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 |
Related structures:
AlphaFold database: E9AQI7
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 |
GO:0007165 | signal transduction | 2 | 1 |
GO:0009966 | regulation of signal transduction | 4 | 1 |
GO:0010646 | regulation of cell communication | 4 | 1 |
GO:0023051 | regulation of signaling | 3 | 1 |
GO:0035556 | intracellular signal transduction | 3 | 1 |
GO:0043408 | regulation of MAPK cascade | 6 | 1 |
GO:0048583 | regulation of response to stimulus | 3 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:1902531 | regulation of intracellular signal transduction | 5 | 1 |
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 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 303 | 307 | PF00656 | 0.547 |
CLV_NRD_NRD_1 | 113 | 115 | PF00675 | 0.279 |
CLV_NRD_NRD_1 | 175 | 177 | PF00675 | 0.345 |
CLV_NRD_NRD_1 | 254 | 256 | PF00675 | 0.279 |
CLV_NRD_NRD_1 | 298 | 300 | PF00675 | 0.427 |
CLV_NRD_NRD_1 | 362 | 364 | PF00675 | 0.598 |
CLV_NRD_NRD_1 | 417 | 419 | PF00675 | 0.480 |
CLV_PCSK_KEX2_1 | 113 | 115 | PF00082 | 0.279 |
CLV_PCSK_KEX2_1 | 175 | 177 | PF00082 | 0.348 |
CLV_PCSK_KEX2_1 | 254 | 256 | PF00082 | 0.279 |
CLV_PCSK_KEX2_1 | 297 | 299 | PF00082 | 0.424 |
CLV_PCSK_KEX2_1 | 304 | 306 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 417 | 419 | PF00082 | 0.480 |
CLV_PCSK_PC1ET2_1 | 304 | 306 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 143 | 147 | PF00082 | 0.271 |
CLV_PCSK_SKI1_1 | 18 | 22 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.279 |
CLV_PCSK_SKI1_1 | 254 | 258 | PF00082 | 0.332 |
CLV_PCSK_SKI1_1 | 362 | 366 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 396 | 400 | PF00082 | 0.591 |
CLV_PCSK_SKI1_1 | 418 | 422 | PF00082 | 0.557 |
CLV_PCSK_SKI1_1 | 583 | 587 | PF00082 | 0.497 |
DEG_APCC_DBOX_1 | 125 | 133 | PF00400 | 0.332 |
DEG_APCC_DBOX_1 | 395 | 403 | PF00400 | 0.586 |
DOC_CDC14_PxL_1 | 397 | 405 | PF14671 | 0.546 |
DOC_CYCLIN_RxL_1 | 251 | 260 | PF00134 | 0.331 |
DOC_CYCLIN_RxL_1 | 415 | 425 | PF00134 | 0.507 |
DOC_CYCLIN_yCln2_LP_2 | 116 | 122 | PF00134 | 0.309 |
DOC_MAPK_DCC_7 | 396 | 405 | PF00069 | 0.579 |
DOC_MAPK_gen_1 | 143 | 152 | PF00069 | 0.332 |
DOC_MAPK_HePTP_8 | 393 | 405 | PF00069 | 0.582 |
DOC_MAPK_MEF2A_6 | 396 | 405 | PF00069 | 0.579 |
DOC_MAPK_MEF2A_6 | 506 | 514 | PF00069 | 0.509 |
DOC_PP1_RVXF_1 | 224 | 231 | PF00149 | 0.309 |
DOC_PP2B_LxvP_1 | 512 | 515 | PF13499 | 0.537 |
DOC_PP4_FxxP_1 | 229 | 232 | PF00568 | 0.306 |
DOC_PP4_FxxP_1 | 275 | 278 | PF00568 | 0.402 |
DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.515 |
DOC_USP7_MATH_1 | 429 | 433 | PF00917 | 0.559 |
DOC_USP7_MATH_1 | 442 | 446 | PF00917 | 0.566 |
DOC_USP7_MATH_2 | 491 | 497 | PF00917 | 0.485 |
DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.279 |
DOC_WW_Pin1_4 | 527 | 532 | PF00397 | 0.593 |
DOC_WW_Pin1_4 | 564 | 569 | PF00397 | 0.469 |
LIG_14-3-3_CanoR_1 | 113 | 119 | PF00244 | 0.298 |
LIG_14-3-3_CanoR_1 | 126 | 130 | PF00244 | 0.381 |
LIG_14-3-3_CanoR_1 | 175 | 180 | PF00244 | 0.286 |
LIG_14-3-3_CanoR_1 | 297 | 302 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 322 | 327 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 39 | 49 | PF00244 | 0.269 |
LIG_14-3-3_CanoR_1 | 417 | 421 | PF00244 | 0.482 |
LIG_Actin_WH2_2 | 249 | 266 | PF00022 | 0.309 |
LIG_Actin_WH2_2 | 605 | 620 | PF00022 | 0.465 |
LIG_AP2alpha_2 | 273 | 275 | PF02296 | 0.279 |
LIG_APCC_ABBA_1 | 272 | 277 | PF00400 | 0.281 |
LIG_APCC_ABBAyCdc20_2 | 138 | 144 | PF00400 | 0.279 |
LIG_BIR_III_4 | 437 | 441 | PF00653 | 0.521 |
LIG_BRCT_BRCA1_1 | 446 | 450 | PF00533 | 0.629 |
LIG_Clathr_ClatBox_1 | 402 | 406 | PF01394 | 0.534 |
LIG_deltaCOP1_diTrp_1 | 243 | 252 | PF00928 | 0.279 |
LIG_eIF4E_1 | 507 | 513 | PF01652 | 0.533 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.320 |
LIG_FHA_1 | 321 | 327 | PF00498 | 0.564 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.313 |
LIG_FHA_1 | 574 | 580 | PF00498 | 0.671 |
LIG_FHA_1 | 593 | 599 | PF00498 | 0.410 |
LIG_FHA_2 | 105 | 111 | PF00498 | 0.281 |
LIG_FHA_2 | 206 | 212 | PF00498 | 0.320 |
LIG_FHA_2 | 55 | 61 | PF00498 | 0.313 |
LIG_FHA_2 | 579 | 585 | PF00498 | 0.434 |
LIG_LIR_Apic_2 | 182 | 188 | PF02991 | 0.332 |
LIG_LIR_Apic_2 | 273 | 278 | PF02991 | 0.404 |
LIG_LIR_Gen_1 | 106 | 116 | PF02991 | 0.257 |
LIG_LIR_Gen_1 | 19 | 29 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 106 | 112 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 407 | 413 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 527 | 532 | PF02991 | 0.599 |
LIG_PCNA_yPIPBox_3 | 284 | 298 | PF02747 | 0.415 |
LIG_Rb_LxCxE_1 | 567 | 584 | PF01857 | 0.461 |
LIG_SH2_CRK | 109 | 113 | PF00017 | 0.279 |
LIG_SH2_STAP1 | 196 | 200 | PF00017 | 0.279 |
LIG_SH2_STAP1 | 594 | 598 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 123 | 126 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 134 | 137 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 219 | 222 | PF00017 | 0.258 |
LIG_SH2_STAT5 | 507 | 510 | PF00017 | 0.483 |
LIG_SH2_STAT5 | 570 | 573 | PF00017 | 0.582 |
LIG_SH2_STAT5 | 591 | 594 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 99 | 102 | PF00017 | 0.316 |
LIG_SH3_3 | 529 | 535 | PF00018 | 0.583 |
LIG_SUMO_SIM_anti_2 | 68 | 73 | PF11976 | 0.298 |
LIG_SUMO_SIM_par_1 | 208 | 214 | PF11976 | 0.279 |
LIG_TRAF2_1 | 282 | 285 | PF00917 | 0.499 |
LIG_TRAF2_1 | 333 | 336 | PF00917 | 0.623 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.281 |
MOD_CK1_1 | 266 | 272 | PF00069 | 0.263 |
MOD_CK1_1 | 312 | 318 | PF00069 | 0.583 |
MOD_CK1_1 | 496 | 502 | PF00069 | 0.544 |
MOD_CK1_1 | 524 | 530 | PF00069 | 0.494 |
MOD_CK2_1 | 205 | 211 | PF00069 | 0.320 |
MOD_CK2_1 | 280 | 286 | PF00069 | 0.482 |
MOD_CK2_1 | 297 | 303 | PF00069 | 0.480 |
MOD_CK2_1 | 533 | 539 | PF00069 | 0.454 |
MOD_CK2_1 | 54 | 60 | PF00069 | 0.279 |
MOD_CK2_1 | 596 | 602 | PF00069 | 0.427 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.279 |
MOD_GlcNHglycan | 277 | 281 | PF01048 | 0.490 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.630 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.435 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.676 |
MOD_GlcNHglycan | 431 | 434 | PF01048 | 0.506 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.681 |
MOD_GlcNHglycan | 461 | 464 | PF01048 | 0.732 |
MOD_GlcNHglycan | 478 | 481 | PF01048 | 0.478 |
MOD_GlcNHglycan | 502 | 505 | PF01048 | 0.742 |
MOD_GlcNHglycan | 516 | 519 | PF01048 | 0.542 |
MOD_GlcNHglycan | 526 | 529 | PF01048 | 0.543 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.279 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.292 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.358 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.396 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.593 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.553 |
MOD_GSK3_1 | 496 | 503 | PF00069 | 0.584 |
MOD_GSK3_1 | 573 | 580 | PF00069 | 0.460 |
MOD_GSK3_1 | 592 | 599 | PF00069 | 0.482 |
MOD_GSK3_1 | 621 | 628 | PF00069 | 0.451 |
MOD_N-GLC_1 | 312 | 317 | PF02516 | 0.574 |
MOD_N-GLC_1 | 494 | 499 | PF02516 | 0.591 |
MOD_N-GLC_2 | 619 | 621 | PF02516 | 0.361 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.433 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.299 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.279 |
MOD_NEK2_1 | 205 | 210 | PF00069 | 0.295 |
MOD_NEK2_1 | 421 | 426 | PF00069 | 0.600 |
MOD_NEK2_1 | 500 | 505 | PF00069 | 0.538 |
MOD_NEK2_1 | 574 | 579 | PF00069 | 0.457 |
MOD_NEK2_1 | 612 | 617 | PF00069 | 0.464 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.306 |
MOD_NEK2_2 | 416 | 421 | PF00069 | 0.557 |
MOD_PIKK_1 | 280 | 286 | PF00454 | 0.387 |
MOD_PK_1 | 322 | 328 | PF00069 | 0.587 |
MOD_PKA_1 | 175 | 181 | PF00069 | 0.279 |
MOD_PKA_1 | 297 | 303 | PF00069 | 0.440 |
MOD_PKA_2 | 125 | 131 | PF00069 | 0.263 |
MOD_PKA_2 | 175 | 181 | PF00069 | 0.332 |
MOD_PKA_2 | 263 | 269 | PF00069 | 0.279 |
MOD_PKA_2 | 297 | 303 | PF00069 | 0.440 |
MOD_PKA_2 | 321 | 327 | PF00069 | 0.536 |
MOD_PKA_2 | 40 | 46 | PF00069 | 0.279 |
MOD_PKA_2 | 416 | 422 | PF00069 | 0.481 |
MOD_Plk_1 | 312 | 318 | PF00069 | 0.572 |
MOD_Plk_1 | 406 | 412 | PF00069 | 0.562 |
MOD_Plk_1 | 574 | 580 | PF00069 | 0.454 |
MOD_Plk_2-3 | 101 | 107 | PF00069 | 0.279 |
MOD_Plk_2-3 | 406 | 412 | PF00069 | 0.529 |
MOD_Plk_4 | 125 | 131 | PF00069 | 0.302 |
MOD_Plk_4 | 175 | 181 | PF00069 | 0.270 |
MOD_Plk_4 | 266 | 272 | PF00069 | 0.268 |
MOD_Plk_4 | 315 | 321 | PF00069 | 0.558 |
MOD_Plk_4 | 322 | 328 | PF00069 | 0.557 |
MOD_Plk_4 | 496 | 502 | PF00069 | 0.570 |
MOD_Plk_4 | 508 | 514 | PF00069 | 0.525 |
MOD_Plk_4 | 521 | 527 | PF00069 | 0.499 |
MOD_Plk_4 | 61 | 67 | PF00069 | 0.263 |
MOD_Plk_4 | 612 | 618 | PF00069 | 0.439 |
MOD_Plk_4 | 83 | 89 | PF00069 | 0.239 |
MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.279 |
MOD_ProDKin_1 | 527 | 533 | PF00069 | 0.592 |
MOD_ProDKin_1 | 564 | 570 | PF00069 | 0.468 |
MOD_SUMO_rev_2 | 14 | 20 | PF00179 | 0.412 |
MOD_SUMO_rev_2 | 162 | 172 | PF00179 | 0.345 |
MOD_SUMO_rev_2 | 599 | 606 | PF00179 | 0.481 |
TRG_AP2beta_CARGO_1 | 407 | 417 | PF09066 | 0.458 |
TRG_DiLeu_BaEn_1 | 554 | 559 | PF01217 | 0.454 |
TRG_DiLeu_BaLyEn_6 | 116 | 121 | PF01217 | 0.495 |
TRG_DiLeu_BaLyEn_6 | 252 | 257 | PF01217 | 0.279 |
TRG_DiLeu_BaLyEn_6 | 398 | 403 | PF01217 | 0.550 |
TRG_ENDOCYTIC_2 | 109 | 112 | PF00928 | 0.289 |
TRG_ENDOCYTIC_2 | 219 | 222 | PF00928 | 0.258 |
TRG_ENDOCYTIC_2 | 87 | 90 | PF00928 | 0.321 |
TRG_ER_diArg_1 | 112 | 114 | PF00400 | 0.279 |
TRG_ER_diArg_1 | 253 | 255 | PF00400 | 0.279 |
TRG_ER_diArg_1 | 297 | 299 | PF00400 | 0.454 |
TRG_ER_diArg_1 | 362 | 364 | PF00400 | 0.515 |
TRG_NES_CRM1_1 | 44 | 58 | PF08389 | 0.278 |
TRG_NES_CRM1_1 | 60 | 73 | PF08389 | 0.320 |
TRG_Pf-PMV_PEXEL_1 | 114 | 118 | PF00026 | 0.279 |
TRG_Pf-PMV_PEXEL_1 | 133 | 137 | PF00026 | 0.438 |
TRG_Pf-PMV_PEXEL_1 | 255 | 260 | PF00026 | 0.258 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEW4 | Leptomonas seymouri | 58% | 100% |
A0A3S5H5G0 | Leishmania donovani | 27% | 100% |
A0A3S7WTT7 | Leishmania donovani | 89% | 100% |
A4H459 | Leishmania braziliensis | 27% | 100% |
A4H8F5 | Leishmania braziliensis | 80% | 99% |
A4HSE2 | Leishmania infantum | 27% | 100% |
A4HWS9 | Leishmania infantum | 89% | 100% |
E9AKB7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
Q4QEZ0 | Leishmania major | 93% | 100% |
Q4QJJ0 | Leishmania major | 27% | 100% |