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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: Q4QEZ0
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 8 |
GO:0006793 | phosphorus metabolic process | 3 | 8 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 8 |
GO:0006807 | nitrogen compound metabolic process | 2 | 8 |
GO:0007165 | signal transduction | 2 | 2 |
GO:0008152 | metabolic process | 1 | 8 |
GO:0009966 | regulation of signal transduction | 4 | 2 |
GO:0009987 | cellular process | 1 | 8 |
GO:0010646 | regulation of cell communication | 4 | 2 |
GO:0016310 | phosphorylation | 5 | 8 |
GO:0019538 | protein metabolic process | 3 | 8 |
GO:0023051 | regulation of signaling | 3 | 2 |
GO:0035556 | intracellular signal transduction | 3 | 2 |
GO:0036211 | protein modification process | 4 | 8 |
GO:0043170 | macromolecule metabolic process | 3 | 8 |
GO:0043408 | regulation of MAPK cascade | 6 | 2 |
GO:0043412 | macromolecule modification | 4 | 8 |
GO:0044237 | cellular metabolic process | 2 | 8 |
GO:0044238 | primary metabolic process | 2 | 8 |
GO:0048583 | regulation of response to stimulus | 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:0071704 | organic substance metabolic process | 2 | 8 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 8 |
GO:1902531 | regulation of intracellular signal transduction | 5 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 8 |
GO:0003824 | catalytic activity | 1 | 8 |
GO:0004672 | protein kinase activity | 3 | 8 |
GO:0005488 | binding | 1 | 8 |
GO:0005524 | ATP binding | 5 | 8 |
GO:0016301 | kinase activity | 4 | 8 |
GO:0016740 | transferase activity | 2 | 8 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 8 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 8 |
GO:0017076 | purine nucleotide binding | 4 | 8 |
GO:0030554 | adenyl nucleotide binding | 5 | 8 |
GO:0032553 | ribonucleotide binding | 3 | 8 |
GO:0032555 | purine ribonucleotide binding | 4 | 8 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 8 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 8 |
GO:0036094 | small molecule binding | 2 | 8 |
GO:0043167 | ion binding | 2 | 8 |
GO:0043168 | anion binding | 3 | 8 |
GO:0097159 | organic cyclic compound binding | 2 | 8 |
GO:0097367 | carbohydrate derivative binding | 2 | 8 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 8 |
GO:1901265 | nucleoside phosphate binding | 3 | 8 |
GO:1901363 | heterocyclic compound binding | 2 | 8 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 303 | 307 | PF00656 | 0.602 |
CLV_C14_Caspase3-7 | 484 | 488 | PF00656 | 0.541 |
CLV_NRD_NRD_1 | 113 | 115 | PF00675 | 0.365 |
CLV_NRD_NRD_1 | 175 | 177 | PF00675 | 0.394 |
CLV_NRD_NRD_1 | 254 | 256 | PF00675 | 0.365 |
CLV_NRD_NRD_1 | 298 | 300 | PF00675 | 0.457 |
CLV_NRD_NRD_1 | 304 | 306 | PF00675 | 0.545 |
CLV_NRD_NRD_1 | 362 | 364 | PF00675 | 0.706 |
CLV_PCSK_KEX2_1 | 113 | 115 | PF00082 | 0.365 |
CLV_PCSK_KEX2_1 | 175 | 177 | PF00082 | 0.397 |
CLV_PCSK_KEX2_1 | 254 | 256 | PF00082 | 0.365 |
CLV_PCSK_KEX2_1 | 297 | 299 | PF00082 | 0.450 |
CLV_PCSK_KEX2_1 | 304 | 306 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.704 |
CLV_PCSK_SKI1_1 | 143 | 147 | PF00082 | 0.353 |
CLV_PCSK_SKI1_1 | 18 | 22 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 254 | 258 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 396 | 400 | PF00082 | 0.658 |
CLV_PCSK_SKI1_1 | 418 | 422 | PF00082 | 0.591 |
CLV_PCSK_SKI1_1 | 583 | 587 | PF00082 | 0.553 |
DEG_APCC_DBOX_1 | 125 | 133 | PF00400 | 0.413 |
DEG_APCC_DBOX_1 | 395 | 403 | PF00400 | 0.652 |
DEG_SPOP_SBC_1 | 442 | 446 | PF00917 | 0.565 |
DOC_CDC14_PxL_1 | 397 | 405 | PF14671 | 0.643 |
DOC_CYCLIN_RxL_1 | 251 | 258 | PF00134 | 0.413 |
DOC_CYCLIN_yCln2_LP_2 | 116 | 122 | PF00134 | 0.371 |
DOC_MAPK_DCC_7 | 396 | 405 | PF00069 | 0.650 |
DOC_MAPK_gen_1 | 143 | 152 | PF00069 | 0.413 |
DOC_MAPK_HePTP_8 | 393 | 405 | PF00069 | 0.652 |
DOC_MAPK_MEF2A_6 | 396 | 405 | PF00069 | 0.650 |
DOC_MAPK_MEF2A_6 | 506 | 514 | PF00069 | 0.592 |
DOC_PP1_RVXF_1 | 224 | 231 | PF00149 | 0.371 |
DOC_PP2B_LxvP_1 | 512 | 515 | PF13499 | 0.620 |
DOC_PP4_FxxP_1 | 229 | 232 | PF00568 | 0.391 |
DOC_PP4_FxxP_1 | 275 | 278 | PF00568 | 0.466 |
DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 429 | 433 | PF00917 | 0.606 |
DOC_USP7_MATH_1 | 442 | 446 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 524 | 528 | PF00917 | 0.645 |
DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.365 |
DOC_WW_Pin1_4 | 362 | 367 | PF00397 | 0.775 |
DOC_WW_Pin1_4 | 564 | 569 | PF00397 | 0.524 |
LIG_14-3-3_CanoR_1 | 113 | 119 | PF00244 | 0.384 |
LIG_14-3-3_CanoR_1 | 126 | 130 | PF00244 | 0.452 |
LIG_14-3-3_CanoR_1 | 175 | 180 | PF00244 | 0.378 |
LIG_14-3-3_CanoR_1 | 297 | 302 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 322 | 327 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 39 | 49 | PF00244 | 0.290 |
LIG_Actin_WH2_2 | 249 | 266 | PF00022 | 0.371 |
LIG_Actin_WH2_2 | 605 | 620 | PF00022 | 0.561 |
LIG_AP2alpha_2 | 273 | 275 | PF02296 | 0.365 |
LIG_APCC_ABBA_1 | 272 | 277 | PF00400 | 0.327 |
LIG_APCC_ABBAyCdc20_2 | 138 | 144 | PF00400 | 0.365 |
LIG_BIR_III_4 | 437 | 441 | PF00653 | 0.559 |
LIG_BRCT_BRCA1_1 | 446 | 450 | PF00533 | 0.678 |
LIG_Clathr_ClatBox_1 | 402 | 406 | PF01394 | 0.634 |
LIG_deltaCOP1_diTrp_1 | 243 | 252 | PF00928 | 0.365 |
LIG_eIF4E_1 | 507 | 513 | PF01652 | 0.581 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.378 |
LIG_FHA_1 | 321 | 327 | PF00498 | 0.644 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.396 |
LIG_FHA_1 | 426 | 432 | PF00498 | 0.628 |
LIG_FHA_1 | 434 | 440 | PF00498 | 0.542 |
LIG_FHA_1 | 574 | 580 | PF00498 | 0.551 |
LIG_FHA_1 | 593 | 599 | PF00498 | 0.580 |
LIG_FHA_2 | 105 | 111 | PF00498 | 0.327 |
LIG_FHA_2 | 190 | 196 | PF00498 | 0.305 |
LIG_FHA_2 | 206 | 212 | PF00498 | 0.339 |
LIG_FHA_2 | 482 | 488 | PF00498 | 0.602 |
LIG_FHA_2 | 55 | 61 | PF00498 | 0.365 |
LIG_FHA_2 | 579 | 585 | PF00498 | 0.550 |
LIG_LIR_Apic_2 | 182 | 188 | PF02991 | 0.413 |
LIG_LIR_Apic_2 | 273 | 278 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 106 | 116 | PF02991 | 0.362 |
LIG_LIR_Gen_1 | 19 | 29 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 106 | 112 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 19 | 24 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 407 | 413 | PF02991 | 0.644 |
LIG_LIR_Nem_3 | 527 | 532 | PF02991 | 0.649 |
LIG_PCNA_yPIPBox_3 | 284 | 298 | PF02747 | 0.477 |
LIG_Rb_LxCxE_1 | 567 | 584 | PF01857 | 0.515 |
LIG_SH2_CRK | 109 | 113 | PF00017 | 0.365 |
LIG_SH2_CRK | 533 | 537 | PF00017 | 0.594 |
LIG_SH2_STAP1 | 196 | 200 | PF00017 | 0.365 |
LIG_SH2_STAP1 | 594 | 598 | PF00017 | 0.587 |
LIG_SH2_STAT5 | 123 | 126 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 134 | 137 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 490 | 493 | PF00017 | 0.605 |
LIG_SH2_STAT5 | 507 | 510 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 570 | 573 | PF00017 | 0.534 |
LIG_SH2_STAT5 | 591 | 594 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 99 | 102 | PF00017 | 0.340 |
LIG_SH3_3 | 529 | 535 | PF00018 | 0.627 |
LIG_SUMO_SIM_anti_2 | 68 | 74 | PF11976 | 0.354 |
LIG_SUMO_SIM_par_1 | 208 | 214 | PF11976 | 0.365 |
LIG_TRAF2_1 | 282 | 285 | PF00917 | 0.606 |
LIG_TRAF2_1 | 333 | 336 | PF00917 | 0.687 |
LIG_WW_1 | 530 | 533 | PF00397 | 0.624 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.327 |
MOD_CK1_1 | 266 | 272 | PF00069 | 0.342 |
MOD_CK1_1 | 312 | 318 | PF00069 | 0.642 |
MOD_CK1_1 | 497 | 503 | PF00069 | 0.595 |
MOD_CK2_1 | 205 | 211 | PF00069 | 0.365 |
MOD_CK2_1 | 280 | 286 | PF00069 | 0.598 |
MOD_CK2_1 | 297 | 303 | PF00069 | 0.525 |
MOD_CK2_1 | 54 | 60 | PF00069 | 0.357 |
MOD_CK2_1 | 578 | 584 | PF00069 | 0.531 |
MOD_CK2_1 | 596 | 602 | PF00069 | 0.581 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.365 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.648 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.481 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.665 |
MOD_GlcNHglycan | 431 | 434 | PF01048 | 0.523 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.729 |
MOD_GlcNHglycan | 461 | 464 | PF01048 | 0.676 |
MOD_GlcNHglycan | 478 | 481 | PF01048 | 0.494 |
MOD_GlcNHglycan | 502 | 505 | PF01048 | 0.797 |
MOD_GlcNHglycan | 516 | 519 | PF01048 | 0.585 |
MOD_GlcNHglycan | 526 | 529 | PF01048 | 0.561 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.365 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.365 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.455 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.561 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.603 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.697 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.665 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.553 |
MOD_GSK3_1 | 496 | 503 | PF00069 | 0.686 |
MOD_GSK3_1 | 574 | 581 | PF00069 | 0.545 |
MOD_GSK3_1 | 592 | 599 | PF00069 | 0.577 |
MOD_GSK3_1 | 621 | 628 | PF00069 | 0.543 |
MOD_N-GLC_1 | 312 | 317 | PF02516 | 0.665 |
MOD_N-GLC_1 | 494 | 499 | PF02516 | 0.663 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.486 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.390 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.365 |
MOD_NEK2_1 | 205 | 210 | PF00069 | 0.334 |
MOD_NEK2_1 | 420 | 425 | PF00069 | 0.693 |
MOD_NEK2_1 | 574 | 579 | PF00069 | 0.493 |
MOD_NEK2_1 | 612 | 617 | PF00069 | 0.535 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.383 |
MOD_NEK2_2 | 416 | 421 | PF00069 | 0.609 |
MOD_PIKK_1 | 280 | 286 | PF00454 | 0.432 |
MOD_PK_1 | 322 | 328 | PF00069 | 0.642 |
MOD_PKA_1 | 175 | 181 | PF00069 | 0.365 |
MOD_PKA_1 | 297 | 303 | PF00069 | 0.467 |
MOD_PKA_2 | 125 | 131 | PF00069 | 0.342 |
MOD_PKA_2 | 175 | 181 | PF00069 | 0.412 |
MOD_PKA_2 | 263 | 269 | PF00069 | 0.365 |
MOD_PKA_2 | 297 | 303 | PF00069 | 0.467 |
MOD_PKA_2 | 321 | 327 | PF00069 | 0.607 |
MOD_PKA_2 | 40 | 46 | PF00069 | 0.365 |
MOD_Plk_1 | 312 | 318 | PF00069 | 0.662 |
MOD_Plk_1 | 406 | 412 | PF00069 | 0.659 |
MOD_Plk_1 | 574 | 580 | PF00069 | 0.545 |
MOD_Plk_2-3 | 101 | 107 | PF00069 | 0.365 |
MOD_Plk_2-3 | 189 | 195 | PF00069 | 0.305 |
MOD_Plk_2-3 | 406 | 412 | PF00069 | 0.641 |
MOD_Plk_4 | 125 | 131 | PF00069 | 0.360 |
MOD_Plk_4 | 175 | 181 | PF00069 | 0.353 |
MOD_Plk_4 | 266 | 272 | PF00069 | 0.328 |
MOD_Plk_4 | 315 | 321 | PF00069 | 0.630 |
MOD_Plk_4 | 322 | 328 | PF00069 | 0.637 |
MOD_Plk_4 | 508 | 514 | PF00069 | 0.695 |
MOD_Plk_4 | 61 | 67 | PF00069 | 0.316 |
MOD_Plk_4 | 612 | 618 | PF00069 | 0.532 |
MOD_Plk_4 | 83 | 89 | PF00069 | 0.340 |
MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.365 |
MOD_ProDKin_1 | 362 | 368 | PF00069 | 0.775 |
MOD_ProDKin_1 | 564 | 570 | PF00069 | 0.525 |
MOD_SUMO_rev_2 | 14 | 20 | PF00179 | 0.467 |
MOD_SUMO_rev_2 | 162 | 172 | PF00179 | 0.396 |
MOD_SUMO_rev_2 | 599 | 606 | PF00179 | 0.569 |
TRG_DiLeu_BaEn_1 | 554 | 559 | PF01217 | 0.552 |
TRG_DiLeu_BaLyEn_6 | 116 | 121 | PF01217 | 0.519 |
TRG_DiLeu_BaLyEn_6 | 252 | 257 | PF01217 | 0.357 |
TRG_DiLeu_BaLyEn_6 | 398 | 403 | PF01217 | 0.643 |
TRG_ENDOCYTIC_2 | 109 | 112 | PF00928 | 0.340 |
TRG_ENDOCYTIC_2 | 87 | 90 | PF00928 | 0.376 |
TRG_ER_diArg_1 | 112 | 114 | PF00400 | 0.365 |
TRG_ER_diArg_1 | 253 | 255 | PF00400 | 0.365 |
TRG_ER_diArg_1 | 297 | 299 | PF00400 | 0.514 |
TRG_NES_CRM1_1 | 44 | 58 | PF08389 | 0.364 |
TRG_NES_CRM1_1 | 60 | 74 | PF08389 | 0.400 |
TRG_Pf-PMV_PEXEL_1 | 114 | 118 | PF00026 | 0.365 |
TRG_Pf-PMV_PEXEL_1 | 133 | 137 | PF00026 | 0.365 |
TRG_Pf-PMV_PEXEL_1 | 18 | 22 | PF00026 | 0.385 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEW4 | Leptomonas seymouri | 59% | 100% |
A0A3S7WTT7 | Leishmania donovani | 91% | 100% |
A4H459 | Leishmania braziliensis | 27% | 100% |
A4H8F5 | Leishmania braziliensis | 82% | 100% |
A4HWS9 | Leishmania infantum | 91% | 100% |
E9AQI7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |