRD_1 | 362 | 364 | PF00675 | 0.713 |
CLV_PCSK_KEX2_1 | 113 | 115 | PF00082 | 0.308 |
CLV_PCSK_KEX2_1 | 175 | 177 | PF00082 | 0.266 |
CLV_PCSK_KEX2_1 | 254 | 256 | PF00082 | 0.328 |
CLV_PCSK_KEX2_1 | 297 | 299 | PF00082 | 0.500 |
CLV_PCSK_KEX2_1 | 361 | 363 | PF00082 | 0.743 |
CLV_PCSK_SKI1_1 | 126 | 130 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 143 | 147 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 18 | 22 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.266 |
CLV_PCSK_SKI1_1 | 254 | 258 | PF00082 | 0.329 |
CLV_PCSK_SKI1_1 | 396 | 400 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 418 | 422 | PF00082 | 0.623 |
CLV_PCSK_SKI1_1 | 536 | 540 | PF00082 | 0.501 |
DEG_APCC_DBOX_1 | 125 | 133 | PF00400 | 0.302 |
DEG_APCC_DBOX_1 | 395 | 403 | PF00400 | 0.571 |
DEG_SPOP_SBC_1 | 437 | 441 | PF00917 | 0.512 |
DOC_ANK_TNKS_1 | 298 | 305 | PF00023 | 0.408 |
DOC_ANK_TNKS_1 | 469 | 476 | PF00023 | 0.516 |
DOC_CDC14_PxL_1 | 397 | 405 | PF14671 | 0.532 |
DOC_CYCLIN_RxL_1 | 250 | 260 | PF00134 | 0.297 |
DOC_CYCLIN_RxL_1 | 415 | 425 | PF00134 | 0.486 |
DOC_CYCLIN_yCln2_LP_2 | 116 | 122 | PF00134 | 0.296 |
DOC_MAPK_DCC_7 | 396 | 405 | PF00069 | 0.566 |
DOC_MAPK_gen_1 | 143 | 152 | PF00069 | 0.315 |
DOC_MAPK_gen_1 | 261 | 271 | PF00069 | 0.466 |
DOC_MAPK_HePTP_8 | 393 | 405 | PF00069 | 0.570 |
DOC_MAPK_MEF2A_6 | 396 | 405 | PF00069 | 0.566 |
DOC_MAPK_MEF2A_6 | 59 | 66 | PF00069 | 0.204 |
DOC_PP1_RVXF_1 | 224 | 231 | PF00149 | 0.298 |
DOC_PP4_FxxP_1 | 229 | 232 | PF00568 | 0.266 |
DOC_PP4_FxxP_1 | 275 | 278 | PF00568 | 0.489 |
DOC_PP4_FxxP_1 | 507 | 510 | PF00568 | 0.504 |
DOC_USP7_MATH_1 | 437 | 441 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 560 | 564 | PF00917 | 0.416 |
DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.266 |
DOC_WW_Pin1_4 | 274 | 279 | PF00397 | 0.312 |
DOC_WW_Pin1_4 | 356 | 361 | PF00397 | 0.654 |
DOC_WW_Pin1_4 | 362 | 367 | PF00397 | 0.765 |
DOC_WW_Pin1_4 | 519 | 524 | PF00397 | 0.651 |
LIG_14-3-3_CanoR_1 | 113 | 119 | PF00244 | 0.298 |
LIG_14-3-3_CanoR_1 | 175 | 180 | PF00244 | 0.270 |
LIG_14-3-3_CanoR_1 | 501 | 510 | PF00244 | 0.466 |
LIG_Actin_WH2_2 | 249 | 266 | PF00022 | 0.298 |
LIG_Actin_WH2_2 | 561 | 577 | PF00022 | 0.398 |
LIG_Actin_WH2_2 | 600 | 615 | PF00022 | 0.518 |
LIG_AP2alpha_2 | 273 | 275 | PF02296 | 0.266 |
LIG_APCC_ABBAyCdc20_2 | 138 | 144 | PF00400 | 0.355 |
LIG_BRCT_BRCA1_1 | 561 | 565 | PF00533 | 0.415 |
LIG_Clathr_ClatBox_1 | 402 | 406 | PF01394 | 0.614 |
LIG_deltaCOP1_diTrp_1 | 243 | 252 | PF00928 | 0.266 |
LIG_eIF4E_1 | 503 | 509 | PF01652 | 0.516 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.355 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.315 |
LIG_FHA_1 | 426 | 432 | PF00498 | 0.689 |
LIG_FHA_1 | 437 | 443 | PF00498 | 0.491 |
LIG_FHA_1 | 548 | 554 | PF00498 | 0.488 |
LIG_FHA_1 | 569 | 575 | PF00498 | 0.692 |
LIG_FHA_1 | 588 | 594 | PF00498 | 0.393 |
LIG_FHA_2 | 206 | 212 | PF00498 | 0.225 |
LIG_FHA_2 | 55 | 61 | PF00498 | 0.346 |
LIG_FHA_2 | 574 | 580 | PF00498 | 0.506 |
LIG_LIR_Apic_2 | 182 | 188 | PF02991 | 0.315 |
LIG_LIR_Apic_2 | 273 | 278 | PF02991 | 0.488 |
LIG_LIR_Apic_2 | 505 | 510 | PF02991 | 0.463 |
LIG_LIR_Gen_1 | 106 | 116 | PF02991 | 0.419 |
LIG_LIR_Gen_1 | 19 | 29 | PF02991 | 0.310 |
LIG_LIR_Gen_1 | 562 | 569 | PF02991 | 0.418 |
LIG_LIR_Gen_1 | 86 | 95 | PF02991 | 0.294 |
LIG_LIR_Nem_3 | 106 | 112 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 19 | 24 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 407 | 413 | PF02991 | 0.564 |
LIG_LIR_Nem_3 | 521 | 527 | PF02991 | 0.571 |
LIG_LIR_Nem_3 | 562 | 568 | PF02991 | 0.422 |
LIG_LYPXL_yS_3 | 524 | 527 | PF13949 | 0.474 |
LIG_NRBOX | 128 | 134 | PF00104 | 0.204 |
LIG_PCNA_PIPBox_1 | 496 | 505 | PF02747 | 0.471 |
LIG_PCNA_yPIPBox_3 | 284 | 298 | PF02747 | 0.404 |
LIG_Pex14_2 | 561 | 565 | PF04695 | 0.415 |
LIG_SH2_CRK | 109 | 113 | PF00017 | 0.327 |
LIG_SH2_CRK | 528 | 532 | PF00017 | 0.563 |
LIG_SH2_STAP1 | 196 | 200 | PF00017 | 0.283 |
LIG_SH2_STAP1 | 589 | 593 | PF00017 | 0.565 |
LIG_SH2_STAT5 | 123 | 126 | PF00017 | 0.296 |
LIG_SH2_STAT5 | 134 | 137 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 586 | 589 | PF00017 | 0.561 |
LIG_SH2_STAT5 | 99 | 102 | PF00017 | 0.299 |
LIG_SH3_3 | 395 | 401 | PF00018 | 0.520 |
LIG_SH3_3 | 468 | 474 | PF00018 | 0.590 |
LIG_SH3_3 | 517 | 523 | PF00018 | 0.611 |
LIG_SH3_3 | 524 | 530 | PF00018 | 0.659 |
LIG_SUMO_SIM_anti_2 | 60 | 66 | PF11976 | 0.285 |
LIG_SUMO_SIM_anti_2 | 68 | 74 | PF11976 | 0.306 |
LIG_SUMO_SIM_par_1 | 208 | 214 | PF11976 | 0.294 |
LIG_TRAF2_1 | 282 | 285 | PF00917 | 0.413 |
LIG_TRAF2_1 | 333 | 336 | PF00917 | 0.628 |
LIG_TRAF2_1 | 576 | 579 | PF00917 | 0.364 |
LIG_WW_1 | 525 | 528 | PF00397 | 0.553 |
MOD_CDC14_SPxK_1 | 359 | 362 | PF00782 | 0.508 |
MOD_CDK_SPK_2 | 356 | 361 | PF00069 | 0.495 |
MOD_CDK_SPxK_1 | 356 | 362 | PF00069 | 0.499 |
MOD_CDK_SPxxK_3 | 356 | 363 | PF00069 | 0.571 |
MOD_CK1_1 | 312 | 318 | PF00069 | 0.536 |
MOD_CK1_1 | 365 | 371 | PF00069 | 0.574 |
MOD_CK1_1 | 424 | 430 | PF00069 | 0.532 |
MOD_CK1_1 | 489 | 495 | PF00069 | 0.518 |
MOD_CK2_1 | 205 | 211 | PF00069 | 0.266 |
MOD_CK2_1 | 297 | 303 | PF00069 | 0.447 |
MOD_CK2_1 | 54 | 60 | PF00069 | 0.355 |
MOD_CK2_1 | 573 | 579 | PF00069 | 0.626 |
MOD_CK2_1 | 591 | 597 | PF00069 | 0.410 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.355 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.535 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.500 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.662 |
MOD_GlcNHglycan | 456 | 459 | PF01048 | 0.723 |
MOD_GlcNHglycan | 461 | 464 | PF01048 | 0.589 |
MOD_GlcNHglycan | 511 | 514 | PF01048 | 0.536 |
MOD_GlcNHglycan | 621 | 624 | PF01048 | 0.416 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.312 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.266 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.577 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.548 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.556 |
MOD_GSK3_1 | 486 | 493 | PF00069 | 0.672 |
MOD_GSK3_1 | 569 | 576 | PF00069 | 0.536 |
MOD_GSK3_1 | 587 | 594 | PF00069 | 0.543 |
MOD_N-GLC_1 | 312 | 317 | PF02516 | 0.587 |
MOD_N-GLC_1 | 489 | 494 | PF02516 | 0.568 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.484 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.244 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.271 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.306 |
MOD_NEK2_1 | 205 | 210 | PF00069 | 0.270 |
MOD_NEK2_1 | 421 | 426 | PF00069 | 0.639 |
MOD_NEK2_1 | 486 | 491 | PF00069 | 0.690 |
MOD_NEK2_1 | 495 | 500 | PF00069 | 0.520 |
MOD_NEK2_1 | 547 | 552 | PF00069 | 0.529 |
MOD_NEK2_1 | 568 | 573 | PF00069 | 0.553 |
MOD_NEK2_1 | 607 | 612 | PF00069 | 0.504 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.408 |
MOD_PIKK_1 | 474 | 480 | PF00454 | 0.485 |
MOD_PIKK_1 | 560 | 566 | PF00454 | 0.435 |
MOD_PK_1 | 297 | 303 | PF00069 | 0.381 |
MOD_PK_1 | 322 | 328 | PF00069 | 0.596 |
MOD_PKA_1 | 175 | 181 | PF00069 | 0.266 |
MOD_PKA_1 | 297 | 303 | PF00069 | 0.533 |
MOD_PKA_2 | 175 | 181 | PF00069 | 0.268 |
MOD_PKA_2 | 263 | 269 | PF00069 | 0.315 |
MOD_PKA_2 | 297 | 303 | PF00069 | 0.533 |
MOD_PKA_2 | 40 | 46 | PF00069 | 0.285 |
MOD_Plk_1 | 312 | 318 | PF00069 | 0.617 |
MOD_Plk_1 | 406 | 412 | PF00069 | 0.574 |
MOD_Plk_1 | 490 | 496 | PF00069 | 0.524 |
MOD_Plk_1 | 569 | 575 | PF00069 | 0.538 |
MOD_Plk_2-3 | 101 | 107 | PF00069 | 0.298 |
MOD_Plk_2-3 | 406 | 412 | PF00069 | 0.574 |
MOD_Plk_4 | 164 | 170 | PF00069 | 0.204 |
MOD_Plk_4 | 175 | 181 | PF00069 | 0.316 |
MOD_Plk_4 | 315 | 321 | PF00069 | 0.508 |
MOD_Plk_4 | 322 | 328 | PF00069 | 0.567 |
MOD_Plk_4 | 491 | 497 | PF00069 | 0.546 |
MOD_Plk_4 | 503 | 509 | PF00069 | 0.510 |
MOD_Plk_4 | 607 | 613 | PF00069 | 0.432 |
MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.266 |
MOD_ProDKin_1 | 274 | 280 | PF00069 | 0.314 |
MOD_ProDKin_1 | 356 | 362 | PF00069 | 0.658 |
MOD_ProDKin_1 | 519 | 525 | PF00069 | 0.646 |
MOD_SUMO_rev_2 | 14 | 20 | PF00179 | 0.400 |
MOD_SUMO_rev_2 | 594 | 601 | PF00179 | 0.538 |
TRG_DiLeu_BaEn_1 | 549 | 554 | PF01217 | 0.574 |
TRG_DiLeu_BaLyEn_6 | 116 | 121 | PF01217 | 0.355 |
TRG_DiLeu_BaLyEn_6 | 252 | 257 | PF01217 | 0.350 |
TRG_DiLeu_BaLyEn_6 | 398 | 403 | PF01217 | 0.562 |
TRG_DiLeu_BaLyEn_6 | 602 | 607 | PF01217 | 0.373 |
TRG_ENDOCYTIC_2 | 109 | 112 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 524 | 527 | PF00928 | 0.474 |
TRG_ENDOCYTIC_2 | 87 | 90 | PF00928 | 0.343 |
TRG_ER_diArg_1 | 112 | 114 | PF00400 | 0.355 |
TRG_ER_diArg_1 | 253 | 255 | PF00400 | 0.319 |
TRG_ER_diArg_1 | 297 | 299 | PF00400 | 0.443 |
TRG_ER_diArg_1 | 360 | 363 | PF00400 | 0.534 |
TRG_ER_diArg_1 | 39 | 42 | PF00400 | 0.204 |
TRG_ER_diArg_1 | 603 | 606 | PF00400 | 0.369 |
TRG_NES_CRM1_1 | 45 | 58 | PF08389 | 0.267 |
TRG_NES_CRM1_1 | 60 | 74 | PF08389 | 0.271 |
TRG_Pf-PMV_PEXEL_1 | 114 | 118 | PF00026 | 0.296 |
TRG_Pf-PMV_PEXEL_1 | 255 | 260 | PF00026 | 0.281 |
TRG_Pf-PMV_PEXEL_1 | 299 | 303 | PF00026 | 0.661 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEW4 | Leptomonas seymouri | 60% | 100% |
A0A0S4IHW4 | Bodo saltans | 46% | 100% |
A0A1X0NFW4 | Trypanosomatidae | 49% | 100% |
A0A3S5H5U5 | Leishmania donovani | 23% | 100% |
A0A3S7WTT7 | Leishmania donovani | 80% | 100% |
A4HWS9 | Leishmania infantum | 80% | 100% |
E9AG71 | Leishmania infantum | 23% | 100% |
E9AKZ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 100% |
E9AQI7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 99% |
Q4QEZ0 | Leishmania major | 82% | 100% |
Q4QIV8 | Leishmania major | 23% | 100% |